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EP1096060A1 - Composition résistante à la froissure - Google Patents

Composition résistante à la froissure Download PDF

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Publication number
EP1096060A1
EP1096060A1 EP99870223A EP99870223A EP1096060A1 EP 1096060 A1 EP1096060 A1 EP 1096060A1 EP 99870223 A EP99870223 A EP 99870223A EP 99870223 A EP99870223 A EP 99870223A EP 1096060 A1 EP1096060 A1 EP 1096060A1
Authority
EP
European Patent Office
Prior art keywords
composition
fabric
water
polymers
fabrics
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.)
Withdrawn
Application number
EP99870223A
Other languages
German (de)
English (en)
Inventor
Markus W. Altmann
Bruno Albert Jean Hubesch
Heidi Simonne Mariette Soyez
Els Goossens
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Procter and Gamble Co
Original Assignee
Procter and Gamble Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Procter and Gamble Co filed Critical Procter and Gamble Co
Priority to EP99870223A priority Critical patent/EP1096060A1/fr
Priority to PCT/US2000/029769 priority patent/WO2001031112A2/fr
Priority to AU12426/01A priority patent/AU1242601A/en
Priority to CA002386928A priority patent/CA2386928A1/fr
Priority to CZ20021397A priority patent/CZ20021397A3/cs
Priority to JP2001533243A priority patent/JP2003513176A/ja
Priority to MXPA02004210A priority patent/MXPA02004210A/es
Priority to EP00973987A priority patent/EP1238137A2/fr
Publication of EP1096060A1 publication Critical patent/EP1096060A1/fr
Priority to US10/924,539 priority patent/US20050015888A1/en
Withdrawn legal-status Critical Current

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Classifications

    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M23/00—Treatment of fibres, threads, yarns, fabrics or fibrous goods made from such materials, characterised by the process
    • D06M23/06—Processes in which the treating agent is dispersed in a gas, e.g. aerosols
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
    • D06M13/224—Esters of carboxylic acids; Esters of carbonic acid
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
    • D06M13/224—Esters of carboxylic acids; Esters of carbonic acid
    • D06M13/2243—Mono-, di-, or triglycerides
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/01—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with natural macromolecular compounds or derivatives thereof
    • D06M15/03—Polysaccharides or derivatives thereof
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/263—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/263—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
    • D06M15/267—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof of unsaturated carboxylic esters having amino or quaternary ammonium groups
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/285—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acid amides or imides
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/356—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of other unsaturated compounds containing nitrogen, sulfur, silicon or phosphorus atoms
    • D06M15/3562—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of other unsaturated compounds containing nitrogen, sulfur, silicon or phosphorus atoms containing nitrogen
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/53—Polyethers
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/564—Polyureas, polyurethanes or other polymers having ureide or urethane links; Precondensation products forming them
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/643—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
    • D06M15/647—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain containing polyether sequences
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M7/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made of other substances with subsequent freeing of the treated goods from the treating medium, e.g. swelling, e.g. polyolefins
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
    • D06M2200/20—Treatment influencing the crease behaviour, the wrinkle resistance, the crease recovery or the ironing ease
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
    • D06M2200/40—Reduced friction resistance, lubricant properties; Sizing compositions

Definitions

  • the present invention relates to fabric care compositions and to a method for treating fabrics in order to improve various properties of fabrics, in particular in-wear wrinkle resistance.
  • Wrinkles in textile fabrics are caused by the bending and creasing of the textile material which places an external portion of a filament in a yarn under tension while the internal portion of that filament in the yarn is placed under compression.
  • the hydrogen bonding that occurs between the cellulose molecules contributes to keeping wrinkles in place.
  • the wrinkling of fabric, in particular clothing, is therefore subject to the inherent tensional elastic deformation and recovery properties of the fibers which constitute the yarn and fabrics.
  • U.S. 5,532,023 discloses aqueous wrinkle control compositions containing non-volatile silicone and film forming polymer.
  • Preferred silicones include reactive silicones and amino-functional silicone, known as "amodimethicone".
  • the composition containing such silicones is applied to fabric from a spray dispenser. It is found that in the spray treatment, an appreciable amount of the aqueous composition misses the fabric, and instead falls on flooring surfaces, such as rugs, carpets, concrete floors, tiled floors, linoleum floors, bathtub floors, which leaves a silicone layer that is accumulated on and/or cured on and/or bonded to the flooring surfaces.
  • U.S. 5,573,695 discloses an aqueous wrinkle removal composition containing a vegetable oil based cationic quaternary ammonium surfactant, and an anionic fluorosurfactant.
  • U.S. 4,661,268 discloses a wrinkle removal spray comprising an aqueous alcoholic composition containing a dialkyl quaternary ammonium salt and a silicone surfactant and/or a fluoro surfactant.
  • 5,100,566 discloses a method of reducing wrinkles in fabric by spraying the fabric with an aqueous alcoholic solution of an anionic siliconate alkali metal salt.
  • U.S. 4,806,254 discloses fabric wrinkle removal aqueous alcoholic solution containing glycerine and a nonionic surfactant.
  • WO98/04772 provides the treatment of fabric against fabric creasing by application of a composition comprising a polycarboxylic acid or derivative thereof; and then curing the composition using a domestic process.
  • Starch is also a conventional ingredient of dewrinkling compositions. However, while starch provides a suitable visual benefit onto the treated fabrics, it also gives fabric with an undesired stiff or starchy feeling.
  • the present invention reduces wrinkles in fabrics, including clothing, dry cleanables, linens, bed clothes, and draperies, by ironing.
  • the present invention can be used on damp or dry clothing to relax wrinkles and give clothes a ready to wear look with lasting benefits that is demanded by today's fast paced world.
  • an additional benefit of the composition of the present invention is an improved garment shape, body and crispness.
  • composition of the present invention acts as an excellent ironing aid.
  • the present invention makes the task of ironing easier and faster by creating less iron drag.
  • the compositions of the present invention help produce a crisp, smooth appearance.
  • the present invention is a wrinkle reducing composition
  • a wrinkle reducing composition comprising a water-soluble lubricant and a component having a deviation of fabric Wrinkle Recovery angle (WRA) versus water of at least +15.
  • WRA fabric Wrinkle Recovery angle
  • an article of manufacture comprising a container and the composition of the invention in association with instructions to use.
  • One essential component of the invention is a water-soluble lubricant.
  • the composition provides an ease of ironing whilst still avoiding the staining of fabric and/or presenting safety hazard to the household members.
  • water-soluble is defined as "a component which when dissolved in water at a level of 0.2% by weight, or less, at 25° C, forms a clear, isotropic liquid".
  • Typical water-soluble lubricants include components selected from nonionic silicone containing surfactants, sorbitan esters, ethoxylated sorbitan esters, and mixtures thereof.
  • the water-soluble lubricants are preferably present in an amount of from 0.1% to 70% by weight of the composition, more preferably of from 1 to 10% % by weight of the composition for diluted composition and of from 20 to 50% by weight of the composition for concentrated compositions.
  • a preferred class of nonionic silicone containing surfactants are the polyalkylene oxide polysiloxanes having a dimethyl polysiloxane hydrophobic moiety and one or more hydrophilic polyalkylene side chains, and having the general formula: R1-(CH3)2SiO-[(CH3)2SiO]a-[(CH3)(R1)SiO]b-Si(CH3)2-R1 wherein a + b are from about 1 to about 50, preferably from about 1 to about 30 , more preferably from about 1 to about 25, and each R1 is the same or different and is selected from the group consisting of methyl and a poly(ethyleneoxide/propyleneoxide) copolymer group having the general formula: -(CH2)n O(C2 H4 O)c (C3 H6 O)d R2 with at least one R1 being a poly(ethyleneoxy/propyleneoxy) copolymer group, and wherein n is 3 or 4, preferably 3; total c (for all poly
  • Nonlimiting examples of this type of surfactants are the Silwet® surfactants which are available OSI Specialties Inc., a Division of Witco, Danbury, Connecticut.
  • Representative Silwet® surfactants which contain only ethyleneoxy (C2H4O) groups are as follows. Name Average MW Average a+b Average total c L-7608 600 1 8 L-7607 1,000 2 17 L-77 600 1 9 L-7605 6,000 20 99 L-7604 4,000 21 53 L-7600 4,000 11 68 L-7657 5,000 20 76 L-7602 3,000 20 29 L-7622 10,000 88 75
  • Nonlimiting examples of Silwet® surfactants which contain both ethyleneoxy (C2 H4 O) and propyleneoxy (C3 H6 O) groups are as follows. Name Average MW EO/PO ratio L-720 12,000 50/50 L-7001 20,000 40/60 L-7002 8,000 50/50 L-7210 13,000 20/80 L-7200 19,000 75/25 L-7220 17,000 20/80
  • the molecular weight of the polyalkyleneoxy group (R1) is less than or equal to about 10,000.
  • the molecular weight of the polyalkyleneoxy group is less than or equal to about 8,000, and most preferably ranges from about 300 to about 5,000.
  • the values of c and d can be those numbers which provide molecular weights within these ranges.
  • the number of ethyleneoxy units (-C2H4O) in the polyether chain (R1) must be sufficient to render the polyalkylene oxide polysiloxane water soluble. If propyleneoxy groups are present in the polyalkylenoxy chain, they can be distributed randomly in the chain or exist as blocks.
  • Silwet® surfactants which contain both ethyleneoxy and propyleneoxy groups, are also preferred.
  • Preferred Silwet® surfactants are the L-7001, L-7087, L-7200, L-7280, L-7600, L-7608, L-7622, L-7657.
  • polyalkylene oxide polysiloxanes of the present invention can be prepared according to the procedure set forth in U.S. Pat. No. 3,299,112, incorporated herein by reference.
  • polyalkylene oxide polysiloxanes of the surfactant blend of the present invention are readily prepared by an addition reaction between a hydrosiloxane (i.e., a siloxane containing silicon-bonded hydrogen) and an alkenyl ether (e.g., a vinyl, allyl, or methallyl ether) of an alkoxy or hydroxy end-blocked polyalkylene oxide).
  • a hydrosiloxane i.e., a siloxane containing silicon-bonded hydrogen
  • an alkenyl ether e.g., a vinyl, allyl, or methallyl ether
  • reaction conditions employed in addition reactions of this type are well known in the art and in general involve heating the reactants (e.g., at a temperature of from about 85° C. to 110° C.) in the presence of a platinum catalyst (e.g., chloroplatinic acid) and a solvent (e.g., toluene).
  • a platinum catalyst e.g., chloroplatinic acid
  • a solvent e.g., toluene
  • Still other preferred water-soluble lubricants of the nonionic type are those from the class of sorbitan esters and/or alkylethoxylate sorbitan ester. These ethoxylated sorbitan esters are formed by ethoxylation of sorbitan or its cyclic derivative sorbitan, followed by esterification of one of the available hydroxy groups to introduce one long chain alkyl or alkenyl group, leaving the remaining hydroxy groups free.
  • a component having a deviation of fabric WRA of at least +15 is another essential component of the invention.
  • these components are present in an amount of at least about 0.01%, preferably from about 0.1% to about 20% by weight of the composition, preferably to about 4% by weight of the diluted composition, preferably to about 12% by weight of the concentrated composition.
  • the WRA Test method is taken from the AATCC 66-1990. This method is an American National Standard method designed for the determination of the wrinkle recovery of woven fabrics, whereby a test specimen, creased and compressed under controlled conditions of time and load, is suspended in the test instrument for a controlled recovery period, after which the recovery angle is measured. Experimental detail on how to measure this WRA is given in AATCC 66-1990, incorporated herein by reference.
  • the WRA method is tested on 100% cotton, woven Oxford pinpoint fabric, free from wrinkles, cut in twelve specimens of 0.59 inch x 1.57 inch, six with their long dimension parallel to the warp, and six with their long dimensional parallel to the filling.
  • the test is carried out on cloth conditioned for 24 hours at 21°C (70°F) and 65% RH. Three specimens from each set are creased on one side and three on the other. Tweezers are used to place the test specimen between the leaves of the specimen holder (2 superimposed leaves 0.63 inch wide, but of different lengths and fastened together at one end) with one end directly under the 0.71-inch mark. With the tweezers, the exposed end of the specimen is lifted over and looped back to the 0.71-inch mark on the shorter, thin metal leaf and holded with the left thumbnail.
  • the holder with the specimen is inserted into a plastic press (2 superimposed leaves of equal length (3.74 inch) and 0.79 inch wide, fastened together at one end ) and a weight of 500g is applied for 5 minutes so that a crease is formed.
  • the plastic press can then be removed and the specimen holder combination can be inserted in the tester with the exposed end of the specimen holder in the mount on the face of the tester.
  • the crease should line up with a spot at the centre of the tester disk, and the dangling specimen leg should be lined up immediately with the vertical guide line. In order to eliminate gravitation effects, keep the dangling specimen leg aligned with the vertical guide line during the 5-min recovery period. Adjust every 15 seconds for the first minute, and once a minute thereafter. Five minutes after the removal of the creasing load, the wrinkle recovery value is read to the nearest degree from the scale. The sum is taken of the average recovery for all warp readings and all filling readings and compared with a cloth treated with water.
  • the fabric WRA obtained with the tested component is compared with the fabric WRA obtained with water, thereby giving a deviation ⁇ .
  • a component which provide a ⁇ of at least positive(+)15, preferably having a ⁇ within the range of 15-30 is a component suitable for the invention.
  • Preferred components which have a deviation of fabric WRA versus water of at least 15 are selected from shape retention polymers, polymers comprising at least one unit which provide a dye transfer inhibiting benefit, polyurethanes, polyamine polymers, Isomaltooligosaccharide, and mixtures thereof. Most preferred are the polymers which are water-soluble.
  • polymers can be natural, or synthetic, and can act by forming a film, and/or by providing adhesive properties.
  • the present invention can optionally use film-forming and/or adhesive polymer to impart shape retention to fabric, particularly clothing.
  • adheresive it is meant that when applied as a solution or a dispersion to a fiber surface and dried, the polymer can attach to the surface.
  • the polymer can form a film on the surface, or when residing between two fibers and in contact with the two fibers, it can bind the two fibers together.
  • Other polymers such as Isomaltose Oligosaccharide can form a film and/or bond the fibers together when the treated fabric is pressed by a hot iron. Such a film will have adhesive strength, cohesive breaking strength, and cohesive breaking strain.
  • Nonlimiting examples for natural polymers are Isomaltose Oligosaccharide and their derivatives, and chitins and their derivatives.
  • the synthetic polymers useful in the present invention are comprised of monomers.
  • monomers which can be used to form the synthetic polymers of the present invention include: low molecular weight C 1 -C 6 unsaturated organic mono-carboxylic and polycarboxylic acids, such as acrylic acid, methacrylic acid, crotonic acid, maleic acid and its half esters, itaconic acid, and mixtures thereof; esters of said acids with C 1 -C 12 alcohols, such as methanol, ethanol, 1-propanol, 2-propanol, 1-butanol, 2-methyl-1-propanol, 1-pentanol, 2-pentanol, 3-pentanol, 2-methyl-1-butanol, 1-methyl-1-butanol, 3-methyl-1-butanol, 1-methyl-1-pentanol, 2-methyl-1-pentanol, 3-methyl-1-pentanol, t-butanol, cyclohexanol, 2-ethyl,
  • Nonlimiting examples of said esters are methyl acrylate, ethyl acrylate, t-butyl acrylate, methyl methacrylate, hydroxyethyl methacrylate, methoxy ethyl methacrylate, and mixtures thereof; amides and imides of said acids, such as N,N-dimethylacrylamide, N-t-butyl acrylamide, maleimides; low molecular weight unsaturated alcohols such as vinyl alcohol (produced by the hydrolysis of vinyl acetate after polymerization), allyl alcohol; esters of said alcohols with low molecular weight carboxylic acids, such as, vinyl acetate, vinyl propionate; ethers of said alcohols such as methyl vinyl ether; aromatic vinyl such as styrene, alpha-methylstyrene, t-butylstyrene, vinyl toluene, polystyrene macromer, and the like; polar vinyl heterocyclics, such as vinyl pyrroli
  • said monomers are selected from the group consisting of vinyl alcohol; acrylic acid; methacrylic acid; methyl acrylate; ethyl acrylate; methyl methacrylate; t-butyl acrylate; t-butyl methacrylate; n-butyl acrylate; n-butyl methacrylate; isobutyl methacrylate; 2-ethylhexyl methacrylate; dimethylaminoethyl methacrylate; N,N-dimethyl acrylamide; N,N-dimethyl methacrylamide; N-t-butyl acrylamide; vinylpyrrolidone; vinyl pyridine; adipic acid; diethylenetriamine; salts thereof and alkyl quaternized derivatives thereof, and mixtures thereof.
  • said monomers form homopolymers and/or copolymers (i.e., the film-forming and/or adhesive polymer) having a glass transition temperature (Tg) of from about -20°C to about 150°C, preferably from about -10°C to about 150°C, more preferably from about 0°C to about 100°C, most preferably, the adhesive polymer hereof, when dried to form a film will have a Tg of at least about 25°C., so that they are not unduly sticky, or "tacky" to the touch.
  • said polymer is soluble and/or dispersible in water and/or alcohol.
  • Said polymer typically has a molecular weight of at least about 500, preferably from about 1,000 to about 2,000,000, more preferably from about 5,000 to about 1,000,000, and even more preferably from about 30,000 to about 300,000 for some polymers.
  • adipic acid/dimethylaminohydroxypropyl diethylenetriamine copolymer adipic acid/epoxypropyl diethylenetriamine copolymer
  • polyvinyl alcohol polyvinylpyridine n-oxide; methacryloyl ethyl betaine/methacrylates copolymer; ethyl acrylate/methyl methacrylate/methacrylic acid/acrylic acid copolymer
  • polyamine resins; and polyquaternary amine resins poly(ethenylformamide); poly(vinylamine) hydrochloride; poly(vinyl alcohol-co-6% vinylamine); poly(vinyl alcohol-co-12% vinylamine); poly(vinyl alcohol-co-6% vinylamine hydrochloride
  • said copolymer and/or homopolymers are selected from the group consisting of adipic acid/dimethylaminohydroxypropyl diethylenetriamine copolymer; poly(vinylpyrrolidone/dimethylaminoethyl methacrylate); polyvinyl alcohol; ethyl acrylate/methyl methacrylate/methacrylic acid/acrylic acid copolymer; methacryloyl ethyl betaine/methacrylates copolymer; polyquaternary amine resins; poly(ethenylformamide); poly(vinylamine) hydrochloride; poly(vinyl alcohol-co-6% vinylamine); poly(vinyl alcohol-co-12% vinylamine); poly(vinyl alcohol-co-6% vinylamine hydrochloride); and poly(vinyl alcohol-co-12% vinylamine hydrochloride).
  • adipic acid/dimethylaminohydroxypropyl diethylenetriamine copolymer poly(vinylpyrrol
  • Preferred polymers useful in the present invention are selected from the group consisting of copolymers of hydrophilic monomers and hydrophobic monomers.
  • the polymer can be linear random or block copolymers, and mixtures thereof.
  • Such hydrophobic/hydrophilic copolymers typically have a hydrophobic monomer/hydrophilic monomer ratio of from about 95:5 to about 20:80, preferably from about 90:10 to about 40:60, more preferably from about 80:20 to about 50:50 by weight of the copolymer.
  • the hydrophobic monomer can comprise a single hydrophobic monomer or a mixture of hydrophobic monomers
  • the hydrophilic monomer can comprise a single hydrophilic monomer or a mixture of hydrophilic monomers.
  • hydrophobic is used herein consistent with its standard meaning of lacking affinity for water, whereas “hydrophilic” is used herein consistent with its standard meaning of having affinity for water.
  • hydrophobic means substantially water insoluble; “hydrophilic” means substantially water soluble.
  • substantially water insoluble shall refer to a material that is not soluble in distilled (or equivalent) water, at 25°C., at a concentration of about 0.2% by weight, and preferably not soluble at about 0.1% by weight (calculated on a water plus monomer or polymer weight basis).
  • substantially water soluble shall refer to a material that is soluble in distilled (or equivalent) water, at 25°C., at a concentration of about 0.2% by weight, and are preferably soluble at about 1% by weight.
  • soluble corresponds to the maximum concentration of monomer or polymer, as applicable, that can dissolve in water or other solvents to form a homogeneous solution, as is well understood to those skilled in the art.
  • Nonlimiting examples of useful hydrophobic monomers are acrylic acid C 1 -C 18 alkyl esters, such as methyl acrylate, ethyl acrylate, t-butyl acrylate; methacrylic C 1 -C 18 alkyl esters, such as methyl methacrylate, 2-ethyl hexyl methacrylate, methoxy ethyl methacrylate; vinyl alcohol esters of carboxylic acids, such as, vinyl acetate, vinyl propionate, vinyl neodecanoate; aromatic vinyls, such as styrene, t-butyl styrene, vinyl toluene; vinyl ethers, such as methyl vinyl ether; vinyl chloride; vinylidene chloride; ethylene, propylene and other unsaturated hydrocarbons; and the like; and mixtures thereof.
  • acrylic acid C 1 -C 18 alkyl esters such as methyl acrylate, ethyl acrylate, t-
  • Some preferred hydrophobic monomers are methyl acrylate, methyl methacrylate, t-butyl acrylate, t-butyl methacrylate, n-butyl acrylate, n-butyl methacrylate, and mixtures thereof.
  • Nonlimiting examples of useful hydrophilic monomers are unsaturated organic mono-carboxylic and polycarboxylic acids, such as acrylic acid, methacrylic acid, crotonic acid, maleic acid and its half esters, itaconic acid; unsaturated alcohols, such as vinyl alcohol, allyl alcohol; polar vinyl heterocyclics, such as vinyl pyrrolidone, vinyl caprolactam, vinyl pyridine, vinyl imidazole; vinyl amine; vinyl sulfonate; unsaturated amides, such as acrylamides, e.g., N,N-dimethylacrylamide, N-t-butyl acrylamide; hydroxyethyl methacrylate; dimethylaminoethyl methacrylate; salts of acids and amines listed above; and the like; and mixtures thereof.
  • unsaturated organic mono-carboxylic and polycarboxylic acids such as acrylic acid, methacrylic acid, crotonic acid, maleic acid and its half esters
  • Some preferred hydrophilic monomers are acrylic acid, methacrylic acid, N,N-dimethyl acrylamide, N,N-dimethyl methacrylamide, N-t-butyl acrylamide, dimethylamino ethyl methacrylate, vinyl pyrrolidone, salts thereof and alkyl quaternized derivatives thereof, and mixtures thereof.
  • the shape retention copolymers contain hydrophobic monomers and hydrophilic monomers which comprise unsaturated organic mono-carboxylic and polycarboxylic acid monomers, such as acrylic acid, methacrylic acid, crotonic acid, maleic acid and its half esters, itaconic acid, and salts thereof, and mixtures thereof; and optionally other hydrophilic monomers.
  • unsaturated organic mono-carboxylic and polycarboxylic acid monomers such as acrylic acid, methacrylic acid, crotonic acid, maleic acid and its half esters, itaconic acid, and salts thereof, and mixtures thereof; and optionally other hydrophilic monomers.
  • hydrophilic unsaturated organic mono-carboxylic and polycarboxylic acid monomers are acrylic acid, methacrylic acid, crotonic acid, maleic acid and its half esters, itaconic acid, and mixtures thereof.
  • Nonlimiting examples of the hydrophobic monomers are esters of the unsaturated organic mono-carboxylic and polycarboxylic acids cited hereinabove with C 1 -C 12 alcohols, such as methanol, ethanol, 1-propanol, 2-propanol, 1-butanol, 2-methyl-1-propanol, 1-pentanol, 2-pentanol, 3-pentanol, 2-methyl-1-butanol, 1-methyl-1-butanol, 3-methyl-1-butanol, 1-methyl-1-pentanol, 2-methyl-1-pentanol, 3-methyl-1-pentanol, t-butanol, cyclohexanol, 2-ethyl-1-butanol, and mixtures thereof, preferably methanol, ethanol, 1-propanol, 2-propanol, 1-butanol, 2-methyl-1-propanol, t-butanol, and mixtures thereof.
  • compositions containing these polymers also can additionally comprise perfume, antibacterial active, odor control agent, static control agent, and mixtures thereof.
  • Highly preferred adhesive and/or film forming polymers that are useful in the composition of the present invention actually contain silicone moieties in the polymers themselves.
  • These preferred polymers include graft and block copolymers of silicone with moieties containing hydrophilic and/or hydrophobic monomers described hereinbefore.
  • the silicone-containing copolymers in the composition of the present invention provide shape retention, body, and/or good, soft fabric feel.
  • Suitable silicone copolymers include the following:
  • Preferred silicone-containing polymers are the silicone graft copolymers comprising acrylate groups described, along with methods of making them, in U.S. Patent No. 5,658,557, Bolich et al., issued Aug. 19, 1997, U.S. Patent No. 4,693,935, Mazurek, issued Sept. 15, 1987, and U.S. Patent No. 4,728,571, Clemens et al., issued Mar. 1, 1988. Additional silicone-containing polymers are disclosed in U.S. Pat. Nos. 5,480,634, Hayama et al, issued Oct. 2, 1996, 5,166,276, Hayama et al., issued Nov. 24, 1992, 5,061,481, issued Oct.
  • These polymers preferably include copolymers having a vinyl polymeric backbone having grafted onto it monovalent siloxane polymeric moieties, and components consisting of non-silicone hydrophilic and hydrophobic monomers.
  • the silicone-containing monomers are exemplified by the general formula: X(Y) n Si(R) 3-m Z m wherein X is a polymerizable group, such as a vinyl group, which is part of the backbone of the polymer; Y is a divalent linking group; R is a hydrogen, hydroxyl, lower alkyl (e.g.
  • Z is a monovalent polymeric siloxane moiety having an average molecular weight of at least about 500, is essentially unreactive under copolymerization conditions, and is pendant from the vinyl polymeric backbone described above; n is 0 or 1; and m is an integer from 1 to 3.
  • the preferred silicone-containing monomer has a weight average molecular weight of from about 1,000 to about 50,000, preferably from about 3,000 to about 40,000, most preferably from about 5,000 to about 20,000.
  • Nonlimiting examples of preferred silicone-containing monomers have the following formulas: X-Si(R 1 ) 3-m Z m
  • Silicone-containing adhesive and/or film-forming copolymers useful in the present invention comprise from 0% to about 90%, preferably from about 10% to about 80%, more preferably from about 40% to about 75% of hydrophobic monomer, from about 0% to about 90%, preferably from about 5% to about 80% of hydrophilic monomer, and from about 5% to about 50%, preferably from about 10% to about 40%, more preferably from about 15% to about 25% of silicone-containing monomer.
  • any particular copolymer will help determine its formulation properties.
  • the copolymer can be optimized for inclusion in specific vehicles.
  • polymers which are soluble in an aqueous formulation preferably contain from 0% to about 70%, preferably from about 5% to about 70% of hydrophobic monomer, and from about 30% to about 98%, preferably from about 30% to about 80%, of hydrophilic monomer, and from about 1% to about 40% of silicone-containing monomer.
  • Polymers which are dispersible preferably contain from 0% to about 70%, more preferably from about 5% to about 70%, of hydrophobic monomer, and from about 20% to about 80%, more preferably from about 20% to about 60%, of hydrophilic monomer, and from about 1% to about 40% of silicone-containing monomer.
  • the silicone-containing copolymers preferably have a weight average molecular weight of from about 10,000 to about 1,000,000, preferably from about 30,000 to about 300,000.
  • the preferred polymers comprise a vinyl polymeric backbone, preferably having a Tg or a Tm as defined above of about -20°C. and, grafted to the backbone, a polydimethylsiloxane macromer having a weight average molecular weight of from about 1,000 to about 50,000, preferably from about 5,000 to about 40,000, most preferably from about 7,000 to about 20,000.
  • the polymer is such that when it is formulated into the finished composition, and then dried, the polymer phase separates into a discontinuous phase which includes the polydimethylsiloxane macromer and a continuous phase which includes the backbone.
  • Exemplary silicone grafted polymers for use in the present invention include the following, where the composition of the copolymer is given with the approximate weight percentage of each monomer used in the polymerization reaction to prepare the copolymer: N,N-dimethylacrylamide/isobutyl methacrylate/(PDMS macromer - 20,000 approximate molecular weight) (20/60/20 w/w/w), copolymer of average molecular weight of about 400,000; N,N-dimethylacrylamide/(PDMS macromer -20,000 approximate molecular weight) (80/20 w/w), copolymer of average molecular weight of about 300,000; and t-butylacrylate/N,N-dimethylacrylamide/(PDMS macromer - 10,000 approximate molecular weight) (70/10/20), copolymer of average molecular weight of about 400,000.
  • Highly preferred shape retention copolymers of this type contain hydrophobic monomers, silicone-containing monomers and hydrophilic monomers which comprise unsaturated organic mono- and polycarboxylic acid monomers, such as acrylic acid, methacrylic acid, crotonic acid, maleic acid and its half esters, itaconic acid, and salts thereof, and mixtures thereof. These preferred polymers surprisingly provide control of certain amine type malodors in fabrics, in addition to providing the fabric wrinkle control benefit.
  • a nonlimiting example of such copolymer is n-butylmethacrylate /acrylic acid/(polydimethylsiloxane macromer, 20,000 approximate molecular weight) copolymer of average molecular weight of about 100,000, and with an approximate monomer weight ratio of about 70/10/20.
  • a highly preferred copolymer is composed of acrylic acid, t-butyl acrylate and silicone-containing monomeric units, preferably with from about 20% to about 90%, preferably from about 30% to about 80%, more preferably from about 50% to about 75% t-butyl acrylate; from about 5% to about 60%, preferably from about 8% to about 45%, more preferably from about 10% to about 30% of acrylic acid; and from about 5% to about 50%, preferably from about 10% to about 40%, more preferably from about 15% to about 30% of polydimethylsiloxane of an average molecular weight of from about 1,000 to about 50,000, preferably from about 5,000 to about 40,000, most preferably from about 7,000 to about 20,000.
  • Nonlimiting examples of acrylic acid/tert-butyl acrylate/polydimethyl siloxane macromer copolymers useful in the present invention, with approximate monomer weight ratio, are: t-butylacrylate/acrylic acid/(polydimethylsiloxane macromer, 10,000 approximate molecular weight) (70/10/20 w/w/w), copolymer of average molecular weight of about 300,000; t-butyl acrylate/acrylic acid/(polydimethylsiloxane macromer, 10,000 approximate molecular weight) (63/20/17), copolymer of average molecular weight of from about 120,000 to about 150,000; and n-butylmethacrylate/acrylic acid/ (polydimethylsiloxane macromer - 20,000 approximate molecular weight) (70/10/20 w/w/w), copolymer of average molecular weight of about 100,000.
  • a useful and commercially available copolymer of this type is Diahold ® ME from Mitsubishi Chemical Corp., which is a t-butyl acrylate/acrylic acid/ (polydimethylsiloxane macromer, 12,000 approximate molecular weight) (60/20/20), copolymer of average molecular weight of about 128,000.
  • silicone block copolymers comprising repeating block units of polysiloxanes.
  • silicone-containing block copolymers examples include U.S. Patent No. 5,523,365, to Geck et al., issued June 4, 1996; U.S. Patent No. 4,689,289, to Crivello, issued Aug. 25, 1987; U.S. Patent No. 4,584,356, to Crivello, issued April 22, 1986; Macromolecular Design, Concept & Practice , Ed: M. K. Mishra, Polymer Frontiers International, Inc., Hopewell Jct., NY (1994), and Block Copolymers, A. Noshay and J. E. McGrath, Academic Press, NY (1977), which are all incorporated by reference herein in their entirety.
  • Other silicone block copolymers suitable for use herein are those described, along with methods of making them, in the above referenced and incorporated U.S. Patent No. 5,658,577.
  • the silicone-containing block copolymers useful in the present invention can be described by the formulas A-B, A-B-A, and -(A-B) n - wherein n is an integer of 2 or greater.
  • A-B represents a diblock structure
  • A-B-A represents a triblock structure
  • -(A-B) n - represents a multiblock structure.
  • the block copolymers can comprise mixtures of diblocks, triblocks, and higher multiblock combinations as well as small amounts of homopolymers.
  • the silicone block portion, B can be represented by the following polymeric structure --(SiR 2 O) m --, wherein each R is independently selected from the group consisting of hydrogen, hydroxyl, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 2 -C 6 alkylamino, styryl, phenyl, C 1 -C 6 alkyl or alkoxy-substituted phenyl, preferably methyl; and m is an integer of about 10 or greater, preferably of about 40 or greater, more preferably of about 60 or greater, and most preferably of about 100 or greater.
  • the non-silicone block, A comprises monomers selected from the monomers as described hereinabove in reference to the non-silicone hydrophilic and hydrophobic monomers for the silicone grafted copolymers. Vinyl blocks are preferred co-monomers.
  • the block copolymers preferably contain one or more non-silicone blocks, and up to about 50%, preferably from about 10% to about 20%, by weight of one or more polydimethyl siloxane blocks.
  • sulfur-linked silicone containing copolymers including block copolymers.
  • the term "sulfur-linked” means that the copolymer contains a sulfur linkage (i.e., -S-), a disulfide linkage (i.e., -S-S-), or a sulfhydryl group (i.e.,-SH).
  • A is a vinyl polymeric segment formed from polymerized free radically polymerizable monomers.
  • the selection of A is typically based upon the intended uses of the composition, and the properties the copolymer must possess in order to accomplish its intended purpose. If A comprises a block in the case of block copolymers, a polymer having AB and/or ABA architecture will be obtained depending upon whether a mercapto functional group -SH is attached to one or both terminal silicon atoms of the mercapto functional silicone compounds, respectively.
  • the weight ratio of vinyl polymer block or segment, to silicone segment of the copolymer can vary.
  • the preferred copolymers are those wherein the weight ratio of vinyl polymer segment to silicone segment ranges from about 98:2 to 50:50, in order that the copolymer possesses properties inherent to each of the different polymeric segments while retaining the overall polymer's solubility.
  • the preferred polymers comprising at least one unit which provide a dye transfer inhibiting benefit are water-soluble polymers.
  • the polymers comprising at least one unit which provide a dye transfer inhibiting benefit useful in the present invention have the formula: [-P(D) m -] n wherein the unit P is a polymer backbone which comprises units which are homopolymeric or copolymeric. D units are defined herein below.
  • the term "homopolymeric” is defined as "a polymer backbone which is comprised of units having the same unit composition, i.e., formed from polymerization of the same monomer”.
  • copolymeric is defined as "a polymer backbone which is comprised of units having a different unit composition, i.e., formed from the polymerization of two or more monomers”.
  • P backbones preferably comprise units having the formula: -[CR 2 -CR 2 ]- or -[(CR 2 ) x -L]- wherein each R unit is independently hydrogen, C 1 -C 12 alkyl, C 6 -C 12 aryl, and D units as described herein below; preferably C 1 -C 4 alkyl.
  • Each L unit is independently selected from heteroatom-containing moieties, non-limiting examples of which are selected from the group consisting of: polysiloxane having the formula: wherein the index p is from 1 to about 6; units which have dye transfer inhibition activity: and mixtures thereof; wherein R 1 is hydrogen, C 1 -C 12 alkyl, C 6 -C 12 aryl, and mixtures thereof.
  • R 2 is C 1 -C 12 alkyl, C 1 -C 12 alkoxy, C 6 -C 12 aryloxy, and mixtures thereof; preferably methyl and methoxy.
  • R 3 is hydrogen C 1 -C 12 alkyl, C 6 -C 12 aryl, and mixtures thereof; preferably hydrogen or C 1 -C 4 alkyl, more preferably hydrogen.
  • R 4 is C 1 -C 12 alkyl, C 6 -C 12 aryl, and mixtures thereof.
  • the backbones of the polymers of the present invention comprise one or more D units which are units which comprise one or more units which provide a dye transfer inhibiting benefit.
  • the D unit can be part of the backbone itself as represented in the general formula: [-P(D) m -] n or the D unit may be incorporated into the backbone as a pendant group to a backbone unit having, for example, the formula:
  • the number of D units depends upon the formulation. For example, the number of D units will be adjusted to provide water solubility of the polymer as well as efficacy of dye transfer inhibition.
  • the molecular weight of the polymers of the present invention are from about 500, preferably from about 1,000, more preferably from about 10,000 most preferably from 200,000 to about 6,000,000, preferably to about 2,000,000, more preferably to about 1,000,000, yet more preferably to about 500,000, most preferably to about 360,000 daltons. Therefore the value of the index n is selected to provide the indicated molecular weight, and providing for a water solubility of at least 100 ppm, preferably at least about 300 ppm, and more preferably at least about 1,000 ppm in water at ambient temperature which is defined herein as 25°C.
  • Non-limiting examples of preferred D units are D units which comprise an amide moiety.
  • Examples of polymers wherein an amide unit is introduced into the polymer via a pendant group includes polyvinylpyrrolidone having the formula: polyvinyloxazolidone having the formula: polyvinylmethyloxazolidone having the formula: polyacrylamides and N-substituted polyacrylamides having the formula: wherein each R' is independently hydrogen, C 1 -C 6 alkyl, or both R' units can be taken together to form a ring comprising 4-6 carbon atoms; polymethacrylamides and N-substituted polymethacrylamides having the general formula: wherein each R' is independently hydrogen, C 1 -C 6 alkyl, or both R' units can be taken together to form a ring comprising 4-6 carbon atoms; poly(N-acrylylglycinamide) having the formula: wherein each R' is independently hydrogen, C 1 -C 6 alkyl, or both R' units can
  • D unit wherein the nitrogen of the dye transfer inhibiting moiety is incorporated into the polymer backbone is a poly(2-ethyl-2-oxazoline) having the formula: wherein the index n indicates the number of monomer residues present.
  • the amino-functional polymers of the present invention can comprise any mixture of dye transfer inhibition units which provides the product with suitable properties.
  • the preferred polymers which comprise D units which are amide moieties are those which have the nitrogen atoms of the amide unit highly substituted so the nitrogen atoms are in effect shielded to a varying degree by the surrounding non-polar groups. This provides the polymers with an amphiphilic character.
  • Non-limiting examples include polyvinyl-pyrrolidones, polyvinyloxazolidones, N,N-disubstituted polyacrylamides, and N,N-disubstituted polymethacrylamides.
  • a detailed description of physico-chemical properties of some of these polymers are given in "Water-Soluble Synthetic Polymers: Properties and Behavior", Philip Molyneux, Vol. I, CRC Press, (1983) included herein by reference.
  • the amide containing polymers may be present partially hydrolyzed and/or crosslinked forms.
  • a preferred polymeric compound for the present invention is polyvinylpyrrolidone (PVP). This polymer has an amphiphilic character with a highly polar amide group conferring hydrophilic and polar-attracting properties, and also has non-polar methylene and methine groups, in the backbone and/or the ring, conferring hydrophobic properties. PVP is readily soluble in aqueous and organic solvent systems.
  • PVP is available ex ISP, Wayne, New Jersey, and BASF Corp., Parsippany, New Jersey, as a powder or aqueous solutions in several viscosity grades, designated as, e.g., K-12, K-15, K-25, and K-30. These K-values indicate the viscosity average molecular weight, as shown below: PVP K-12, K-15, and K-30 are also available ex Polysciences, Inc. Warrington, Pennsylvania, PVP K-15, K-25, and K-30 and poly(2-ethyl-2-oxazoline) are available ex Aldrich Chemical Co., Inc., Milwaukee, Wisconsin.
  • PVP K30 (40,000) through to K90 (360,000) are also commercially available ex BASF under the tradename Luviskol or commercially available ex ISP. Still higher molecular PVP like PVP 1.3MM, commercially available ex Aldrich is also suitable for use herein.
  • PVP-type of material suitable for use in the present invention are polyvinylpyrrolidone-co-dimethylaminoethylmethacrylate, commercially available ex ISP in a quaternised form under the tradename Gafquat® or commercially available ex Aldrich Chemical Co.
  • N-oxide units having the formula: wherein R 1 , R 2 , and R 3 can be any hydrocarbyl unit (for the purposes of the present invention the term "hydrocarbyl" does not include hydrogen atom alone).
  • the N-oxide unit may be part of a polymer, such as a polyamine, i.e., polyalkyleneamine backbone, or the N-oxide may be part of a pendant group attached to the polymer backbone.
  • An example of a polymer which comprises an the N-oxide unit as a part of the polymer backbone is polyethyleneimine N-oxide.
  • Non-limiting examples of groups which can comprise an N-oxide moiety include the N-oxides of certain heterocycles inter alia pyridine, pyrrole, imidazole, pyrazole, pyrazine, pyrimidine, pyridazine, piperidine, pyrrolidine, pyrrolidone, azolidine, morpholine.
  • a preferred polymer is poly(4-vinylpyriding N-oxide, PVNO).
  • the N-oxide unit may be pendant to the ring, for example, aniline oxide.
  • N-oxide comprising polymers of the present invention will preferably have a ratio of N-oxidized amine nitrogen to non-oxidized amine nitrogen of from about 1:0 to about 1:2, preferably to about 1:1, more preferably to about 3:1.
  • the amount of N-oxide units can be adjusted by the formulator.
  • the formulator may co-polymerize N-oxide comprising monomers with non N-oxide comprising monomers to arrive at the desired ratio of N-oxide to non N-oxide amino units, or the formulator may control the oxidation level of the polymer during preparation.
  • the amine oxide unit of the polyamine N-oxides of the present invention have a Pk a less than or equal to 10, preferably less than or equal to 7, more preferably less than or equal to 6.
  • the average molecular weight of the N-oxide comprising polymers which provide a dye transfer inhibitor benefit to polymers is from about 500 daltons, preferably from about 10,000 daltons, more preferably from about 20,000 daltons to about 6,000,000 daltons, preferably to about 2,000,000 daltons, more preferably to about 360,000 daltons.
  • polymers which have dye transfer inhibition benefits are polymers which comprise both amide units and N-oxide units as described herein above.
  • Non-limiting examples include co-polymers of two monomers wherein the first monomer comprises an amide unit and the second monomer comprises an N-oxide unit.
  • oligomers or block polymers comprising these units can be taken together to form the mixed amide/N-oxide polymers.
  • Polymers of the urethane type are also suitable components for use herein.
  • a typical disclosure of polyurethane polymer can be found in EP844274A1 as well as in EP839903.
  • Isomaltooligosaccharides (including mixtures), the individual components of said mixtures, substituted versions thereof, derivatised versions thereof, and mixtures thereof are suitable components for use herein.
  • IMO is used as corn syrup.
  • cellulosic fibers/fabrics such as cotton, rayon, ramie, jute, flax, linen, polynosic-fibers, Lyocell (Tencel ® ), polyester/cotton blends, other cotton blends, and the like, especially cotton, rayon, linen, polyester/cotton blends, and mixtures thereof.
  • Suitable fabric improving actives that are useful in the present invention include oligosaccharides with a degree of polymerization (DP) of from about 1 to about 15, preferably from about 2 to about 10, and wherein each monomer is selected from the group consisting of reducing saccharide containing 5 and/or 6 carbon atoms, including isomaltose, isomaltotriose, isomaltotetraose, isomaltooligosaccharide, fructooligosaccharide, levooligosaccharides, galactooligosaccharide, xylooligosaccharide, gentiooligosaccharides, disaccharides, glucose, fructose, galactose, xylose, mannose, arabinose, rhamnose, maltose, sucrose, lactose, maltulose, ribose, lyxose, allose, altrose, gulose, idose, talose, tre
  • Oligosaccharides containing b-linkages are also preferred.
  • Preferred oligosaccharides are acyclic and have at least one linkage that is not an ⁇ -1,4-glycosidic bond.
  • a preferred oligosaccharide is a mixture containing IMO: from 0 to about 20 % by weight of glucose, from about 10 to about 65 % of isomaltose, from about 1% to about 45% of each of isomaltotriose, isomaltetraose and isomaltopentaose, from 0 to about 3 % of each of isomaltohexaose, isomaltoheptaose, isomaltooctaose and isomaltononaose, from about 0.2% to about 15% of each of isomaltohexaose and isomaltoheptaose, and from 0 to about 50 % by weight of said mixture being isomaltooli
  • Oligosaccharide mixtures are either prepared by enzymatic reactions or separated as natural products from plant materials.
  • the enzymatic synthesis of oligosaccharides involves either adding monosaccharides, one at a time, to a di- or higher saccharide to produce branched oligosaccharides, or it can involve the degradation of polysaccharides followed by transfer of saccharides to branching positions.
  • Oligosaccharide Mixtures I and II are prepared by enzymatic hydrolysis of starch to maltooligosaccharides, which are then converted to isomaltooligosaccharides by a transglucosidase reaction.
  • Oligosaccharide Mixture III for example, is a mixture of oligosaccharides isolated from soybean. Soybean oligosaccharides such as Mixture III, are of pure natural origin.
  • Substituted and/or derivatised materials of the oligosaccharides listed hereinabove are also suitable in the present invention.
  • Nonlimiting examples of these materials include: carboxyl and hydroxymethyl substitutions (e.g., glucuronic acid instead of glucose); amino oligosaccharides (amine substitution, e.g., glucosamine instead of glucose); cationic quaternized oligosaccharides; C 1 -C 6 alkylated oligosaccharides; acetylated oligosaccharide ethers; oligosaccharides having amino acid residues attached (small fragments of glycoprotein); oligosaccharides containing silicone moieties.
  • substituted and/or derivatised oligosaccharides can provide additional benefits, such as: carboxyl and hydroxymethyl substitutions can introduce readily oxidizable materials on and in the fiber, thus reducing the probability of the fiber itself being oxidized by oxidants, such as bleaches; amine substitution can bind and/or condense with oxidatively damaged regions of the fiber to rejuvenate aged fabrics; acetylated sugar ethers can serve as bleach activators in subsequent processes where hydrogen peroxide is present; oligosaccharides having amino acid residues can improve delivery of fabric care benefits for fabrics containing proteinaceous fibers, e.g., wool and silk; and silicone-derivatised oligosaccharides can provide additional fabric softness and lubricity.
  • C 6 alkyl oligosaccharide is disclosed (along with other higher, viz., C 6 -C 30 , alkyl polysaccharides) in U.S. Pat. 4,565,647. Typical disclosure of C 1 -C 6 alkylated oligosaccharides can also be found in U.S. 4,488,981. These patents are incorporated herein by reference.
  • One preferred isomaltooligosaccharide is IMO 900 commercially available from Showa Sangyo Co.)
  • Polyvinylamines polymers are also suitable component giving a deviation of fabric WRA of at least 15.
  • Typical polyvinylamines polymers include the the quaternized and non-quaternized polyvinylamines having the formula: wherein R is hydrogen, C1-C12 linear or branched alkyl, benzyl, or alkyleneoxy having the formula (R10)zY, wherein R1 is C1-C6 linear or branched alkylene, Y is hydrogen or an anionic unit, non-limiting examples of which include,-(CH2)fCO2M, -C(O)(CH2)fCO2M, -(CH2)fPO3M, -(CH2)fOPO3M,-(CH2)fSO3M, -CH2(CHSO3M)-(CH2)fSO3M, -CH2(CHSO2M)(CH2)fSO3M,-C(O)CH2CH(SO3M)CO2M, -C(O)CH2CH(CO2
  • the index x has the value from about 50 to about 1,500; preferably the index x has a value such that the resulting polymeric suds stabilizer has an average molecular weight of from about 2,500, preferably from about 10,000, more preferably from about 20,000 to about 150,000, preferably to about 90,000, more preferably to about 80,000 daltons.
  • Most preferred polymers for use in the present invention are water-soluble, including IMO 900 (Isomaltose Oligosaccharide ex. Showa Sangyo Co.), Avalure AC 120 (Polyacrylate ex. BF Goodrich), Luviskol K30, K60 and K85 (Polyvinylpyrrolidone MW 40.000, 400.000 and 1.250.000 ex. BASF), Luvitec VPC 55K65W (copolymer Vinylpyrrolidone & Vinylcaprolactam ex. BASF), Luvitec Quat 73W (copolymer 1-methyl-3-vinyl-imidazolium-methylsulfate & 1-vinyl-2-pyrrolidone ex.
  • IMO 900 Isomaltose Oligosaccharide ex. Showa Sangyo Co.
  • Avalure AC 120 Polyacrylate ex. BF Goodrich
  • Luviskol K30, K60 and K85 Polyvinylpyrrolidone MW 40.000, 400.000 and 1.25
  • Luviquat FC 905 copolymer Vinylimidazolium methochloride & Vinylpyrrolidone ex. BASF
  • Sedipur 520 modified Polyacrylamide ex. BASF
  • Chitanide 222 Chitosan succinamide ex. MIP
  • Mirasil ADM-E Amphomer HC (Acrylate / Octylacrylamide copolymer ex. National Starch), and mixtures thereof.
  • the water-soluble lubricant and the component, preferably polymer, having a deviation of fabric WRA of at least +15 are present in weight ratios of water-soluble lubricant to component of from 10:1 to 1:1. Indeed, it has been found that within these ratio ranges the resulting composition provides best in wear wrinkle benefit.
  • composition of the invention may also comprises one or more of the following optional ingredients.
  • Durable press polymers are optional components of the invention. These polymers can be a cross-linking resin having the property of being cationic. By “cross-linking resin having the property of being cationic”, it is meant that the resin is at least partially positively charged. It is not however necessary that the reactive part of the molecule carries the positive charge. Indeed, polymeric resins can be based on positively charged monomers which help the deposition on the fibers.
  • Cross-linking resins having the property of being cationic suitable for use herein are those commonly known as having wet strength in the paper field. At least two mechanisms have been postulated to account for the mechanism by which wet strength resin act. One is that wet strength resins form covalent bonds between adjacent fibers while another is that the wet strength resin places a layer over the hydrogen bonds formed between adjacent paper fibers and thus prevents water from breaking the hydrogen bonds.
  • wet-strength agents suitable for use herein include compounds made of epichlorohydrin adducts of polyamine resins, polyethyleneimine resins, cationic starch, polydiallyldimethylammonium chloride, and mixtures thereof, amine-aldehyde resins such as melamine-formaldehyde resin, amide-aldehyde resins, and mixtures thereof.
  • amine-aldehyde resins such as melamine-formaldehyde resin, amide-aldehyde resins, and mixtures thereof.
  • the preferred components are the polymeric amine-epichlorohydrin resins selected from the group consisting of a polyamide-epichlorohydrin (PAE) resin, a polyalkylenepolyamine-epichlorohydrin (PAPAE) resin, and an amine polymer-epichlorohydrin (APE) resin, in which the amine groups have been alkylated with epichlorohydrin to produce a polyamine-epichlorohydrin resin that has azetidinium or epoxide functionality.
  • PAE polyamide-epichlorohydrin
  • PAPAE polyalkylenepolyamine-epichlorohydrin
  • APE amine polymer-epichlorohydrin
  • the cross-linking resin having cationic properties is a cationic wet strength resin that is produced by reacting a saturated aliphatic dicarboxylic acid containing three to ten carbon atoms with a polyalkylenepolyamine, containing from two to four ethylene groups, two primary amine groups, and one to three secondary amine groups (such as diethylenetriamine, triethylenetetramine and tetraethylenepentamine), to form a poly(aminoamide) having secondary amine groups that are alkylated with epichlorohydrin to form a PAE resin.
  • a saturated aliphatic dicarboxylic acid containing three to ten carbon atoms with a polyalkylenepolyamine, containing from two to four ethylene groups, two primary amine groups, and one to three secondary amine groups (such as diethylenetriamine, triethylenetetramine and tetraethylenepentamine), to form a poly(aminoamide) having secondary amine groups that are alkylated with epic
  • cross-linking resin having cationic properties from this class are the wet strength resin Kymene 557H (available from Hercules Incorporated), in which adipic acid is reacted with diethylenetriamine to form a poly(aminoamide) that is alkylated and crosslinked with epichlorohydrin to form a PAE resin.
  • Still another preferred cross-linking resin having cationic properties made of epichlorohydrin are Luresin.RTM and Etadurin which both are polyamidoamine-epichlorohydrin resins.
  • Amine-aldehyde resins are suitable cross-linking resins for the present invention and are made by condensation of amine or amide monomers with aldehydes such as formaldehyde or glyoxal.
  • Preferred amines are those having low molecular weight amines e.g. melamine or polymeric amines e.g. poly-diallylamine, preferably quarternized.
  • Preferred amides are those polymeric amides such as polyacrylamide. All these suitable amine/amide monomers can also be copolymerized with cationic monomers.
  • amine-aldehyde cross-linking resin preferred are those from the class of melamine-formaldehyde resin.
  • Melamine-formaldehyde resins of this type are known as crosslinking agents of this type in the coating industry and are also described, for example, in German Auslegeschrift Nos. 2,457,387 (U.S. Pat. No. 4,035,213 incorporated herein by reference) and 1,719,324 and, in particular, in U.S. Pat. No. 3,242,230 incorporated herein by reference.
  • Preferred melamine-formaldehyde resin are those commercially available under the tradenames Madurit, and Cassurit from Clariant.
  • Still other preferred cross-linking resin having the property of being cationic among the class of amine-aldehyde cross-linking resin are the Poly(acrylamide-glyoxal) resin commercially available under the tradename SOLIDURIT KM from Clariant.
  • the cross-linking resin having cationic properties have a molecular weight between 200 and 1,000,000, preferably between 500 and 100,000, most preferably between 1000 and 25,000.
  • Cross-linking resin having a low molecular weight are most preferred for use in the present invention as they are more water-soluble and have a better fiber penetration.
  • low molecular weight it is meant a molecular weight within the range of from 25 to 2000, preferably from 50 to 1000, and more preferably from 50 to 500.
  • the level of cross-linking components or derivative thereof is present in an amount of from 0.01% to 60%, preferably from 0.01% to 30% by weight of the total composition
  • catalysts includes organic acids such as citric acid, succinic acid, and tartaric acids, as well as conventional Lewis acid such as Al Cl 3 or MgCl 2 , or salts thereof, or mixtures thereof.
  • organic acids such as citric acid, succinic acid, and tartaric acids
  • Lewis acid such as Al Cl 3 or MgCl 2
  • catalyst NKD made of a mixture of salts and organic acid, and commercially available from Hoechst.
  • the level of catalyst is from 10% to 50%, preferably from 20 to 40% by weight of the cross-linking components or derivative thereof.
  • the liquid carrier employed in the instant compositions is preferably at least primarily water due to its low cost, relative availability, safety, and environmental compatibility.
  • the level of water in the liquid carrier is preferably at least about 50%, most preferably at least about 60%, by weight of the carrier.
  • Mixtures of water and low molecular weight, e.g., ⁇ about 200, organic solvent, e.g., lower alcohols such as ethanol, propanol, isopropanol or butanol are useful as the carrier liquid.
  • Low molecular weight alcohols include monohydric, dihydric (glycol, etc.) trihydric (glycerol, etc.), and higher polyhydric (polyols) alcohols.
  • compositions containing both saturated and unsaturated diester quaternary ammonium compounds can be prepared that are stable without the addition of concentration aids.
  • the compositions of the present invention may require organic and/or inorganic concentration aids to go to even higher concentrations and/or to meet higher stability standards depending on the other ingredients.
  • concentration aids which typically can be viscosity modifiers may be needed, or preferred, for ensuring stability under extreme conditions when particular softener active levels are used.
  • the surfactant concentration aids are typically selected from the group consisting of (1) single long chain alkyl cationic surfactants; (2) nonionic surfactants; (3) amine oxides; (4) fatty acids; and (5) mixtures thereof.
  • the total level is from 0.1% to 20%, preferably from 0.2% to 10%, more preferably from 0.5% to 5%, and even more preferably from 1% to 2% by weight of the composition.
  • These materials can either be added as part of the active softener raw material, (I), e.g., the mono-long chain alkyl cationic surfactant and/or the fatty acid which are reactants used to form the biodegradable fabric softener active as discussed hereinbefore, or added as a separate component.
  • the total level of dispersibility aid includes any amount that may be present as part of component (I).
  • Inorganic viscosity/dispersibility control agents which can also act like or augment the effect of the surfactant concentration aids, include water-soluble, ionizable salts which can also optionally be incorporated into the compositions of the present invention.
  • ionizable salts can be used. Examples of suitable salts are the halides of the Group IA and IIA metals of the Periodic Table of the Elements, e.g., calcium chloride, magnesium chloride, sodium chloride, potassium bromide, and lithium chloride.
  • the ionizable salts are particularly useful during the process of mixing the ingredients to make the compositions herein, and later to obtain the desired viscosity.
  • the amount of ionizable salts used depends on the amount of active ingredients used in the compositions and can be adjusted according to the desires of the formulator. Typical levels of salts used to control the composition viscosity are from about 20 to about 20,000 parts per million (ppm), preferably from about 20 to about 11,000 ppm, by weight of the composition.
  • Alkylene polyammonium salts can be incorporated into the composition to give viscosity control in addition to or in place of the water-soluble, ionizable salts above.
  • these agents can act as scavengers, forming ion pairs with anionic detergent carried over from the main wash, in the rinse, and on the fabrics, and may improve softness performance.
  • alkylene polyammonium salts include l-lysine monohydrochloride and 1,5-diammonium 2-methyl pentane dihydrochloride.
  • Stabilizers can be present in the compositions of the present invention.
  • the term "stabilizer,” as used herein, includes antioxidants and reductive agents. These agents are present at a level of from 0% to about 2%, preferably from about 0.01% to about 0.2%, more preferably from about 0.035% to about 0.1% for antioxidants, and more preferably from about 0.01% to about 0.2% for reductive agents. These assure good odor stability under long term storage conditions for the compositions and compounds stored in molten form.
  • the use of antioxidants and reductive agent stabilizers is especially critical for low scent products (low perfume).
  • antioxidants examples include a mixture of ascorbic acid, ascorbic palmitate, propyl gallate, available from Eastman Chemical Products, Inc., under the trade names Tenox® PG and Tenox S-1; a mixture of BHT (butylated hydroxytoluene), BHA (butylated hydroxyanisole), propyl gallate, and citric acid, available from Eastman Chemical Products, Inc., under the trade name Tenox-6; butylated hydroxytoluene, available from UOP Process Division under the trade name Sustane® BHT; tertiary butylhydroquinone, Eastman Chemical Products, Inc., as Tenox TBHQ; natural tocopherols, Eastman Chemical Products, Inc., as Tenox GT-1/GT-2; and butylated hydroxyanisole, Eastman Chemical Products, Inc., as BHA; long chain esters (C 8 -C 22 ) of gallic acid, e.g., dodecyl
  • reductive agents examples include sodium borohydride, hypophosphorous acid, Irgafos® 168, and mixtures thereof.
  • antimicrobial preservative can be added to the composition of the present invention. Contamination by certain microorganisms with subsequent microbial growth can result in an unsightly and/or malodorous solution. Because microbial growth in solutions is highly objectionable when it occurs, it is highly preferable to include an antimicrobial preservative, which is effective for inhibiting and/or regulating microbial growth in order to increase storage stability of the composition.
  • a broad spectrum preservative e.g., one that is effective on both bacteria (both gram positive and gram negative) and fungi.
  • a limited spectrum preservative e.g., one that is only effective on a single group of microorganisms, e.g., fungi, can be used in combination with a broad spectrum preservative or other limited spectrum preservatives with complimentary and/or supplementary activity.
  • a mixture of broad spectrum preservatives can also be used.
  • aminocarboxylate chelators such as those described hereinbefore, can be used alone or as potentiators in conjunction with other preservatives.
  • chelators which include, e.g., ethylenediaminetetraacetic acid (EDTA), hydroxyethylenediaminetriacetic acid, diethylenetriaminepentaacetic acid, and other aminocarboxylate chelators, and mixtures thereof, and their salts, and mixtures thereof, can increase preservative effectiveness against Gram-negative bacteria, especially Pseudomonas species.
  • EDTA ethylenediaminetetraacetic acid
  • hydroxyethylenediaminetriacetic acid hydroxyethylenediaminetriacetic acid
  • diethylenetriaminepentaacetic acid diethylenetriaminepentaacetic acid
  • other aminocarboxylate chelators and mixtures thereof, and their salts, and mixtures thereof, can increase preservative effectiveness against Gram-negative bacteria, especially Pseudomonas species.
  • Antimicrobial preservatives useful in the present invention include biocidal compounds, i.e., substances that kill microorganisms, or biostatic compounds, i.e., substances that inhibit and/or regulate the growth of microorganisms.
  • biocidal compounds i.e., substances that kill microorganisms
  • biostatic compounds i.e., substances that inhibit and/or regulate the growth of microorganisms.
  • Well known preservatives such as short chain alkyl esters of p-hydroxybenzoic acid, commonly known as parabens; N-(4-chlorophenyl)-N'-(3,4-dichlorophenyl) urea, also known as 3,4,4'-trichlorocarbanilide or triclocarban; 2,4,4'-trichloro-2'-hydroxy diphenyl ether, commonly known as triclosan are useful preservative in the present invention.
  • Still other preferred preservatives are the water-soluble preservatives, i.e. those that have a solubility in water of at least about 0.3 g per 100 ml of water, i.e., greater than about 0.3% at room temperature, preferably greater than about 0.5% at room temperature.
  • the preservative in the present invention is included at an effective amount.
  • effective amount means a level sufficient to prevent spoilage, or prevent growth of inadvertently added microorganisms, for a specific period of time.
  • the preservative is not being used to kill microorganisms on the surface onto which the composition is deposited in order to eliminate odors produced by microorganisms. Instead, it is preferably being used to prevent spoilage of the solution in order to increase the shelf-life of the composition.
  • Preferred levels of preservative are from about 0.0001% to about 0.5%, more preferably from about 0.0002% to about 0.2%, most preferably from about 0.0003% to about 0.1%, by weight of the usage composition.
  • the preservative can be any organic preservative material which will not cause damage to fabric appearance, e.g., discoloration, coloration, bleaching.
  • Preferred water-soluble preservatives include organic sulfur compounds, halogenated compounds, cyclic organic nitrogen compounds, low molecular weight aldehydes, quaternary ammonium compounds, dehydroacetic acid, phenyl and phenolic compounds, and mixtures thereof.
  • Non-limiting examples of preferred water-soluble preservatives for use in the present invention can be found in U.S. Patent 5,714,137, incorporated hereinbefore by reference, as well as co-pending application PCT/US 98/12154 pages 29 to 36.
  • Preferred water-soluble preservatives for use in the present invention are organic sulfur compounds.
  • organic sulfur compounds suitable for use in the present invention are:
  • a preferred preservative is an antimicrobial, organic preservative containing 3-isothiazolone groups. This class of compounds is disclosed in U.S. Pat. No. 4,265,899, Lewis et al., issued May 5, 1981, and incorporated herein by reference.
  • a preferred preservative is a water-soluble mixture of 5-chloro-2-methyl-4-isothiazolin-3-one and 2-methyl-4-isothiazolin-3-one, more preferably a mixture of about 77% 5-chloro-2-methyl-4-isothiazolin-3-one and about 23% 2-methyl-4-isothiazolin-3-one, a broad spectrum preservative available as a 1.5% aqueous solution under the trade name Kathon ® CG by Rohm and Haas Company.
  • Kathon ® When Kathon ® is used as the preservative in the present invention it is present at a level of from about 0.0001% to about 0.01%, preferably from about 0.0002% to about 0.005%, more preferably from about 0.0003% to about 0.003%, most preferably from about 0.0004% to about 0.002%, by weight of the composition.
  • isothiazolins include 1,2-benzisothiazolin-3-one, available under the trade name Proxel ® products; and 2-methyl-4,5-trimethylene-4-isothiazolin-3-one, available under the trade name Promexal ® . Both Proxel and Promexal are available from Zeneca. They have stability over a wide pH range (i.e., 4-12). Neither contain active halogen and are not formaldehyde releasing preservatives.
  • Proxel and Promexal are effective against typical Gram negative and positive bacteria, fungi and yeasts when used at a level from about 0.001% to about 0.5%, preferably from about 0.005% to about 0.05%, and most preferably from about 0.01% to about 0.02% by weight of the usage composition.
  • Another preferred organic sulfur preservative is sodium pyrithione, with water solubility of about 50%.
  • sodium pyrithione is typically present at a level of from about 0.0001% to about 0.01%, preferably from about 0.0002% to about 0.005%, more preferably from about 0.0003% to about 0.003%, by weight of the usage composition.
  • Mixtures of the preferred organic sulfur compounds can also be used as the preservative in the present invention.
  • composition may suitably use an optional solubilized, water-soluble antimicrobial active, useful in providing protection against organisms that become attached to the treated material.
  • an optional solubilized, water-soluble antimicrobial active useful in providing protection against organisms that become attached to the treated material.
  • the free, uncomplexed antimicrobial, e.g., antibacterial, active provides an optimum antibacterial performance.
  • compositions of the present invention containing, antimicrobial materials, e.g., antibacterial halogenated compounds, quaternary compounds, and phenolic compounds.
  • antimicrobial materials e.g., antibacterial halogenated compounds, quaternary compounds, and phenolic compounds.
  • Some of the more robust antimicrobial halogenated compounds which can function as disinfectants/sanitizers as well as finish product preservatives (vide infra), and are useful in the compositions of the present invention include 1,1'-hexamethylene bis(5-(p-chlorophenyl)biguanide), commonly known as chlorhexidine, and its salts, e.g., with hydrochloric, acetic and gluconic acids.
  • the digluconate salt is highly water-soluble, about 70% in water, and the diacetate salt has a solubility of about 1.8% in water.
  • chlorhexidine When used as a sanitizer in the present invention it is typically present at a level of from about 0.001% to about 0.4%, preferably from about 0.002% to about 0.3%, and more preferably from about 0.01% to about 0.1%, by weight of the usage composition. In some cases, a level of from about 1% to about 2% may be needed for virucidal activity.
  • Other useful biguanide compounds include Cosmoci ® CQ ® , Vantocil ® IB, including poly (hexamethylene biguanide) hydrochloride.
  • Other useful cationic antimicrobial agents include the bis-biguanide alkanes. Usable water soluble salts of the above are chlorides, bromides, sulfates, alkyl sulfonates such as methyl sulfonate and ethyl sulfonate, phenylsulfonates such as p-methylphenyl sulfonates, nitrates, acetates, gluconates, and the like.
  • the bis biguanide of choice is chlorhexidine and its salts, e.g., digluconate, dihydrochloride, diacetate, and mixtures thereof.
  • Quaternary Compounds A wide range of quaternary compounds can also be used as antimicrobial actives, in conjunction with the preferred surfactants, for compositions of the present invention that do not contain cyclodextrin.
  • useful quaternary compounds include: (1) benzalkonium chlorides and/or substituted benzalkonium chlorides such as commercially available Barquat ® (available from Lonza), Maquat ® (available from Mason), Variquat ® (available from Witco/Sherex), and Hyamine ® (available from Lonza); (2) dialkyl quaternary such as Bardac ® products of Lonza, (3) N-(3-chloroallyl) hexaminium chlorides such as Dowicide ® and Dowicil ® available from Dow; (4) benzethonium chloride such as Hyamine ® 1622 from Rohm & Haas; (5) methylbenzethonium chloride represented by Hyamine ® 10X supplied by Rohm &
  • Typical concentrations for biocidal effectiveness of these quaternary compounds range from about 0.001% to about 0.8%, preferably from about 0.005% to about 0.3%, more preferably from about 0.01% to 0.2%, by weight of the usage composition.
  • the corresponding concentrations for the concentrated compositions are from about 0.003% to about 2%, preferably from about 0.006% to about 1.2%, and more preferably from about 0.1 % to about 0.8% by weight of the concentrated compositions.
  • the present invention can contain a perfume. Suitable perfumes are disclosed in U.S. Pat. 5,500,138, said patent being incorporated herein by reference.
  • perfume includes fragrant substance or mixture of substances including natural (i.e., obtained by extraction of flowers, herbs, leaves, roots, barks, wood, blossoms or plants), artificial (i.e., a mixture of different nature oils or oil constituents) and synthetic (i.e., synthetically produced) odoriferous substances.
  • natural i.e., obtained by extraction of flowers, herbs, leaves, roots, barks, wood, blossoms or plants
  • artificial i.e., a mixture of different nature oils or oil constituents
  • synthetic i.e., synthetically produced
  • perfumes are complex mixtures of a plurality of organic compounds.
  • perfume ingredients useful in the perfumes of the present invention compositions include, but are not limited to, hexyl cinnamic aldehyde; amyl cinnamic aldehyde; amyl salicylate; hexyl salicylate; terpineol; 3,7-dimethyl- cis -2,6-octadien-1-ol; 2,6-dimethyl-2-octanol; 2,6-dimethyl-7-octen-2-ol; 3,7-dimethyl-3-octanol; 3,7-dimethyl- trans -2,6-octadien-1-ol; 3,7-dimethyl-6-octen-1-ol; 3,7-dimethyl-1-octanol; 2-methyl-3-(para-tert-butylphenyl)-propionaldehyde; 4-(4-hydroxy-4-methylpentyl)-3-cyclohexene-1-carbox
  • fragrance materials include, but are not limited to, orange oil; lemon oil; grapefruit oil; bergamot oil; clove oil; dodecalactone gamma; methyl-2-(2-pentyl-3-oxo-cyclopentyl) acetate; beta-naphthol methylether; methyl-beta-naphthylketone; coumarin; decylaldehyde; benzaldehyde; 4-tert-butylcyclohexyl acetate; alpha,alpha-dimethylphenethyl acetate; methylphenylcarbinyl acetate; Schiff's base of 4-(4-hydroxy-4-methylpentyl)-3-cyclohexene-1-carboxaldehyde and methyl anthranilate; cyclic ethyleneglycol diester of tridecandioic acid; 3,7-dimethyl-2,6-octadiene-1-nitrile; i
  • perfume components are geraniol; geranyl acetate; linalool; linalyl acetate; tetrahydrolinalool; citronellol; citronellyl acetate; dihydromyrcenol; dihydromyrcenyl acetate; tetrahydromyrcenol; terpinyl acetate; nopol; nopyl acetate; 2-phenylethanol; 2-phenylethyl acetate; benzyl alcohol; benzyl acetate; benzyl salicylate; benzyl benzoate; styrallyl acetate; dimethylbenzylcarbinol; trichloromethylphenylcarbinyl methylphenylcarbinyl acetate; isononyl acetate; vetiveryl acetate; vetiverol; 2-methyl-3-(p-tert-butylphenyl)-propanal; 2-methyl-3-(
  • the perfumes useful in the present invention compositions are substantially free of halogenated materials and nitromusks.
  • Suitable solvents, diluents or carriers for perfumes ingredients mentioned above are for examples, ethanol, isopropanol, diethylene glycol, monoethyl ether, dipropylene glycol, diethyl phthalate, triethyl citrate, etc.
  • the amount of such solvents, diluents or carriers incorporated in the perfumes is preferably kept to the minimum needed to provide a homogeneous perfume solution.
  • Perfume can be present at a level of from 0% to 10%, preferably from 0.1% to 5%, and more preferably from 0.2% to 3%, by weight of the finished composition.
  • Fabric softener compositions of the present invention provide improved fabric perfume deposition.
  • Perfume ingredients may also be suitably added as releasable fragrances, for example, as pro-perfumes or pro-fragrances as described in U.S. 5,652,205 Hartman et al., issued July 29, 1997, WO95/04809, WO96/02625, PCT US97/14610 filed 19 August 1997 and claiming priority of 19 August 1996, EP-A-0,752,465, co-pending application EP 98870227.0, EP 98870226.2, EP 99870026.4, and EP 99870025.6; all incorporated herein by reference.
  • Soil Release agents are desirably used in compositions of the instant invention. Any polymeric soil release agent known to those skilled in the art can optionally be employed in the compositions of this invention. Polymeric soil release agents are characterized by having both hydrophilic segments, to hydrophilize the surface of hydrophobic fibers, such as polyester and nylon, and hydrophobic segments, to deposit upon hydrophobic fibers and remain adhered thereto through completion of washing and rinsing cycles and, thus, serve as an anchor for the hydrophilic segments. This can enable stains occurring subsequent to treatment with the soil release agent to be more easily cleaned in later washing procedures.
  • soil release agents will generally comprise from about 0.01% to about 10.0%, by weight, of the detergent compositions herein, typically from about 0.1% to about 5%, preferably from about 0.2% to about 3.0%.
  • soil release agents include the METOLOSE SM100, METOLOSE SM200 manufactured by Shin-etsu Kagaku Kogyo K.K., SOKALAN type of material, e.g., SOKALAN HP-22, available from BASF (Germany), ZELCON 5126 (from Dupont) and MILEASE T (from ICI).
  • compositions according to the present invention are optional requirements of the compositions according to the present invention.
  • the pH as measured in the neat compositions at 20 °C is greater than 3, preferably between 3 and 12, more preferably between 4 and 8, most preferably is of 5. This range is preferred for fabric safety.
  • the pH of these compositions herein can be regulated by the addition of a Bronsted acid.
  • the present invention can include optional components conventionally used in textile treatment compositions, for example, humectants like diethylene glycol, and/or salts like lithium salts, colorants, bactericides, optical brighteners, opacifiers, anti-shrinkage agents, germicides, fungicides, anti-oxidants, color protection agent like dye fixing agent as described in EP 931133, enzymes, chelating agents, cyclodextrin as described in WO 98/56888, metallic salts to absorb amine and sulfur-containing compounds and selected from the group consisting of copper salts, zinc salts, and mixtures thereof, water-soluble polyionic polymers, e.g., water-soluble cationic polymer like polyamines, and water-soluble anionic polymers like polyacrylic acids, other antistatic agent, insect and/or moth repelling agents, colorants and dyes, anti-clogging agent, and the like; typical disclosure of which can be found in WO 98/56888.
  • compositions are preferably free of any material that would soil or stain fabric, and are also substantially free of starch. Typically, there should be less than about 0.5%, by weight of the composition, preferably less than about 0.3%, more preferably less than about 0.1%, by weight of the composition, of starch and/or modified starch.
  • composition of the invention may take a variety of physical form including liquid, liquid-gel, paste-like, foam in either aqueous or non-aqueous form, powder like granular and tablet forms.
  • a preferred form of the composition is in a liquid form.
  • the composition When in a liquid form, the composition is preferably dispensed by a dispensing means such as a spray dispenser, aerosol dispenser, or refill thereof. Still another preferred dispensing means is by incorporation of the composition of the invention in the ironing tank per se, or via a cartridge preferably adapted for the iron.
  • a dispensing means such as a spray dispenser, aerosol dispenser, or refill thereof.
  • Still another preferred dispensing means is by incorporation of the composition of the invention in the ironing tank per se, or via a cartridge preferably adapted for the iron.
  • the present invention also relates to such compositions incorporated into a spray dispenser to create an article of manufacture that can facilitate treatment of fabric articles and/or surfaces with the compositions according to the invention at a level that is effective.
  • the spray dispenser comprises manually activated and non-manual powered (operated) spray means and a container containing the treating composition. Typical disclosure of such spray dispenser can be found in WO 96/04940 page 19 line 21 to page 22 line 27.
  • the spray dispenser is selected from spray dispenser comprising battery operated pump, spray dispenser comprising a trigger spray device, spray dispenser comprising a pressurized aerosol spray dispenser.
  • the use of the water-soluble lubricant provided a reduction of the WRA compared to water. Accordingly, there is provided a method of increasing the WRA of fabrics, which comprises the steps of contacting the fabrics with a water-soluble lubricant as defined herein before, using a domestic process.
  • the use of the water-soluble lubricant or composition of the invention provides surprisingly good benefit on the dewrinkling performance upon wearing. This benefit is particularly achieved while spraying the compound or composition from the iron. Accordingly, there is also provided a method of treating fabrics, in particular to provide in wear wrinkle resistance on fabrics, which comprises the steps of contacting the fabrics with a water-soluble lubricant or composition according to the invention, as defined herein before, using a domestic process.
  • contacting it is meant any steps that is suitable for providing a contact of the composition with the fabric. This can include by soaking, washing, rinsing, and/or spraying as well as by means of a dryer sheet onto which is adsorbed the composition.
  • the contacting occurs after the laundering and optional drying of the fabrics, e.g. by spraying, more preferably by spraying from the iron spray dispenser and/or via the vaporisation holes from the iron sole.
  • the composition of the present invention is used as an ironing aid.
  • An effective amount of the composition can be sprayed onto fabric, wherein said fabric should not be sprayed to saturation.
  • Still another preferred way of treating the fabrics is when the fabric can be sprayed with an effective amount of the composition, allowed to dry and then ironed, or sprayed and ironed immediately.
  • the composition of the invention can also be sprayed onto the fabrics by means of an iron spraying means, whereby the composition is incorporated into the iron as is or via a cartridge, preferably adapted for the iron.
  • the spraying means should preferably be capable of providing droplets with a weight average diameter of from about 40 to about 200 ⁇ m, preferably from about 70 to about 150 ⁇ m.
  • the loading of moisture on fabrics made of natural and synthetic fibers is from about 5 to about 25%, more preferably from about 5 to about 10% by weight of the dried fabric.
  • cylinder test By “wrinkle reducing composition”, it is meant that the composition is tested on 100% cotton, woven Oxford pinpoint fabric according to the procedure given in W. Garner, Textile Laboratory Manual Vol. 6, Ed. 3, Elsevier Inc., 1967, p. 105, so called “cylinder test”.
  • Wrinkle reducing compositions are compositions which provide a better crease resistance versus water, i.e fabrics that have been treated with a composition of the invention show less wrinkles compared to fabrics which have only been treated with water.
  • the composition can be sprayed onto fabrics by an in-home de-wrinkling chamber containing the fabric to be dewrinkled, thereby providing ease of operation.
  • Conventional personal as well as industrial de-wrinkling apparatuses are suitable for use herein. Traditionally, these apparatuses act by a steaming process which effects a relaxation of the fibers. Examples of home dewrinkling chambers include shower stalls.
  • the spraying of the composition or compounds onto the fabrics can then occur within the chamber of the apparatus or before placing the fabrics into the chamber.
  • the spraying means should preferably be capable of providing droplets with a weight average diameter of from about 8 to about 100 ⁇ m, preferably from about 10 to about 50 ⁇ m.
  • the loading of moisture on fabrics made of natural and synthetic fibers is from about 5 to about 25%, more preferably from about 5 to about 10% by weight of the dried fabric.
  • Other conventional steps that can be carried out in the dewrinkling apparatus can be applied such as heating which will provide the curing step and drying.
  • the temperature profile inside the chamber ranges from about 40°C to about 80°C, more preferably from about 50°C to about 70°C.
  • the preferred length of the drying cycle is from about 15 to about 60 minutes, more preferably from about 20 to about 45 minutes.
  • the steaming step in the dewrinkling apparatus can also be eliminated if the composition is maintained at a temperature range from about 22°C (about 72° F) to about 76°C (170°F) before spraying.
  • the present invention encompasses the method of spraying a mist of an effective amount of solution of the invention composition onto fabric and/or fabric articles.
  • said fabric and/or fabric articles include, but are not limited to, clothes, curtains, drapes, upholstered furniture, carpeting, bed linens, bath linens, tablecloths, sleeping bags, tents, car interiors, etc.
  • compositions herein are especially useful, when used to treat garments for extending the time before another wash cycle is needed, and/or even reducing the time involved in ironing.
  • Such garments include uniforms and other garments which are normally treated in an industrial process, which can be dewrinkled and the time between treatments extended.
  • an article of manufacture comprising a container and the composition of the invention in association with a set of instructions to use the composition in an amount effective to provide a solution to problems involving and/or provision of a benefit related to those selected from reducing wrinkles; imparting in-wear resistance to fabrics. It is important that the consumer be aware of these additional benefits, since otherwise the consumer would not know that the composition would solve these problems and/or provide these benefits.
  • the phrase " in association with” means the set of instructions are either directly printed on the container itself or presented in a separate manner including, but not limited to, a brochure, print advertisement, electronic advertisement, and/or verbal communication, so as to communicate the set of instructions to a consumer of the article of manufacture.
  • the set of instructions preferably comprises the instruction to apply an effective amount of the composition, preferably by spraying, to provide the indicated benefit, e.g. wrinkles reduction; imparting in-wear resistance to fabrics.

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  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Dispersion Chemistry (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Detergent Compositions (AREA)
  • Lubricants (AREA)
EP99870223A 1999-10-27 1999-10-27 Composition résistante à la froissure Withdrawn EP1096060A1 (fr)

Priority Applications (9)

Application Number Priority Date Filing Date Title
EP99870223A EP1096060A1 (fr) 1999-10-27 1999-10-27 Composition résistante à la froissure
PCT/US2000/029769 WO2001031112A2 (fr) 1999-10-27 2000-10-27 Composition resistant aux plis
AU12426/01A AU1242601A (en) 1999-10-27 2000-10-27 Wrinkle resistant composition
CA002386928A CA2386928A1 (fr) 1999-10-27 2000-10-27 Composition resistant aux plis
CZ20021397A CZ20021397A3 (cs) 1999-10-27 2000-10-27 Nemačkavý prostředek
JP2001533243A JP2003513176A (ja) 1999-10-27 2000-10-27 しわ抵抗組成物
MXPA02004210A MXPA02004210A (es) 1999-10-27 2000-10-27 Composicion contra las arrugas.
EP00973987A EP1238137A2 (fr) 1999-10-27 2000-10-27 Composition resistant aux plis
US10/924,539 US20050015888A1 (en) 1999-10-27 2004-08-24 Wrinkle resistant composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP99870223A EP1096060A1 (fr) 1999-10-27 1999-10-27 Composition résistante à la froissure

Publications (1)

Publication Number Publication Date
EP1096060A1 true EP1096060A1 (fr) 2001-05-02

Family

ID=8243917

Family Applications (2)

Application Number Title Priority Date Filing Date
EP99870223A Withdrawn EP1096060A1 (fr) 1999-10-27 1999-10-27 Composition résistante à la froissure
EP00973987A Withdrawn EP1238137A2 (fr) 1999-10-27 2000-10-27 Composition resistant aux plis

Family Applications After (1)

Application Number Title Priority Date Filing Date
EP00973987A Withdrawn EP1238137A2 (fr) 1999-10-27 2000-10-27 Composition resistant aux plis

Country Status (7)

Country Link
EP (2) EP1096060A1 (fr)
JP (1) JP2003513176A (fr)
AU (1) AU1242601A (fr)
CA (1) CA2386928A1 (fr)
CZ (1) CZ20021397A3 (fr)
MX (1) MXPA02004210A (fr)
WO (1) WO2001031112A2 (fr)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002086049A1 (fr) * 2001-04-23 2002-10-31 The Procter & Gamble Company Compositions aqueuses pour l'entretien des tissus permettant une utilisation efficace hors de chez soi et accessoires associés
WO2004018765A1 (fr) * 2002-08-19 2004-03-04 Unilever Plc Composition d'entretien de tissu
AU2003260168B2 (en) * 2002-10-04 2005-07-07 Tenix Investments Pty Ltd Data quality & integrity engine
DE102004015376A1 (de) * 2004-03-26 2005-10-13 Henkel Kgaa Verwendung von Silizium-haltigen Verbindungen zur Behandlung von textilen Flächengebilden
WO2006017503A1 (fr) * 2004-08-03 2006-02-16 Johnsondiversey, Inc. Compositions lubrifiantes pour conteneur ou piste de convoyeur
EP1746153A1 (fr) 2005-07-22 2007-01-24 Unilever Plc Perfectionnements au lavage du linge
US7429558B2 (en) 2002-01-18 2008-09-30 Unilever Home & Personal Care Division Of Conopco, Inc. Azetidinium modified polymers and fabric treatment composition
CN106592249A (zh) * 2016-11-25 2017-04-26 山东黄河三角洲纺织科技研究院有限公司 一种棉织物的抗皱整理剂及其制备方法和抗皱整理工艺
CN109342311A (zh) * 2018-10-08 2019-02-15 浙江染化宝检测服务有限公司 一种高精度织物折皱回复角检测仪

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4843022B2 (ja) 2005-04-07 2011-12-21 コーニンクレッカ フィリップス エレクトロニクス エヌ ヴィ アイロンをかけられる物品の布地の種類を識別する識別手段を有するアイロン装置
JP4652126B2 (ja) * 2005-05-23 2011-03-16 花王株式会社 アイロン仕上げ剤
KR20100110732A (ko) * 2009-04-03 2010-10-13 라이온 가부시키가이샤 섬유 제품용 수성 주름 감소제 조성물
US11019902B2 (en) 2014-05-01 2021-06-01 Cornell University Green technology for crosslinking protein molecules for various uses
US11530300B2 (en) 2014-05-01 2022-12-20 Cornell University Residual soy flour sugars as crosslinkers for enhancing mechanical performance of protein fibers

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GB674948A (en) * 1948-03-27 1952-07-02 Monsanto Chemicals Improvements in or relating to the production of a glazed finish on textile fabrics
GB827647A (en) * 1955-11-01 1960-02-10 Tootal Broadhurst Lee Co Ltd Process for the treatment of native cellulosic texí¡í¡ with a synthetic resin
US4376802A (en) * 1980-01-24 1983-03-15 Allied Corporation Finish composition for polyester yarn
US4661268A (en) * 1985-12-24 1987-04-28 Very Incredible Products, Inc. Wrinkle removing solution and process for using same
US5100566A (en) * 1991-02-04 1992-03-31 Dow Corning Corporation Fabric wrinkle reduction composition and method
US5573695A (en) * 1995-12-19 1996-11-12 Targosz; Eugene F. Compositions for removal of wrinkles in fabrics

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Publication number Priority date Publication date Assignee Title
US3965014A (en) * 1972-12-07 1976-06-22 Colgate-Palmolive Company Anionic fabric conditioners
JPH0411288A (ja) * 1990-04-27 1992-01-16 Brother Ind Ltd 楽曲検索機能付きカラオケ装置

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB674948A (en) * 1948-03-27 1952-07-02 Monsanto Chemicals Improvements in or relating to the production of a glazed finish on textile fabrics
GB827647A (en) * 1955-11-01 1960-02-10 Tootal Broadhurst Lee Co Ltd Process for the treatment of native cellulosic texí¡í¡ with a synthetic resin
US4376802A (en) * 1980-01-24 1983-03-15 Allied Corporation Finish composition for polyester yarn
US4661268A (en) * 1985-12-24 1987-04-28 Very Incredible Products, Inc. Wrinkle removing solution and process for using same
US5100566A (en) * 1991-02-04 1992-03-31 Dow Corning Corporation Fabric wrinkle reduction composition and method
US5573695A (en) * 1995-12-19 1996-11-12 Targosz; Eugene F. Compositions for removal of wrinkles in fabrics

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002086049A1 (fr) * 2001-04-23 2002-10-31 The Procter & Gamble Company Compositions aqueuses pour l'entretien des tissus permettant une utilisation efficace hors de chez soi et accessoires associés
US7429558B2 (en) 2002-01-18 2008-09-30 Unilever Home & Personal Care Division Of Conopco, Inc. Azetidinium modified polymers and fabric treatment composition
WO2004018765A1 (fr) * 2002-08-19 2004-03-04 Unilever Plc Composition d'entretien de tissu
AU2003260168B2 (en) * 2002-10-04 2005-07-07 Tenix Investments Pty Ltd Data quality & integrity engine
DE102004015376A1 (de) * 2004-03-26 2005-10-13 Henkel Kgaa Verwendung von Silizium-haltigen Verbindungen zur Behandlung von textilen Flächengebilden
WO2006017503A1 (fr) * 2004-08-03 2006-02-16 Johnsondiversey, Inc. Compositions lubrifiantes pour conteneur ou piste de convoyeur
US7592296B2 (en) 2004-08-03 2009-09-22 Johnsondiversey, Inc. Conveyor track or container lubricant compositions
AU2005271573B2 (en) * 2004-08-03 2010-05-27 Johnsondiversey, Inc. Conveyor track or container lubricant compositions
EP1746153A1 (fr) 2005-07-22 2007-01-24 Unilever Plc Perfectionnements au lavage du linge
CN106592249A (zh) * 2016-11-25 2017-04-26 山东黄河三角洲纺织科技研究院有限公司 一种棉织物的抗皱整理剂及其制备方法和抗皱整理工艺
CN106592249B (zh) * 2016-11-25 2019-02-22 山东黄河三角洲纺织科技研究院有限公司 一种棉织物的抗皱整理剂及其制备方法和抗皱整理工艺
CN109342311A (zh) * 2018-10-08 2019-02-15 浙江染化宝检测服务有限公司 一种高精度织物折皱回复角检测仪

Also Published As

Publication number Publication date
AU1242601A (en) 2001-05-08
WO2001031112A3 (fr) 2001-11-22
MXPA02004210A (es) 2002-10-17
EP1238137A2 (fr) 2002-09-11
JP2003513176A (ja) 2003-04-08
CZ20021397A3 (cs) 2002-09-11
CA2386928A1 (fr) 2001-05-03
WO2001031112A2 (fr) 2001-05-03

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