WO2014195201A1 - Cosmetic composition containing non-ionic associative polymers and non-ionic surfactants, and method for cosmetic treatment - Google Patents

Cosmetic composition containing non-ionic associative polymers and non-ionic surfactants, and method for cosmetic treatment Download PDF

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WO2014195201A1
WO2014195201A1 PCT/EP2014/061038 EP2014061038W WO2014195201A1 WO 2014195201 A1 WO2014195201 A1 WO 2014195201A1 EP 2014061038 W EP2014061038 W EP 2014061038W WO 2014195201 A1 WO2014195201 A1 WO 2014195201A1
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weight
nonionic
polymers
composition according
chain
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PCT/EP2014/061038
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French (fr)
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Marie-Florence D'ARRAS
Estelle Mathonneau
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L'oreal
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/02Preparations for cleaning the hair
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/39Derivatives containing from 2 to 10 oxyalkylene groups
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73Polysaccharides
    • A61K8/731Cellulose; Quaternized cellulose derivatives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73Polysaccharides
    • A61K8/737Galactomannans, e.g. guar; Derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8141Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • A61K8/8152Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/87Polyurethanes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/90Block copolymers

Definitions

  • Cosmetic composition comprising nonionic associative polymers and nonionic surfactants, and cosmetic treatment method
  • the present invention relates to a cosmetic composition, in particular a capillary composition, comprising at least one nonionic associative polymer and at least one particular nonionic surfactant, as well as a cosmetic treatment method using said composition.
  • Hair tends to lose some of its qualities under the action of factors such as natural regreasing, sweat, the elimination of dander, pollution or moisture in particular.
  • the visual appearance and the feel of the hair can be degraded.
  • Regreasing for example, weighs down the hair, which then tends to pack.
  • the hair may be more difficult to comb, and have a greasy shine or an unpleasant waxed touch.
  • shampoos which are generally aqueous compositions containing large amounts of surfactants, which are generally anionic surfactants, alone or in combination with amphoteric and / or nonionic surfactants.
  • the total amounts of surfactants used generally exceed 10% by weight of active material, relative to the total weight of the cosmetic composition.
  • surfactants can alter, as and when applications, the cosmetic properties of the hair which leads to the need to also use conditioning agents such as cationic polymers, silicones or non-silicone oils.
  • shampoos should generally be thickened; but their thickening may cause problems of stability of the composition.
  • the object of the present invention is to provide cosmetic hair compositions which overcome these drawbacks, and in particular capable of generating an adequate foam, both in quality and in quantity, and providing the hair with satisfactory cosmetic properties, especially on dry hair.
  • the subject of the invention is therefore a cosmetic composition, in particular a capillary, non-coloring composition comprising:
  • nonionic surfactants of C 12 -C 18 fatty chain type, polyoxyalkylenated having a number of alkylene oxide units ranging from 4 to 10.
  • non-coloring composition is intended to mean a composition which does not contain a dye for keratin fibers, such as direct dyes or oxidation dye precursors (bases and / or couplers). If they are present, their content does not exceed 0.005% by weight relative to the total weight of the composition. Indeed, at such a content, only the composition would be tinted, that is to say, one would not observe staining effect of keratin fibers.
  • composition according to the invention thus comprises one or more associative nonionic polymers.
  • the term "polymer” means any compound resulting from the polymerization by polycondensation or the radical polymerization of monomers, at least one of which is different from an alkylene oxide and a monofunctional compound of formula RX, R denotes a C10-C30 alkyl or alkenyl group, optionally hydroxylated, and X denoting a carboxylic acid, amine, amide, hydroxyl or ester group.
  • RX denotes a C10-C30 alkyl or alkenyl group, optionally hydroxylated
  • X denoting a carboxylic acid, amine, amide, hydroxyl or ester group.
  • association polymer means an amphiphilic polymer capable, in an aqueous medium, of reversibly associating with itself or with other molecules, it generally comprising in its chemical structure at least one zone or group, hydrophilic and at least one hydrophobic zone or group.
  • hydrophobic group is meant a radical or a hydrocarbon-based polymer, saturated or unsaturated, linear or branched.
  • the hydrophobic group comprises at least 10 carbon atoms, preferably from 10 to 30 carbon atoms, in particular from 12 to 30 carbon atoms and preferably from 18 to 30 carbon atoms.
  • the hydrophobic hydrocarbon group comes from a monofunctional compound.
  • the hydrophobic group may be derived from a fatty alcohol such as stearyl alcohol, dodecyl alcohol, decyl alcohol or a polyalkylene fatty alcohol such as steareth-100. It can also denote a hydrocarbon polymer such as for example polybutadiene.
  • the associative nonionic polymers that may be used in the context of the invention are preferably chosen from:
  • celluloses modified with groups comprising at least one fatty chain we can cite as an example:
  • hydroxyethyl celluloses modified with groups comprising at least one fatty chain such as alkyl, arylalkyl or alkylaryl groups, or mixtures thereof, and in which the alkyl groups are preferably C8-C22, such as NATROSOL PLUS GRADE products 330 CS (C16 alkyls) or POLYSURF 67 CS sold by the company ASHLAND, or the product BERMOCOLL EHM 100 sold by the company BEROL NOBEL,
  • celluloses modified with alkyl phenol polyalkylene glycol ether groups such as the product AMERCELL POLYMER HM-1500 (polyethylene glycol (15) nonyl phenol ether) sold by the company AMERCHOL.
  • hydroxypropyl guars modified with groups comprising at least one C8-C30 fatty chain such as the product ESAFLOR HM 22 (C22 alkyl chain) sold by the company LAMBERTI, the products RE210-18 (C14 alkyl chain) and RE205-1 (C20 alkyl chain) sold by Rhodia;
  • copolymers of C 1 -C 6 alkyl methacrylates or acrylates and of amphiphilic monomers comprising at least one fatty chain such as, for example, the oxyethylenated methyl acrylate / stearyl acrylate copolymer sold by GOLDSCHMIDT under the name ANTIL 208;
  • copolymers of hydrophilic methacrylates or acrylates and monomers hydrophobic compounds comprising at least one fatty chain such as, for example, polyethylene glycol methacrylate / lauryl methacrylate co-polymer
  • polyether polyurethanes comprising in their chain both hydrophilic sequences of a most often polyoxyethylenated nature and hydrophobic sequences which may be aliphatic chains alone and / or cycloaliphatic and / or aromatic chains.
  • polymers having an aminoplast ether skeleton having at least one fatty chain such as the PURE THIX compounds proposed by the company SUD-CHEMIE;
  • copolymers of vinyipyrrolidone and hydrophobic fatty-chain monomers such as ANTARON V216 or GANEX V216 (vinyipyrrolidone / hexadecene copolymer) sold by the company I.S.P .; the ANTARON V220 or GANEX V220 products (vinyipyrrolidone / eicosene copolymer) sold by the company I.S.P.
  • the at least one nonionic associative polymer is preferably chosen from polyether polyurethanes.
  • the associative nonionic polyether polyurethanes according to the invention comprise at least two hydrocarbon-based lipophilic chains having from 6 to 30 carbon atoms, separated by a hydrophilic sequence, the hydrocarbon chains possibly being pendant chains or end chains. - hydrophilic quence.
  • the polymer may comprise a hydrocarbon chain at one end or both ends of a hydrophilic block.
  • the polyether polyurethanes associative according to the invention can be multisequenced, in particular in the form of triblock or multiblock.
  • the hydrophobic sequences may be located at each end of the chain (hydrophilic central block triblock copolymer) or distributed at both the ends and in the chain (multiblock copolymer for example). These polymers may also be graft or star.
  • the associative polyether polyurethanes according to the invention are triblock copolymers whose hydrophilic sequence is a polyoxyethylenated chain comprising from 50 to 1000 oxyethylenated groups.
  • the associative nonionic polyether polyurethanes according to the invention carry the hydrophobic grafts at the end of the chain (telescopic polymers).
  • the associative nonionic polyether polyurethanes according to the invention are triblock copolymers whose hydrophilic sequence is a polyoxyethylenated chain comprising from 50 to 1000, in particular from 100 to 300, oxyethylenated groups; and comprising at least two hydrocarbon lipophilic chains having from 6 to 30 carbon atoms, separated by said hydrophilic sequence, said hydrocarbon lipophilic chains being pendant chains or end chains of hydrophilic sequence.
  • the associative nonionic polyether polyurethanes comprise a urethane bond between the hydrophilic blocks, hence the origin of the name.
  • hydrophobic chain associative nonionic polyether polyurethanes those whose hydrophilic sequences are linked to the hydrophobic blocks by other chemical bonds.
  • the associative nonionic polyether polyurethanes according to the invention have a weight average molecular weight (Mw) of less than or equal to 500,000, better still less than or equal to 100,000.
  • Mw weight average molecular weight
  • the associative nonionic polyether polyurethanes that may be used according to the invention may also be chosen from those described in the article by G. Fonnum, J. Bakke and Fk. Hansen - Colloid Polym. Sci 271, 380, 389 (1993).
  • an associative nonionic polyether polyurethane which can be obtained by polycondensation of at least three compounds comprising (i) at least one polyethylene glycol comprising from 100 to 180 moles of ethylene oxide, (ii) an alcohol polyoxyethylenated stearyl comprising 100 moles of ethylene oxide and (iii) a diisocyanate.
  • Such a polymer is in particular proposed by the company ELEMENTIS under the name RHEOLATE FX 1 100 ® which is a polyethylene glycol polycondensate containing 136 moles of ethylene oxide, stearyl alcohol polyoxyethylenated to 100 moles of ethylene oxide and hexamethylene diisocyanate (HDI) having a weight average molecular weight (Mw) of 30000 (INCI name: PEG-136 / STEARETH- 100 / HDI COPOLYMER).
  • RHEOLATE FX 1 100 ® is a polyethylene glycol polycondensate containing 136 moles of ethylene oxide, stearyl alcohol polyoxyethylenated to 100 moles of ethylene oxide and hexamethylene diisocyanate (HDI) having a weight average molecular weight (Mw) of 30000 (INCI name: PEG-136 / STEARETH- 100 / HDI COPOLYMER).
  • an associative nonionic polyether polyurethane obtainable by polycondensation of at least three compounds comprising (i) at least one polyethylene glycol comprising from 150 to 180 moles of ethylene oxide, (ii) stearyl alcohol or decyl alcohol and (iii) at least one diisocyanate.
  • Such polymers are in particular proposed by Rohm & Haas under the names Aculyn 46® and Aculyn 44®.
  • Aculyn 46 ® is a polyethylene glycol polycondensate containing 150 or 180 moles of ethylene oxide, stearyl alcohol and methylene bis (4-cyclohexyl isocyanate) (SMDI) at 15% by weight in a maltodextrin matrix. (4%) and water (81%) (INCI name: PEG-150 / STEARYL ALCOHOL / SMDI COPOLYMER).
  • Aculyn 44 ® is a polycondensate of polyethylene glycol containing 150 or 180 moles of ethylene oxide, decyl alcohol and methylene bis (4-cyclohexyl isocyanate) (SMDI), at 35% by weight in a propylene glycol mixture ( 39%) and water (26%) (INCI name: PEG-150 / DECYL ALCOHOL / SMDI COPOLYMER).
  • composition according to the invention comprises associative nonionic polymers in an amount ranging from 2 to 60% by weight, preferably from 2.5 to 40% by weight, more preferably from 2.7 to 20% by weight, or even from 2.75 to 15% by weight, relative to the total weight of the composition.
  • composition according to the invention also comprises one or more nonionic surfactants of polyoxyalkylenated C12-C18 chain fatty alcohol type having an alkylene oxide unit number ranging from 4 to 10.
  • the polyoxyalkylenated fatty alcohols according to the invention preferably comprise oxyethylene groups, and in particular have a number of oxyethylene groups ranging from 4 to 10.
  • the polyoxyalkylenated fatty alcohols according to the invention are therefore preferably polyoxyethylenated fatty alcohols.
  • the fatty chain of the polyoxyalkylenated fatty alcohol according to the invention is C 12 -C 18, preferably C 14 -C 16, and may be saturated or unsaturated, linear or branched.
  • the polyoxyalkylene, especially polyoxyethylenated, C12-C18 fatty alcohol is saturated and linear.
  • the composition according to the invention comprises one or more non-ionic surfactants of the C 12 -C 18 saturated linear chain fatty alcohol type, polyoxyethylenated with a number of ethylene oxide units ranging from 4 to 10.
  • ethylene with lauryl alcohol especially those containing from 4 to 10 oxyethylene groups
  • adducts of ethylene oxide with cetearyl alcohol mixture of cetyl alcohol and stearyl alcohol
  • adducts of ethylene oxide with cetyl alcohol especially those containing from 4 to 10 oxyethylene groups
  • adducts of ethylene oxide with stearyl alcohol especially those containing from 4 to 10 oxyethylene groups
  • adducts of ethylene oxide with isostearyl alcohol especially those containing from 4 to 10 oxyethylene groups
  • adducts of ethylene oxide with oleyl alcohol in particular those containing from 4 to 10 oxyethylene groups
  • adducts of ethylene oxide with oleyl alcohol in particular
  • composition according to the invention preferably comprises the said polyoxyalkylenated C12-C18 chain fatty alcohol nonionic surfactant (s) having a number of alkylene oxide units ranging from 4 to 10, in a smaller amount or equal to 10% by weight, especially ranging from 0.1 to 10% by weight, preferably from 1 to 8% by weight, preferably from 1.5 to 7.5% by weight, relative to the total weight of the composition .
  • s polyoxyalkylenated C12-C18 chain fatty alcohol nonionic surfactant
  • composition according to the invention may further comprise one or more additional surfactants, preferably chosen from nonionic surfactants other than the polyoxyalkylenated fatty alcohols above, anionic surfactants and amphoteric surfactants.
  • additional surfactants preferably chosen from nonionic surfactants other than the polyoxyalkylenated fatty alcohols above, anionic surfactants and amphoteric surfactants.
  • anionic surfactants that can be used in the composition according to the invention, mention may be made of alkyl sulphates, alkyl ether sulphates, alkyl amidoether sulphates, alkylaryl polyether sulphates, monoglyceride sulphates, alkyl sulphonates, alkyl amide sulphonates and alkyl aryl sulphonates.
  • alpha-olefin sulfonates paraffin-sulfonates, alkylsulfosuccinates, alkylethersulphonates, succinates, alkylamide-sulfosuccinates, alkylsulfoacetates, acylsarconids, acylglutamates, alkylsulfosuccinamates, acylisethionates and N-acyltaurates, salts of alkyl monoesters and polyglycoside-polycarboxylic acids, acyllactylates, N-acyl glycinates, D-galactoside uronic acid salts, alkyl ether carboxylic acid salts, alkyl aryl ether carboxylic acid salts, alkyl amido ether carboxylic acid salts, and the like.
  • the alkyl and acyl groups of all these compounds having from 6 to 40 carbon atoms and the aryl group denoting a phenyl group.
  • These compounds can be oxyethylenated and then preferably comprise from 1 to 50 ethylene oxide units.
  • the salts of C 6 -C 24 alkyl monoesters and of polyglycoside-polycarboxylic acids may be chosen from C 6 -C 24 alkyl polyglycoside-citrates, C 6 -C 24 alkyl polyglycoside-tartrates and polyglycoside-sulphosuccinates. C6-C24 alkyl.
  • anionic surfactants when they are in salt form, they may be chosen from alkali metal salts such as the sodium or potassium salt and preferably sodium salt, the ammonium salts, the amine salts and, in particular, aminoalcohols or alkaline earth metal salts such as magnesium salts.
  • the alkali metal or alkaline earth metal salts and in particular the sodium or magnesium salts are preferably used.
  • the additional nonionic surfactants that may be used may be chosen from alcohols, alpha-diols and (C 1 -C 20) alkyl phenols, these compounds being polyethoxylated, polypropoxylated or having a fatty chain comprising, for example, from 8 to 30 atoms. carbon, in particular from 16 to 30 carbon atoms, the number of ethylene oxide and / or propylene oxide groups possibly ranging from 2 to 50 and the number of glycerol groups that can range from 2 to 30, in particular from 2 to 30; exclusion of course fatty alcohols to C12-C18 chain, polyoxyalkylenated having a number of alkylene oxide units ranging from 4 to 10 described above.
  • ethylene oxide and propylene oxide condensates on fatty alcohols there may also be mentioned ethylene oxide and propylene oxide condensates on fatty alcohols; the polyethoxylated fatty amides preferably having from 2 to 30 ethylene oxide units, the polyglycerolated fatty amides comprising on average from 1 to 5 glycerol groups and in particular from 1.5 to 4; ethoxylated sorbitan fatty acid esters preferably having from 2 to 40 ethylene oxide units, sucrose fatty acid esters, polyethylene glycol fatty acid esters, N-alkyl derivatives; C6-24) glucamine, amine oxides such as (C10-14 alkyl) amine oxides or N- (C10-14 acyl) aminopropylmorpholine oxides.
  • nonionic surfactants of alkylpolyglycoside type in particular represented by the following general formula: RiO- (R 2 O) t - (G) v
  • R 1 represents a linear or branched alkyl or alkenyl radical containing 6 to 24 carbon atoms, in particular 8 to 18 carbon atoms, or an alkyl-phenyl radical whose linear or branched alkyl radical contains 6 to 24 carbon atoms, especially 8 at 18 carbon atoms;
  • R2 represents an alkylene radical containing 2 to 4 carbon atoms
  • G represents a sugar unit comprising 5 to 6 carbon atoms
  • - 1 denotes a value ranging from 0 to 10, preferably from 0 to 4,
  • v denotes a value ranging from 1 to 15, preferably from 1 to 4.
  • the alkylpolyglycoside surfactants are compounds of the formula described above in which R 1 denotes a saturated or unsaturated, linear or branched alkyl radical containing from 8 to 18 carbon atoms, t denotes a value ranging from 0 to 3, preferably 0, G denotes glucose, fructose or galactose, preferably glucose; the degree of polymerization, i.e., the value of v, ranging from 1 to 15, preferably from 1 to 4; the average degree of polymerization being more particularly between 1 and 2.
  • the glucosidic linkages between the sugar units are generally of the 1 -6 or 1 -4 type, preferably of the 1 -4 type.
  • the alkylpolyglycoside surfactant is an alkylpolyglucoside surfactant.
  • the additional amphoteric surfactants that may be used in the invention may be derivatives of secondary or tertiary aliphatic amines, optionally quaternized, in which the aliphatic group is a linear or branched chain containing 8 to 22 carbon atoms, said derivatives of amines containing at least one anionic group such as, for example, a carboxylate, sulfonate, sulfate, phosphate or phosphonate group.
  • R a represents a C 10 -C 30 alkyl or alkenyl group derived from a R a -COOH acid, preferably present in hydrolysed coconut oil, a heptyl, nonyl or undecyl group,
  • Rb represents a beta-hydroxyethyl group
  • R c represents a carboxymethyl group
  • n 0.1 or 2
  • Z represents a hydrogen atom or a hydroxyethyl or carboxymethyl group
  • B represents -CH 2 CH 2 OX ', with X' representing -CH 2 -COOH, CH 2 -COOZ ', -CH 2 CH 2 -COOH, -CH 2 CH 2 -COOZ', or a hydrogen atom,
  • Z represents a hydrogen atom or a hydroxyethyl or carboxymethyl group
  • Z ' represents an ion derived from an alkali metal or alkaline earth metal, such as sodium, potassium or magnesium; an ammonium ion; or an ion derived from an organic amine and in particular an aminoalcohol, such as mono-, di- and triethanolamine, mono-, di- or tri-isopropanolamine, 2-amino-2-methyl-1-propanol 2-amino-2-methyl-1,3-propanediol and tris (hydroxymethyl) amino methane.
  • an alkali metal or alkaline earth metal such as sodium, potassium or magnesium
  • an ammonium ion or an ion derived from an organic amine and in particular an aminoalcohol, such as mono-, di- and triethanolamine, mono-, di- or tri-isopropanolamine, 2-amino-2-methyl-1-propanol 2-amino-2-methyl-1,
  • R a ' represents a C 10 -C 30 alkyl or alkenyl group of an R a COOH acid preferably present in coconut oil or in hydrolysed linseed oil, an alkyl group, especially C 17, and its form iso, an unsaturated C17 group.
  • Compounds of formula (A3) are preferred. These compounds are classified in the CTFA dictionary, 5 th edition, 1993, under the names disodium cocoamphodiacetate, disodium lauroamphodiacetate, disodium caprylamphodiacetate, disodium capryloamphodiacetate, disodium co-coamphodipropionate, disodium lauroamphodipropionate, disodium caprylamphodipropionate, disodium capryloamphodipropionate, lauroamphodipropionic acid, cocoamphodipropionic acid.
  • Examples include the marketed by Rhodia cocoamphodiacetate under the trade name Miranol ® C2M concentrate or under the trade name MIRANOL ULTRA C 32 and the product sold by the company Chimex under the trade name Chimexane HA.
  • R a - represents a C10-C30 alkyl or alkenyl group of an acid R a - C (O) OH, preferably present in coconut oil or in hydrolysed linseed oil;
  • Y represents the group -C (O) OH, -C (O) OZ", -CH 2 -CH (OH) -SO 3 H or the group -CH 2 -CH (OH) -SO 3 -Z "with Z "representing a cationic counterion derived from an alkaline or alkaline earth metal, such as sodium, an ammonium ion or an ion derived from an organic amine;
  • Rd and R e independently of one another, represent a C1-C4 alkyl or hydroxyalkyl radical
  • n and n ' independently of one another, denote an integer ranging from 1 to 3.
  • the compound classified in the CTFA dictionary under the name sodium diethylaminopropyl cocoaspartamide and marketed by Chimex under the name Chimexane HB may be mentioned in particular.
  • amphoteric surfactants are chosen from (C 8 -C 20) alkyl betaines, (C 8 -C 20) alkylamido (C 1 -C 6) alkyl betaines and (C 8 -C 20) alkyl amphodiacetates, as well as the sodium salt of laurylaminosuccinamate. diethylaminopropyl; and their mixtures.
  • the composition according to the invention comprises a total amount of nonionic surfactants (total, that is to say polyoxyalkylenated fatty alcohols according to the invention and optional additional nonionic), anionic (possible) and amphoteric (possible) , ranging from 0.1 to 10% by weight, preferably ranging from 1 to 8% by weight, preferably from 1.5 to 7.5% by weight, relative to the total weight of the composition.
  • nonionic surfactants total, that is to say polyoxyalkylenated fatty alcohols according to the invention and optional additional nonionic
  • anionic possibly ranging from 1 to 8% by weight, preferably from 1.5 to 7.5% by weight, relative to the total weight of the composition.
  • the composition according to the invention comprises a total amount of surfactants (cationic, anionic, nonionic, amphoteric, zwitterionic) ranging from 0.1 to 10% by weight, preferably ranging from 1 to 8% by weight, preferably from 1.5 to 7.5% by weight, based on the total weight of the composition.
  • the ratio (% by weight) "nonionic surfactants (total) + anionic surfactants (optional) + amphoteric surfactants (optional)” / "nonionic associative polymers” is less than or equal to 3; preferably it varies from 0.01 to 3, especially from 0.01 to 2.8, preferably from 0.1 to 2.5.
  • composition according to the invention may also comprise one or more polymers, different from the nonionic associative polymers according to the invention, and especially selected from amphoteric or cationic polymers, as well as their mixture.
  • cationic polymer means any polymer comprising cationic groups and / or ionizable groups into cationic groups.
  • the cationic polymer is hydrophilic or amphiphilic.
  • the preferred cationic polymers are chosen from those containing units containing primary, secondary, tertiary and / or quaternary amine groups that may either be part of the main polymer chain or may be borne by a lateral substituent directly connected thereto.
  • the cationic polymers which may be used preferably have a weight average molecular weight (Mw) of between approximately 500 and 5 ⁇ 10 6 , preferably between 10 3 and 3 ⁇ 10 6 approximately.
  • cationic polymers mention may be made more particularly of:
  • R3 which may be identical or different, denote a hydrogen atom or a CH3 radical
  • A which may be identical or different, represent a divalent alkyl group, linear or branched, of 1 to 6 carbon atoms, preferably 2 or 3 carbon atoms or a hydroxyalkyl group of 1 to 4 carbon atoms;
  • R4, R5, R6, which may be identical or different, represent an alkyl group having from 1 to 18 carbon atoms or a benzyl radical; preferably an alkyl group having 1 to 6 carbon atoms;
  • R1 and R2 identical or different, represent a hydrogen atom or an alkyl group having 1 to 6 carbon atoms, preferably methyl or ethyl;
  • X denotes an anion derived from an inorganic or organic acid such as an anion methosulphate or a halide such as chloride or bromide.
  • the copolymers of the family (1) may also contain one or more units derived from comonomers which may be chosen from the family of acrylamides, methacrylamides, acrylamide diacetones, acrylamides and methacrylamides substituted on the nitrogen by lower alkyls (C1-C4).
  • comonomers which may be chosen from the family of acrylamides, methacrylamides, acrylamide diacetones, acrylamides and methacrylamides substituted on the nitrogen by lower alkyls (C1-C4).
  • copolymers of acrylamide and of dimethylaminoethyl methacrylate quaternized with dimethyl sulphate or with a dimethyl halide such as that sold under the name HERCOFLOC by the company HERCULES,
  • copolymers of acrylamide and of methacryloyloxyethyltrimethylammonium chloride such as those sold under the name BINA QUAT P 100 by the company CIBA GEIGY,
  • vinylpyrrolidone / dialkylaminoalkyl acrylate or methacrylate copolymers whether or not quaternized, such as the products sold under the name "GAFQUAT” by ISP, for example “GAFQUAT 734" or “GAFQUAT 755", or the products referred to as "COPOLYMER 845"; , 958 and 937 ".
  • dimethylaminoethyl methacrylate / vinylcaprolactam / vinylpyrrolidone terpolymers such as the product sold under the name GAFFIX VC 713 by the company ISP,
  • vinyipyrrolidone / methacrylamidopropyldimethylamine copolymers such as those sold under the name STYLEZE CC 10 by ISP;
  • the vinyipyrrolidone / dimethylaminopropyl methacrylamide quaternized copolymers such as the product sold under the name "GAFQUAT HS 100" by the company ISP,
  • the polymers preferably crosslinked, of methacryloyloxyalkyl (C1 -C4) trialkyl (C1 -C4) ammonium salts, such as the polymers obtained by homopolymerization of dimethylaminoethyl methacrylate quaternized with methyl chloride, or by copolymerization of acrylamide with dimethylaminoethyl methacrylate; quaternized by methyl chloride, the homo- or copolymerization being followed by crosslinking with an olefinically unsaturated compound, in particular methylenebisacrylamide.
  • methacryloyloxyalkyl (C1 -C4) trialkyl (C1 -C4) ammonium salts such as the polymers obtained by homopolymerization of dimethylaminoethyl methacrylate quaternized with methyl chloride, or by copolymerization of acrylamide with dimethylaminoethyl methacrylate; quaternized by methyl
  • an acrylically crosslinked copolymer lamide / methacryloyloxyethyl trimethylannononiun chloride (20/80 by weight) in the form of a dispersion comprising 50% by weight of said copolymer in mineral oil.
  • This dispersion is marketed under the name "SALCARE® SC 92" by the company CIBA.
  • a crosslinked homopolymer of methacryloyloxyethyltrimethylammonium chloride comprising about 50% by weight of the homopolymer in mineral oil or in a liquid ester.
  • cationic polysaccharides especially cationic celluloses and galactomannan gums.
  • cationic polysaccharides mention may be made more particularly of cellulose ether derivatives containing quaternary ammonium groups, cationic cellulose copolymers or cellulose derivatives grafted with a water-soluble quaternary ammonium monomer and cationic galactomannan gums. .
  • the cellulose ether derivatives containing quaternary ammonium groups are especially described in FR1492597, and mention may be made of the polymers sold under the name "UCARE POLYMER JR” (JR 400 LT, JR 125, JR 30M) or "LR” (LR). 400, LR 30M) by the company AMERCHOL. These polymers are also defined in the CTFA dictionary as quaternary ammoniums of hydroxyethylcellulose reacted with an epoxide substituted with a trimethylammonium group.
  • cationic cellulose copolymers or cellulose derivatives grafted with a water-soluble quaternary ammonium monomer are described in particular in the US4131576 patent, and mention may be made of hydroxyalkylcelluloses, such as hydroxymethyl-, hydroxyethyl- or hydroxypropyl cellulose grafted in particular with a salt methacryloylethyl trimethylammonium, methacrylamidopropyl trimethylammonium, dimethyl diallylammonium.
  • marketed products corresponding to this definition are more particularly the products sold under the name "Celquat L 200" and "Celquat H 100" by the company National Starch.
  • guar gums comprising cationic trialkylammonium groups.
  • guar gums modified with a salt for example a chloride
  • Such products are marketed in particular under the names Jaguar C13 S, Jaguar C 15, Jaguar C 17 or Jaguar C162 by Rhodia.
  • water-soluble polyamino amides prepared in particular by polycondensation of an acidic compound with a polyamine; these polyaminoamides may be crosslinked by an epihalohydrin, a diepoxide, a dianhydride, an unsaturated di-hydride, a bis-unsaturated derivative, a bis-halohydrin, a bis-azetidinium, a bis-haloacyldiamine, a bis-alkyl halide.
  • a bis-halohydrin, a bis-azetidinium, a bis-haloacyldiamine or an alkyl bis-halide an epilhalohydrin, a diepoxide or a bis-unsaturated derivative; the crosslinking agent being used in proportions ranging from 0.025 to 0.35 moles per amine group of the polyaminoamide; these polyaminoamides can be alkylated or if they comprise one or more tertiary amino functions, quaternized.
  • polyamino amide derivatives resulting from the condensation of polyalkylene polyamines with polycarboxylic acids followed by alkylation with difunctional agents.
  • adipic acid-diacoylaminohydroxyalkyldialoylene triamine polymers in which the alkyl radical contains from 1 to 4 carbon atoms and preferably denotes methyl, ethyl or propyl.
  • alkyl radical contains from 1 to 4 carbon atoms and preferably denotes methyl, ethyl or propyl.
  • Polymers of this type are in particular sold under the name "Hercosett 57” by the company Hercules Inc. or under the name “PD 170” or “Delsette 101” by the company Hercules in the case of the adipic acid copolymer / epoxypropyl / diethylenetriamine.
  • cyclopolymers of alkyl diallyl amine or of dialkyl diallyl ammonium such as homopolymers or copolymers comprising, as main constituent of the chain, units corresponding to formulas (I) or (II): (CH 2 ) k (CH 2 ) k
  • R12 denotes a hydrogen atom or a methyl radical
  • R10 and R1 independently of each other, denote an alkyl group having from 1 to 6 carbon atoms, a hydroxyalkyl group in which the alkyl group has 1 to 5 carbon atoms, a C1-C6 amidoalkyl group; C4; or R10 and R1 may together with the nitrogen atom to which they are attached, designate heterocyclic groups, such as piperidinyl or morpholinyl; R10 and R1, independently of one another, preferably denote an alkyl group having from 1 to 4 carbon atoms.
  • - Y is an anion such as bromide, chloride, acetate, borate, citrate, tartrate, bisulphate, bisulphite, sulphate, phosphate.
  • R13, R14, R15 and R16 which may be identical or different, represent aliphatic, alicyclic or arylaliphatic radicals comprising from 1 to 20 carbon atoms or lower hydroxyalkylaliphatic radicals, or R13, R14, R15 and R16, together or separately, together with the nitrogen atoms to which they are attached, are heterocycles optionally comprising a second heteroatom other than nitrogen, or else R13, R14, R15 and R16 represent a linear or branched C1-C6 alkyl radical substituted with a nitrile, ester, acyl, amide or -CO-O-R17-D or -CO-NH-R17-D group where R17 is alkylene and D is a quaternary ammonium group;
  • A1 and B1 represent divalent polymethylenic groups comprising from 2 to 20 carbon atoms which may be linear or branched, saturated or unsaturated, and which may contain, bound to or intercalated in the main
  • X denotes an anion derived from a mineral or organic acid
  • A1, R13 and R15 can form with the two nitrogen atoms to which they are attached a piperazine ring;
  • A1 denotes a linear or branched, saturated or unsaturated alkylene or hydroxyalkylene radical
  • B1 may also denote a (CH2) n -CO-D-OC- (CH2) n- group in which D denotes:
  • a glycol residue of formula -OZO- where Z denotes a linear or branched hydrocarbon radical or a group corresponding to one of the following formulas: - (CH 2 -CH 2 -O) x -CH 2 -CH 2 - and - [CH 2 -CH (CH 3) -O] y -CH 2 -CH (CH 3) - where x and y denote an integer of 1 to 4, representing a defined and unique degree of polymerization or any number from 1 to 4 representing a degree of average polymerization;
  • a bis-secondary diamine residue such as a piperazine derivative
  • X " is an anion such as chloride or bromide
  • Mn number-average molar mass
  • R 1, R 2, R 3 and R 4 which may be identical or different, denote an alkyl or hydroxyalkyl radical having from 1 to 4 carbon atoms, n and p are integers ranging from 2 to approximately 20 and, X- is an anion derived from a mineral or organic acid.
  • CTFA Hexadimethrin chloride
  • R18, R19, R20 and R21 which may be identical or different, represent a hydrogen atom or a methyl, ethyl, propyl, ⁇ -hydroxyethyl, ⁇ -hydroxypropyl or -CH2CH2 (OCH2CH2) pOH radical, where p is 0 or to an integer between 1 and 6, provided that R18, R19, R20 and R21 do not simultaneously represent a hydrogen atom,
  • r and s which are identical or different, are integers between 1 and 6,
  • q is equal to 0 or to an integer between 1 and 34
  • X - denotes an anion such as a halide
  • - A denotes a radical of a dihalide or is preferably -CH2-CH2-O-CH2-CH2-.
  • Quaternary polymers of vinyipyrrolidone and of vinylimidazole such as, for example, the products sold under the names Luviquat® FC 905, FC 550 and FC 370 by the company B.A.S.F.
  • these polymers may in particular be chosen from homo- or copolymers comprising one or more units derived from vinylamine and possibly one or more units derived from vinylformamide.
  • these cationic polymers are chosen from polymers comprising, in their structure, from 5 to 100 mol% of units corresponding to formula (A) and from 0 to 95 mol% of units corresponding to formula (B) preferably 10 to 100 mol% of units of formula (A) and 0 to 90 mol% of units of formula (B).
  • These polymers can be obtained for example by partial hydrolysis of polyvinylformamide. This hydrolysis can be done in acidic or basic medium.
  • the weight average molecular weight of said polymer measured by diffraction of light, can vary from 1000 to 3,000,000 g / mol, preferably from 10,000 to 1,000,000 and more particularly from 100,000 to 500,000 g / mol.
  • the cationic charge density of these polymers can vary from 2 meq / g to 20 meq / g, preferably from 2.5 to 15 and more particularly from 3.5 to 10 meq / g.
  • the polymers comprising units of formula (A) and optionally units of formula (B) are in particular sold under the name LUPAMIN by BASF, such as, for example, and without limitation, the products offered under the name LUPAMIN 9095, LUPAMIN 5095, LUPAMIN 1095, LUPAMIN 9030 (or LUVIQUAT 9030) and LUPAMIN 9010.
  • cationic polymers which may be used in the context of the invention are cationic proteins or hydrolysates of cationic proteins, polyalkyleneimines, in particular polyethyleneimines, polymers comprising vinylpyridine or vinylpyridinium units, polyamine and polyamine condensates. epichlorohydrin, quaternary polyureylenes and chitin derivatives.
  • the cationic polymers are chosen from those of families (1), (2), (7) and (10) mentioned above.
  • cationic polysaccharides in particular cationic celluloses and galactomannan gums, and in particular quaternary cellulose ether derivatives such as the products sold under the name "JR 400.
  • cationic cyclopolymers in particular homopolymers or copolymers of salts (for example chloride) dimethyldiallylammonium, sold under the names MERQUAT 100, MERQUAT 550 and MER-QUAT S by the company NALCO and their homologues of low molecular weight by weight, quaternary polymers of vinyipyrrolidone and vinylimidazole, optionally crosslinked homopolymers or copolymers of methacryloyloxyalkyl (C1 -C4) trialkyl (C1 -C4) ammonium salts; and their mixtures.
  • amphoteric polymers which may preferably be selected from amphoteric polymers comprising the repetition of:
  • the units derived from a monomer of (i) (meth) acrylamide type are units of the following structure (Ia): wherein R 1 is H or CH 3 , and R 2 is selected from amino, dimethylamino, tert-butylamino, dodecylamino, or -NH-CH 2 OH.
  • said amphoteric polymer comprises the repetition of only one unit of formula (Ia).
  • the unit resulting from a (meth) acrylamide type monomer of formula (Ia) in which R 1 denotes H and R 2 is an amino (NH 2) radical is particularly preferred. It corresponds to the acrylamide monomer itself.
  • the units derived from a monomer of (ii) (meth) acrylamidoalkyltrialkylammonium type are units of the following structure (Ma)
  • R 3 denotes H or CH 3 ,
  • R 4 denotes a group (CH 2 ) k with k an integer ranging from 1 to 6, and preferably from 2 to 4;
  • R 5 , R 6 and R 7 identical or different, each denote an alkyl group having 1 to 4 carbon atoms;
  • - Y is an anion such as bromide, chloride, acetate, borate, citrate, tartrate, bisulphate, bisulphite, sulphate, phosphate.
  • said amphoteric polymer comprises the repetition of only one unit of formula (Ma).
  • the units derived from a monomer of (iii) (meth) acrylic acid type are units of formula (IIIa):
  • R 9 denotes a hydroxyl radical or a radical -NH-C (CH 3 ) 2 -CH 2 -SO 3 H.
  • the preferred units of formulas (IIIa) correspond to the monomers acrylic acid, methacrylic acid and 2-acrylamino-2-methyl propane sulfonic acid.
  • the unit derived from an acid monomer (meth) acrylic acid of formula (IIIa) is that derived from acrylic acid, wherein Rs denotes a hydrogen atom and R 9 denotes a hydroxyl radical.
  • the acid monomer (s) of the (meth) acrylic acid type may be unneutralized, or partially or completely neutralized with an organic or inorganic base.
  • said amphoteric polymer comprises the repetition of only one unit of formula (IIIa).
  • the amphopolymeric polymer or polymers of this type comprise at least 30 mol% of units derived from a monomer of (i) (meth) acrylamide type. Preferably, they comprise from 30 to 70 mol% of units derived from a (meth) acrylamide type monomer, more preferably from 40 to 60 mol%.
  • the content of units derived from a monomer of the type (ii) (meth) acrylamido alkyltrialkylammonium may advantageously be from 10 to 60%, preferably from 20 to 55% by moles.
  • the content of units derived from an acidic monomer of (iii) (meth) acrylic acid type may advantageously be from 1 to 20%, preferably from 5 to 15% by mole.
  • the amphoteric polymer of this type comprises:
  • amphoteric polymers may also comprise additional units, different from the units derived from a monomer of (meth) acrylamide type, of (meth) acrylamidoalkyltrialkylammonium type and (meth) acrylic acid type as described above.
  • said amphoteric polymers consist solely of units derived from monomers of (i) (meth) acrylamide type, (ii) (meth) acrylamidoalkyltrialkylammonium type and (iii) acid type. (meth) acrylic acid.
  • amphoteric polymers As an example of particularly preferred amphoteric polymers, mention may be made of acrylamide / methacrylamidopropyltrimethylammonium chloride / acrylic acid terpolymers. Such polymers are listed in the CTFA International Cosmetic Ingredient Dictionary, io th edition, 2004, under the name "Polyquaternium 53". Corresponding products are in particular sold under the names MERQUAT 2003 and MERQUAT 2003 PR by the company NALCO.
  • amphoteric polymer As another type of amphoteric polymer that may be used, mention may also be made of copolymers based on (meth) acrylic acid and on a dialkyl-diallylammonium salt, such as copolymers of (meth) acrylic acid and of dimethyldiallyl ammonium chloride.
  • copolymers based on (meth) acrylic acid and on a dialkyl-diallylammonium salt such as copolymers of (meth) acrylic acid and of dimethyldiallyl ammonium chloride.
  • composition according to the invention may comprise cationic and / or amphoteric polymers in an amount of between 0.01 and 5% by weight, in particular from 0.05 to 3% by weight, preferably from 0.1 to 2% by weight. , relative to the total weight of the composition.
  • the cosmetic composition according to the invention may be in any of the galenical forms conventionally used, and especially in the form of an aqueous, alcoholic or aqueous-alcoholic solution or suspension, or an oily solution; a solution or dispersion of the lotion or serum type; an emulsion, an aqueous or anhydrous gel, or any other cosmetic form.
  • the composition according to the invention is preferably aqueous and then comprises water at a concentration preferably ranging from 5 to 98% by weight, in particular from 20 to 95% by weight, better still from 50 to 90% by weight, by weight. relative to the total weight of the composition.
  • the composition may also comprise one or more organic solvents liquid at 25 ° C., 1 atm.,
  • organic solvents liquid such as C 1 -C 7 alcohols, and in particular C 1 -C 7 aliphatic or aromatic monoalcohols, polyols and polyethers.
  • C3-C7 polyols which can be used alone or mixed with water.
  • the organic solvent can be chosen among ethanol, isopropanol and mixtures thereof.
  • composition according to the invention may further comprise at least one usual cosmetic ingredient, different from the compounds of the invention, and especially chosen from vegetable, mineral, animal or synthetic oils; solid fatty substances and in particular waxes, C8-C40 esters, C8-C40 acids; C8-C40 alcohols; cationic surfactants, anionic polymers; solar filters; moisturizing agents; antidandruff agents; antioxidants; chelating agents; pearlescent and opacifying agents; plasticizing or coalescing agents; hydroxy acids; the charges; silicones and in particular polydimethylsiloxanes (PDMS); the perfumes; alkalizing or acidifying agents; aldehydes, DHA; the thickeners other than the nonionic associative polymers according to the invention, and preferably chosen from non-polymeric thickeners and non-associative polymeric thickeners.
  • the composition may of course include several cosmetic ingredients listed above. Those skilled in the art will take care to choose the ingredients in the composition, as well as their amounts, so that they
  • the pH of the composition if it is aqueous, is preferably between 3 and 9, especially between 3 and 6.
  • the cosmetic composition according to the invention finds particular application particularly interesting in the field of care and hair hygiene, especially for the care and / or cleaning of hair and / or scalp.
  • the cosmetic composition may be rinsed or not rinsed after being applied to the hair and / or the scalp; preferably it is rinsed after a possible exposure time.
  • the composition according to the invention may be packaged in a tube, in a bottle with or without a pump, or in an aerosol. In the case of an aerosol, the composition may then contain one or more conventional propellants.
  • the subject of the invention is also a process for the cosmetic treatment, in particular of care and / or cleaning, of the hair and / or the scalp, comprising the application to the hair and / or the scalp of a cosmetic composition according to the invention, optionally followed by rinsing, after a possible exposure time.
  • Foaming detergent compositions are obtained which can be used for cleaning the hair and leading to good cosmetic properties on dry hair.

Abstract

The present invention relates to a cosmetic composition, in particular a capillary composition, comprising: one or more non-ionic associative polymers, in particular of the polyurethane polyether type in an amount of 2 to 60 wt % relative to the total weight of the composition; and one or more non-ionic surfactants composed of polyoxyalkylenated fatty alcohol having a C12-C18 chain and a number of alkylene oxide units of 4 and 10. The invention also relates to a cosmetic treatment method using said composition, in particular to a hair-care treatment method, particularly for cleaning hair and/or scalp.

Description

Composition cosmétique comprenant des polymères associatifs non ioniques et des tensioactifs non ioniques, et procédé de traitement cosmétique  Cosmetic composition comprising nonionic associative polymers and nonionic surfactants, and cosmetic treatment method
La présente invention concerne une composition cosmétique, notamment capillaire, comprenant au moins un polymère associatif non ionique et au moins un tensioactif non ionique particulier, ainsi qu'un procédé de traitement cosmétique mettant en œuvre ladite composition. The present invention relates to a cosmetic composition, in particular a capillary composition, comprising at least one nonionic associative polymer and at least one particular nonionic surfactant, as well as a cosmetic treatment method using said composition.
Les chevelures ont tendance à perdre certaines de leurs qualités sous l'action de facteurs tels que le regraissage naturel, la sueur, l'élimination de squames, la pollution ou l'humidité notamment. L'aspect visuel ainsi que le toucher des cheveux peut ainsi être dégradé. Le regraissage, par exemple, alourdit les cheveux qui ont alors tendance à se mettre en paquets. Les cheveux peuvent être plus difficiles à coiffer, et avoir une brillance grasse ou un toucher ciré désagréable. Hair tends to lose some of its qualities under the action of factors such as natural regreasing, sweat, the elimination of dander, pollution or moisture in particular. The visual appearance and the feel of the hair can be degraded. Regreasing, for example, weighs down the hair, which then tends to pack. The hair may be more difficult to comb, and have a greasy shine or an unpleasant waxed touch.
Il est connu de nettoyer les cheveux avec des shampooings qui sont généralement des compositions aqueuses contenant de grandes quantités de tensioactifs, qui sont généralement des tensioactifs anioniques, seuls ou en associations avec des tensioactifs amphotères et/ou non ioniques. Les quantités totales de tensioactifs mises en œuvre dépassent le plus souvent 10% en poids de matière active, par rapport au poids total de la composition cosmétique. It is known to clean the hair with shampoos which are generally aqueous compositions containing large amounts of surfactants, which are generally anionic surfactants, alone or in combination with amphoteric and / or nonionic surfactants. The total amounts of surfactants used generally exceed 10% by weight of active material, relative to the total weight of the cosmetic composition.
Ces shampooings à base de quantités importantes de tensioactifs anioniques peuvent générer des désagréments tels que des picotements du cuir chevelu ou bien des yeux, lorsqu'ils sont mis en contact avec le shampoing.  These shampoos based on significant amounts of anionic surfactants can cause discomfort such as tingling of the scalp or eyes when they come into contact with the shampoo.
Par ailleurs, ces tensioactifs peuvent altérer, au fur et à mesure des applications, les propriétés cosmétiques des cheveux ce qui conduit à la nécessité d'utiliser également des agents conditionneurs comme des polymères cationiques, des sili- cônes ou des huiles non siliconées.  Furthermore, these surfactants can alter, as and when applications, the cosmetic properties of the hair which leads to the need to also use conditioning agents such as cationic polymers, silicones or non-silicone oils.
En outre, le rinçage des compositions cosmétiques à forte teneur en tensioactifs peut être souvent long.  In addition, the rinsing of cosmetic compositions with high surfactant content can often be long.
Enfin, pour éviter les coulures à l'application et notamment les coulures dans les yeux, les shampooings doivent généralement être épaissis; mais leur épaississe- ment peut poser des problèmes de stabilité de la composition.  Finally, to avoid application dripping and especially eye drops, shampoos should generally be thickened; but their thickening may cause problems of stability of the composition.
Afin de pallier ces différents problèmes, il a été proposé, par exemple par la demande FR2935267, d'ajouter des polymères associatifs aux compositions de shampoing, ce qui permettait de diminuer leur teneur en tensioactifs classiques. A partir d'une certaine concentration, ces polymères associatifs ont un pouvoir détergent suffisant pour permettre le nettoyage des cheveux en présence de très faibles quantités de tensioactifs voire même en l'absence de ces tensioactifs. Toutefois, les compositions ainsi obtenues, même si elles permettent une déter- gence similaire à celle obtenue avec un shampoing classique, présentent encore un caractère moussant insuffisant; en outre, les propriétés cosmétiques conférées aux cheveux ne sont pas encore totalement satisfaisantes, en particulier sur che- veux secs. In order to overcome these various problems, it has been proposed, for example by the application FR2935267, to add associative polymers to shampoo compositions, which makes it possible to reduce their content of conventional surfactants. From a certain concentration, these associative polymers have sufficient detergency to allow the cleaning of the hair in the presence of very small amounts of surfactants or even in the absence of these surfactants. However, the compositions thus obtained, even if they allow a detergency similar to that obtained with a conventional shampoo, still have insufficient foaming character; in addition, the cosmetic properties imparted to the hair are not yet completely satisfactory, in particular on dry hair.
La présente invention a pour but de proposer des compositions cosmétiques capillaires palliant ces inconvénients, et notamment susceptibles de générer une mousse adéquate, en qualité comme en quantité, et apportant aux cheveux, des propriétés cosmétiques satisfaisantes, tout particulièrement sur cheveux secs. The object of the present invention is to provide cosmetic hair compositions which overcome these drawbacks, and in particular capable of generating an adequate foam, both in quality and in quantity, and providing the hair with satisfactory cosmetic properties, especially on dry hair.
L'invention a donc pour objet une composition cosmétique, notamment capillaire, non colorante comprenant : The subject of the invention is therefore a cosmetic composition, in particular a capillary, non-coloring composition comprising:
- 2 à 60% en poids par rapport au poids total de la composition, d'un ou plusieurs polymères non ioniques associatifs, et  2 to 60% by weight relative to the total weight of the composition, of one or more associative nonionic polymers, and
- un ou plusieurs tensioactifs non ioniques de type alcool gras à chaîne en C12- C18, polyoxyalkyléné ayant un nombre d'unité d'oxyde d'alkylène allant de 4 à 10.  one or more nonionic surfactants of C 12 -C 18 fatty chain type, polyoxyalkylenated having a number of alkylene oxide units ranging from 4 to 10.
La composition selon l'invention est non colorante. Par composition non colorante, on entend selon la présente invention, une composition ne contenant pas de colorant des fibres kératiniques tels que les colorants directs ou les précurseurs de colorant d'oxydation (bases et/ou coupleurs). S'ils sont présents, leur teneur ne dépasse pas 0,005% en poids par rapport au poids total de la composition. En effet, à une telle teneur, seule la composition serait teintée, c'est-à-dire qu'on n'observerait pas d'effet de coloration des fibres kératiniques. The composition according to the invention is non-coloring. According to the present invention, the term "non-coloring composition" is intended to mean a composition which does not contain a dye for keratin fibers, such as direct dyes or oxidation dye precursors (bases and / or couplers). If they are present, their content does not exceed 0.005% by weight relative to the total weight of the composition. Indeed, at such a content, only the composition would be tinted, that is to say, one would not observe staining effect of keratin fibers.
Dans la présente description, l'expression "au moins un" est équivalente à l'expression "un ou plusieurs" et peut y être substituée. In the present description, the term "at least one" is equivalent to the term "one or more" and may be substituted therefor.
Dans la présente description, l'expression "compris entre" est équivalente à l'expression "allant de" et peut y être substituée; dans ces expressions, les bornes sont considérées comme incluses.  In the present description, the term "between" is equivalent to and may be substituted for "from"; in these expressions, the bounds are considered included.
Polymère non ionique associatif Nonionic associative polymer
La composition selon l'invention comprend donc un ou plusieurs polymères non ioniques associatifs.  The composition according to the invention thus comprises one or more associative nonionic polymers.
Au sens de la présente invention, on entend par "polymère" tout composé issu de la polymérisation par polycondensation ou de la polymérisation radicalaire de monomères dont l'un au moins est différent d'un oxyde d'alkylène et d'un composé monofonctionnel de formule RX, R désignant un groupe alkyle ou alkényle en C10-C30, éventuellement hydroxylé, et X désignant un groupement acide car- boxylique, aminé, amide, hydroxylé, ester. Sont en particulier exclus tous les composés issus uniquement de la simple condensation d'un oxyde d'alkylène sur un alcool gras, un ester gras, un acide gras, un amide gras, une aminé grasse. For the purposes of the present invention, the term "polymer" means any compound resulting from the polymerization by polycondensation or the radical polymerization of monomers, at least one of which is different from an alkylene oxide and a monofunctional compound of formula RX, R denotes a C10-C30 alkyl or alkenyl group, optionally hydroxylated, and X denoting a carboxylic acid, amine, amide, hydroxyl or ester group. In particular, all compounds derived solely from the simple condensation of an alkylene oxide on a fatty alcohol, a fatty ester, a fatty acid, a fatty amide, a fatty amine.
Au sens de la présente invention, on entend par "polymère associatif un polymère amphiphile capable, dans un milieu aqueux, de s'associer réversiblement avec lui- même ou avec d'autres molécules. Il comporte généralement dans sa structure chimique au moins une zone ou groupement, hydrophile et au moins une zone ou groupement, hydrophobe. For the purposes of the present invention, the term "associative polymer" means an amphiphilic polymer capable, in an aqueous medium, of reversibly associating with itself or with other molecules, it generally comprising in its chemical structure at least one zone or group, hydrophilic and at least one hydrophobic zone or group.
Par "groupement hydrophobe", on entend un radical ou un polymère à chaîne hydrocarbonée, saturée ou non, linéaire ou ramifiée. Lorsqu'il désigne un radical hydrocarboné, le groupement hydrophobe comporte au moins 10 atomes de car- bone, de préférence de 10 à 30 atomes de carbone, en particulier de 12 à 30 atomes de carbone et préférentiellement de 18 à 30 atomes de carbone. Préféren- tiellement, le groupement hydrophobe hydrocarboné provient d'un composé monofonctionnel. A titre d'exemple, le groupement hydrophobe peut être issu d'un alcool gras tel que l'alcool stéarylique, l'alcool dodécylique, l'alcool décylique ou bien d'un alcool gras polyalkyléné comme le stéareth-100. Il peut également désigner un polymère hydrocarboné tel que par exemple le polybutadiène.  By "hydrophobic group" is meant a radical or a hydrocarbon-based polymer, saturated or unsaturated, linear or branched. When it refers to a hydrocarbon radical, the hydrophobic group comprises at least 10 carbon atoms, preferably from 10 to 30 carbon atoms, in particular from 12 to 30 carbon atoms and preferably from 18 to 30 carbon atoms. Preferably, the hydrophobic hydrocarbon group comes from a monofunctional compound. By way of example, the hydrophobic group may be derived from a fatty alcohol such as stearyl alcohol, dodecyl alcohol, decyl alcohol or a polyalkylene fatty alcohol such as steareth-100. It can also denote a hydrocarbon polymer such as for example polybutadiene.
Les polymères non ioniques associatifs susceptibles d'être utilisés dans le cadre de l'invention sont choisis de préférence parmi : The associative nonionic polymers that may be used in the context of the invention are preferably chosen from:
(1 ) les celluloses modifiées par des groupements comportant au moins une chaîne grasse; on peut citer à titre d'exemple : (1) celluloses modified with groups comprising at least one fatty chain; we can cite as an example:
- les hydroxyéthyl celluloses modifiées par des groupements comportant au moins une chaîne grasse tels que des groupes alkyle, arylalkyle, alkylaryle, ou leurs mé- langes, et dans lesquels les groupes alkyle sont de préférence en C8-C22, comme les produits NATROSOL PLUS GRADE 330 CS (alkyles en C16) ou POLYSURF 67 CS vendus par la société ASHLAND, ou le produit BERMOCOLL EHM 100 vendu par la société BEROL NOBEL,  hydroxyethyl celluloses modified with groups comprising at least one fatty chain, such as alkyl, arylalkyl or alkylaryl groups, or mixtures thereof, and in which the alkyl groups are preferably C8-C22, such as NATROSOL PLUS GRADE products 330 CS (C16 alkyls) or POLYSURF 67 CS sold by the company ASHLAND, or the product BERMOCOLL EHM 100 sold by the company BEROL NOBEL,
- les celluloses modifiées par des groupes polyalkyléné glycol éther d'alkyl phénol, tel que le produit AMERCELL POLYMER HM-1500 (polyéthylène glycol (15) éther de nonyl phénol) vendu par la société AMERCHOL.  celluloses modified with alkyl phenol polyalkylene glycol ether groups, such as the product AMERCELL POLYMER HM-1500 (polyethylene glycol (15) nonyl phenol ether) sold by the company AMERCHOL.
(2) les hydroxypropylguars modifiés par des groupements comportant au moins une chaîne grasse en C8-C30, tel que le produit ESAFLOR HM 22 (chaîne alkyle en C22) vendu par la société LAMBERTI, les produits RE210-18 (chaîne alkyle en C14) et RE205-1 (chaîne alkyle en C20) vendus par la société RHODIA; (2) hydroxypropyl guars modified with groups comprising at least one C8-C30 fatty chain, such as the product ESAFLOR HM 22 (C22 alkyl chain) sold by the company LAMBERTI, the products RE210-18 (C14 alkyl chain) and RE205-1 (C20 alkyl chain) sold by Rhodia;
(3) les copolymères de méthacrylates ou d'acrylates d'alkyles en C1 -C6 et de monomères amphiphiles comportant au moins une chaîne grasse tels que par exemple le copolymère acrylate de méthyle/acrylate de stéaryle oxyéthyléné vendu par la société GOLDSCHMIDT sous la dénomination ANTIL 208; (3) copolymers of C 1 -C 6 alkyl methacrylates or acrylates and of amphiphilic monomers comprising at least one fatty chain, such as, for example, the oxyethylenated methyl acrylate / stearyl acrylate copolymer sold by GOLDSCHMIDT under the name ANTIL 208;
(4) les copolymères de méthacrylates ou d'acrylates hydrophiles et de monomères hydrophobes comportant au moins une chaîne grasse tels que par exemple le co- polymère méthacrylate de polyéthylèneglycol/méthacrylate de lauryle; (4) copolymers of hydrophilic methacrylates or acrylates and monomers hydrophobic compounds comprising at least one fatty chain, such as, for example, polyethylene glycol methacrylate / lauryl methacrylate co-polymer;
(5) les polyuréthanes polyéthers comportant dans leur chaîne, à la fois des sé- quences hydrophiles de nature le plus souvent polyoxyéthylénée et des séquences hydrophobes qui peuvent être des enchaînements aliphatiques seuls et/ou des enchaînements cycloaliphatiques et/ou aromatiques. (5) polyether polyurethanes comprising in their chain both hydrophilic sequences of a most often polyoxyethylenated nature and hydrophobic sequences which may be aliphatic chains alone and / or cycloaliphatic and / or aromatic chains.
(6) les polymères à squelette aminoplaste éther possédant au moins une chaîne grasse, tels que les composés PURE THIX proposés par la société SUD-CHEMIE; (6) polymers having an aminoplast ether skeleton having at least one fatty chain, such as the PURE THIX compounds proposed by the company SUD-CHEMIE;
(7) les copolymères de vinyipyrrolidone et de monomères hydrophobes à chaîne grasse, tels que les produits ANTARON V216 ou GANEX V216 (copolymère vinyipyrrolidone / hexadécène) vendus par la société I.S.P.; les produits ANTARON V220 ou GANEX V220 (copolymère vinyipyrrolidone / eicosène) vendus par la société I.S.P. (7) copolymers of vinyipyrrolidone and hydrophobic fatty-chain monomers, such as ANTARON V216 or GANEX V216 (vinyipyrrolidone / hexadecene copolymer) sold by the company I.S.P .; the ANTARON V220 or GANEX V220 products (vinyipyrrolidone / eicosene copolymer) sold by the company I.S.P.
Le ou les polymères associatifs non ioniques sont de préférence choisis parmi les polyuréthanes polyéthers. The at least one nonionic associative polymer is preferably chosen from polyether polyurethanes.
De préférence, les polyuréthanes polyéthers non ioniques associatifs selon l'invention comportent au moins deux chaînes lipophiles hydrocarbonées ayant de 6 à 30 atomes de carbone, séparées par une séquence hydrophile, les chaînes hydrocarbonées pouvant être des chaînes pendantes ou des chaînes en bout de sé- quence hydrophile. En particulier, il est possible qu'une ou plusieurs chaînes pendantes soient prévues. En outre, le polymère peut comporter une chaîne hydrocarbonée à un bout ou aux deux bouts d'une séquence hydrophile. Preferably, the associative nonionic polyether polyurethanes according to the invention comprise at least two hydrocarbon-based lipophilic chains having from 6 to 30 carbon atoms, separated by a hydrophilic sequence, the hydrocarbon chains possibly being pendant chains or end chains. - hydrophilic quence. In particular, it is possible that one or more pendant chains are provided. In addition, the polymer may comprise a hydrocarbon chain at one end or both ends of a hydrophilic block.
Les polyuréthanes polyéthers associatifs selon l'invention peuvent être multisé- quencés en particulier sous forme de tribloc ou de multibloc. Les séquences hydrophobes peuvent être situées à chaque extrémité de la chaîne (copolymère tri- bloc à séquence centrale hydrophile) ou réparties à la fois aux extrémités et dans la chaîne (copolymère multiséquencé par exemple). Ces polymères peuvent être également en greffons ou en étoile. The polyether polyurethanes associative according to the invention can be multisequenced, in particular in the form of triblock or multiblock. The hydrophobic sequences may be located at each end of the chain (hydrophilic central block triblock copolymer) or distributed at both the ends and in the chain (multiblock copolymer for example). These polymers may also be graft or star.
De préférence, les polyuréthanes polyéthers associatifs selon l'invention sont des copolymères triblocs dont la séquence hydrophile est une chaîne polyoxyéthylénée comportant de 50 à 1000 groupements oxyéthylénés. Preferably, the associative polyether polyurethanes according to the invention are triblock copolymers whose hydrophilic sequence is a polyoxyethylenated chain comprising from 50 to 1000 oxyethylenated groups.
De préférence, les polyuréthanes polyéthers non ioniques associatifs selon l'invention portent les greffons hydrophobes en bout de chaîne (polymères téléché- liques). Preferably, the associative nonionic polyether polyurethanes according to the invention carry the hydrophobic grafts at the end of the chain (telescopic polymers).
Préférentiellement, les polyuréthanes polyéthers non ioniques associatifs selon l'invention sont des copolymères triblocs dont la séquence hydrophile est une chaîne polyoxyéthylénée comportant de 50 à 1000, notamment de 100 à 300, groupements oxyéthylénés; et comportant au moins deux chaînes lipophiles hydrocarbonées ayant de 6 à 30 atomes de carbone, séparées par ladite séquence hydrophile, lesdites chaînes lipophiles hydrocarbonées pouvant être des chaînes pendantes ou des chaînes en bout de séquence hydrophile. Preferably, the associative nonionic polyether polyurethanes according to the invention are triblock copolymers whose hydrophilic sequence is a polyoxyethylenated chain comprising from 50 to 1000, in particular from 100 to 300, oxyethylenated groups; and comprising at least two hydrocarbon lipophilic chains having from 6 to 30 carbon atoms, separated by said hydrophilic sequence, said hydrocarbon lipophilic chains being pendant chains or end chains of hydrophilic sequence.
Les polyuréthanes polyéthers non ioniques associatifs comportent une liaison uré- thane entre les séquences hydrophiles, d'où l'origine du nom. The associative nonionic polyether polyurethanes comprise a urethane bond between the hydrophilic blocks, hence the origin of the name.
Par extension figurent aussi parmi les polyuréthanes polyéthers non ioniques as- sociatifs à chaîne hydrophobe, ceux dont les séquences hydrophiles sont liées aux séquences hydrophobes par d'autres liaisons chimiques. By extension are also included among the hydrophobic chain associative nonionic polyether polyurethanes, those whose hydrophilic sequences are linked to the hydrophobic blocks by other chemical bonds.
De préférence, les polyuréthanes polyéthers non ioniques associatifs selon l'invention présentent un poids moléculaire moyen en masse (Mw) inférieur ou égal à 500 000, mieux inférieur ou égal à 100 000. Preferably, the associative nonionic polyether polyurethanes according to the invention have a weight average molecular weight (Mw) of less than or equal to 500,000, better still less than or equal to 100,000.
Comme exemples de polyéthers polyuréthanes non ioniques associatifs selon l'invention, on peut citer : As examples of associative nonionic polyurethane polyethers according to the invention, mention may be made of:
- le Rhéolate 205 ® à fonction urée vendu par la société RHEOX ou encore les Rhéolates ® 208 , 204 ou 212, ainsi que l'Acrysol RM 184 ®;  - Rheolate 205 ® urea function sold by Rheox or Rheolates ® 208, 204 or 212, and Acrysol RM 184 ®;
- le produit ELFACOS T210® à chaîne alkyle en C12-C14 et le produit ELFACOS T212® à chaîne alkyle en C18 d'AKZO;  the product ELFACOS T210® with a C12-C14 alkyl chain and the product ELFACOS T212® with a C18 alkyl chain of AKZO;
- le produit DW 1206B® de ROHM & HAAS à chaîne alkyle en C20 et à liaison uréthane (proposé à 20% en matière sèche dans l'eau.  the product DW 1206B® from ROHM & HAAS with a C20 alkyl chain and a urethane bond (proposed at 20% solids content in water.
On peut aussi utiliser des solutions ou dispersions de ces polymères notamment dans l'eau ou en milieu hydroalcoolique. Comme exemples de tels polymères, on peut citer : It is also possible to use solutions or dispersions of these polymers, especially in water or in an aqueous-alcoholic medium. Examples of such polymers include:
- le Rhéolate ® 255, le Rhéolate ® 278 et le Rhéolate ® 244 de la société RHEOX;  - Rheolate ® 255, Rheolate ® 278 and Rheolate ® 244 from RHEOX;
- les produits DW 1206F et DW 1206J proposés par la société ROHM & HAAS.  the products DW 1206F and DW 1206J proposed by the company ROHM & HAAS.
Les polyuréthanes polyéthers non ioniques associatifs susceptibles d'être utilisés selon l'invention peuvent aussi être choisis parmi ceux décrits dans l'article de G. Fonnum, J. Bakke et Fk. Hansen - Colloid Polym. Sci 271 , 380.389 (1993). The associative nonionic polyether polyurethanes that may be used according to the invention may also be chosen from those described in the article by G. Fonnum, J. Bakke and Fk. Hansen - Colloid Polym. Sci 271, 380, 389 (1993).
De préférence, on utilise un polyuréthane polyéther non ionique associatif susceptible d'être obtenu par polycondensation d'au moins trois composés comprenant (i) au moins un polyéthylèneglycol comprenant de 100 à 180 moles d'oxyde d'éthylène, (ii) un alcool stéarylique polyoxyéthyléné comprenant 100 moles d'oxyde d'éthylène et (iii) un diisocyanate. Preferably, an associative nonionic polyether polyurethane is used which can be obtained by polycondensation of at least three compounds comprising (i) at least one polyethylene glycol comprising from 100 to 180 moles of ethylene oxide, (ii) an alcohol polyoxyethylenated stearyl comprising 100 moles of ethylene oxide and (iii) a diisocyanate.
Un tel polymère est notamment proposé par la société ELEMENTIS sous l'appellation RHEOLATE FX 1 100 ® qui est un polycondensat de polyéthylèneglycol à 136 moles d'oxyde d'éthylène, d'alcool stéarylique polyoxyéthyléné à 100 moles d'oxyde d'éthylène et de hexaméthylène diisocyanate (HDI) ayant poids moléculaire moyen en poids (Mw) de 30000 (nom INCI: PEG-136/STEARETH-100/HDI COPOLYMER). Such a polymer is in particular proposed by the company ELEMENTIS under the name RHEOLATE FX 1 100 ® which is a polyethylene glycol polycondensate containing 136 moles of ethylene oxide, stearyl alcohol polyoxyethylenated to 100 moles of ethylene oxide and hexamethylene diisocyanate (HDI) having a weight average molecular weight (Mw) of 30000 (INCI name: PEG-136 / STEARETH- 100 / HDI COPOLYMER).
Selon une autre préférence, on utilise un polyuréthane polyéther non ionique associatif susceptible d'être obtenu par polycondensation d'au moins trois composés comprenant (i) au moins un polyéthylèneglycol comprenant de 150 à 180 moles d'oxyde d'éthylène, (ii) de l'alcool stéarylique ou de l'alcool décylique et (iii) au moins un diisocyanate. According to another preference, an associative nonionic polyether polyurethane obtainable by polycondensation of at least three compounds comprising (i) at least one polyethylene glycol comprising from 150 to 180 moles of ethylene oxide, (ii) stearyl alcohol or decyl alcohol and (iii) at least one diisocyanate.
De tels polymères sont notamment proposés par la société ROHM & HAAS sous les appellations Aculyn 46 ® et Aculyn 44 ® .  Such polymers are in particular proposed by Rohm & Haas under the names Aculyn 46® and Aculyn 44®.
L'Aculyn 46 ® est un polycondensat de polyéthylèneglycol à 150 ou 180 moles d'oxyde d'éthylène, d'alcool stéarylique et de méthylène bis(4-cyclohexyl- isocyanate) (SMDI) à 15% en poids dans une matrice de maltodextrine (4%) et d'eau (81 %) (nom INCI : PEG-150/STEARYL ALCOHOL/SMDI COPOLYMER). L'Aculyn 44 ® est un polycondensat de polyéthylèneglycol à 150 ou 180 moles d'oxyde d'éthylène, d'alcool décylique et de méthylène bis(4-cyclohexylisocyanate) (SMDI), à 35% en poids dans un mélange de propylèneglycol (39%) et d'eau (26%) (nom INCI : PEG-150/DECYL ALCOHOL/SMDI COPOLYMER).  Aculyn 46 ® is a polyethylene glycol polycondensate containing 150 or 180 moles of ethylene oxide, stearyl alcohol and methylene bis (4-cyclohexyl isocyanate) (SMDI) at 15% by weight in a maltodextrin matrix. (4%) and water (81%) (INCI name: PEG-150 / STEARYL ALCOHOL / SMDI COPOLYMER). Aculyn 44 ® is a polycondensate of polyethylene glycol containing 150 or 180 moles of ethylene oxide, decyl alcohol and methylene bis (4-cyclohexyl isocyanate) (SMDI), at 35% by weight in a propylene glycol mixture ( 39%) and water (26%) (INCI name: PEG-150 / DECYL ALCOHOL / SMDI COPOLYMER).
La composition selon l'invention comprend les polymères non ioniques associatifs en une quantité allant de 2 à 60% en poids, de préférence de 2,5 à 40% en poids, encore mieux de 2,7 à 20% en poids, voire de 2,75 à 15% en poids, par rapport au poids total de la composition. The composition according to the invention comprises associative nonionic polymers in an amount ranging from 2 to 60% by weight, preferably from 2.5 to 40% by weight, more preferably from 2.7 to 20% by weight, or even from 2.75 to 15% by weight, relative to the total weight of the composition.
Alcools gras polvoxyalkylénés Polyoxyalkylenated fatty alcohols
La composition selon l'invention comprend également un ou plusieurs tensioactifs non ioniques de type alcools gras à chaîne en C12-C18, polyoxyalkylénés ayant un nombre d'unité d'oxyde d'alkylène allant de 4 à 10.  The composition according to the invention also comprises one or more nonionic surfactants of polyoxyalkylenated C12-C18 chain fatty alcohol type having an alkylene oxide unit number ranging from 4 to 10.
Les alcools gras polyoxyalkylénés selon l'invention comprennent de préférence des groupements oxyéthylène, et ont notamment un nombre de groupements oxyéthylène allant de 4 à 10. The polyoxyalkylenated fatty alcohols according to the invention preferably comprise oxyethylene groups, and in particular have a number of oxyethylene groups ranging from 4 to 10.
Les alcools gras polyoxyalkylénés selon l'invention sont donc préférentiellement des alcools gras polyoxyéthylénés. The polyoxyalkylenated fatty alcohols according to the invention are therefore preferably polyoxyethylenated fatty alcohols.
La chaîne grasse de l'alcool gras polyoxyalkyléné selon l'invention est en C12- C18, de préférence en C14-C16, et peut être saturée ou non, linéaire ou ramifiée. De préférence, l'alcool gras polyoxyalkyléné, notamment polyoxyéthyléné, en C12-C18, est saturé et linéaire. The fatty chain of the polyoxyalkylenated fatty alcohol according to the invention is C 12 -C 18, preferably C 14 -C 16, and may be saturated or unsaturated, linear or branched. Preferably, the polyoxyalkylene, especially polyoxyethylenated, C12-C18 fatty alcohol is saturated and linear.
Ainsi, préférentiellement, la composition selon l'invention comprend un ou plu- sieurs tensioactifs non ioniques de type alcools gras à chaîne linéaire saturée en C12-C18, polyoxyéthylénés ayant un nombre d'unité d'oxyde d'éthylène allant de 4 à 10. On peut notamment citer les produits d'addition d'oxyde d'éthylène avec l'alcool laurylique, notamment ceux comportant de 4 à 10 groupes oxyéthylène; les produits d'addition d'oxyde d'éthylène avec l'alcool cétéarylique (mélange d'alcool cétylique et d'alcool stéarylique), notamment ceux comportant de 4 à 10 groupes oxyéthylène; les produits d'addition d'oxyde d'éthylène avec l'alcool cétylique, no- tamment ceux comportant de 4 à 10 groupes oxyéthylène; les produits d'addition d'oxyde d'éthylène avec l'alcool stéarylique, notamment ceux comportant de 4 à 10 groupes oxyéthylène; les produits d'addition d'oxyde d'éthylène avec l'alcool isostéarylique, notamment ceux comportant de 4 à 10 groupes oxyéthylène; les produits d'addition d'oxyde d'éthylène avec l'alcool oléylique, notamment ceux comportant de 4 à 10 groupes oxyéthylène; les produits d'addition d'oxyde d'éthylène avec l'alcool isocétylique comportant de 4 à 10 groupes oxyéthylène, et leurs mélanges. Thus, preferably, the composition according to the invention comprises one or more non-ionic surfactants of the C 12 -C 18 saturated linear chain fatty alcohol type, polyoxyethylenated with a number of ethylene oxide units ranging from 4 to 10. Particular mention may be made of the addition products of ethylene with lauryl alcohol, especially those containing from 4 to 10 oxyethylene groups; adducts of ethylene oxide with cetearyl alcohol (mixture of cetyl alcohol and stearyl alcohol), in particular those comprising from 4 to 10 oxyethylene groups; adducts of ethylene oxide with cetyl alcohol, especially those containing from 4 to 10 oxyethylene groups; adducts of ethylene oxide with stearyl alcohol, especially those containing from 4 to 10 oxyethylene groups; adducts of ethylene oxide with isostearyl alcohol, especially those containing from 4 to 10 oxyethylene groups; adducts of ethylene oxide with oleyl alcohol, in particular those containing from 4 to 10 oxyethylene groups; adducts of ethylene oxide with isocetyl alcohol having from 4 to 10 oxyethylene groups, and mixtures thereof.
La composition selon l'invention comprend de préférence le ou lesdits tensioactifs non ioniques de type alcools gras à chaîne en C12-C18, polyoxyalkylénés ayant un nombre d'unité d'oxyde d'alkylène allant de 4 à 10, en une quantité inférieure ou égale à 10% en poids, notamment allant de 0,1 à 10% en poids, de préférence de 1 à 8% en poids, préférentiellement de 1 ,5 à 7,5% en poids, par rapport au poids total de la composition. The composition according to the invention preferably comprises the said polyoxyalkylenated C12-C18 chain fatty alcohol nonionic surfactant (s) having a number of alkylene oxide units ranging from 4 to 10, in a smaller amount or equal to 10% by weight, especially ranging from 0.1 to 10% by weight, preferably from 1 to 8% by weight, preferably from 1.5 to 7.5% by weight, relative to the total weight of the composition .
Tensioactifs additionnels Additional surfactants
La composition selon l'invention peut comprendre en outre un ou plusieurs tensioactifs additionnels, de préférence choisis parmi les tensioactifs non ioniques autres que les alcools gras polyoxyalkylénés ci-dessus, les tensioactifs anioniques et les tensioactifs amphotères.  The composition according to the invention may further comprise one or more additional surfactants, preferably chosen from nonionic surfactants other than the polyoxyalkylenated fatty alcohols above, anionic surfactants and amphoteric surfactants.
On entend par "tensioactif anionique", un tensioactif ne comportant à titre de groupements ioniques ou ionisables que des groupements anioniques. Ces groupements anioniques sont choisis de préférence parmi les groupements -C(O)OH, -C(O)O-, -SO3H, -S(O)2O-, -OS(O)2OH, -OS(O)2O-, -P(O)OH2, - P(O)2O-, -P(O)O2-, -P(OH)2, =P(O)OH, -P(OH)O-, =P(O)O-, =POH, =PO-, les parties anioniques comprenant un contre ion cationique tel que un métal alcalin, un métal alcalino-terreux, ou un ammonium. The term "anionic surfactant" is understood to mean a surfactant comprising as ionic or ionizable groups only anionic groups. These anionic groups are preferably chosen from the groups -C (O) OH, -C (O) O-, -SO 3 H, -S (O) 2 O-, -OS (O) 2 OH, -OS (O) 2 O- , -P (O) OH2, -P (O) 2O-, -P (O) O2-, -P (OH) 2, = P (O) OH, -P (OH) O-, = P (O O-, = POH, = PO-, the anionic parts comprising a cationic counterion such as an alkali metal, an alkaline earth metal, or an ammonium.
Comme exemple de tensioactifs anioniques utilisables dans la composition selon l'invention, on peut citer les alkyl sulfates, les alkyl éther sulfates, les alkylamidoé- thersulfates, les alkylarylpolyéthersulfates, les monoglycéride-sulfates, les alkylsul- fonates, les alkylamidesulfonates, les alkylarylsulfonates, les alpha-oléfine- sulfonates, les paraffine-sulfonates, les alkylsulfosuccinates, les alkyléthersulfo- succinates, les alkylamide-sulfosuccinates, les alkylsulfo-acétates, les acylsarco- sinates, les acylglutamates, les alkylsulfosuccinamates, les acyliséthionates et les N-acyltaurates, les sels de monoesters d'alkyle et d'acides polyglycoside- polycarboxyliques, les acyllactylates, les N-acyl glycinates, les sels d'acides D- galactoside-uroniques, les sels d'acides alkyl éther-carboxyliques, les sels d'acides alkyl aryl éther-carboxyliques, les sels d'acides alkyl amidoéther- carboxyliques, et les formes non salifiées correspondantes de tous ces composés, les groupes alkyle et acyle de tous ces composés comportant de 6 à 40 atomes de carbone et le groupe aryle désignant un groupe phényle. Ces composés peu- vent être oxyéthylénés et comportent alors de préférence de 1 à 50 motifs oxyde d'éthylène. As examples of anionic surfactants that can be used in the composition according to the invention, mention may be made of alkyl sulphates, alkyl ether sulphates, alkyl amidoether sulphates, alkylaryl polyether sulphates, monoglyceride sulphates, alkyl sulphonates, alkyl amide sulphonates and alkyl aryl sulphonates. alpha-olefin sulfonates, paraffin-sulfonates, alkylsulfosuccinates, alkylethersulphonates, succinates, alkylamide-sulfosuccinates, alkylsulfoacetates, acylsarconids, acylglutamates, alkylsulfosuccinamates, acylisethionates and N-acyltaurates, salts of alkyl monoesters and polyglycoside-polycarboxylic acids, acyllactylates, N-acyl glycinates, D-galactoside uronic acid salts, alkyl ether carboxylic acid salts, alkyl aryl ether carboxylic acid salts, alkyl amido ether carboxylic acid salts, and the like. corresponding non-salified compounds of all these compounds, the alkyl and acyl groups of all these compounds having from 6 to 40 carbon atoms and the aryl group denoting a phenyl group. These compounds can be oxyethylenated and then preferably comprise from 1 to 50 ethylene oxide units.
Les sels de monoesters d'alkyle en C6-C24 et d'acides polyglycoside- polycarboxyliques peuvent être choisis parmi les polyglycoside-citrates d'alkyle en C6-C24, les polyglycosides-tartrates d'alkyle en C6-C24 et les polyglycoside- sulfosuccinates d'alkyle en C6-C24.  The salts of C 6 -C 24 alkyl monoesters and of polyglycoside-polycarboxylic acids may be chosen from C 6 -C 24 alkyl polyglycoside-citrates, C 6 -C 24 alkyl polyglycoside-tartrates and polyglycoside-sulphosuccinates. C6-C24 alkyl.
Lorsque les tensioactifs anioniques sont sous forme de sel, ils peuvent être choisis parmi les sels de métaux alcalins tels que le sel de sodium ou de potassium et de préférence de sodium, les sels d'ammonium, les sels d'amines et en particulier d'aminoalcools ou les sels de métaux alcalino-terreux tel que les sels de magné- sium.  When the anionic surfactants are in salt form, they may be chosen from alkali metal salts such as the sodium or potassium salt and preferably sodium salt, the ammonium salts, the amine salts and, in particular, aminoalcohols or alkaline earth metal salts such as magnesium salts.
Corne exemple de sels d'aminoalcools, on peut citer les sels de mono-, di- et trié- thanolamine, les sels de mono-, di- ou triisopropanolamine, les sels de 2-amino-2- méthyl-1 -propanol, 2-amino-2-méthyl-1 ,3-propanediol et tris(hydroxy-méthyl)amino méthane.  Mention may be made, for example, of the salts of mono-, di- and triethanolamine, the salts of mono-, di- or triisopropanolamine, the salts of 2-amino-2-methyl-1-propanol, 2-amino-2-methyl-1,3-propanediol and tris (hydroxymethyl) amino methane.
On utilise de préférence les sels de métaux alcalins ou alcalino-terreux et en particulier les sels de sodium ou de magnésium. The alkali metal or alkaline earth metal salts and in particular the sodium or magnesium salts are preferably used.
Parmi les tensioactifs anioniques, on préfère tout particulièrement les alkyl(C6- C24)sulfates, les alkyl(C6-C24)éthersulfates comprenant de 2 à 50 motifs oxyde d'éthylène, notamment sous forme de sels de métaux alcalins, d'ammonium, d'aminoalcools, et de métaux alcalino-terreux, ou un mélange de ces composés. Encore mieux, on préfère les alkyl(C12-C20)sulfates, les alkyl(C12- C20)éthersulfates comprenant de 2 à 20 motifs oxyde d'éthylène, notamment sous forme de sels de métaux alcalins, d'ammonium, d'aminoalcools, et de métaux alcalino-terreux, ou un mélange de ces composés. Mieux encore, on préfère le lauryl éther sulfate de sodium à 2,2 moles d'oxyde d'éthylène.  Among the anionic surfactants, C6-C24 alkyl sulphates, C6-C24 alkyl ether sulphates comprising from 2 to 50 ethylene oxide units, in particular in the form of alkali metal salts, ammonium salts, are particularly preferred. aminoalcohols, and alkaline earth metals, or a mixture of these compounds. Even better, the (C 12 -C 20) alkyl sulphates, the (C 12 -C 20) alkyl ether sulphates comprising from 2 to 20 ethylene oxide units, in particular in the form of alkali metal, ammonium or aminoalcohol salts, are preferred. and alkaline earth metals, or a mixture of these compounds. More preferably, sodium lauryl ether sulfate is preferred to 2.2 moles of ethylene oxide.
Les tensioactifs non ioniques additionnels susceptibles d'être utilisés peuvent être choisis parmi les alcools, les alpha-diols, les alkyl(Ci_2o)phénols, ces composés étant polyéthoxylés, polypropoxylés ou ayant une chaîne grasse comportant, par exemple, de 8 à 30 atomes de carbone, notamment de 16 à 30 atomes de carbone, le nombre de groupements oxyde d'éthylène et/ou oxyde de propylène pouvant aller notamment de 2 à 50 et le nombre de groupements glycérol pouvant aller notamment de 2 à 30, à l'exclusion bien évidemment des alcools gras à chaîne en C12-C18, polyoxyalkylénés ayant un nombre d'unité d'oxyde d'alkylène allant de 4 à 10 décrits ci-dessus. The additional nonionic surfactants that may be used may be chosen from alcohols, alpha-diols and (C 1 -C 20) alkyl phenols, these compounds being polyethoxylated, polypropoxylated or having a fatty chain comprising, for example, from 8 to 30 atoms. carbon, in particular from 16 to 30 carbon atoms, the number of ethylene oxide and / or propylene oxide groups possibly ranging from 2 to 50 and the number of glycerol groups that can range from 2 to 30, in particular from 2 to 30; exclusion of course fatty alcohols to C12-C18 chain, polyoxyalkylenated having a number of alkylene oxide units ranging from 4 to 10 described above.
On peut également citer les condensais d'oxyde d'éthylène et d'oxyde de propy- lène sur des alcools gras; les amides gras polyéthoxylés ayant de préférence de 2 à 30 motifs d'oxyde d'éthylène, les amides gras polyglycérolés comportant en moyenne de 1 à 5 groupements glycérol et en particulier de 1 ,5 à 4; les esters d'acides gras du sorbitane éthoxylés ayant de préférence de 2 à 40 motifs d'oxyde d'éthylène, les esters d'acides gras du saccharose, les esters d'acides gras du polyéthylèneglycol, les dérivés de N-(alkyl en C6-24)glucamine, les oxydes d'amines tels que les oxydes d'(alkyl en C10-14)amines ou les oxydes de N-(acyl en C10-14)-aminopropylmorpholine.  There may also be mentioned ethylene oxide and propylene oxide condensates on fatty alcohols; the polyethoxylated fatty amides preferably having from 2 to 30 ethylene oxide units, the polyglycerolated fatty amides comprising on average from 1 to 5 glycerol groups and in particular from 1.5 to 4; ethoxylated sorbitan fatty acid esters preferably having from 2 to 40 ethylene oxide units, sucrose fatty acid esters, polyethylene glycol fatty acid esters, N-alkyl derivatives; C6-24) glucamine, amine oxides such as (C10-14 alkyl) amine oxides or N- (C10-14 acyl) aminopropylmorpholine oxides.
On peut encore citer les tensioactifs non ioniques de type alkylpolyglycoside, notamment représentés par la formule générale suivante : RiO-(R2O)t-(G)v Mention may also be made of nonionic surfactants of alkylpolyglycoside type, in particular represented by the following general formula: RiO- (R 2 O) t - (G) v
dans laquelle: in which:
- Ri représente un radical alkyle ou alcényle linéaire ou ramifié comportant 6 à 24 atomes de carbone, notamment 8 à 18 atomes de carbone, ou un radical alkyl- phényle dont le radical alkyle linéaire ou ramifié comporte 6 à 24 atomes de carbone, notamment 8 à 18 atomes de carbone;  R 1 represents a linear or branched alkyl or alkenyl radical containing 6 to 24 carbon atoms, in particular 8 to 18 carbon atoms, or an alkyl-phenyl radical whose linear or branched alkyl radical contains 6 to 24 carbon atoms, especially 8 at 18 carbon atoms;
- R2 représente un radical alkylène comportant 2 à 4 atomes de carbone, R2 represents an alkylene radical containing 2 to 4 carbon atoms,
- G représente un motif sucre comportant 5 à 6 atomes de carbone,  G represents a sugar unit comprising 5 to 6 carbon atoms,
- 1 désigne une valeur allant de 0 à 10, de préférence de 0 à 4, - 1 denotes a value ranging from 0 to 10, preferably from 0 to 4,
- v désigne une valeur allant de 1 à 15, de préférence de 1 à 4.  v denotes a value ranging from 1 to 15, preferably from 1 to 4.
De préférence, les tensioactifs alkylpolyglycoside sont des composés de formule décrite ci-dessus dans laquelle Ri désigne un radical alkyle saturé ou insaturé, linéaire ou ramifié comportant de 8 à 18 atomes de carbone, t désigne une valeur allant de 0 à 3, de préférence égale à 0, G désigne le glucose, le fructose ou le galactose, de préférence le glucose; le degré de polymérisation, c'est-à-dire la valeur de v, pouvant aller de 1 à 15, de préférence de 1 à 4; le degré moyen de polymérisation étant plus particulièrement compris entre 1 et 2.  Preferably, the alkylpolyglycoside surfactants are compounds of the formula described above in which R 1 denotes a saturated or unsaturated, linear or branched alkyl radical containing from 8 to 18 carbon atoms, t denotes a value ranging from 0 to 3, preferably 0, G denotes glucose, fructose or galactose, preferably glucose; the degree of polymerization, i.e., the value of v, ranging from 1 to 15, preferably from 1 to 4; the average degree of polymerization being more particularly between 1 and 2.
Les liaisons glucosidiques entre les motifs sucre sont généralement de type 1 -6 ou 1 -4, de préférence de type 1 -4. De préférence, le tensioactif alkylpolyglycoside est un tensioactif alkylpolyglucoside.  The glucosidic linkages between the sugar units are generally of the 1 -6 or 1 -4 type, preferably of the 1 -4 type. Preferably, the alkylpolyglycoside surfactant is an alkylpolyglucoside surfactant.
Parmi les produits commerciaux, on peut citer les produits vendus par la société COGNIS sous les dénominations PLANTAREN® (600 CS/U, 1200 et 2000) ou PLANTACARE® (818, 1200 et 2000); les produits vendus par la société SEPPIC sous les dénominations TRITON CG1 10 (ou ORAMIX CG 10) et TRITON CG312 (ou ORAMIX® NS 10); les produits vendus par la société BASF sous la dénomination LUTENSOL GD 70 ou encore les produits vendus par la société CHEM Y sous la dénomination AG10 LK. De préférence, on utilise les alkyl C8/C16- polyglycoside 1 ,4, notamment en solution aqueuse à 53%, tels que ceux commercialisés par COGNIS sous la référence PLANTACARE® 818 UP. Les tensioactifs amphotères additionnels susceptibles d'être utilisés dans l'invention peuvent être des dérivés d'aminés aliphatiques secondaire ou tertiaire, éventuellement quaternisées, dans lesquels le groupe aliphatique est une chaîne linéaire ou ramifiée comportant 8 à 22 atomes de carbone, lesdits dérivés d'amines contenant au moins un groupe anionique tel que, par exemple, un groupe car- boxylate, sulfonate, sulfate, phosphate ou phosphonate. Among the commercial products, mention may be made of the products sold by the company COGNIS under the names PLANTAREN® (600 CS / U, 1200 and 2000) or PLANTACARE® (818, 1200 and 2000); the products sold by the company SEPPIC under the trade names TRITON CG1 10 (or ORAMIX CG 10) and TRITON CG312 (or ORAMIX® NS 10); the products sold by BASF under the name LUTENSOL GD 70 or the products sold by CHEM Y under the name AG10 LK. Preferably, the alkyl C8 / C16-polyglycoside 1, 4, in particular in aqueous solution at 53%, such as those marketed by COGNIS under the reference PLANTACARE® 818 UP. The additional amphoteric surfactants that may be used in the invention may be derivatives of secondary or tertiary aliphatic amines, optionally quaternized, in which the aliphatic group is a linear or branched chain containing 8 to 22 carbon atoms, said derivatives of amines containing at least one anionic group such as, for example, a carboxylate, sulfonate, sulfate, phosphate or phosphonate group.
On peut citer en particulier les alkyl(C8-C20)bétaïnes, les sulfobétaïnes, les al- kyl(C8-C2o)sulfobétaïnes, les alkyl(C8-C20)amidoalkyl(C1 -C6)bétaïnes telles que la cocoamidopropylbétaïne, les alkyl(C8-C20)amidoalkyl(C1 -C6)sulfobétaïnes. Mention may in particular be made of (C 8 -C 20 ) alkyl betaines, sulphobetaines, (C 8 -C 20 ) alkylsulfobetaines, (C 8 -C 20 ) alkylamido (C 1 -C 6 ) alkyl betaines such as cocoamidopropylbetaine, (C 8 -C 20) alkylamido (C 1 -C 6) alkyl sulfobetaines.
Parmi les dérivés d'amines aliphatiques secondaires ou tertiaires éventuellement quaternisées susceptibles d'être employés, on peut également citer les produits de structures respectives (A2) et (A3) suivantes : Among the derivatives of aliphatic amines, secondary or tertiary, which may be quaternized, which may be employed, there may also be mentioned the following products of structures (A2) and (A3):
(A2) Ra-CON(Z)CH2-(CH2)m-N+(Rb)(Rc)(CH2COO-) (A2) Ra-CON (Z) CH 2- (CH 2 ) m -N + (R b ) (R c ) (CH 2 COO-)
dans laquelle : in which :
Ra représente un groupe alkyle ou alkényle en C10-C30 dérivé d'un acide Ra-COOH de préférence présent dans l'huile de coprah hydrolysée, un groupe heptyle, nonyle ou undécyle, R a represents a C 10 -C 30 alkyl or alkenyl group derived from a R a -COOH acid, preferably present in hydrolysed coconut oil, a heptyl, nonyl or undecyl group,
Rb représente un groupe beta-hydroxyéthyle,  Rb represents a beta-hydroxyethyl group,
Rc représente un groupe carboxyméthyle ; R c represents a carboxymethyl group;
m est égal à 0,1 ou 2, m is equal to 0.1 or 2,
Z représente un atome d'hydrogène ou un groupe hydroxyéthyl ou carboxyméthyl;  Z represents a hydrogen atom or a hydroxyethyl or carboxymethyl group;
(A3) Ra-CON(Z)CH2-(CH2)m -N(B)(B') (A3) R a -CON (Z) CH 2- (CH 2 ) m -N (B) (B ')
dans laquelle : in which :
B représente -CH2CH2OX', avec X' représentant -CH2-COOH, CH2-COOZ', - CH2CH2-COOH, -CH2CH2-COOZ', ou un atome d'hydrogène, B represents -CH 2 CH 2 OX ', with X' representing -CH 2 -COOH, CH 2 -COOZ ', -CH 2 CH 2 -COOH, -CH 2 CH 2 -COOZ', or a hydrogen atom,
B' représente -(CH2)Z-Y\ avec z = 1 ou 2, et Y' représentant -COOH, -COOZ', - CH2-CHOH-SO3H ou -CH2-CHOH-SO3Z', B 'represents - (CH 2 ) Z -Y \ with z = 1 or 2, and Y' represents -COOH, -COOZ ', -CH 2 -CHOH-SO 3 H or -CH 2 -CHOH-SO 3 Z' ,
m' est égal à 0,1 ou 2, m 'is equal to 0.1 or 2,
Z représente un atome d'hydrogène ou un groupe hydroxyéthyl ou carboxyméthyl, Z' représente un ion issu d'un métal alcalin ou alcalinoterreux, tel que le sodium, le potassium ou le magnésium; un ion ammonium; ou un ion issu d'une aminé organique et notamment d'un aminoalcool, tel que la mono-, di- et triéthanolamine, la mono-, di- ou tri-isopropanol-amine, le 2-amino 2-méthyl 1 -propanol, le 2-amino 2- méthyl 1 ,3-propanediol et le tris(hydroxyméthyl)amino méthane.  Z represents a hydrogen atom or a hydroxyethyl or carboxymethyl group, Z 'represents an ion derived from an alkali metal or alkaline earth metal, such as sodium, potassium or magnesium; an ammonium ion; or an ion derived from an organic amine and in particular an aminoalcohol, such as mono-, di- and triethanolamine, mono-, di- or tri-isopropanolamine, 2-amino-2-methyl-1-propanol 2-amino-2-methyl-1,3-propanediol and tris (hydroxymethyl) amino methane.
Ra' représente un groupe alkyle ou alkényle en C10-C30 d'un acide RaCOOH de préférence présent dans l'huile de coprah ou dans l'huile de lin hydrolysée, un groupe alkyle, notamment en C17 et sa forme iso, un groupe en C17 insaturé. R a 'represents a C 10 -C 30 alkyl or alkenyl group of an R a COOH acid preferably present in coconut oil or in hydrolysed linseed oil, an alkyl group, especially C 17, and its form iso, an unsaturated C17 group.
Les composés répondant à la formule (A3) sont préférés. Ces composés sont également classés dans le dictionnaire CTFA, 5eme édition, 1993, sous les dénominations cocoamphodiacétate de disodium, lauroamphodiacétate de disodium, caprylamphodiacétate de disodium, capryloamphodiacétate de disodium, co- coamphodipropionate de disodium, lauroamphodipropionate de disodium, capry- lamphodipropionate de disodium, capryloamphodipropionate de disodium, acide lauroamphodipropionique, acide cocoamphodipropionique. Compounds of formula (A3) are preferred. These compounds are classified in the CTFA dictionary, 5 th edition, 1993, under the names disodium cocoamphodiacetate, disodium lauroamphodiacetate, disodium caprylamphodiacetate, disodium capryloamphodiacetate, disodium co-coamphodipropionate, disodium lauroamphodipropionate, disodium caprylamphodipropionate, disodium capryloamphodipropionate, lauroamphodipropionic acid, cocoamphodipropionic acid.
A titre d'exemple, on peut citer le cocoamphodiacétate commercialisé par la société RHODIA sous la dénomination commerciale MIRANOL® C2M concentré ou sous la dénomination commerciale MIRANOL ULTRA C 32 et le produit commercialisé par la société CHIMEX sous la dénomination commerciale CHIMEXANE HA. Examples include the marketed by Rhodia cocoamphodiacetate under the trade name Miranol ® C2M concentrate or under the trade name MIRANOL ULTRA C 32 and the product sold by the company Chimex under the trade name Chimexane HA.
On peut aussi utiliser des composés de formule (A4) : It is also possible to use compounds of formula (A4):
(A4) Ra"-NH-CH(Y")-(CH2)n-C(O)-NH-(CH2)n'-N(Rd)(Re) (A4) Ra "-NH-CH (Y") - (CH2) nC (O) -NH- (CH 2 ) n -N (Rd) (Re)
dans laquelle : in which :
- Ra- représente un groupe alkyle ou alcényle en C10-C30 d'un acide Ra"-C(O)OH, de préférence présent dans l'huile de coprah ou dans l'huile de lin hydrolysée; - R a - represents a C10-C30 alkyl or alkenyl group of an acid R a - C (O) OH, preferably present in coconut oil or in hydrolysed linseed oil;
- Y" représente le groupe -C(O)OH, -C(O)OZ", -CH2-CH(OH)-SO3H ou le groupe -CH2-CH(OH)-SO3-Z" avec Z" représentant un contre ion cationique issu d'un métal alcalin ou alcalinoterreux, tel que le sodium, un ion ammonium ou un ion issu d'une aminé organique; Y "represents the group -C (O) OH, -C (O) OZ", -CH 2 -CH (OH) -SO 3 H or the group -CH 2 -CH (OH) -SO 3 -Z "with Z "representing a cationic counterion derived from an alkaline or alkaline earth metal, such as sodium, an ammonium ion or an ion derived from an organic amine;
- Rd et Re, indépendamment l'un de l'autre, représentent un radical alkyle ou hy- droxyalkyle en C1 -C4; et Rd and R e , independently of one another, represent a C1-C4 alkyl or hydroxyalkyl radical; and
- n et n', indépendamment l'un de l'autre, désignent un nombre entier allant de 1 à 3.  n and n ', independently of one another, denote an integer ranging from 1 to 3.
On peut notamment citer le composé classé dans le dictionnaire CTFA sous la dénomination sodium diethylaminopropyl cocoaspartamide et commercialisé par la société CHIMEX sous l'appellation CHIMEXANE HB. The compound classified in the CTFA dictionary under the name sodium diethylaminopropyl cocoaspartamide and marketed by Chimex under the name Chimexane HB may be mentioned in particular.
De préférence, les tensioactifs amphotères sont choisis parmi les alkyl(C8- C20)bétaïnes, les alkyl(C8-C20)amidoalkyl(C1 -C6)bétaïnes et les alkyl(C8-C20) amphodiacétates, ainsi que le sel de sodium du laurylaminosuccinamate de dié- thylaminopropyle; et leurs mélanges. Preferably, the amphoteric surfactants are chosen from (C 8 -C 20) alkyl betaines, (C 8 -C 20) alkylamido (C 1 -C 6) alkyl betaines and (C 8 -C 20) alkyl amphodiacetates, as well as the sodium salt of laurylaminosuccinamate. diethylaminopropyl; and their mixtures.
De préférence, la composition selon l'invention comprend une quantité totale de tensioactifs non ioniques (totaux, c'est-à-dire alcools gras polyoxyalkylénés selon l'invention et non ioniques additionnels éventuels), anioniques (éventuels) et amphotères (éventuels), allant de 0,1 à 10% en poids, de préférence allant de 1 à 8% en poids, préférentiellement de 1 ,5 à 7,5% en poids, par rapport au poids total de la composition. Preferably, the composition according to the invention comprises a total amount of nonionic surfactants (total, that is to say polyoxyalkylenated fatty alcohols according to the invention and optional additional nonionic), anionic (possible) and amphoteric (possible) , ranging from 0.1 to 10% by weight, preferably ranging from 1 to 8% by weight, preferably from 1.5 to 7.5% by weight, relative to the total weight of the composition.
De préférence, la composition selon l'invention comprend une quantité totale de tensioactifs (cationiques, anioniques, non ioniques, amphotères, zwittérioniques) allant de 0,1 à 10% en poids, de préférence allant de 1 à 8% en poids, préférentiellement de 1 ,5 à 7,5% en poids, par rapport au poids total de la composition. De préférence, le ratio (% en poids) "tensioactifs non ioniques (totaux) + tensioac- tifs anioniques (éventuels) + tensioactifs amphotères (éventuels)" / "polymères associatifs non ioniques" est inférieur ou égal à 3; de préférence il varie de 0,01 à 3, notamment de 0,01 à 2,8, préférentiellement de 0,1 à 2,5. Preferably, the composition according to the invention comprises a total amount of surfactants (cationic, anionic, nonionic, amphoteric, zwitterionic) ranging from 0.1 to 10% by weight, preferably ranging from 1 to 8% by weight, preferably from 1.5 to 7.5% by weight, based on the total weight of the composition. Preferably, the ratio (% by weight) "nonionic surfactants (total) + anionic surfactants (optional) + amphoteric surfactants (optional)" / "nonionic associative polymers" is less than or equal to 3; preferably it varies from 0.01 to 3, especially from 0.01 to 2.8, preferably from 0.1 to 2.5.
Polymères polymers
La composition selon l'invention peut comprendre en outre un ou plusieurs polymères, différents des polymères associatifs non ioniques selon l'invention, et no- tamment choisis parmi les polymères amphotères ou cationiques, ainsi que leur mélange.  The composition according to the invention may also comprise one or more polymers, different from the nonionic associative polymers according to the invention, and especially selected from amphoteric or cationic polymers, as well as their mixture.
On entend par "polymère cationique", tout polymère comprenant des groupements cationiques et/ou des groupements ionisables en groupements cationiques. De préférence, le polymère cationique est hydrophile ou amphiphile. Les polymères cationiques préférés sont choisis parmi ceux qui contiennent des motifs comportant des groupements aminés primaires, secondaires, tertiaires et/ou quaternaires pouvant soit faire partie de la chaîne principale polymère, soit être portés par un substituant latéral directement relié à celle-ci. The term "cationic polymer" means any polymer comprising cationic groups and / or ionizable groups into cationic groups. Preferably, the cationic polymer is hydrophilic or amphiphilic. The preferred cationic polymers are chosen from those containing units containing primary, secondary, tertiary and / or quaternary amine groups that may either be part of the main polymer chain or may be borne by a lateral substituent directly connected thereto.
Les polymères cationiques susceptibles d'être utilisés ont de préférence une masse molaire moyenne en poids (Mw) comprise entre 500 et 5.106 environ, de préférence comprise entre 103 et 3.106 environ. The cationic polymers which may be used preferably have a weight average molecular weight (Mw) of between approximately 500 and 5 × 10 6 , preferably between 10 3 and 3 × 10 6 approximately.
Parmi les polymères cationiques, on peut citer plus particulièrement : Among the cationic polymers, mention may be made more particularly of:
(1 ) les homopolymères ou copolymères dérivés d'esters ou d'amides acryliques ou méthacryliques et comportant au moins un des motifs de formule suivante : (1) homopolymers or copolymers derived from acrylic or methacrylic esters or amides and comprising at least one of the following units of formula:
Figure imgf000013_0001
Figure imgf000013_0001
dans lesquelles: in which:
- R3, identiques ou différents, désignent un atome d'hydrogène ou un radical CH3;R3, which may be identical or different, denote a hydrogen atom or a CH3 radical;
- A, identiques ou différents, représentent un groupe divalent alkyle, linéaire ou ramifié, de 1 à 6 atomes de carbone, de préférence 2 ou 3 atomes de carbone ou un groupe hydroxyalkyle de 1 à 4 atomes de carbone ; A, which may be identical or different, represent a divalent alkyl group, linear or branched, of 1 to 6 carbon atoms, preferably 2 or 3 carbon atoms or a hydroxyalkyl group of 1 to 4 carbon atoms;
- R4, R5, R6, identiques ou différents, représentent un groupe alkyle ayant de 1 à 18 atomes de carbone ou un radical benzyle; de préférence un groupe alkyle ayant de 1 à 6 atomes de carbone; R4, R5, R6, which may be identical or different, represent an alkyl group having from 1 to 18 carbon atoms or a benzyl radical; preferably an alkyl group having 1 to 6 carbon atoms;
- R1 et R2, identiques ou différents, représentent un atome d'hydrogène ou un groupe alkyle ayant de 1 à 6 atomes de carbone, de préférence méthyle ou éthyle; - X désigne un anion dérivé d'un acide minéral ou organique tel qu'un anion mé- thosulfate ou un halogénure tel que chlorure ou bromure.  - R1 and R2, identical or different, represent a hydrogen atom or an alkyl group having 1 to 6 carbon atoms, preferably methyl or ethyl; X denotes an anion derived from an inorganic or organic acid such as an anion methosulphate or a halide such as chloride or bromide.
Les copolymères de la famille (1 ) peuvent contenir en outre un ou plusieurs motifs dérivant de comonomères pouvant être choisis dans la famille des acrylamides, méthacrylamides, diacétones acrylamides, acrylamides et méthacrylamides substitués sur l'azote par des alkyles inférieurs (C1 -C4), des acides acryliques ou mé- thacryliques ou leurs esters, des vinyllactames tels que la vinyipyrrolidone ou le vinylcaprolactame, des esters vinyliques. The copolymers of the family (1) may also contain one or more units derived from comonomers which may be chosen from the family of acrylamides, methacrylamides, acrylamide diacetones, acrylamides and methacrylamides substituted on the nitrogen by lower alkyls (C1-C4). acrylic or methacrylic acids or their esters, vinyllactams such as vinyipyrrolidone or vinylcaprolactam, vinyl esters.
Parmi ces copolymères de la famille (1 ), on peut citer : Among these copolymers of family (1), mention may be made of:
- les copolymères d'acrylamide et de diméthylaminoéthyl méthacrylate quaternisé au sulfate de diméthyle ou avec un halogénure de diméthyle, tels que celui vendu sous la dénomination HERCOFLOC par la société HERCULES, copolymers of acrylamide and of dimethylaminoethyl methacrylate quaternized with dimethyl sulphate or with a dimethyl halide, such as that sold under the name HERCOFLOC by the company HERCULES,
- les copolymères d'acrylamide et de chlorure de méthacryloyloxyéthyltriméthyl- ammonium, tels que ceux vendus sous la dénomination BINA QUAT P 100 par la société CIBA GEIGY,  copolymers of acrylamide and of methacryloyloxyethyltrimethylammonium chloride, such as those sold under the name BINA QUAT P 100 by the company CIBA GEIGY,
- le copolymère d'acrylamide et de méthosulfate de méthacryloyloxyéthyltriméthyl- ammonium, tel que celui vendu sous la dénomination RETEN par la société HERCULES,  the copolymer of acrylamide and methacryloyloxyethyltrimethylammonium methosulphate, such as that sold under the name Reten by the company Hercules,
- les copolymères vinylpyrrolidone/acrylate ou méthacrylate de dialkylaminoalkyle, quaternisés ou non, tels que les produits vendus sous la dénomination "GAFQUAT" par la société ISP comme par exemple "GAFQUAT 734" ou "GAFQUAT 755" ou bien les produits dénommés "COPOLYMER 845, 958 et 937". Ces polymères sont décrits en détail dans les brevets français 2.077.143 et 2.393.573, vinylpyrrolidone / dialkylaminoalkyl acrylate or methacrylate copolymers, whether or not quaternized, such as the products sold under the name "GAFQUAT" by ISP, for example "GAFQUAT 734" or "GAFQUAT 755", or the products referred to as "COPOLYMER 845"; , 958 and 937 ". These polymers are described in detail in French Patents 2,077,143 and 2,393,573.
- les terpolymères méthacrylate de diméthylaminoéthyle/ vinylcaprolactame/ vinyl- pyrrolidone, tel que le produit vendu sous la dénomination GAFFIX VC 713 par la société ISP, dimethylaminoethyl methacrylate / vinylcaprolactam / vinylpyrrolidone terpolymers, such as the product sold under the name GAFFIX VC 713 by the company ISP,
- les copolymères vinyipyrrolidone/ méthacrylamidopropyldimethylamine, tels que ceux commercialisés sous la dénomination STYLEZE CC 10 par ISP;  vinyipyrrolidone / methacrylamidopropyldimethylamine copolymers, such as those sold under the name STYLEZE CC 10 by ISP;
- les copolymères vinyipyrrolidone/ méthacrylamide de diméthylaminopropyle qua- ternisé, tel que le produit vendu sous la dénomination "GAFQUAT HS 100" par la société ISP,  the vinyipyrrolidone / dimethylaminopropyl methacrylamide quaternized copolymers, such as the product sold under the name "GAFQUAT HS 100" by the company ISP,
- les polymères, de préférence réticulés, de sels de méthacryloyloxyalkyl(C1 -C4) trialkyl(C1 -C4)ammonium tels que les polymères obtenus par homopolymérisation du diméthylaminoéthylméthacrylate quaternisé par le chlorure de méthyle, ou par copolymérisation de l'acrylamide avec le diméthylaminoéthylméthacrylate quaternisé par le chlorure de méthyle, l'homo- ou la copolymérisation étant suivie d'une réticulation par un composé à insaturation oléfinique, en particulier le méthylène bis acrylamide. On peut plus particulièrement utiliser un copolymère réticulé acry- lamide/chlorure de méthacryloyloxyéthyl triméthylannnnoniunn (20/80 en poids) sous forme de dispersion comprenant 50% en poids dudit copolymère dans de l'huile minérale. Cette dispersion est commercialisée sous le nom de "SALCARE® SC 92" par la société CIBA. On peut également utiliser un homopolymère réticulé du chlorure de méthacryloyloxyéthyl triméthylammonium comprenant environ 50% en poids de l'homopolymère dans de l'huile minérale ou dans un ester liquide. Ces dispersions sont commercialisées sous les noms "SALCARE® SC 95" et "SALCARE® SC 96" par la société CIBA. (2) Les polysaccharides cationiques, notamment les celluloses et les gommes de galactomannanes cationiques. Parmi les polysaccharides cationiques, on peut citer plus particulièrement les dérivés d'éthers de cellulose comportant des groupements ammonium quaternaires, les copolymères de cellulose cationiques ou les dérivés de cellulose greffés avec un monomère hydrosoluble d'ammonium quater- naire et les gommes de galactomannanes cationiques. the polymers, preferably crosslinked, of methacryloyloxyalkyl (C1 -C4) trialkyl (C1 -C4) ammonium salts, such as the polymers obtained by homopolymerization of dimethylaminoethyl methacrylate quaternized with methyl chloride, or by copolymerization of acrylamide with dimethylaminoethyl methacrylate; quaternized by methyl chloride, the homo- or copolymerization being followed by crosslinking with an olefinically unsaturated compound, in particular methylenebisacrylamide. It is more particularly possible to use an acrylically crosslinked copolymer lamide / methacryloyloxyethyl trimethylannononiun chloride (20/80 by weight) in the form of a dispersion comprising 50% by weight of said copolymer in mineral oil. This dispersion is marketed under the name "SALCARE® SC 92" by the company CIBA. It is also possible to use a crosslinked homopolymer of methacryloyloxyethyltrimethylammonium chloride comprising about 50% by weight of the homopolymer in mineral oil or in a liquid ester. These dispersions are sold under the names "SALCARE® SC 95" and "SALCARE® SC 96" by the company CIBA. (2) cationic polysaccharides, especially cationic celluloses and galactomannan gums. Among the cationic polysaccharides, mention may be made more particularly of cellulose ether derivatives containing quaternary ammonium groups, cationic cellulose copolymers or cellulose derivatives grafted with a water-soluble quaternary ammonium monomer and cationic galactomannan gums. .
Les dérivés d'éthers de cellulose comportant des groupements ammonium quaternaires sont notamment décrits dans FR1492597, et on peut citer les polymères commercialisés sous la dénomination "UCARE POLYMER JR" (JR 400 LT, JR 125, JR 30M) ou "LR" (LR 400, LR 30M) par la Société AMERCHOL. Ces poly- mères sont également définis dans le dictionnaire CTFA comme des ammonium quaternaires d'hydroxyéthylcellulose ayant réagi avec un époxyde substitué par un groupement triméthylammonium.  The cellulose ether derivatives containing quaternary ammonium groups are especially described in FR1492597, and mention may be made of the polymers sold under the name "UCARE POLYMER JR" (JR 400 LT, JR 125, JR 30M) or "LR" (LR). 400, LR 30M) by the company AMERCHOL. These polymers are also defined in the CTFA dictionary as quaternary ammoniums of hydroxyethylcellulose reacted with an epoxide substituted with a trimethylammonium group.
Les copolymères de cellulose cationiques ou les dérivés de cellulose greffés avec un monomère hydrosoluble d'ammonium quaternaire, sont décrits notamment dans le brevet US4131576, et on peut citer les hydroxyalkylcelluloses, comme les hydroxyméthyl-, hydroxyéthyl- ou hydroxypropyl celluloses greffées notamment avec un sel de méthacryloyléthyl triméthylammonium, de méthacrylamidopropyl triméthylammonium, de diméthyl-diallylammonium. Les produits commercialisés répondant à cette définition sont plus particulièrement les produits vendus sous la dénomination "Celquat L 200" et "Celquat H 100" par la Société National Starch. Les gommes de galactomannane cationiques sont décrites plus particulièrement dans les brevets US3589578 et US4031307, et on peut citer les gommes de guar comprenant des groupements cationiques trialkylammonium. On utilise par exemple des gommes de guar modifiées par un sel (par exemple un chlorure) de 2,3-époxypropyl triméthylammonium. De tels produits sont commercialisés notamment sous les dénominations JAGUAR C13 S, JAGUAR C 15, JAGUAR C 17 ou JAGUAR C162 par la société RHODIA.  The cationic cellulose copolymers or cellulose derivatives grafted with a water-soluble quaternary ammonium monomer, are described in particular in the US4131576 patent, and mention may be made of hydroxyalkylcelluloses, such as hydroxymethyl-, hydroxyethyl- or hydroxypropyl cellulose grafted in particular with a salt methacryloylethyl trimethylammonium, methacrylamidopropyl trimethylammonium, dimethyl diallylammonium. The marketed products corresponding to this definition are more particularly the products sold under the name "Celquat L 200" and "Celquat H 100" by the company National Starch. The cationic galactomannan gums are described more particularly in the patents US Pat. No. 3,098,578 and US Pat. No. 4,031,307, and mention may be made of guar gums comprising cationic trialkylammonium groups. For example, guar gums modified with a salt (for example a chloride) of 2,3-epoxypropyltrimethylammonium are used. Such products are marketed in particular under the names Jaguar C13 S, Jaguar C 15, Jaguar C 17 or Jaguar C162 by Rhodia.
(3) les polymères constitués de motifs pipérazinyle et de radicaux divalents alky- lène ou hydroxyalkylène à chaînes linéaires ou ramifiées, éventuellement interrompues par des atomes d'oxygène, de soufre, d'azote ou par des cycles aromatiques ou hétérocycliques, ainsi que les produits d'oxydation et/ou de quaternisa- tion de ces polymères. (4) les polyaminoamides solubles dans l'eau, préparés en particulier par polycon- densation d'un composé acide avec une polyamine; ces polyaminoamides peuvent être réticulés par une épihalohydrine, un diépoxyde, un dianhydride, un dian- hydride non saturé, un dérivé bis-insaturé, une bis-halohydrine, un bis-azétidinium, une bis-haloacyldiamine, un bis-halogénure d'alkyle ou encore par un oligomère résultant de la réaction d'un composé bifonctionnel réactif vis-à-vis d'une bis- halohydrine, d'un bis-azétidinium, d'une bis-haloacyldiamine, d'un bis-halogénure d'alkyle, d'une épilhalohydrine, d'un diépoxyde ou d'un dérivé bis-insaturé; l'agent réticulant étant utilisé dans des proportions allant de 0,025 à 0,35 mole par groupement aminé du polyaminoamide; ces polyaminoamides peuvent être alcoylés ou s'ils comportent une ou plusieurs fonctions aminés tertiaires, quaternisés. (3) Polymers consisting of piperazinyl units and linear or branched chain alkylene or hydroxyalkylene divalent radicals, optionally interrupted by oxygen, sulfur, nitrogen or aromatic or heterocyclic rings, as well as oxidation and / or quaternization products of these polymers. (4) water-soluble polyamino amides, prepared in particular by polycondensation of an acidic compound with a polyamine; these polyaminoamides may be crosslinked by an epihalohydrin, a diepoxide, a dianhydride, an unsaturated di-hydride, a bis-unsaturated derivative, a bis-halohydrin, a bis-azetidinium, a bis-haloacyldiamine, a bis-alkyl halide. or alternatively by an oligomer resulting from the reaction of a bifunctional compound which is reactive with a bis-halohydrin, a bis-azetidinium, a bis-haloacyldiamine or an alkyl bis-halide. an epilhalohydrin, a diepoxide or a bis-unsaturated derivative; the crosslinking agent being used in proportions ranging from 0.025 to 0.35 moles per amine group of the polyaminoamide; these polyaminoamides can be alkylated or if they comprise one or more tertiary amino functions, quaternized.
(5) les dérivés de polyaminoamides résultant de la condensation de polyalcoy- lènes polyamines avec des acides polycarboxyliques suivie d'une alcoyiation par des agents bifonctionnels. On peut citer par exemple les polymères acide adi- pique-diacoylaminohydroxyalcoyldialoylène triamine dans lesquels le radical al- coyle comporte de 1 à 4 atomes de carbone et désigne de préférence méthyle, éthyle, propyle. Parmi ces dérivés, on peut citer plus particulièrement les poly- mères acide adipique/diméthylaminohydroxypropyl/diéthylène triamine vendus sous la dénomination "Cartaretine F, F4 ou F8" par la société Sandoz. (5) polyamino amide derivatives resulting from the condensation of polyalkylene polyamines with polycarboxylic acids followed by alkylation with difunctional agents. There may be mentioned, for example, adipic acid-diacoylaminohydroxyalkyldialoylene triamine polymers in which the alkyl radical contains from 1 to 4 carbon atoms and preferably denotes methyl, ethyl or propyl. Among these derivatives, mention may be made more particularly of the adipic acid / dimethylaminohydroxypropyl / diethylene triamine polymers sold under the name "Cartaretine F, F4 or F8" by the company Sandoz.
(6) les polymères obtenus par réaction d'une polyalkylène polyamine comportant deux groupements aminé primaire et au moins un groupement aminé secondaire avec un acide dicarboxylique choisi parmi l'acide diglycolique et les acides dicar- boxyliques aliphatiques saturés ayant de 3 à 8 atomes de carbone; le rapport molaire entre le polyalkylène polyamine et l'acide dicarboxylique étant de préférence compris entre 0,8:1 et 1 ,4:1 ; le polyaminoamide en résultant étant amené à réagir avec l'épichlorhydrine dans un rapport molaire d'épichlorhydrine par rapport au groupement aminé secondaire du polyaminoamide compris de préférence entre 0,5:1 et 1 ,8:1 . Des polymères de ce type sont en particulier commercialisés sous la dénomination "Hercosett 57" par la société Hercules Inc. ou bien sous la dénomination de "PD 170" ou "Delsette 101 " par la société Hercules dans le cas du copolymère d'acide adipique/époxypropyl/diéthylène-triamine. (6) polymers obtained by reaction of a polyalkylene polyamine comprising two primary amine groups and at least one secondary amine group with a dicarboxylic acid chosen from diglycolic acid and saturated aliphatic dicarboxylic acids having from 3 to 8 carbon atoms. carbon; the molar ratio between the polyalkylene polyamine and the dicarboxylic acid being preferably between 0.8: 1 and 1, 4: 1; the polyaminoamide resulting therefrom being reacted with epichlorohydrin in a molar ratio of epichlorohydrin relative to the secondary amine group of the polyaminoamide preferably between 0.5: 1 and 1, 8: 1. Polymers of this type are in particular sold under the name "Hercosett 57" by the company Hercules Inc. or under the name "PD 170" or "Delsette 101" by the company Hercules in the case of the adipic acid copolymer / epoxypropyl / diethylenetriamine.
(7) les cyclopolymères d'alkyl diallyl aminé ou de dialkyl diallyl ammonium tels que les homopolymères ou copolymères comportant comme constituant principal de la chaîne des motifs répondant aux formules (I) ou (II) : (CH2)k (CH2)k (7) cyclopolymers of alkyl diallyl amine or of dialkyl diallyl ammonium, such as homopolymers or copolymers comprising, as main constituent of the chain, units corresponding to formulas (I) or (II): (CH 2 ) k (CH 2 ) k
C(R12)-CH2 CH C (R 12 ) -CH 2 CH
(CH2)t- CR -(CH2)t- CR C(R12)-(CH 2 ) t - CR - (CH 2 ) t - CR C (R 12 ) -
12 12 12 12
H2C H 2 C
CH CH2 CH CH 2
/ 2 / 2
(I) N÷ γ- <">  (I) N ÷ γ- <">
Rio Rn R10 R io R n R 10
dans lesquelles in which
- k et t sont égaux à 0 ou 1 , la somme k + t étant égale à 1 ;  - k and t are equal to 0 or 1, the sum k + t being equal to 1;
- R12 désigne un atome d'hydrogène ou un radical méthyle ;  - R12 denotes a hydrogen atom or a methyl radical;
- R10 et R1 1 , indépendamment l'un de l'autre, désignent un groupement alkyle ayant de 1 à 6 atomes de carbone, un groupement hydroxyalkyle dans lequel le groupement alkyle a 1 à 5 atomes de carbone, un groupement amidoalkyle en C1 - C4; ou bien R10 et R1 1 peuvent désigner conjointement avec l'atome d'azote auquel ils sont rattachés, des groupement hétérocycliques, tels que pipéridinyle ou morpholinyle ; R10 et R1 1 , indépendamment l'un de l'autre, désignent de préférence un groupement alkyle ayant de 1 à 4 atomes de carbone. - R10 and R1 1, independently of each other, denote an alkyl group having from 1 to 6 carbon atoms, a hydroxyalkyl group in which the alkyl group has 1 to 5 carbon atoms, a C1-C6 amidoalkyl group; C4; or R10 and R1 may together with the nitrogen atom to which they are attached, designate heterocyclic groups, such as piperidinyl or morpholinyl; R10 and R1, independently of one another, preferably denote an alkyl group having from 1 to 4 carbon atoms.
- Y" est un anion tel que bromure, chlorure, acétate, borate, citrate, tartrate, bisulfate, bisulfite, sulfate, phosphate. - Y "is an anion such as bromide, chloride, acetate, borate, citrate, tartrate, bisulphate, bisulphite, sulphate, phosphate.
On peut citer plus particulièrement l'homopolymère de sels (par exemple chlorure) de diméthyldiallylammonium par exemple vendu sous la dénomination "MER- QUAT 100" par la société NALCO (et leurs homologues de faibles masses molaires moyenne en poids) et les copolymères de sels (par exemple chlorure) de diallyldiméthylammonium et d'acrylamide commercialisés notamment sous la dénomination "MERQUAT 550" ou "MERQUAT 7SPR".  Mention may more particularly be made of the homopolymer of salts (for example chloride) of dimethyldiallylammonium, for example sold under the name "Merquat 100" by the company Nalco (and their counterparts of low molecular weight average weight) and the salt copolymers (For example chloride) diallyldimethylammonium and acrylamide sold in particular under the name "MERQUAT 550" or "MERQUAT 7SPR".
(8) les polymères de diammonium quaternaire comprenant des motifs récurrents de formule : (8) quaternary diammonium polymers comprising recurring units of formula:
R13 R15
Figure imgf000017_0001
R 13 R 15
Figure imgf000017_0001
dans laquelle : in which :
- R13, R14, R15 et R16, identiques ou différents, représentent des radicaux ali- phatiques, alicycliques, ou arylaliphatiques comprenant de 1 à 20 atomes de carbone ou des radicaux hydroxyalkylaliphatiques inférieurs, ou bien R13, R14, R15 et R16, ensemble ou séparément, constituent avec les atomes d'azote auxquels ils sont rattachés des hétérocycles comprenant éventuellement un second hété- roatome autre que l'azote ou bien R13, R14, R15 et R16 représentent un radical alkyle en C1 -C6 linéaire ou ramifié substitué par un groupement nitrile, ester, acyle, amide ou -CO-O-R17-D ou -CO-NH-R17-D où R17 est un alkylène et D un groupement ammonium quaternaire ; - A1 et B1 représentent des groupements divalents polyméthyléniques comprenant de 2 à 20 atomes de carbone pouvant être linéaires ou ramifiés, saturés ou insaturés, et pouvant contenir, liés à ou intercalés dans la chaîne principale, un ou plusieurs cycles aromatiques, ou un ou plusieurs atomes d'oxygène, de soufre ou des groupements sulfoxyde, sulfone, disulfure, amino, alkylamino, hydroxyle, ammonium quaternaire, uréido, amide ou ester, et R13, R14, R15 and R16, which may be identical or different, represent aliphatic, alicyclic or arylaliphatic radicals comprising from 1 to 20 carbon atoms or lower hydroxyalkylaliphatic radicals, or R13, R14, R15 and R16, together or separately, together with the nitrogen atoms to which they are attached, are heterocycles optionally comprising a second heteroatom other than nitrogen, or else R13, R14, R15 and R16 represent a linear or branched C1-C6 alkyl radical substituted with a nitrile, ester, acyl, amide or -CO-O-R17-D or -CO-NH-R17-D group where R17 is alkylene and D is a quaternary ammonium group; A1 and B1 represent divalent polymethylenic groups comprising from 2 to 20 carbon atoms which may be linear or branched, saturated or unsaturated, and which may contain, bound to or intercalated in the main chain, one or more aromatic rings, or one or more oxygen, sulfur or sulfoxide, sulfone, disulfide, amino, alkylamino, hydroxyl, quaternary ammonium, ureido, amide or ester groups, and
- X" désigne un anion dérivé d'un acide minéral ou organique; X " denotes an anion derived from a mineral or organic acid;
Etant entendu que A1 , R13 et R15 peuvent former avec les deux atomes d'azote auxquels ils sont rattachés un cycle pipérazinique ;  It being understood that A1, R13 and R15 can form with the two nitrogen atoms to which they are attached a piperazine ring;
en outre si A1 désigne un radical alkylène ou hydroxyalkylène linéaire ou ramifié, saturé ou insaturé, B1 peut également désigner un groupement (CH2)n-CO-D- OC-(CH2)n- dans lequel D désigne : in addition, if A1 denotes a linear or branched, saturated or unsaturated alkylene or hydroxyalkylene radical, B1 may also denote a (CH2) n -CO-D-OC- (CH2) n- group in which D denotes:
a) un reste de glycol de formule -O-Z-O-, où Z désigne un radical hydrocarboné linéaire ou ramifié ou un groupement répondant à l'une des formules sui- vantes: -(CH2-CH2-O)x-CH2-CH2- et -[CH2-CH(CH3)-O]y-CH2-CH(CH3)- où x et y désignent un nombre entier de 1 à 4, représentant un degré de polymérisation défini et unique ou un nombre quelconque de 1 à 4 représentant un degré de polymérisation moyen ;  a) a glycol residue of formula -OZO-, where Z denotes a linear or branched hydrocarbon radical or a group corresponding to one of the following formulas: - (CH 2 -CH 2 -O) x -CH 2 -CH 2 - and - [CH 2 -CH (CH 3) -O] y -CH 2 -CH (CH 3) - where x and y denote an integer of 1 to 4, representing a defined and unique degree of polymerization or any number from 1 to 4 representing a degree of average polymerization;
b) un reste de diamine bis-secondaire tel qu'un dérivé de pipérazine ;  b) a bis-secondary diamine residue such as a piperazine derivative;
c) un reste de diamine bis-primaire de formule : -NH-Y-NH-, où Y désigne un radical hydrocarboné linéaire ou ramifié, ou bien le radical divalent -CH2-CH2- c) a bis-primary diamine residue of formula: -NH-Y-NH-, where Y denotes a linear or branched hydrocarbon radical, or the divalent radical -CH2-CH2-
S-S-CH2-CH2- ; S-S-CH 2 -CH 2 -;
d) un groupement uréylène de formule : -NH-CO-NH- ;  d) a ureylene group of formula: -NH-CO-NH-;
De préférence, X" est un anion tel que le chlorure ou le bromure. Ces polymères ont une masse molaire moyenne en nombre (Mn) généralement comprise entrePreferably, X " is an anion such as chloride or bromide These polymers have a number-average molar mass (Mn) generally between
1000 et 100000. 1000 and 100000.
On peut citer plus particulièrement les polymères qui sont constitués de motifs récurrents répondant à la formule : Mention may be made more particularly of polymers which consist of repeating units corresponding to the formula:
- 2)p — (IV)- 2 ) p - (IV)
Figure imgf000018_0001
Figure imgf000018_0001
dans laquelle R1 , R2, R3 et R4, identiques ou différents, désignent un radical al- kyle ou hydroxyalkyle ayant de 1 à 4 atomes de carbone environ, n et p sont des nombres entiers variant de 2 à 20 environ et, X- est un anion dérivé d'un acide minéral ou organique. in which R 1, R 2, R 3 and R 4, which may be identical or different, denote an alkyl or hydroxyalkyl radical having from 1 to 4 carbon atoms, n and p are integers ranging from 2 to approximately 20 and, X- is an anion derived from a mineral or organic acid.
Un composé de formule (IV) particulièrement préféré est celui pour lequel R1 , R2, R3 et R4 représentent un radical méthyle, n=3, p=6 et X = Cl, dénommé Hexadi- methrine chloride selon la nomenclature INCI (CTFA). (9) les polymères de polyammonium quaternaires comprenant des motifs de for- mule (V): A compound of formula (IV) which is particularly preferred is that for which R 1, R 2, R 3 and R 4 represent a methyl radical, n = 3, p = 6 and X = Cl, called Hexadimethrin chloride according to the INCI nomenclature (CTFA). (9) quaternary polyammonium polymers comprising mule (V):
^18 20 ^ 18 20
— N+ - (CH2)r - NH - CO - (CH2)q CO - NH (CH2)S - N+ - A— - N + - (CH 2 ) r - NH - CO - (CH 2 ) q CO - NH (CH 2 ) S - N + - A -
R19 (V) χ_ 21 R19 (V) χ _ 21
dans laquelle : in which :
- R18, R19, R20 et R21 , identiques ou différents, représentent un atome d'hydrogène ou un radical méthyle, éthyle, propyle, β-hydroxyéthyle, β-hydroxypropyle ou -CH2CH2(OCH2CH2)pOH, où p est égal à 0 ou à un nombre entier compris entre 1 et 6, sous réserve que R18, R19, R20 et R21 ne représentent pas simultanément un atome d'hydrogène, R18, R19, R20 and R21, which may be identical or different, represent a hydrogen atom or a methyl, ethyl, propyl, β-hydroxyethyl, β-hydroxypropyl or -CH2CH2 (OCH2CH2) pOH radical, where p is 0 or to an integer between 1 and 6, provided that R18, R19, R20 and R21 do not simultaneously represent a hydrogen atom,
- r et s, identiques ou différents, sont des nombres entiers compris entre 1 et 6,r and s, which are identical or different, are integers between 1 and 6,
- q est égal à 0 ou à un nombre entier compris entre 1 et 34, q is equal to 0 or to an integer between 1 and 34,
- X- désigne un anion tel qu'un halogénure,  X - denotes an anion such as a halide,
- A désigne un radical d'un dihalogénure ou représente de préférence -CH2-CH2-O-CH2-CH2-.  - A denotes a radical of a dihalide or is preferably -CH2-CH2-O-CH2-CH2-.
On peut par exemple citer les produits "Mirapol® A 15", "Mirapol® AD1 ", "Mira- pol® AZ1 " et "Mirapol® 175" vendus par la société Miranol. For example, the products "Mirapol® A 15", "Mirapol® AD1", "Mirapol® AZ1" and "Mirapol® 175" sold by the company Miranol can be mentioned.
(10) Les polymères quaternaires de vinyipyrrolidone et de vinylimidazole tels que par exemple les produits commercialisés sous les dénominations Luviquat® FC 905, FC 550 et FC 370 par la société B.A.S.F. (10) Quaternary polymers of vinyipyrrolidone and of vinylimidazole such as, for example, the products sold under the names Luviquat® FC 905, FC 550 and FC 370 by the company B.A.S.F.
(1 1 ) Les polyamines comme le Polyquart® H vendu par COGNIS, référencé sous le nom de "POLYETHYLENEGLYCOL (15) TALLOW POLYAMINE" dans le dictionnaire CTFA. (1 1) Polyamines such as Polyquart® H sold by COGNIS, referenced under the name "POLYETHYLENEGLYCOL (15) TALLOW POLYAMINE" in the CTFA dictionary.
(12) les polymères comportant dans leur structure : (12) polymers having in their structure:
(a) un ou plusieurs motifs répondant à la formule (A) suivante :  (a) one or more of the following Forms (A):
— CH2— CH— - CH 2 - CH-
NH2 (A) NH 2 (A)
(b) éventuellement un ou plusieurs motifs répondant à la formule (B) suivante : (b) optionally one or more units of the following formula (B):
— CHô— CH— - CH-CH-
(B)  (B)
NH— C-H  NH- C-H
I I I I
O O
Autrement dit, ces polymères peuvent être notamment choisis parmi les homo- ou copolymères comportant un ou plusieurs motifs issus de la vinylamine et éventuel- lement un ou plusieurs motifs issus du vinylformamide. De préférence, ces polymères cationiques sont choisis parmi les polymères comportant, dans leur structure, de 5 à 100% en moles de motifs répondant à la formule (A) et de 0 à 95% en moles de motifs répondant à la formule (B), préféren- tiellement de 10 à 100% en moles de motifs répondant à la formule (A) et de 0 à 90% en moles de motifs répondant à la formule (B). In other words, these polymers may in particular be chosen from homo- or copolymers comprising one or more units derived from vinylamine and possibly one or more units derived from vinylformamide. Preferably, these cationic polymers are chosen from polymers comprising, in their structure, from 5 to 100 mol% of units corresponding to formula (A) and from 0 to 95 mol% of units corresponding to formula (B) preferably 10 to 100 mol% of units of formula (A) and 0 to 90 mol% of units of formula (B).
Ces polymères peuvent être obtenus par exemple par hydrolyse partielle du poly- vinylformamide. Cette hydrolyse peut se faire en milieu acide ou basique.  These polymers can be obtained for example by partial hydrolysis of polyvinylformamide. This hydrolysis can be done in acidic or basic medium.
La masse moléculaire moyenne en poids dudit polymère, mesurée par diffraction de la lumière, peut varier de 1000 à 3.000.000 g/mole, de préférence de 10 000 à 1 .000.000 et plus particulièrement de 100 000 à 500.000 g/mole. The weight average molecular weight of said polymer, measured by diffraction of light, can vary from 1000 to 3,000,000 g / mol, preferably from 10,000 to 1,000,000 and more particularly from 100,000 to 500,000 g / mol.
La densité de charge cationique de ces polymères peut varier de 2 meq/g à 20 meq/g, de préférence de 2,5 à 15 et plus particulièrement de 3,5 à 10 meq/g.  The cationic charge density of these polymers can vary from 2 meq / g to 20 meq / g, preferably from 2.5 to 15 and more particularly from 3.5 to 10 meq / g.
Les polymères comportant des motifs de formule (A) et éventuellement des motifs de formule (B) sont notamment vendus sous la dénomination LUPAMIN par la so- ciété BASF, tels que par exemple, et de manière non limitative, les produits proposés sous la dénomination LUPAMIN 9095, LUPAMIN 5095, LUPAMIN 1095, LUPAMIN 9030 (ou LUVIQUAT 9030) et LUPAMIN 9010. The polymers comprising units of formula (A) and optionally units of formula (B) are in particular sold under the name LUPAMIN by BASF, such as, for example, and without limitation, the products offered under the name LUPAMIN 9095, LUPAMIN 5095, LUPAMIN 1095, LUPAMIN 9030 (or LUVIQUAT 9030) and LUPAMIN 9010.
D'autres polymères cationiques utilisables dans le cadre de l'invention sont des protéines cationiques ou des hydrolysats de protéines cationiques, des polyalky- lèneimines, en particulier des polyéthylèneimines, des polymères comprenant des motifs vinylpyridine ou vinylpyridinium, des condensais de polyamines et d'épichlorhydrine, des polyuréylènes quaternaires et les dérivés de la chitine. De préférence, les polymères cationiques sont choisis parmi ceux des familles (1 ), (2), (7) et (10) ci-dessus citées. Other cationic polymers which may be used in the context of the invention are cationic proteins or hydrolysates of cationic proteins, polyalkyleneimines, in particular polyethyleneimines, polymers comprising vinylpyridine or vinylpyridinium units, polyamine and polyamine condensates. epichlorohydrin, quaternary polyureylenes and chitin derivatives. Preferably, the cationic polymers are chosen from those of families (1), (2), (7) and (10) mentioned above.
Parmi les polymères cationiques mentionnés ci-dessus, on peut utiliser de préférence les polysaccharides cationiques, notamment les celluloses et les gommes de galactomannanes cationiques, et en particulier les dérivés d'éther de cellulose quaternaires tels que les produits vendus sous la dénomination "JR 400" par la Société AMERCHOL, les cyclopolymères cationiques, en particulier les homopo- lymères ou copolymères de sels (par exemple chlorure) de diméthyldiallylammo- nium, vendus sous les dénominations MERQUAT 100, MERQUAT 550 et MER- QUAT S par la société NALCO et leurs homologues de faibles poids moléculaires en poids, les polymères quaternaires de vinyipyrrolidone et de vinylimidazole, les homopolymères ou copolymères éventuellement réticulés de sels de méthacryloy- loxyalkyl(C1 -C4) trialkyl(C1 -C4)ammonium; et leurs mélanges.  Among the cationic polymers mentioned above, it is preferable to use cationic polysaccharides, in particular cationic celluloses and galactomannan gums, and in particular quaternary cellulose ether derivatives such as the products sold under the name "JR 400. "By the company AMERCHOL, cationic cyclopolymers, in particular homopolymers or copolymers of salts (for example chloride) dimethyldiallylammonium, sold under the names MERQUAT 100, MERQUAT 550 and MER-QUAT S by the company NALCO and their homologues of low molecular weight by weight, quaternary polymers of vinyipyrrolidone and vinylimidazole, optionally crosslinked homopolymers or copolymers of methacryloyloxyalkyl (C1 -C4) trialkyl (C1 -C4) ammonium salts; and their mixtures.
Il est également possible d'utiliser des polymères amphotères, qui peuvent de pré- férence être choisis parmi les polymères amphotères comprenant la répétition de :It is also possible to use amphoteric polymers, which may preferably be selected from amphoteric polymers comprising the repetition of:
(i) un ou plusieurs motifs issus d'un monomère de type (méth)acrylamide, (i) one or more units derived from a monomer of (meth) acrylamide type,
(ii) un ou plusieurs motifs issus d'un monomère de type (méth)acrylamidoalkyl- trialkylammonium, et (iii) un ou plusieurs motifs issus d'un monomère acide de type acide (méth)acrylique. (ii) one or more units derived from a monomer of the (meth) acrylamidoalkyltrialkylammonium type, and (iii) one or more units derived from an acid monomer of (meth) acrylic acid type.
De préférence, les motifs issus d'un monomère de type (i) (méth)acrylamide sont des motifs de structure (la) suivante :
Figure imgf000021_0001
dans laquelle Ri désigne H ou CH3, et R2 est choisi parmi un radical amino, dimé- thylamino, tert-butylamino, dodécylamino, ou -NH-CH2OH.
Preferably, the units derived from a monomer of (i) (meth) acrylamide type are units of the following structure (Ia):
Figure imgf000021_0001
wherein R 1 is H or CH 3 , and R 2 is selected from amino, dimethylamino, tert-butylamino, dodecylamino, or -NH-CH 2 OH.
De préférence, ledit polymère amphotère ne comprend la répétition que d'un seul motif de formule (la). Preferably, said amphoteric polymer comprises the repetition of only one unit of formula (Ia).
Le motif issu d'un monomère de type (méth)acrylamide de formule (la) dans laquelle Ri désigne H et R2 est un radical amino (NH2) est particulièrement préféré. Il correspond au monomère acrylamide proprement dit. De préférence, les motifs issus d'un monomère de type (ii) (méth)acrylamidoalkyltrialkylammonium sont des motifs de structure (Ma) suivante The unit resulting from a (meth) acrylamide type monomer of formula (Ia) in which R 1 denotes H and R 2 is an amino (NH 2) radical is particularly preferred. It corresponds to the acrylamide monomer itself. Preferably, the units derived from a monomer of (ii) (meth) acrylamidoalkyltrialkylammonium type are units of the following structure (Ma)
Figure imgf000021_0002
Figure imgf000021_0002
dans laquelle : in which :
- R3 désigne H ou CH3, R 3 denotes H or CH 3 ,
- R4 désigne un groupement (CH2)k avec k un nombre entier allant de 1 à 6, et de préférence de 2 à 4 ; - R 4 denotes a group (CH 2 ) k with k an integer ranging from 1 to 6, and preferably from 2 to 4;
- R5, R6 et R7, identiques ou différents, désignent chacun un groupement alkyle ayant de 1 à 4 atomes de carbone; - R 5 , R 6 and R 7 , identical or different, each denote an alkyl group having 1 to 4 carbon atoms;
- Y" est un anion tel que bromure, chlorure, acétate, borate, citrate, tartrate, bisulfate, bisulfite, sulfate, phosphate. - Y "is an anion such as bromide, chloride, acetate, borate, citrate, tartrate, bisulphate, bisulphite, sulphate, phosphate.
De préférence, ledit polymère amphotère ne comprend la répétition que d'un seul motif de formule (Ma).  Preferably, said amphoteric polymer comprises the repetition of only one unit of formula (Ma).
Parmi ces motifs issus d'un monomère de type (méth)acryl- amidoalkyltrialkylammonium de formule (Ma), on préfère ceux issus du monomère chlorure de méthacrylamidopropyltriméthylammonium, pour lequel R3 désigne un radical méthyle, k vaut 3, R5, R6 et R7 désignent un radical méthyle, et Y" désigne un anion chlorure. Among these units resulting from a (meth) acrylamidoalkyltrialkylammonium type monomer of formula (Ma), those derived from methacrylamidopropyltrimethylammonium chloride monomer, for which R 3 denotes a methyl radical, k is 3, R 5 , R 6 and R 7 denote a methyl radical, and Y " denotes a chloride anion.
De préférence, les motifs issus d'un monomère de type (iii) acide (méth)acrylique sont des motifs de formule (llla) : Preferably, the units derived from a monomer of (iii) (meth) acrylic acid type are units of formula (IIIa):
Figure imgf000022_0001
Figure imgf000022_0001
dans laquelle Rs désigne H ou CH3, et R9 désigne un radical hydroxyle ou un radical -NH-C(CH3)2-CH2-SO3H. in which Rs denotes H or CH 3 , and R 9 denotes a hydroxyl radical or a radical -NH-C (CH 3 ) 2 -CH 2 -SO 3 H.
Les motifs préférés de formules (llla) correspondent aux monomères acide acrylique, acide méthacrylique et acide 2-acrylamino 2-méthyl propane sulfonique. De préférence, le motif issu d'un monomère de type acide (méth)acrylique de formule (llla) est celui issu de l'acide acrylique, pour lequel Rs désigne un atome d'hydrogène et R9 désigne un radical hydroxyle. The preferred units of formulas (IIIa) correspond to the monomers acrylic acid, methacrylic acid and 2-acrylamino-2-methyl propane sulfonic acid. Preferably, the unit derived from an acid monomer (meth) acrylic acid of formula (IIIa) is that derived from acrylic acid, wherein Rs denotes a hydrogen atom and R 9 denotes a hydroxyl radical.
Le ou les monomères acides de type acide (méth)acrylique peuvent être non neutralisés, ou partiellement ou totalement neutralisés par une base organique ou minérale. The acid monomer (s) of the (meth) acrylic acid type may be unneutralized, or partially or completely neutralized with an organic or inorganic base.
De préférence, ledit polymère amphotère ne comprend la répétition que d'un seul motif de formule (llla).  Preferably, said amphoteric polymer comprises the repetition of only one unit of formula (IIIa).
Selon un mode de réalisation préféré de l'invention, le ou les polymères ampho- tères de ce type comprennent au moins 30% en mole de motifs issus d'un monomère de type (i) (méth)acrylamide. De préférence, ils comprennent de 30 à 70% en mole de motifs issus d'un monomère de type (méth)acrylamide, de manière plus préférée de 40 à 60% en mole. According to a preferred embodiment of the invention, the amphopolymeric polymer or polymers of this type comprise at least 30 mol% of units derived from a monomer of (i) (meth) acrylamide type. Preferably, they comprise from 30 to 70 mol% of units derived from a (meth) acrylamide type monomer, more preferably from 40 to 60 mol%.
La teneur en motifs issus d'un monomère de type (ii) (méth)acrylamido alkyltrialky- lammonium peut avantageusement être de 10 à 60%, préférentiellement de 20 à 55% en moles.  The content of units derived from a monomer of the type (ii) (meth) acrylamido alkyltrialkylammonium may advantageously be from 10 to 60%, preferably from 20 to 55% by moles.
La teneur en motifs issus d'un monomère acide de type (iii) acide (méth)acrylique peut avantageusement être de 1 à 20%, préférentiellement de 5 à 15% en moles. Selon un mode de réalisation particulièrement préféré de l'invention, le polymère amphotère de ce type comprend :  The content of units derived from an acidic monomer of (iii) (meth) acrylic acid type may advantageously be from 1 to 20%, preferably from 5 to 15% by mole. According to a particularly preferred embodiment of the invention, the amphoteric polymer of this type comprises:
- de 30 à 70% en moles de motifs issus d'un monomère de type (i) (méth)acrylamide, de manière plus préférée de 40 à 60% en moles,  from 30 to 70 mol% of units derived from a monomer of (i) (meth) acrylamide type, more preferably from 40 to 60 mol%,
- de 10 à 60% en moles, préférentiellement de 20 à 55% en moles, de motifs issus d'un monomère de type (ii) (méth)acrylamidoalkyltrialkylammonium, et from 10 to 60 mol%, preferably from 20 to 55 mol%, of units derived from a monomer of (ii) (meth) acrylamidoalkyltrialkylammonium type, and
- de 1 à 20% en moles, préférentiellement de 5 à 15% en moles, de motifs issus d'un monomère de type (iii) acide (méth)acrylique. Ce type de polymères amphotères peut également comprendre des motifs additionnels, différents des motifs issus d'un monomère de type (méth)acrylamide, de type (méth)acrylamidoalkyltrialkylammonium et de type acide (méth)acrylique tels que décrits ci-avant. from 1 to 20 mol%, preferably from 5 to 15 mol%, of units derived from a monomer of (iii) (meth) acrylic acid type. This type of amphoteric polymers may also comprise additional units, different from the units derived from a monomer of (meth) acrylamide type, of (meth) acrylamidoalkyltrialkylammonium type and (meth) acrylic acid type as described above.
Toutefois, selon un mode de réalisation préféré de l'invention, lesdits polymères amphotères sont constitués uniquement de motifs issus de monomères de type (i) (méth)acrylamide, de type (ii) (méth)acrylamidoalkyltrialkylammonium et de type (iii) acide (méth)acrylique. However, according to a preferred embodiment of the invention, said amphoteric polymers consist solely of units derived from monomers of (i) (meth) acrylamide type, (ii) (meth) acrylamidoalkyltrialkylammonium type and (iii) acid type. (meth) acrylic acid.
Comme exemple de polymères amphotères particulièrement préférés, on peut citer les terpolymères acrylamide/chlorure de méthacrylamidopropyltriméthy- lammonium/acide acrylique. De tels polymères sont répertoriés dans le dictionnaire C.T.F.A. International Cosmetic Ingrédient Dictionary, i oeme édition 2004, sous la dénomination "Polyquaternium 53". Des produits correspondants sont notamment commercialisés sous les dénominations MERQUAT 2003 et MERQUAT 2003 PR par la société NALCO. As an example of particularly preferred amphoteric polymers, mention may be made of acrylamide / methacrylamidopropyltrimethylammonium chloride / acrylic acid terpolymers. Such polymers are listed in the CTFA International Cosmetic Ingredient Dictionary, io th edition, 2004, under the name "Polyquaternium 53". Corresponding products are in particular sold under the names MERQUAT 2003 and MERQUAT 2003 PR by the company NALCO.
Comme autre type de polymère amphotère susceptible d'être utilisé, on peut également citer les copolymères à base d'acide (méth)acrylique et d'un sel de dialkyl- diallylammonium, tels que les copolymères d'acide (méth)acrylique et de chlorure de diméthyldiallyl ammonium. On peut citer par exemple le Merquat 280 proposé par la société NALCO. As another type of amphoteric polymer that may be used, mention may also be made of copolymers based on (meth) acrylic acid and on a dialkyl-diallylammonium salt, such as copolymers of (meth) acrylic acid and of dimethyldiallyl ammonium chloride. We can cite for example the Merquat 280 proposed by the company NALCO.
La composition selon l'invention peut comprendre les polymères cationiques et/ou amphotères en une quantité comprise entre 0,01 et 5% en poids, notamment de 0,05 à 3% en poids, préférentiellement de 0,1 à 2% en poids, par rapport au poids total de la composition. The composition according to the invention may comprise cationic and / or amphoteric polymers in an amount of between 0.01 and 5% by weight, in particular from 0.05 to 3% by weight, preferably from 0.1 to 2% by weight. , relative to the total weight of the composition.
Autres ingrédients Other ingredients
La composition cosmétique selon l'invention peut se présenter sous toutes les formes galéniques classiquement utilisées, et notamment sous forme d'une solution ou suspension aqueuse, alcoolique ou hydroalcoolique, ou huileuse; d'une solution ou d'une dispersion du type lotion ou sérum; d'une émulsion, d'un gel aqueux ou anhydre, ou de toute autre forme cosmétique. La composition selon l'invention est de préférence aqueuse et comprend alors de l'eau à une concentration allant de préférence de 5 à 98% en poids, notamment de 20 à 95% en poids, mieux de 50 à 90% en poids, par rapport au poids total de la composition.  The cosmetic composition according to the invention may be in any of the galenical forms conventionally used, and especially in the form of an aqueous, alcoholic or aqueous-alcoholic solution or suspension, or an oily solution; a solution or dispersion of the lotion or serum type; an emulsion, an aqueous or anhydrous gel, or any other cosmetic form. The composition according to the invention is preferably aqueous and then comprises water at a concentration preferably ranging from 5 to 98% by weight, in particular from 20 to 95% by weight, better still from 50 to 90% by weight, by weight. relative to the total weight of the composition.
La composition peut également comprendre un ou plusieurs solvants organiques liquides à 25°C, 1 atm., notamment hydrosolubles, tels que les alcools en C1 -C7, et notamment les monoalcools aliphatiques ou aromatiques en C1 -C7, les polyols et les éthers de polyols en C3-C7, qui peuvent donc être employés seuls ou en mélange avec de l'eau. Avantageusement, le solvant organique peut être choisi parmi l'éthanol, l'isopropanol et leurs mélanges. The composition may also comprise one or more organic solvents liquid at 25 ° C., 1 atm., In particular water-soluble, such as C 1 -C 7 alcohols, and in particular C 1 -C 7 aliphatic or aromatic monoalcohols, polyols and polyethers. C3-C7 polyols, which can be used alone or mixed with water. Advantageously, the organic solvent can be chosen among ethanol, isopropanol and mixtures thereof.
La composition selon l'invention peut en outre comprendre au moins un ingrédient cosmétique usuel, différent des composés de l'invention, et notamment choisi parmi les huiles végétales, minérales, animales ou de synthèse; les corps gras solides et notamment les cires, les esters en C8-C40, les acides en C8-C40; les alcools en C8-C40; les tensioactifs cationiques, les polymères anioniques; les filtres solaires; les agents hydratants; les agents antipelliculaires; les agents antioxydants; les agents chélatants; les agents nacrants et opacifiants; les agents plastifiants ou de coalescence; les hydroxyacides; les charges; les silicones et en particulier les polydiméthylsiloxanes (PDMS); les parfums; les agents d'alcalinisation ou d'acidification; les aldéhydes, la DHA; les épaississants autres que les polymères associatifs non ioniques selon l'invention, et de préférence choisis parmi les épaississants non polymériques et les épaississants polymé- riques non associatifs. La composition peut bien évidemment comprendre plusieurs ingrédients cosmétiques figurant dans la liste ci-dessus. L'homme de métier veillera à choisir les ingrédients entrant dans la composition, ainsi que leurs quantités, de manière à ce qu'ils ne nuisent pas aux propriétés des compositions de la présente invention. The composition according to the invention may further comprise at least one usual cosmetic ingredient, different from the compounds of the invention, and especially chosen from vegetable, mineral, animal or synthetic oils; solid fatty substances and in particular waxes, C8-C40 esters, C8-C40 acids; C8-C40 alcohols; cationic surfactants, anionic polymers; solar filters; moisturizing agents; antidandruff agents; antioxidants; chelating agents; pearlescent and opacifying agents; plasticizing or coalescing agents; hydroxy acids; the charges; silicones and in particular polydimethylsiloxanes (PDMS); the perfumes; alkalizing or acidifying agents; aldehydes, DHA; the thickeners other than the nonionic associative polymers according to the invention, and preferably chosen from non-polymeric thickeners and non-associative polymeric thickeners. The composition may of course include several cosmetic ingredients listed above. Those skilled in the art will take care to choose the ingredients in the composition, as well as their amounts, so that they do not adversely affect the properties of the compositions of the present invention.
Le pH de la composition, si elle est aqueuse, est de préférence compris entre 3 et 9, notamment entre 3 et 6. The pH of the composition, if it is aqueous, is preferably between 3 and 9, especially between 3 and 6.
La composition cosmétique selon l'invention trouve notamment une application particulièrement intéressante dans le domaine du soin et de l'hygiène capillaire, notamment pour le soin et/ou le nettoyage des cheveux et/ou du cuir chevelu. La composition cosmétique peut être rincée ou non rincée après avoir été appliquée sur les cheveux et/ou le cuir chevelu; de préférence elle est rincée, après un éventuel temps de pose. The cosmetic composition according to the invention finds particular application particularly interesting in the field of care and hair hygiene, especially for the care and / or cleaning of hair and / or scalp. The cosmetic composition may be rinsed or not rinsed after being applied to the hair and / or the scalp; preferably it is rinsed after a possible exposure time.
La composition selon l'invention peut être conditionnée dans un tube, dans un flacon muni ou non d'une pompe, ou encore dans un aérosol. Dans le cas d'un aérosol, la composition peut alors contenir un ou plusieurs agents propulseurs classiques. L'invention a également pour objet un procédé de traitement cosmétique, notamment de soin et/ou de nettoyage, des cheveux et/ou du cuir chevelu, comprenant l'application sur les cheveux et/ou le cuir chevelu, d'une composition cosmétique selon l'invention, suivie éventuellement d'un rinçage, après un éventuel temps de pose. The composition according to the invention may be packaged in a tube, in a bottle with or without a pump, or in an aerosol. In the case of an aerosol, the composition may then contain one or more conventional propellants. The subject of the invention is also a process for the cosmetic treatment, in particular of care and / or cleaning, of the hair and / or the scalp, comprising the application to the hair and / or the scalp of a cosmetic composition according to the invention, optionally followed by rinsing, after a possible exposure time.
L'invention est illustrée plus en détails dans les exemples suivants. Exemples 1 à 4 On prépare les compositions capillaires suivantes (% en poids de matière commerciale) : The invention is further illustrated in the following examples. Examples 1 to 4 The following hair compositions are prepared (% by weight of commercial material):
Figure imgf000025_0001
Figure imgf000025_0001
On obtient des compositions détergentes à effet moussant, susceptibles d'être employées pour le nettoyage des cheveux et conduisant à de bonnes propriétés cosmétiques sur cheveux secs. Foaming detergent compositions are obtained which can be used for cleaning the hair and leading to good cosmetic properties on dry hair.

Claims

REVENDICATIONS
1 . Composition cosmétique non colorante comprenant : 1. Non-coloring cosmetic composition comprising:
- 2 à 60% en poids par rapport au poids total de la composition, d'un ou plusieurs polymères non ioniques associatifs, et 2 to 60% by weight relative to the total weight of the composition, of one or more associative nonionic polymers, and
- un ou plusieurs tensioactifs non ioniques de type alcools gras à chaîne en C12- C18, polyoxyalkylénés ayant un nombre d'unité d'oxyde d'alkylène allant de 4 à 10.  one or more nonionic surfactants of C 12 -C 18 chain fatty alcohol type, polyoxyalkylenated having a number of alkylene oxide units ranging from 4 to 10.
2. Composition selon la revendication 1 , dans laquelle les polymères associatifs non ioniques sont choisis parmi : 2. Composition according to claim 1, in which the nonionic associative polymers are chosen from:
(1 ) les celluloses modifiées par des groupements comportant au moins une chaîne grasse; et notamment :  (1) celluloses modified with groups comprising at least one fatty chain; and especially :
- les hydroxyéthyl celluloses modifiées par des groupements comportant au moins une chaîne grasse tels que des groupes alkyle, arylalkyle, alkylaryle, ou leurs mélanges, et dans lesquels les groupes alkyle sont de préférence en C8-C22,hydroxyethyl celluloses modified with groups comprising at least one fatty chain, such as alkyl, arylalkyl or alkylaryl groups, or mixtures thereof, and in which the alkyl groups are preferably C8-C22,
- les celluloses modifiées par des groupes polyalkylène glycol éther d'alkyl phénol;celluloses modified with alkyl phenol polyalkylene glycol ether groups;
(2) les hydroxypropylguars modifiés par des groupements comportant au moins une chaîne grasse en C8-C30; (2) hydroxypropyl guars modified with groups having at least one C8-C30 fatty chain;
(3) les copolymères de méthacrylates ou d'acrylates d'alkyles en C1 -C6 et de monomères amphiphiles comportant au moins une chaîne grasse;  (3) copolymers of C 1 -C 6 alkyl methacrylates or acrylates and of amphiphilic monomers comprising at least one fatty chain;
(4) les copolymères de méthacrylates ou d'acrylates hydrophiles et de monomères hydrophobes comportant au moins une chaîne grasse tels que par exemple le co- polymère méthacrylate de polyéthylèneglycol/méthacrylate de lauryle;  (4) copolymers of hydrophilic methacrylates or acrylates and of hydrophobic monomers comprising at least one fatty chain, such as, for example, polyethylene glycol methacrylate / lauryl methacrylate co-polymer;
(5) les polyuréthanes polyéthers comportant dans leur chaîne, à la fois des séquences hydrophiles de nature le plus souvent polyoxyéthylénée et des séquences hydrophobes qui peuvent être des enchaînements aliphatiques seuls et/ou des enchaînements cycloaliphatiques et/ou aromatiques;  (5) polyether polyurethanes comprising in their chain, both hydrophilic sequences most often polyoxyethylenated nature and hydrophobic sequences which may be aliphatic sequences alone and / or cycloaliphatic and / or aromatic sequences;
(6) les polymères à squelette aminoplaste éther possédant au moins une chaîne grasse; (6) Aminoplast ether backbone polymers having at least one fatty chain;
(7) les copolymères de vinylpyrrolidone et de monomères hydrophobes à chaîne grasse.  (7) copolymers of vinylpyrrolidone and hydrophobic fatty-chain monomers.
3. Composition selon l'une quelconque des revendications précédentes, dans laquelle le polymère associatif non ionique est choisi parmi les polyuréthanes polyéthers non ioniques associatifs comportant au moins deux chaînes lipophiles hydrocarbonées ayant de 6 à 30 atomes de carbone, séparées par une séquence hydrophile, les chaînes hydrocarbonées pouvant être des chaînes pendantes ou des chaînes en bout de séquence hydrophile. 3. Composition according to any one of the preceding claims, wherein the nonionic associative polymer is chosen from associative nonionic polyether polyurethanes comprising at least two hydrocarbon lipophilic chains having from 6 to 30 carbon atoms, separated by a hydrophilic block, the hydrocarbon chains may be pendant chains or chains at the end of the hydrophilic sequence.
4. Composition selon l'une quelconque des revendications précédentes, dans laquelle les polymères associatifs non ioniques sont des polyuréthanes polyéthers copolymères triblocs dont la séquence hydrophile est une chaîne polyoxyéthy- lénée comportant de 50 à 1000 groupements oxyéthylénés. 4. Composition according to any one of the preceding claims, in which the nonionic associative polymers are polyurethane polyethers. triblock copolymers whose hydrophilic sequence is a polyoxyethylenated chain containing from 50 to 1000 oxyethylenated groups.
5. Composition selon l'une quelconque des revendications précédentes, dans la- quelle les polymères non ioniques associatifs sont des polyuréthanes polyéthers copolymères triblocs dont la séquence hydrophile est une chaîne polyoxyéthy- lénée comportant de 50 à 1000, notamment de 100 à 300, groupements oxyéthylénés; et comportant au moins deux chaînes lipophiles hydrocarbonées ayant de 6 à 30 atomes de carbone, séparées par ladite séquence hydrophile, lesdites chaînes lipophiles hydrocarbonées pouvant être des chaînes pendantes ou des chaînes en bout de séquence hydrophile. 5. Composition according to any one of the preceding claims, in which the associative nonionic polymers are triblock copolymer polyurethane polyurethanes whose hydrophilic sequence is a polyoxyethylenated chain comprising from 50 to 1000, in particular from 100 to 300, groups. oxyethylenated; and comprising at least two hydrocarbon lipophilic chains having from 6 to 30 carbon atoms, separated by said hydrophilic sequence, said hydrocarbon lipophilic chains being pendant chains or end chains of hydrophilic sequence.
6. Composition selon l'une quelconque des revendications précédentes, dans laquelle les polymères non ioniques associatifs sont choisis parmi : 6. Composition according to any one of the preceding claims, in which the associative nonionic polymers are chosen from:
- les polyuréthanes polyéthers non ioniques associatifs susceptibles d'être obtenus par polycondensation d'au moins trois composés comprenant (i) au moins un polyéthylèneglycol comprenant de 100 à 180 moles d'oxyde d'éthylène, (ii) un alcool stéarylique polyoxyéthyléné comprenant 100 moles d'oxyde d'éthylène et (iii) un diisocyanate. the associative nonionic polyether polyurethanes obtainable by polycondensation of at least three compounds comprising (i) at least one polyethylene glycol comprising from 100 to 180 moles of ethylene oxide, (ii) a polyoxyethylenated stearyl alcohol comprising 100 moles of ethylene oxide and (iii) a diisocyanate.
- les polyuréthanes polyéthers non ioniques associatifs susceptibles d'être obtenus par polycondensation d'au moins trois composés comprenant (i) au moins un polyéthylèneglycol comprenant de 150 à 180 moles d'oxyde d'éthylène, (ii) de l'alcool stéarylique ou de l'alcool décylique et (iii) au moins un diisocyanate. the associative nonionic polyether polyurethanes obtainable by polycondensation of at least three compounds comprising (i) at least one polyethylene glycol comprising from 150 to 180 moles of ethylene oxide, (ii) stearyl alcohol or decyl alcohol and (iii) at least one diisocyanate.
7. Composition selon l'une quelconque des revendications précédentes, comprenant les polymères non ioniques associatifs en une quantité allant de 2,5 à 40% en poids, encore mieux de 2,7 à 20% en poids, voire de 2,75 à 15% en poids, par rapport au poids total de la composition. A composition according to any one of the preceding claims comprising the associative nonionic polymers in an amount of from 2.5 to 40% by weight, more preferably from 2.7 to 20% by weight, or even from 2.75 to 15% by weight, relative to the total weight of the composition.
8. Composition selon l'une quelconque des revendications précédentes, dans laquelle les tensioactifs non ioniques sont choisis parmi les alcools gras à chaîne linéaire saturée en C12-C18, polyoxyéthylénés ayant un nombre d'unité d'oxyde d'éthylène allant de 4 à 10. 8. Composition according to any one of the preceding claims, in which the nonionic surfactants are chosen from linear polyunsaturated C12-C18 saturated fatty alcohols having a number of units of ethylene oxide ranging from 4 to 10.
9. Composition selon l'une quelconque des revendications précédentes, comprenant les tensioactifs non ioniques alcools gras à chaîne en C12-C18, polyoxyalky- lénés ayant un nombre d'unité d'oxyde d'alkylène allant de 4 à 10, en une quantité inférieure ou égale à 10% en poids, notamment allant de 0,1 à 10% en poids, de préférence de 1 à 8% en poids, préférentiellement de 1 ,5 à 7,5% en poids, par rapport au poids total de la composition. A composition according to any one of the preceding claims, comprising the nonionic, C 12 -C 18, polyoxyalkylenated chain fatty alcohol surfactants having an alkylene oxide unit number of from 4 to 10, in an amount of less than or equal to 10% by weight, especially ranging from 0.1 to 10% by weight, preferably from 1 to 8% by weight, preferably from 1.5 to 7.5% by weight, relative to the total weight of the composition.
10. Composition selon l'une quelconque des revendications précédentes, comprenant en outre un ou plusieurs tensioactifs additionnels choisis parmi les tensioac- tifs non ioniques autres que les alcools gras à chaîne en C12-C18, polyoxyalkylé- nés ayant un nombre d'unité d'oxyde d'alkylène allant de 4 à 10, les tensioactifs anioniques et les tensioactifs amphotères. 10. Composition according to any one of the preceding claims, further comprising one or more additional surfactants chosen from surfactants. nonionic acids other than C12-C18 chain fatty alcohols, polyoxyalkylenes having an alkylene oxide unit number of from 4 to 10, anionic surfactants and amphoteric surfactants.
1 1 . Composition selon l'une quelconque des revendications précédentes, comprenant une quantité totale de tensioactifs non ioniques, anioniques et amphotères, allant de 0,1 à 10% en poids, de préférence allant de 1 à 8% en poids, préférentiellement de 1 ,5 à 7,5% en poids, par rapport au poids total de la composition. 1 1. Composition according to any one of the preceding claims, comprising a total amount of nonionic, anionic and amphoteric surfactants, ranging from 0.1% to 10% by weight, preferably ranging from 1% to 8% by weight, preferably from 1.5% by weight. at 7.5% by weight, relative to the total weight of the composition.
12. Composition selon l'une quelconque des revendications précédentes, comprenant une quantité totale de tensioactifs allant de 0,1 à 10% en poids, de préférence allant de 1 à 8% en poids, préférentiellement de 1 ,5 à 7,5% en poids, par rapport au poids total de la composition. 12. Composition according to any one of the preceding claims, comprising a total amount of surfactants ranging from 0.1 to 10% by weight, preferably from 1 to 8% by weight, preferably from 1.5 to 7.5% by weight. by weight, relative to the total weight of the composition.
13. Composition selon l'une quelconque des revendications précédentes, dans laquelle le ratio (% en poids) "tensioactifs non ioniques + tensioactifs anioniques + tensioactifs amphotères" / "polymères associatifs non ioniques" est inférieur ou égal à 3; de préférence varie de 0,01 à 3, notamment de 0,01 à 2,8, préférentiellement de 0,1 à 2,5. 13. Composition according to any one of the preceding claims, wherein the ratio (% by weight) "nonionic surfactants + anionic surfactants + amphoteric surfactants" / "nonionic associative polymers" is less than or equal to 3; preferably ranges from 0.01 to 3, especially from 0.01 to 2.8, preferably from 0.1 to 2.5.
14. Composition selon l'une quelconque des revendications précédentes, comprenant en outre un ou plusieurs polymères, notamment choisis parmi les polymères amphotères et cationiques, ainsi que leur mélange. 14. Composition according to any one of the preceding claims, further comprising one or more polymers, especially chosen from amphoteric and cationic polymers, and their mixture.
15. Composition selon l'une quelconque des revendications précédentes, comprenant de l'eau à une concentration allant de préférence de 5 à 98% en poids, notamment de 20 à 95% en poids, mieux de 50 à 90% en poids, par rapport au poids total de la composition. 15. A composition according to any one of the preceding claims, comprising water at a concentration preferably ranging from 5 to 98% by weight, in particular from 20 to 95% by weight, better still from 50 to 90% by weight, by weight. relative to the total weight of the composition.
16. Procédé de traitement cosmétique, notamment de soin et/ou de nettoyage, des cheveux et/ou du cuir chevelu, comprenant l'application sur les cheveux et/ou le cuir chevelu, d'une composition cosmétique telle que définie à l'une des revendications 1 à 15, suivie éventuellement d'un rinçage, après un éventuel temps de pose. 16. A method of cosmetic treatment, particularly care and / or cleaning, of the hair and / or scalp, comprising the application to the hair and / or the scalp, of a cosmetic composition as defined in one of claims 1 to 15, optionally followed by rinsing, after a possible exposure time.
PCT/EP2014/061038 2013-06-03 2014-05-28 Cosmetic composition containing non-ionic associative polymers and non-ionic surfactants, and method for cosmetic treatment WO2014195201A1 (en)

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