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    • 专利摘要:
    The invention relates to multiphasic polymers comprising from 45% to 95% by weight of a first polymer P1 and from 5% to 55% by weight of a second polymer P2, said polymers P1 and P2 being of distinct compositions, - said polymer P1 being obtained by polymerization from a monomer mixture comprising at least one anionic monomer (a) having a polymerizable vinyl function; at least one nonionic hydrophobic monomer (b) having a polymerizable vinyl function, at least one crosslinking monomer (c) and at least one associative monomer (d) having a polymerizable vinyl function and a hydrophobic hydrocarbon chain and said polymer P2 being obtained by polymerization from a monomer mixture comprising at least one anionic monomer (a ') having a polymerizable vinyl function, at least one nonionic hydrophobic monomer (b') having a polymerizable vinyl function and at least one monomer (c ') ) crosslinking agent. It also relates to a process for preparing these polymers, aqueous compositions containing them and their use as thickeners and suspensives.
    公开号:FR3030307A1
    申请号:FR1463229
    申请日:2014-12-23
    公开日:2016-06-24
    发明作者:Clementine Champagne；Jean-Marc Suau；Benoit Magny；Delphine Bony；Yves Kensicher
    申请人:Coatex SAS；
    IPC主号:
    专利说明:

    [0001] BACKGROUND OF THE INVENTION The present invention relates to novel polymers useful as rheology modifying agents for aqueous formulations and for inducing both good thickening, clarity and good performance properties. suspensivantes. Rheology modifying agents, also known as thickening or viscosity agents, are present in the cleaning compositions, whether in the care or hygiene compositions of the person, for example the cosmetic compositions, or in the care compositions. such as detergent products. These agents influence the rheological (especially viscosity) and aesthetic (such as clarity) properties of the formulation generally rich in surfactants, as well as the ability to suspend and stabilize particles within the formulation.
    [0002] Among the rheology modifying agents commonly used in aqueous formulations, mention may be made of soluble or swellable polymers in an alkaline medium, better known under the name "ASE" (for "Alkali-Soluble or Swellable Emulsions" in English) and polymers. soluble or swellable in alkaline medium and hydrophobic modified, better known under the name "HASE" (for "Hydrophobically modified Alkali-Soluble or Swellable Emulsions"). The ASE-type polymers are linear or branched copolymers synthesized from (meth) acrylic acid and alkyl acrylates. The HASE polymers are linear or branched copolymers synthesized from (meth) acrylic acid, alkyl acrylates and at least one associative monomer.
    [0003] These rheology modifiers provide good suspensivative properties, viscosity and clarity in surfactant-rich formulations with near-neutral pH values. Unfortunately, they do not allow to combine, under conditions of acidic pH, good suspensive properties, viscosity and clarity.
    [0004] However, it is desirable to be able to formulate compositions based on surfactants in a pH range corresponding to that of the skin, that is to say at pH values between 4 and 6 depending on whether the cosmetic product is intended to an application on the body, the face or the mucous membranes. In addition, conventionally used preservatives, such as formaldehyde donors, halogenated compounds and paraben compounds are either banned from use or suspected of having adverse health effects. To replace them, organic acids (eg sorbic, citric and benzoic acid), as used in the food industry, are an interesting alternative. However, the antimicrobial activity of organic acids is related to the associated or protonated species of the acid molecule. As the pH of the organic acid-containing formulation increases, acid salts are formed by dissociation of the proton. However, the dissociated form of the organic acids has no antimicrobial activity when used alone, which does not allow the use of these organic acid compounds in formulations having pH values greater than 6.
    [0005] It has furthermore been suggested in the literature that the formulation of products in an acid pH range makes it possible to reduce the amount of preservatives required in the product by improving its effectiveness, stabilizing and increasing the effectiveness of ingredients. cosmetic actives, is beneficial in the repair and maintenance of the skin barrier and strengthens the skin flora (Cosmetics & Toiletries®, vol 123, No. 12 of December 2008, "Formulating at pH 4-5: How Lower pH Benefits the Skin and Formulations "). WO 2012/006402 discloses core-shell type polymers comprising a linear core polymer based on acrylic units and a crosslinked shell polymer based on acrylic units. These core-bark polymers are provided to provide good aesthetics, rheology and clarity in aqueous compositions comprising surfactants under acidic pH conditions. However, it appears difficult to obtain a composition incorporating the described core-bark polymers and combining both good suspensive performance, viscosity and clarity under acidic pH conditions. The present invention aims to propose novel rheology modifying agents, having both good properties in terms of thickening effect (viscosity) and leading to formulations having good suspensive performance and high clarity (clear continuous phase). even under acidic pH conditions (pH <6). The inventors have discovered that it is possible to access a formulation that meets all of these criteria (viscosity, suspensive performance, and clarity) by using a specific multiphasic polymer as a rheology modifier. More particularly, the present invention relates, according to a first aspect, to a multiphasic polymer comprising from 45% to 95% by weight of a first polymer, denoted P1, and from 5% to 55% by weight of a second polymer. , noted P2, polymers P1 and P2 being of distinct compositions. (1) Said polymer P1 being obtained by polymerization from a monomer mixture comprising: - at least one anionic monomer (a) having a polymerizable vinyl function, - at least one nonionic hydrophobic monomer (b) having a vinyl function polymerizable, - at least one crosslinking monomer (c), - at least one associative monomer (d) having a polymerizable vinyl function and a hydrophobic hydrocarbon chain and - optionally at least one additional nonionic monomer (e), distinct from the monomer (b) ). (2) Said polymer P2 being obtained by polymerization from a monomer mixture comprising: at least one anionic monomer (a ') having a polymerizable vinyl function; at least one nonionic hydrophobic monomer (b') having a polymerizable vinyl function, - at least one crosslinking monomer (c '), - optionally at least one associative (d') monomer having a polymerizable vinyl function and a hydrophobic hydrocarbon chain and - optionally at least one additional nonionic monomer (e ') , distinct from the monomer (b ').
    [0006] Advantageously, as illustrated in the examples which follow, the multiphase polymers according to the invention provide the formulation in which they are used with good suspensive properties, thickening and clarity, even when formulated at pH. acid. A multiphasic polymer having the specific compositions P1 and P2 specified above is referred to more simply in the rest of the text under the name "polymer according to the invention". The term "multiphase polymer" is intended to denote, in the sense of the invention, a multiphase particle of polymer, in other words a polymer particle having a non-homogeneous composition, prepared by a sequential polymerization process in at least two stages from at least two separate monomer compositions. The multiphase particles according to the invention may in particular be structured in core / shell (or "core / shell" in English), the first polymer forming the "core" and the second polymer forming the "bark". This term "heart / bark" should not, however, be interpreted as designating a particle in which the "core" part is totally coated or encapsulated by a "bark" part, but as designating a particle with a controlled morphology having two distinct phases. The expression "polymer P1" can be understood to mean a single polymer P1 as defined above or several polymers P1 obtained by sequential polymerization. Similarly, the term "polymer P2" can be understood to mean a single polymer P2 as defined above or several polymers P2 obtained by sequential polymerization. By "suspending properties" or "suspensive power" is meant the ability of the composition to keep particles in suspension in its continuous phase, particularly stably in time, for example during storage of the composition. "Particles" to be suspended means solid bodies, solid or hollow, liquid immiscible with the formulation or encapsulated or gaseous, which may be characterized by shapes, textures, structures, compositions, colors and final properties. different. As an indication, mention may be made of exfoliating particles (for example polyethylene particles, looted fruit shells, pumice stones), nourishing particles (for example collagen spheres), pearling particles (for example titanium mica). distearate glycols) and aesthetic particles (for example air bubbles, flakes, optionally colored pigments). As regards the suspension of air bubbles in the composition, the particles may especially have a size of 1, 2 or 3 mm. The suspensive performance can be evaluated by observing the stability of the suspension of standardized particles in a composition stored in an oven at 45 ° C, as described in the following examples. The "clarity" or "clarity" of the composition can be evaluated by measuring the transmittance of the composition. A method of determining transmittance is described in the following examples. It is expressed as a percentage. A composition is considered clear or limpid if it has a transmittance, for a wavelength of 500 nm, of at least 60%, preferably at least 70% and more preferably at least 80%. Other characteristics, advantages and modes of application of the multiphasic polymer according to the invention will emerge more clearly on reading the description and the examples which follow, given by way of illustration and not limitation. In the remainder of the text, the expressions "between ... and ...", "ranging from ... to ..." and "varying from ... to ..." are equivalent and mean to mean that terminals are included unless otherwise stated.
    [0007] Unless otherwise indicated, the expression "comprising / including a" shall be understood as "comprising / including at least one". Multiphasic Polymer As indicated above, the multiphasic polymer according to the invention comprises, in particular is formed, from 45% to 95% by weight of a first polymer P1 and from 5% to 55% by weight of a second polymer P2, the compositions of polymers P1 and P2 being different. (1) Said polymer P1 being obtained by polymerization from a monomer mixture comprising: - at least one anionic monomer (a) having a polymerizable vinyl function, - at least one nonionic hydrophobic monomer (b) having a vinyl function polymerizable, - at least one crosslinking monomer (c), - at least one associative monomer (d) having a polymerizable vinyl function and a hydrophobic hydrocarbon chain and - optionally at least one additional nonionic monomer (e), distinct from the monomer (b) ). (2) Said polymer P2 being obtained by polymerization from a monomer mixture comprising: at least one anionic monomer (a ') having a polymerizable vinyl function; at least one nonionic hydrophobic monomer (b') having a polymerizable vinyl function, - at least one crosslinking monomer (c '), - optionally at least one associative (d') monomer having a polymerizable vinyl function and a hydrophobic hydrocarbon chain and - optionally at least one additional nonionic monomer (e ') , distinct from the monomer (b '). In the remainder of the text, the proportions in monomers entering into the composition of the polymer P1 (respectively polymer P2) are expressed in percentage by weight relative to the total weight of monomers used to form the polymer P1 (respectively the polymer P2) .
    [0008] According to one particular embodiment, the polymer P1 does not comprise any monomeric unit other than the monomers (a), (b), (c) and (d) (with the exception of the optional presence of fragments of agents transfer or polymerization initiators). According to one particular embodiment, the polymer P2 does not comprise any monomeric unit other than the monomers (a '), (b'), (c ') and (d') (with the exception of the optional presence of fragments of transfer agents or polymerization initiators). In other words, according to an alternative embodiment, the sum of the monomer contents (a), (b), (c) and (d) of the composition of the polymer P1 (respectively (a '), (b'), (c ') and optionally (d') of the composition of the polymer P2) is equal to 100%. According to another variant embodiment, the polymer P1 and / or the polymer P2 may further comprise one or more additional monomeric unit (s) separate from the monomers (a), ( b), (c) and (d) (respectively (a '), (b'), (c ') and (d')). In particular, the composition of the polymer P1 (respectively of the polymer P2) may further comprise one or more additional monomer (s) nonionic (s) (e) (respectively (e ')) as detailed more precisely in the following text.
    [0009] On the other hand, it is understood that the monomers (a) and (a ') (respectively (b) and (b'), respectively (c) and (c '), respectively (d) and (d'), respectively ( e) and (e ')) used in the composition of the polymer P1 and the polymer P2 may be of the same kind in the polymer P1 and in the polymer P2 or of different natures. The monomers (a), (b), (c), (d) and (e) of the composition of the polymer P1 are different.
    [0010] In particular, the one or more monomers (b) are different from the one or more monomers (d). The same applies to the monomers (a '), (b'), (c '), (d') and (e ') of the composition of the polymer P2.
    [0011] According to a particular embodiment, the weight ratio polymer P1 / polymer P2 of the multiphasic polymer according to the invention is between 45/55 and 95/5, in particular between 60/40 and 95/5.
    [0012] Anionic Monomer Having a Polymeric Vinyl Function According to one particular embodiment, the anionic monomers (a) and (a ') having a polymerizable vinyl function, more simply called in the remainder of the text "anionic monomers", comprise at least one carboxylic group . In particular, the anionic monomers may be chosen from acrylic acid, methacrylic acid, maleic acid, itaconic acid, crotonic acid and mixtures thereof, and / or the salts of these acids. According to a particular embodiment, the anionic monomers may be chosen from acrylic acid and / or methacrylic acid monomers and / or one of their salts.
    [0013] Preferably, the anionic monomer (a) of the polymer P1 and (a ') of the polymer P2 of the multiphasic polymer according to the invention is methacrylic acid (AMA). The at least one anionic monomer (a) may represent from 20% to 53% by weight, in particular from 25% to 48% by weight, and more particularly from 30% to 43% by weight, relative to the total weight of monomers forming the polymer Pl.
    [0014] The at least one anionic monomer (a ') may represent from 10% to 53% by weight, in particular from 15% to 48% by weight, and more particularly from 20% to 43% by weight, relative to the total weight of monomers. forming the polymer P2. The at least one anionic monomer (a) and (a ') may represent from 14.5% to 53% by weight, in particular from 19.5% to 48% by weight and more particularly from 24.5% to 43% by weight. weight, of the total weight of monomers forming the multiphasic polymer of the invention. Nonionic hydrophobic monomer having a polymerizable vinyl function The nonionic hydrophobic monomers (b) and (b ') having a polymerizable vinyl function, more simply called in the following text "hydrophobic nonionic monomers", are monomers having no charge positive or negative charge in aqueous solution.
    [0015] They may be chosen from esters, amides or nitriles of acrylic or methacrylic acids or from acrylonitrile, styrene, methylstyrene, diisobutylene, vinylpyrrolidone or vinylcaprolactam. More particularly, the nonionic hydrophobic monomers may be chosen from C1-C8 alkyl acrylates or C1-C8 alkyl methacrylates, such as methyl acrylate, ethyl acrylate, acrylate and the like. butyl, 2-ethyl hexyl acrylate, methyl methacrylate, ethyl methacrylate, butyl methacrylate and mixtures thereof. According to a particular embodiment, the nonionic hydrophobic monomers may be chosen from ethyl acrylate, butyl acrylate, ethyl methacrylate and mixtures thereof. In particular, the nonionic hydrophobic monomer (b) of the polymer P1 and (b ') of the polymer P2 of the multiphasic polymer according to the invention may be ethyl acrylate (AE).
    [0016] The at least one nonionic hydrophobic monomer (b) may represent from 40% to 75% by weight, in particular from 45% to 70% by weight and more particularly from 50% to 65% by weight, relative to the total weight of monomers. forming the polymer P1. The at least one nonionic hydrophobic monomer (b ') may represent from 50% to 85% by weight, in particular from 55% to 80% by weight, and more particularly from 60% to 75% by weight. relative to the total weight of monomers forming the polymer P2. The at least one nonionic hydrophobic monomer (b) and (b ') may represent from 40% to 83% by weight, in particular from 45% to 78% by weight and more particularly from 50% to 73% by weight of the total weight. of monomers forming the multiphasic polymer of the invention. According to a particularly preferred embodiment, the mass proportion of monomers (b ') in the polymer P2 (mass content of monomers (b') relative to the total weight of monomers forming the polymer P2) is greater than that in the polymer. P1 (mass content of monomers (b) relative to the total weight of monomers forming the polymer P1). The at least one anionic monomer (a) and (a ') and the at least one nonionic hydrophobic monomer (b) and (b') may represent more than 83% by weight, in particular between 83% and 99.3% by weight. of the overall composition of the multiphasic polymer of the invention. By "overall composition" is meant the total weight of the monomers used for the synthesis of the multiphasic polymer.
    [0017] Preferably, the weight ratio non-ionic hydrophobic monomers (b ') / anionic monomers (a') of the composition of the polymer P2 is between 60/40 and 85/15, in particular between 65/35 and 80/20.
    [0018] According to one particular embodiment, the weight ratio of nonionic hydrophobic monomers (b) / anionic monomers (a) of the composition of polymer P1 is between 53/47 and 70/30, in particular between 55/45 and 68/32. . According to one particular embodiment, the multiphasic polymer according to the invention is such that: the anionic monomers (a) and (a ') polymers P1 and P2 are chosen from acrylic acid and / or methacrylic acid and or one of their salts, in particular the monomer (a) and the monomer (a ') are methacrylic acid and the nonionic hydrophobic monomers (b) and (b') polymers P1 and P2 are chosen among ethyl acrylate, butyl acrylate, ethyl methacrylate or mixtures thereof, in particular monomer (b) and monomer (b ') are ethyl acrylate. Crosslinking Monomer The polymer P1 and the polymer P2 of the multiphasic polymer according to the invention are partially or completely crosslinked. The compositions of the polymer P1 and the polymer P2 thus both further comprise one or more crosslinking monomers. According to a particular embodiment, the multiphasic polymer according to the invention comprises a single crosslinking monomer. According to another embodiment, it comprises two different crosslinking monomers. The crosslinking monomer (s) is (are) used to generate a polymer in the form of a three-dimensional network.
    [0019] According to the present invention, a monomer which is a polyunsaturated compound is used as the crosslinking monomer. This compound may comprise two, three or more ethylenic unsaturations. The crosslinking monomer may have a hydrophilic, hydrophobic or amphiphilic character.
    [0020] Examples of these compounds include di (meth) acrylate compounds such as polyalkylene glycol di (meth) acrylate, especially polypropylene glycol di (meth) acrylate, ethylene glycol di (meth) acrylate, di (meth) ) polyethylene glycol acrylate, triethylene glycol di (meth) acrylate, 1,3-butylene glycol di (meth) acrylate, 1,6-butylene glycol di (meth) acrylate, di (meth) acrylate 1,6-hexanediol, neopentyl glycol di (meth) acrylate, 1,9-nonanediol di (meth) acrylate, but also 2,2'-bis (4- (acryloxypropyloxyphenyl) propane, 2,2'-bis (4- (acryloxydiethoxy-phenyl) propane and zinc acrylate, tri (meth) acrylate compounds such as trimethylolpropane tri (meth) acrylate, tri (meth) acrylate trimethylolethane, tri pentaerythritol (meth) acrylate and tetramethylolmethane tri (meth) acrylate; tetra (meth) acrylate compounds such as ditrimethylolpropane tetra (meth) acrylate, tetra (met) h) tetramethylolmethane acrylate and pentaerythritol tetra (meth) acrylate; hexa (meth) acrylate compounds such as dipentaerythritol hexa (meth) acrylate; penta (meth) acrylate compounds such as dipentaerythritol penta (meth) acrylate; allyl compounds such as any '(meth) acrylate, diallylphthalate, diallyl itaconate, diallyl fumarate and diallyl maleate; polyallyl sucrose ethers having 2 to 8 groups per molecule, polyallyl pentaerythritol ethers such as pentaerythritol diallyl ether, pentaerythritol triallyl ether and pentaerythritol tetraallyl ether; polyallyl ethers of trimethylolpropane such as diallyl trimethylolpropane ether and triallyl trimethylolpropane ether. Other polyunsaturated compounds include divinyl glycol, divinyl benzene, divinylcyclohexyl and methylenebisacrylamide. In another aspect, the crosslinking monomers may be prepared by an esterification reaction of a polyol with an unsaturated anhydride such as maleic anhydride or itaconic anhydride or by an addition reaction with an isocyanate such as 3 isopropenyl-dimethylbenzene isocyanate. The following compounds can also be used to obtain crosslinking monomers: polyhaloalkanols such as 1,3-dichloroisoprop anol and 1,3-dibromois oprop anol haloepoxyalkanes such as epichlorohydrin, epibromohydrin, 2-methyl epichlorohydrin and epiiodohydrin; polyglycidyl ethers such as 1,4-butanediol diglycidyl ether, glycerin-1,3-diglycidyl ether, ethylene glycol diglycidyl ether, propylene glycol diglycidyl ether, diethylene glycol diglycidyl ether, neopentyl glycol diglycidyl ether, polypropylene glycol diglycidyl ether, bisphenol A- epichlorohydrin epoxy resin and mixtures.
    [0021] According to a particular embodiment, the crosslinking monomers used in the polymer P1 and in the polymer P2 are chosen from trifunctional crosslinking agents. It may be in particular trimethylolpropane triacrylate (TMPTA). The content of monomer (s) crosslinking (s) (c) in the composition of the polymer P 1 can be more particularly greater than or equal to 0.3% by weight, relative to the total weight of the monomers forming the polymer P 1, in particular higher or equal to 0.4% by weight and preferably between 0.4% and 5% by weight. The content of monomer (s) crosslinking (s) (c ') in the composition of the polymer P2 may be more particularly greater than or equal to 0.2% by weight, relative to the total weight of the monomers forming the polymer P2, in particular greater than or equal to 0.3% and especially between 0.3% and 5% by weight. The one or more crosslinking monomers (c) and (c ') may represent from 0.2% to 5% by weight, in particular from 0.3% to 5% by weight, of the total weight of monomers forming the multiphasic polymer of the 'invention.
    [0022] Associative Monomer The associative monomers having a polymerizable vinyl function and a hydrophobic hydrocarbon chain are preferably chosen from oxyalkylated monomers. They may be more particularly chosen from the following monomers of formula (I): ## STR3 ## in which: T represents an end allowing the copolymerization of the associative monomer, - RE0 ) (P0) (B0) 1 represents a polyalkoxylated chain consisting of alkoxylated units, divided into blocks, alternating or random, chosen from ethoxylated units EO, propoxylated units PO and butoxylated units BO, - n, n ', n "represent, independently of each other, 0 or an integer ranging from 150 to -Z represents a fatty chain, linear or branched, of at least 12 carbon atoms and optionally comprising one or more cyclic groups of 5 to 7-membered, saturated, partially unsaturated or aromatic, said groups may be optionally substituted.
    [0023] Equivalently, the associative monomer may be represented according to the following formula (II): TAZ (II) in which: - T represents an end allowing the copolymerization of the associative monomer, - A represents a polymeric chain consisting of: - m units of alkylene oxide of formula -CH 2 CHR 10 - with R 1 representing an alkyl group comprising from 1 to 4 carbons, for example a methyl or ethyl group, and m ranging from 0 to 150, - p alkylene oxide units of formula -CH2CHR20- with R2 representing an alkyl group comprising 1 to 4 carbons, for example a methyl or ethyl group, and p ranging from 0 to 150, n-ethylene oxide units with n ranging from 0 to 150, or from 10, or 15, to 150, or from 10, or 15, to 100, or from 15 to 50, or from 15 to 30, wherein m + n + p> 0 and wherein the alkylene oxide units of the formula -CH2CHR10-, the alkylene oxide units of formula -CH2CHR20- and the ethylene oxide units are in blocks, alternated or statistics and - Z is as defined above.
    [0024] By "propoxylated units PO" and "butoxylated units BO" is meant ethoxylated units bearing on one or other of their carbons, a methyl or ethyl radical respectively. An ethoxylated unit is a -CH2-CH2-0 unit. By "fatty chain" is meant an aliphatic hydrocarbon chain of a linear or branched fatty acid comprising at least 12 carbon atoms, or from 12 to 36 carbon atoms, or from 12 to 32 carbon atoms. The Z chain may comprise, for example, from 2 to 10 aromatic cyclic groups. According to a particular embodiment, the fatty chain Z may comprise one or more phenol group (s) bearing (s) one or more styryl groups, such as, for example, distyrylphenol, tristyrylphenol and / or pentastyrylcumylphenol groups.
    [0025] Preferably, the Z chain is a branched chain containing 16 carbon atoms. The end T is more particularly a radical containing a polymerizable unsaturated functional group belonging to the group of acrylic, methacrylic, maleic, itaconic or crotonic esters. The end T may in particular be chosen from acrylate, methacrylate, allylic, vinyl, methacrylurethane and alpha, alpha-dimethyl-m-isopropenyl benzyl urethane groups. According to a particular embodiment, the associative monomer corresponds to formula (III): ## STR2 ## in which: R 1 represents H or CH 3 and - n, n ', n "and Z have the same definition as in formula (I) above.
    [0026] Equivalently, the associative monomer has the following formula (IV): CH 2 = C (R 1) -000-AZ (IV) in which: - R 1 represents H or CH 3 and - A and Z have the same definition as in formula (II) above.
    [0027] According to a particular embodiment, n 'and n "in formula (I) or (III) above are zero, and n preferably varies from 15 to 150, in particular from 15 to 50 and in particular from 15 to 30. A in formulas (II) and (IV) above represents a polymer chain consisting of from 15 to 150, in particular from 15 to 50 and in particular from 15 to 30 ethylene oxide units. the associative monomer may have the formula (III) wherein n 'and n "are nil, n is 25, R1 is CH3, Z is a branched chain having 16 carbon atoms. As indicated above, the at least one associative monomer may be present only in the polymer P1. Alternatively, the at least one associative monomer may be present in both the polymer P1 and in the polymer P2 of the multiphasic polymer of the invention.
    [0028] The at least one associative monomer (d) and optionally (d ') may represent at least 0.5% by weight of the overall composition of the multiphasic polymer of the invention. By "overall composition" is meant the total weight of the monomers used for the synthesis of the multiphasic polymer. In particular, the at least one associative monomer (d) may be used in a proportion of at least 0.5% by weight, in particular from 0.5% to 12% by weight, relative to the total weight of monomers forming the polymer Pl.
    [0029] Additional Nonionic Monomers The polymers P1 and P2 may comprise one or more additional nonionic monomers (e) and / or (e '). These additional nonionic monomers (e) and (e ') may be more particularly chosen from: - 2-acrylamido-2-methylpropanesulphonic acid (AMPS), - unsaturated telomers of acrylic acid, - the monomers of in which: Ra, Rb and 12, independently of one another, are H or CH3, n is an integer of 1 or 2 and the monomers of formula (II) e2): (e2) in which: - Ra ', Rb', and Rd 'represent, independently of one another, H or CH3, - X represents (C = O) or (CH2), with r = 0, 1 or 2, - (AO) represents a polyalkoxylated chain consisting of alkoxylated units, divided into blocks, alternating or random, chosen from the ethoxylated units E0, the propoxylated units PO, and the butoxylated units BO and -q represents 0 or a number integer ranging from 1 to 150.
    [0030] In particular, the additional monomers of formula (el) may be chosen from allyl alcohol (n = 1), methallylic alcohol (n = 1) and isoprenol (n = 2). Advantageously, the optional monomer is isoprenol. By "unsaturated telomers of acrylic acid" is meant oligomers of acrylic acid or acryloxypropionic acid, of formula (V): ## STR2 ## = CH-C-n (V) where n is an integer ranging from 1 to 10. These different oligomers can be in a mixture. When n = 1, the oligomer is a dimer of acrylic acid. It is understood that the various particular modes described for each of the anionic, hydrophobic nonionic, crosslinking and associative monomers of the multiphasic polymer according to the invention can be combined. The additional nonionic monomer (s) and (e ') may represent less than 50% by weight of the overall composition of the multiphasic polymer of the invention, in particular less than 40% by weight and more particularly from 1% to 30% by weight.
    [0031] According to a particularly preferred embodiment, the multiphasic polymer according to the invention is formed: (1) of a polymer P 1 obtained by polymerization from a monomer mixture comprising, if not being formed: from 30% to 43% by weight of at least one anionic monomer (a) having a polymerizable vinyl function, - from 50% to 65% by weight of at least one nonionic hydrophobic monomer (b) having a polymerizable vinyl function, - 0.4 % to 5% by weight of at least one monomer (c) crosslinking, - at least 0.5% by weight of at least one associative monomer (d) having a polymerizable vinyl function and a hydrophobic hydrocarbon chain and optionally at least one additional nonionic monomer (e), distinct from the monomer (b) and (2), of a polymer P2 obtained by polymerization from a monomer mixture comprising, or even being formed: - by 20% at 43% by weight of at least one anionic monomer (a ') having a polymerizable vinyl function, - from 60% to 75% by weight of at least one nonionic hydrophobic monomer (b ') having a polymerizable vinyl function, - from 0.3% to 5% by weight of at least one monomer (c ') crosslinking, - optionally at least one associative monomer (d') having a polymerizable vinyl function and a hydrophobic hydrocarbon chain and - optionally at least one additional nonionic monomer (e), distinct from the monomer ( b ').
    [0032] According to a particular embodiment, the multiphasic polymer according to the invention is obtained from at least the following monomers: one or more anionic monomers chosen from acrylic acid and / or methacrylic acid and / or one of their salts, in particular methacrylic acid, one or more nonionic hydrophobic monomers chosen from ethyl acrylate, butyl acrylate, ethyl methacrylate or their mixtures, in particular the acrylate, ethyl, - one or more crosslinking monomers, in particular as defined above and more particularly trimethylolpropane triacrylate, - one or more associative monomers of formula (II) or (III) above, in particular of formula (IV) or ( V) above, and more particularly as described above and optionally one or more additional nonionic monomers as defined above.
    [0033] Preparation of the Multiphase Polymer According to the Invention The multiphase polymers according to the invention can be prepared sequentially by a radical polymerization process in emulsion, dispersion or solution.
    [0034] Preferably, they are prepared by radical polymerization in at least two stages, the polymer P1 and the polymer P2 being produced in two sequential emulsion polymerization stages, in particular in this order P1 then P2. The polymerization is carried out in suitable solvents, in the presence of known initiators. By way of example, the polymerization initiator may be a persulfate salt, such as ammonium persulfate. The radical emulsion polymerization may advantageously be carried out in the presence of at least one surfactant and optionally at least one chain transfer agent, making it possible to regulate the molecular mass of the chains produced during the polymerization. Surfactants which may be used include anionic surfactants, such as a fatty acid salt, an alkyl sulphate salt (such as sodium lauryl sulphate), an alkyl ether sulphate salt (such as sodium lauryl ether sulphate). ), an alkylbenzenesulfate salt (such as sodium dodecylbenzenesulfonate), an alkyl phosphate salt or a diester sulfosuccinate salt or nonionic surfactants, such as a polyoxyethylene alkyl ether or a polyoxyethylene fatty acid ester, cationic surfactants such as halides quaternary alkyl- and / or arylammoniums, zwitterionic or amphoteric surfactants, such as surfactants comprising a betaine group.
    [0035] As chain transfer agents, there may be mentioned, advantageously, mercaptan compounds comprising at least four carbon atoms, such as butyl mercaptan, n-octyl mercaptan, n-dodecyl mercaptan, tert-dodecyl mercaptan. The emulsion polymerization is conventionally carried out in an aqueous dispersion medium.
    [0036] Thus, the invention more particularly relates to a process for preparing a multiphase polymer according to the invention, comprising at least the following consecutive steps: (i) polymerization of the polymer P1 from a first monomer mixture comprising: at least one anionic monomer (a) having a polymerizable vinyl function, at least one nonionic hydrophobic monomer (b) having a polymerizable vinyl function, at least one crosslinking monomer, at least one associative monomer having a polymerizable vinyl function and a hydrophobic hydrocarbon chain and - optionally at least one additional nonionic monomer (e), distinct from the monomer (b) and (ii) polymerization in the presence of the previously obtained polymer P1 of a second monomer mixture comprising: at least one anionic monomer (a ') having a polymerizable vinyl function; at least one nonionic hydrophobic monomer (b') e having a polymerizable vinyl function, - at least one crosslinking monomer (c '), - optionally an associative monomer (d') having a polymerizable vinyl function and a hydrophobic hydrocarbon chain and - optionally an additional nonionic monomer (e '), distinct from the monomer (b '). From a practical point of view, the first step consists in contacting the monomers intended to enter the composition of the polymer P1 with a polymerization initiator, this contacting being able to be carried out in batch mode (or batch mode) or in semi-continuous mode (the contacting being performed over a period of time ranging from several minutes to several hours). From a practical point of view, the second step (step of producing the polymer P2) can proceed as follows: a step of adding the monomers intended to enter the composition of the polymer P2 to a dispersion medium comprising the polymer P1 already formed, this addition being able to be done in a discontinuous or semi-continuous mode (the bringing into contact being carried out over a period ranging from several minutes to several hours) and - simultaneously for the semi-continuous mode or after this adding step for the batch mode, a step of introducing a polymerization initiator.
    [0037] Applications The multiphasic polymers according to the invention are particularly effective as rheology modifiers in a wide range of aqueous compositions, particularly surfactant-containing washing compositions, such as care compositions or maintenance compositions. The term "care compositions" includes, for example, cosmetic, personal hygiene, toiletry and cleaning compositions for application to the body (including skin, hair, nails) of humans or animals. , for example shampoo compositions. The term "maintenance compositions" includes compositions used for cleaning or maintaining sanitary conditions, for example in the kitchen, bathroom, detergent products, laundry products, etc. The invention thus relates, according to yet another of its aspects, an aqueous composition comprising at least one multiphasic polymer according to the invention or as obtained according to the method described above. The multiphasic polymer according to the invention may be used in the aqueous composition in a proportion of 0.1 to 20% by weight, in particular from 0.5 to 12% by weight, relative to the total weight of the composition.
    [0038] As illustrated in the following examples, the polymer according to the invention advantageously combines performance in terms of thickening effect, clarity and suspensive properties. In other words, it makes it possible to obtain an aqueous composition having the desired viscosity and comprising a clear continuous phase and particles in suspension distributed homogeneously in the continuous phase.
    [0039] The invention thus relates more particularly to the use of a multiphase polymer according to the invention in an aqueous composition as a thickening and suspending agent. It also relates to the use for the preparation of a stable aqueous composition, comprising a clear continuous phase and particles in suspension distributed in the continuous phase, preferably having a pH of less than or equal to 6, of a multiphasic polymer such as previously defined. The invention also relates to an agent for obtaining a stable aqueous composition, comprising a clear continuous phase and suspended particles distributed in the continuous phase, in particular of a pH of less than or equal to 6, comprising a multiphasic polymer according to the invention. 'invention. In addition to the clarity it provides, the agent of the invention thus allows to maintain in suspension the particles present in the composition. The use of a composition thus formulated therefore requires no mixing step, even if the composition has been stored for several weeks or even several months.
    [0040] A composition according to the invention may comprise ingredients conventionally used in the formulations mentioned above. It may comprise one or more active ingredients (or active agents), in any form whatsoever, and whatever the field of application of the composition, as indicated above. The active ingredient (s) may be dissolved in the continuous phase of the composition and / or they may be in particulate form, not soluble in the continuous phase, and constitute all or part of the particles in suspension. It may comprise one or more surfactants, in particular chosen from anionic, zwitterionic or amphoteric surfactants, cationic or nonionic surfactants, and mixtures thereof. The invention relates more particularly to an aqueous cosmetic composition, comprising a continuous phase and particles suspended in the continuous phase, said continuous phase and / or said particles comprising and / or consisting of a cosmetic active ingredient, said composition comprising a multiphasic polymer as defined above. As a principle (s) active (s), it may include a washing base for the body and / or hair. Advantageously, the rheology modifying agent according to the invention makes it possible to obtain the properties of viscosity, clarity and suspensive effect desired for a wide pH range, especially when it is formulated in compositions having a high pH range. pH less than or equal to 6, in particular less than or equal to 5.5, in particular less than or equal to 5, in particular between 4 and 5. Such pHs are close to the average pH value of human skin. The rheology modifying agent according to the invention thus has a major interest in cosmetics. The invention will now be described by means of the following examples, given of course by way of illustration and not limitation of the invention.
    [0041] EXAMPLES The following abbreviations are used: AMA: (meth) acrylic acid.
    [0042] AE: ethyl acrylate. MA: associative monomer of formula (IV) in which n 'and n "are zero, n is 25, R1 is CH3, Z is a branched chain containing 16 carbon atoms TMPTA: trimethylolpropane triacrylate.
    [0043] Synthesis of Multiphasic Polymers The protocol for the synthesis of the multiphasic polymer denoted "Po1.1" of Example 1 is as follows: It is introduced into a 1 L reactor, stirred and heated with the aid of an oil bath, 430 g of water and 4.65 g of sodium lauryl ether sulphate (Texapon NSO at 28%).
    [0044] The premix comprising the monomers corresponding to the polymer P1 is prepared in a beaker. It contains 141.0 g of water, 4.9 g of 28% Texapon NSO, 82.5 g of AMA, 131.7 g. of EA, 19.3 g of MA and 2.1 g of TMPTA. In a second beaker is prepared the premix comprising the monomers corresponding to the polymer P2. It contains 43.4 g of water, 1.5 g of 28% Texapon NSO, 26.9 g of AMA, 54.8 g of AE, 6.0 g of MA and 0.7 g of TMPTA . The polymerization initiator solution is prepared in a third beaker. It contains 0.587 g of ammonium persulfate and 55 g of water. The polymerization initiator solution is injected into the reactor maintained at 86 ± 2 ° C. in parallel for 2 hours and the monomer pre-mixture corresponding to the polymer P1 for 1 hour and 30 minutes followed by the pre-mixing of monomers corresponding to polymer P2 for 30 minutes. This polymerization step is followed by the injection over 1 hour of a mixture containing 0.1 g of ammonium persulfate and 35 g of water. The whole is then cooled to room temperature.
    [0045] The set of multiphase polymers presented in the following examples were synthesized under the conditions described above, by varying the monomer compositions and the injection times of the monomer premixes.
    [0046] The composition of the polymer P1 (respectively polymer P2) is indicated in percentage by weight of each of the monomers relative to the total weight of the monomers of P1 (respectively P2).
    [0047] Evaluation in an aqueous formulation The polymers are tested in an aqueous formulation, of composition indicated in the following Table 1 (2% or 2.4% by weight of multiphasic polymer relative to the total weight of the composition). Compounds Amount (% by weight) Sodium lauryl ether sulfate 9 Cocamidopropylbetaine 3 Polymer tested 2 or 2.4 water Qs 100 Table 1 The pH of the formulation is adjusted to a value of 4, 5 or 6 by adding lactic acid or of sodium hydroxide. Properties evaluated The compositions are evaluated for their properties of clarity, viscosity and suspensive performance. Clarity The clarity of the composition is evaluated by measurement of the transmittance according to the following protocol: The measurements are carried out on a Genesys UV UV Spectrometer UV (Cole Parmer), equipped with Rotilabo-Einmal Kuvetten PS vats, 4.5 ml. Conveniently, the apparatus is preheated 10 minutes before use. A first measurement is made by means of a tank filled with 3.8 ml of bipermuted water (the "white"). The measurement is then carried out with a vat filled with 3.8 ml of the cosmetic composition solution to be tested. The transmittance is then measured at the wavelength of 500 nm. The higher the transmittance value, expressed in%, the higher the cosmetic composition is clear. As indicated previously, it is estimated that at a transmittance value at 500 nm of at least 60%, the composition is clear.
    [0048] Viscosity The viscosity of said formulations is measured using a Brookfield viscometer, model LVT. Before measuring the viscosity, each of the formulations is allowed to stand for 24 hours at 25.degree. The mobile must be centered with respect to the opening of the bottle.
    [0049] The viscosity is then measured at 6 rpm using the appropriate module. The viscometer is allowed to rotate until the viscosity is stable. The rheology modifier must provide sufficient viscosity to the formulation in which it is used. In general, the desired viscosity for the thickened formulations is greater than 2000 mPa.s, in particular greater than 3000 mPa.s and more particularly greater than 4000 mPa.s. Suspensive performance Suspensive performance is evaluated by observation of the stability of polyethylene balls of 800 μm diameter, in the cosmetic formulation after storage in an oven at 45 ° C. As soon as a particle displacement is noted, the test is stopped. The results are noted as follows: Stability time Suspension note Up to 7 days 1 Up to 30 days 2 Up to 60 days 3 Up to 75 days 4 Over 90 days 5 Suspensive performance of the formulation are satisfactory for a stability period of at least 75 days, ie a suspension score> 4.
    [0050] EXAMPLE 1 Influence of the presence of the crosslinking monomer in the polymer P1 and in the polymer P2 Polymer tested Pol. 1 Cl (outside the invention) Composition Pl AE 55.92 56.42 AMA 35.00 35.31 MA 8.19 8.26 TMPTA 0.89 0.00 Composition AE 62.01 62.01 P2 AMA 30.50 30 , 50 MA 6.76 6.76 TMPTA 0.74 0.74 Overall composition AE 57.58 57.95 AMA 33.77 33.99 MA 7.80 7.85 TMPTA 0.85 0.20 Proportion Pl 72, 74 72.56 Proportion P2 27.26 27.44 2.4% active, pH = 5 Visco Brook 17400 12600 (mPa $) Note of 5 3 suspension T (500nm) (%) 87 93 Table 2 Polymer tested Pol. 2 C2 (outside the invention) Composition Pl AE 55.92 55.92 AMA 35.00 35.00 MA 8.19 8.19 TMPTA 0.89 0.89 Composition AE 62.01 62.47 P2 AMA 30.50 30 , 72 MA 6.76 6.81 TMPTA 0.74 0.00 Overall composition AE 57.58 57.69 AMA 33.77 33.84 MA 7.80 7.82 TMPTA 0.85 0.65 Proportion Pl 72, 74 72.88 Proportion P2 27.26 27.12 Visco Brook at 2% active pH = 4 8400 7100 (mPa. $) PH = 5 7400 6500 pH = 6 5800 4900 Suspension note pH = 4 5 3 at 2% active pH = 5 5 2 pH = 6 4 2 T (500nm) pH = 4881 to 2% active (%) pH = 5 84 85 pH = 6 91 90 Table 3 The results presented in Tables 2 and 3 show that the presence crosslinking monomer in both the polymer P1 and the polymer P2 provides improved viscosity and suspensivative properties, while maintaining the desired clarity properties.
    [0051] EXAMPLE 2 Influence of the presence of the associative monomer in the multiphasic polymer Polymer tested Pol. 2 C3 (excluding Pol 3 Pol 4 C4 (outside the invention) invention) Composition Pl AE 55.92 60.91 55.92 54.53 66.58 AMA 35.00 38.12 35.00 34.14 32, 36 MA 8.19 0.00 8.19 10.46 0.00 TMPTA 0.89 0.97 0.89 0.87 1.06 Composition P2 AE 62.01 63.30 66.50 66.50 43 44 AMA 30.50 35.95 32.71 32.71 35.99 MA 6.76 0.00 0.00 0.00 20.05 TMPTA 0.74 0.75 0.79 0.79 0.52 Composition Total AE 57.58 61.59 58.66 57.57 57.58 AMA 33.77 37.50 34.41 33.77 33.77 MA 7.80 0.00 6.07 7.80 7.80 TMPTA 0.85 0.91 0.86 0.85 0.85 Proportion P1 72.74 71.44 74.11 74.58 61.09 Proportion P2 27.26 28.56 25.90 25.42 38.91 Visco Brook pH = 4 8400 2800 7300 7200 12200 at 2% active (mPa. $) - 5 7400 7400 2400 6100 6200 10800 pH rating = 4 5 1 4 4 1 suspension at 2% active P ". =" '4 1 4 4 1 T (500nm) at pH = 4 82 85 82 81 93 2% active (%) pH = 5 84 85 83 81 94 Table 4 The results presented in Table 4 show that the absence of associative monomer in the Polymer P1 does not provide access to good suspending performance. On the other hand, the presence of associative monomer according to the invention in the polymer P1, and possibly also in the polymer P 2, of the multiphase polymer, leads to good properties both in terms of viscosity, transmittance and suspensive performance.
    [0052] EXAMPLE 3 Influence of the Multiphase Structure According to the Invention The C5 polymer was synthesized by simple radical polymerization in emulsion (non-sequential process). Polymer tested Pol. 5 C5 (outside the invention) Composition P AE 55.92 60.44 AMA 35.00 30.91 MA 8.18 7.80 TMPTA 0.89 0.85 Composition P2 AE 72.50 AMA 20.00 MA 6.76 TMPTA 0.74 Overall composition AE 60.44 60.44 AMA 30.91 30.91 MA 7.80 7.80 TMPTA 0.85 0.85 Proportion P1 72.74 100.00 Proportion P2 27.26 0.00 2.4% active, pH = 5 Visco Brook (mPa. $) 9400 11100 Suspension note 5 3 T (500 nm) (%) 84 92 Table 5 These results show that the implementation of a polymer with a multiphasic structure according to the invention, compared to a single polymer, provides access to improved suspensive performance of the formulation, while maintaining satisfactory viscosity and transmittance properties.
    [0053] EXAMPLE 4 Influence of the Pol / Polymer Polymer Polymer Ratio Tested Pol.
    [0054] 6 Pol 7 C6 (outside the invention) Composition AE 55.92 55.92 55.92 Pl AMA 35.00 35.00 35.00 MA 8.19 8.19 8.19 TMPTA 0.89 0.89 0.89 Composition P2 AE 62,01 62,01 62,01 AMA 30,50 30,49 30,50 MA 6.76 6.76 6.77 TMPTA 0.74 0.74 0.7 Overall composition AE 57.58 58, 17 60.46 AMA 33.77 33.33 31.64 MA 7.80 7.66 7.12 TMPTA 0.85 0.83 0.78 Proportion P1 72.74 62.98 25.32 Proportion P2 27.26 37.02 74.68 Visco Brook pH = 4 9300 8500 7600 at 2% active (mPa. $) PH = 5 8000 7200 6300 pH rating = 4 5 5 3 suspension at 2% active pH = 5 5 5 3 T ( 500nm) at pH = 84 84 87 2% active (%) pH = 5 83 84 87 Table 6
    权利要求:
    Claims (21)
    [0001]
    REVENDICATIONS1. A multiphasic polymer comprising from 45% to 95% by weight of a first polymer P1 and from 5% to 55% by weight of a second polymer P2, said polymers P1 and P2 being of different compositions, (1) said polymer P1 being obtained by polymerization from a monomer mixture comprising: at least one anionic monomer (a) having a polymerizable vinyl function, at least one nonionic hydrophobic monomer (b) having a polymerizable vinyl function, at least one monomer (c) crosslinker, - at least one associative monomer (d) having a polymerizable vinyl function and a hydrophobic hydrocarbon chain and - optionally at least one additional nonionic monomer (e), distinct from the monomer (b) and (2) said polymer P2 being obtained by polymerization from a monomer mixture comprising: at least one anionic monomer (a ') having a polymerizable vinyl function, at least one monomer (b') hydrophobic nonionic polymer having a polymerizable vinyl function, - at least one crosslinking monomer (c '), - optionally at least one associative monomer (d') having a polymerizable vinyl function and a hydrophobic hydrocarbon chain and - optionally at least one monomer (e) ') additional nonionic, distinct from the monomer (b').
    [0002]
    2. Polymer according to the preceding claim, wherein the weight ratio polymer P1 / polymer P2 is between 45/55 and 95/5, in particular between 60/40 and 95/5.
    [0003]
    3. Polymer according to any one of the preceding claims, wherein said anionic monomer or monomers are selected from acrylic acid monomers and / or methacrylic acid and / or a salt thereof.
    [0004]
    Polymer according to any one of the preceding claims, wherein said anionic monomer (s) (a) represents from 20% to 53% by weight, in particular from 25% to 48% by weight, and more particularly from 30% to 30% by weight. 43% by weight, based on the total weight of monomers forming the polymer P1.
    [0005]
    Polymer according to any one of the preceding claims, in which the said anionic monomer (s) (a ') represent from 10% to 53% by weight, in particular from 15% to 48% by weight, and more particularly of 20%. to 43% by weight, based on the total weight of monomers forming the polymer P2.
    [0006]
    6. Polymer according to any one of the preceding claims, wherein said one or more nonionic hydrophobic monomers are chosen from C1-C8 alkyl acrylates or C1-C8 alkyl methacrylates, such as methyl, ethyl acrylate, butyl acrylate, 2-ethylhexyl acrylate, methyl methacrylate, ethyl methacrylate, butyl methacrylate, and mixtures thereof.
    [0007]
    Polymer according to any one of the preceding claims, wherein said one or more nonionic hydrophobic monomers (b) represent from 40% to 75% by weight, in particular from 45% to 70% by weight, and more particularly from 50% to 50% by weight. % to 65% by weight, based on the total weight of monomers forming the polymer P1.
    [0008]
    Polymer according to any one of the preceding claims, wherein the one or more nonionic hydrophobic monomers (b ') represent from 50% to 85% by weight, in particular from 55% to 80% by weight and more particularly 60% by weight. % to 75% by weight, based on the total weight of monomers forming the polymer P2.
    [0009]
    9. Polymer according to any one of the preceding claims, in which the weight ratio of nonionic hydrophobic monomers (b ') / anionic monomers (a') of the composition of the polymer P2 is between 60/40 and 85/15, in particular between 65/35 and 80/20. 30
    [0010]
    10. Polymer according to any one of the preceding claims, wherein said one or more crosslinking monomers are chosen from trifunctional crosslinking agents, in particular trimethylolpropane triacrylate.
    [0011]
    11. Polymer according to any one of the preceding claims, wherein the content of monomer (s) crosslinking (s) (c) in the composition of the polymer P1 is greater than or equal to 0.3% by weight, relative to the weight total monomers forming the polymer P1, in particular greater than or equal to 0.4% by weight and preferably between 0.4% and 5% by weight.
    [0012]
    12. Polymer according to any one of the preceding claims, wherein the content of monomer (s) crosslinking (s) (c ') in the composition of the polymer P2 may be more particularly greater than or equal to 0.2% by weight, relative to the total weight of the monomers forming the polymer P2, in particular greater than or equal to 0.3% and in particular between 0.3% and 5% by weight.
    [0013]
    13. The polymer as claimed in any one of the preceding claims, in which the one or more associative monomers are chosen from the following monomers of formula (I): ## STR5 ## (P0) (B0) ',, I -Z (I) in which: T represents an end allowing the copolymerization of the associative monomer, - RE0) '(PO) (B0) 1 represents a polyalkoxylated chain consisting of alkoxylated units, divided into blocks, alternating or random, chosen from ethoxylated units EO, the propoxylated units PO and the butoxylated units BO, - n, n ', n "represent, independently of each other, 0 or an integer ranging from 1 to 150 and - Z represents a fatty chain, linear or branched, of at least 12 carbon atoms and optionally comprising one or more cyclic groups of 5 to 7 members, saturated, partially unsaturated or aromatic, said groups possibly being optionally substituted.
    [0014]
    14. The polymer as claimed in any one of the preceding claims, in which the at least one associative monomer is used in a proportion of at least 0.5% by weight, in particular from 0.5% to 12% by weight, by weight. relative to the total weight of monomers forming the polymer P1.
    [0015]
    15. Polymer according to any one of the preceding claims, in which the additional nonionic monomers (e) and (e ') are chosen from: 2-acrylamido-2-methylpropanesulphonic acid (AMPS), telomers unsaturated acrylic acid, - the monomers of formula (el): (e1) in which: Ra, Rb and 12 represent, independently of one another, H or CH3 and n is an integer equal to 1 or to 2 and - the monomers of formula (e2): (e2) in which: - Ra ', Rb ,, Rc, and Rd, represent, independently of one another, H or CH3, - X represents (C = 0) or (CH2), with r = 0, 1 or 2, - (AO) represents a polyalkoxylated chain consisting of alkoxylated units, divided into blocks, alternating or random, selected from the ethoxylated units EO, the propoxylated units PO, and the Butoxylated units BO and - q represents 0 or an integer ranging from 1 to 150.
    [0016]
    16. Polymer according to any one of the preceding claims, said polymer being formed: (1) a polymer P1 obtained by polymerization from a monomer mixture comprising or being formed: - from 30 to 43% by weight at least one anionic monomer (a) having a polymerizable vinyl function, - from 50 to 65% by weight of at least one nonionic hydrophobic monomer (b) having a polymerizable vinyl function, - from 0.4 to 5% by weight of at least one monomer (c) crosslinking, - at least 0.5% by weight of at least one associative monomer (d) having a polymerizable vinyl function and a hydrophobic hydrocarbon chain and - optionally at least one additional monomer (e) nonionic, distinct from the monomer (b) and (2) of a polymer P2 obtained by polymerization from a monomer mixture comprising, or being formed: - from 20 to 43% by weight of at least one anionic monomer (a ') having a function v polymerizable inylic, - from 60 to 75% by weight of at least one nonionic hydrophobic monomer (b ') having a polymerizable vinyl function, - from 0.3 to 5% by weight of at least one monomer (c') crosslinker, - optionally at least one associative monomer (d ') having a polymerizable vinyl function and a hydrophobic hydrocarbon chain and - optionally at least one additional nonionic monomer (e'), distinct from the monomer (b ').
    [0017]
    17. A process for preparing a multiphasic polymer as defined in any one of claims 1 to 16, comprising at least the following consecutive steps: (i) polymerization of the polymer P1 from a first monomer mixture comprising: at least one anionic monomer (a) having a polymerizable vinyl function; at least one nonionic hydrophobic monomer (b) having a polymerizable vinyl function; at least one crosslinking monomer; at least one monomer (d); associative having a polymerizable vinyl function and a hydrophobic hydrocarbon chain and - optionally at least one additional nonionic monomer (e), distinct from the monomer (b) and (ii) polymerization in the presence of the previously obtained polymer P1 of a second monomer mixture comprising: - at least one anionic monomer (a ') having a polymerizable vinyl function, - at least one nonionic hydrophobic monomer (b') having a polymerizable vinyl function, at least one crosslinking monomer, optionally an associative monomer having a polymerizable vinyl functional group and a hydrophobic hydrocarbon chain and optionally at least one nonionic monomer additional, distinct from the monomer (b ').
    [0018]
    18. An aqueous composition comprising at least one multiphasic polymer as defined in any one of claims 1 to 16 or as obtained according to the process of claim 17.
    [0019]
    19. Composition according to the preceding claim, said composition having a pH value of less than or equal to 6, in particular less than or equal to 5.5, and more particularly less than or equal to 5.
    [0020]
    20. Composition according to claim 18 or 19, comprising from 0.1% to 20% by weight, in particular from 0.5% to 12% by weight of polymer (s) multiphasic (s) relative to its total weight.
    [0021]
    21. Use of a multiphase polymer as defined in any one of claims 1 to 16 or as obtained according to the process of claim 17, as thickening and suspensing agent.
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    法律状态:
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    优先权:
    申请号 | 申请日 | 专利标题
    FR1463229A|FR3030307B1|2014-12-23|2014-12-23|MULTIPHASIC POLYMER AS A THICKENING AND SUSPENDING AGENT|FR1463229A| FR3030307B1|2014-12-23|2014-12-23|MULTIPHASIC POLYMER AS A THICKENING AND SUSPENDING AGENT|
    BR112017011278-7A| BR112017011278A2|2014-12-23|2015-10-30|multiphase polymer as a thickener and suspending agent|
    KR1020177015432A| KR20170098814A|2014-12-23|2015-10-30|Multiphase polymer as a thickening and suspending agent|
    US15/532,299| US10470994B2|2014-12-23|2015-10-30|Multiphasic polymer as a thickening and suspending agent|
    ES15800882T| ES2826375T3|2014-12-23|2015-10-30|Multiphase polymer as a thickening and suspending agent|
    JP2017526659A| JP6771460B2|2014-12-23|2015-10-30|Polyphasic polymer as a thickener and suspending agent|
    PCT/FR2015/052934| WO2016102790A1|2014-12-23|2015-10-30|Multiphase polymer as a thickening and suspending agent|
    CN201580067219.6A| CN107001536B|2014-12-23|2015-10-30|Heterophasic polymers as thickeners and suspending agents|
    MX2017006809A| MX2017006809A|2014-12-23|2015-10-30|Multiphase polymer as a thickening and suspending agent.|
    EP15800882.1A| EP3237470B1|2014-12-23|2015-10-30|Multiphase polymer as a thickening and suspending agent|
    CA2969945A| CA2969945A1|2014-12-23|2015-10-30|Multiphase polymer as a thickening and suspending agent|
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