EP3082967A2 - Composition comprising a specific acrylic copolymer and a fixing polymer chosen from anionic fixing polymers comprising crotonic acid as a monomer, non ionic and non silicone fixing polymers, and amphoteric fixing polymers - Google Patents
Composition comprising a specific acrylic copolymer and a fixing polymer chosen from anionic fixing polymers comprising crotonic acid as a monomer, non ionic and non silicone fixing polymers, and amphoteric fixing polymersInfo
- Publication number
- EP3082967A2 EP3082967A2 EP14835708.0A EP14835708A EP3082967A2 EP 3082967 A2 EP3082967 A2 EP 3082967A2 EP 14835708 A EP14835708 A EP 14835708A EP 3082967 A2 EP3082967 A2 EP 3082967A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- monomer
- polymers
- weight
- composition according
- alkyl group
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8105—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- A61K8/8117—Homopolymers or copolymers of aromatic olefines, e.g. polystyrene; Compositions of derivatives of such polymers
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8129—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical; Compositions of hydrolysed polymers or esters of unsaturated alcohols with saturated carboxylic acids; Compositions of derivatives of such polymers, e.g. polyvinylmethylether
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8135—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid or of a haloformic acid; Compositions of derivatives of such polymers, e.g. vinyl esters (polyvinylacetate)
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- A61K8/8147—Homopolymers or copolymers of acids; Metal or ammonium salts thereof, e.g. crotonic acid, (meth)acrylic acid; Compositions of derivatives of such polymers
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- A61K8/8158—Homopolymers or copolymers of amides or imides, e.g. (meth) acrylamide; Compositions of derivatives of such polymers
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/817—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen; Compositions or derivatives of such polymers, e.g. vinylimidazol, vinylcaprolactame, allylamines (Polyquaternium 6)
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/817—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen; Compositions or derivatives of such polymers, e.g. vinylimidazol, vinylcaprolactame, allylamines (Polyquaternium 6)
- A61K8/8176—Homopolymers of N-vinyl-pyrrolidones. Compositions of derivatives of such polymers
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/817—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen; Compositions or derivatives of such polymers, e.g. vinylimidazol, vinylcaprolactame, allylamines (Polyquaternium 6)
- A61K8/8182—Copolymers of vinyl-pyrrolidones. Compositions of derivatives of such polymers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/88—Polyamides
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/59—Mixtures
- A61K2800/594—Mixtures of polymers
Definitions
- the present invention relates to a composition for the treatment of keratinous fibers, in particular human keratinous fibers such as the hair, comprising one or more particular acrylic copolymers and one or more fixing polymers.
- the present invention also relates to a method for shaping and / or maintaining the hairstyle using said composition and the use of said composition for shaping and / or maintaining the hairstyle.
- compositions consisting essentially of a solution most often alcoholic or hydroalcoholic and one or more polymers, called fixing polymers, which are generally film-forming polymers. These polymers thus have the function of making welds between the hair so as to be able to structure the hairstyle and bring it a lasting hold.
- JP2007-223943 and JP2007-63186 disclose hair compositions associating a silicone-fixing polymer.
- JP2007-223943 describes hair compositions comprising a film-forming acrylic copolymer, wherein the film-forming acrylic copolymer can be combined with an alkyl acrylate / methacrylic acid / silicone copolymer.
- the compositions obtained make it possible to obtain good strength properties without adding stiffness or stickiness.
- JP2007-63186 also discloses hair compositions comprising a film-forming acrylic copolymer, the film-forming acrylic copolymer being capable of being associated with a methylpolysiloxane or a methylphenylpolysiloxane.
- the compositions obtained provide fixation and a cosmetic feel, especially softness.
- JP2007-217314 discloses hair compositions comprising a film-forming acrylic copolymer, the film-forming acrylic copolymer being capable of being associated with an alkyl acrylate copolymer.
- the compositions obtained make it possible to give a natural rendering without generating stickiness.
- compositions especially for styling, which allow a good level of fixation and maintenance of the hairstyle, durable, while providing a cosmetic touch to the hair.
- the Applicant has found surprisingly and unexpectedly that the combination of a particular acrylic copolymer and a fixing polymer allowed to obtain a hair not having the above disadvantages.
- this combination provides a strong attachment of the hair, lasting on the day, while providing a cosmetic touch to the hair.
- the surface of the hair is smoother and the hair is held in the desired shape without being fixed or hardened.
- composition comprising:
- Another object of the present invention is a method of shaping and / or maintaining the hairstyle using the composition according to the invention.
- the invention also relates to a use of the composition according to the invention for shaping and / or maintaining the hairstyle.
- composition according to the invention comprises one or more acrylic copolymers capable of being obtained (s) by copolymerization of the following monomers:
- the acrylic copolymer is preferably film-forming.
- film-forming polymer is meant a polymer capable of forming, by itself or in the presence of an auxiliary film-forming agent, a macroscopically continuous film on a support, in particular on keratin materials, and preferably a cohesive film.
- the acrylic copolymer comprises at least one monomer chosen from acrylic or methacrylic acids or their salts.
- the acrylic or methacrylic acids or their salts are present in a content ranging from 2 to 10% by weight, preferably from 5 to 9% by weight relative to the total weight of the copolymer.
- the acrylic copolymer also comprises one or more acrylate or methacrylate unsaturated ester monomers having in their structure or structure a fatty-chain alkyl group. These monomers are therefore esters of acrylic or methacrylic acid and a monoalcohol of fatty alcohol type, the monoalcohol providing the alkyl group of the ester.
- the alkyl group can be linear or branched.
- the unsaturated ester monomer of the acrylate or methacrylate type having in its structure a fatty-chain alkyl group is an alkyl acrylate or methacrylate with a C 8 -C 3 O alkyl group, more preferably a C 10 -C 15 alkyl group. better in C12-C13.
- the unsaturated ester monomer (s) of the acrylate or methacrylate type having in its structure at least one fatty-chain alkyl group is or are present in a content ranging from From 1 to 5% by weight, preferably from 0.5 to 3% by weight, more preferably from 1 to 2% by weight relative to the total weight of the copolymer.
- the acrylic copolymer is also derived from at least one unsaturated ester monomer of the acrylate or methacrylate type having in its structure at least one short chain alkyl group. These monomers are therefore esters of acrylic or methacrylic acid and a short chain monohydric alcohol, the monohydric alcohol providing the alkyl group of the ester.
- the alkyl group may be linear or branched, preferably branched.
- the unsaturated ester monomer of the acrylate or methacrylate type having in its structure a short-chain alkyl group is an alkyl acrylate or methacrylate with a C 2 -C 6 alkyl group, more preferably a C 3 -C 6 alkyl group. 5 , better in C 4 .
- the acrylic copolymer comprises, as monomer, a tert-butyl acrylate or methacrylate.
- the monomer (s) unsaturated ester (s) of acrylate or methacrylate type having in its structure at least one short chain alkyl group is or are present in a content ranging from 50 to 95% by weight, preferably 60 to 90% by weight, more preferably 70 to 85% by weight relative to the total weight of the copolymer.
- the acrylic copolymer also comprises at least one acrylamide monomer substituted with at least one alkyl group.
- the alkyl group may be linear or branched, preferably branched.
- the alkyl group is C 3 -C 10 , even more preferably C 4 -C 8 .
- the acrylic copolymer comprises, as monomer, tert-butylacrylamide or tert-octylacrylamide.
- the acrylic copolymer comprises, as monomer, tert-butylacrylamide and tert-octylacrylamide.
- the acrylamide monomer (s) substituted with at least one alkyl group is or are present in a content ranging from 0.01% to 10% by weight, preferably from 1% to 5% by weight. % by weight relative to the weight of the copolymer.
- the acrylic copolymer may further comprise as monomer one or more hydroxylated ester monomers of acrylic or methacrylic acid.
- the ester is a hydroxylated alkyl acrylate or methacrylate of C 2 -C 6 , more preferably C 2 such as acrylate or hydroxyethyl methacrylate.
- the acrylic copolymer may have an average molecular weight of from 20000 to 500000 g / mol, preferably from 100000 to 250000 g / mol.
- the copolymer according to the invention is in salt form by neutralization of acid residues derived from acrylic or methacrylic acids.
- the copolymer may be partially or completely neutralized with a mineral base (sodium hydroxide, potassium hydroxide, ammonia) or an organic base such as mono-, di- or tri-ethanolamine, aminomethylpropanol, N-methyl-glucamine, basic amino acids such as arginine and lysine, and mixtures of these compounds.
- the acrylic copolymer is neutralized with a neutralization agent chosen from aminomethylpropanol, tri-ethanolamine and sodium hydroxide.
- the degree of neutralization of the acrylic copolymer ranges from 50 to 100%, preferably from 80 to 100%, and more particularly acrylic copolymer is neutralized to 100%.
- an AMP-acrylates copolymer / Ci C 8 alkyl acrylate / -C 8 alkyl acrylamide / hydroxyethyl acrylate marketed by GOO Chemical under the trade reference PLASCIZE® L-9700 or L PLASCIZE® -9700U.
- the acrylic copolymer may be present in the composition in a content ranging from 0.5 to 20% by weight, preferably from 1 to 10% by weight relative to the total weight of the composition.
- the composition according to the invention comprises one or more fixing polymers chosen from anionic fixing polymers comprising a crotonic acid monomer, nonionic and non-silicone fixing polymers and amphoteric fixing polymers.
- composition according to the invention may comprise an anionic fixing polymer comprising a crotonic acid monomer.
- the anionic fixing polymer comprising a crotonic acid monomer can have an average molecular weight of from 20,000 to 200,000, preferably from 30,000 to 150,000 g / mole, more preferably from 40,000 to 100,000 g / mole.
- the anionic fixing polymer comprising a crotonic acid monomer may be chosen from crotonic acid copolymers comprising in their chain, acetate or vinyl propionate units, and possibly other monomers such as allyl or methallyl esters, vinyl ethers or vinyl esters of a saturated carboxylic acid, linear or branched, with a long hydrocarbon chain, such as those containing at least 5 carbon atoms, these polymers possibly being grafted or crosslinked, or still another vinyl, allyl or methallyl ester monomer of an ⁇ - or ⁇ -cyclic carboxylic acid.
- LUVISET ® CA 66 sold by the company BASF
- ARISTOFLEX ® A60 sold by CLARIANT (INCI VA / crotonates copolymer)
- MEXOMERE ® PW or PAM sold by CHIMEX (INCI VA / vinyl butyl) may also be mentioned.
- benzoate / crotonates copolymer BELSIL P1 101 sold by the company Wacker (INCI name crotonic acid / vinyl C8-12 isoalkyl esters / VA / bis-vinyldimethicone crosspolymer) can also be mentioned.
- a copolymer of crotonic acid comprising in its chain of vinyl acetate units and a vinyl ester, especially a vinyl acetate copolymer / crotonic acid / vinyl neodecanoate such as the product RESYN 28-2930 ® marketed by the company AKZO NOBEL.
- composition according to the invention may comprise one or more nonionic and non-silicone fixing polymers.
- non-silicone polymer a polymer containing no silicon atom (Si) in its structure.
- the nonionic and non-silicone fixing polymer may have an average molecular weight of from 500 to 5,000,000, preferably from 10,000 to 500,000, more preferably from 25,000 to 300,000.
- nonionic and non-silicone fixing polymers that can be used according to the present invention are chosen, for example, from:
- vinyl acetate copolymers such as, for example, copolymers of vinyl acetate and acrylic ester, vinyl acetate copolymers and ethylene, or copolymers of vinyl acetate and maleic ester, for example, dibutyl maleate,
- acrylic esters such as, for example, alkyl acrylates and copolymers of alkyl methacrylates, such as the products sold by the company Rohm & Haas under the names Primal AC-261 ® K and EUDRAGIT ® NE 30 D, by BASF under the name 8845, by Hoechst under the name APPRETAN ® N9212,
- styrene such as, for example, copolymers of styrene and (meth) acrylate, such as Mowilith LDM ® products 691 1 Mowilith ® DM 61 1 and Mowilith ® LDM 6070 sold by the company Hoechst, RHODOPAS ® SD 215 and RHODOPAS ® DS 910 products offered by the company RHONE POULENC, copolymers of styrene, of alkyl methacrylate and of alkyl acrylate, copolymers of styrene and butadiene, or styrene copolymers, butadiene and vinylpyridine,
- vinylpyrrolidone homopolymers such as vinylpyrrolidone homopolymers marketed for example under the Luviskol ® K30 powder names by BASF or PVP K30L or K60 solution or K90 by ISP, polyvinylcaprolactam sold under the name Luviskol ® PLUS by BASF company,
- - vinyllactam copolymers such as a poly (vinylpyrrolidone / vinyllactam) copolymer sold under the trade name Luvitec® ® VPC 55K65W by BASF, poly (vinylpyrrolidone / vinyl acetate) as those marketed under the name PVPA A ® S630L by the company ISP, Luviskol ® VA 73, VA 64, VA 55, VA 37 and VA 28 by the company BASF, and poly terpolymers (vinylpyrrolidone / vinyl acetate / vinyl propionate), for example, that marketed under the name Luviskol ® VAP 343 by BASF and
- the alkyl groups of the nonionic polymers mentioned above preferably have from 1 to 6 carbon atoms.
- the non-silicone non-silicone polymer is chosen from homopolymers and copolymers of vinyllactam. More preferably, the non-silicone non-silicone polymer is chosen from polymers comprising at least one vinylpyrrolidone monomer.
- the non-silicone nonionic polymer comprises a vinylpyrrolidone monomer and a vinyl acetate monomer.
- the ratio vinylpyrrolidone / vinyl acetate ranges from 25/75 to 75/25.
- composition according to the invention may comprise one or more amphoteric fixing polymers.
- the amphoteric fixing polymer can have an average molecular weight of from 70,000 to 1,700,000, preferably from 100,000 to 500,000, more preferably from 100,000 to 200,000, g / mol.
- amphoteric fixing polymers that may be used in accordance with the invention may be chosen from polymers comprising units B and C statistically distributed in the polymer chain, where B denotes a unit derived from a monomer comprising at least one basic nitrogen atom and C denotes a unit derived from an acidic monomer having one or more carboxylic or sulphonic groups or else B and C may denote groups derived from zwitterionic monomers of carboxybetaines or of sulphobetaines; B and C may also designate a cationic polymer chain comprising primary, secondary, tertiary or quaternary amine groups, in which at least one of the amine groups carries a carboxylic or sulfonic group connected via a hydrocarbon group, or B and C are part of a chain of an ethylene-dicarboxylic-containing polymer having one of the carboxylic groups reacted with a polyamine having one or more primary or secondary amine groups.
- amphoteric polymers as defined above which are more particularly preferred, are chosen from the following polymers:
- a monomer derived from a vinyl compound carrying a carboxylic group such as, more particularly, acrylic acid, methacrylic acid, maleic acid, alpha-chloro acrylic acid
- a basic monomer derived from a substituted vinyl compound containing at least one basic atom such as, more particularly, dialkylaminoalkylmethacrylate and acrylate, dialkylaminoalkyl-methacrylamide and acrylamide.
- the vinyl compound may also be a dialkyldiallylammonium salt such
- At least one basic comonomer such as primary, secondary, tertiary and quaternary amine substituent esters of acrylic and methacrylic acids, and the quaternization product of dimethylaminoethyl methacrylate with dimethyl or diethyl sulfate.
- N-substituted acrylamides or methacrylamides which are more particularly preferred according to the invention are the groups in which the alkyl groups contain from 2 to 12 carbon atoms and more particularly N-ethylacrylamide, N-tert-butylacrylamide, N-tert-octylacrylamide, N octyl. N-decylacrylamide, N-dodecylacrylamide and the corresponding methacrylamides.
- the acidic comonomers are chosen more particularly from acrylic, methacrylic, crotonic, itaconic, maleic and fumaric acids as well as alkyl monoesters having 1 to 4 carbon atoms of maleic or fumaric acids or anhydrides.
- Preferred basic comonomers are aminoethyl, butylaminoethyl, ⁇ , ⁇ '-dimethylaminoethyl, N-tert-butylaminoethyl methacrylates.
- copolymers whose CTFA (4th Ed., 1991) name is octylacrylamide / acrylates / butylaminoethylmethacrylate copolymer, such as the products sold under the name AMPHOMER®, AMPHOMER® LV 71, AMPHOMER® SOL or BALANCE® 47 by the company AKZO, are particularly used. NOBEL.
- R 4 represents a divalent group derived from a saturated dicarboxylic acid, an aliphatic mono or dicarboxylic acid with an ethylenic double bond, an ester of an alcohol having 1 to 6 carbon atoms of these acids or a group deriving from the addition of any of said acids with a bis primary or bis secondary amine
- Z denotes a group of a bis-primary, mono or bis-secondary polyalkylene polyamine and preferably represents:
- this group derived from diethylene triamine, triethylene tetraamine or dipropylene triamine;
- the saturated carboxylic acids are preferably chosen from acids having 6 to 10 carbon atoms such as adipic acid, 2,2,4-trimethyladipic acid and 2,4,4-trimethyladipic acid, terephthalic acid, ethylenically double-bonded acids such as for example, acrylic, methacrylic, itaconic acids.
- the alkanesultones used in the alkylation are preferably propane or butanesultone
- the salts of the alkylating agents are preferably the sodium or potassium salts.
- R 5 denotes a polymerizable unsaturated group such as an acrylate, methacrylate, acrylamide or methacrylamide group
- y and z each represent an integer of 1 to 3
- R 6 and R 7 represent a hydrogen atom, a methyl group, , ethyl or propyl
- R 8 and R 9 represent a hydrogen atom or an alkyl group such that the sum of the carbon atoms in Rio and Ru does not exceed 10.
- Polymers comprising such units may also comprise units derived from non-zwitterionic monomers, such as dimethyl- or diethylaminoethyl acrylate or methacrylate, or alkyl acrylates or methacrylates, acrylamides or methacrylamides, or vinyl acetate. .
- Ru, R12 and R 13 each represents a hydrogen atom, as well as the salts formed by these compounds with bases or acids.
- R14 is hydrogen, CH 3 0, CH 3 CH 2 0, phenyl
- R 5 is hydrogen or C 1-4 alkyl such as methyl and ethyl
- R 6 is hydrogen or a Ci -4 alkyl group such as methyl and ethyl
- R17 denotes a Ci -4 alkyl group such as methyl and ethyl or a group of the formula: -Ri8-N (R 6)
- Ris representing a group -CH 2 -CH 2 -, -CH 2 -CH 2 -CH 2 -, -CH 2 -CH (CH 3 ) -, R 16 having the meanings mentioned above, as well as the higher homologs of these groups and containing up to 6 carbon atoms.
- D is a group and X denotes the symbol E or ⁇ ', E or E', which may be identical or different, denote a divalent group which is a straight or branched chain alkylene group having up to 7 carbon atoms in the unsubstituted or substituted primary chain.
- hydroxyl groups and which may further comprise oxygen, nitrogen, sulfur atoms, 1 to 3 aromatic and / or heterocyclic rings; the oxygen, nitrogen and sulfur atoms being present in the form of ether, thioether, sulphoxide, sulphone, sulphonium, alkylamine, alkenylamine, hydroxyl groups, benzylamine, amine oxide, quaternary ammonium, amide, imide groups, alcohol, ester and / or urethane.
- D is a group and X denotes the symbol E or E 'and at least once ⁇ '; E having the meaning indicated above and E 'is a bivalent group which is a straight or branched chain alkylene group having up to 7 carbon atoms in the main chain, substituted or unsubstituted by one or more hydroxyl groups and having a or a plurality of nitrogen atoms, the nitrogen atom being substituted by an optionally interrupted alkyl chain by an oxygen atom and necessarily comprising one or more carboxyl functions or one or more hydroxyl functions and betaineized by reaction with chloroacetic acid or chloroacetate of soda.
- amphoteric polymers are polymers having units derived from:
- At least one basic comonomer such as primary, secondary, tertiary and quaternary amine substituent esters of acrylic and methacrylic acids, and the quaternization product of dimethylaminoethyl methacrylate with dimethyl or diethyl sulfate.
- composition according to the invention may comprise one or more fixing polymer (s) chosen from anionic fixing polymers comprising a crotonic acid monomer, nonionic and non-silicone fixing polymers and amphoteric fixing polymers in an amount ranging from from 0.5 to 20%, preferably from 0.5 to 10% by weight, relative to the total weight of the composition.
- fixing polymer chosen from anionic fixing polymers comprising a crotonic acid monomer, nonionic and non-silicone fixing polymers and amphoteric fixing polymers in an amount ranging from from 0.5 to 20%, preferably from 0.5 to 10% by weight, relative to the total weight of the composition.
- composition according to the invention may further comprise one or more solvents.
- the solvent may be chosen from water, an organic solvent or a mixture of water and one or more organic solvents, preferably water-soluble.
- organic solvent means an organic compound which is liquid at a temperature of 25 ° C. and at atmospheric pressure (760 mmHg).
- water-soluble is intended to mean a compound which is soluble to at least 5% by weight in water at a temperature of 25 ° C. and at atmospheric pressure (760 mmHg).
- the organic compound is polar.
- the organic solvents may be chosen from short-chain monohydric alcohols, for example C 1 -C 4 alcohols, such as ethanol or isopropanol; diols or polyols such as ethylene glycol, 1,2-propylene glycol, 1,3-butylene glycol, hexylene glycol, diethylene glycol, dipropylene glycol, 2-ethoxyethanol, diethylene glycol monomethyl ether, triethylene glycol monomethyl ether and sorbitol.
- C 1 -C 4 alcohols such as ethanol or isopropanol
- diols or polyols such as ethylene glycol, 1,2-propylene glycol, 1,3-butylene glycol, hexylene glycol, diethylene glycol, dipropylene glycol, 2-ethoxyethanol, diethylene glycol monomethyl ether, triethylene glycol monomethyl ether and sorbitol.
- the composition comprises water.
- composition comprises or not one or more water-soluble organic solvents such as ethanol or isopropanol.
- the composition does not comprise water.
- composition according to the invention may comprise one or more solvents in an amount ranging from 30 to 95%, preferably from 40 to 95% by weight, relative to the total weight of the composition.
- composition according to the invention may further comprise one or more surfactants, which may be chosen in particular from nonionic, cationic, anionic and amphoteric or zwitterionic surfactants.
- the surfactant (s) according to the invention preferably comprise one or more nonionic surfactant (s).
- nonionic surfactant (s) usable in the present composition are described, for example, in "Handbook of Surfactants” by MR PORTER, Blackie & Son editions (Glasgow and London), 1991, pp. 16-178.
- nonionic surfactants mention may be made of the following nonionic surfactants:
- esters of fatty acids and of sucrose alkyl (C 8 -C 3 ) (poly) glucosides, alkenyl (C 8 -C 3 ) (poly) glucosides, optionally oxyalkylenated (0 to 10 oxyalkylenated units) and comprising from 1 to 15 glucose units, alkyl (C 8 -C 3 O) (poly) glucosides,
- ethylene oxide and / or propylene oxide condensates inter alia, alone or in mixtures;
- N-alkyl C 8 -C 3 o
- N-acyl C 8 -C 30
- the oxyalkylenated units are more particularly oxyethylenated units, oxypropylene, or their combination, preferably oxyethylenated.
- the number of moles of ethylene oxide and / or propylene oxide is preferably from 1 to 250, more preferably from 2 to 100; better from 2 to 50; the number of moles of glycerol ranges from 1 to 50, more preferably from 1 to 10.
- nonionic surfactants according to the invention do not comprise oxypropylene units.
- nonionic glycerolated surfactants it is preferable to use C 8 -C 4 o, mono- or polyglycerolated alcohols comprising from 1 to 50 moles of glycerol, preferably from 1 to 10 moles of glycerol.
- lauryl alcohol with 4 moles of glycerol (INCI name: POLYGLYCERYL-4 LAURYL ETHER), lauric alcohol with 1.5 moles of glycerol, alcohol oleic acid with 4 moles of glycerol (INCI name: POLYGLYCERYL-4 OLEYL ETHER), oleic alcohol with 2 moles of glycerol (INCI name: POLYGLYCERYL-2 OLEYL ETHER), cetearyl alcohol with 2 moles of glycerol, alcohol 6 moles of glycerol, oleocetyl alcohol with 6 moles of glycerol, and octadecanol with 6 moles of glycerol.
- the C 8 / C 10 alcohol with one mole of glycerol
- the C 10 / C 12 alcohol with 1 mole of glycerol
- the C 12 alcohol with 1.5 moles of glycerol.
- the at least one nonionic surfactant (s) according to the invention are preferably chosen from:
- oxyethylenated C 4 -C 40 alcohols comprising from 1 to 100 moles of ethylene oxide, preferably from 2 to 50, more particularly from 2 to 40 moles of ethylene oxide; saturated or unsaturated oxyethylenated vegetable oils comprising from 1 to 100 moles of ethylene oxide, preferably from 2 to 50;
- C 8 -C 4 o mono- or poly-glycerol, comprising from 1 to 50 moles of glycerol, preferably from 1 to 10 moles of glycerol;
- agent (s) surfactant (s) nonionic (s) are selected from:
- composition according to the invention may comprise one or more cationic surfactant (s).
- cationic surfactant means a surfactant positively charged when it is contained in the composition according to the invention. This surfactant may carry one or more positive permanent charges or contain one or more cationizable functions within the composition according to the invention.
- the cationic surfactant (s) is (are) preferably chosen from primary, secondary or tertiary fatty amines, optionally polyoxyalkylenated, or their salts, quaternary ammonium salts, and mixtures thereof.
- the fatty amines generally comprise at least one C 8 -C 30 hydrocarbon chain.
- quaternary ammonium salts there may be mentioned, for example:
- R 8 to Ru which may be identical or different, represent a linear or branched aliphatic group containing from 1 to 30 carbon atoms, or an aromatic group such as aryl or alkylaryl, at least one of the R groups. 8 to Ru denoting a group having from 8 to 30 carbon atoms, preferably from 12 to 24 carbon atoms.
- the aliphatic groups can comprise heteroatoms such as in particular oxygen, nitrogen, sulfur and halogens.
- the aliphatic groups are for example selected from alkyl C1-C30, C1-C30, polyoxy (C 2 -C 6) alkylamide C1-C30 alkyl (Ci2-C22) amidoalkyl (C 2 -C 6) C 1 -C 2 alkyl, C 1 -C 30 hydroxyalkyl;
- X " is an anion chosen from the group of halides, phosphates, acetates, lactates, alkyl (CrC 4 ) sulphates, alkyl (dC 4 ) - or alkyl (CrC 4 ) aryl sulphonates.
- tetraalkylammonium salts for example dialkyl dimethylammonium or alkyltrimethylammonium salts, in which the alkyl group contains from about 12 to 22 carbon atoms, are preferred.
- R12 represents an alkenyl or alkyl group having 8 to 30 carbon atoms, for example derived from tallow fatty acids
- R 3 represents a hydrogen atom, a C1-C4 alkyl or alkenyl or alkyl comprising from 8 to 30 carbon atoms
- R 4 represents a C 1 -C 4 alkyl group
- R 6 represents a hydrogen atom or a C 1 -C 4 alkyl group
- X " is an anion chosen from the group of halides, phosphates and acetates; , lactates, alkyl sulphates, alkyl- or alkylaryl-sulphonates in which the alkyl and aryl groups preferably comprise respectively 1 to 20 carbon atoms and 6 to 30 carbon atoms.
- R 12 and R 13 denote a mixture of alkenyl groups or alkyl having from 12 to 21 carbon atoms, for example fatty acid derivatives of tallow, R 4 denotes a methyl group, R 5 denotes a hydrogen atom, such a product is for example marketed under the name REWOQUAT ® W 75 by the company REWO;
- R 16 denotes an alkyl radical containing about 16 to 30 carbon atoms, optionally hydroxylated and / or interrupted by one or more oxygen atoms
- R 17 is chosen from hydrogen or an alkyl radical containing from 1 to 4 atoms atoms or a (Ri6a) (Ri7a) (Ri8a) N- (CH 2) 3, Rie, Ri?
- Risa, R 18, Rig, R20 and R 2 i are identical or different, are chosen from hydrogen or an alkyl radical having from 1 to 4 carbon atoms, and X " is an anion chosen from the group of the halides, acetates, phosphates, nitrates and methylsulfates
- X " is an anion chosen from the group of the halides, acetates, phosphates, nitrates and methylsulfates
- Such compounds are, for example, the Finquat CT-P proposed by FINETEX company (Quaternium 89), the Finquat CT proposed by FINETEX (Quaternium 75), the quaternary ammonium salts containing at least one ester function, such as those of formula IV) below:
- R22 is selected from alkyl and -C 6 hydroxyalkyl or dihydroxyalkyl groups -C 6;
- R23 is selected from:
- R27 groups which are linear or branched, saturated or unsaturated C1-C22 hydrocarbon groups
- R25 is selected from:
- R 24, R 26 and R 2 8, identical or different, are selected from hydrocarbon groups C7-C21 linear or branched, saturated or unsaturated;
- r, s and t are integers ranging from 2 to 6;
- y is an integer from 1 to 10;
- x and z which are identical or different, are integers ranging from 0 to 10;
- X " is a simple or complex anion, organic or inorganic
- R 23 denotes R 27 and that when z is 0, then R 25 denotes R 2 g.
- the alkyl groups R 22 may be linear or branched and more particularly linear.
- R 22 denotes a methyl, ethyl, hydroxyethyl or dihydroxypropyl group, and more particularly a methyl or ethyl group.
- the sum x + y + z is from 1 to 10.
- R 23 is a hydrocarbon R 27 group, it may be long and have 12 to 22 carbon atoms, or short and have 1 to 3 carbon atoms.
- R 25 is a hydrocarbon R 29 group, it preferably has 1 to 3 carbon atoms.
- R 24 , R 26 and R 28 which are identical or different, are chosen from linear or branched, saturated or unsaturated C 11 -C 21 hydrocarbon-based groups, and more particularly from linear or branched C 11 -C 21 alkyl and alkenyl groups. , saturated or unsaturated.
- x and z are 0 or 1.
- y is 1.
- r, s and t which are identical or different, are equal to 2 or 3, and even more particularly are equal to 2.
- the anion X " is preferably a halide (chloride, bromide or iodide) or an alkyl sulphate, more particularly methyl sulphate, but methanesulphonate, phosphate, nitrate, tosylate, an anion derived from an organic acid such as acetate or lactate or any other anion compatible with ester-function ammonium.
- the anion X - is even more particularly chloride or methylsulfate.
- R 22 denotes a methyl or ethyl group
- x and y are equal to 1;
- z is 0 or 1;
- R 23 is chosen from:
- R 25 is selected from:
- R24, R26 and R 2 8 are selected from hydrocarbon groups C13-C17 linear or branched, saturated or unsaturated, and preferably from alkyl groups and alkenyl C13-C17 linear or branched, saturated or unsaturated.
- the hydrocarbon groups are linear.
- the compounds of formula (IV) such as the salts (in particular chloride or methylsulfate) of diacyloxyethyl-dimethylammonium, diacyloxyethyl-hydroxyethyl-methylammonium, monoacyloxyethyl-dihydroxyethyl-methylammonium, triacyloxyethyl-methylammonium, monoacyloxyethyl-hydroxyethyl dimethylammonium and mixtures thereof.
- the acyl groups preferably have from 14 to 18 carbon atoms and come more particularly from a vegetable oil such as palm oil or sunflower oil. When the compound contains more than one acyl group, the latter groups may be identical or different.
- These products are obtained, for example, by direct esterification of triethanolamine, triisopropanolamine, alkyldiethanolamine or alkyldiisopropanolamine, optionally oxyalkylenated, with C 10 -C 30 fatty acids or mixtures of C 10 -C 30 fatty acids. of vegetable or animal origin, or by transesterification of their methyl esters.
- This esterification is followed by quaternization using an alkylating agent such as an alkyl halide (preferably methyl or ethyl), a dialkyl sulphate (preferably methyl or ethyl), methanesulfonate. methyl, para-toluenesulfonate methyl, chlorohydrin glycol or glycerol.
- Such compounds are for example marketed under the names DEHYQUART ® by Henkel, Stepanquat® ® by the company Stepan, Noxamium ® by CECA Rewoquat ® WE 18 by the company Witco REWO-.
- composition according to the invention may contain, for example, a mixture of quaternary ammonium mono-, di- and triester salts with a majority by weight of diester salts.
- ammonium salts containing at least one ester function described in US-A-4874554 and US-A-4137180.
- the behenoylhydroxypropyltrimethylammonium chloride proposed by KAO can be used under the name Quatarmin BTC 131.
- ammonium salts containing at least one ester function contain two ester functions.
- the quaternary ammonium salts containing at least one useful ester function it is preferred to use dipalmitoylethylhydroxyethylmethylammonium salts.
- the cationic surfactants are preferably chosen from those of formula (I) and those of formula (IV), and even more preferably from those of formula (I).
- composition according to the invention may comprise one or more anionic surfactant (s).
- anionic surfactant means a surfactant comprising as ionic or ionizable groups only anionic groups. These anionic groups are preferably chosen from groups
- anionic surfactants that may be used in the composition according to the invention, mention may be made of alkyl sulphates, alkyl ether sulphates, alkylamido ether sulphates, alkylaryl polyether sulphates, monoglyceride sulphates, alkyl sulphonates, alkyl amide sulphonates and alkyl aryl sulphonates.
- alpha-olefin sulfonates paraffin sulfonates, alkylsulfosuccinates, alkylethersulfosuccinates, alkylamide-sulfosuccinates, alkylsulfoacetates, acylsarcosinates, acylglutamates, alkylsulfosuccinamates, acylisethionates and N-acyltaurates, and salts thereof.
- alkyl monoesters and polyglucoside polycarboxylic acids acyllactylates, D-galactoside uronic acid salts, alkyl ether carboxylic acid salts, alkyl aryl ether carboxylic acid salts, of alkyl amidoether carboxylic acids, alkyl or alkenyl phosphates and the corresponding non-salified forms of all these alkyl and acyl groups of all these compounds having from 6 to 40 carbon atoms and the aryl group denoting a phenyl group.
- These compounds may be oxyethylenated and then preferably comprise from 1 to 50 ethylene oxide units.
- Alkyl monoesters, salts of C 6 -C 2 4 and polyglucoside- polycarboxylic acids may be selected from alkyl polyglucoside citrates C 6 - C 2 4, C 6 -C 2 4 alkyl polyglucoside tartrates and C 6 -C 24 alkyl polyglucoside sulfosuccinates.
- anionic surfactant (s) When the anionic surfactant (s) are in the salt form, they may be chosen from alkali metal salts such as sodium or potassium salt and preferably sodium salt, sodium salts or ammonium, salts of amines and in particular of aminoalcohols or salts of alkaline earth metals such as magnesium salts.
- alkali metal salts such as sodium or potassium salt and preferably sodium salt, sodium salts or ammonium, salts of amines and in particular of aminoalcohols or salts of alkaline earth metals such as magnesium salts.
- aminoalcohol salts By way of example of aminoalcohol salts, mention may be made in particular of the salts of mono-, di- and triethanolamine, the salts of mono-, di- or triisopropanolamine, the salts of 2-amino-2-methyl-1 - propanol, 2-amino-2-methyl-1,3-propanediol and tris (hydroxymethyl) amino methane.
- the alkali metal or alkaline earth metal salts and in particular the sodium or magnesium salts are preferably used.
- anionic surfactants it is preferable to use (C 6 -C 2 4) alkyl sulphates, (C 6 -C 2 4) alkyl ethersulphates, (C 6 -C 24 ) alkyls or (C 6 -C alkenyl) alkenyls. 24 ) phosphates comprising from 2 to 50 ethylene oxide units, especially in the form of alkali metal salts, ammonium, aminoalcohols, and alkaline earth metals, or a mixture of these compounds.
- composition according to the invention may comprise one or more surfactant (s) amphoteric (s) or zwitterionic (s).
- amphoteric (s) or zwitterionic (s) surfactant (s), preferably non-silicone surfactants, that may be used in the present invention may in particular be derivatives of secondary or tertiary aliphatic amines, optionally quaternized, in which the aliphatic group is a linear or branched chain having 8 to 22 carbon atoms, said amine derivatives containing at least one anionic group such as, for example, a carboxylate group, sulfonate, sulfate, phosphate or phosphonate.
- alkyl (C 8 -C 20) betaines examples include alkyl (C 8 -C 20) betaines, (C 8 - C 20) sulfobetaines, (C8-C 2 o) alkylamido (C 3 -C 8) alkylbetaines and alkyl (C 8 -C 20 ) - amidalkyl (C 6 -C 8 ) sulfobetaines.
- the derivatives of secondary or tertiary aliphatic amines optionally quaternized, which may be used, as defined above, there may also be mentioned the compounds of respective structures (V) and (VI):
- R a represents an alkyl or alkenyl group containing 1 0 C30 derived from an acid R a COOH, preferably present in hydrolysed coconut oil or a heptyl, nonyl or undecyl radical;
- R b represents a beta-hydroxyethyl group
- R c represents a carboxymethyl group
- M + represents a cationic counterion derived from an alkali metal, alkaline earth metal, such as sodium, an ammonium ion or an ion derived from an organic amine, and
- X " represents an organic or inorganic anionic counterion, such as that chosen from halides, acetates, phosphates, nitrates, alkyl (d-C 4 ) sulphates, alkyl (dC 4 ) - or alkyl (CrC 4 ) aryl sulphonates; especially methylsulfate and ethylsulfate, or M + and X " are absent;
- B represents the group -CH 2 CH 2 OX '
- X ' represents the group -CH 2 COOH, -CH 2 -COOZ', -CH 2 CH 2 COOH, -CH 2 CH 2 -COOZ ', or a hydrogen atom;
- Y ' represents the group -COOH, -COOZ', -CH 2 CH (OH) SO 3 H or the group CH 2 CH (OH) SO 3 Z ';
- Z ' represents a cationic counterion derived from an alkaline or alkaline earth metal, such as sodium, an ammonium ion or an ion derived from an organic amine;
- R a ' represents a C10-C30 alkyl or alkenyl group of an acid R a ' - COOH, preferably present in coconut oil or hydrolyzed linseed oil, an alkyl group, especially a C17 group, and iso form, an unsaturated C 7 group .
- Examples include the cocoamphodiacetate sold by Rhodia under the trade name Miranol ® C2M concentrate.
- Y represents the group -COOH, -COOZ", -CH 2 -CH (OH) SO 3 H or the group CH 2 CH (OH) SO 3 -Z ";
- R d and R e independently of one another, represent a C 1 -C 4 alkyl or hydroxyalkyl radical
- Z represents a cationic counterion derived from an alkaline or alkaline earth metal, such as sodium, an ammonium ion or an ion derived from an organic amine;
- R a represents a C10-C30 alkyl or alkenyl group of a R a " - COOH acid, preferably present in coconut oil or in hydrolysed linseed oil;
- n and n ' independently of each other, denote an integer ranging from 1 to 3.
- alkyl (C 8 -C 20 ) betaines such as cocobetaine, (C 8 -C 2 O) alkylamido (C 3 -C 8 ) alkylbetaines, are preferably used.
- alkyl (C 8 -C 20 ) betaines such as cocobetaine, (C 8 -C 2 O) alkylamido (C 3 -C 8 ) alkylbetaines
- cocamidopropylbetaine and mixtures thereof
- compounds of formula (VII) such as the sodium salt of diethylaminopropyl laurylamino succinamate (INCI name sodium diethylaminopropyl cocoaspartamide).
- surfactant s
- surfactant (s) surfactant (s) nonionic preferably oxyethylenated (s) such as oxyethylenated C4-C40 alcohols comprising from 1 to 100 moles of ethylene oxide, preferably from 2 to 50, more particularly from 2 to 40 moles of ethylene oxide, and phosphated anionic surfactants such as alkyls; (C 6 -C 2 4) or alkenyl (C 6 -C 2 4) phosphates comprising from 2 to 50 ethylene oxide units.
- oxyethylenated such as oxyethylenated C4-C40 alcohols comprising from 1 to 100 moles of ethylene oxide, preferably from 2 to 50, more particularly from 2 to 40 moles of ethylene oxide
- phosphated anionic surfactants such as alkyls; (C 6 -C 2 4) or alkenyl (C 6 -C 2 4) phosphates comprising from 2 to 50 ethylene oxide units
- the surfactant (s) represent from 0.001 to
- the composition may also comprise one or more thickeners.
- the thickening agents may be chosen from fatty acid amides obtained from C 10 -C 30 carboxylic acids, such as monoisopropanol, diethanol or coconut acid monoethanol amide and alkyl ether acid monoethanolamide.
- the associative polymers that can be used according to the invention are water-soluble or water-dispersible polymers capable, in an aqueous medium, of reversibly associating with each other or with other molecules.
- Their chemical structure comprises hydrophilic zones, and hydrophobic zones characterized by the presence of at least one fatty chain preferably comprising from 10 to 30 carbon atoms.
- They may be of anionic, cationic, amphoteric or nonionic type, such as, for example, the polymers sold under the names Pemulen TR1 or TR2 by the company Goodrich, whose INCI name is Acrylates / CI O-30 Alkyl Acrylate Crosspolymer, SALCARE SC90 by CIBA, ACULYN 22, 28, 33, 44, 46 or 88 by the company ROHM & HAAS and ELFACOS T210 and T212 by the company AKZO.
- Pemulen TR1 or TR2 by the company Goodrich, whose INCI name is Acrylates / CI O-30 Alkyl Acrylate Crosspolymer, SALCARE SC90 by CIBA, ACULYN 22, 28, 33, 44, 46 or 88 by the company ROHM & HAAS and ELFACOS T210 and T212 by the company AKZO.
- acrylic associative thickeners are preferably used.
- the thickeners may be present in an amount ranging from 0.01% to 20% by weight, preferably from 0.1% to 10% by weight, better still from 0.2% to 5% by weight relative to the weight.
- the composition according to the invention may further contain one or more additives chosen from anionic fixing polymers different from the acrylic copolymers according to the invention and anionic fixing polymers comprising a crotonic acid monomer, the cationic fixing polymers.
- conditioning agents such as cationic polymers, fats, silicones, ceramides and pseudo-ceramides, vitamins and pro-vitamins including panthenol, water-soluble and fat-soluble sunscreens, pearlescent and opacifying agents, sequestering agents , solubilizing agents, antioxidants, hydroxy acids, penetrating agents, perfumes, peptizers, amino acids and preservatives, alone or in admixture, and any other additive conventionally used in the cosmetics field.
- conditioning agents such as cationic polymers, fats, silicones, ceramides and pseudo-ceramides, vitamins and pro-vitamins including panthenol, water-soluble and fat-soluble sunscreens, pearlescent and opacifying agents, sequestering agents , solubilizing agents, antioxidants, hydroxy acids, penetrating agents, perfumes, peptizers, amino acids and preservatives, alone or in admixture, and any other additive conventionally used in the cosmetics field.
- additives may be present in the composition according to the invention in an amount ranging from 0 to 20% by weight relative to the total weight of the composition.
- compositions according to the invention may be present inter alia in the form of more or less thickened liquids, gels, creams, pastes or foams.
- compositions in accordance with the invention may be packaged for example in a jar, in a tube, in a pump bottle or in an aerosol device that is usual in cosmetics.
- compositions according to the invention may, when they are intended to be packaged in an aerosol type device, contain one or more propellants.
- the propellant gas may then be chosen for example from volatile hydrocarbons, such as in particular C 1 -C 4 alkanes and preferably n-butane, propane, isobutane and mixtures thereof, chlorinated and / or fluorinated hydrocarbons, especially 1,1-difluoroethane, dimethyl ether and mixtures of these gases.
- the propellant is selected from 1,1-difluoroethane, dimethyl ether, n-butane, propane, isobutane and mixtures thereof.
- the composition comprises a propellant in a content ranging from 2 to 75% by weight, more preferably from 2 to 60% by weight, relative to the total weight of said composition.
- the composition When the composition is distributed in the form of an aerosol spray, the composition comprises a propellant in a content preferably ranging from 20 to 60% by weight, relative to the total weight of said composition.
- the composition When the composition is distributed in the form of an aerosol foam, the composition comprises a propellant in a content preferably ranging from 2 to 10% by weight, relative to the total weight of said composition.
- the present invention also relates to a method for shaping and / or maintaining the hairstyle comprising the implementation of the composition as defined above.
- the method of shaping and / or maintaining the hairstyle comprises a step of application to human keratinous fibers, in particular the hair, dry or wet, of a composition as defined previously pulverized, to rinse or not after a possible exposure time or after any drying.
- the composition according to the invention is not rinsed.
- the cosmetic composition according to the invention can thus be applied to dry or wet hair.
- the cosmetic composition is applied to clean hair.
- the application of the composition may be followed by drying at room temperature or at a temperature above 40 ° C.
- Drying can be carried out immediately after application or after a laying time ranging from 1 minute to 30 minutes.
- the composition is applied from an aerosol device.
- the aerosol device comprises a pressurized container containing the composition described above, the container being surmounted by a diffuser.
- the container may be equipped with a valve.
- the diffuser may be provided with an outlet port of the composition, in particular of a nozzle with simple orifice or vortex channels, or of several outlet orifices, in particular three orifices.
- the present invention also relates to the use of a composition as defined above, for shaping and / or maintaining the hairstyle.
- compositions A and B according to the invention were prepared from the ingredients indicated in the table below in gram of active material:
- PLASCIZE L-9700U sold by the company GOO CHEMICAL (Copolymer AMP-acrylates / Ci-C-18 alkylacrylate / Ci-Ce alkylacrylamide / hydroxyethylacrylate 38%, Oleth-20 phosphate 1%, PPG-7-Buteth-10 at 1% and 60% ethanol)
- compositions prepared above were introduced into an aerosol dispensing device which has the following characteristics:
- valve equipped with a nozzle having an orifice size of 0.64 mm and an internal restriction orifice size of 0.64 mm, with an additional gas intake of 0.64 mm,
- a diffuser comprising three direct-output orifices of 0.4 mm in diameter.
- compositions were sprayed on dry hair.
- compositions A and B After drying, hair is obtained having a significant fixation, durable over time.
- the touch is very satisfying (softness, flexibility).
- compositions C to F according to the invention can be prepared from the ingredients indicated in the table below in grams of active material: Lacquer composition according to the invention:
- compositions can be introduced into an aerosol dispensing device.
- a valve may be used comprising:
- a diffuser with a 0.45 mm diameter outlet channel vortex nozzle can be used.
- compositions can be sprayed on dry hair.
- Vinylpyrrolidone / vinyl acetate copolymer 3 (38% AMP-acrylates / C1-C18alkylacrylate / C1-C18 alkylacrylamide / hydroxyethylacrylate copolymer, 1% Oleth-20 Phosphate, 1% PPG-7-Buteth-10 and 60% Ethanol)
- the above composition can be introduced into an aerosol dispensing device comprising a monoblock aluminum container provided with a warhead (45x128).
- the container is equipped with a precision valve P73 without dip tube surmounted by an axial diffuser pusher for conical cup.
- composition can be dispensed on dry or wet hair.
- composition F prepared above was applied as a styling gel to wet hair.
- compositions G and H according to the invention were prepared from the ingredients indicated in the table below in grams of active material: Lacquer composition according to the invention:
- PLASCIZE L-9700U marketed by the company GOO CHEMICAL (Copolymer AMP-acrylates / Ci-C-18 alkylacrylate / Ci-Ce alkylacrylamide / hydroxyethylacrylate 38%, Oleth-20 phosphate 1%, PPG-7-Buteth-10 to 1 % and 60% ethanol)
- valve equipped with a nozzle having an orifice size of 0.64 mm and an internal restriction orifice size of 0.64 mm, with an additional gas intake of 0.64 mm,
- a diffuser comprising three direct-output orifices of 0.4 mm in diameter.
- compositions were sprayed on dry hair.
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Abstract
Description
COMPOSITION COMPRENANT UN COPOLYMERE ACRYLIQUE PARTICULIER ET UN POLYMERE FIXANT ANIONIQUE COMPRENANT UN MONOMERE D'ACIDE COMPOSITION COMPRISING A PARTICULAR ACRYLIC COPOLYMER AND ANIONIC FIXING POLYMER COMPRISING AN ACID MONOMER
CROTONIQUE CROTONIC
La présente invention concerne une composition pour le traitement des fibres kératiniques, en particulier des fibres kératiniques humaines telles que les cheveux, comprenant un ou plusieurs copolymères acryliques particuliers et un ou plusieurs polymères fixants. La présente invention concerne également un procédé pour la mise en forme et/ou le maintien de la coiffure mettant en uvre ladite composition ainsi que l'utilisation de ladite composition pour la mise en forme et/ou le maintien de la coiffure. The present invention relates to a composition for the treatment of keratinous fibers, in particular human keratinous fibers such as the hair, comprising one or more particular acrylic copolymers and one or more fixing polymers. The present invention also relates to a method for shaping and / or maintaining the hairstyle using said composition and the use of said composition for shaping and / or maintaining the hairstyle.
Dans le domaine du coiffage, en particulier parmi les produits destinés à la mise en forme et/ou au maintien de la coiffure, les compositions capillaires les plus répandues sur le marché de la cosmétique sont des compositions essentiellement constituées d'une solution le plus souvent alcoolique ou hydroalcoolique et d'un ou plusieurs polymères, appelés polymères fixants, qui sont généralement des polymères filmogènes. Ces polymères ont ainsi pour fonction de réaliser des soudures entre les cheveux de manière à pouvoir structurer la coiffure et lui apporter une tenue durable. In the field of styling, in particular among products intended for shaping and / or maintaining the hairstyle, the most popular hair compositions on the cosmetics market are compositions consisting essentially of a solution most often alcoholic or hydroalcoholic and one or more polymers, called fixing polymers, which are generally film-forming polymers. These polymers thus have the function of making welds between the hair so as to be able to structure the hairstyle and bring it a lasting hold.
Cependant, certains polymères fixants entraînent un durcissement de la chevelure. Cet inconvénient conduit à une coiffure figée et à un démêlage souvent difficile en fin de journée, les cheveux présentant un toucher sec. However, some fixing polymers cause a hardening of the hair. This inconvenience leads to a fixed hairstyle and a difficult disentangling at the end of the day, the hair having a dry touch.
Pour améliorer le toucher cosmétique des cheveux, il est connu d'ajouter des composés siliconés ou oxyéthylénés. Toutefois, ce type d'association a tendance à faire diminuer le niveau de fixation des compositions et à diminuer la tenue de la coiffure. To improve the cosmetic feel of the hair, it is known to add silicone or oxyethylenated compounds. However, this type of association tends to decrease the level of fixation of the compositions and to reduce the behavior of the hairstyle.
Les documents JP2007-223943 et JP2007-63186 décrivent des compositions capillaires associant un polymère fixant à un composé siliconé. JP2007-223943 and JP2007-63186 disclose hair compositions associating a silicone-fixing polymer.
Le document JP2007-223943 décrit par exemple des compositions pour cheveux comprenant un copolymère acrylique filmogène, le copolymère acrylique filmogène pouvant être associé à un copolymère acrylate d'alkyle/acide méthacrylique/silicone. Les compositions obtenues permettent d'obtenir de bonnes propriétés de résistance mécanique sans apporter de raidissement ni de poisseux. For example, JP2007-223943 describes hair compositions comprising a film-forming acrylic copolymer, wherein the film-forming acrylic copolymer can be combined with an alkyl acrylate / methacrylic acid / silicone copolymer. The compositions obtained make it possible to obtain good strength properties without adding stiffness or stickiness.
Le document JP2007-63186 décrit aussi des compositions pour cheveux comprenant un copolymère acrylique filmogène, le copolymère acrylique filmogène pouvant être associé à un méthylpolysiloxane ou un méthylphénylpolysiloxane. Les compositions obtenues apportent de la fixation et un toucher cosmétique, notamment de la douceur. Par ailleurs, le document JP2007-217314 décrit des compositions pour cheveux comprenant un copolymère acrylique filmogène, le copolymère acrylique filmogène pouvant être associé à un copolymère d'acrylate d'alkyle. Les compositions obtenues permettent de donner un rendu naturel sans générer de collant. JP2007-63186 also discloses hair compositions comprising a film-forming acrylic copolymer, the film-forming acrylic copolymer being capable of being associated with a methylpolysiloxane or a methylphenylpolysiloxane. The compositions obtained provide fixation and a cosmetic feel, especially softness. Furthermore, JP2007-217314 discloses hair compositions comprising a film-forming acrylic copolymer, the film-forming acrylic copolymer being capable of being associated with an alkyl acrylate copolymer. The compositions obtained make it possible to give a natural rendering without generating stickiness.
Cependant, les propriétés obtenues en termes de fixation (niveau, durabilité), et de cosmétique (toucher lisse, démêlage) ne sont pas optimales. However, the properties obtained in terms of fixation (level, durability), and cosmetics (smooth touch, disentangling) are not optimal.
Il existe donc un réel besoin de trouver des compositions, notamment pour le coiffage, qui permettent un bon niveau de fixation et de maintien de la coiffure, durable, tout en apportant un toucher cosmétique aux cheveux. There is therefore a real need to find compositions, especially for styling, which allow a good level of fixation and maintenance of the hairstyle, durable, while providing a cosmetic touch to the hair.
La Demanderesse a trouvé de manière surprenante et inattendue que l'association d'un copolymère acrylique particulier et d'un polymère fixant permettait d'obtenir une chevelure ne présentant pas les inconvénients ci-dessus. The Applicant has found surprisingly and unexpectedly that the combination of a particular acrylic copolymer and a fixing polymer allowed to obtain a hair not having the above disadvantages.
En effet, cette association permet d'obtenir une fixation forte de la chevelure, durable sur la journée, tout en apportant un toucher cosmétique aux cheveux. La surface de la chevelure est plus lisse et les cheveux sont maintenus dans la forme désirée sans être figés ni durcis. Indeed, this combination provides a strong attachment of the hair, lasting on the day, while providing a cosmetic touch to the hair. The surface of the hair is smoother and the hair is held in the desired shape without being fixed or hardened.
En outre, le démêlage en fin de journée est facilité, le toucher est non collant et les cheveux plus doux, sont souples et lisses. In addition, detangling at the end of the day is easier, the touch is non-sticky and the hair softer, are soft and smooth.
L'invention a donc pour objet une composition, comprenant : The subject of the invention is therefore a composition, comprising:
(i) un ou plusieurs copolymères acryliques comprenant à titre de monomères : (i) one or more acrylic copolymers comprising as monomers:
(a) au moins un monomère acide insaturé choisi parmi les acides acrylique ou méthacrylique ou leurs sels ; (a) at least one unsaturated acidic monomer selected from acrylic or methacrylic acids or their salts;
(b) au moins un monomère ester insaturé de type acrylate ou méthacrylate ayant dans sa structure au moins un groupe alkyl à chaîne grasse, linéaire ou ramifié, de préférence ayant un groupe alkyl en C8-C3o, de préférence encore en(b) at least one unsaturated ester monomer of the acrylate or methacrylate type having in its structure at least one linear or branched chain fatty alkyl group, preferably having a C 8 -C 3 o alkyl group, more preferably
C10-C15, mieux en C12-C13 ; C10-C15, better C12-C13;
(c) au moins un monomère ester insaturé de type acrylate ou méthacrylate ayant dans sa structure au moins un groupe alkyl à chaîne courte, linéaire ou ramifié, de préférence ramifié, de préférence ayant un groupe alkyl en C2-C6, de préférence encore en C3-C5, mieux en C4 ; et (c) at least one unsaturated ester monomer of the acrylate or methacrylate type having in its structure at least one linear or branched, preferably branched, short chain alkyl group, preferably having a C 2 -C 6 alkyl group, preferably still in C 3 -C 5 , better in C 4 ; and
(d) au moins un monomère d'acrylamide ayant un groupe alkyl, linéaire ou ramifié, de préférence ramifié, de préférence ayant un groupe alkyl en C3-C10, de préférence en C4-C8 ; (d) at least one acrylamide monomer having a linear or branched, preferably branched, alkyl group, preferably having a C 3 -C 10 , preferably C 4 -C 8, alkyl group;
(ii) un ou plusieurs polymère(s) fixant(s) choisis parmi les polymères fixants anioniques comprenant un monomère d'acide crotonique, les polymères fixants non ioniques et non siliconés et les polymères fixants amphotères. Un autre objet de la présente invention consiste en un procédé de mise en forme et/ou de maintien de la coiffure mettant en œuvre la composition selon l'invention. (ii) one or more fixing polymer (s) chosen from anionic fixing polymers comprising a crotonic acid monomer, nonionic and non-silicone fixing polymers and amphoteric fixing polymers. Another object of the present invention is a method of shaping and / or maintaining the hairstyle using the composition according to the invention.
L'invention a encore pour objet une utilisation de la composition selon l'invention pour la mise en forme et/ou le maintien de la coiffure. The invention also relates to a use of the composition according to the invention for shaping and / or maintaining the hairstyle.
D'autres objets, caractéristiques, aspects et avantages de l'invention apparaîtront encore plus clairement à la lecture de la description et de l'exemple qui suit. Other objects, features, aspects and advantages of the invention will emerge even more clearly on reading the description and the example which follows.
Comme indiqué précédemment, la composition selon l'invention comprend un ou plusieurs copolymères acryliques susceptible(s) d'être obtenu(s) par copolymérisation des monomères suivants: As indicated above, the composition according to the invention comprises one or more acrylic copolymers capable of being obtained (s) by copolymerization of the following monomers:
(a) au moins un monomère acide insaturé choisi parmi les acides acrylique ou méthacrylique ou leurs sels; (a) at least one unsaturated acidic monomer selected from acrylic or methacrylic acids or their salts;
(b) au moins un monomère ester insaturé de type acrylate ou méthacrylate ayant dans sa structure au moins un groupe alkyl à chaîne grasse; (b) at least one acrylate or methacrylate-type unsaturated ester monomer having in its structure at least one fatty-chain alkyl group;
(c) au moins un monomère ester insaturé de type acrylate ou méthacrylate ayant dans sa structure un groupe alkyl à chaîne courte; et (c) at least one acrylate or methacrylate unsaturated ester monomer having in its structure a short chain alkyl group; and
(d) au moins un monomère d'acrylamide substitué par au moins un groupe alkyl. (d) at least one acrylamide monomer substituted with at least one alkyl group.
Le copolymère acrylique est de préférence filmogène. The acrylic copolymer is preferably film-forming.
Par polymère "filmogène", on entend un polymère apte à former à lui seul ou en présence d'un agent auxiliaire de filmification, un film macroscopiquement continu sur un support, notamment sur les matières kératiniques, et de préférence un film cohésif. By "film-forming" polymer is meant a polymer capable of forming, by itself or in the presence of an auxiliary film-forming agent, a macroscopically continuous film on a support, in particular on keratin materials, and preferably a cohesive film.
Le copolymère acrylique comprend au moins un monomère choisi parmi les acides acrylique ou méthacrylique ou leurs sels. The acrylic copolymer comprises at least one monomer chosen from acrylic or methacrylic acids or their salts.
De préférence, les acides acrylique ou méthacrylique ou leurs sels sont présents dans une teneur allant de 2 à 10% en poids, de préférence de 5 à 9% en poids par rapport au poids total du copolymère. Preferably, the acrylic or methacrylic acids or their salts are present in a content ranging from 2 to 10% by weight, preferably from 5 to 9% by weight relative to the total weight of the copolymer.
Le copolymère acrylique comprend également un ou plusieurs monomères ester insaturé acrylate ou méthacrylate ayant dans sa ou leur structure un groupe alkyl à chaîne grasse. Ces monomères sont donc des esters d'acide acrylique ou méthacrylique et d'un monoalcool de type alcool gras, le monoalcool fournissant le groupe alkyle de l'ester. Le groupe alkyl peut être linéaire ou ramifié. De préférence, le monomère ester insaturé de type acrylate ou méthacrylate ayant dans sa structure un groupe alkyl à chaîne grasse est un acrylate ou un méthacrylate d'alkyle avec un groupe alkyl en C8-C3o, de préférence encore en C10-C15, mieux en C12-C13. De préférence, le ou les monomère(s) ester(s) insaturé(s) de type acrylate ou méthacrylate ayant dans sa ou leur structure au moins un groupe alkyl à chaîne grasse est ou sont présent(s) dans une teneur allant de 0,1 à 5% en poids, de préférence de 0,5 à 3% en poids, mieux de 1 à 2% en poids par rapport au poids total du copolymère. The acrylic copolymer also comprises one or more acrylate or methacrylate unsaturated ester monomers having in their structure or structure a fatty-chain alkyl group. These monomers are therefore esters of acrylic or methacrylic acid and a monoalcohol of fatty alcohol type, the monoalcohol providing the alkyl group of the ester. The alkyl group can be linear or branched. Preferably, the unsaturated ester monomer of the acrylate or methacrylate type having in its structure a fatty-chain alkyl group is an alkyl acrylate or methacrylate with a C 8 -C 3 O alkyl group, more preferably a C 10 -C 15 alkyl group. better in C12-C13. Preferably, the unsaturated ester monomer (s) of the acrylate or methacrylate type having in its structure at least one fatty-chain alkyl group is or are present in a content ranging from From 1 to 5% by weight, preferably from 0.5 to 3% by weight, more preferably from 1 to 2% by weight relative to the total weight of the copolymer.
Le copolymère acrylique est issu aussi d'au moins un monomère ester insaturé de type acrylate ou méthacrylate ayant dans sa structure au moins un groupe alkyl à chaîne courte. Ces monomères sont donc des esters d'acide acrylique ou méthacrylique et d'un monoalcool à chaîne courte, le monoalcool fournissant le groupe alkyle de l'ester. Le groupe alkyl peut être linéaire ou ramifié, de préférence ramifié. The acrylic copolymer is also derived from at least one unsaturated ester monomer of the acrylate or methacrylate type having in its structure at least one short chain alkyl group. These monomers are therefore esters of acrylic or methacrylic acid and a short chain monohydric alcohol, the monohydric alcohol providing the alkyl group of the ester. The alkyl group may be linear or branched, preferably branched.
De préférence, le monomère ester insaturé de type acrylate ou méthacrylate ayant dans sa structure un groupe alkyl à chaîne courte est un acrylate ou un méthacrylate d'alkyle avec un groupe alkyl en C2-C6, de préférence encore en C3-C5, mieux en C4. Preferably, the unsaturated ester monomer of the acrylate or methacrylate type having in its structure a short-chain alkyl group is an alkyl acrylate or methacrylate with a C 2 -C 6 alkyl group, more preferably a C 3 -C 6 alkyl group. 5 , better in C 4 .
Selon un mode de réalisation préféré, le copolymère acrylique comprend à titre de monomère un acrylate ou méthacrylate de tertiobutyle. According to a preferred embodiment, the acrylic copolymer comprises, as monomer, a tert-butyl acrylate or methacrylate.
De préférence, le ou les monomère(s) ester(s) insaturé(s) de type acrylate ou méthacrylate ayant dans sa ou leur structure au moins un groupe alkyl à chaîne courte est ou sont présents dans une teneur allant de 50 à 95% en poids, de préférence de 60 à 90% en poids, mieux de 70 à 85% en poids par rapport au poids total du copolymère. Preferably, the monomer (s) unsaturated ester (s) of acrylate or methacrylate type having in its structure at least one short chain alkyl group is or are present in a content ranging from 50 to 95% by weight, preferably 60 to 90% by weight, more preferably 70 to 85% by weight relative to the total weight of the copolymer.
Le copolymère acrylique comprend aussi au moins un monomère d'acrylamide substitué par au moins un groupe alkyl. Le groupe alkyl peut être linéaire ou ramifié, de préférence ramifié. De préférence, le groupe alkyl est en C3-C10, encore plus préférentiellement en C4-C8. The acrylic copolymer also comprises at least one acrylamide monomer substituted with at least one alkyl group. The alkyl group may be linear or branched, preferably branched. Preferably, the alkyl group is C 3 -C 10 , even more preferably C 4 -C 8 .
Selon un mode de réalisation préféré, le copolymère acrylique comprend à titre de monomère du tertiobutylacrylamide ou du tertiooctylacrylamide. According to a preferred embodiment, the acrylic copolymer comprises, as monomer, tert-butylacrylamide or tert-octylacrylamide.
Encore plus préférentiellement, le copolymère acrylique comprend à titre de monomère du tertiobutylacrylamide et du tertiooctylacrylamide. Even more preferably, the acrylic copolymer comprises, as monomer, tert-butylacrylamide and tert-octylacrylamide.
De préférence, le ou les monomère(s) d'acrylamide substitué(s) par au moins un groupe alkyl est ou sont présent(s) dans une teneur allant de 0,01 à 10% en poids, de préférence de 1 à 5% en poids par rapport au poids du copolymère. Preferably, the acrylamide monomer (s) substituted with at least one alkyl group is or are present in a content ranging from 0.01% to 10% by weight, preferably from 1% to 5% by weight. % by weight relative to the weight of the copolymer.
Le copolymère acrylique peut en outre comprendre à titre de monomère un ou plusieurs monomères esters hydroxylés d'acide acrylique ou méthacrylique. De préférence, l'ester est un acrylate ou un méthacrylate d'alkyle hydroxylé en C2-C6, de préférence encore en C2 tel que l'acrylate ou le méthacrylate d'hydroxyéthyle. The acrylic copolymer may further comprise as monomer one or more hydroxylated ester monomers of acrylic or methacrylic acid. Of preferably, the ester is a hydroxylated alkyl acrylate or methacrylate of C 2 -C 6 , more preferably C 2 such as acrylate or hydroxyethyl methacrylate.
Le copolymère acrylique peut avoir un poids moléculaire moyen allant de 20000 à 500000 g/mole, de préférence de 100000 à 250000 g/mole. The acrylic copolymer may have an average molecular weight of from 20000 to 500000 g / mol, preferably from 100000 to 250000 g / mol.
De façon préférentielle, le copolymère conforme à l'invention est sous forme de sel de par la neutralisation des résidus acides issus des acides acrylique ou méthacrylique. Le copolymère peut être neutralisé partiellement ou totalement par une base minérale (soude, potasse, ammoniaque) ou une base organique telle que la mono-, di- ou tri-éthanolamine, un aminométhylpropanol, la N-méthyl-glucamine, les acides aminés basiques comme l'arginine et la lysine, et les mélanges de ces composés. De préférence, le copolymère acrylique est neutralisé par un agent de neutralisation choisi parmi l'aminométhylpropanol, la tri-éthanolamine et la soude. Preferably, the copolymer according to the invention is in salt form by neutralization of acid residues derived from acrylic or methacrylic acids. The copolymer may be partially or completely neutralized with a mineral base (sodium hydroxide, potassium hydroxide, ammonia) or an organic base such as mono-, di- or tri-ethanolamine, aminomethylpropanol, N-methyl-glucamine, basic amino acids such as arginine and lysine, and mixtures of these compounds. Preferably, the acrylic copolymer is neutralized with a neutralization agent chosen from aminomethylpropanol, tri-ethanolamine and sodium hydroxide.
De préférence, le taux de neutralisation du copolymère acrylique varie de 50 à 100%, de préférence de 80 à 100%, et plus particulièrement copolymère acrylique est neutralisé à 100%. Preferably, the degree of neutralization of the acrylic copolymer ranges from 50 to 100%, preferably from 80 to 100%, and more particularly acrylic copolymer is neutralized to 100%.
On utilisera par exemple, en tant que copolymère acrylique selon l'invention, un copolymère AMP-acrylates / C Ci8 alkylacrylate / CrC8 alkylacrylamide / hydroxyéthylacrylate commercialisé par la société GOO CHEMICAL sous la référence commerciale PLASCIZE® L-9700 ou PLASCIZE® L-9700U. For example be used as the acrylic copolymer according to the invention, an AMP-acrylates copolymer / Ci C 8 alkyl acrylate / -C 8 alkyl acrylamide / hydroxyethyl acrylate marketed by GOO Chemical under the trade reference PLASCIZE® L-9700 or L PLASCIZE® -9700U.
Le copolymère acrylique peut être présent dans la composition dans une teneur allant de 0,5 à 20% en poids, de préférence de 1 à 10% en poids par rapport au poids total de la composition. Comme indiqué précédemment, la composition selon l'invention comprend un ou plusieurs polymères fixants choisis parmi les polymères fixants anioniques comprenant un monomère d'acide crotonique, les polymères fixants non ioniques et non siliconés et les polymères fixants amphotères. The acrylic copolymer may be present in the composition in a content ranging from 0.5 to 20% by weight, preferably from 1 to 10% by weight relative to the total weight of the composition. As indicated above, the composition according to the invention comprises one or more fixing polymers chosen from anionic fixing polymers comprising a crotonic acid monomer, nonionic and non-silicone fixing polymers and amphoteric fixing polymers.
La composition selon l'invention peut comprendre un polymère fixant anionique comprenant un monomère d'acide crotonique. The composition according to the invention may comprise an anionic fixing polymer comprising a crotonic acid monomer.
Le polymère fixant anionique comprenant un monomère d'acide crotonique peut avoir un poids moléculaire moyen allant de 20 000 à200 000, de préférence de 30 000 à 150 000 g/mole, mieux de 40 000 à 100 000 g/mole. The anionic fixing polymer comprising a crotonic acid monomer can have an average molecular weight of from 20,000 to 200,000, preferably from 30,000 to 150,000 g / mole, more preferably from 40,000 to 100,000 g / mole.
Le polymère fixant anionique comprenant un monomère d'acide crotonique peut être choisi parmi les copolymères d'acide crotonique comportant dans leur chaîne des motifs acétate ou propionate de vinyle, et éventuellement d'autres monomères tels que les esters allylique ou méthallylique, éther vinylique ou ester vinylique d'un acide carboxylique saturé, linéaire ou ramifié, à longue chaîne hydrocarbonée, comme ceux comportant au moins 5 atomes de carbone, ces polymères pouvant éventuellement être greffés ou réticulés, ou encore un autre monomère ester vinylique, allylique ou méthallylique d'un acide carboxylique a- ou β-cyclique. The anionic fixing polymer comprising a crotonic acid monomer may be chosen from crotonic acid copolymers comprising in their chain, acetate or vinyl propionate units, and possibly other monomers such as allyl or methallyl esters, vinyl ethers or vinyl esters of a saturated carboxylic acid, linear or branched, with a long hydrocarbon chain, such as those containing at least 5 carbon atoms, these polymers possibly being grafted or crosslinked, or still another vinyl, allyl or methallyl ester monomer of an α- or β-cyclic carboxylic acid.
De tels polymères sont décrits entre autres dans les brevets français nos 1 222 944, 1 580 545, 2 265 782, 2 265 781 , 1 564 1 10 et 2 439 798. Des produits commerciaux entrant dans cette classe sont les produits RESYN® 28-2930 et 28- 1310 commercialisées par la société AKZO NOBEL (dénominations INCI VA / crotonates / vinyl neodecanoate copolymer et VA / crotonates copolymer respectivement) . On peut également citer les produits LUVISET® CA 66 vendu par la société BASF, ARISTOFLEX® A60 vendu par la société CLARIANT (dénomination INCI VA / crotonates copolymer) et MEXOMERE® PW ou PAM vendus par la société CHIMEX (dénomination INCI VA / vinyl butyl benzoate / crotonates copolymer). On peut aussi citer le produit BELSIL P1 101 vendu par la société WACKER (dénomination INCI crotonic acid/vinyl C8-12 isoalkyl esters/VA/bis-vinyldimethicone crosspolymer). Such polymers are described, inter alia, in French Patent Nos 1222944, 1580545, 2265782, 2265781, 1564 and January 10 2439 798. Commercial products falling into this class are the RESYN ® products 28-2930 and 28-1310 sold by AKZO NOBEL (names INCI VA / crotonates / vinyl neodecanoate copolymer and VA / crotonates copolymer respectively). LUVISET ® CA 66 sold by the company BASF, ARISTOFLEX ® A60 sold by CLARIANT (INCI VA / crotonates copolymer) and MEXOMERE ® PW or PAM sold by CHIMEX (INCI VA / vinyl butyl) may also be mentioned. benzoate / crotonates copolymer). BELSIL P1 101 sold by the company Wacker (INCI name crotonic acid / vinyl C8-12 isoalkyl esters / VA / bis-vinyldimethicone crosspolymer) can also be mentioned.
De préférence, on utilisera un copolymère d'acide crotonique comprenant dans sa chaîne des motifs d'acétate de vinyle et un ester de vinyl, et en particulier un copolymère vinyl acétate / acide crotonique /vinyl néodécanoate tel que le produit RESYN® 28-2930 commercialisé par la société AKZO NOBEL. Preferably, a copolymer of crotonic acid comprising in its chain of vinyl acetate units and a vinyl ester, especially a vinyl acetate copolymer / crotonic acid / vinyl neodecanoate such as the product RESYN 28-2930 ® marketed by the company AKZO NOBEL.
La composition selon l'invention peut comprendre un ou plusieurs polymères fixants non ioniques et non siliconés. The composition according to the invention may comprise one or more nonionic and non-silicone fixing polymers.
Par polymère non siliconé on entend un polymère ne contenant pas d'atome de silicium (Si) dans sa structure. By non-silicone polymer is meant a polymer containing no silicon atom (Si) in its structure.
Le polymère fixant non ionique et non siliconé peut avoir un poids moléculaire moyen allant de 500 à 5 000 000, de préférence de 10 000 à 500 000 g/mole, mieux de 25 000 à 300 000 g/mole. The nonionic and non-silicone fixing polymer may have an average molecular weight of from 500 to 5,000,000, preferably from 10,000 to 500,000, more preferably from 25,000 to 300,000.
Les polymères fixants non ioniques et non siliconés utilisables selon la présente invention sont choisis, par exemple, parmi : The nonionic and non-silicone fixing polymers that can be used according to the present invention are chosen, for example, from:
- les polyalkyloxazolines, polyalkyloxazolines,
- les homopolymères d'acétate de vinyle, homopolymers of vinyl acetate,
- les copolymères d'acétate de vinyle, tels que, par exemple, les copolymères d'acétate de vinyle et d'ester acrylique, les copolymères d'acétate de vinyle et d'éthylène, ou les copolymères d'acétate de vinyle et d'ester maléïque, par exemple, de maléate de dibutyle, vinyl acetate copolymers, such as, for example, copolymers of vinyl acetate and acrylic ester, vinyl acetate copolymers and ethylene, or copolymers of vinyl acetate and maleic ester, for example, dibutyl maleate,
- les homopolymères et copolymères d'esters acryliques, tels que, par exemple, les copolymères d'acrylates d'alkyle et de méthacrylates d'alkyle, tels que les produits proposés par la société ROHM & HAAS sous les dénominations PRIMAL® AC-261 K et EUDRAGIT® NE 30 D, par la société BASF sous la dénomination 8845, par la société HOECHST sous la dénomination APPRETAN® N9212, - homopolymers and copolymers of acrylic esters such as, for example, alkyl acrylates and copolymers of alkyl methacrylates, such as the products sold by the company Rohm & Haas under the names Primal AC-261 ® K and EUDRAGIT ® NE 30 D, by BASF under the name 8845, by Hoechst under the name APPRETAN ® N9212,
- les copolymères d'acrylonitrile et d'un monomère non ionique choisis, par exemple, parmi le butadiène et les (méth)acrylates d'alkyle, tels que les produits proposés sous la dénomination CJ 0601 B par la société ROHM & HAAS, copolymers of acrylonitrile and of a nonionic monomer chosen, for example, from butadiene and alkyl (meth) acrylates, such as the products sold under the name CJ 0601 B by the company Rohm & Haas,
- les homopolymères de styrène, homopolymers of styrene,
- les copolymères de styrène comme, par exemple, les copolymères de styrène et de (méth)acrylate d'alkyle, tels que les produits MOWILITH® LDM 691 1 , MOWILITH® DM 61 1 et MOWILITH® LDM 6070 proposés par la société HOECHST, les produits RHODOPAS® SD 215 et RHODOPAS® DS 910 proposés par la société RHONE POULENC, les copolymères de styrène, de méthacrylate d'alkyle et d'acrylate d'alkyle, les copolymères de styrène et de butadiène, ou les copolymères de styrène, de butadiène et de vinylpyridine, - copolymers of styrene such as, for example, copolymers of styrene and (meth) acrylate, such as Mowilith LDM ® products 691 1 Mowilith ® DM 61 1 and Mowilith ® LDM 6070 sold by the company Hoechst, RHODOPAS ® SD 215 and RHODOPAS ® DS 910 products offered by the company RHONE POULENC, copolymers of styrene, of alkyl methacrylate and of alkyl acrylate, copolymers of styrene and butadiene, or styrene copolymers, butadiene and vinylpyridine,
- les polyamides, polyamides,
- les homopolymères de vinyllactame, tels que les homopolymères de vinylpyrrolidone commercialisés par exemple sous les dénominations Luviskol® K30 poudre par la société BASF ou PVP K30L ou K60 solution ou K90 par la société ISP, le polyvinylcaprolactame commercialisé sous la dénomination Luviskol® PLUS par la société BASF, - homopolymers of vinyllactams such as vinylpyrrolidone homopolymers marketed for example under the Luviskol ® K30 powder names by BASF or PVP K30L or K60 solution or K90 by ISP, polyvinylcaprolactam sold under the name Luviskol ® PLUS by BASF company,
- les copolymères de vinyllactame, tels qu'un copolymère poly(vinylpyrrolidone/vinyllactame) vendu sous le nom commercial Luvitec® VPC 55K65W par la société BASF, les copolymères poly(vinylpyrrolidone/acétate de vinyle) comme ceux commercialisés sous la dénomination PVPA A® S630L par la société ISP, Luviskol® VA 73, VA 64, VA 55, VA 37 et VA 28 par la société BASF, et les terpolymères poly(vinylpyrrolidone/acétate de vinyle/propionate de vinyle) comme, par exemple, celui commercialisé sous la dénomination Luviskol® VAP 343 par la société BASF, et - vinyllactam copolymers such as a poly (vinylpyrrolidone / vinyllactam) copolymer sold under the trade name Luvitec® ® VPC 55K65W by BASF, poly (vinylpyrrolidone / vinyl acetate) as those marketed under the name PVPA A ® S630L by the company ISP, Luviskol ® VA 73, VA 64, VA 55, VA 37 and VA 28 by the company BASF, and poly terpolymers (vinylpyrrolidone / vinyl acetate / vinyl propionate), for example, that marketed under the name Luviskol ® VAP 343 by BASF and
- les poly(alcool vinylique). polyvinyl alcohol.
- les polymères polyvinylformamides non hydrolysés. non-hydrolysed polyvinylformamide polymers.
Les groupes alkyles des polymères non ioniques mentionnés ci-dessus ont, de préférence, de 1 à 6 atomes de carbone. De préférence, le polymère non ionique non siliconé est choisi parmi les homopolymères et copolymères de vinyllactame. De préférence encore, le polymère non ionique non siliconé est choisi parmi les polymères comprenant au moins un monomère vinylpyrrolidone. The alkyl groups of the nonionic polymers mentioned above preferably have from 1 to 6 carbon atoms. Preferably, the non-silicone non-silicone polymer is chosen from homopolymers and copolymers of vinyllactam. More preferably, the non-silicone non-silicone polymer is chosen from polymers comprising at least one vinylpyrrolidone monomer.
Selon un mode de réalisation préféré, le polymère non ionique non siliconé comprend un monomère vinylpyrrolidone et un monomère acétate de vinyle. De préférence, le ratio vinylpyrrolidone / acétate de vinyle va de 25/75 à 75/25. According to a preferred embodiment, the non-silicone nonionic polymer comprises a vinylpyrrolidone monomer and a vinyl acetate monomer. Preferably, the ratio vinylpyrrolidone / vinyl acetate ranges from 25/75 to 75/25.
La composition selon l'invention peut comprendre un ou plusieurs polymères fixants amphotères. The composition according to the invention may comprise one or more amphoteric fixing polymers.
Le polymère fixant amphotère peut avoir un poids moléculaire moyen allant de 70 000 à 1 700 000, de préférence de 100 000 à 500 000, mieux de 100 000 à 200 000 g/mole. The amphoteric fixing polymer can have an average molecular weight of from 70,000 to 1,700,000, preferably from 100,000 to 500,000, more preferably from 100,000 to 200,000, g / mol.
Les polymères fixants amphotères utilisables conformément à l'invention peuvent être choisis parmi les polymères comportant des motifs B et C répartis statistiquement dans la chaîne polymère où B désigne un motif dérivant d'un monomère comportant au moins un atome d'azote basique et C désigne un motif dérivant d'un monomère acide comportant un ou plusieurs groupements carboxyliques ou sulfoniques ou bien B et C peuvent désigner des groupements dérivant de monomères zwittérioniques de carboxybétaïnes ou de sulfobétaïnes ; B et C peuvent également désigner une chaîne polymère cationique comportant des groupements aminé primaire, secondaire, tertiaire ou quaternaire, dans laquelle au moins l'un des groupements aminé porte un groupement carboxylique ou sulfonique relié par l'intermédiaire d'un groupe hydrocarboné, ou bien B et C font partie d'une chaîne d'un polymère à motif éthylène-dicarboxylique dont l'un des groupements carboxyliques a été amené à réagir avec une polyamine comportant un ou plusieurs groupements aminé primaire ou secondaire. The amphoteric fixing polymers that may be used in accordance with the invention may be chosen from polymers comprising units B and C statistically distributed in the polymer chain, where B denotes a unit derived from a monomer comprising at least one basic nitrogen atom and C denotes a unit derived from an acidic monomer having one or more carboxylic or sulphonic groups or else B and C may denote groups derived from zwitterionic monomers of carboxybetaines or of sulphobetaines; B and C may also designate a cationic polymer chain comprising primary, secondary, tertiary or quaternary amine groups, in which at least one of the amine groups carries a carboxylic or sulfonic group connected via a hydrocarbon group, or B and C are part of a chain of an ethylene-dicarboxylic-containing polymer having one of the carboxylic groups reacted with a polyamine having one or more primary or secondary amine groups.
Les polymères amphotères répondant à la définition donnée ci-dessus que l'on préfère plus particulièrement, sont choisis parmi les polymères suivants : The amphoteric polymers as defined above, which are more particularly preferred, are chosen from the following polymers:
1 ) les polymères résultant de la copolymérisation d'un monomère dérivé d'un composé vinylique portant un groupement carboxylique tel que plus particulièrement l'acide acrylique, l'acide méthacrylique, l'acide maléique, l'acide alpha-chloracrylique, et d'un monomère basique dérivé d'un composé vinylique substitué contenant au moins un atome basique tel que plus particulièrement les dialkylaminoalkylméthacrylate et acrylate, les dialkylaminoalkyl-méthacrylamide et acrylamide. De tels composés sont décrits dans le brevet américain n° 3 836 537. Le composé vinylique peut être également un sel de dialkyldiallylammonium tel que le chlorure de diéthyldiallyl-ammonium. 1) polymers resulting from the copolymerization of a monomer derived from a vinyl compound carrying a carboxylic group such as, more particularly, acrylic acid, methacrylic acid, maleic acid, alpha-chloro acrylic acid, and a basic monomer derived from a substituted vinyl compound containing at least one basic atom such as, more particularly, dialkylaminoalkylmethacrylate and acrylate, dialkylaminoalkyl-methacrylamide and acrylamide. Such compounds are described in U.S. Patent No. 3,836,537. The vinyl compound may also be a dialkyldiallylammonium salt such as diethyldiallyl ammonium chloride.
2) les polymères comportant des motifs dérivant : 2) polymers comprising units derived from:
a) d'au moins un monomère choisi parmi les acrylamides ou les méthacrylamides substitués sur l'azote par un groupe alkyle, a) at least one monomer chosen from acrylamides or methacrylamides substituted on the nitrogen with an alkyl group,
b) d'au moins un comonomère acide contenant un ou plusieurs groupements carboxyliques réactifs, et b) at least one acidic comonomer containing one or more reactive carboxylic groups, and
c) d'au moins un comonomère basique tel que des esters à substituants aminé primaire, secondaire, tertiaire et quaternaire des acides acrylique et méthacrylique, et le produit de quaternisation du méthacrylate de diméthylaminoéthyle avec le sulfate de diméthyle ou de diéthyle. c) at least one basic comonomer such as primary, secondary, tertiary and quaternary amine substituent esters of acrylic and methacrylic acids, and the quaternization product of dimethylaminoethyl methacrylate with dimethyl or diethyl sulfate.
Les acrylamides ou méthacrylamides N-substitués plus particulièrement préférés selon l'invention sont les groupements dont les groupes alkyle contiennent de 2 à 12 atomes de carbone et plus particulièrement le N-éthylacrylamide, le N- tertiobutylacrylamide, le N-tertiooctylacrylamide, le N-octylacrylamide. le N- décylacrylamide, le N-dodécylacrylamide ainsi que les méthacrylamides correspondants. The N-substituted acrylamides or methacrylamides which are more particularly preferred according to the invention are the groups in which the alkyl groups contain from 2 to 12 carbon atoms and more particularly N-ethylacrylamide, N-tert-butylacrylamide, N-tert-octylacrylamide, N octyl. N-decylacrylamide, N-dodecylacrylamide and the corresponding methacrylamides.
Les comonomères acides sont choisis plus particulièrement parmi les acides acrylique, méthacrylique, crotonique, itaconique, maléique, fumarique ainsi que les monoesters d'alkyle ayant 1 à 4 atomes de carbone des acides ou des anhydrides maléique ou fumarique. Les comonomères basiques préférés sont des méthacrylates d'aminoéthyle, de butylaminoéthyle, de Ν,Ν'-diméthylaminoéthyle, de N-tertio-butylaminoéthyle. The acidic comonomers are chosen more particularly from acrylic, methacrylic, crotonic, itaconic, maleic and fumaric acids as well as alkyl monoesters having 1 to 4 carbon atoms of maleic or fumaric acids or anhydrides. Preferred basic comonomers are aminoethyl, butylaminoethyl, Ν, Ν'-dimethylaminoethyl, N-tert-butylaminoethyl methacrylates.
On utilise particulièrement les copolymères dont la dénomination CTFA (4ème Ed, 1991 ) est Octylacrylamide / acrylates / butylaminoethylmethacrylate copolymer tels que les produits vendus sous la dénomination AMPHOMER® , AMPHOMER® LV 71 , AMPHOMER® SOL ou encore BALANCE® 47 par la société AKZO NOBEL. The copolymers whose CTFA (4th Ed., 1991) name is octylacrylamide / acrylates / butylaminoethylmethacrylate copolymer, such as the products sold under the name AMPHOMER®, AMPHOMER® LV 71, AMPHOMER® SOL or BALANCE® 47 by the company AKZO, are particularly used. NOBEL.
3) les polyaminoamides réticulés et acylés partiellement ou totalement dérivant de polyaminoamides de formule générale : 3) polyaminoamides crosslinked and partially or completely acylated deriving from polyaminoamides of general formula:
CO— R CO— z- (I) CO-R COZ- (I)
dans laquelle R4 représente un groupe divalent dérivé d'un acide dicarboxylique saturé, d'un acide aliphatique mono ou dicarboxylique à double liaison éthylénique, d'un ester d'un alcool ayant 1 à 6 atomes de carbone de ces acides ou d'un groupe dérivant de l'addition de l'un quelconque desdits acides avec une amine bis primaire ou bis dérivé secondaire, et Z désigne un groupe d'une polyalkylène-polyamine bis-primaire, mono ou bis-secondaire et représente de préférence : in which R 4 represents a divalent group derived from a saturated dicarboxylic acid, an aliphatic mono or dicarboxylic acid with an ethylenic double bond, an ester of an alcohol having 1 to 6 carbon atoms of these acids or a group deriving from the addition of any of said acids with a bis primary or bis secondary amine, and Z denotes a group of a bis-primary, mono or bis-secondary polyalkylene polyamine and preferably represents:
a) dans les proportions de 60 à 100 % en moles, le groupe a) in the proportions of 60 to 100 mol%, the group
NH-HCH,)— NH-NH-HCH, - NH-
(II) où x=2 et p=2 ou 3, ou bien x=3 et p=2 (II) where x = 2 and p = 2 or 3, or x = 3 and p = 2
ce groupe dérivant de la diéthylène-triamine, de la triéthylène-tétraamine ou de la dipropylène-triamine; this group derived from diethylene triamine, triethylene tetraamine or dipropylene triamine;
b) dans les proportions de 0 à 40 % en moles, le groupe (II) ci-dessus, dans lequel x=2 et p=1 et qui dérive de l'éthylènediamine, ou le groupe dérivant de la pipérazine c) dans les proportions de 0 à 20 % en moles, le groupe -NH-(CH2)6-NH- dérivant de l'hexaméthylènediamine, ces polyaminoamines étant réticulées par addition d'un agent réticulant bifonctionnel choisi parmi les épihalohydrines, les diépoxydes, les dianhydrides, les dérivés bis insaturés, au moyen de 0,025 à 0,35 mole d'agent réticulant par groupement amine du polyaminoamide et alcoylés par action d'acide acrylique, d'acide chloracétique ou d'une alcane-sultone ou de leurs sels. b) in the proportions of 0 to 40 mol%, the group (II) above, in which x = 2 and p = 1 and which is derived from ethylenediamine, or the group derived from piperazine c) in the proportions of 0 to 20 mol%, the -NH- (CH 2 ) 6 -NH- group derived from hexamethylenediamine, these polyaminoamines being crosslinked by addition of a bifunctional crosslinking agent chosen from epihalohydrins, diepoxides, dianhydrides, bis unsaturated derivatives, by means of 0.025 to 0.35 mole of crosslinking agent per amine group of the polyaminoamide and alkylated by the action of acrylic acid, chloroacetic acid or an alkane-sultone or of their salts.
Les acides carboxyliques saturés sont choisis de préférence parmi les acides ayant 6 à 10 atomes de carbone tels que les acides adipique, 2,2,4-triméthyladipique et 2,4,4-triméthyladipique, téréphtalique, les acides à double liaison éthylénique comme, par exemple, les acides acrylique, méthacrylique, itaconique. Les alcane- sultones utilisées dans l'alcoylation sont de préférence la propane- ou la butane- sultone, les sels des agents d'alcoylation sont de préférence les sels de sodium ou de potassium. The saturated carboxylic acids are preferably chosen from acids having 6 to 10 carbon atoms such as adipic acid, 2,2,4-trimethyladipic acid and 2,4,4-trimethyladipic acid, terephthalic acid, ethylenically double-bonded acids such as for example, acrylic, methacrylic, itaconic acids. The alkanesultones used in the alkylation are preferably propane or butanesultone, the salts of the alkylating agents are preferably the sodium or potassium salts.
4) les polymères comportant des motifs zwittérioniques de formule : 4) polymers comprising zwitterionic units of formula:
dans laquelle R5 désigne un groupement insaturé polymérisable tel qu'un groupement acrylate, méthacrylate, acrylamide ou méthacrylamide, y et z représentent chacun un nombre entier de 1 à 3, R6 et R7 représentent un atome d'hydrogène, un groupement méthyle, éthyle ou propyle, R8 et R9 représentent un atome d'hydrogène ou un groupe alkyle de telle façon que la somme des atomes de carbone dans Rio et Ru ne dépasse pas 10. in which R 5 denotes a polymerizable unsaturated group such as an acrylate, methacrylate, acrylamide or methacrylamide group, y and z each represent an integer of 1 to 3, R 6 and R 7 represent a hydrogen atom, a methyl group, , ethyl or propyl, R 8 and R 9 represent a hydrogen atom or an alkyl group such that the sum of the carbon atoms in Rio and Ru does not exceed 10.
Les polymères comprenant de tels motifs peuvent également comporter des motifs dérivés de monomères non zwittérioniques tels que l'acrylate ou le méthacrylate de diméthyl- ou diéthylaminoéthyle, ou des acrylates ou méthacrylates d'alkyle, des acrylamides ou méthacrylamides, ou l'acétate de vinyle. Polymers comprising such units may also comprise units derived from non-zwitterionic monomers, such as dimethyl- or diethylaminoethyl acrylate or methacrylate, or alkyl acrylates or methacrylates, acrylamides or methacrylamides, or vinyl acetate. .
5) les polymères dérivés du chitosane comportant des motifs monomères répondant aux formules suivantes : 5) polymers derived from chitosan having monomeric units corresponding to the following formulas:
(IV) (V) (VI) le motif (IV) étant présent dans des proportions comprises entre 0 et 30 %, le motif (V) dans des proportions comprises entre 5 et 50 % et le motif (VI) dans des proportions comprises entre 30 et 90 %, étant entendu que dans ce motif (VI), R10 représente un groupe de formule: dans laquelle si q=0, Ru , R12 et R13, identiques ou différents, représentent chacun un atome d'hydrogène, un reste méthyle, hydroxyle, acétoxy ou amino, un reste monoalkylamine ou un reste dialkylamine éventuellement interrompus par un ou plusieurs atomes d'azote et/ou éventuellement substitués par un ou plusieurs groupes amine, hydroxyle, carboxyle, alkylthio, sulfonique, un reste alkylthio dont le groupe alkyle porte un reste amino, l'un au moins des groupes Ru , R12 et R13 étant dans ce cas un atome d'hydrogène ; (IV) (V) (VI) the unit (IV) being present in proportions of between 0 and 30%, the unit (V) in proportions of between 5 and 50% and the unit (VI) in proportions of between 30 and 90%, it being understood that in this unit (VI), R 10 represents a group of formula: in which if q = 0, Ru, R12 and R 13 , which may be identical or different, each represent a hydrogen atom, a methyl, hydroxyl, acetoxy or amino residue, a monoalkylamine residue or a dialkylamine residue optionally interrupted by one or more atoms nitrogen and / or optionally substituted with one or more amine, hydroxyl, carboxyl, alkylthio, sulfonic, alkylthio radical whose alkyl group carries an amino residue, at least one of Ru, R12 and R 13 groups being in this case a hydrogen atom;
ou si q=1 , Ru , R12 et R13 représentent chacun un atome d'hydrogène, ainsi que les sels formés par ces composés avec des bases ou des acides. or if q = 1, Ru, R12 and R 13 each represents a hydrogen atom, as well as the salts formed by these compounds with bases or acids.
6) Les polymères dérivés de la N-carboxyalkylation du chitosane. 6) The polymers derived from the N-carboxyalkylation of chitosan.
7) Les polymères de motifs répondant à la formule générale (VIII) décrits par exemple, dans le brevet français 1 400 366 : 7) The polymers of units corresponding to the general formula (VIII) described for example in the French patent 1,400,366:
(VIII) dans laquelle R14 représente un atome d'hydrogène, un groupe CH30, CH3CH20, phényle, Ri5 désigne l'hydrogène ou un groupe alkyle en Ci-4 tel que méthyle et éthyle, Ri6 désigne l'hydrogène ou un groupe alkyle en Ci-4 tel que méthyle et éthyle, R17 désigne un groupe alkyle en Ci-4 tel que méthyle et éthyle ou un groupe répondant à la formule: -Ri8-N(Ri6)2, Ris représentant un groupement -CH2-CH2-, -CH2-CH2-CH2-, -CH2-CH(CH3)-, R16 ayant les significations mentionnées ci-dessus, ainsi que les homologues supérieurs de ces groupes et contenant jusqu'à 6 atomes de carbone. (VIII) wherein R14 is hydrogen, CH 3 0, CH 3 CH 2 0, phenyl, R 5 is hydrogen or C 1-4 alkyl such as methyl and ethyl, R 6 is hydrogen or a Ci -4 alkyl group such as methyl and ethyl, R17 denotes a Ci -4 alkyl group such as methyl and ethyl or a group of the formula: -Ri8-N (R 6) 2, Ris representing a group -CH 2 -CH 2 -, -CH 2 -CH 2 -CH 2 -, -CH 2 -CH (CH 3 ) -, R 16 having the meanings mentioned above, as well as the higher homologs of these groups and containing up to 6 carbon atoms.
8) Les polymères amphotères du type -D-X-D-X- choisis parmi: 8) amphoteric polymers of the type -D-X-D-X- selected from:
a) les polymères obtenus par action de l'acide chloracétique ou le chloracétate de sodium sur les composés comportant au moins un motif de formule: a) the polymers obtained by the action of chloroacetic acid or sodium chloroacetate on compounds comprising at least one unit of formula:
-D-X-D-X-D- (IX) -D-X-D-X-D- (IX)
où D désigne un groupe et X désigne le symbole E ou Ε', E ou E', identiques ou différents, désignent un groupe bivalent qui est un groupe alkylène à chaîne droite ou ramifiée comportant jusqu'à 7 atomes de carbone dans la chaîne principale non substituée ou substituée par des groupements hydroxyle, et pouvant comporter en outre des atomes d'oxygène, d'azote, de soufre, 1 à 3 cycles aromatiques et/ou hétérocycliques ; les atomes d'oxygène, d'azote et de soufre étant présents sous forme de groupements éther, thioéther, sulfoxyde, sulfone, sulfonium, alkylamine, alcénylamine, des groupements hydroxyle, benzylamine, oxyde d'amine, ammonium quaternaire, amide, imide, alcool, ester et/ou uréthanne. where D is a group and X denotes the symbol E or Ε ', E or E', which may be identical or different, denote a divalent group which is a straight or branched chain alkylene group having up to 7 carbon atoms in the unsubstituted or substituted primary chain. hydroxyl groups, and which may further comprise oxygen, nitrogen, sulfur atoms, 1 to 3 aromatic and / or heterocyclic rings; the oxygen, nitrogen and sulfur atoms being present in the form of ether, thioether, sulphoxide, sulphone, sulphonium, alkylamine, alkenylamine, hydroxyl groups, benzylamine, amine oxide, quaternary ammonium, amide, imide groups, alcohol, ester and / or urethane.
b) Les polymères de formule : b) polymers of formula:
-D-X-D-X- (X) -D-X-D-X- (X)
où D désigne un groupe et X désigne le symbole E ou E' et au moins une fois Ε'; E ayant la signification indiquée ci-dessus et E' est un groupe bivalent qui est un groupe alkylène à chaîne droite ou ramifiée ayant jusqu'à 7 atomes de carbone dans la chaîne principale, substitué ou non par un ou plusieurs groupes hydroxyle et comportant un ou plusieurs atomes d'azote, l'atome d'azote étant substitué par une chaîne alkyle interrompue éventuellement par un atome d'oxygène et comportant obligatoirement une ou plusieurs fonctions carboxyle ou une ou plusieurs fonctions hydroxyle et bétaïnisées par réaction avec l'acide chloracétique ou du chloracétate de soude. 9) Les copolymères alkyl(Ci-C5)vinyléther/anhydride maléique modifié partiellement par semiamidification avec une Ν,Ν-dialkylaminoalkylamine telle que la Ν,Ν-diméthylaminopropyl-amine ou par semiestérification avec une N,N- dialcanolamine Ces copolymères peuvent également comporter d'autres comonomères vinyliques tels que le vinylcaprolactame. where D is a group and X denotes the symbol E or E 'and at least once Ε'; E having the meaning indicated above and E 'is a bivalent group which is a straight or branched chain alkylene group having up to 7 carbon atoms in the main chain, substituted or unsubstituted by one or more hydroxyl groups and having a or a plurality of nitrogen atoms, the nitrogen atom being substituted by an optionally interrupted alkyl chain by an oxygen atom and necessarily comprising one or more carboxyl functions or one or more hydroxyl functions and betaineized by reaction with chloroacetic acid or chloroacetate of soda. 9) (C 1 -C 5 ) alkyl vinyl ether / maleic anhydride copolymers partially modified by semiamidation with a Ν, Ν-dialkylaminoalkylamine such as Ν, Ν-dimethylaminopropylamine or by semi-esterification with an N, N-dialkanolamine These copolymers may also be include other vinyl comonomers such as vinylcaprolactam.
Les polymères amphotères préférés sont les polymères comportant des motifs dérivant : The preferred amphoteric polymers are polymers having units derived from:
a) d'au moins un monomère choisi parmi les acrylamides ou les méthacrylamides substitués sur l'azote par un groupe alkyle, a) at least one monomer chosen from acrylamides or methacrylamides substituted on the nitrogen with an alkyl group,
b) d'au moins un comonomère acide contenant un ou plusieurs groupements carboxyliques réactifs, et b) at least one acidic comonomer containing one or more reactive carboxylic groups, and
c) d'au moins un comonomère basique tel que des esters à substituants aminé primaire, secondaire, tertiaire et quaternaire des acides acrylique et méthacrylique, et le produit de quaternisation du méthacrylate de diméthylaminoéthyle avec le sulfate de diméthyle ou de diéthyle. c) at least one basic comonomer such as primary, secondary, tertiary and quaternary amine substituent esters of acrylic and methacrylic acids, and the quaternization product of dimethylaminoethyl methacrylate with dimethyl or diethyl sulfate.
On peut citer, en particulier, les polymères vendus sous la dénomination AMPHOMER® , AMPHOMER® LV 71 , AMPHOMER® SOL ou encore BALANCE® 47 par la société AKZO NOBEL. La composition selon l'invention peut comprendre un ou plusieurs polymère(s) fixant(s) choisis parmi les polymères fixants anioniques comprenant un monomère d'acide crotonique, les polymères fixants non ioniques et non siliconés et les polymères fixants amphotères dans une quantité allant de 0,5 à 20%, de préférence, de 0,5 à 10 % en poids, par rapport au poids total de la composition. Mention may in particular be made of the polymers sold under the name AMPHOMER®, AMPHOMER® LV 71, AMPHOMER® SOL or BALANCE® 47 by the company AKZO NOBEL. The composition according to the invention may comprise one or more fixing polymer (s) chosen from anionic fixing polymers comprising a crotonic acid monomer, nonionic and non-silicone fixing polymers and amphoteric fixing polymers in an amount ranging from from 0.5 to 20%, preferably from 0.5 to 10% by weight, relative to the total weight of the composition.
La composition selon l'invention peut en outre comprendre un ou plusieurs solvants. The composition according to the invention may further comprise one or more solvents.
Le solvant peut être choisi parmi l'eau, un solvant organique ou un mélange d'eau et d'un ou plusieurs solvants organiques de préférence hydrosolubles. The solvent may be chosen from water, an organic solvent or a mixture of water and one or more organic solvents, preferably water-soluble.
Par « solvant organique », on entend au sens de la présente invention un composé organique liquide à la température de 25 °C et à la pression atmosphérique (760 mm Hg). For the purposes of the present invention, the term "organic solvent" means an organic compound which is liquid at a temperature of 25 ° C. and at atmospheric pressure (760 mmHg).
Par « hydrosoluble », on entend au sens de la présente invention un composé soluble à au moins 5% en poids dans l'eau à la température de 25 °C et à la pression atmosphérique (760 mm Hg). For the purposes of the present invention, the term "water-soluble" is intended to mean a compound which is soluble to at least 5% by weight in water at a temperature of 25 ° C. and at atmospheric pressure (760 mmHg).
De préférence, le composé organique est polaire. Les solvants organiques peuvent être choisis parmi les mono alcools à chaîne courte par exemple en C1-C4 comme l'éthanol, l'isopropanol ; les diols ou les polyols comme l'éthylèneglycol, le 1 ,2-propylèneglycol, le 1 ,3-butylène glycol, l'hexylèneglycol, le diéthylèneglycol, le dipropylene glycol, le 2-éthoxyéthanol, le diéthylène glycol monométhyléther, le triéthylène glycol monométhyléther et le sorbitol. Preferably, the organic compound is polar. The organic solvents may be chosen from short-chain monohydric alcohols, for example C 1 -C 4 alcohols, such as ethanol or isopropanol; diols or polyols such as ethylene glycol, 1,2-propylene glycol, 1,3-butylene glycol, hexylene glycol, diethylene glycol, dipropylene glycol, 2-ethoxyethanol, diethylene glycol monomethyl ether, triethylene glycol monomethyl ether and sorbitol.
Dans une variante de l'invention, la composition comprend de l'eau. In a variant of the invention, the composition comprises water.
Dans cette variante la composition comprend ou non un ou plusieurs solvants organiques hydrosolubles tels que l'éthanol ou l'isopropanol. In this variant the composition comprises or not one or more water-soluble organic solvents such as ethanol or isopropanol.
Dans une autre variante de l'invention, la composition ne comprend pas d'eau. In another variant of the invention, the composition does not comprise water.
La composition selon l'invention peut comprendre un ou plusieurs solvants dans une quantité allant de 30 à 95%, de préférence, de 40 à 95 % en poids, par rapport au poids total de la composition. The composition according to the invention may comprise one or more solvents in an amount ranging from 30 to 95%, preferably from 40 to 95% by weight, relative to the total weight of the composition.
La composition selon l'invention peut en outre comprendre un ou plusieurs tensioactifs, qui peuvent être notamment choisis parmi les agents tensioactifs non- ioniques, cationiques, anioniques et amphotères ou zwittérioniques. The composition according to the invention may further comprise one or more surfactants, which may be chosen in particular from nonionic, cationic, anionic and amphoteric or zwitterionic surfactants.
Le ou lesdits agent(s) tensioactif(s) selon l'invention comprennent de préférence un ou plusieurs agent(s) tensioactif(s) non-ionique(s). The surfactant (s) according to the invention preferably comprise one or more nonionic surfactant (s).
Les agent(s) tensioactif(s) non-ionique(s) utilisable(s) dans la présente composition sont décrits par exemple dans "Handbook of Surfactants" par M.R. PORTER, éditions Blackie & Son (Glasgow and London), 1991 , pp 1 16-178. The nonionic surfactant (s) usable in the present composition are described, for example, in "Handbook of Surfactants" by MR PORTER, Blackie & Son editions (Glasgow and London), 1991, pp. 16-178.
A titre d'exemples d'agents tensioactifs non-ioniques, on peut citer les agents tensioactifs non-ioniques suivants : As examples of nonionic surfactants, mention may be made of the following nonionic surfactants:
- les alkyl(C8-C24)phénols oxyalkylénés ; oxyalkylenated (C 8 -C 2 4) alkyl phenols;
- les alcools en C4-C40, saturés ou non, linéaires ou ramifiés, oxyalkylénés ou glycérolés; saturated or unsaturated, linear or branched, oxyalkylenated or glycerolated C4-C40 alcohols;
- les amides d'acide gras en C8-C3o, saturés ou non, linéaires ou ramifiés, oxyalkylénés ; - C 8 -C 3 O fatty acid amides, saturated or unsaturated, linear or branched, oxyalkylenated;
- les esters d'acides en C8-C3o, saturés ou non, linéaires ou ramifiés, et de polyéthylèneglycols ; saturated or unsaturated, linear or branched C 8 -C 3 0 esters of polyethylene glycols;
- les esters d'acides en C8-C3o, saturés ou non, linéaires ou ramifiés, et de sorbitol de préférence oxyéthylénés ; saturated or unsaturated, linear or branched C 8 -C 3 0 esters of acids, and of sorbitol, preferably oxyethylenated;
- les esters d'acides gras et de saccharose, les alkyl(C8-C3o)(poly)glucosides, alcényl(C8-C3o)(poly)glucosides, éventuellement oxyalkylénés (0 à 10 motifs oxyalkylénés) et comprenant de 1 à 15 motifs glucose, les esters d'alkyl (C8-C3o)(poly)glucosides, esters of fatty acids and of sucrose, alkyl (C 8 -C 3 ) (poly) glucosides, alkenyl (C 8 -C 3 ) (poly) glucosides, optionally oxyalkylenated (0 to 10 oxyalkylenated units) and comprising from 1 to 15 glucose units, alkyl (C 8 -C 3 O) (poly) glucosides,
- les huiles végétales oxyéthylénées, saturées ou non ; vegetable oils oxyethylenated, saturated or not;
- les condensais d'oxyde d'éthylène et/ou d'oxyde de propylène, entre autres, seuls ou en mélanges ; ethylene oxide and / or propylene oxide condensates, inter alia, alone or in mixtures;
- les dérivés de N-alkyl(C8-C3o)glucamine et de N-acyl(C8-C30)-méthylglucamine ;derivatives of N-alkyl (C 8 -C 3 o) glucamine and N-acyl (C 8 -C 30 ) -methylglucamine;
- les aldobionamides ; aldobionamides;
- les oxydes d'amine ; amine oxides;
- les silicones oxyéthylénées et/ou oxypropylénées, oxyethylenated and / or oxypropylenated silicones,
- et leurs mélanges. - and their mixtures.
Les motifs oxyalkylénés sont plus particulièrement des motifs oxyéthylénés, oxypropylénés, ou leur combinaison, de préférence oxyéthylénés. The oxyalkylenated units are more particularly oxyethylenated units, oxypropylene, or their combination, preferably oxyethylenated.
Le nombre de moles d'oxyde d'éthylène et/ou de propylène va de préférence de 1 à 250, plus particulièrement de 2 à 100 ; mieux de 2 à 50 ; le nombre de moles de glycérol va notamment de 1 à 50, mieux de 1 à 10. The number of moles of ethylene oxide and / or propylene oxide is preferably from 1 to 250, more preferably from 2 to 100; better from 2 to 50; the number of moles of glycerol ranges from 1 to 50, more preferably from 1 to 10.
De manière avantageuse, les agents tensioactifs non-ioniques selon l'invention ne comprennent pas de motifs oxypropylénés. Advantageously, the nonionic surfactants according to the invention do not comprise oxypropylene units.
A titre d'exemple d'agents tensioactifs non-ioniques glycérolés, on utilise de préférence les alcools en C8-C4o, mono- ou poly-glycérolés, comprenant de 1 à 50 moles de glycérol, de préférence de 1 à 10 moles de glycérol. By way of example of nonionic glycerolated surfactants, it is preferable to use C 8 -C 4 o, mono- or polyglycerolated alcohols comprising from 1 to 50 moles of glycerol, preferably from 1 to 10 moles of glycerol.
A titre d'exemple de composés de ce type, on peut citer, l'alcool laurique à 4 moles de glycérol (nom INCI : POLYGLYCERYL-4 LAURYL ETHER), l'alcool laurique à 1 ,5 moles de glycérol, l'alcool oléique à 4 moles de glycérol (nom INCI : POLYGLYCERYL-4 OLEYL ETHER), l'alcool oléique à 2 moles de glycérol (Nom INCI : POLYGLYCERYL-2 OLEYL ETHER), l'alcool cétéarylique à 2 moles de glycérol, l'alcool cétéarylique à 6 moles de glycérol, l'alcool oléocétylique à 6 moles de glycérol, et l'octadécanol à 6 moles de glycérol. By way of example of compounds of this type, mention may be made of lauryl alcohol with 4 moles of glycerol (INCI name: POLYGLYCERYL-4 LAURYL ETHER), lauric alcohol with 1.5 moles of glycerol, alcohol oleic acid with 4 moles of glycerol (INCI name: POLYGLYCERYL-4 OLEYL ETHER), oleic alcohol with 2 moles of glycerol (INCI name: POLYGLYCERYL-2 OLEYL ETHER), cetearyl alcohol with 2 moles of glycerol, alcohol 6 moles of glycerol, oleocetyl alcohol with 6 moles of glycerol, and octadecanol with 6 moles of glycerol.
Parmi les alcools glycérolés, on préfère plus particulièrement utiliser l'alcool en C8/Cio à une mole de glycérol, l'alcool en C10/C12 à 1 mole de glycérol et l'alcool en C12 à 1 ,5 mole de glycérol. Among the glycerolated alcohols, it is more particularly preferred to use the C 8 / C 10 alcohol with one mole of glycerol, the C 10 / C 12 alcohol with 1 mole of glycerol and the C 12 alcohol with 1.5 moles of glycerol.
Le ou les agent(s) tensioactif(s) non-ionique(s) selon l'invention sont préférentiellement choisis parmi : The at least one nonionic surfactant (s) according to the invention are preferably chosen from:
- les alcools en C4-C40, oxyéthylénés comprenant de 1 à 100 moles d'oxyde d'éthylène, de préférence de 2 à 50, plus particulièrement de 2 à 40 moles d'oxyde d'éthylène ; - les huiles végétales oxyéthylénées, saturées ou non comprenant de 1 à 100 moles d'oxyde d'éthylène, de préférence de 2 à 50 ; oxyethylenated C 4 -C 40 alcohols comprising from 1 to 100 moles of ethylene oxide, preferably from 2 to 50, more particularly from 2 to 40 moles of ethylene oxide; saturated or unsaturated oxyethylenated vegetable oils comprising from 1 to 100 moles of ethylene oxide, preferably from 2 to 50;
- les alkyl(C8-C3o)(poly)glucosides, éventuellement oxyalkylénés (0 à 10 OE) et comprenant 1 à 15 motifs glucose ; - (C 8 -C 3 ) alkyl (poly) glucosides, optionally oxyalkylenated (0 to 10 EO) and comprising 1 to 15 glucose units;
- les alcools en C8-C4o, mono- ou poly-glycérolés, comprenant de 1 à 50 moles de glycérol, de préférence de 1 à 10 moles de glycérol ; - Alcohols C 8 -C 4 o, mono- or poly-glycerol, comprising from 1 to 50 moles of glycerol, preferably from 1 to 10 moles of glycerol;
- les amides d'acides gras en C8-C3o, saturés ou non, linéaires ou ramifiés, oxyalkylénés ; saturated or unsaturated, linear or branched, oxyalkylenated C 8 -C 3 0 fatty acid amides;
- les esters d'acides en C8-C3o, saturés ou non, linéaires ou ramifiés, et de polyéthylèneglycols ; saturated or unsaturated, linear or branched C 8 -C 3 0 esters of polyethylene glycols;
- et leurs mélanges. - and their mixtures.
De manière encore plus préférentielle, le ou les agent(s) tensioactif(s) non- ionique(s) selon l'invention sont choisis parmi : Even more preferably, the agent (s) surfactant (s) nonionic (s) according to the invention are selected from:
- les alcools en C4-C40, saturés ou non, linéaires ou ramifiés, oxyalkylénés, notamment le PPG-7-BUTETH-10.; saturated or unsaturated, linear or branched, oxyalkylenated C 4 -C 40 alcohols, in particular PPG-7-BUTETH-10;
- les alkyl(C8-C3o)(poly)glucosides, notamment le caprylyl/capryl glucoside ;- (C 8 -C 3 ) alkyls (poly) glucosides, especially caprylyl / capryl glucoside;
- les esters d'acides en C8-C30, saturés ou non, linéaires ou ramifiés, et de polyéthylèneglycols et notamment l'isostearate de PEG-8 ; saturated or unsaturated, linear or branched, C 8 -C 30 acid esters of polyethylene glycols and in particular PEG-8 isostearate;
- et leurs mélanges. - and their mixtures.
La composition selon l'invention peut comporter un ou plusieurs agent(s) tensioactif(s) cationique(s). The composition according to the invention may comprise one or more cationic surfactant (s).
On entend par « agent tensioactif cationique », un agent tensioactif chargé positivement lorsqu'il est contenu dans la composition selon l'invention. Cet agent tensioactif peut porter une ou plusieurs charges permanentes positives ou contenir une ou plusieurs fonctions cationisables au sein de la composition selon l'invention. The term "cationic surfactant" means a surfactant positively charged when it is contained in the composition according to the invention. This surfactant may carry one or more positive permanent charges or contain one or more cationizable functions within the composition according to the invention.
Le ou les agent(s) tensioactif(s) cationique(s) sont de préférence choisis parmi les aminés grasses primaires, secondaires ou tertiaires, éventuellement polyoxyalkylénées, ou leurs sels, les sels d'ammonium quaternaire, et leurs mélanges. The cationic surfactant (s) is (are) preferably chosen from primary, secondary or tertiary fatty amines, optionally polyoxyalkylenated, or their salts, quaternary ammonium salts, and mixtures thereof.
Les aminés grasses comprennent en général au moins une chaîne hydrocarbonée en C8-C30. The fatty amines generally comprise at least one C 8 -C 30 hydrocarbon chain.
A titre de sels d'ammonium quaternaire, on peut notamment citer, par exemple : As quaternary ammonium salts, there may be mentioned, for example:
- ceux répondant à la formule générale (I) suivante : dans laquelle les groupes R8 à Ru, qui peuvent être identiques ou différents, représentent un groupe aliphatique, linéaire ou ramifié, comportant de 1 à 30 atomes de carbone, ou un groupe aromatique tel que aryle ou alkylaryle, au moins un des groupes R8 à Ru désignant un groupe comportant de 8 à 30 atomes de carbones, de préférence de 12 à 24 atomes de carbone. Les groupes aliphatiques peuvent comporter des hétéroatomes tels que notamment l'oxygène, l'azote, le soufre et les halogènes. Les groupes aliphatiques sont par exemple choisis parmi les groupes alkyle en C1-C30, alcoxy en C1-C30, polyoxyalkylène (C2-C6), alkylamide en C1-C30, alkyl(Ci2-C22)amidoalkyle(C2-C6), alkyl(Ci2-C22)acétate, et hydroxyalkyle en C1-C30 ; X" est un anion choisi dans le groupe des halogénures, phosphates, acétates, lactates, alkyl(CrC4)sulfates, alkyl(d-C4)- ou alkyl(CrC4)aryl-sulfonates. - those corresponding to the following general formula (I): in which the groups R 8 to Ru, which may be identical or different, represent a linear or branched aliphatic group containing from 1 to 30 carbon atoms, or an aromatic group such as aryl or alkylaryl, at least one of the R groups. 8 to Ru denoting a group having from 8 to 30 carbon atoms, preferably from 12 to 24 carbon atoms. The aliphatic groups can comprise heteroatoms such as in particular oxygen, nitrogen, sulfur and halogens. The aliphatic groups are for example selected from alkyl C1-C30, C1-C30, polyoxy (C 2 -C 6) alkylamide C1-C30 alkyl (Ci2-C22) amidoalkyl (C 2 -C 6) C 1 -C 2 alkyl, C 1 -C 30 hydroxyalkyl; X " is an anion chosen from the group of halides, phosphates, acetates, lactates, alkyl (CrC 4 ) sulphates, alkyl (dC 4 ) - or alkyl (CrC 4 ) aryl sulphonates.
Parmi les sels d'ammonium quaternaire de formule (I), on préfère d'une part, les sels de tétraalkylammonium comme, par exemple, les sels de dialkyldiméthylammonium ou d'alkyltriméthylammonium dans lesquels le groupe alkyle comporte environ de 12 à 22 atomes de carbone, en particulier les sels de béhényltriméthylammonium, de distéaryldiméthylammonium, de cétyltriméthylammonium, de benzyldiméthylstéarylammonium ou encore, d'autre part, les sels de palmitylamidopropyltriméthylammonium, de stéaramidopropyltriméthylammonium, les sels de stéaramidopropyldiméthylcétéarylammonium, ou les sels de stéaramidopropyldiméthyl-(myristylacétate)-ammonium commercialisé sous la dénomination CERAPHYL® 70 par la société VAN DYK. On préfère en particulier utiliser les sels de chlorure de ses composés. Among the quaternary ammonium salts of formula (I), tetraalkylammonium salts, for example dialkyl dimethylammonium or alkyltrimethylammonium salts, in which the alkyl group contains from about 12 to 22 carbon atoms, are preferred. carbon, in particular the salts of behenyltrimethylammonium, distearyldimethylammonium, cetyltrimethylammonium, benzyldimethylstearylammonium or, on the other hand, the salts of palmitylamidopropyltrimethylammonium, of stearamidopropyltrimethylammonium, the salts of stearamidopropyldimethylcétéaryl ammonium, or the salts of stearamidopropyldimethyl- (myristylacetate) -ammonium marketed under the name CERAPHYL ® 70 by the company Van Dyk. It is particularly preferred to use the chloride salts of its compounds.
- les sels d'ammonium quaternaire de l'imidazoline, comme par exemple ceux de formule (II) suivante : the quaternary ammonium salts of imidazoline, for example those of formula (II) below:
(il) (he)
dans laquelle R12 représente un groupe alcényle ou alkyle comportant de 8 à 30 atomes de carbone, par exemple dérivés des acides gras du suif, Ri3 représente un atome d'hydrogène, un groupe alkyle en C1-C4 ou un groupe alcényle ou alkyle comportant de 8 à 30 atomes de carbone, Ri4 représente un groupe alkyle en Ci-C4, Ris représente un atome d'hydrogène, un groupe alkyle en CrC4, X" est un anion choisi dans le groupe des halogénures, phosphates, acétates, lactates, alkylsulfates, alkyl- ou alkylaryl-sulfonates dont les groupements alkyl et aryl comprennent de préférence respectivement de 1 à 20 atomes de carbone et de 6 à 30 atomes de carbone. De préférence, R12 et R13 désignent un mélange de groupes alcényle ou alkyle comportant de 12 à 21 atomes de carbone, par exemple dérivés des acides gras du suif, Ri4 désigne un groupe méthyle, Ri5 désigne un atome d'hydrogène. Un tel produit est par exemple commercialisé sous la dénomination REWOQUAT® W 75 par la société REWO ; wherein R12 represents an alkenyl or alkyl group having 8 to 30 carbon atoms, for example derived from tallow fatty acids, R 3 represents a hydrogen atom, a C1-C4 alkyl or alkenyl or alkyl comprising from 8 to 30 carbon atoms, R 4 represents a C 1 -C 4 alkyl group, R 6 represents a hydrogen atom or a C 1 -C 4 alkyl group; X " is an anion chosen from the group of halides, phosphates and acetates; , lactates, alkyl sulphates, alkyl- or alkylaryl-sulphonates in which the alkyl and aryl groups preferably comprise respectively 1 to 20 carbon atoms and 6 to 30 carbon atoms. preferably, R 12 and R 13 denote a mixture of alkenyl groups or alkyl having from 12 to 21 carbon atoms, for example fatty acid derivatives of tallow, R 4 denotes a methyl group, R 5 denotes a hydrogen atom, such a product is for example marketed under the name REWOQUAT ® W 75 by the company REWO;
- les sels de di ou de triammonium quaternaire en particulier de formule (III) : the di or quaternary triammonium salts, in particular of formula (III):
dans laquelle Ri6 désigne un radical alkyle comportant environ de 16 à 30 atomes de carbone éventuellement hydroxylé et/ou interrompu par un ou plusieurs atomes d'oxygène, Ri7 est choisi parmi l'hydrogène ou un radical alkyle comportant de 1 à 4 atomes de carbone ou un groupe (Ri6a)(Ri7a)(Ri8a)N-(CH2)3, Riea, Ri?a, Risa, R18, Rig, R20 et R2i , identiques ou différents, sont choisis parmi l'hydrogène ou un radical alkyle comportant de 1 à 4 atomes de carbone, et X" est un anion choisi dans le groupe des halogénures, acétates, phosphates, nitrates et méthylsulfates. De tels composés sont par exemple le Finquat CT-P proposé par la société FINETEX (Quaternium 89), le Finquat CT proposé par la société FINETEX (Quaternium 75), - les sels d'ammonium quaternaire contenant au moins une fonction ester, tels que ceux de formule IV) suivante : in which R 16 denotes an alkyl radical containing about 16 to 30 carbon atoms, optionally hydroxylated and / or interrupted by one or more oxygen atoms, R 17 is chosen from hydrogen or an alkyl radical containing from 1 to 4 atoms atoms or a (Ri6a) (Ri7a) (Ri8a) N- (CH 2) 3, Rie, Ri? a, Risa, R 18, Rig, R20 and R 2 i are identical or different, are chosen from hydrogen or an alkyl radical having from 1 to 4 carbon atoms, and X " is an anion chosen from the group of the halides, acetates, phosphates, nitrates and methylsulfates Such compounds are, for example, the Finquat CT-P proposed by FINETEX company (Quaternium 89), the Finquat CT proposed by FINETEX (Quaternium 75), the quaternary ammonium salts containing at least one ester function, such as those of formula IV) below:
dans laquelle : in which :
R22 est choisi parmi les groupes alkyles en CrC6 et les groupes hydroxyalkyles ou dihydroxyalkyles en CrC6 ; R22 is selected from alkyl and -C 6 hydroxyalkyl or dihydroxyalkyl groups -C 6;
R23 est choisi parmi : R23 is selected from:
- le groupe - the group
- les groupes R27 qui sont des groupes hydrocarbonés en C1-C22, linéaires ou ramifiés, saturés ou insaturés, the R27 groups which are linear or branched, saturated or unsaturated C1-C22 hydrocarbon groups,
- l'atome d'hydrogène, - the hydrogen atom,
R25 est choisi parmi : R25 is selected from:
O O
- le groupe ΰ - the group ΰ
- les groupes R2g qui sont des groupes hydrocarbonés en CrC6, linéaires ou ramifiés, saturés ou insaturés, the groups R 2 g which are linear or branched, saturated or unsaturated C 1 -C 6 hydrocarbon-based groups,
- l'atome d'hydrogène, - the hydrogen atom,
R24, 26 et R28, identiques ou différents, sont choisis parmi les groupes hydrocarbonés en C7-C21 , linéaires ou ramifiés, saturés ou insaturés ; R 24, R 26 and R 2 8, identical or different, are selected from hydrocarbon groups C7-C21 linear or branched, saturated or unsaturated;
r, s et t, identiques ou différents, sont des entiers valant de 2 à 6 ; r, s and t, identical or different, are integers ranging from 2 to 6;
y est un entier valant de 1 à 10 ; y is an integer from 1 to 10;
x et z, identiques ou différents, sont des entiers valant de 0 à 10 ; x and z, which are identical or different, are integers ranging from 0 to 10;
X" est un anion simple ou complexe, organique ou inorganique ; X " is a simple or complex anion, organic or inorganic;
sous réserve que la somme x + y + z vaut de 1 à 15, que lorsque x vaut 0 alors R23 désigne R27 et que lorsque z vaut 0 alors R25 désigne R2g- Les groupes alkyles R22 peuvent être linéaires ou ramifiés et plus particulièrement linéaires. with the proviso that the sum x + y + z is from 1 to 15, that when x is 0, then R 23 denotes R 27 and that when z is 0, then R 25 denotes R 2 g. The alkyl groups R 22 may be linear or branched and more particularly linear.
De préférence, R22 désigne un groupe méthyle, éthyle, hydroxyéthyle ou dihydroxypropyle, et plus particulièrement un groupe méthyle ou éthyle. Preferably, R 22 denotes a methyl, ethyl, hydroxyethyl or dihydroxypropyl group, and more particularly a methyl or ethyl group.
Avantageusement, la somme x + y + z vaut de 1 à 10. Lorsque R23 est un groupe R27 hydrocarboné, il peut être long et avoir de 12 à 22 atomes de carbone, ou court et avoir de 1 à 3 atomes de carbone. Advantageously, the sum x + y + z is from 1 to 10. When R 23 is a hydrocarbon R 27 group, it may be long and have 12 to 22 carbon atoms, or short and have 1 to 3 carbon atoms.
Lorsque R25 est un groupe R29 hydrocarboné, il a de préférence 1 à 3 atomes de carbone. When R 25 is a hydrocarbon R 29 group, it preferably has 1 to 3 carbon atoms.
Avantageusement, R24, R26 et R28, identiques ou différents, sont choisis parmi les groupes hydrocarbonés en C11-C21 , linéaires ou ramifiés, saturés ou insaturés, et plus particulièrement parmi les groupes alkyle et alcényle en C11-C21 , linéaires ou ramifiés, saturés ou insaturés. Advantageously, R 24 , R 26 and R 28 , which are identical or different, are chosen from linear or branched, saturated or unsaturated C 11 -C 21 hydrocarbon-based groups, and more particularly from linear or branched C 11 -C 21 alkyl and alkenyl groups. , saturated or unsaturated.
De préférence, x et z, identiques ou différents, valent 0 ou 1 . Preferably, x and z, identical or different, are 0 or 1.
Avantageusement, y est égal à 1 . Advantageously, y is 1.
De préférence, r, s et t, identiques ou différents, valent 2 ou 3, et encore plus particulièrement sont égaux à 2. Preferably, r, s and t, which are identical or different, are equal to 2 or 3, and even more particularly are equal to 2.
L'anion X" est de préférence un halogénure (chlorure, bromure ou iodure) ou un alkylsulfate plus particulièrement méthylsulfate. On peut cependant utiliser le méthanesulfonate, le phosphate, le nitrate, le tosylate, un anion dérivé d'acide organique tel que l'acétate ou le lactate ou tout autre anion compatible avec l'ammonium à fonction ester. The anion X " is preferably a halide (chloride, bromide or iodide) or an alkyl sulphate, more particularly methyl sulphate, but methanesulphonate, phosphate, nitrate, tosylate, an anion derived from an organic acid such as acetate or lactate or any other anion compatible with ester-function ammonium.
L'anion X" est encore plus particulièrement le chlorure ou le méthylsulfate. The anion X - is even more particularly chloride or methylsulfate.
On utilise plus particulièrement dans la composition selon l'invention, les sels d'ammonium de formule (IV) dans laquelle : In the composition according to the invention, the ammonium salts of formula (IV) in which:
R22 désigne un groupe méthyle ou éthyle, R 22 denotes a methyl or ethyl group,
x et y sont égaux à 1 ; x and y are equal to 1;
z est égal à 0 ou 1 ; z is 0 or 1;
r, s et t sont égaux à 2 ; r, s and t are 2;
R23 est choisi parmi : R 23 is chosen from:
- le groupe - the group
- les groupes méthyle, éthyle ou hydrocarbonés en Ci4-C22, methyl, ethyl or C 4 -C 22 hydrocarbon groups,
- l'atome d'hydrogène ; - the hydrogen atom;
R25 est choisi parmi : R 25 is selected from:
O - le groupe ^28 ^ O - the group ^ 28 ^
- l'atome d'hydrogène ; R24, R26 et R28, identiques ou différents, sont choisis parmi les groupes hydrocarbonés en C13-C17, linéaires ou ramifiés, saturés ou insaturés, et de préférence parmi les groupes alkyles et alcényles en C13-C17, linéaires ou ramifiés, saturés ou insaturés. - the hydrogen atom; R24, R26 and R 2 8, identical or different, are selected from hydrocarbon groups C13-C17 linear or branched, saturated or unsaturated, and preferably from alkyl groups and alkenyl C13-C17 linear or branched, saturated or unsaturated.
Avantageusement, les groupes hydrocarbonés sont linéaires. Advantageously, the hydrocarbon groups are linear.
On peut citer par exemple les composés de formule (IV) tels que les sels (chlorure ou méthylsulfate notamment) de diacyloxyéthyl-diméthylammonium, de diacyloxyéthyl-hydroxyéthyl-méthylammonium, de monoacyloxyéthyl-dihydroxyéthyl- méthylammonium, de triacyloxyéthyl-méthylammonium, de monoacyloxyéthyl- hydroxyéthyl-diméthylammonium et leurs mélanges. Les groupes acyles ont de préférence 14 à 18 atomes de carbone et proviennent plus particulièrement d'une huile végétale comme l'huile de palme ou de tournesol. Lorsque le composé contient plusieurs groupes acyles, ces derniers peuvent être identiques ou différents. There may be mentioned, for example, the compounds of formula (IV) such as the salts (in particular chloride or methylsulfate) of diacyloxyethyl-dimethylammonium, diacyloxyethyl-hydroxyethyl-methylammonium, monoacyloxyethyl-dihydroxyethyl-methylammonium, triacyloxyethyl-methylammonium, monoacyloxyethyl-hydroxyethyl dimethylammonium and mixtures thereof. The acyl groups preferably have from 14 to 18 carbon atoms and come more particularly from a vegetable oil such as palm oil or sunflower oil. When the compound contains more than one acyl group, the latter groups may be identical or different.
Ces produits sont obtenus, par exemple, par estérification directe de la triéthanolamine, de la triisopropanolamine, d'alkyldiéthanolamine ou d'alkyldiisopropanolamine éventuellement oxyalkylénées sur des acides gras en C10- C3o ou sur des mélanges d'acides gras en C10-C30 d'origine végétale ou animale, ou par transestérification de leurs esters méthyliques. Cette estérification est suivie d'une quaternisation à l'aide d'un agent d'alkylation tel qu'un halogénure d'alkyle (méthyle ou éthyle de préférence), un sulfate de dialkyle (méthyle ou éthyle de préférence), le méthanesulfonate de méthyle, le para-toluènesulfonate de méthyle, la chlorhydrine du glycol ou du glycérol. These products are obtained, for example, by direct esterification of triethanolamine, triisopropanolamine, alkyldiethanolamine or alkyldiisopropanolamine, optionally oxyalkylenated, with C 10 -C 30 fatty acids or mixtures of C 10 -C 30 fatty acids. of vegetable or animal origin, or by transesterification of their methyl esters. This esterification is followed by quaternization using an alkylating agent such as an alkyl halide (preferably methyl or ethyl), a dialkyl sulphate (preferably methyl or ethyl), methanesulfonate. methyl, para-toluenesulfonate methyl, chlorohydrin glycol or glycerol.
De tels composés sont par exemple commercialisés sous les dénominations DEHYQUART® par la société HENKEL, STEPANQUAT® par la société STEPAN, NOXAMIUM® par la société CECA, REWOQUAT® WE 18 par la société REWO- WITCO. Such compounds are for example marketed under the names DEHYQUART ® by Henkel, Stepanquat® ® by the company Stepan, Noxamium ® by CECA Rewoquat ® WE 18 by the company Witco REWO-.
La composition selon l'invention peut contenir par exemple un mélange de sels de mono-, di- et triester d'ammonium quaternaire avec une majorité en poids de sels de diester. The composition according to the invention may contain, for example, a mixture of quaternary ammonium mono-, di- and triester salts with a majority by weight of diester salts.
On peut aussi utiliser les sels d'ammonium contenant au moins une fonction ester décrits dans les brevets US-A-4874554 et US-A-4137180. It is also possible to use the ammonium salts containing at least one ester function described in US-A-4874554 and US-A-4137180.
On peut utiliser le chlorure de béhénoylhydroxypropyltriméthylammonium proposé par KAO sous la dénomination Quatarmin BTC 131 . The behenoylhydroxypropyltrimethylammonium chloride proposed by KAO can be used under the name Quatarmin BTC 131.
De préférence les sels d'ammonium contenant au moins une fonction ester contiennent deux fonctions esters. Parmi les sels d'ammonium quaternaire contenant au moins une fonction ester utilisables, on préfère utiliser les sels de dipalmitoyléthylhydroxyéthylméthylammonium. Preferably the ammonium salts containing at least one ester function contain two ester functions. Among the quaternary ammonium salts containing at least one useful ester function, it is preferred to use dipalmitoylethylhydroxyethylmethylammonium salts.
Les agents tensioactifs cationiques sont choisis de préférence parmi ceux de formule (I) et ceux de formule (IV), et encore plus préférentiellement parmi ceux de formule (I). The cationic surfactants are preferably chosen from those of formula (I) and those of formula (IV), and even more preferably from those of formula (I).
La composition selon l'invention peut comporter un ou plusieurs agent(s) tensioactif(s) anionique(s). The composition according to the invention may comprise one or more anionic surfactant (s).
On entend par « agent tensioactif anionique », un agent tensioactif ne comportant à titre de groupements ioniques ou ionisables que des groupements anioniques. Ces groupements anioniques sont choisis de préférence parmi les groupements The term "anionic surfactant" means a surfactant comprising as ionic or ionizable groups only anionic groups. These anionic groups are preferably chosen from groups
-COOH, -COO", -S03H, -SO3 ", -OSO3H, -OSO3 ", -P02H2, -PO2H", -PO22", -P(OH)2, =P(0)OH, -P(OH)0", =P(0)0", =POH, =PO", les parties anioniques comprenant un contre ion cationique tel qu'un métal alcalin, un métal alcalino-terreux, ou un ammonium. -COOH, -COO ", -S0 3 H, -SO 3", -OSO 3 H, -OSO 3 ", -P0 2 H 2, -PO2H" -PO2 2 ", -P (OH) 2, = P (O) OH, -P (OH) O " , = P (O) O " , = POH, = PO " , the anionic parts comprising a cationic counterion such as an alkali metal, an alkaline earth metal, or an ammonium.
A titre d'exemples d'agents tensioactifs anioniques utilisables dans la composition selon l'invention, on peut citer les alkyl sulfates, les alkyl éther sulfates, les alkylamidoéthersulfates, les alkylarylpolyéthersulfates, les monoglycéride-sulfates, les alkylsulfonates, les alkylamidesulfonates, les alkylarylsulfonates, les alpha-oléfine- sulfonates, les paraffine-sulfonates, les alkylsulfosuccinates, les alkyléthersulfo- succinates, les alkylamide-sulfosuccinates, les alkylsulfo-acétates, les acylsarcosinates, les acylgiutamates, les alkyisulfosuccinamates, les acyliséthionates et les N-acyltaurates, les sels de monoesters d'alkyle et d'acides polyglucoside- polycarboxyliques, les acyllactylates, les sels d'acides D-galactoside-uroniques, les sels d'acides alkyl éther-carboxyliques, les sels d'acides alkyl aryl éther-carboxyliques, les sels d'acides alkyl amidoéther-carboxyliques, les alkyl ou alkényl phosphates et les formes non salifiées correspondantes de tous ces composés, les groupes alkyle et acyle de tous ces composés comportant de 6 à 40 atomes de carbone et le groupe aryle désignant un groupe phényle. As examples of anionic surfactants that may be used in the composition according to the invention, mention may be made of alkyl sulphates, alkyl ether sulphates, alkylamido ether sulphates, alkylaryl polyether sulphates, monoglyceride sulphates, alkyl sulphonates, alkyl amide sulphonates and alkyl aryl sulphonates. , alpha-olefin sulfonates, paraffin sulfonates, alkylsulfosuccinates, alkylethersulfosuccinates, alkylamide-sulfosuccinates, alkylsulfoacetates, acylsarcosinates, acylglutamates, alkylsulfosuccinamates, acylisethionates and N-acyltaurates, and salts thereof. alkyl monoesters and polyglucoside polycarboxylic acids, acyllactylates, D-galactoside uronic acid salts, alkyl ether carboxylic acid salts, alkyl aryl ether carboxylic acid salts, of alkyl amidoether carboxylic acids, alkyl or alkenyl phosphates and the corresponding non-salified forms of all these alkyl and acyl groups of all these compounds having from 6 to 40 carbon atoms and the aryl group denoting a phenyl group.
Ces composés peuvent être oxyéthylénés et comportent alors de préférence de 1 à 50 motifs oxyde d'éthylène. These compounds may be oxyethylenated and then preferably comprise from 1 to 50 ethylene oxide units.
Les sels de monoesters d'alkyle en C6-C24 et d'acides polyglucoside- polycarboxyliques peuvent être choisis parmi les polyglucoside-citrates d'alkyle en C6- C24, les polyglucosides-tartrates d'alkyle en C6-C24 et les polyglucoside- sulfosuccinates d'alkyle en C6-C24. Alkyl monoesters, salts of C 6 -C 2 4 and polyglucoside- polycarboxylic acids may be selected from alkyl polyglucoside citrates C 6 - C 2 4, C 6 -C 2 4 alkyl polyglucoside tartrates and C 6 -C 24 alkyl polyglucoside sulfosuccinates.
Lorsque le ou les agent(s) tensioactif(s) anionique(s) sont sous forme de sel, ils peuvent être choisis parmi les sels de métaux alcalins tels que le sel de sodium ou de potassium et de préférence de sodium, les sels d'ammonium, les sels d'amines et en particulier d'aminoalcools ou les sels de métaux alcalino-terreux tel que les sels de magnésium. When the anionic surfactant (s) are in the salt form, they may be chosen from alkali metal salts such as sodium or potassium salt and preferably sodium salt, sodium salts or ammonium, salts of amines and in particular of aminoalcohols or salts of alkaline earth metals such as magnesium salts.
A titre d'exemple de sels d'aminoalcools, on peut citer notamment les sels de mono-, di- et triéthanolamine, les sels de mono-, di- ou triisopropanolamine, les sels de 2-amino-2-méthyl-1 -propanol, 2-amino-2-méthyl-1 ,3-propanediol et tris(hydroxy- méthyl)amino méthane. By way of example of aminoalcohol salts, mention may be made in particular of the salts of mono-, di- and triethanolamine, the salts of mono-, di- or triisopropanolamine, the salts of 2-amino-2-methyl-1 - propanol, 2-amino-2-methyl-1,3-propanediol and tris (hydroxymethyl) amino methane.
On utilise de préférence les sels de métaux alcalins ou alcalino-terreux et en particulier les sels de sodium ou de magnésium. The alkali metal or alkaline earth metal salts and in particular the sodium or magnesium salts are preferably used.
Parmi les agents tensioactifs anioniques cités, on préfère utiliser les alkyl(C6- C24)sulfates, les alkyl(C6-C24)éthersulfates, les alkyl(C6-C24) ou alkényl(C6-C24) phosphates comprenant de 2 à 50 motifs oxyde d'éthylène, notamment sous forme de sels de métaux alcalins, d'ammonium, d'aminoalcools, et de métaux alcalino-terreux, ou un mélange de ces composés. Among the anionic surfactants mentioned, it is preferable to use (C 6 -C 2 4) alkyl sulphates, (C 6 -C 2 4) alkyl ethersulphates, (C 6 -C 24 ) alkyls or (C 6 -C alkenyl) alkenyls. 24 ) phosphates comprising from 2 to 50 ethylene oxide units, especially in the form of alkali metal salts, ammonium, aminoalcohols, and alkaline earth metals, or a mixture of these compounds.
En particulier, on préfère utiliser les alkyl(Ci2-C20)sulfates, les alkyl(Ci2- C20)éthersulfates, les alkyl(d2-C24) ou alkényl(Ci2-C24) phosphates comprenant de 2 à 20 motifs oxyde d'éthylène, notamment sous forme de sels de métaux alcalins, d'ammonium, d'aminoalcools, et de métaux alcalino-terreux, ou un mélange de ces composés. Mieux encore, on préfère utiliser l'oleth-20 phosphate. In particular, it is preferred to use alkyl (Ci 2 -C 20 ) sulphates, alkyl (Ci 2 -C 20 ) ethersulfates, alkyl (d 2 -C 24 ) or alkenyl (Ci 2 -C 24 ) phosphates comprising from 2 to 20 ethylene oxide units, especially in the form of alkali metal salts, ammonium, aminoalcohols, and alkaline earth metals, or a mixture of these compounds. More preferably, it is preferred to use oleth-20 phosphate.
La composition selon l'invention peut comporter un ou plusieurs agent(s) tensioactif(s) amphotère(s) ou zwittérionique(s). The composition according to the invention may comprise one or more surfactant (s) amphoteric (s) or zwitterionic (s).
En particulier, le ou les tensioactif(s) amphotère(s) ou zwittérionique(s), de préférence non-siliconés, utilisables dans la présente invention, peuvent être notamment des dérivés d'amines aliphatiques secondaire ou tertiaire, éventuellement quaternisées, dans lesquels le groupe aliphatique est une chaîne linéaire ou ramifiée comportant de 8 à 22 atomes de carbone, lesdits dérivés d'amines contenant au moins un groupe anionique tel que, par exemple, un groupe carboxylate, sulfonate, sulfate, phosphate ou phosphonate. In particular, the amphoteric (s) or zwitterionic (s) surfactant (s), preferably non-silicone surfactants, that may be used in the present invention may in particular be derivatives of secondary or tertiary aliphatic amines, optionally quaternized, in which the aliphatic group is a linear or branched chain having 8 to 22 carbon atoms, said amine derivatives containing at least one anionic group such as, for example, a carboxylate group, sulfonate, sulfate, phosphate or phosphonate.
On peut citer en particulier les alkyl(C8-C20)bétaïnes, les alkyl(C8- C20)sulfobétaïnes, les alkyl(C8-C2o)amidoalkyl(C3-C8)bétaïnes et les alkyl(C8-C20)- amidalkyl(C6-C8)sulfobétaïnes. Parmi les dérivés d'amines aliphatiques secondaires ou tertiaires, éventuellement quaternisées utilisables, tels que définis ci-dessus, on peut également citer les composés de structures respectives (V) et (VI) suivantes : Mention may in particular alkyl (C 8 -C 20) betaines, (C 8 - C 20) sulfobetaines, (C8-C 2 o) alkylamido (C 3 -C 8) alkylbetaines and alkyl (C 8 -C 20 ) - amidalkyl (C 6 -C 8 ) sulfobetaines. Among the derivatives of secondary or tertiary aliphatic amines, optionally quaternized, which may be used, as defined above, there may also be mentioned the compounds of respective structures (V) and (VI):
Ra-CONHCH2CH2-N+(Rb)(Rc)-CH2COO", M+ , X" (V) R a -CONHCH 2 CH 2 -N + (R b ) (R c ) -CH 2 COO " , M + , X " (V)
Formule dans laquelle : Formula in which:
- Ra représente un groupe alkyle ou alcényle en C10-C30 dérivé d'un acide RaCOOH, de préférence présent dans l'huile de coprah hydrolysée, un groupe heptyle, nonyle ou undécyle ; - R a represents an alkyl or alkenyl group containing 1 0 C30 derived from an acid R a COOH, preferably present in hydrolysed coconut oil or a heptyl, nonyl or undecyl radical;
- Rb représente un groupe bêta-hydroxyéthyle ; et - R b represents a beta-hydroxyethyl group; and
- Rc représente un groupe carboxyméthyle ; - R c represents a carboxymethyl group;
- M+ représente un contre ion cationique issu d'un métal alcalin, alcalinoterreux, tel que le sodium, un ion ammonium ou un ion issu d'une aminé organique, et M + represents a cationic counterion derived from an alkali metal, alkaline earth metal, such as sodium, an ammonium ion or an ion derived from an organic amine, and
- X" représente un contre ion anionique organique ou inorganique, tel que celui choisi parmi les halogénures, acétates, phosphates, nitrates, alkyl(d- C4)sulfates, alkyl(d-C4)- ou alkyl(CrC4)aryl-sulfonates, en particulier méthylsulfate et éthylsulfate ; ou alors M+ et X" sont absents ; X " represents an organic or inorganic anionic counterion, such as that chosen from halides, acetates, phosphates, nitrates, alkyl (d-C 4 ) sulphates, alkyl (dC 4 ) - or alkyl (CrC 4 ) aryl sulphonates; especially methylsulfate and ethylsulfate, or M + and X " are absent;
-CONHCH2CH2-N(B)(B') -CONHCH 2 CH 2 -N (B) (B ')
Formule dans laquelle : Formula in which:
- B représente le groupe -CH2CH2OX' ; B represents the group -CH 2 CH 2 OX ';
- B' représente le groupe -(CH2)ZY\ avec z = 1 ou 2 ; - B 'represents the group - (CH 2 ) Z Y \ with z = 1 or 2;
X' représente le groupe -CH2COOH, -CH2-COOZ', -CH2CH2COOH, -CH2CH2-COOZ', ou un atome d'hydrogène ; X 'represents the group -CH 2 COOH, -CH 2 -COOZ', -CH 2 CH 2 COOH, -CH 2 CH 2 -COOZ ', or a hydrogen atom;
Y' représente le groupe -COOH, -COOZ', -CH2CH(OH)S03H ou le groupe CH2CH(OH)S03-Z' ; Y 'represents the group -COOH, -COOZ', -CH 2 CH (OH) SO 3 H or the group CH 2 CH (OH) SO 3 Z ';
- Z' représente un contre ion cationique issu d'un métal alcalin ou alcalinoterreux, tel que le sodium, un ion ammonium ou un ion issu d'une aminé organique ; Z 'represents a cationic counterion derived from an alkaline or alkaline earth metal, such as sodium, an ammonium ion or an ion derived from an organic amine;
- Ra' représente un groupe alkyle ou alcényle en C10-C30 d'un acide Ra'- COOH de préférence présent dans l'huile de coprah ou dans l'huile de lin hydrolysée, un groupe alkyle, notamment en C17 et sa forme iso, un groupe en Ci7 insaturé. Ces composés sont classés dans le dictionnaire CTFA, 5ème édition, 1993, sous les dénominations cocoamphodiacétate de disodium, lauroamphodiacétate de disodium, caprylamphodiacétate de disodium, capryloamphodiacétate de disodium, cocoamphodipropionate de disodium, lauroamphodipropionate de disodium, caprylamphodipropionate de disodium, capryloamphodipropionate de disodium, acide lauroamphodipropionique, acide cocoamphodipropionique. - R a 'represents a C10-C30 alkyl or alkenyl group of an acid R a ' - COOH, preferably present in coconut oil or hydrolyzed linseed oil, an alkyl group, especially a C17 group, and iso form, an unsaturated C 7 group . These compounds are classified in the CTFA dictionary, 5th edition, 1993, under the names cocoamphodiacétate disodium, lauroamphodiacétate disodium, caprylamphodiacétate disodium, capryloamphodiacétate disodium, cocoamphodipropionate disodium, lauroamphodipropionate disodium, caprylamphodipropionate disodium, capryloamphodipropionate disodium, acid lauroamphodipropionic, cocoamphodipropionic acid.
A titre d'exemple, on peut citer le cocoamphodiacétate commercialisé par la société RHODIA sous la dénomination commerciale MIRANOL® C2M concentré. Examples include the cocoamphodiacetate sold by Rhodia under the trade name Miranol ® C2M concentrate.
On peut aussi utiliser des composés de formule (VII) ; It is also possible to use compounds of formula (VII);
Ra"-NHCH(Y")-(CH2)nCONH(CH2)n'-N(Rd)(Re) (VII) R a "-NHCH (Y") - (CH 2 ) n CONH (CH 2 ) n '-N (R d ) (R e ) (VII)
Formule dans laquelle : Formula in which:
- Y" représente le groupe -COOH, -COOZ", -CH2-CH(OH)S03H ou le groupe CH2CH(OH)S03-Z" ; Y "represents the group -COOH, -COOZ", -CH 2 -CH (OH) SO 3 H or the group CH 2 CH (OH) SO 3 -Z ";
- Rd et Re, indépendamment l'un de l'autre, représentent un radical alkyle ou hydroxyalkyle en CrC4 ; - R d and R e , independently of one another, represent a C 1 -C 4 alkyl or hydroxyalkyl radical;
- Z" représente un contre ion cationique issu d'un métal alcalin ou alcalinoterreux, tel que le sodium, un ion ammonium ou un ion issu d'une aminé organique ; Z "represents a cationic counterion derived from an alkaline or alkaline earth metal, such as sodium, an ammonium ion or an ion derived from an organic amine;
- Ra" représente un groupe alkyle ou alcényle en C10-C30 d'un acide Ra"- COOH de préférence présent dans l'huile de coprah ou dans l'huile de lin hydrolysée ; - R a "represents a C10-C30 alkyl or alkenyl group of a R a " - COOH acid, preferably present in coconut oil or in hydrolysed linseed oil;
- n et n', indépendamment l'un de l'autre, désigne un nombre entier allant de 1 à 3. n and n ', independently of each other, denote an integer ranging from 1 to 3.
Parmi les composés de formule (VII) on peut citer le composé classé dans le dictionnaire CTFA sous la dénomination sodium diethylaminopropyl cocoaspartamide et commercialisé par la société CHIMEX sous l'appellation CHIMEXANE HB. Among the compounds of formula (VII), mention may be made of the compound classified in the CTFA dictionary under the name sodium diethylaminopropyl cocoaspartamide and marketed by CHIMEX under the name CHIMEXANE HB.
Ces composés peuvent être utilisés seuls ou en mélanges. These compounds can be used alone or in mixtures.
Parmi les agents tensioactifs amphotères ou zwittérioniques cités ci-dessus, on utilise de préférence les alkyl(C8-C20)bétaïnes telles que la cocobétaïne, les alkyl(C8- C2o)amidoalkyl(C3-C8)bétaïnes telles que la cocamidopropylbétaïne, et leurs mélanges, les composés de formule (VII) tels que le sel de sodium du lauryl amino succinamate de diéthylaminopropyle (nom INCI sodium diethylaminopropyl cocoaspartamide). Among the amphoteric or zwitterionic surfactants mentioned above, alkyl (C 8 -C 20 ) betaines such as cocobetaine, (C 8 -C 2 O) alkylamido (C 3 -C 8 ) alkylbetaines, are preferably used. such as cocamidopropylbetaine, and mixtures thereof, compounds of formula (VII) such as the sodium salt of diethylaminopropyl laurylamino succinamate (INCI name sodium diethylaminopropyl cocoaspartamide).
Parmi tous les agents tensioactifs cités, on préfère utiliser un ou plusieurs agent(s) tensioactif(s) non-ionique(s), de préférence oxyéthyléné(s) tels que les alcools en C4-C40, oxyéthylénés comprenant de 1 à 100 moles d'oxyde d'éthylène, de préférence de 2 à 50, plus particulièrement de 2 à 40 moles d'oxyde d'éthylène, et les tensioactifs anioniques phosphatés tels que les alkyl(C6-C24) ou alkényl(C6-C24) phosphates comprenant de 2 à 50 motifs oxyde d'éthylène. Among all the surfactants mentioned, it is preferred to use one or more surfactant (s) surfactant (s) nonionic (s), preferably oxyethylenated (s) such as oxyethylenated C4-C40 alcohols comprising from 1 to 100 moles of ethylene oxide, preferably from 2 to 50, more particularly from 2 to 40 moles of ethylene oxide, and phosphated anionic surfactants such as alkyls; (C 6 -C 2 4) or alkenyl (C 6 -C 2 4) phosphates comprising from 2 to 50 ethylene oxide units.
Lorsqu'ils sont présents, le ou les agent(s) tensioactif(s) représentent de 0,001 à When present, the surfactant (s) represent from 0.001 to
20 %, de préférence de 0,005 à 15 %, mieux de 0,01 à 10 % en poids, par rapport au poids total de la composition. 20%, preferably from 0.005 to 15%, more preferably from 0.01 to 10% by weight, relative to the total weight of the composition.
La composition peut également comprendre un ou plusieurs épaississants. Au sens de la présente invention, on entend par "épaississant", un agent qui, introduit à 1 % en poids dans une solution aqueuse ou hydroalcoolique à 30% d'éthanol, et à pH=7, permet d'atteindre une viscosité d'au moins 100 mPa.s (100 cPs), de préférence au moins 500 mPa.s (500 cPs), à 25°C et à un taux de cisaillement de 1 s" Cette viscosité peut être mesurée à l'aide d'un viscosimètre cône/plan (Rhéomètre Haake R600 ou analogue). The composition may also comprise one or more thickeners. For the purposes of the present invention, the term "thickener" is understood to mean an agent which, introduced at 1% by weight in an aqueous or aqueous-alcoholic solution containing 30% of ethanol, and at pH = 7, makes it possible to attain a viscosity of at least 100 mPa.s (100 cPs), preferably at least 500 cPs, at 25 ° C and at a shear rate of 1 s " This viscosity can be measured with the aid of a cone / plane viscometer (Haake R600 Rheometer or the like).
Les agents épaississants peuvent être choisis parmi les amides d'acides gras obtenus à partir d'acide carboxylique en C10-C30, tels que le monoisopropanol-, diéthanol- ou monoéthanol-amide d'acide de coprah et le monoéthanolamide d'acide alkyl éther carboxylique oxyéthyléné, les épaississants cellulosiques de préférence non ioniques, tels que l'hydroxyéthylcellulose, l'hydroxypropylcellulose et la carboxyméthylcellulose, la gomme de guar et ses dérivés non ioniques tels que l'hydroxypropylguar, les gommes d'origine microbienne, telles que la gomme de xanthane, la gomme de scléroglucane, les homo- et copolymères réticulés à base d'acide acrylique ou d'acide méthacrylique ou d'acide acrylamidopropanesulfonique, et les polymères associatifs, notamment acryliques ou polyuréthanes, tels que décrits ci-dessous. The thickening agents may be chosen from fatty acid amides obtained from C 10 -C 30 carboxylic acids, such as monoisopropanol, diethanol or coconut acid monoethanol amide and alkyl ether acid monoethanolamide. carboxylic oxyethylenated, preferably nonionic cellulosic thickeners, such as hydroxyethylcellulose, hydroxypropylcellulose and carboxymethylcellulose, guar gum and its nonionic derivatives such as hydroxypropylguar, gums of microbial origin, such as gum xanthan, scleroglucan gum, crosslinked homopolymers and copolymers based on acrylic acid or methacrylic acid or acrylamidopropanesulfonic acid, and associative polymers, especially acrylic or polyurethanes, as described below.
Les polymères associatifs utilisables selon l'invention sont des polymères hydrosolubles ou hydrodispersibles capables, dans un milieu aqueux, de s'associer réversiblement entre eux ou avec d'autres molécules. Leur structure chimique comprend des zones hydrophiles, et des zones hydrophobes caractérisées par la présence d'au moins une chaîne grasse comportant de préférence de 10 à 30 atomes de carbone. Ils peuvent être de type anionique, cationique, amphotère ou non ionique, tels que par exemple les polymères commercialisés sous les appellations PEMULEN TR1 ou TR2 par la société GOODRICH, dont la dénomination INCI est Acrylates/CI O-30 Alkyl Acrylate Crosspolymer, SALCARE SC90 par la société CIBA, ACULYN 22, 28, 33, 44, 46 ou 88 par la société ROHM & HAAS et ELFACOS T210 et T212 par la société AKZO. The associative polymers that can be used according to the invention are water-soluble or water-dispersible polymers capable, in an aqueous medium, of reversibly associating with each other or with other molecules. Their chemical structure comprises hydrophilic zones, and hydrophobic zones characterized by the presence of at least one fatty chain preferably comprising from 10 to 30 carbon atoms. They may be of anionic, cationic, amphoteric or nonionic type, such as, for example, the polymers sold under the names Pemulen TR1 or TR2 by the company Goodrich, whose INCI name is Acrylates / CI O-30 Alkyl Acrylate Crosspolymer, SALCARE SC90 by CIBA, ACULYN 22, 28, 33, 44, 46 or 88 by the company ROHM & HAAS and ELFACOS T210 and T212 by the company AKZO.
Parmi les épaississants cités, on utilise de préférence les épaississants associatifs acryliques. Among the thickeners mentioned, acrylic associative thickeners are preferably used.
S'ils sont présents, les épaississants peuvent être présents en une quantité allant de 0,01 à 20 % en poids, préférentiellement de 0, 1 à 10 % en poids, mieux de 0,2 à 5 % en poids par rapport au poids de la composition les comprenant La composition selon l'invention peut en outre contenir un ou plusieurs additifs choisis parmi les polymères fixants anioniques différents des copolymères acryliques selon l'invention et des polymères fixants anioniques comprenant un monomère d'acide crotonique, les polymères fixants cationiques, les agents conditionneurs tels que les polymères cationiques, les corps gras, les silicones, les céramides et pseudo- céramides, les vitamines et pro-vitamines dont le panthénol, les filtres solaires hydrosolubles et liposolubles, les agents nacrants et opacifiants, les agents séquestrants, les agents solubilisants, les agents anti-oxydants, les hydroxyacides, les agents de pénétration, les parfums, les peptisants, les acides-aminés et les agents conservateurs, seuls ou en mélange, et tout autre additif classiquement utilisé dans le domaine cosmétique. If they are present, the thickeners may be present in an amount ranging from 0.01% to 20% by weight, preferably from 0.1% to 10% by weight, better still from 0.2% to 5% by weight relative to the weight. The composition according to the invention may further contain one or more additives chosen from anionic fixing polymers different from the acrylic copolymers according to the invention and anionic fixing polymers comprising a crotonic acid monomer, the cationic fixing polymers. , conditioning agents such as cationic polymers, fats, silicones, ceramides and pseudo-ceramides, vitamins and pro-vitamins including panthenol, water-soluble and fat-soluble sunscreens, pearlescent and opacifying agents, sequestering agents , solubilizing agents, antioxidants, hydroxy acids, penetrating agents, perfumes, peptizers, amino acids and preservatives, alone or in admixture, and any other additive conventionally used in the cosmetics field.
L'homme de métier veillera à choisir les éventuels additifs et leurs quantités de manière à ce qu'ils ne nuisent pas aux propriétés des compositions de la présente invention. Those skilled in the art will take care to choose the possible additives and their amounts so that they do not adversely affect the properties of the compositions of the present invention.
Ces additifs peuvent être présents dans la composition selon l'invention en une quantité allant de 0 à 20 % en poids par rapport au poids total de la composition. These additives may be present in the composition according to the invention in an amount ranging from 0 to 20% by weight relative to the total weight of the composition.
Les compositions selon l'invention peuvent se présenter entre autres sous forme de liquides plus ou moins épaissis, de gels, de crèmes, de pâtes ou de mousses. The compositions according to the invention may be present inter alia in the form of more or less thickened liquids, gels, creams, pastes or foams.
Les compositions conformes à l'invention peuvent être conditionnées par exemple dans un pot, dans un tube, un flacon pompe ou dans un dispositif aérosol usuel en cosmétique. The compositions in accordance with the invention may be packaged for example in a jar, in a tube, in a pump bottle or in an aerosol device that is usual in cosmetics.
Les compositions selon l'invention peuvent, lorsqu'elles ont destinées à être conditionnées dans un dispositif de type aérosol, contenir un ou plusieurs gaz propulseurs. The compositions according to the invention may, when they are intended to be packaged in an aerosol type device, contain one or more propellants.
Le gaz propulseur peut alors être choisi par exemple parmi les hydrocarbures volatiles, tels que notamment les alcanes en Ci à C4 et de préférence le n-butane, le propane, l'isobutane et leurs mélanges, les hydrocarbures chlorés et/ou fluorés, notamment le 1 , 1 -difluoroéthane, le diméthyléther et les mélanges de ces gaz. De préférence, le gaz propulseur est choisi parmi le 1 , 1 -difluoroéthane, le diméthyléther, le n-butane, le propane, l'isobutane et leurs mélanges. The propellant gas may then be chosen for example from volatile hydrocarbons, such as in particular C 1 -C 4 alkanes and preferably n-butane, propane, isobutane and mixtures thereof, chlorinated and / or fluorinated hydrocarbons, especially 1,1-difluoroethane, dimethyl ether and mixtures of these gases. Preferably, the propellant is selected from 1,1-difluoroethane, dimethyl ether, n-butane, propane, isobutane and mixtures thereof.
Lorsqu'elle en contient, la composition comprend un gaz propulseur dans une teneur allant de 2 à 75 % en poids, plus préférentiellement de 2 à 60 % en poids, par rapport au poids total de ladite composition. When it contains, the composition comprises a propellant in a content ranging from 2 to 75% by weight, more preferably from 2 to 60% by weight, relative to the total weight of said composition.
Lorsque la composition est distribuée sous forme de spray aérosol, la composition comprend un gaz propulseur dans une teneur allant de préférence de 20 à 60 % en poids, par rapport au poids total de ladite composition. When the composition is distributed in the form of an aerosol spray, the composition comprises a propellant in a content preferably ranging from 20 to 60% by weight, relative to the total weight of said composition.
Lorsque la composition est distribuée sous forme de mousse aérosol, la composition comprend un gaz propulseur dans une teneur allant de préférence de 2 à 10% en poids, par rapport au poids total de ladite composition. La présente invention concerne également un procédé pour la mise en forme et/ou le maintien de la coiffure comprenant la mise en œuvre de la composition telle que définie ci-avant. When the composition is distributed in the form of an aerosol foam, the composition comprises a propellant in a content preferably ranging from 2 to 10% by weight, relative to the total weight of said composition. The present invention also relates to a method for shaping and / or maintaining the hairstyle comprising the implementation of the composition as defined above.
En particulier, le procédé de mise en forme et/ou de maintien de la coiffure comporte une étape d'application sur les fibres kératiniques humaines, en particulier les cheveux, secs ou humides, d'une composition telle que définie précédemment pulvérisée, à rincer ou non après un éventuel temps de pose ou après un éventuel séchage. In particular, the method of shaping and / or maintaining the hairstyle comprises a step of application to human keratinous fibers, in particular the hair, dry or wet, of a composition as defined previously pulverized, to rinse or not after a possible exposure time or after any drying.
De préférence, la composition selon l'invention n'est pas rincée. Preferably, the composition according to the invention is not rinsed.
La composition cosmétique selon l'invention peut ainsi être appliquée sur cheveux secs ou humides. De préférence, la composition cosmétique est appliquée sur cheveux propres. The cosmetic composition according to the invention can thus be applied to dry or wet hair. Preferably, the cosmetic composition is applied to clean hair.
Selon un mode de réalisation particulier de l'invention, l'application de la composition peut être suivie d'un séchage à température ambiante ou à une température supérieure à 40°C. According to a particular embodiment of the invention, the application of the composition may be followed by drying at room temperature or at a temperature above 40 ° C.
Le séchage peut être réalisé immédiatement après l'application ou après un temps de pose pouvant aller de 1 minute à 30 minutes. Drying can be carried out immediately after application or after a laying time ranging from 1 minute to 30 minutes.
Selon un mode de réalisation, la composition est appliquée à partir d'un dispositif aérosol. Le dispositif aérosol comprend un récipient pressurisé contenant la composition décrite ci-dessus, le récipient étant surmonté d'un diffuseur. Le récipient peut être équipé d'une valve. Le diffuseur peut être muni d'un orifice de sortie de la composition, notamment d'une buse à orifice simple ou à canaux tourbillonnaires, ou de plusieurs orifices de sortie, notamment trois orifices. According to one embodiment, the composition is applied from an aerosol device. The aerosol device comprises a pressurized container containing the composition described above, the container being surmounted by a diffuser. The container may be equipped with a valve. The diffuser may be provided with an outlet port of the composition, in particular of a nozzle with simple orifice or vortex channels, or of several outlet orifices, in particular three orifices.
Tout type de récipient et système de valve pour composition aérosol est approprié pour la mise en oeuvre de la présente invention. Any type of container and valve system for aerosol composition is suitable for carrying out the present invention.
La présente invention porte aussi sur l'utilisation d'une composition telle que définie ci-avant, pour la mise en forme et/ou le maintien de la coiffure. The present invention also relates to the use of a composition as defined above, for shaping and / or maintaining the hairstyle.
Les exemples qui suivent servent à illustrer l'invention sans toutefois présenter un caractère limitatif. Exemples The examples which follow serve to illustrate the invention without, however, being limiting in nature. Examples
Les compositions suivantes A et B selon l'invention ont été préparées à partir des ingrédients indiqués dans le tableau ci-dessous en gramme de matière active : The following compositions A and B according to the invention were prepared from the ingredients indicated in the table below in gram of active material:
( ' PLASCIZE L-9700U commercialisé par la société GOO CHEMICAL (Copolymère AMP- acrylates/Ci-C-i8 alkylacrylate/C-i-Ce alkylacrylamide/hydroxyéthylacrylate à 38%, Oleth-20 phosphate à 1 %, PPG-7-Buteth-10 à 1 % et éthanol à 60%) PLASCIZE L-9700U sold by the company GOO CHEMICAL (Copolymer AMP-acrylates / Ci-C-18 alkylacrylate / Ci-Ce alkylacrylamide / hydroxyethylacrylate 38%, Oleth-20 phosphate 1%, PPG-7-Buteth-10 at 1% and 60% ethanol)
(2) Resyn 28-2930 commercialisé par la société AKZO NOBEL On a introduit les compositions préparées ci-dessus dans un dispositif de distribution aérosol qui a les caractéristiques suivantes : (2) Resyn 28-2930 sold by the company AKZO NOBEL The compositions prepared above were introduced into an aerosol dispensing device which has the following characteristics:
- une valve équipée d'un gicleur présentant une taille d'orifice de 0,64 mm et une taille d'orifice de restriction interne 0,64 mm, avec une prise de gaz additionnelle de 0,64 mm, a valve equipped with a nozzle having an orifice size of 0.64 mm and an internal restriction orifice size of 0.64 mm, with an additional gas intake of 0.64 mm,
- un diffuseur comprenant trois orifices à sortie directe de 0,4 mm de diamètre. a diffuser comprising three direct-output orifices of 0.4 mm in diameter.
On a vaporisé les compositions sur des cheveux secs. The compositions were sprayed on dry hair.
Avec les compositions A et B, on obtient, après séchage, une chevelure présentant une fixation importante, durable dans le temps. Le toucher est très satisfaisant (douceur, souplesse). Les compositions suivantes C à F selon l'invention peuvent être préparées à partir des ingrédients indiqués dans le tableau ci-dessous en gramme de matière active : Composition de laque selon l'invention : With the compositions A and B, after drying, hair is obtained having a significant fixation, durable over time. The touch is very satisfying (softness, flexibility). The following compositions C to F according to the invention can be prepared from the ingredients indicated in the table below in grams of active material: Lacquer composition according to the invention:
( ' PLASCIZE L-9700U commercialisé par la société GOO CHEMICAL (Copolymère AMP- acrylates/Ci-C-i8 alkylacrylate/C-i-Ce alkylacrylamide/hydroxyéthylacrylate à 38%, Oleth-20 phosphate à 1 %, PPG-7-Buteth-10 à 1 % et éthanol à 60%) ( 'PLASCIZE L-9700U marketed by GOO CHEMICAL (Copolymer AMP-acrylates / Ci-C-i8 alkyl acrylate / alkylacrylamide Ci-Ce / 38% hydroxyethylacrylate, oleth-20 phosphate 1%, PPG-7-Buteth-10 at 1% and 60% ethanol)
(2) LUVISKOL VA 64 commercialisé par la société BASF (2) LUVISKOL VA 64 sold by the company BASF
On peut introduire les compositions ci-dessus dans un dispositif de distribution aérosol. The above compositions can be introduced into an aerosol dispensing device.
On peut utiliser une valve comprenant: A valve may be used comprising:
- un orifice de gicleur de 0,33 mm, - a nozzle orifice of 0.33 mm,
- pas d'orifice de prise de gaz additionnelle, - no additional gas intake port,
- un orifice de restriction interne de 0,33 mm. an internal restriction orifice of 0.33 mm.
On peut utiliser un diffuseur muni d'une buse à canaux tourbillonnaires d'orifice de sortie de 0,45 mm de diamètre. A diffuser with a 0.45 mm diameter outlet channel vortex nozzle can be used.
On peut vaporiser les compositions sur des cheveux secs. The compositions can be sprayed on dry hair.
Composition de mousse selon l'invention : Foam composition according to the invention
E E
Copolymère AMP-acrylates/CrCi8 alkylacrylate/d-AMP-acrylates / CrCi 8 alkylacrylate / d-copolymer
3 3
C8 alkylacrylamide/hydroxyéthylacrylate(1) C 8 alkylacrylamide / hydroxyethylacrylate (1)
Copolymère vinylpyrrolidone / acétate de vinyle 3 (Copolymère AMP- acrylates/Ci-C-i8 alkylacrylate/C-i-Ce alkylacrylamide/hydroxyéthylacrylate à 38%, Oleth-20 phosphate à 1 %, PPG-7-Buteth-10 à 1 % et éthanol à 60%) Vinylpyrrolidone / vinyl acetate copolymer 3 (38% AMP-acrylates / C1-C18alkylacrylate / C1-C18 alkylacrylamide / hydroxyethylacrylate copolymer, 1% Oleth-20 Phosphate, 1% PPG-7-Buteth-10 and 60% Ethanol)
(2) LUVISKOL VA 64 commercialisé par la société BASF (2) LUVISKOL VA 64 sold by the company BASF
On peut introduire la composition ci-dessus dans un dispositif de distribution aérosol comprenant un récipient en aluminium monobloc muni d'un col ogive (45x128). Le récipient est équipé d'une valve Précision P73 sans tube plongeur surmonté d'un poussoir diffuseur axial pour coupelle conique. The above composition can be introduced into an aerosol dispensing device comprising a monoblock aluminum container provided with a warhead (45x128). The container is equipped with a precision valve P73 without dip tube surmounted by an axial diffuser pusher for conical cup.
On peut distribuer la composition sur des cheveux secs ou humides. The composition can be dispensed on dry or wet hair.
Compositions de gel selon l'invention : Gel compositions according to the invention:
( ' PLASCIZE L-9700U commercialisé par la société GOO CHEMICAL (Copolymère AMP- acrylates/Ci-C-i8 alkylacrylate/C-i-Ce alkylacrylamide/hydroxyéthylacrylate à 38%, Oleth-20 phosphate à 1 %, PPG-7-Buteth-10 à 1 % et éthanol à 60%) ( 'PLASCIZE L-9700U marketed by GOO CHEMICAL (Copolymer AMP-acrylates / Ci-C-i8 alkyl acrylate / alkylacrylamide Ci-Ce / 38% hydroxyethylacrylate, oleth-20 phosphate 1%, PPG-7-Buteth-10 at 1% and 60% ethanol)
(2) (2)
PVP K 30L commercialisé par la société ISP PVP K 30L marketed by the company ISP
(4) (4)
Aculyn® 88 vendu par la société Rohm & Haas Aculyn® 88 sold by Rohm & Haas
On a appliqué la composition F préparée ci-dessus sous forme de gel de coiffage sur des cheveux humides. The composition F prepared above was applied as a styling gel to wet hair.
On obtient, après séchage, une chevelure présentant une fixation importante, durable dans le temps. Le toucher est très satisfaisant (douceur, souplesse). En outre, la composition D ne laisse pas de résidus à la surface des cheveux. Les compositions suivantes G et H selon l'invention ont été préparées à partir des ingrédients indiqués dans le tableau ci-dessous en gramme de matière active : Composition de laque selon l'invention : After drying, hair is obtained having a significant fixation, durable over time. The touch is very satisfying (softness, flexibility). In addition, composition D leaves no residue on the surface of the hair. The following compositions G and H according to the invention were prepared from the ingredients indicated in the table below in grams of active material: Lacquer composition according to the invention:
PLASCIZE L-9700U commercialisé par la société GOO CHEMICAL (Copolymère AMP- acrylates/Ci-C-i8 alkylacrylate/C-i-Ce alkylacrylamide/hydroxyéthylacrylate à 38%, Oleth-20 phosphate à 1 %, PPG-7-Buteth-10 à 1 % et éthanol à 60%) PLASCIZE L-9700U marketed by the company GOO CHEMICAL (Copolymer AMP-acrylates / Ci-C-18 alkylacrylate / Ci-Ce alkylacrylamide / hydroxyethylacrylate 38%, Oleth-20 phosphate 1%, PPG-7-Buteth-10 to 1 % and 60% ethanol)
(2) AMPHOMER® commercialisé par la société AKZO NOBEL (2) AMPHOMER® marketed by the company AKZO NOBEL
On a introduit les compositions préparées ci-dessus dans un dispositif de distribution aérosol qui a les caractéristiques suivantes : The compositions prepared above have been introduced into an aerosol dispensing device which has the following characteristics:
- une valve équipée d'un gicleur présentant une taille d'orifice de 0,64 mm et une taille d'orifice de restriction interne 0,64 mm, avec une prise de gaz additionnelle de 0,64 mm, a valve equipped with a nozzle having an orifice size of 0.64 mm and an internal restriction orifice size of 0.64 mm, with an additional gas intake of 0.64 mm,
- un diffuseur comprenant trois orifices à sortie directe de 0,4 mm de diamètre. a diffuser comprising three direct-output orifices of 0.4 mm in diameter.
On a vaporisé les compositions sur des cheveux secs. The compositions were sprayed on dry hair.
On obtient, après séchage, une chevelure présentant une fixation importante, durable dans le temps. Le toucher est très satisfaisant (douceur, souplesse). After drying, hair is obtained having a significant fixation, durable over time. The touch is very satisfying (softness, flexibility).
Claims
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR1363196A FR3015269B1 (en) | 2013-12-20 | 2013-12-20 | COMPOSITION COMPRISING A PARTICULAR ACRYLIC COPOLYMER AND A POLYMER FIXING AMPHOTERE |
| FR1363193A FR3015266B1 (en) | 2013-12-20 | 2013-12-20 | COMPOSITION COMPRISING A PARTICULAR ACRYLIC COPOLYMER AND A NON-SILICONE NONIONIC FIXING POLYMER |
| FR1363194A FR3015267B1 (en) | 2013-12-20 | 2013-12-20 | COMPOSITION COMPRISING A PARTICULAR ACRYLIC COPOLYMER AND ANIONIC FIXING POLYMER COMPRISING A MONOMER OF CROTONIC ACID |
| PCT/FR2014/053457 WO2015092322A2 (en) | 2013-12-20 | 2014-12-19 | Composition containing a specific acrylic copolymer and an anionic fixing polymer that contains a crotonic acid monomer |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP3082967A2 true EP3082967A2 (en) | 2016-10-26 |
Family
ID=52469230
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP14835708.0A Withdrawn EP3082967A2 (en) | 2013-12-20 | 2014-12-19 | Composition comprising a specific acrylic copolymer and a fixing polymer chosen from anionic fixing polymers comprising crotonic acid as a monomer, non ionic and non silicone fixing polymers, and amphoteric fixing polymers |
Country Status (2)
| Country | Link |
|---|---|
| EP (1) | EP3082967A2 (en) |
| WO (1) | WO2015092322A2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR3141334A1 (en) * | 2022-10-28 | 2024-05-03 | L'oreal | AEROSOL DEVICE BASED ON ANIONIC FIXING POLYMER, DIRECT DYE, MONOALCOHOL AND A HALOGENATED HYDROCARBON |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1400366A (en) | 1963-05-15 | 1965-05-28 | Oreal | New compounds which can be used in particular for the treatment of hair |
| GB1567947A (en) | 1976-07-02 | 1980-05-21 | Unilever Ltd | Esters of quaternised amino-alcohols for treating fabrics |
| DE3623215A1 (en) | 1986-07-10 | 1988-01-21 | Henkel Kgaa | NEW QUARTERS OF AMMONIUM COMPOUNDS AND THEIR USE |
| JP4104790B2 (en) * | 1999-08-10 | 2008-06-18 | 日本エヌエスシー株式会社 | Cosmetics |
| ATE248574T1 (en) * | 2001-12-01 | 2003-09-15 | Wella Ag | HAIR TREATMENT WITH A COMBINATION OF THREE POLYMERS |
| JP5164318B2 (en) | 2005-08-31 | 2013-03-21 | 株式会社アリミノ | Hairdressing composition |
| JP2007217314A (en) | 2006-02-15 | 2007-08-30 | Kracie Home Products Kk | Misty hair cosmetics |
| JP4930683B2 (en) | 2006-02-23 | 2012-05-16 | ライオン株式会社 | Hair cosmetic composition |
| JP4889795B2 (en) * | 2009-04-28 | 2012-03-07 | 株式会社 資生堂 | Hairdressing cosmetics |
| JP5557234B2 (en) * | 2009-07-17 | 2014-07-23 | 株式会社 資生堂 | Aerosol hair cosmetics |
| WO2013081055A1 (en) * | 2011-11-29 | 2013-06-06 | ライオン株式会社 | Deodorant composition |
-
2014
- 2014-12-19 WO PCT/FR2014/053457 patent/WO2015092322A2/en not_active Ceased
- 2014-12-19 EP EP14835708.0A patent/EP3082967A2/en not_active Withdrawn
Non-Patent Citations (2)
| Title |
|---|
| None * |
| See also references of WO2015092322A2 * |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2015092322A3 (en) | 2015-08-27 |
| WO2015092322A2 (en) | 2015-06-25 |
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