[go: up one dir, main page]

EP2388308A1 - Composition de nettoyage avec des propriétés detachantes améliorees - Google Patents

Composition de nettoyage avec des propriétés detachantes améliorees Download PDF

Info

Publication number
EP2388308A1
EP2388308A1 EP10163222A EP10163222A EP2388308A1 EP 2388308 A1 EP2388308 A1 EP 2388308A1 EP 10163222 A EP10163222 A EP 10163222A EP 10163222 A EP10163222 A EP 10163222A EP 2388308 A1 EP2388308 A1 EP 2388308A1
Authority
EP
European Patent Office
Prior art keywords
group
branched
linear
cleaning composition
cyclic
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Withdrawn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
EP10163222A
Other languages
German (de)
English (en)
Inventor
Isabelle Léonard
Valérie Kochowski
Geneviève Bonnechere - Delstanche
Olivier Henry
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.)
Dequest AG
Original Assignee
Dequest AG
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 Dequest AG filed Critical Dequest AG
Priority to EP10163222A priority Critical patent/EP2388308A1/fr
Priority to BR112012029448A priority patent/BR112012029448A8/pt
Priority to ES11720503.9T priority patent/ES2545222T3/es
Priority to PL11720503T priority patent/PL2571971T3/pl
Priority to CN201180024251.8A priority patent/CN103080291B/zh
Priority to EP11720503.9A priority patent/EP2571971B1/fr
Priority to US13/696,620 priority patent/US8883711B2/en
Priority to JP2013510626A priority patent/JP6174996B2/ja
Priority to PCT/EP2011/058154 priority patent/WO2011144699A1/fr
Priority to RU2012150152/04A priority patent/RU2571083C2/ru
Publication of EP2388308A1 publication Critical patent/EP2388308A1/fr
Priority to JP2015149127A priority patent/JP2015232139A/ja
Withdrawn legal-status Critical Current

Links

Images

Classifications

    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/26—Organic compounds containing nitrogen
    • C11D3/33—Amino carboxylic acids
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/20—Organic compounds containing oxygen
    • C11D3/22—Carbohydrates or derivatives thereof
    • C11D3/222—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/20—Organic compounds containing oxygen
    • C11D3/22—Carbohydrates or derivatives thereof
    • C11D3/222—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin
    • C11D3/225—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin etherified, e.g. CMC
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/37—Polymers
    • C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3719—Polyamides or polyimides

Definitions

  • the present invention relates generally to the field of cleaning composition.
  • the present invention relates to a cleaning composition suitable for stain removal.
  • the present invention also relates to the use of the cleaning composition in domestic and/or institutional and industrial surfaces cleaning.
  • NTA nitrilotriacetic acid
  • EDTA ethylenediaminetetraacetic acid
  • phosphonates to control water hardness ions.
  • NTA is by far the most widely used in these applications.
  • Chelating agents are used to control water hardness ions such as Ca 2+ and Mg 2+ providing scale inhibition formation in hard water by keeping these ions in solution. Chelating agents further provide control of other bivalent and trivalent ions such as manganese, copper and iron ions. This is of primary importance when cleaning compositions contain oxygen bleaches. Indeed, these ions act as catalysts for the decomposition of such bleach.
  • the addition of efficient metal ion chelating agents provides bleach stabilization.
  • Cleaning compositions sometimes also contain polycarboxylic polymers that provide soil dispersion. This further increases the cleaning performance by keeping the soil in solution. Soil is then easily rinsed away.
  • the most widely used polymers in such application are polyacrylate homo polymers of relatively low molecular weights and/or polyacrylate co-polymers of higher molecular weights.
  • WO 2008/132133 discloses a phosphate-free dishwasher detergent containing 0.01 - 20% by weight of at least one specific alcohol alkoxylate, 0.01 - 10% by weight of at least one specific alcohol ethoxylate, 0 - 15% by weight of at least one sulfonate group-containing polymer, 0 - 15% by weight of at least one hydrophilically modified polycarboxylate, 0 - 8% by weight of at least one polycarboxylate, 1 - 50% by weight of at least one complexing agent and 0.1 - 60% by weight of at least one further additive, components (A), (B), (C), (D), (E), (F) and (G) adding up to 100%.
  • WO 2006/029806 discloses a phosphate-free cleaning formulation for a dish cleaning machine containing the following components: (a) 1-20 % by weight hydrophobically modified polycarboxylate, (b) 1-50 % by weight complexing agent, (c) 1-15 % by weight non-ionic low-foaming detergents, (d) 0.1-30 % by weight bleaching and optionally a bleaching activator, (e) 0-60 % by weight additional detergents, (f) 0-8 % by weight enzymes, (g) 0-50 % by weight one or several types of additives, wherein from (a) to (g) is equal to 100 % by weight.
  • US 2008/0221006 discloses an alkaline cleaning composition comprising a source of alkalinity, a biodegradable surfactant system and a biodegradable chelating agent.
  • the influence of the biodegradable agent on antimicrobial activity is negligible at room or elevated temperature.
  • WO 2009/020546 discloses an aqueous, concentrated neutral detergent composition for use in cleaning medical instruments and metal components having scale control and corrosion inhibition properties.
  • the composition comprises at least one surfactant, at least one scale control component, at least one corrosion inhibitor, a buffer system and water.
  • Cleaning compositions known in the art have several disadvantages such as the low efficiency in stain removal, toxicity or low biodegradable properties. There is thus a need for an effective cleaning composition suitable for domestic and/or industrial and institutional surface cleaning. In short, there is a need for effective cleaning composition for surface cleaning which have enhanced cleaning performance to currently available products, are biodegradable, non-toxic, non-carcinogenic or cost effective.
  • the present invention aims at providing cleaning compositions that overcome the above-discussed drawbacks of the prior art.
  • the present invention aims at providing cleaning compositions which are environmentally friendly and exhibit enhanced stain removal.
  • the invention provides a cleaning composition characterized in that the cleaning composition comprises:
  • composition of the present invention may optionally further contain a component (III) comprising any one, or combination of, conventional ingredients well known in the art of cleaning compositions.
  • hydrolysable as used herein means that the backbone of the polymer is susceptible to hydrolysis, i. e. that the polymer comprises a polycondensate containing ether, ester and/or amide bonds.
  • dispersing as used herein means that the polymer is capable of dispersing soil particles in the aqueous cleaning medium.
  • biodegradable as used herein means that the amino carboxylate chelating agent can be degraded by micro-organisms, preferably that it is readily biodegradable in accordance with either of OECD Guideline for Testing of Chemicals 301 methods A to F.
  • chelating agent as used herein means that the compound is able to bind a single positively charged central atom, preferably a metal cation such as Ca 2+ or Mg 2+ .
  • the cleaning composition of the present invention enhances stain removal due to the synergistic and specific combination of a dispersing polymer and one or more chelating agents. Another advantage of the cleaning composition is that the aqueous cleaning composition may be free of various phosphorous compounds, such as phosphonates, phosphates, polyphosphates and the like. As mentioned above cleaning compositions of the present invention surprisingly yield synergistic results with regard to cleaning performance. Unexpected results with respect to soil removal are obtained.
  • the use of the cleaning composition according to the present invention for stain removal is provided.
  • a method for cleaning a surface comprising the step of contacting the surface with a composition of the invention.
  • FIG. 1A and FIG. 1B are comparative charts representing stain removal ( ⁇ E) obtained in presence of various compositions on starch mix and coffee stains respectively. These figures illustrate the synergy observed between one hydrolysable dispersing polymer (carboxymethylinulin) and one biodegradable aminocarboxylate chelating agent (methylglycin diacetic acid - MGDA).
  • FIG. 2A and FIG. 2B are comparative charts representing stain removal ( ⁇ E) obtained in presence of various compositions on starch mix and coffee stains respectively. These figures illustrate the synergy observed between one hydrolysable dispersing polymer (carboxymethylinulin) and one biodegradable aminocarboxylate chelating agent (glutamic diacetic acid - GLDA).
  • FIG. 3A and FIG. 3B are comparative charts representing stain removal ( ⁇ E) obtained on starch mix by various compositions in presence of 75% of sodium hydroxide solution.
  • the invention provides a cleaning composition characterized in that the composition comprises:
  • the number of biodegradable aminocarboxylate chelating agents within the cleaning composition may range from 1 to 10, preferably from 1 to 5. More preferably, the cleaning composition comprises one biodegradable aminocarboxylate chelating agent. Alternatively, the cleaning composition may comprise two biodegradable aminocarboxylate chelating agents.
  • substituted means that one or more hydrogen of the corresponding atom is replaced with a selection of substituents, provided that the valence of said corresponding atom does not exceed the normal valence thereof, and that the substitution gives rise to a chemically stable compound, i.e. a robust compound able to survive to its identification at an acceptable degree of purity from the reaction mixture.
  • the term "one or more" means from one substituent to the highest possible number of substitution, i.e. replacement of one hydrogen up to replacement of all hydrogen by substituents.
  • C 1 -C 10 linear, branched, cyclic hydrocarbon radical refers to a hydrocarbyl radical having from 1 to 10 carbon atoms.
  • the hydrocarbon radical refers to, but is not limited to, the radicals methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, s-butyl, t-butyl, 1-pentyl, 2-pentyl, 3-pentyl, i-pentyl, neo-pentyl, t-pentyl, 1-hexyl, 2-hexyl, 3-hexyl, 1-methyl-1-ethyl-n-pentyl, 1,1,2-trimethyl-n-propyl, 1,2,2-trimethyl-npropyl, 3,3-dimethyl-n-butyl, 1-heptyl, 2-heptyl, 1-ethyl-1,2-dimethyl-methyl-butyl, 1-h
  • C 1-6 hydrocarbon radical refers to a hydrocarbon radical having from 1 to 6 carbon atoms and includes but is not limited to, methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, s-butyl, t-butyl, 1-pentyl, 2-pentyl, 3-pentyl, i-pentyl, neo-pentyl, t-pentyl, 1-hexyl, 2-hexyl, 3-hexyl.
  • C 1-3 hydrocarbon radical denotes a hydrocarbon radical having from 1 to 3 carbon atoms and refers to, but is not limited to, methyl, ethyl, n-propyl, i-propyl.
  • heterocyclic refers to a heterocycloalkyl or a heteroaryl radical.
  • heterocycloalkyl refers to a monovalent saturated or partially unsaturated monocyclic ring system.
  • the heterocycloalkyl may be 5- or 6-membered heterocycloalkyl, i.e. a monovalent monocyclic ring containing one or two ring heteroatoms selected from N, O, and S.
  • Examples for 5- or 6-membered heterocycloalkyl moieties are tetrahydropyranyl, tetrahydrothiopyranyl, tetrahydrofuranyl, tetrahydrothiophenyl, pyrrolidinyl, imidazolidinyl, morpholinyl, thiomorpholinyl, piperidinyl, and piperazinyl. Preferred examples are morpholinyl, piperidinyl or piperazinyl.
  • heteroaryl denotes a monovalent monocyclic or bicyclic, preferably monocyclic, aromatic ring system of 5 or 6 ring atoms containing one, two, or three ring heteroatoms selected from N, O, and S, the remaining ring atoms being carbon atoms.
  • heteroaryl moieties include, but are not limited to thiophenyl, furanyl, pyrrolyl, imidazolyl, pyrazolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, [1,2,4]oxadiazolyl, [1,3,4]oxadiazolyl, [1,2,4]triazolyl, [1,2,3]triazolyl, tetrazolyl, pyridinyl, pyrimidinyl, pyrazinyl or pyridazinyl.
  • aromatic groups refers to polyunsaturated groups having one or more fused rings or covalently linked, containing from 6 to 10 carbon atoms, wherein the ring is aromatic.
  • the aromatic group can be substituted.
  • the aromatic group can be phenyl or naphtyl.
  • said one or more biodegradable aminocarboxylate chelating agents (II) is of general formula (A), or salt thereof: wherein
  • the aminocarboxylate chelating agents (II) of general formula (A) may not be a compound wherein the substituents R 1 and R 2 are simultaneously hydrogen.
  • methylene group refers to a hydrocarbyl radical having one carbon atom.
  • the methylene group may be unsubstituted and may be a -CH 2 -moiety.
  • the methylene group may be substituted by one or two substituents selected from the group consisting of OH, COOH, COOR', F, Br, Cl, I, OR', SO 3 H, SO 3 R', SH, SR', NH 2 , NR' 2 , CONH 2 , CONR' 2 , C 5 -C 6 heterocyclic groups and C 1 -C 10 linear, branched, cyclic or aromatic groups unsubstituted or substituted by one or more OH, COOH, COOR', F, Br, Cl, I, OR', SO 3 H, SO 3 R', SH and/or SR' moieties wherein R' is a C 1 -C 10 linear, branched, cyclic or aromatic hydrocarbon group.
  • said one or more biodegradable aminocarboxylate chelating agents (II) are of general formula (A), or a salt thereof:
  • said one or more biodegradable aminocarboxylate chelating agents (II) is of general formula (A), or a salt thereof:
  • said one or more biodegradable aminocarboxylate chelating agents (II) is of general formula (A), or a salt thereof: wherein
  • said one or more biodegradable aminocarboxylate chelating agents have at least two carboxylic acid substituents on carbon atom(s) in ⁇ -position or in ⁇ -position of the nitrogen atom.
  • said one or more biodegradable aminocarboxylate chelating agents have at least two carboxylic acid substituents on carbon atom(s) in ⁇ -position of the nitrogen atom.
  • said one or more biodegradable aminocarboxylate chelating agents (II) are selected from the group consisting of methylglycin diacetic acid (MGDA), glutamic diacetic acid (GLDA), iminodisuccinic acid (IDS), salts thereof, and mixtures thereof.
  • the biodegradable aminocarboxylate chelating agent (II) may be in form of a salt.
  • the salt is an alkali, ammonia and amine salt, especially sodium or potassium salt.
  • the chelating agent has more than one carboxylic acid moiety, the one or more carboxylic acid moieties can be in form of a salt.
  • the cleaning composition of the present invention comprises a hydrolysable dispersing polymer (I) which is preferably selected from the group consisting of carboxylated fructan components, polyaspartic acid, salts thereof, chitosan, block copolymers having polyacrylic acid moiety and chitosan and/or polysaccharide moiety(ies).
  • a hydrolysable dispersing polymer (I) which is preferably selected from the group consisting of carboxylated fructan components, polyaspartic acid, salts thereof, chitosan, block copolymers having polyacrylic acid moiety and chitosan and/or polysaccharide moiety(ies).
  • the cleaning composition of the present invention comprises a hydrolysable dispersing polymer (I) selected from the group consisting of polyaspartic acid and a carboxylated fructan component selected from the group consisting of:
  • Fructans used as starting material for producing the carboxylated fructans used as component (I) are oligo- and polysaccharides which have a majority of anhydrofructose units, and can have a polydisperse chain length distribution and can be of straight- or branched-chain.
  • the fructan contains mainly beta-2,1 bonds, as in inulin.
  • the fructans, and the preferred inulin, used as starting material for producing component (I) can be products obtained directly from a vegetable source or other sources as well as products in which the average chain length has been modified, increased or reduced, by fractionation, enzymatic synthesis or hydrolysis.
  • Carboxylated fructans with modified average chain length can be made from fructans with enzymatically increased chain length, fructan hydrolysis products having shortened chains and fractionated products having a modified chain length. Fractionating of fructans such as inulin can be achieved, for example, by means of known techniques including low temperature crystallization (see WO 94/01849 ), column chromatography (see WO 94/12541 ), membrane filtration (see EP-A-0440074 , EP-A-0627490 ) or selective precipitation with alcohol.
  • Hydrolysis to yield shorter fructans can be carried out, for example, enzymatically (endo-insulase), chemically (water and acid) or by heterogeneous catalysis (acid column).
  • Reduced, oxidized, hydroxyalkylated and/or crosslinked fructans can also represent suitable starting materials to produce the carboxylated fructans used as component (I).
  • the fructans have an average chain length (degree of polymerization, DP) of at least 3 to about 1000.
  • the average chain length is from 3 to 60, in particular of from 5 to 30 monosaccharide units.
  • a preferred fructan is inulin (beta-2,1-fructan) or a modified inulin, and these preferred carboxylated inulins and modified inulins are made accordingly.
  • Dicarboxyfructans can be obtained through oxidation of the fructan raw material, and accordingly the preferred dicarboxyinulins can be obtained through oxidation of the inulin raw material.
  • the anhydrofructose units are converted, with ring opening, into dicarboxy(hydroxyethoxy)ethyleneoxy units.
  • the oxidation can proceed in one step with hypohalite, as described in WO 91/17189 , or in two steps with periodate and chlorite, as described in WO 95/12619 .
  • Preferred degrees of oxidation (DO) are in the range of from 20 to 90%, the DO being the (molar) percentage of monosaccharide units converted into the corresponding dicarboxy analogues.
  • Fructan polycarboxylic acid is preferably inulin polycarboxylic acid which can be prepared by successive oxidation and carboxyalkylation of the selected starting material.
  • the material has a DO (degree of oxidation) of from 0.2 to 2.0 and a degree of carboxy-alkyl/-acyl substitution of from 0.2 to 3, preferably from 1.5 to 2.7.
  • 6-carboxyfructan is preferably 6-Carboxy inulin, which is a well known material. It can be obtained by oxidation in accordance with the method of WO 95/07303 .
  • polyaspartic acid refers to a homo or co - polymer having at least one block comprising repetitive unit of aspartic acid.
  • Polyaspartic acid may be in form of a salt.
  • the term encompasses polymer from both L and D-aspartic acid monomer.
  • chitosan refers to a linear polysaccharide composed of randomly distributed ⁇ -(1-4)-linked D-glucosamine.
  • chitosan encompasses chitosan wherein part or whole amine moities are substituted.
  • the carboxylated fructan component is selected from carboxyalkylinulin having 1 or 2 carbon atoms in the alkyl moiety (e.g. carboxymethylinulin and/or carboxyethylinulin) and having a degree of substitution of from 1.5 to 2.7.
  • Carboxymethylinulin can be prepared by reaction of the fructan with chloroacetic acid as described in WO 95/15984 or in EP 1 713 831 .
  • Carboxylethylinulin can be prepared in accordance with the method of WO 96/34017 .
  • the dispersing polymer (I) is selected from the group consisting of polyaspartic acid or a salt thereof, and carboxyalkylinulin having 1 or 2 carbon atoms in the alkyl moiety and having a degree of substitution of from 1.5 to 2.7.
  • the carboxylated fructan component is carboxymethylinulin having a degree of substitution of from 1.5 to 2.7.
  • the hydrolysable dispersing polymer (I) is preferably selected from the group consisting of polyaspartic acid, a salt thereof, and carboxymethylinulin having a degree of substitution of from 1.5 to 2.7. More preferably, the hydrolysable dispersing polymer (I) is carboxymethylinulin having a degree of substitution of from 1.5 to 2.7. Alternatively, more preferably, the hydrolysable dispersing polymer (I) is polyaspartic acid or a salt thereof.
  • the weight ratio between components (I) and (II) may be in the range of 30 : 1 to 1 : 100.
  • the weight ratio between components (I) and (II) is in the range of 1 : 1 to 1 : 100.
  • the cleaning composition is an aqueous alkaline composition.
  • the pH of the cleaning composition may be higher than 9, preferably higher than 11.
  • the cleaning compositions of the present invention may be used at temperature ranging from 20°C to 95°C, preferably from 40°C to 90°C.
  • the percentage in active ingredient of biodegradable aminocarboxylate chelating agents (II), in the cleaning composition is in the range from 0.5 to 50%.
  • the percentage in active ingredient of biodegradable aminocarboxylate chelating agents is in the range from 2% to 30%.
  • the percentage in active ingredient of dispersing polymer, in the cleaning composition is in the range from 0.15% to about 5%.
  • the percentage in active ingredient of dispersing polymer (I) is in the range from 0.3% to 2%.
  • the cleaning composition of the present invention is used for stain removal.
  • the cleaning composition according to the invention may be used in institutional and industrial surfaces cleaning.
  • the cleaning composition according to the invention may be used in domestic surfaces cleaning.
  • industrial applications comprises any cleaning application made in the industry, including without limitation the cleaning and washing of vehicles, walls, floors, tiles and the like, stainless steel surfaces, toilets, machines including, for example, storage tanks, tubes and pipelines, as used in the industry, subjects in processing and production facilities, such as used in the food processing industry, canteen kitchens, or slaughter houses.
  • institutional applications comprises any cleaning application made outside industry, including without limitation the cleaning and washing of subjects in housekeeping, hotels, hospitals, airports and the like, such as cleaning and washing of walls, floors, tiles and the like, stainless steel surfaces, toilets, plates and dishes, silverware, pots and pans, china and crystalware.
  • domestic hard surfaces cleaning comprises any cleaning application outside industry that is executed by a non-professional housekeeper (such as housewife, etc.). The cleaning method of the invention may be applied in all such uses.
  • Cleaning compositions of the present invention optionally furthermore contain ingredients and auxiliaries of a component (III) comprising any one, or combinations of, detergent ingredients selected from builders, solvents, perfumes, optical brighteners, other dispersing agents, pH adjusting agents, fiber softeners, suds regulants, dyes, dye transfer inhibitors, enzymes and anti-redeposition agents and additional detergent components well known in the art. Any of such components is used for its known functionality in known levels. The choice of any such component will, of course, vary depending upon the physical state, pH and application properties of a given composition.
  • component (III) and, thus, the composition of the invention, does not contain NTA and/or EDTA, more preferably neither NTA nor EDTA.
  • composition of the invention is free of phosphorous compounds, such as phosphonates, phosphates, polyphosphates and the like.
  • composition of the invention is free of phosphorous compounds, NTA and EDTA.
  • the test principle is the following: the standardized colored soiled melamine tiles are soaked, under constant and defined agitation, in beaker containing the cleaning composition to be evaluated at 2g/L.
  • the beaker (containing the soiled tile and the cleaning composition) is placed into an oven equipped with agitating plate. The temperature is kept constant.
  • the percentage of active ingredient mentions in the following examples is the percentage calculated in the cleaning composition before dilution at 2g/L.
  • methylglycin diacetic acid was purchased by BASF (Trilon ® M series), glutamic diacetic acid (GLDA) by Akzo Nobel (Dissolvine ® GL #3).
  • Carboxymethylinulin was provided by Dequest AG (Dequest ® PB #3) and polyacrylic acid polymer by Rohm&Haas (Acusol ® 445N). Examples 1 to 4 were performed under institutional and industrial conditions.
  • compositions were tested on starch mix and coffee stains. Stain removal ( ⁇ E) are listed in Table 1. The results are represented in FIG. 1A for tests on starch mix and in FIG. 1B for coffee stains.
  • Composition 1 contained 10% of sodium hydroxide (NaOH) solution.
  • Composition 2 contained 10% of sodium hydroxide (NaOH) solution and 3.3% of carboxymethylinulin having a degree of substitution (DS) of 2.5.
  • Composition 3 contained 10% of sodium hydroxide (NaOH) solution and 75% of methylglycin diacetic acid (MGDA).
  • Composition 4 was a composition of the present invention and contained 10% of sodium hydroxide (NaOH) solution, 3.3% of carboxymethylinulin (DS of 2.5), and 75% of methylglycin diacetic acid (MGDA). All compositions were completed with water to reach 100%. With regard to the sodium hydroxide (NaOH) solution, the percentage in active ingredient was 5%. With regard to the biodegradable aminocarboxylate chelating agent (MGDA), the percentage in active ingredient was 30%. With regard to the hydrolysable dispersing polymer (carboxymethylinulin), the percentage in active ingredient was 0.5%.
  • Stain removal ( ⁇ E) expected for the composition 4 was calculated by adding to stain removal value of composition 3 the difference between stain removal value of composition 2 and stain removal value of composition 1.
  • the stain removal ( ⁇ E) experimentally obtained with the composition 4 according to the present invention is noted 4b in FIG. 1A and 1 B .
  • stain removal ( ⁇ E) obtained with the composition 4 of the present invention was 37.8 which was far from the expected value (27.6). Therefore, a synergic effect was observed when combining a hydrolysable dispersing polymer, such as carboxymethyl inulin, and an biodegradable aminocarboxylate chelating agent, such as methylglycine diacetic acid. A synergism was also observed on coffee stains. Stain removal ( ⁇ E) obtained (60.3) was surprisingly higher than the expected value (51.9).
  • compositions were tested on starch mix and coffee stains. Stain removal ( ⁇ E) are listed in Table 2. The results are represented in FIG. 2A for tests on starch mix and FIG. 2B for tests on coffee.
  • Composition 1 contained 10% of sodium hydroxide (NaOH) solution.
  • Composition 2 contained 10% of sodium hydroxide (NaOH) solution and 3.3% of carboxymethylinulin having a degree of substitution (DS) of 2.5.
  • Composition 5 contained 10% of sodium hydroxide (NaOH) solution and 75% of glutamic diacetic acid (GLDA).
  • Composition 6 was a composition of the present invention and contained 10% of sodium hydroxide (NaOH) solution, 3.3% of carboxymethylinulin (DS of 2.5), and 75% of glutamic diacetic acid (GLDA). All compositions were completed with water to reach 100%. With regard to the sodium hydroxide (NaOH) solution, the percentage in active ingredient was 5%. With regard to the biodegradable aminocarboxylate chelating agent (GLDA), the percentage in active ingredient was 30%. With regard to the hydrolysable dispersing polymer (carboxymethylinulin), the percentage in active ingredient was 0.5%.
  • Stain removal ( ⁇ E) expected for the composition 6 was calculated by adding to stain removal of composition 5 the difference between stain removal value of composition 2 and stain removal value of composition 1.
  • the stain removal ( ⁇ E) experimentally obtained with the composition 6 according to the present invention is noted 6b in FIG. 2A and 2B .
  • Table 2 Comp.1 Comp. 2 Comp. 5 Comp. 6 Exected value
  • Comp. 6 obtained value
  • a synergism was also observed when using the composition 6 according to the invention on starch mix or coffee stains.
  • the expected stain removal ( ⁇ E) of the composition 6 was 27.7, and a stain removal ( ⁇ E) of 38.7 was obtained.
  • stain removal ( ⁇ E) expected was 51.2 and stain removal ( ⁇ E) of 59.8 was obtained.
  • Tests were performed on starch mix with two different aminocarboxylate chelating agents (II) in presence of 75% of sodium hydroxide (NaOH) solution. Stain removal ( ⁇ E) are listed in Table 3.
  • Composition 7 contained 75% of sodium hydroxide (NaOH) solution.
  • Composition 8 contained 75% of sodium hydroxide (NaOH) solution and 3.3% of carboxymethylinulin having a degree of substitution (DS) of 2.5.
  • Composition 9 contained 75% of sodium hydroxide (NaOH) solution and 10% of an biodegradable aminocarboxylate chelating agent (II).
  • Composition 10 was a composition of the present invention and contained 75% of sodium hydroxide (NaOH) solution, 3.3% of carboxymethylinulin (DS of 2.5), and 10% of biodegradable aminocarboxylate chelating agent (II). All compositions are completed with water to reach 100%. Stain removal ( ⁇ E) expected for composition 10 (noted 10a in FIG. 3A and FIG. 3B ) was calculated by adding to the stain removal ( ⁇ E) value of composition 9 the difference between the stain removal value of composition 8 and of composition 7. The stain removal ( ⁇ E) observed with the composition 10 according to the present invention is noted 10b in FIG. 3A and 3B .
  • sodium hydroxide (NaOH) solution the percentage in active ingredient was 37.5%.
  • biodegradable aminocarboxylate chelating agent (II) the percentage in active ingredient was 4%.
  • the hydrolysable dispersing polymer (carboxymethylinulin) the percentage in active ingredient was 0.5%.
  • FIG. 3A reported the results when the biodegradable aminocarboxylate chelating agent was methylglycin diacetic acid (MGDA).
  • FIG. 3B reported the results when the biodegradable aminocarboxylate chelating agent was glutamic diacetic acid (GLDA).
  • Table 3 Comp. 7 Comp. 8 Comp. 9 Comp. 10 (Expected value) Comp. 10 (Obtained value) Aminocarboxylate Chelating agent (II) : MGDA 13.8 18.4 19.4 24.0 31.3 Aminocarboxylate Chelating agent (II) : GLDA 13.8 18.4 19.9 24.5 33.5
  • Stain removal ( ⁇ E) obtained with composition 10 was higher than the expected value for both biodegradable aminocarboxylate chelating agents.
  • combining a biodegradable aminocarboxylate chelating agent and a hydrolysable dispersing polymer allows an improvement in stain removal. A synergism between both components was observed in cleaning compositions of the present invention even if the percentage in active ingredient of the biodegradable aminocarboxylate chelating agent was low.
  • Comparative example 4 aims to compare the performance of cleaning compositions of the present invention with a composition wherein carboxymethylinulin was replaced by polyacrylic acid. Tests were performed with GLDA or MGDA as biodegradable aminocarboxylate chelating agent. Stain removal ( ⁇ E) are listed in table 4 and table 5.
  • Composition 12 contained 10% of sodium hydroxide (NaOH) solution, 1.1 % of polyacrylic acid, and 75% of MGDA.
  • Composition 13 contained 10% of sodium hydroxide (NaOH) solution, 1.1% of polyacrylic acid, and 75% of GLDA.
  • compositions 12 and 13 comprising polyacrylic acid instead of a hydrolysable dispersing polymer such as carboxymethylinulin.
  • a hydrolysable dispersing polymer such as carboxymethylinulin.
  • the same results were observed when the amount of NaOH was 75% and the amount of biodegradable aminocarboxylate chelating agent was 10%.
  • the cleaning composition added to the auto dishwasher, contained 45 wt% of biodegradable aminocarboxylate chelating agent (MGDA, GLDA, or IDS), 22.5 wt% of soda ash, 3 wt% of non-ionic 7EO, 7.5 wt% of Disilicate de Sodium, 7.5 wt% of perborate de sodium, 3 wt% of tetra-acetyl ethylene diamine, 3 wt% of enzymes (1.5wt% amylase and 1.5wt% protease).
  • the composition further comprised either carboxymethylinulin (2 wt%) or polyacrylate (3 wt%).
  • the active ingredient percentage was 0.3% for carboxymethylinulin and 1.2% for polyacrylate. Glasses were soiled with 50g of ballast soil and placed into the autodishwasher. Tests were performed at 50°C for 78 minutes. Water hardness was at 300 ppm CaCO 3 After the washing was completed, a panel of five peoples gave independently a quote from 0 (soil glass) to 10 (clean glass). An average quote was then calculated. The results are listed in Table 6 for the spotting tests. The control was based on a composition containing one biodegradable aminocarboxylate chelating agent (II) (either MGDA or GLDA) and without hydrolysable dispersing polymer. The same value was obtained when MGDA or GLDA was used. Table 6 Control MGDA + Polyacrylate GLDA + Polyacrylate MGDA + CMI GLDA + CMI Spotting quote 6.7 6.3 7.3 7.5 8.5

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Molecular Biology (AREA)
  • Emergency Medicine (AREA)
  • Detergent Compositions (AREA)
EP10163222A 2010-05-19 2010-05-19 Composition de nettoyage avec des propriétés detachantes améliorees Withdrawn EP2388308A1 (fr)

Priority Applications (11)

Application Number Priority Date Filing Date Title
EP10163222A EP2388308A1 (fr) 2010-05-19 2010-05-19 Composition de nettoyage avec des propriétés detachantes améliorees
EP11720503.9A EP2571971B1 (fr) 2010-05-19 2011-05-19 Composition de nettoyage présentant un détachage amélioré
ES11720503.9T ES2545222T3 (es) 2010-05-19 2011-05-19 Composición de limpieza con eliminación de manchas mejorada
PL11720503T PL2571971T3 (pl) 2010-05-19 2011-05-19 Kompozycje czyszczące z polepszonym usuwaniem plam
CN201180024251.8A CN103080291B (zh) 2010-05-19 2011-05-19 改善去污的清洗组合物
BR112012029448A BR112012029448A8 (pt) 2010-05-19 2011-05-19 Composição de limpeza com remoção de manchas melhorada
US13/696,620 US8883711B2 (en) 2010-05-19 2011-05-19 Cleaning composition with improved stain removal
JP2013510626A JP6174996B2 (ja) 2010-05-19 2011-05-19 ステイン除去が改善された洗浄組成物
PCT/EP2011/058154 WO2011144699A1 (fr) 2010-05-19 2011-05-19 Composition de nettoyage présentant un détachage amélioré
RU2012150152/04A RU2571083C2 (ru) 2010-05-19 2011-05-19 Очищающая композиция для улучшенного удаления загрязнений
JP2015149127A JP2015232139A (ja) 2010-05-19 2015-07-29 ステイン除去が改善された洗浄組成物

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP10163222A EP2388308A1 (fr) 2010-05-19 2010-05-19 Composition de nettoyage avec des propriétés detachantes améliorees

Publications (1)

Publication Number Publication Date
EP2388308A1 true EP2388308A1 (fr) 2011-11-23

Family

ID=42941905

Family Applications (1)

Application Number Title Priority Date Filing Date
EP10163222A Withdrawn EP2388308A1 (fr) 2010-05-19 2010-05-19 Composition de nettoyage avec des propriétés detachantes améliorees

Country Status (1)

Country Link
EP (1) EP2388308A1 (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9416095B2 (en) 2013-07-16 2016-08-16 Akzo Nobel Chemicals International B.V. Salts, crystals, complexes, and derivatives of threonine diacetic acid, a process to prepare threonine diacetic acid, and the use thereof
WO2019152208A1 (fr) * 2018-01-30 2019-08-08 Eastman Chemical Company Compositions comprenant des agents de chélation de type aminocarboxylate

Citations (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0440074A1 (fr) 1990-02-02 1991-08-07 Südzucker Aktiengesellschaft Mannheim/Ochsenfurt Procédé de préparation d'un produit inulooligosaccharide pauvre en glucose, fructose et saccharose
WO1991017189A1 (fr) 1990-04-27 1991-11-14 Nederlandse Organisatie Voor Toegepast-Natuurwetenschappelijk Onderzoek Tno Procede de preparation de composes polycarboxy se liant au calcium forme a base de polysaccharides et agents de remplacement des phosphates dans des detergents, formes a base de ces composes polycarboxy
WO1994001849A1 (fr) 1992-07-13 1994-01-20 Michael Baum Test psychometrique
WO1994012541A1 (fr) 1992-11-24 1994-06-09 Raffinerie Tirlemontoise S.A. Procede de separation d'une composition polydispersee de saccharides, produits obtenus par ce procede et utilisation des produits obtenus dans des compositions alimentaires
EP0627490A1 (fr) 1993-05-17 1994-12-07 Südzucker Aktiengesellschaft Mannheim/Ochsenfurt Procédé pour la préparation d'inuline à longue chaîne
WO1995007303A1 (fr) 1993-09-07 1995-03-16 Nederlandse Organisatie Voor Toegepast-Natuurwetenschappelijk Onderzoek Tno Procede d'oxydation des glucides
WO1995012619A1 (fr) 1993-11-04 1995-05-11 Instituut Voor Agrotechnologisch Onderzoek (Ato-Dlo) Procede d'oxydation de glucides
WO1995015984A1 (fr) 1993-12-10 1995-06-15 Akzo Nobel N.V. Inuline carboxymethylique
WO1996034017A1 (fr) 1995-04-27 1996-10-31 Coöperatie Suiker Unie U.A. Derives d'inuline
DE19741721A1 (de) * 1997-09-22 1999-03-25 Huels Chemische Werke Ag Wasch- und Reinigungsmittelformulierungen mit Chitin/Chitosan-Derivaten als Schmutzlösepolymer
WO2006029806A1 (fr) 2004-09-14 2006-03-23 Basf Aktiengesellschaft Formulations de nettoyage pour un nettoyage de la vaisselle en machine contenant du polycarboxylate modifie de maniere hydrophobe
EP1655362A1 (fr) * 2004-11-03 2006-05-10 Lanxess Deutschland GmbH Composition de nettoyage pour enlever la suie
EP1713831A1 (fr) 2004-01-30 2006-10-25 Koninklijke Coöperatie Cosun U.A. Methode de fabrication d'inuline carboxyalkylique
US20080221006A1 (en) 2007-03-08 2008-09-11 Heisig Christopher C Biodegradable alkaline disinfectant cleaner with analyzable surfactant
WO2008132133A1 (fr) 2007-04-25 2008-11-06 Basf Se Détergent pour lave-vaisselle sans phosphate à pouvoir de rinçage remarquable
US20090032058A1 (en) * 2007-08-03 2009-02-05 Mcrae Ann Kneipp Biodegradable detergent concentrate for medical instruments and equipment
EP2045317A1 (fr) * 2007-10-04 2009-04-08 Lanxess Deutschland GmbH Moyen de lavage et de nettoyage liquide

Patent Citations (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0440074A1 (fr) 1990-02-02 1991-08-07 Südzucker Aktiengesellschaft Mannheim/Ochsenfurt Procédé de préparation d'un produit inulooligosaccharide pauvre en glucose, fructose et saccharose
WO1991017189A1 (fr) 1990-04-27 1991-11-14 Nederlandse Organisatie Voor Toegepast-Natuurwetenschappelijk Onderzoek Tno Procede de preparation de composes polycarboxy se liant au calcium forme a base de polysaccharides et agents de remplacement des phosphates dans des detergents, formes a base de ces composes polycarboxy
WO1994001849A1 (fr) 1992-07-13 1994-01-20 Michael Baum Test psychometrique
WO1994012541A1 (fr) 1992-11-24 1994-06-09 Raffinerie Tirlemontoise S.A. Procede de separation d'une composition polydispersee de saccharides, produits obtenus par ce procede et utilisation des produits obtenus dans des compositions alimentaires
EP0627490A1 (fr) 1993-05-17 1994-12-07 Südzucker Aktiengesellschaft Mannheim/Ochsenfurt Procédé pour la préparation d'inuline à longue chaîne
WO1995007303A1 (fr) 1993-09-07 1995-03-16 Nederlandse Organisatie Voor Toegepast-Natuurwetenschappelijk Onderzoek Tno Procede d'oxydation des glucides
WO1995012619A1 (fr) 1993-11-04 1995-05-11 Instituut Voor Agrotechnologisch Onderzoek (Ato-Dlo) Procede d'oxydation de glucides
WO1995015984A1 (fr) 1993-12-10 1995-06-15 Akzo Nobel N.V. Inuline carboxymethylique
WO1996034017A1 (fr) 1995-04-27 1996-10-31 Coöperatie Suiker Unie U.A. Derives d'inuline
DE19741721A1 (de) * 1997-09-22 1999-03-25 Huels Chemische Werke Ag Wasch- und Reinigungsmittelformulierungen mit Chitin/Chitosan-Derivaten als Schmutzlösepolymer
EP1713831A1 (fr) 2004-01-30 2006-10-25 Koninklijke Coöperatie Cosun U.A. Methode de fabrication d'inuline carboxyalkylique
WO2006029806A1 (fr) 2004-09-14 2006-03-23 Basf Aktiengesellschaft Formulations de nettoyage pour un nettoyage de la vaisselle en machine contenant du polycarboxylate modifie de maniere hydrophobe
EP1655362A1 (fr) * 2004-11-03 2006-05-10 Lanxess Deutschland GmbH Composition de nettoyage pour enlever la suie
US20080221006A1 (en) 2007-03-08 2008-09-11 Heisig Christopher C Biodegradable alkaline disinfectant cleaner with analyzable surfactant
WO2008132133A1 (fr) 2007-04-25 2008-11-06 Basf Se Détergent pour lave-vaisselle sans phosphate à pouvoir de rinçage remarquable
US20090032058A1 (en) * 2007-08-03 2009-02-05 Mcrae Ann Kneipp Biodegradable detergent concentrate for medical instruments and equipment
WO2009020546A1 (fr) 2007-08-03 2009-02-12 American Sterilizer Company Concentré de détergent biodégradable pour instruments et matériel médicaux
EP2045317A1 (fr) * 2007-10-04 2009-04-08 Lanxess Deutschland GmbH Moyen de lavage et de nettoyage liquide

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9416095B2 (en) 2013-07-16 2016-08-16 Akzo Nobel Chemicals International B.V. Salts, crystals, complexes, and derivatives of threonine diacetic acid, a process to prepare threonine diacetic acid, and the use thereof
WO2019152208A1 (fr) * 2018-01-30 2019-08-08 Eastman Chemical Company Compositions comprenant des agents de chélation de type aminocarboxylate
US11713435B2 (en) 2018-01-30 2023-08-01 Eastman Chemical Company Aminocarboxylate chelating agents and detergent compositions containing them

Similar Documents

Publication Publication Date Title
EP2571971B1 (fr) Composition de nettoyage présentant un détachage amélioré
CA2748533C (fr) Mise au point d'un adjuvant a base d'hydroxycarboxylate d'aluminium
EP3122786B1 (fr) Ester de carboxylate de polysaccharide
AU2006310249B2 (en) Detergent composition
JP7292309B2 (ja) ポリアスパラギン酸並びにオリゴ糖及び多糖をベースとするグラフトポリマーをフィルム抑制添加剤として含む食器洗い用洗剤製剤
KR20160055917A (ko) 식기세척 세제에서의 개질된 폴리아스파르트산의 용도
EP2519623B2 (fr) Produits de remplacement de phosphate pour des compositions de détergent et/ou de nettoyage compatibles avec des membranes
KR20180130513A (ko) 킬레이트제의 혼합물, 및 이러한 혼합물의 제조 방법
EP4352191A1 (fr) Additif d'agent de nettoyage d'origine biologique
CN110462015A (zh) 具有分散剂共混物的自动餐具洗涤组合物
AU2008299653B2 (en) Pyrrolidone containing detergent composition
KR102694078B1 (ko) 거울상이성질체의 혼합물의 제조 방법, 및 거울상이성질체의 혼합물
EP2388308A1 (fr) Composition de nettoyage avec des propriétés detachantes améliorees
JP2006265463A (ja) 自動食器洗浄機用洗浄剤組成物
NL2004743C2 (en) Cleaning composition with improved stain removal.
EP4172297B1 (fr) Formulation de détergent à lessive comprenant un agent anti-redéposition biodégradable
GB2610026A (en) Compositions
US20220010239A1 (en) Detergent polymer and composition
EP0625567A2 (fr) Agent de nettoyage sous phosphate pour le lavage de la vaisselle en machine
WO2025223955A1 (fr) Procédé de production d'acide polyaspartique, acide polyaspartique et son utilisation
JP2025500419A (ja) 水溶性グラフトポリマー、その調製、使用及びそのようなポリマーを含む組成物
CN118434782A (zh) 水溶性接枝聚合物、其制备、用途及包含这类聚合物的组合物

Legal Events

Date Code Title Description
AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO SE SI SK SM TR

AX Request for extension of the european patent

Extension state: BA ME RS

PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20120524