A hair coloring process comprising the application of a treatment with an alkaline agent and a composition comprising a (poly)carbodiimide compound and a coloring agent

Abstract

The present invention relates to a hair coloring process comprising: (i) a step of treating the hair with a composition T comprising at least one alkaline agent selected from mineral alkaline agents, which are selected from alkali or alkaline-earth metal phosphates, mineral hydroxides, alkali or alkaline-earth metal silicates or metasilicates, hydroxylamine, ammonia and their mineral and / or organic salts; and organic alkaline agents and their mineral and / or organic salts, and mixtures thereof, and then (ii) a step of applying to the hair at least one coloring composition C comprising: (1) at least one (poly)carbodiimide compound; and (2) at least one coloring agent selected from pigments, direct dyes, and mixtures thereof.

Description

Description Title of the invention: Process for coloring hair comprising the application of a treatment with an alkaline agent and a composition comprising a (poly)carbodiimide compound and an agent dye

[0001] — The present invention relates to a method for coloring hair comprising the application of a treatment with a composition comprising at least one agent particular alkaline, then the application to the hair of a coloring composition C comprising a (poly)carbodiimide compound and a coloring agent. Technical field

[0002] In the field of coloring hair keratin fibers, it is already known to color hair keratin fibers using different techniques from direct dyes or pigments for non-permanent or pre-coloring dye sliders for permanent coloring.

[0003] There are essentially three types of hair coloring process:

[0004] a) so-called permanent coloring which has the function of bringing about a modification sensitive to natural color and which uses oxidation dyes which penetrate the hair fiber and form the dye through a condensation process oxidative;

[0005] b) non-permanent, semi-permanent or direct coloring, which does not put in implements the oxidative condensation process and withstands 4 or 5 shampoos; consists of dyeing keratin fibers with dye compositions containing direct dyes;

[0006] — c) temporary coloring which results in a modification of the natural color hair that lasts from one shampoo to the next and is used to enhance or correct a shade already obtained. It can also be likened to a “makeup” process.

[0007] — Another coloring method consists of using pigments. Indeed, the use of pigments on the surface of keratin fibers generally allows to obtain visible colorations on dark hair since the pigment on the surface masks the natural color of the fiber. However, the colors obtained by this coloring method have the disadvantage of having low resistance to shampoos as well as external agents such as sebum, perspiration, brushing and / or rubbing. The resulting colors may also be too selective, that is to say that the difference in coloration is too great along the same keratin fiber which is differently sensitized between its tip and its root.

[0008] There therefore remains a need to have a hair coloring process, which has the advantage of obtaining a homogeneous colored coating on the hair, while forming a coating that is resistant to shampoos and various aggressions that the hair may be subjected to such as brushing and / or rubbing, and which also has the advantage of leading to good dyeing properties, particularly in terms of selectivity. Thus, the aim of the present invention is to develop a hair coloring process which has the advantage of obtaining a homogeneous and smooth colored coating on the hair, while forming a coating which is resistant to shampooing and to various aggressions which the hair may be subjected to such as brushing and / or rubbing, and which also has the advantage of leading to good dyeing properties, in particular low selectivity. Statement of the invention The present invention therefore relates to a hair coloring process comprising: (i) a step consisting of treating the hair with a composition T comprising at least one alkaline agent chosen from mineral alkaline agents, which are chosen from alkali or alkaline-earth metal phosphates, mineral hydroxides, alkali or alkaline-earth metal silicates or metasilicates, hydroxylamine, ammonia and their mineral and / or organic salts; organic alkaline agents, their mineral and / or organic salts, and their mixtures, then (ii) a step consisting of applying to the hair at least one coloring composition C comprising: l. at least one (poly)carbodiimide compound; 2 at least one coloring agent chosen from pigments, direct dyes and their mixtures. Thanks to the hair coloring process according to the invention, colored coatings are obtained on the hair, making it possible to obtain a visible coloring on all types of hair, with little selectiveness, that is to say homogeneous along the fiber, and lasting after shampooing. Such a coating can be resistant to external aggressions that the hair may be subjected to, such as blow-drying and perspiration. The coloring process according to the invention makes it possible in particular to obtain a homogeneous coating. The expression "at least one" means one or more. Unless otherwise indicated, the limits of a domain of values ​​are included in this domain, notably in the expressions "between" and "ranging from ... to seen Di The invention is not limited to the examples illustrated. The characteristics of the different examples may in particular be combined within non-exhaustive variants. illustrated. For the purposes of the present invention and, unless otherwise indicated, - an “alkyl” radical designates a saturated linear or branched radical containing, for example, from 1 to 20 carbon atoms; - an “aminoalkyl” radical denotes an alkyl radical as defined above, said alkyl radical comprising an NH group; - an “Aydroxyalkyl” radical denotes an alkyl radical as defined above, said alkyl radical comprising an OH group; - an “alkylene” radical denotes a divalent saturated C1-C4 hydrocarbon group, linear or branched, such as methylene, ethylene, or propylene; - a “cycloalkyl” or “alicycloalkyl” radical denotes a mono- or polycyclic, preferably monocyclic, bicyclic or tricyclic, saturated cyclic hydrocarbon group comprising from 1 to 3 rings, preferably 2 rings, and comprising from 3 to 24 carbon atoms, in particular comprising from 3 to 20 carbon atoms, more particularly from 3 to 13 carbon atoms, even more particularly from 3 to 12 carbon atoms, preferably between 5 and 10 carbon atoms, such as cyclopropyl, cyclopentyl, cyclohexyl, cycloheptyl, or norbornyl, in particular cyclopropyl, cyclopentyl or cyclohexyl, it being understood that the cycloalkyl radical may be substituted by one or more (C,-C4)alkyl groups such as methyl, preferably the cycloalkyl radical is then an isobornyl group, - a “cycloalkylene” radical denotes a divalent cycloalkyl group with “cycloalkyl” as defined previously, preferably C4-C,; ; - an “aryl” radical is an unsaturated and aromatic hydrocarbon cyclic radical, comprising from 6 to 14 carbon atoms, preferably between 6 and 12 carbon atoms, mono / bi / or tri / cyclic, fused or not, preferably the aryl group comprises 1 cycle with 6 carbon atoms such as phenyl, naphthlyl, anthryl, phenanthryl and biphenyl, it being understood that the aryl radical may be substituted by one or more (C,-C,)alkyl groups such as methyl, preferably tolyl, xylyl, or methylnaphthyl, preferably the aryl group represents phenyl; - an “arylene” radical is a divalent aryl radical with “aryl” as defined above, preferably arylene represents phenylene; - a “heterocyclic” radical designates a mono- or polycyclic, saturated or unsaturated, non-aromatic or aromatic hydrocarbon radical, comprising one or more heteroatoms, preferably from 1 to 5 atoms chosen from O, S or N, comprising from 3 to 20 links, preferably between 5 and 10 links, such as imidazolyl, pyrrolyl and furanyl; - a “heterocycloalkylene” radical is a divalent heterocyclic group with “heterocyclic” as defined previously; - an “aryloxy” radical denotes an aryl-oxy radical with “aryl” as defined previously; - an “alkoxy” radical denotes an alkyl-oxy radical with “alkyl” as defined previously; - an “acyloxy” radical denotes an ester radical RC(O)-O- with R an alkyl group as defined previously; - a “reactive” group is a group capable of forming a covalent bond with another group, identical or different, by chemical reaction. Unless otherwise indicated, when compounds are mentioned in this application, their optical isomers, their geometric isomers, their tautomers, their salts, alone or in mixture, are also meant. By "keratin (hair) fibers" is meant hair. In other words, the expressions "keratin (hair) fibers" and "hair" are equivalent in the remainder of the description. For the purposes of the present invention, the term "hair" means the hair of the head. This term does not correspond to body hair, eyebrows, or eyelashes. Treatment with a particular alkaline agent The method according to the invention comprises a step consisting of treating the hair with a composition T comprising at least one alkaline agent chosen from mineral alkaline agents, which are chosen from alkali or alkaline-earth metal phosphates, mineral hydroxides, alkali or alkaline-earth metal silicates or metasilicates, hydroxylamine, ammonia and their mineral and / or organic salts; organic alkaline agents, their mineral and / or organic salts, and mixtures thereof. For the purposes of the present invention, alkali or alkaline earth metal carbonates such as sodium or potassium carbonate and alkali or alkaline earth metal bicarbonates such as sodium or potassium bicarbonate are not considered to be “organic alkaline agents”. Thus, the alkaline agent(s) according to the invention are not chosen from alkali or alkaline earth metal carbonates or alkali or alkaline earth metal bicarbonates. As indicated above, the alkaline agent(s) according to the invention may be chosen from mineral alkaline agents, which are chosen from alkali or alkaline earth metal phosphates, mineral hydroxides, alkali or alkaline earth metal silicates or metasilicates, hydroxylamine, ammonia and their mineral and / or organic salts, and mixtures thereof. The alkali or alkaline earth metal phosphates can be chosen from the lithium phosphates, sodium phosphates, potassium phosphates, magnesium phosphates, calcium phosphates, and mixtures thereof. Among the mineral hydroxides, mention may in particular be made of alkali metal hydroxides, alkaline earth metal hydroxides, transition metal hydroxides and mixtures thereof. More preferably, the alkaline agent may be chosen from sodium hydroxide, lithium hydroxide, calcium hydroxide, magnesium hydroxide, barium hydroxide, strontium hydroxide, manganese hydroxide, zinc hydroxide and mixtures thereof. Even more preferably, the alkaline agent is sodium hydroxide or calcium hydroxide. The silicates or metasilicates of alkali or alkaline earth metals may be chosen from sodium silicate, sodium disilicate, sodium metasilicate, and mixtures thereof. The alkaline agent(s) according to the invention may also be chosen from hydroxylamine and its mineral and / or organic salts. Inorganic salts of hydroxylamine include addition salts with hydrochloric acid, phosphoric acid, or sulfuric acid. Organic salts of hydroxylamine include addition salts with an organic acid such as acetic acid, formic acid, oxalic acid, tartaric acid, fumaric acid, maleic acid, succinic acid, or cinnamic acid. Preferably, the alkaline agent(s) may be chosen from sodium hydroxide, calcium hydroxide, hydroxylamine, mineral and / or organic salts of hydroxylamine, and mixtures thereof. More preferably, the alkaline agent(s) may be chosen from sodium hydroxide, calcium hydroxide, hydroxylamine, hydroxylamine hydrochloride, and mixtures thereof. Even more preferably, the alkaline agent(s) may be chosen from hydroxylamine, hydroxylamine hydrochloride, and mixtures thereof. And better, the alkaline agent can be hydroxylamine hydrochloride. The organic alkaline agent(s) according to the invention may be chosen from alkanolamines, organic amines other than said alkanolamines, oxyethylenated and / or oxypropylenated ethylenediamines, compounds of formula (IIT) below, and mixtures thereof. The organic alkaline agent(s) may be chosen from alkanolamines. By alkanolamine is meant an organic amine comprising a primary, secondary or tertiary amine function, and one or more linear or branched C; to C; alkyl groups carrying one or more hydroxyl radicals. Particularly suitable for carrying out the invention are organic amines chosen from alkanolamines such as mono-, di- or tri-alkanolamines, comprising one to three hydroxyalkyl radicals, identical or not, in C, to C4. In particular, the alkanolamine(s) are chosen from monethanolamine, diethanolamine, triethanolamine, monoisopropanolamine, diisopropanolamine, N,N-dimethylethanolamine, 2-amino-2-methyl-1-propanol, triisopropanolamine, 2-amino-2-methyl-1,3-propanediol, 3-amino-1,2-propanediol, 3-dimethylamino-1,2-propanediol, tris-hydroxymethylamino-methane and mixtures thereof. The organic amines may be aliphatic organic amines such as spermine, spermidine and 1,3-diaminopropane. The organic amines may also be chosen from heterocyclic organic amines. In particular, mention may be made of pyridine, piperidine, imidazole, triazole, tetrazole and benzimidazole. The organic amines may also be chosen from amino acid dipeptides. As amino acid dipeptides that may be used in the present invention, mention may be made in particular of carnosine, anserine and balenine. The organic amines may also be chosen from compounds comprising a guanidine function. As amines of this type other than arginine which may be used in the present invention, mention may in particular be made of creatine, creatinine, 1,1-dimethylguanidine, 1,1-diethylguanidine, glycocyamine, metformin, agmatine, n-amidinoalanine, 3-guanidinopropionic acid, 4-guanidinobutyric acid and 2-([amino(imino)methyl]amino)ethane-1-sulfonic acid). The organic alkaline agent(s) according to the invention may be chosen from oxyethylenated and / or oxypropylenated ethylenediamines. The organic alkaline agent(s) may also be chosen from urea and its derivatives, such as dimethylurea, N,N-dimethylpropyleneurea, or guanylurea. The organic alkaline agent(s) according to the invention may be chosen from the compounds of the following formula (III) as well as their salts: (D, {MH R5 R in which R1, R2, R3, R4, R5 represent, independently of each other: (i) a hydrogen atom or (ii) a linear or branched C1-C4 lower alkyl or alkenyl radical, optionally substituted by one or two radicals chosen from: hydroxyl, amino, dimethylamino, methoxy, ethoxy, carboxyl, carboxamide, N-methylcarboxamide or SO3H, when R1, R2 and R3 and R4 represent a hydrogen atom, R5 can also denote an amino radical; acetyl; chloroacetyl; carboxamide; methoxy; ethoxy; 1,2,4-triazolyl; cyclopentyl; methoxycarbonyl; ethoxycarbonyl; CO- CH=CH-COOH; phenyl optionally substituted by a chlorine atom or a hydroxyl radical; benzyl; thiazolidone; benzimidazole; benzoxazole; benzothiazole; or C(FNH)-NR6R7 in which R6 and R7 denote, independently of each other, a hydrogen atom or a linear or branched C1-C4 lower alkyl radical, optionally substituted by one or two radicals chosen from: hydroxyl, amino, dimethylamino, carboxyl or carboxamide; or N-methylcarboxamide; or a phenyl radical, when R1=R3=R5=H, R2 and R4 can also denote an amino radical, when R1=R2=R3=H, R4 and RS can also form, with the nitrogen atom which carries them, a pyrrolidine, piperidine, pyrazole or 1,2,4-triazole ring, said ring being optionally substituted by 1 or 2 radicals chosen from: hydroxyl, amino or carboxyl, when R1=R2=H, and R4=H or methyl, R3 and RS can also together form a 5-membered ring possibly containing an oxo group. Preferably, the compounds of formula (III) are chosen from: - guanidine; - aminoguanidine; - 1,3-diaminoguanidine; -- 1-methylguanidine; - 1,1-dimethylguanidine; - 1-ethylguanidine; - - N-(2-hydroxyethyl)guanidine; - N-(3-hydroxypropyl)guanidine; - biguanide; - N-methyl biguanide; - N-ethyl] biguanide; -1,1-dimethylbiguanide; - 1,1,3,3-tetramethylguanidine; - 2-tert-butyl-1,1,3,3-tetramethylguanidine; - L-arginine; - DL-arginine; - and their mixtures. More preferably, the compounds of formula (III) are chosen from guanidine, 1,3-diaminoguanidine, arginine (L-arginine and DL-arginine), and 1,1,3,3-tetramethylguanidine. The organic alkaline agent(s) according to the invention may also be chosen from mineral and / or organic salts of organic alkaline agents. In particular, mention may be made of alkali and alkaline-earth metal salts and mineral acid salts of alkanolamines, such as monoethanolamine hydrochloride, alkali and alkaline-earth metal salts and mineral acid salts of oxyethylenated and / or oxypropylenated ethylenediamines, organic acid salts of urea or its derivatives, such as guanylurea phosphate, alkali metal salts of compounds of formula (III), mineral acid salts of compounds of formula (II), in particular hydrochloric acid salts, phosphoric acid salts, sulfuric acid salts, organic acid salts of compounds of formula (II), and hydroxides, carbonates and bicarbonates of compounds of formula (II), such as for example: - guanidine hydrochloride; - guanidine acetate; - guanidine sulfate; - guanidine, carbonate; - guanidine, bicarbonate; - guanidine, phosphate; - guanidine, sulfamate; - aminoguanidine hydrochloride; - aminoguanidine sulfate; - aminoguanidine, bicarbonate; - 1,3-diaminoguanidine hydrochloride; - 1-methylguanidine hydrochloride; - 1,1-dimethylguanidine hydrochloride; - 1-ethylguanidine hydrochloride; - biguanide, hydrochloride; - N-methyl biguanide, hydrochloride; - N-ethyl biguanide, hydrochloride; - 1,1-dimethylbiguanide hydrochloride; - 1,1,3,3-tetramethylguanidine hydrochloride; - 2-tert-butyl-1,1,3,3-tetramethylguanidine, hydrochloride; - guanidinium hydroxide (or guanidine hydroxide); - and their mixtures. Guanidinium hydroxide is generally obtained by mixing, at the time of use, a composition comprising guanidine carbonate with a composition comprising calcium hydroxide. Guanidinium hydroxide can therefore be formed in situ at the time of use. Preferably, the alkaline agent(s) are chosen from sodium hydroxide, calcium hydroxide, hydroxylamine, hydroxylamine hydrochloride, guanidine, 1,1,3,3-tetramethylguanidine, diguanidinium carbonate, guanidinium hydroxide, and mixtures thereof. Even more preferably, the alkaline agent(s) are chosen from sodium hydroxide, calcium hydroxide, hydroxylamine, hydroxylamine hydrochloride, diguanidinium carbonate, guanidinium hydroxide, and mixtures thereof. Composition T may be an aqueous composition. Water may be present in a content ranging from 90 to 99% by weight relative to the total weight of composition T. When composition T is aqueous, it can have a pH ranging from 7 to 10, and more preferably from 8 to 9. When the alkaline agent(s) is (are) present in an aqueous composition, the concentration of alkaline agent(s) may in particular be adjusted according to the desired pH for the composition, or a pH adjuster may be added to the aqueous composition. Preferably, the alkaline agent(s) as defined above is (are) present in a content of 0.05% to 15% by weight, preferably 0.05% to 10% by weight, more preferably 0.1% to 10% by weight, better still 0.1% to 7% by weight, even better still 0.5% to 5% by weight relative to the total weight of the composition T according to the invention. Polycarbodiimide compound The composition CÇ used in the context of the process according to the invention comprises at least one (poly)carbodiimide compound, The composition may comprise at least two distinct (poly)carbodiimide compounds, present as a mixture in the composition. The term “(poly)carbodiimide compound” means a compound comprising one or more carbodiimide groups, preferably at least two carbodiimide groups, more preferably at least three carbodiimide groups; in particular, the number of carbodiimide groups does not exceed 200, preferably 150, more preferably 100. The term "carbodiimide group" means a divalent linear triatomic moiety of general formula - (N=C=N) -. The (poly)carbodiimide compound(s) according to the invention may optionally comprise in their structure one or more reactive groups different from the carbodiimide groups, chosen from alkoxysilyl, hydroxysilyl, acetoxysilyl, vinylsilyl, acrylalkylsilyl, methacrylalkylsilyl, crotonylalkylsilyl, carboxyanhydridoalkylsilyl, carboxyalkylsilyl, hydroxyalkylsilyl, aldehydoal- alkylsilyl, mercaptoalkylsilyl, norbornenylsilyl, acylpentadienylalkylsilyl, maleimidoalkylsilyl, sulphonylalkylsilyl, (meth)acrylalkyl, crotonylalkyl, alkylepoxide such as propylepoxide or butylepoxide and azacyclopropane. The reactive group(s) other than the carbodiimide groups may be pendant or terminal. Preferably, the (poly)carbodiimide compound(s) comprise one or more terminal groups other than the carbodiimide groups, preferably one or more terminal groups chosen from alkoxysilyl, hydroxysilyl, acetoxysilyl, vinylsilyl, acrylalkylsilyl, methacrylalkylsilyl, crotonylalkylsilyl, carboxyanhydridoalkylsilyl, carboxyalkylsilyl, hydroxyalkylsilyl, aldehydoalkylsilyl, mercaptoalkylsilyl, norbornenylsilyl, acylpentadienylalkylsilyl, maleimidoalkylsilyl, sulphonylalkylsilyl, (meth)acrylalkyl, crotonylalkyl, alkylepoxide groups such as propylepoxide or butylepoxide and azacyclopropane. According to a particular embodiment, the (poly)carbodiimide compound is chosen from the compounds of the following formula (I): (D, Re A vod Creme 9-2 Taken rm CN; ü ANS —N { 2a-—Ra in which: - X, and X; represent, independently, an oxygen atom O, a sulfur atom S or an NH group; - R, and Ra independently represent a group chosen from a hydrocarbon radical, preferably alkyl, optionally interrupted by one or more heteroatom(s), a group chosen from alkoxysilyl, hydroxysilyl, acetoxysilyl, vinylsilyl, acrylalkylsilyl, methacrylalkylsilyl, crotonylalkylsilyl, carboxyanhydridoalkylsilyl, carboxyalkylsilyl, hydroxyalkylsilyl, aldehydoalkylsilyl, mercaptoalkylsilyl, norbornenylsilyl, acylpentadienylalkylsilyl, maleimidoalkylsilyl, sulphonylalkylsilyl, (meth)acrylalkyl, crotonylalkyl, alkylepoxide such as propylepoxide or butylepoxide, and azacyclopropane, and a hydrocarbon radical, preferably alkyl, optionally interrupted by one or more heteroatom(s) and by one or more groups chosen from alkoxysilyl, hydroxysilyl, acetoxysilyl, vinylsilyl, acrylalkylsilyl, methacrylaalkylsilyl, crotonylalkylsilyl, carboxyanhydridoalkylsilyl groups,carboxyalkylsilyl, hydroxyalkylsilyl, aldehydoalkylsilyl, mercaptoalkylsilyl, norbornenylsilyl, acylpentadienylalkylsilyl, maleimidoalkylsilyl, sulphonylalkylsilyl, (meth)acrylalkyl, crotonylalkyl, alkylepoxide such as propylepoxide or butylepoxide, and azacyclopropane; , - n denotes an integer ranging from 1 to 1000; and - A is a monomer chosen from the compounds below: LA, Sad, AN OS TT will do *1=1200 S1=t-i00 l fs ad, ; “}=+-150 * 2 "221545 121-400 41-380 L “ a di an A0 ; se * ss, to SES, + a Ne TN YUSTS : * = *, » DST Se na Ne y Ÿ See « y : ï *Ê 1 D sk ST x A 5 "4 ER, Fi a FA ra, SET SU ee SOYS Ts tr be Led a” SNAA; “ kids di kde “ar Se ÇîÎ S Le 1" Le DS pe be Se “ag Se F SR as (> Ame AND TS CO ° y 5 + KP l, ) x A 8 Ke 4, According to another embodiment, the (poly)carbodiimide compound is chosen from the compounds of the following formula (I): Ÿ ' Ï Ë r + f À dt SA tite lucas Aa Apr L 'æt fe} 5 (Tr) in which: - X, and X; represent, independently, an oxygen atom O, a sulfur atom S or an NH group; - Y, and Yz represent, independently, a divalent organic radical selected from a saturated C, to C;5 aliphatic group or a C, to C, aromatic or alkylaromatic group, the aliphatic or aromatic group optionally comprising one or more non-pendant heteroatoms, such as the nitrogen atom, the oxygen atom, the sulfur atom, or combinations thereof; - Z; and Za represent, independently, a reactive terminal group or an inert terminal group; - as an inert terminal group, Z, and Z, may independently represent a saturated, linear or branched or cyclic aliphatic group, C, to Csp, or an aromatic group C5 to Cys, said aliphatic and aromatic groups optionally comprising from 1 to 10 heteroatoms chosen from nitrogen, oxygen, sulfur and combinations thereof, and the aliphatic or aromatic group may be partially or totally fluorinated; in this variant, Z, and Z; comprise a CG linking group linking Z, to Y, and Z; to Y,, the CG group possibly being a single covalent bond, a saturated CC bond, an unsaturated covalent CC bond, an amide group, an ester group, a carbonate group, a thioester group, an ether group, a urethane group, a thiourethane group or a urea group; - as a reactive terminal group, Z, and Z; may be chosen from alkoxysilyl, hydroxysilyl, acetoxysilyl, vinylsilyl, acrylalkylsilyl, methacrylalkylsilyl, crotonylalkylsilyl, carboxyanhydridoalkylsilyl, carboxyalkylsilyl, hydroxyalkylsilyl, aldehydoalkylsilyl, mercaptoalkylsilyl, norbornenylsilyl, acylpentadienylalkylsilyl, maleimidoalkylsilyl, sulfonylalkylsilyl, (meth)acrylalkyl, crotonylalkyl, alkylepoxide groups such as propylepoxide or butylepoxide and azacyclopropane; - Q represents an organopolymer or an organo-oligomer comprising repeating units of saturated, linear or branched or cyclic aliphatic groups, or of aromatic groups or of alkylaromatic groups, coupled by repeating carbonate, ester, ether, amide, urethane or urea bonds or their combinations; - A represents a divalent aliphatic, aromatic, alkylaromatic or linear, saturated, branched or cyclic radical having from 2 to 30 carbon atoms, which may optionally comprise one or more non-pendant heteroatoms, such as the nitrogen atom, the oxygen atom, the sulfur atom, or their combinations, in the aliphatic chain or the aromatic chain; -r denotes an integer equal to A or ! ; - m denotes an integer ranging from 0 to 1000, preferably equal to 0 or |; - m' denotes an integer ranging from 0 to 1000, preferably equal to 0 or 1; - n denotes an integer ranging from 0 to 1000, preferably equal to 0 or 1, with m+ (m'*n )>2. Preferably, Z; and Z» represent, independently, a reactive terminal group, more preferably, Zy and Z» represent, independently, a group chosen from alkoxysilyl, hydroxysilyl, acetoxysilyl, vinylsilyl, acrylalkylsilyl, methacrylalkylsilyl, crotonylalkylsilyl, carboxyanhydridoalkylsilyl, carboxyalkylsilyl, hydroxyalkylsilyl, aldehydoalkylsilyl, mercaptoalkylsilyl, norbornylsilyl, acylpentadienylalkylsilyl, maleimidoalkylsilyl, sulfonylalkylsilyl, (meth)acrylalkyl, crotonylalkyl, alkylepoxide groups such as propylepoxide or butyl- epoxide, and azacyclopropane. Such (poly)carbodiimide compounds are, for example, marketed by Stahl BV under the name Permutex XR, or under the name RelcaLink10, under the name Picassian XL and Nisshinbo compounds marketed under the name CARBODILITE with the series V-02, V-02-L2, SV-02, E-02, V-10, SW-12G, E-03A, E-04DG-T, E-05, V-04, V-02B, V-04PF, V-05. Preferably, the (poly)carbodiimide compound(s) is (are) chosen from the compounds of the following formula (IT): (M, Las 5 s compounds of formula (II) following: cr . SA AS 7 Pr 5, La RA, ü Fc ° > 4.7 “AN LA N° >, na > 8 ÿ AE À pe * Ry HAaAnëé LA Teal les in which: - X, and X; represent, independently, an oxygen atom O, a sulfur atom S or an NH group; - R, and R independently represent a hydrocarbon radical optionally interrupted by one or more heteroatom(s); - net z denotes an integer ranging from 1 to 20, with n+z = 2 and w denotes an integer ranging from 1 to 3; - L, independently represents a divalent aliphatic hydrocarbon radical in C, - Cys, a cycloalkylene radical in C;-C;s, a heterocycloalkylene group in C;-C,2, or a arylene group in C,-C;4, and mixtures thereof; - E independently represents a group chosen from: - -OR;-O-; -S-R4-S-; -R<-N(R5)-R4-N(R5)-R+-, in which R3 and R4 independently represent a divalent hydrocarbon radical optionally interrupted by one or more heteroatom(s); - Rs independently represents a covalent bond or a divalent saturated hydrocarbon radical, optionally interrupted by one or more heteroatom(s); - Rs independently represents a hydrogen atom, or a hydrocarbon radical possibly interrupted by one or more heteroatom(s). The term “hydrocarbon radical” means a saturated or unsaturated, linear or branched radical having from 1 to 300 carbon atoms, preferably from 1 to 250 carbon atoms, more preferably from 1 to 200 carbon atoms. Preferably, the hydrocarbon radical is a linear and saturated radical. The hydrocarbon radical may comprise one or more cyclic groups. The hydrocarbon radical may be interrupted by one or more heteroatom(s), in particular chosen from O, S or N and / or substituted by one or more cation(s), anion(s), or zwitterion(s) or cationic group(s) such as ammonium, anionic group(s) such as carboxylate, or zwitterionic group(s), and / or comprising a metal ion which may be incorporated in the form of a salt. The term "heteroatom(s)" means an oxygen O, sulfur S or nitrogen N atom, as well as halogen atoms such as Cl, F, Br and I. If the heteroatom is included in the chain of the hydrocarbon radical, the heteroatom is preferably chosen from oxygen O, sulfur S or nitrogen N atoms. Preferably, X, and X; independently represent an oxygen atom. Preferably, R, and Rz are independently selected from dialkylamino alcohols, hydroxycarboxylic acid alkyl esters and (poly)alkylene glycol monoalkyl ethers, in which a hydroxy group has been removed, and mixtures thereof. According to a preferred embodiment, R, and Rz are independently chosen from the following groups (i) to (iv): (i) the compound of formula (IIT) following: R7-OC(O)-C(R2)(H)- (ID, wherein Ry represents a C1-C3 alkyl group, and Rs represents a hydrogen atom or a C1-C3 alkyl group, preferably R, is a methyl and Rs is a hydrogen atom or a methyl. (ii) the compound of formula (IV) following: Ro-[O-CH:-C(H)(R10)],- (IV), in which R, represents a C,-C4 alkyl group, Ry0 represents a hydrogen atom or a C,-C alkyl group, and p denotes an integer ranging from 1 to 3; preferably, Ry is methyl, ethyl or butyl and Rp is a hydrogen atom or methyl and p is equal to 1. (lil) the compound of formula (V) following: (R,1):N-CHz-C(H)(R12)- (V), in which R;; represents a C,-C4 alkyl group and Ry2 represents a hydrogen atom or a C,-C, alkyl group; preferably R, is methyl, ethyl or butyl and Ry7 is a hydrogen atom or methyl. (iv) the compound of formula (VI) following: R,-[O-CH,-C(HA(R14)]e- (VD, in which Ry; represents a C,-C4 alkyl group or a phenyl, R;4 represents a hydrogen atom or a C,-C alkyl group, and q denotes an integer ranging from 4 to 30; preferably R,; is a methyl, ethyl or butyl and R,, is a hydrogen atom or a methyl. Preferably, R, and Ra independently represent a compound of formula (VI) in which R,; represents a C,-C, alkyl group or a phenyl, preferably a C,-C, alkyl group, more preferably a methyl, R,4 represents a hydrogen atom or a C,-C, alkyl group, preferably a hydrogen atom and q denotes an integer ranging from 4 to 30. According to an alternative embodiment, R, and R are different and one of the radicals R; or R, represents a compound of formula (IV) as described above and the other radical R, or R» represents a compound of formula (VI) as described above. Preferably, in formula (IV), Ry is methyl, ethyl or butyl and Ryp is hydrogen or methyl and p is 1. Preferably, in formula (VI), Ry3 is methyl, ethyl or butyl and R,4 is hydrogen or methyl and q denotes an integer ranging from 4 to 30. According to another alternative embodiment, R, and Ra are identical and represent a compound of formula (VI) in which R,; represents a C,-C, alkyl group; or a phenyl, preferably a C,-C, alkyl group, more preferably a methyl, R,; represents a hydrogen atom or a C,-C, alkyl group, preferably a hydrogen atom and q denotes an integer ranging from 4 to 30. Preferably, n denotes an integer ranging from 1 to 20, more preferably from 2 to 20. Preferably, z denotes an integer ranging from 1 to 20, more preferably from 23 to 320. Preferably, w is equal to 1. Preferably, w is equal to 1, n+z denotes an integer ranging from 4 to 10. Preferably, L is chosen from a divalent C-Cys aliphatic hydrocarbon radical such as methylene, ethylene, and propylene, a C-Cys cycloalkylene radical such as cyclopentylene, cycloheptylene, and cyclohexylene, a C-Cys heterocycloalkylene group such as imidazolene, pyrrolene, and furanylene, or a C-Cys arylene group, such as phenylene, and mixtures thereof. For example, L; may be selected from a radical derived from tolylene diisocyanate, hexamethylene diisocyanate, xylylene diisocyanate, 2,2,4-trimethylhexamethylene diisocyanate, 1,12-dodecane diisocyanate, norbornane diisocyanate, 2,4-bis-(8-isocyanateoctyl)-1,3-dioctylcyclobutane, 4,4'-dicylclohexylmethane diisocyanate, tetramethylxylylene diisocyanate, isophorone diisocyanate, 1,5-naphthylene diisocyanate, 4,4'-diphenylmethane diisocyanate, 4,4*-diphenyldimethylmethane diisocyanate and phenylene diisocyanate and mixtures thereof. Preferably, L; is chosen from a C3-C5 cycloalkylene radical, where a C1-C1 arylene group, and mixtures thereof, such as the compounds of formula (VID) below: Se VA ” NN TS SV 4 Évoed hoc y A 7 J — Kb A; ; mt YU is 40 + Ÿ * t to 5 $ t $ = Set<e PS Se sr oo SE Da L ; uw Ù 5 C Ï j ee X “, x ; *æ J Ve Nas Sene 74 F2 > LS “re map y Sue” + Preferably, [LI] is 4,4-dicyclohexylene methane corresponding to the following formula (VIII): (VIII). PS 000 [TS no ST According to another embodiment, when L] is a Ce-C14 arylene group, L, is not the m-tetramethylxylylene radical represented by the following formula (IX): (IX). yes As previously indicated, E independently represents a group chosen from: - -OR;-O-; -S-R4-S-; -Rs<-N(Rç)-R4-N(Rs)-Rs-; in which R3 and R, independently represent a divalent hydrocarbon radical optionally interrupted by one or more heteroatom(s); - Rs independently represents a covalent bond or a divalent saturated hydrocarbon radical, optionally interrupted by one or more heteroatom(s); and - Rs independently represents a hydrogen atom, or a hydrocarbon radical optionally interrupted by one or more heteroatom(s). Preferably, R3 and R4 are independently selected from a C3-C4 arylene radical such as phenylene, a C3-C4 cycloalkylene radical; such as cyclopropylene and cyclobutylene, a linear or branched C1-Cy alkylene radical; such as methylene and ethylene, optionally interrupted by one or more heteroatom(s) and mixtures thereof. More preferably, R3 and R4 are independently chosen from a linear or branched C;-C; alkylene radical such as methylene, butylene, propylene, ethylene, optionally interrupted by one or more heteroatom(s). Preferably, when Rs is not a covalent bond, Rs is selected from a C5-C4 arylene radical such as phenylene, a Cz-C cycloalkylene radical; such as cyclopropylene and cyclobutylene, a linear or branched C;-Cys alkylene radical such as methylene and ethylene, optionally interrupted by one or more heteroatom(s), and mixtures thereof. Preferably, Rs is chosen from a Cs-Cy4 arylene radical such as phenylene, a C1-C1 cycloalkylene radical such as cyclopropylene and cyclobutylene, a linear or branched C1-C1 alkylene radical such as methylene and ethylene, optionally interrupted by one or more heteroatom(s), and mixtures thereof. Preferably, E represents a group -O-R4-O- in which R3 is chosen from a C1-C14 arylene radical, a C1-C14 cycloalkylene radical, a linear or branched C1-Cys alkylene radical, optionally interrupted by one or more heteroatom(s), and mixtures thereof. More preferably, E represents a group - -O-R4-O- in which R3 represents a linear or branched C,-C; alkylene radical; such as methylene, butylene, propylene, ethylene, optionally interrupted by one or more heteroatom(s). According to a particular embodiment, the (poly)carbodiimide compound is a copolymer derived from alpha-methylstyryl-isocyanates of the following formula (X): (x), cp EC 10 LS TO NRC NN wherein R independently represents an alkyl group having from 1 to 24 carbon atoms, a cycloalkyl group having from 3 to 24 carbon atoms or an aryl group having from 6 to 24 carbon atoms, ct, n denotes an integer ranging from 2 to 100. In this embodiment, the term “alkyl group” is as defined above. In this embodiment, the term “cycloalkyl group” is as defined above. In this embodiment, n may denote an integer ranging from 2 to 50, preferably from 3 to 30, more preferably from 5 to 10. According to another particular embodiment, the (poly)carbodiimide compound is a compound of the following formula (XI): (XI), RoSNSSS BREAK = A asijhiiïçirç.çe DEF OH y NS EE # Re rock RE ER Re rome And wherein R independently represents an alkyl group having from 1 to 24 carbon atoms, a cycloalkyl group having from 3 to 24 carbon atoms, or an aryl group having from 6 to 24 carbon atoms. “Alkyl group”, “cycloalkyl group” and “aryl group” are as defined above. According to a preferred embodiment, the (poly)carbodiimide compound is chosen from the compounds of formula (I) or formula (II) in which: - X, and X, independently represent an oxygen atom; - R, and R, are independently selected from dialkylaminoalcohols, hydroxycarboxylic acid alkyl esters and (poly)alkylene glycol monoalkyl ethers, in which a hydroxy group has been removed, and mixtures thereof, preferably (poly)alkylene glycol monoalkyl ethers, in which a hydroxy group has been removed, more preferably, the compound of formula (VI) as described above in which Ry3 represents a C,-C, alkyl group or a phenyl, preferably a C,-C, alkyl group, more preferably a methyl, R;4 represents a hydrogen atom or a C,-C, alkyl group, preferably a hydrogen atom and q denotes an integer ranging from 4 to 30 - net z, when present, denotes an integer ranging from 1 to 20, with n+z > 2 and w equal to 1; - L,, when present, is chosen from a divalent aliphatic hydrocarbon radical in C,-Cys, a cycloalkylene radical in C,-C;s, a heterocycloalkylene group in C3-C,2, or a arylene group in C1,4, and mixtures thereof, preferably, a cycloalkylene radical in C4-C;5; - A, when present, is chosen from a divalent aliphatic hydrocarbon radical in C,-Cys, a cycloalkylene radical in C,-C;s, a heterocycloalkylene group in C3-C,2, or a arylene group in Cs-C,4, and mixtures thereof, preferably, a cycloalkylene radical in C3-Cys; - E, when present, independently represents a group chosen from: - -OR;-O-; -S-R4-S-; -R<-N(R5)-R4-N(R5)-Rs-; in which R3 and R4 are independently chosen from a Cs-Cu4 arylene radical, a C3-C2 cycloalkylene radical, a linear or branched C1-C1s alkylene radical, optionally interrupted by one or more heteroatom(s), and mixtures thereof; - when Rs is not a covalent bond, Rs, when present, is chosen from a C,-C,4 arylene radical, a C,-C,; cycloalkylene radical, a linear or branched C,-Cys alkylene radical, optionally interrupted by one or more heteroatom(s), and mixtures thereof; and - Re, when present, is chosen from a Cs-C,4 arylene radical, a C;-C,2 cycloalkylene radical, a linear or branched C,-C,; alkylene radical, optionally interrupted by one or more heteroatom(s), and mixtures thereof. Preferably, the (poly)carbodiimide compound is chosen from the compounds of formula (II) in which: - X, and X, independently represent an oxygen atom; - R, and Ra, are independently selected from dialkylaminoalcohols, hydroxycarboxylic acid alkyl esters and (poly)alkylene glycol monoalkyl ethers, in which a hydroxy group has been removed, and mixtures thereof; - net z denotes an integer ranging from 1 to 20, with n+z = 2 and w is equal to 1; - L; is chosen from a divalent aliphatic hydrocarbon radical in C,-C;3, a cycloalkylene radical in C3-C;s, a heterocycloalkylene group in C3-C;2, or an arylene group in C5-C,4, and mixtures thereof; - E independently represents a group chosen from: - -OR,-O-; -S-R4-S-; -R<-N(R5)-R4-N(R5)-Rs+-; in which R3 and R, are independently chosen from a Cs-C14 arylene radical, a C;-C,, cycloalkylene radical, a linear or branched C;-C;3 alkylene radical, optionally interrupted by one or more heteroatom(s), and mixtures thereof; - when Rs is not a covalent bond, Rs is chosen from a C1-Cy4 arylene radical, a C1-Cy2 cycloalkylene radical, a C1-Cy3 linear or branched alkylene radical, optionally interrupted by one or more heteroatom(s), and mixtures thereof; and - Rs is chosen from a Ce-C,4 arylene radical, a Cz-C;2 cycloalkylene radical, a linear or branched C,-C,; alkylene radical, optionally interrupted by one or more heteroatom(s), and mixtures thereof. More preferably, the (poly)carbodiimide compound is chosen from the compounds of formula (II) in which: - X, and X, independently represent an oxygen atom; - R, and Ra, are independently monoalkyl ethers of (poly)alkylene glycol, in which a hydroxy group has been removed; - net z denotes an integer ranging from 1 to 20, with n+z > 2 and w is equal to | ; - L, is a C4-C5 cycloalkylene radical; - E independently represents a group chosen from: - -O-R1-O-; -S-R4-5-; -Rs5-N(R5)-R4-N(R5)-Rs-; in which R3 and R4 are independently chosen from a Cs-C14 arylene radical, a C;-C;1 cycloalkylene radical, a linear or branched C,-C1s alkylene radical, optionally interrupted by one or more heteroatom(s), and mixtures thereof; - when Rs is not a covalent bond, Rs is chosen from a C1-C4 arylene radical, a C1-C1 cycloalkylene radical, a linear or branched C1-C15 alkylene radical, optionally interrupted by one or more heteroatoms, and mixtures thereof; and - Rs is chosen from a C5-C4 arylene radical, a C3-C2 cycloalkylene radical, a linear or branched C1-C3 alkylene radical, optionally interrupted by one or more heteroatom(s), and mixtures thereof. Even more preferably, the (poly)carbodiimide compound is chosen from the compounds of formula (II) in which: - X, and X, independently represent an oxygen atom; - R, and R>, independently represent the compound of formula (VI) following: Rir-[O-CH>-C(H(R14)]a- (VD, in which R;3 represents a C,-C4 alkyl group or a phenyl, preferably a C,-C, alkyl group, more preferably a methyl, R;4 represents an atom hydrogen or a C1-C4 alkyl group, preferably a hydrogen atom and q denotes an integer ranging from 4 to 30; - net z denotes an integer ranging from 1 to 20, with n+z ranging from 4 to 10 and w is equal to l; - L; is a Cz-C;s cycloalkylene radical such as cyclopentylene, cycloheptylene, cyclohexylene and 4,4-dicyclohexylene methane; and - E represents a group -O-R3-O- in which R; is chosen from a Cs-C,4 arylene radical, a C;-C,, cycloalkylene radical, a linear or branched C,-C;3 alkylene radical, optionally interrupted by one or more heteroatom(s), and mixtures thereof. Even more preferably, the (poly)carbodiimide compound is chosen from the compounds of formula (II) in which: - X, and X, independently represent an oxygen atom; - R, and R>, independently represent the compound of formula (VI) following: R1r-[O-CH--C(HA(R14)]a- (VD in which Ry3 represents a C1-C4 alkyl group or a phenyl, preferably a C1-C4 alkyl group, more preferably a methyl, R,4 represents a hydrogen atom or a C1-C4 alkyl group, preferably a hydrogen atom and q denotes an integer ranging from 4 to 30; - net z denotes an integer ranging from 1 to 20, with n+z ranging from 4 to 10 and w is equal to 1; - L; is a C3-C5 cycloalkylene radical such as cyclopentylene, cycloheptylene, cyclohexylene, 4,4-dicyclohexylene methane, preferably 4,4-dicyclohexylene methane; and - E represents a group - -O-R4-O- in which R; represents a linear or branched C,-C, alkylene radical; such as methylene, propylene, butylene ethylene, optionally interrupted by one or more heteroatom(s). According to a preferred embodiment, the (poly)carbodiimide compound is a compound of the following formula (XII): (KID, . ( Die sa p0 pi nbPa gr NF 9 AT % a: Î-E ï 0e te 2° * Pa AA 'Gad s+ in which LI is 4,4-dicyclohexylene methane, n and z denote an integer ranging from 1 to 20, with n+z ranging from 4 to 10, E represents a group -O-R3-O- in which R3 represents a linear or branched C;-C1; alkylene radical such as methylene, propylene, butylene ethylene, optionally interrupted by one or more heteroatom(s), and r and s denote an integer ranging from 4 to 30. Advantageously, the total quantity of the (poly)carbodiimide compound(s) ranges from 0.01 to 20% by weight, preferably from 0.1 to 15% by weight, more preferably from 0.2 to 10% by weight, even more preferably from 0.5 to 8%, better still from 1 to 6% by weight relative to the total weight of composition C. Coloring agent The composition € used in the context of the process according to the invention comprises at least one coloring agent chosen from pigments, direct dyes, and their mixtures. Preferably, the composition C used in the context of the process according to the invention comprises one or more pigments. Preferably, the composition C used in the context of the process according to the invention comprises at least one pigment. The term "pigment" means all pigments that provide color to keratin materials. Their solubility in water at 25°C and atmospheric pressure (760 mmHg) is less than 0.05% by weight, and preferably less than 0.01%. The pigments which can be used are chosen in particular from pigments organic and / or mineral materials known to the art, in particular those described in Kirk-Othmer's Encyclopedia of Chemical Technology and in Ullmann's Encyclopedia of Industrial Chemistry. They can be natural, of natural origin, or not. These pigments can be in the form of powder or pigment paste. They can be coated or uncoated. Pigments can, for example, be chosen from mineral pigments, organic pigments, lakes, special effect pigments such as mother-of-pearl or glitter, and mixtures thereof. The pigment may be a mineral pigment. A mineral pigment is any pigment that meets the definition in the Ullmann Encyclopedia in the inorganic pigment chapter. Mineral pigments useful in the present invention include iron or chromium oxides, manganese violet, ultramarine blue, chromium hydrate, ferric blue, and titanium oxide. The pigment may be an organic pigment. By "organic pigment" we mean any pigment that meets the definition in the Ullmann Encyclopedia in the organic pigment chapter. The organic pigment may in particular be chosen from nitroso, nitro, azo, xanthene, pyrene, quinoline, quinoline, anthraquinone, triphenylmethane, fluorane, phthalocyanine, metal complex type compounds, isoindolinone, isoindoline, quinacridone, perinone, perylene, diketopyrrolopyrrole, indigo, thioindigo, dioxazine, triphenylmethane, quinophthalone. In particular, the white or colored organic pigments may be chosen from carmine, carbon black, aniline black, azo yellow, quinacridone, phthalocyanine blue, the blue pigments codified in the Color Index under the references CI 42090, 69800, 69825, 74100, 74160, the yellow pigments codified in the Color Index under the references CI 11680, 11710, 19140, 20040, 21100, 21108, 47000, 47005, the green pigments codified in the Color Index under the references CI 61565, 61570, 74260, the orange pigments codified in the Color Index under the references CI 11725, 45370, 71105, the red pigments codified in the Color Index under the references CI 12085, 12120, 12370, 12420, 12490, 14700, 15525, 15580, 15620, 15630, 15800, 15850, 15865, 15880, 26100, 45380, 45410, 58000, 73360, 73915, 75470, the pigments obtained by oxidative polymerization of indole, phenolic derivatives as described in patent FR 2 679 771. As an example, we can also cite organic pigment pigment pastes such as the products sold by the company HOECHST under the name: - COSMENYL YELLOW IOG: Pigment YELLOW 3 (C1 11710); - COSMENYL YELLOW G: Pigment YELLOW 1 (CI 11680); - ORANGE COSMENYL GR: Pigment ORANGE 43 (CI 71105); - COSMENYL RED R: Pigment RED 4 (CI 12085); - CARMIN COSMENYL FB: Pigment RED 5 (CI 12490); - VIOLET COSMENYL RL: Pigment VIOLET 23 (CI 51319); - COSMENYL BLUE A2R: Pigment BLUE 15.1 (C1 74160); - VERT COSMENYL GG: Pigment GREEN 7 (CI 74260); - COSMENYL BLACK R: Pigment BLACK 7 (C1 77266). The pigments in accordance with the invention may also be in the form of composite pigments as described in patent EP 1 184 426. These composite pigments may be composed in particular of particles comprising an inorganic core, at least one binder ensuring the fixing of the organic pigments on the core, and at least one organic pigment at least partially covering the core. Organic pigment can also be a lake. Lake refers to dyes adsorbed onto insoluble particles, the resulting mixture remaining insoluble during use. Inorganic substrates on which dyes are adsorbed include, for example, alumina, silica, calcium sodium borosilicate or calcium aluminum borosilicate, and aluminum. Among the colorants, we can cite carminic acid. We can also cite the colorants known under the following names: D & C Red 21 (CI 45 380), D & C Orange 5 (CI 45 370), D & C Red 27 (CI 45 410), D & C Orange 10 (CI 45 425), D & C Red 3 (CI 45 430), D & C Red 4 (CI 15 510), D & C Red 33 (CI 17 200), D & C Yellow 5 (CI 19 140), D & C Yellow 6 (CI 15 985), D & C Green (CI 61 570) D&C Yellow 1 O (CI 77 002), D & C Green 3 (CI 42 053), D & C Blue 1 (CI 42 090). Examples of lacquers include the product known as D & C Red 7 (CI 15850:1). The pigment can also be a special effect pigment. Special effect pigments are pigments that generally create a colored appearance (characterized by a certain shade, vibrancy and clarity) that is non-uniform and changes depending on the viewing conditions (light, temperature, viewing angles, etc.). They are therefore opposed to colored pigments that provide a conventional uniform opaque, semi-transparent or transparent shade. There are several types of special effect pigments, those with a low refractive index such as fluorescent or photochromic pigments, and those with a higher refractive index such as pearlescent pigments, interference pigments or glitter. Examples of special effect pigments include pearlescent pigments such as mica coated with titanium, or bismuth oxychloride, pearlescent pigments colored such as mica coated with titanium and iron oxides, mica coated with iron oxide, mica coated with titanium and in particular with ferric blue or chromium oxide, mica coated with titanium and an organic pigment as defined above as well as pearlescent pigments based on bismuth oxychloride. As pearlescent pigments, mention may be made of Cellini pearlescent pigments marketed by BASF (Mica-TiO lake), Prestige marketed by Eckart (Mica-TiOz), Prestige Bronze marketed by Eckart (Mica-Fe,O;) Colorona marketed by Merck (Mica-TiO,-Fe, 03). We can also cite the gold-colored mother-of-pearls marketed in particular by the company BASF under the name Brillant gold 212G (Timica), Gold 222C (Cloisonne), Sparkle Gold (Timica), Gold 4504 (Chromalite) and Monarch gold 233X (Cloisonne); the bronze mother-of-pearls marketed in particular by the company MERCK under the name Bronze fine (17384) (Colorona) and Bronze (17353) (Colorona) and by the company BASF under the name Super bronze (Cloisonne); the orange mother-of-pearls marketed in particular by the company BASF under the name Orange 363C (Cloisonne) and Orange MCR 101 (Cosmica) and by the company MERCK under the name Passion orange (Colorona) and Matte orange (17449) (Microna); brown-tinted mother-of-pearls marketed in particular by BASF under the name Nu-antique Copper 340XB (Cloisonne) and Brown CL4509 (Chromalite); copper-reflecting mother-of-pearls marketed in particular by BASF under the name Copper 340A (Timica);red-tinted mother-of-pearl, notably marketed by MERCK under the name Sienna Fine (17386) (Colorona); yellow-tinted mother-of-pearl, notably marketed by BASF under the name Yellow (4502) (Chromalite); red-tinted mother-of-pearl with a gold tint, notably marketed by BASF under the name Sunstone G012 (Gemtone); pink mother-of-pearl, notably marketed by BASF under the name Tan opale G005 (Gemtone);black mother-of-pearl with a gold sheen, notably marketed by BASF under the name Nu antique bronze 240 AB (Timica), blue mother-of-pearl notably marketed by MERCK under the name Matte Blue (17433) (Microna), white mother-of-pearl with a silver sheen, notably marketed by MERCK under the name Xirona Silver and pinkish-orange, golden-green mother-of-pearl notably marketed by MERCK under the name Indian Summer (Xirona) and their mixtures.; Still as an example of nacres, we can also cite particles comprising a borosilicate substrate coated with titanium oxide. Particles with a glass substrate coated with titanium oxide are sold in particular under the name METASHINE MC1080RY by the company TOYAL. Finally, as examples of mother-of-pearl, we can also cite poly- glitters. ethylene terephthalate, including those marketed by Meadowbrook Inventions under the name Silver 1P 0.004X0.004 (silver flakes). Multi-layer pigments based on synthetic substrates such as alumina, silica, calcium sodium borosilicate or calcium aluminum borosilicate, and aluminum can also be considered. Special effect pigments may also be chosen from reflective particles, that is to say in particular particles whose size, structure, in particular the thickness of the layer(s) which constitute them and their physical and chemical nature, and surface condition, enable them to reflect incident light. This reflection may, where appropriate, have sufficient intensity to create on the surface of the composition or mixture, when it is applied to the support to be made up, highlights visible to the naked eye, that is to say brighter points which contrast with their environment by appearing to shine. The reflective particles may be selected so as not to significantly alter the coloring effect generated by the coloring agents associated with them and more particularly so as to optimize this effect in terms of color rendering. They may more particularly have a yellow, pink, red, bronze, orange, brown, gold and / or copper color or reflection. These particles can have various shapes, including being platelet-shaped or globular, particularly spherical. The reflective particles, whatever their shape, may have a multi-layer structure or not and, in the case of a multi-layer structure, for example at least one layer of uniform thickness, in particular of a reflective material. When the reflective particles do not have a multi-layer structure, they may be composed, for example, of metal oxides, in particular synthetically obtained titanium or iron oxides. When the reflective particles have a multi-layer structure, they may, for example, comprise a natural or synthetic substrate, in particular a synthetic substrate at least partially coated with at least one layer of a reflective material, in particular at least one metal or metallic material. The substrate may be single-material, multi-material, organic and / or inorganic. More particularly, it can be chosen from glasses, ceramics, graphite, metal oxides, aluminas, silicas, silicates, in particular aluminosilicates and borosilicates, synthetic mica and their mixtures, this list not being limiting. The reflective material may include a layer of metal or a metallic material. Reflective particles are described in particular in documents JP- A-09188830, JP-A-10158450, JP-A-10158541, JP-A-07258460 and JP-A-05017710. Still as an example of reflective particles comprising a mineral substrate coated with a layer of metal, we can also cite particles comprising a borosilicate substrate coated with silver. Platelet-shaped particles with a silver-coated glass substrate are sold under the name MICROGLASS METASHINE REFSX 2025 PS by TOYAL. Particles with a nickel / chromium / molybdenum alloy-coated glass substrate are sold under the name CRYSTAL STAR GF 550, GF 2525 by the same company. It is also possible to use particles comprising a metallic substrate such as silver, aluminum, iron, chromium, nickel, molybdenum, gold, copper, zinc, tin, magnesium, steel, bronze, titanium, said substrate being coated with at least one layer of at least one metallic oxide such as titanium oxide, aluminum oxide, iron oxide, cerium oxide, chromium oxide, silicon oxides and mixtures thereof. Examples include aluminum, bronze or copper powders coated with SiO, marketed under the name VISIONAIRE by the ECKART company. Other examples include interference pigments that are not fixed to a substrate, such as liquid crystals (Helicones HC from Wacker), and holographic interference flakes (Geometric Pigments or Spectra f / x from Spectratek). Special effect pigments also include fluorescent pigments, whether they are substances that fluoresce in daylight or produce ultraviolet fluorescence, phosphorescent pigments, photochromic pigments, thermochromic pigments, and quantum dots, marketed for example by the company Quantum Dots Corporation. The variety of pigments that can be used in the present invention makes it possible to obtain a rich palette of colors, as well as particular optical effects such as metallic and interference effects. The size of the pigment used in the composition according to the present invention is generally between 10 nm and 200 um, preferably between 20 nm and 80 um, and more preferably between 30 nm and 50 um. The pigments can be dispersed in the composition using a dispersing agent. The dispersing agent serves to protect the dispersed particles from agglomeration or flocculation. This dispersing agent may be a surfactant, an oligomer, a polymer or a mixture of several of them, carrying one or more functionalities having a strong affinity for the surface of the particles to be dispersed. In particular, they can attach physically or chemically to the surface of the pigments. These dispersants have, in addition, at least one functional group compatible or soluble in the continuous medium. In particular, esters of 12-hydroxystearic acid in particular and of C8 to C20 fatty acid and polyol such as glycerol, diglycerin, such as poly(12-hydroxystearic acid) stearate with a molecular weight of approximately 750g / mol such as that sold under the name Solsperse 21 000 by the company Avecia, polyglyceryl-2 dipolyhydroxystearate (CTFA name) sold under the reference Dehymyls PGPH by the company Henkel or polyhydroxystearic acid such as that sold under the reference Arlacel P100 by the company Unigema and their mixtures are used. As another dispersant that can be used in the compositions of the invention, mention may be made of quaternary ammonium derivatives of polycondensed fatty acids such as Solsperse 17 000 sold by the company Avecia, poly dimethylsiloxane / oxypropylene mixtures such as those sold by the company Dow Corning under the references DC2-5185, DC2-5225 C. The pigments used in the composition can be surface treated with an organic agent. Thus, the previously surface-treated pigments useful in the context of the invention are pigments which have undergone totally or partially a surface treatment of a chemical, electronic, electrochemical, mechanochemical or mechanical nature, with an organic agent such as those which are described in particular in Cosmetics and Toiletries, February 1990, Vol. 105, p. 53-64 before being dispersed in the composition in accordance with the invention.These organic agents may be chosen, for example, from waxes, for example carmauba wax and beeswax; fatty acids, fatty alcohols and their derivatives, such as stearic acid, hydroxystearic acid, stearyl alcohol, hydroxystearyl alcohol, lauric acid and their derivatives; anionic surfactants; lecithins; sodium, potassium, magnesium, iron, titanium, zinc or aluminum salts of fatty acids, for example aluminum stearate or laurate; metal alkoxides; polyethylene; (meth)acrylic polymers, for example polymethylmethacrylates; polymers and copolymers containing acrylate units; alkanoamines; silicone compounds, for example silicones, in particular polydimethylsiloxanes; fluorinated organic compounds, for example perfluoroalkyl ethers; fluorosilicone compounds. The surface-treated pigments useful in the composition may also have been treated with a mixture of these compounds and / or have undergone several surface treatments. The surface-treated pigments useful in the context of the present invention can be prepared according to surface treatment techniques well known to those skilled in the art or found as such commercially. Preferably, the surface-treated pigments are covered by an organic layer. The organic agent with which the pigments are treated can be deposited on the pigments by solvent evaporation, chemical reaction between the surfactant molecules or creation of a covalent bond between the surfactant and the pigments. Surface treatment can thus be carried out, for example, by chemical reaction of a surfactant with the surface of the pigments and creation of a covalent bond between the surfactant and the pigments or fillers. This method is described in particular in US patent 4,578,266. Preferably, an organic agent covalently bound to the pigments will be used. The surface treatment agent may represent from 0.1 to 50% by weight of the total weight of the surface-treated pigment, preferably from 0.5 to 30% by weight, and even more preferably from 1 to 20% by weight of the total weight of the surface-treated pigment. Preferably, the surface treatments of the pigments are chosen from the following treatments: - a PEG-Silicone treatment like the AQ surface treatment marketed by LCW: - a Methicone treatment such as the SI surface treatment marketed by LCW: - a Dimethicone treatment such as the Covasil 3.05 surface treatment marketed by LCW; - a Dimethicone / Trimethylsiloxysilicate treatment such as the Covasil 4.05 surface treatment marketed by LCW: - a Magnesium Myristate treatment such as the MM surface treatment marketed by LCW; - an Aluminum Dimyristate treatment like the MI surface treatment marketed by Miyoshi; - a Perfluoropolymethylisopropyl ether treatment such as the FHC surface treatment marketed by LCW; - an Isostearyl Sebacate treatment like the HS surface treatment marketed by Miyoshi; - a Perfluoroalkyl Phosphate treatment such as the PF surface treatment marketed by Daito; - an acrylate / Dimethicone and Perfluoroalkyl Phosphate Copolymer treatment like the FSA surface treatment marketed by Daito; - a Polymethylhydrogen siloxane / Perfluoroalkyl Phosphate treatment such as the FS01 surface treatment marketed by Daito; - an Acrylate / Dimethicone Copolymer treatment such as the ASC surface treatment marketed by Daito; - an Isopropyl Titanium Triisostearate treatment like the ITT surface treatment marketed by Daito; - an Acrylate copolymer treatment such as the APD surface treatment marketed by Daito; - a Perfluoroalkyl Phosphate / Isopropyl Titanium Triisostearate treatment like the PF + ITT surface treatment marketed by Daito. According to a particular embodiment of the invention, the dispersing agent is present with organic or inorganic pigments in particulate form of sub-micron size. By "sub-micronic" or in English "sub-micronic" is meant pigments whose particle size has been micronized by micronization method and whose average particle size is less than one micrometer (um), in particular between 0.1 and 0.9 um, and preferably between 0.2 and 0.6 um. According to one embodiment, the dispersing agent and the pigment(s) are present in an amount (dispersant: pigment), according to a weight ratio, of between 1:4 and 4:1, particularly between 1.5:3.5 and 3.5:1 or better between 1.75:3 and 3:1. The dispersing agent(s) may therefore have a silicone backbone, such as silicone polyether and amino-silicone dispersants. Suitable dispersing agents include: - amino-silicones i.e. silicones comprising one or more amino groups such as those marketed under the names and references: BYK LPX 21879, by BYK, GP-4, GP-6, GP-344, GP-851, GP-965, GP-967 and GP-988-1, marketed by Genesee polymers, - silicone acrylates such as Tego ® RC 902, Tego ® RC 922, Tego ® RC 1041, and Tego ® RC 1043, marketed by Evonik, - polydimethylsiloxane (PDMS) silicones with carboxylic groups such as X- 22162 and X-22370 by Shin-Etsu, silicone epoxy such as GP-29, GP-32, GP-502, GP-504, GP-514, GP-607, GP-682, and GP-695, by Genesee Polymers, or Tego ® RC 1401, Tego ® RC 1403, Tego ® RC 1412, by Evonik. According to a particular embodiment, the dispersing agent(s) are of the amino-silicone type and are cationic. Preferably, the pigment(s) is (are) chosen from mineral, mixed mineral-organic or organic pigments. In a variant of the invention, the pigment(s) are organic pigments, preferably organic pigments surface-treated with an organic agent. chosen from silicone compounds. In another variant of the invention, the pigment(s) are mineral pigments. Preferably, the pigment(s) are chosen from iron oxides, in particular red, brown or black. As an example of iron oxide, mention may be made of iron oxide sold by the company Sun Chemical under the name SunPuro® Red Iron Oxide. Direct dye The composition CÇ used in the context of the process according to the invention may comprise one or more direct dye(s). By "direct dye" we mean natural and / or synthetic dyes, different from oxidation dyes. These are dyes that will diffuse superficially onto the fiber. They can be ionic or non-ionic, preferably cationic or non-ionic. Examples of suitable direct dyes that may be mentioned include azo direct dyes; (poly)methine dyes such as cyanines, hemicyanines and styryls; carbonyl dyes; azine dyes; nitro(hetero)aryl dyes; tri(hetero)arylmethane dyes; porphyrin dyes; phthalocyanine dyes and natural direct dyes, alone or in the form of mixtures. Direct dyes are preferably cationic direct dyes. Mention may be made of cationic hydrazono dyes of formulae (XIII) and (XIV), cationic azo dyes (XV) and (XVI) below: Hét-N{Ra)-N=CRb}-Ar, HQ. X1D, (XIV). Het*-C(Ra}=NN(Rb}-As, Q Hér-N=N-Ar, Q. (XV) AN g=N Ar” , Q. (XVD formulas (XIII) to (XVI) in which: - Het+ represents a cationic heteroaryl radical, preferably with an endocyclic cationic charge such as imidazolium, indolium, or pyridinium, optionally substituted preferably by at least one (C,-C;)alkyl group such as methyl; - Ar+ represents an aryl radical, such as phenyl or naphthyl, with an exocyclic cationic charge, preferably ammonium, particularly tri(C,-C,)alkyl-ammonium such as trimethylammonium; - Ar represents an aryl group, in particular phenyl, optionally substituted, preferably by one or more electron-donating groups such as i) (C,-C; )alkyl optionally substituted, ii) (C,-C:)alkoxy optionally substituted, iii) (di)(C; -Cs)(alkyl)amino optionally substituted on the alkyl group(s) by a hydroxyl group, iv) aryK(C,-C,)alkylamino, v) N-(C,-C;)alkyl-N-ary1(C,-C; )alkylamino optionally substituted or Ar represents a julolidine group; - Ar” represents an optionally substituted (hetero)aryl group such as phenyl or pyrazolyl optionally substituted, preferably by one or more (C,-Cz)alkyl, hydroxyl, (di)(C,-Cs)(alkyl)amino, (C;-C; Jalkoxy or phenyl groups; - Ra and Rb, identical or different, representing a hydrogen atom or a (C,-C;)alkyl group optionally substituted, preferably by a hydroxyl group; or the substituent Ra with a substituent of Het+ and / or Rb with a substituent of Ar form together with the atoms which carry them a (hetero)cycloalkyl; particularly Ra and Rb, representing a hydrogen atom or a (C;-C;)alkyl group optionally substituted by a hydroxyl group; - Q- represents an organic or inorganic anionic counterion such as a halide or an alkyl sulfate. In particular, mention may be made of the direct dyes with endocyclic azo and hydrazono cationic charge of formula (XIII) to (XVI) as defined above; more particularly, the direct dyes with endocyclic cationic charge described in patent applications WO 95 / 15144, WO 95 / 01772 and EP-714954; preferably the following direct dyes: R° (XVII), 114 _ = A a of a Q n R! (XVI, R° Zn M N* = F » = - NN A Mk N _ 8 Q | R! Formulas (XVII) and (XVIIT) in which: - R! represents a (C,-C,)alkyl group such as methyl; - R? and R3, identical or different, represent a hydrogen atom or a (C,-C,)alkyl group such as methyl; and - R* represents a hydrogen atom or an electron-donating group such as (C, - Cy)alkyl optionally substituted, (C,-Cp)alkoxy optionally substituted, (di)(C,-C; \(alkyl)amino optionally substituted on the alkyl group(s) by a hydroxyl group; particularly R is a hydrogen atom, - Z represents a CH group or a nitrogen atom, preferably CH, - Q- is an anionic counterion as defined above, particularly halide such as chloride or an alkylsulfate such as methylsulfate or mesyl. In particular, the dyes of formula (XV) and (XVI) are chosen from Basic Red 51, Basic Yellow 87 and Basic Orange 31 or their derivatives with Q' an anionic counterion as defined above, particularly halide such as chloride or an alkylsulfate such as methylsulfate or mesyl. The direct dyes may be chosen from anionic direct dyes. The anionic direct dyes of the invention are dyes commonly called “acid” direct dyes for their affinity with alkaline substances. Anionic direct dyes means any direct dye comprising in its structure at least one COR or SOzR substituent with R denoting a hydrogen atom or a cation originating from a metal or an amine, or an ammonium ion. The anionic dyes may be chosen from acid nitro direct dyes, acid azo dyes, acid azine dyes, acid triarylmethane dyes, acid indoamine dyes, acid anthraquinone dyes, indigoids and acid natural dyes. As acid dyes useful in the invention, mention may be made of the dyes of formulae (XIX), (XIX"), (XX), (XX), (XXI), (XXI), (XXII), (XXI), (XXII), (XXIV), (XXV) and (XXVI) following: (a) diaryl anionic azo dyes of formula (XIX) or (XIX"): (XTX), Rae R5 Ra eat 75) Ki 7 Re 3 & (XX), R, ; R7 from 4%; W'Rs Ras formulas (XIX) and (XIX") in which: - R7, Rs, Ro, Rio, R°7, R°3, R°9 and R°1p, identical or different, represent a hydrogen atom or a group chosen from: - alkyl; - alkoxy, alkylthio; - hydroxy, mercapto; - nitro, nitroso; - R°-C(X)-X"-, R°-X"-C(X)-, R°-X"-C(X)-X""- with R° representing a hydrogen atom, an alkyl or aryl group; X, X” and X”', identical or different, representing an oxygen, sulfur or NR atom with R representing a hydrogen atom or an alkyl group; - (0),S(O-)-, M+ with M+ representing a hydrogen atom or a cationic counterion; - (O)CO--, M+ with M+ as defined previously; - R°'-S(O)z-, with R'' representing a hydrogen atom, an alkyl group, an aryl group, (di)(alkyl)amino, aryl(alkyl)amino; preferably a phenylamino or phenyl group; - R°-S(O),-X"- with R°”" representing an alkyl group, optionally substituted aryl, X° as defined previously; - (di)(alkyl)amino; - aryl(alkyl)amino optionally substituted by one or more groups chosen from i) nitro; ii) nitroso; iii) (O)S(O-)-, M+ and iv) alkoxy with M+ as defined above; - optionally substituted heteroaryl; preferably a benzothiazolyl group; - cycloalkyl, in particular cyclohexyl; - Ar-N=N- with Ar representing an optionally substituted aryl group; preferably a phenyl optionally substituted by one or more alkyl groups, (O):S(O-)-, M+ or phenylamino; - or two contiguous groups R; with Rs or Rs with Ry or Ry with Rio together form a fused benzo group A'; and R°, with R°; or R°; with R'9 or R'9 with R',0 together form a fused benzo group B°; with A' and B° optionally substituted by one or more groups chosen from i) nitro; ii) nitroso; iii) (O):S(O-)-, M+; iv) hydroxy; v) mercapto; vi) (di)(alkyl)amino; vii) R°-C(X)-X"-; viii) R°-X°-C(X)-; ix) R°-X°-C(X)-X""-; x) Ar-N=N- and xi) optionally substituted aryl(alkyl)amino; with M+, R°, X, X”, X°” and Ar as defined above; - W represents a sigma 0 bond, an oxygen atom, sulfur, or a radical divalent 1) —NR- with R as defined above, or ii) methylene -C(Ra)(Rb)- with Ra and Rb identical or different, representing a hydrogen atom or an aryl group, or Ra and Rb together form with the carbon atom which carries them a spiro cycloalkyl; preferably W represents a sulfur atom or Ra and Rb together form a cyclohexyl; it being understood that formulas (XIX) and (XIX") comprise at least one sulfonate radical (0),S(O-)-, M+ or one carboxylate radical (O0)CO--, M+ on one of the rings A, A', B, B' or C; preferably sodium sulfonate. À titre d'exemple de colorants de formule (XIX) on peut citer : Acid Red 1, Acid Red 4, Acid Red 13, Acid Red 14, Acid Red 18, Acid Red 27, Acid Red 28, Acid Red 32, Acid Red 33, Acid Red 35, Acid Red 37, Acid Red 40, Acid Red 41, Acid Red 42, Acid Red 44, Pigment red 57, Acid Red 68, Acid Red 73, Acid Red 135, Acid Red 138, Acid Red 184, Food Red 1, Food Red 13, Acid Orange 6, Acid Orange 7, Acid Orange 10, Acid Orange 19, Acid Orange 20, Acid Orange 24, Yellow 6, Acid Yellow 9, Acid Yellow 36, Acid Yellow 199, Food Yellow 3; Acid Violet 7, Acid Violet 14, Acid Blue 113, Acid Blue 117, Acid Black 1, Acid Brown 4, Acid Brown 20, Acid Black 26, Acid Black 52, Food Black 1, Food Black 2 ; Food yellow 3 ou sunset yellow; et à titre d'exemple de colorants de formule (XIX") on peut citer : Acid Red 111, Acid Red 134, Acid yellow 38 ; les colorants azo anioniques pyrrazolone de formule (XX) et (XX) : (XX), ReBis Re Ras Res N EV—Rs N# R Bus, 7 , 18 = NL Ré RaoRe RD Ÿ BR. Ra (XX), AR R R, P 5 Ras Ru #5N / F) N,}=n _ vAUÊTTSE R / R AK A ' 15 Ru Ps; ; … 657; J Ra formulas (XX) and (XX) in which: - R;1, R;2 and R;3, identical or different, represent a hydrogen atom, of halogen, an alkyl group or -(O):S(O-), M+ with M+ as defined previously; - R,4 represents a hydrogen atom, an alkyl group or a -C(O)O-, M+ group with M+ as defined previously; - R,s represents a hydrogen atom; - Rys represents an oxo group in which case R',5 is absent, or else Rs with Ri6 together form a double bond: - Ry7 and Rys, identical or different, represent a hydrogen atom, or a group chosen from: - (0),S(O-)-, M+ with M+ as defined previously; - Ar-OS(O)z- with Ar representing an optionally substituted aryl group; preferably a phenyl optionally substituted by one or more alkyl groups; - Ris and Ra, together form either a double bond or a benzo D' group, possibly substituted; - R'16, R°19 and R'20, identical or different, represent a hydrogen atom or an alkyl or hydroxy group; - R», represents a hydrogen atom, an alkyl or alkoxy group; - Ra and Rb, identical or different, are as defined previously, preferably Ra represents a hydrogen atom and Rb represents an aryl group; - Y represents either a hydroxy group or an oxo group; - ==> represents a single bond when Y is an oxo group; and represents a double bond when Y represents a hydroxy group; it being understood that formulas (XX) and (XX”) comprise at least one sulfonate radical (O)2S(O-)-, M+ or one carboxylate radical -C(O)O-, M+ on one of rings D or E; preferably sodium sulfonate; Examples of dyes of formula (XX) include: Acid Red 195, Acid Yellow 23, Acid Yellow 27, Acid Yellow 76, and examples of dyes of formula (XX) include: Acid Yellow 17; c) anthraquinone dyes of formula (XXI) and (XXI): (XXI), o £Z Rz © 7 Ras Î = => R= 2 LP Ra R5: nn +. R, 9 z (XXT), formulas (XXI) and (XXI) in which: - R22, R23, Raas Ras, Rag and R37, identical or different, represent a hydrogen atom, halogen atom, or a group chosen from: - alkyl; - hydroxy, mercapto; - alkoxy, alkylthio; - optionally substituted aryloxy or arylthio, preferably substituted by one or more groups chosen from alkyl and (O),S(O-)-, M+ with M+ as defined above; - aryl(alkyl)amino optionally substituted by one or more groups chosen from alkyl and (O),S(O-)-, M+ with M+ as defined previously; - (di)(alkyl)amino; - (di)(hydroxyalkyl)amino - (0):S(0-)-, M+ with M+ as defined previously; - Z' represents a hydrogen atom or a group NRz3R29 with Ras and Ro, identical or different, represent a hydrogen atom or a group chosen from: - alkyl; - polyhydroxyalkyl such as hydroxyethyl; - aryl optionally substituted by one or more groups, particularly i) alkyl such as methyl, n-dodecyl, n-butyl; ii) (O)2S(O-)-, M+ with M+ as defined above; iii) R°-C(X)-X"-, R°-X°-C(X)-, R°-X*-C(X)-X""- with R°, X, X' and X”” as defined above, preferably R° represents an alkyl group; - cycloalkyl, in particular cyclohexyl; - Z represents a group chosen from hydroxy and NR'23R”29 with R'23 and R°29, identical or different, representing the same atoms or groups as R3; and Ra9 as defined previously; it being understood that formulas (XXI) and (XXI) comprise at least one sulfonate radical (O),S(O-)-, M+ or one carboxylate radical -C(O)O-, M+; preferably sodium sulfonate: Examples of dyes of formula (XXI) include: Acid Blue 25, Acid Blue 43, Acid Blue 62, Acid Blue 78, Acid Blue 129, Acid Blue 138, Acid Blue 140, Acid Blue 251, Acid Green 25, Acid Green 41, Acid Violet 42, Acid Violet 43, Mordant Red 3; EXT violet No. 2; and examples of dyes of formula (XXI) include: Acid Black 48; (d) nitrated dyes of formula (XXII), (XXII): (XXII), 1 M so, ve MR R. R, FR u J PA cu Re Ra Re Rz Ch (XXI), Rod | W—Aux—S0, M |, of the NO, formulas (XXII) and (XXIT) in which: - Rao, R3; and Ra, identical or different, represent a hydrogen atom, halogen atom, or a group chosen from: - alkyl; - alkoxy optionally substituted by one or more hydroxy groups, alkylthio optionally substituted by one or more hydroxy groups; - hydroxy, mercapto; - nitro, nitroso; - polyhaloalkyl; - R°-C(X)-X"-, R°-X"-C(X)-, R°-X"-C(X)-X""- with R°; X, X' and X”' as defined previously; - (0),S(O-)-, M+ with M+ as defined previously; - (O)CO--, M+ with M+ as defined previously; - (di)(alkyl)amino; - (di)(hydroxyalkyl)amino; - heterocycloalkyl such as piperidino, piperazino or morpholino; particularly R 30, R3, and R3 represent a hydrogen atom; - Rc and Rd, identical or different, represent a hydrogen atom or an alkyl group; - W is as defined previously; W particularly represents a _NH= group. - ALK represents a linear or branched divalent alkylene group, C,-C6; particularly ALK represents a -CH,-CH-- group; -is worth 1 or 2; - represents an integer between 1 and 5 inclusive; - q represents an integer between 1 and 4 inclusive; -u is 0 or | ; - when n is 1, J represents a nitro, or nitroso group; particularly nitro; - when n is 2, J represents an oxygen atom, a sulfur atom, or a divalent radical —S(O)m- with m representing an integer 1 or 2; preferably J represents a radical -SO—; - M' represents a hydrogen atom or a cationic counterion; … = Present or absent represents a benzo group optionally substituted by one or more R4 groups as defined previously, it being understood that formulas (XXII) and (XXIT') comprise at least one sulfonate radical (O),S(O-)-, M+ or a carboxylate radical -C(O)O-, M+; preferably sodium sulfonate. Examples of dyes of formula (XXII) include: Acid Brown 13; Acid Orange 3; examples of dyes of formula (XXII) include: Acid Yellow 1, 2,4-dinitro-1-naphthol-7-sulfonic acid sodium salt, 2-piperidino 5-nitro benzene sulfonic acid, Acid 2(4-N,N(2"-hydroxyethyl)amino-2-nitro)aniline ethane sulfonic acid, 4-B-hydroxyethylamino-3-nitrobenzene sulfonic acid; EXT D&C yellow 7; €) triarylmethane dyes of formula (XXIIT): (XXIID, R Ras BR j | ” = N° AE PS Rai 6) » ef Ras Re 54 "0e p fo . Las Se Ra formula (XXII) in which: - R33, Ra, Ras and Ras, identical or different, represent a hydrogen atom or a group chosen from alkyl, optionally substituted aryl and optionally substituted arylalkyl; particularly an alkyl and benzyl group optionally substituted by a (O)mS(O-)-, M+ group with M+ and m as defined previously; - Ra7, Ras, Rao, Raos Rai, Ra, Ra43 and Ru, identical or different, represent a hydrogen atom or a group chosen from: - alkyl; - alkoxy, alkylthio; - (di)(alkyl)amino; - hydroxy, mercapto; - nitro, nitroso; - R°-C(X)-X"-, R°-X'-C(X)-, R°-X"-C(X)-X""- with R° representing a hydrogen atom, an alkyl or aryl group; X, X° and X”', identical or different, representing an oxygen, sulfur or NR atom with R representing a hydrogen atom or an alkyl group; - (0)2S(O-)-, M+ with M+ representing a hydrogen atom or a cationic counterion; - (O)CO--, M+ with M+ as defined previously; - or two contiguous groups R4; with R42 OR Rz2 With R43 OR R43 With Ra together form a fused benzo group: I'; with optionally substituted by one or more groups chosen from i) nitro; ii) nitroso; iii) (O): S(O-)-, M+; iv) hydroxy; v) mercapto; vi) (di)(alkyl)amino; vii) R°-C(X)-X"-; viii) R°-X'-C(X)-; ix) R°-X°-C(X)-X""-; with M+, R°, X, X°, X°' as defined previously; particularly R37 to Rap represent a hydrogen atom, and R4; to R44, identical or different, represent a hydroxy group or (O),S(O-)-, M+; and when R43 with R4 together form a benzo group, it is preferentially substituted by a grouping (0),S(O-)-: it being understood that at least one of the cycles G, H, I or I comprise at least one sulfonate radical (O),S(O-)- or one carboxylate radical -C(O)O-; preferably sulfonate. Examples of dyes of formula (XXIIT) include: Acid Blue 1; Acid Blue 3; Acid Blue 7, Acid Blue 9; Acid Violet 49; Acid green 3; Acid green S; Acid Green 50. (f) dyes derived from xanthene of formula (XXIV): (XXIV), Ras Re =e Pa Pa LE fe Re Or ,— To | a ee Reg Re Rat formula (XXIV) in which: - Ras, Ra6, R47 and Rus, identical or different, represent a hydrogen atom or a halogen atom; - R49, Rso, Rs; and Rs), identical or different, represent a hydrogen atom, halogen atom, or a group chosen from: - alkyl; - alkoxy, alkylthio; - hydroxy, mercapto; - nitro, nitroso; - (0),S(O-)-, M+ with M+ representing a hydrogen atom or a cationic counterion; - (O)CO--, M+ with M+ as defined previously; particularly R49, Rso, Rs, and Rsz represent a hydrogen or halogen atom - G represents an oxygen atom, sulfur atom or an NRe group with Re as defined previously; particularly G represents an oxygen atom; - L represents an alcoholate O-, M+; a thioalcoholate S-, M+ or an NRf group, with Rf representing a hydrogen atom or an alkyl group, and M+ as defined previously; M+ is particularly sodium or potassium; - L' represents an oxygen atom, sulfur or an ammonium group: N+RfRg, with Rf and Rg, identical or different, representing a hydrogen atom, an alkyl group, an optionally substituted aryl group; L' particularly represents an oxygen atom or a phenylamino group optionally substituted by one or more alkyl groups or (O)mS(O-)-, M+ with m and M+ as defined previously; - Q and Q', identical or different, represent an oxygen or sulfur atom; particularly Q and Q' represent an oxygen atom; - M+ is as defined previously. Examples of dyes of formula (XXIV) include: Acid Yellow 73; Acid Red 51: Acid Red 52, Acid Red 87: Acid Red 92; Acid Red 95; Acid Violet 9; g) dyes derived from indole of formula (XXV): {(XXV). v RG Re Ra 6 R, Res Ra Î 4 200 2 4 Ree NOR R, MG Re formula (XXV) in which: - Rs3, Rs4, Rss, Rs6, Rs7, Rs, Rs9 and Rey, identical or different, represent a hydrogen atom or a group chosen from: - alkyl; - alkoxy, alkylthio; - hydroxy, mercapto; - nitro, nitroso; - R°-C(X)-X"-, R°-X'-C(X)-, R°-X"-C(X)-X""- with R° representing a hydrogen atom, an alkyl or aryl group; X, X” and X”', identical or different, representing an oxygen, sulfur or NR atom with R representing a hydrogen atom or an alkyl group; - (0),S(O-)-, M+ with M+ representing a hydrogen atom or a cationic counterion; - (O)CO--, M+ with M+ as defined previously; - G represents an oxygen atom, sulfur atom or an NRe group with Re as defined previously; particularly G represents an oxygen atom; - Riet Rh, identical or different, represent a hydrogen atom or an alkyl group; it being understood that the formula (XXIIT) comprises at least one sulfonate radical (O)2S(O-)-, M+ or a carboxylate radical -C(O)O-, M+; preferably sodium sulfonate. Examples of dyes of formula (XXV) include: Acid Blue 74; h) dyes derived from quinoline of formula (XXVI): (XXVD. EN Res f Res = bo LA, Res HUE; Res 8 HG Taussus la 2 S'VYUT\ Anna Tansalla + formula (XXVI) in which: - Rs, represents a hydrogen atom, halogen or an alkyl group; - Rez, Res, and Ra, identical or different, represent a hydrogen atom or a group (0):S(O-)-, M+ with M+ representing a hydrogen atom or a cationic counterion; or Rs; with Re2, or Rç; with Re, together form a benzo group optionally substituted by one or more groups (0),S(O-)-, M+ with M+ representing a hydrogen atom or a cationic counterion; it being understood that formula (XXVI) comprises at least one sulfonate radical (O). S(O-)-, M+ preferably sodium sulfonate. Examples of dyes of formula (XXVI) include: Acid Yellow 2, Acid Yellow 3 and Acid Yellow 5. Among the natural direct dyes that can be used according to the invention, mention may be made of lawsone, juglone, alizarin, purpurin, carminic acid, kermesic acid, purpurogallin, protocatechaldehyde, indigo, isatin, curcumin, spinulosin, apigenidin, orceins. Extracts or decoctions containing these natural dyes and in particular poultices or extracts based on henna may also be used. Preferably, the direct dyes are chosen from anionic direct dyes. The coloring agent(s) may be present in a total amount ranging from 0.001 to 20% by weight, preferably from 0.005 to 15% by weight relative to the total weight of composition C, preferably the coloring agent(s) are chosen from pigments. The pigment(s) may be present in a total amount ranging from 0.05 to 20% by weight, preferably from 0.1 to 15% by weight, better still from 0.5 to 10% by weight relative to the total weight of composition C. The direct dye(s) may be present in a total amount ranging from 0.001 at 10% by weight, preferably from 0.005 to 5% by weight relative to the total weight of composition C. Compound having at least one carboxylic function Composition C used in the context of the process according to the invention may further comprise at least one compound having at least one carboxylic function. Preferably, the compound having at least one carboxylic function is chosen from silicone compounds comprising at least one carboxylic group, polyurethanes, acrylic polymers and mixtures thereof. Polyurethanes and acrylic polymers: According to a preferred embodiment, composition C comprises at least one compound having at least one carboxylic function chosen from polyurethanes, acrylic polymers and their mixtures. Preferably, the compound(s) having at least one carboxylic function are in the form of aqueous dispersions of particles of polymer(s) chosen from polyurethanes, acrylic polymers, and their mixtures. Preferably, composition C comprises at least one compound having at least one carboxylic function in the form of aqueous dispersions of polyurethane particles, acrylic polymers, and mixtures thereof. The dispersion(s) may be simple dispersions in the aqueous medium of the cosmetic composition. As a particular case of dispersions, latexes may be mentioned. The aqueous dispersion(s) of polymer particles may be chosen from aqueous dispersions of polyurethane particles. More particularly, the polyurethane(s) present in the aqueous dispersions used in the present invention are derived from the reaction of - a prepolymer of the following formula (A): Ÿs è $ s to $ Ÿ sweudk a if SNS Poe te ie Nate tn gr em ee fairy be EE PA (HAS), in which: - R, represents a bivalent radical of a dihydroxylated compound; - Ra represents a radical of an aliphatic or cycloaliphatic polyisocyanate; - R; represents a radical of a low molecular weight diol, optionally substituted by one or more ionic groups; - n represents an integer ranging from 1 to 5, and - mest greater than | ; - at least one chain extender according to the following formula (B): H,NR,-NH; (B), in which R represents an alkylene or alkylene oxide radical which is not substituted by one or more ionic or potentially ionic groups; and - at least one chain extender according to the following formula (C): H,N-Rs-NH; (C), in which Rs represents an alkylene radical substituted by one or more ionic or potentially ionic groups. Among the dihydroxylated compounds that can be used according to the present invention, mention may in particular be made of compounds having two hydroxyl groups and a number-average molecular weight of approximately 700 to approximately 16,000, and preferably of approximately 750 to approximately 5,000. As examples of dihydroxylated compounds having a high molecular weight, mention may be made of polyol polyesters, polyol polyethers, polyhydroxylated polycarbonates, polyhydroxylated polyacetates, polyhydroxylated polyacrylates, polyhydroxylated amide polyesters, polyhydroxylated polyalkadienes, polyhydroxylated polythioethers and mixtures thereof. Preferably, the hydroxylated compounds are chosen from polyol polyesters, polyol polyethers, polyhydroxylated polycarbonates and mixtures thereof. The polyisocyanates which can be used according to the present invention are in particular chosen from organic diisocyanates having a molecular weight of approximately 112 to 1000, and preferably of approximately 140 to 400. Preferably, the polyisocyanates are chosen from diisocyanates and more particularly from those represented by the general formula R,(NCO),, in which R, represents a divalent aliphatic hydrocarbon group having from 4 to 18 carbon atoms, a divalent cycloaliphatic hydrocarbon group having from 5 to 15 carbon atoms, a divalent araliphatic hydrocarbon group having from 7 to 15 carbon atoms or a divalent aromatic hydrocarbon group having 6 to 15 carbon atoms. Preferably, Rz represents an organic diisocyanate. Examples of organic diisocyanates that may be chosen include tetramethylene diisocyanate, 1,6-hexamethylene diisocyanate, dodecamethylene diisocyanate, 1,3-diisocyanatocyclohexane, 1,4-diisocyanatocyclohexane, 3-isocyanatomethyl-3,5,5-trimethylcyclohexane isocyanate (isophorone diisocyanate or IPDI), bis-(4-isocyanatocyclohexyl)-methane, 1,3-bis(isocyanatomethyl)-cyclohexane, 1,4-bis(isocyanatomethyl)-cyclohexane, bis- (4-isocyanato-3-methyl-cyclohexyl)-methane, isomers of toluene diisocyanate (TDD) such as 2,4-toluene diisocyanate, 2,6-toluene diisocyanate and mixtures thereof, hydrogenated toluene diisocyanate, 4,4'-diphenyl methane diisocyanate and mixtures with its isomers 2,4-diphenylmethane diisocyanate and optionally 2,2"-diphenylmethane diisocyanate, naphthalene-1,5-diisocyanate, and mixtures thereof. Preferably, the diisocyanates are aliphatic and cycloaliphatic diisocyanates, and are more preferably chosen from 1,6-hexamethylene diisocyanate, 3-isocyanatomethyl-3,5,5-trimethylcyclohexane isocyanate and mixtures thereof. By "low molecular weight diol" is meant, according to the present invention, a diol having a molecular weight of about 62 to 700, and preferably 62 to 200. These diols may comprise aliphatic, alicyclic or aromatic groups. Preferably, they comprise only aliphatic groups. Preferably, R3 represents a low molecular weight diol, having more than 20 carbon atoms, more preferably chosen from ethylene glycol, diethylene glycol, propane 1,2-diol, propane 1,3-diol, butane 1,4-diol, butylene 1,3-glycol, neopentyl glycol, butyl-ethyl-propane diol, cyclohexane diol, 1,4-cyclohexane dimethanol, hexane 1,6-diol, bisphenol A (2,2-bis(4-hydroxyphenyl)propane), hydrogenated bisphenol A (2,2-bis(4-hydroxycyclohexyl)propane), and mixtures thereof. The low molecular weight diols may optionally comprise ionic or potentially ionic groups. Examples of low molecular weight diols containing ionic or potentially ionic groups are described in particular in US patent 3,412,054. Such compounds are preferably selected from dimethylol butanoic acid, dimethylol propionic acid, polycaprolactone diols containing a carboxyl group and mixtures thereof. If lower molecular weight diols containing ionic or potentially ionic groups are used, they are preferably used in an amount such that less than 0.30 meq of COOH per gram of polyurethane in the polyurethane dispersion is present. The prepolymer is extended using two families of chain extenders. The first family of chain extenders corresponds to compounds of general formula @B). The chain extenders of formula (B) are preferably selected from alkylene diamines, such as hydrazine, ethylenediamine, propylenediamine, 1,4-butylenediamine, piperazine; alkylene oxide diamines, such as 3-{2-[2-(3-aminopropoxy)ethoxy]-ethoxy}propylamine (also called dipropylamine diethylene glycol or DPA-DEG ​​available from Tomah Products, Milton, Wis.), 2-methyl-1,5-pentanediamine (Dytec ® from DuPont), hexane diamine, isophorone diamine, 4,4-methylenedi-(cyclohexylamine), ether amines of DPA series available from Tomah Products, Milton, Wis., such as dipropylamine propylene glycol, dipropylamine dipropylene glycol, dipropylamine tripropylene glycol, dipropylamine poly(propylene glycol), dipropylamine ethylene glycol, dipropylamine poly(ethylene glycol), dipropylamine 1,3-propane diol, dipropylamine 2-methyl-1,3-propane diol, dipropylamine 1,4-butane diol, dipropylamine 1,3-butane diol, dipropylamine 1,6-hexane diol and dipropylamine cyclohexane-1,4-dimethanol; and mixtures thereof. The second family of chain extenders corresponds to compounds of general formula (C). Such compounds preferably have one ionic or potentially ionic group and two groups capable of reacting with isocyanate groups. Such compounds may optionally comprise two groups reactive with isocyanate groups and one ionic group or one capable of forming an ionic group. The ionic or potentially ionic group may preferably be selected from ternary or quaternary ammonium groups or groups convertible into such groups, a carboxyl group, a carboxylate group, a sulfonic acid group and a sulfonate group. The at least partial conversion of the groups convertible into a salt of ternary or quaternary ammonium groups may take place before or during mixing with water. The chain extenders of formula (C) are preferably chosen from diaminosulfonates, such as for example the sodium salt of N- @-aminoethyl)-2-aminoethanesulfonic acid (AAS), N-(2-aminoethyl)-2-aminopropionic acid sodium salt, and mixtures thereof. The polyurethane usable according to the present invention may optionally further comprise compounds which are respectively located at the ends of the chains and terminate said chains (chain terminators). Such compounds are described in particular in US patents 7,445,770 and / or US 7,452,770. Preferably, the aqueous dispersion of polyurethane particles has a viscosity of less than 2000 mPa.s at 23°C, more preferably less than 1500, and even better less than 1000. Even more preferably, the aqueous dispersion of polyurethane has a glass transition temperature of less than 0°C. Also preferably, the aqueous polyurethane dispersion has a polyurethane content (or active material, or dry matter) based on the weight of the dispersion of 20 to 60% by weight, more preferably 25 to 55% by weight and more preferably 30 to 50% by weight. This means that the polyurethane content (dry matter) of the aqueous dispersion is preferably 20% to 60% by weight, more preferably 25% to 55% by weight and more preferably 30% to 50% by weight, relative to the total weight of the dispersion. Also preferably, the aqueous dispersion of polyurethane particles has a glass transition temperature (Tg) equal to or less than -25°C, preferably less than -35°C, and more preferably less than -40°C. The polyurethane particles may have an average diameter of up to about 1000 nm, for example from about 50 nm to about 800 nm, more preferably from about 100 nm to about 500 nm. These particle sizes can be measured with a laser particle size analyzer (e.g. Brookhaven BI90). By way of non-limiting example of aqueous polyurethane dispersions, mention may be made of those sold under the name Baycusan® by Bayer such as, for example, Baycusan® C1000 (INCI name: polyurethane-34), Baycusan® C1001 (INCI name: polyurethane-34), Baycusan® C1003 (INCI name: polyurethane-32), Baycusan® C1004 (INCI name: polyurethane-35) and Baycusan® C1008 (INCI name: polyurethane-48). Other examples include aqueous dispersions of polyurethane of isophthalic acid / adipic acid copolymer / hexylene glycol / neopentyl glycol / dimethylol acid / isophorone diisocyanate (INCI name: Polyurethane-1, such as Luviset® PUR, BASF), polyurethane of polycarbonate, polyurethane and aliphatic polyester polyurethane (such as NEOREZ® series, DSM, such as NEOREZ® R989, NEOREZ® and R-2202). According to a preferred embodiment, the aqueous dispersion of polyurethane particles may be chosen from aqueous dispersions of particles of compounds having the INCI name polyurethane-35 or compounds having the INCI name polyurethane-34. Preferably, the compound(s) having at least one carboxylic function are in the form of aqueous dispersions of acrylic polymer particles, more preferably in the form of aqueous dispersions of film-forming acrylic polymer particles. For the purposes of the invention, the term "polymer" means a compound corresponding to the repetition of one or more units (these units being derived from compounds called monomers). This or these units are repeated at least twice and preferably at least 3 times. By "film-forming polymer" is meant a polymer capable of forming, on its own or in the presence of an auxiliary film-forming agent, a macroscopically continuous film on a support, in particular on the hair, and preferably a cohesive film. By "acrylic polymer", is meant, within the meaning of the present invention, a polymer synthesized from at least one monomer chosen from (meth)acrylic acid and / or (meth)acrylic acid ester and / or (meth)acrylic acid amide. The unit(s) derived from the (meth)acrylic acid monomers of the polymer may optionally be in the form of salt(s), in particular of alkali metal, alkaline earth metal, ammonium or organic base. The esters of (meth)acrylic acid (also called (meth)acrylates) are advantageously chosen from alkyl (meth)acrylates, in particular C to C 39 alkyl, preferably C to C 1 , better still C to C 1 p, aryl (meth)acrylates, in particular C to C 1 p aryl, hydroxyalkyl (meth)acrylates, in particular C to C 5 hydroxyalkyl. Among the alkyl (meth)acrylates, mention may be made of methyl (meth)acrylate, ethyl (meth)acrylate, butyl (meth)acrylate, isobutyl (meth)acrylate, 2-ethylhexyl (meth)acrylate, lauryl (meth)acrylate, cyclohexyl (meth)acrylate. Among the hydroxyalkyl (meth)acrylates, mention may be made of hydroxyethyl acrylate, 2-hydroxypropyl acrylate, hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate. Among the aryl (meth)acrylates, we can cite benzyl acrylate and phenyl acrylate. Particularly preferred esters of (meth)acrylic acid are alkyl (meth)acrylates, preferably C to C10 alkyl, more preferably C to C10, even better C to C10, and even more particularly C to C4. According to the present invention, the alkyl group of the esters can be fluorinated, or even perfluorinated, that is to say that some or all of the hydrogen atoms of the alkyl group are substituted by fluorine atoms. Examples of amides of (meth)acrylic acid include (meth)acrylamides and N-alkyl (meth)acrylamides, particularly C 2 to C 12 alkyl. Examples of N-alkyl (meth)acrylamides include N-ethyl acrylamide, N-t-butyl acrylamide, Nt-octyl acrylamide and N-undecylacrylamide. The acrylic polymer according to the invention may be a homopolymer or a copolymer, advantageously a copolymer, even better a copolymer of (meth)acrylic acid and (meth)acrylic acid esters. Preferably, the acrylic polymer(s) according to the invention comprise one or more units derived from the following monomers: (a) (meth)acrylic acid; and b) C, to C10, more preferably C12, to C14, even better C16, to C18, and even more particularly C18, to C19, alkyl (meth)acrylate Preferably, the aqueous dispersion of acrylic polymer particles does not comprise a surfactant. The term "fensioactive" means any agent capable of modifying the surface tension between two surfaces. Among the acrylic polymers according to the invention, mention may be made of copolymers of (meth)acrylic acid and methyl or ethyl (meth)acrylate, in particular copolymers of methacrylic acid and ethyl acrylate such as the compound sold under the trade name LUVIMER MAE by the company BASF, or the compound Polyacrylate-2 crosspolymer sold under the trade name FIXATE SUPERHOLD POLYMER by the company LUBRIZOL, or the compound Acrylate Copolymer sold under the trade name DAITOSOL 3000VP3 by the company DAITO KASEI KOGYO, or the compound Acrylate Copolymer sold under the trade name DAITOSOL 3000SLPN-PE1 by the company DAITO KASFI KOGYO. The acrylic polymer may optionally comprise one or more additional monomers, other than the (meth)acrylic acid and / or (meth)acrylic acid ester and / or (meth)acrylic acid amide monomers. Examples of additional monomers that may be mentioned are styrenic monomers, in particular styrene and alpha-methylstyrene, and preferably styrene. In particular, the acrylic polymer may be a styrene / (meth)acrylate copolymer, and in particular a polymer chosen from copolymers resulting from the polymerization of at least one styrene monomer and at least one C1 to C2, preferably C1 to C10, alkyl (meth)acrylate monomer. The C1-C10 alkyl (meth)acrylate monomer may be chosen from methyl acrylate, ethyl acrylate, propyl acrylate, butyl acrylate, hexyl acrylate, octyl acrylate, 2-ethyl hexyl acrylate. Examples of acrylic polymers include styrene / (meth)acrylate(s) copolymers marketed under the name JONCRYL 77 by BASF, under the name YODOSOL GH41F by AKZO NOBEL and under the name SYNTRAN 5760 CG by INTERPOLYMER. Preferably, composition C comprises at least one aqueous dispersion of acrylic polymer particles. More preferably, composition C comprises at least one aqueous dispersion of acrylic polymer particles comprising one or more units derived from the following monomers: (a) (meth)acrylic acid; and b) C, to C10, more preferably C12, to C14, even better C16, to C18, and even more particularly C18, to C19, alkyl (meth)acrylate Preferably, the aqueous dispersion of acrylic polymer particles has an acrylic polymer (or active material, or dry matter) content based on the weight of the dispersion of 20 to 60% by weight, more preferably of 22 to 55% by weight and more preferably of 25 to 50% by weight. Silicone acrylic copolymer According to a particular embodiment, the silicone compound(s) comprising at least at least one carboxylic group are chosen from silicone acrylic copolymers. Thus, according to a particular embodiment, the compound(s) having at least one carboxylic function are chosen from silicone acrylic copolymers. Preferably, said silicone acrylic copolymer(s) comprise: - at least one acrylic or methacrylic or crotonic unit; and - at least one polydimethylsiloxane (PDMS) unit. For the purposes of the present invention, the term "polydimethylsiloxanes" (also abbreviated as PDMS), in accordance with general acceptance, means any organosilicon polymer or oligomer with a linear structure, of variable molecular weight, obtained by polymerization and / or polycondensation of suitably functionalized silanes, and consisting essentially of a repetition of main units in which the silicon atoms are linked together by oxygen atoms (Si-O-Si siloxane bond), comprising methyl radicals directly linked via a carbon atom to said silicon atoms. The PDMS chains that can be used to obtain the copolymer used according to the invention comprise at least one polymerizable radical group, preferably located on at least one of the ends of the chain, that is to say that the PDMS can have, for example, a polymerizable radical group on each of the two ends of the chain or have a polymerizable radical group on one end of the chain and a trimethylsilyl terminal group on the other end of the chain. By polymerizable radical group is meant a radical capable of polymerizing with other polymerizable radical groups or monomers. Preferably, the polydimethylsiloxane unit comprises at least one polymerizable radical group. Preferably, the polymerizable radical group comprises at least one vinyl group. Preferably, the polydimethylsiloxane (PDMS) unit comprises at least one polymerizable radical group comprising a vinyl group, preferably at least two polymerizable radical groups comprising a vinyl group, preferably located on at least one of the ends of the chain. As indicated previously, said silicone acrylic copolymer(s) preferably comprise at least one acrylic or methacrylic or crotonic unit, i.e. at least one unit comprising a carboxylic group. The term “carboxylic group” means a functional group COOH or COO, the counterion of the COO- group being able to be chosen from alkali metals, alkaline earth metals, quaternary ammoniums. Preferably, said silicone acrylic copolymer(s) comprise: - at least one acrylic or methacrylic or crotonic motif, and at least one motif acrylic ester or methacrylic ester or vinyl ester; and - at least one polydimethylsiloxane (PDMS) unit. More preferably, the composition comprises one or more silicone acrylic copolymers comprising: - at least one crotonic unit and at least one unit chosen from an alkyl crotonate unit, the alkyl radical being a linear or branched, saturated radical containing from 1 to 20 carbon atoms; a vinyl acetate unit; a vinyl alkyl ester unit, the alkyl radical being a linear or branched, saturated radical containing from 2 to 20 carbon atoms; and mixtures thereof; and - at least one polydimethylsiloxane (PDMS) unit. A crotonic unit is a unit derived from a crotonic acid monomer or one of its salts. By alkyl crotonate unit is meant a unit derived from a crotonic acid ester monomer, having a linear or branched, saturated alkyl radical containing from 1 to 20 carbon atoms. By vinyl alkyl ester unit is meant a unit derived from a vinyl ester monomer having a linear or branched, saturated alkyl radical containing from 2 to 20 carbon atoms. A vinyl acetate unit is a unit derived from a vinyl acetate monomer. According to a preferred embodiment, said silicone acrylic copolymer(s) comprise: - at least one crotonic unit, at least one vinyl acetate unit and at least one vinyl alkyl ester unit, the alkyl radical being a linear or branched, saturated radical containing from 2 to 20 carbon atoms, preferably from 2 to 18 carbon atoms, and - at least one polydimethylsiloxane (PDMS) unit, preferably comprising at least one polymerizable radical group comprising at least one vinyl group. According to a particularly preferred embodiment, said silicone acrylic copolymer(s) comprise: - at least one crotonic unit, at least one vinyl acetate unit and at least one vinyl alkyl ester unit, the alkyl radical being a linear or branched, saturated radical containing from 6 to 16 carbon atoms, and - at least one polydimethylsiloxane (PDMS) mold comprising at least one polymerizable radical group comprising at least one vinyl group. More preferably, the composition comprises one or more silicone acrylic copolymers comprising: - at least one crotonic unit, at least one vinyl acetate unit and at least one vinyl alkyl ester unit, the alkyl radical being a linear or branched, saturated radical containing from 2 to 20 carbon atoms, preferably from 2 to 18 carbon atoms; and - at least one polydimethylsiloxane (PDMS) unit comprising at least one polymerizable radical group comprising at least one vinyl group. Even more preferably, the composition comprises one or more silicone acrylic co-polymers comprising: - at least one crotonic unit, at least one vinyl acetate unit and at least one vinyl alkyl ester unit, the alkyl radical being a linear or branched, saturated radical containing from 6 to 16 carbon atoms; and - at least one polydimethylsiloxane (PDMS) unit comprising at least one polymerizable radical group comprising at least one vinyl group. Among the silicone acrylic copolymers that can be used in the context of the invention, mention may be made of the compound sold by the company Wacker Chemie AG under the trade name Belsil® P1101, with the INCI name Crotonic Acid / Vinyl C8-12 Isoalkyl Esters / VA / Bis-Vinyldimethicone Crosspolymer. The total amount of the compound(s) having at least one carboxylic function preferably ranges from 0.1 to 35% by weight, more preferably from 0.5 to 30% by weight, better still from 1 to 20% by weight, and even more preferably from 3 to 15% by weight relative to the total weight of composition C. The total quantity of the aqueous dispersion(s) of polymer particles chosen from polyurethanes, acrylic polymers, and their mixtures preferably ranges from 0.1 to 35% by weight, more preferably from 0.5 to 30% by weight, better still from 1 to 20% by weight, and even more preferably from 3 to 15% by weight relative to the total weight of composition C. According to a particular embodiment, the total quantity of the aqueous dispersion(s) of acrylic polymer particles preferably ranges from 0.1 to 35% by weight, more preferably from 0.5 to 30% by weight, better still from 1 to 20% by weight, and even more preferably from 3 to 15% by weight relative to the total weight of composition C. Advantageously, the total quantity of silicone acrylic copolymer(s) ranges from 0.1 to 35% by weight, more preferably from 0.5 to 30% by weight, better still from 1 to 20% by weight, and even more preferably from 3 to 15% by weight relative to the total weight of composition C. Solvents Composition C used in the process according to the invention may be aqueous. The water content may range from 1 to 90% by weight, preferably from 10 to 80% by weight, more preferably from 20 to 75% by weight relative to the total weight of composition C. In addition, composition C may comprise one or more organic solvents. Examples of organic solvents that may be mentioned are C1-C4 lower alkanols such as ethanol and isopropanol; polyols and polyol ethers such as 2-butoxyethanol, 1,2-hexanediol, propylene glycol, pentylene glycol, propylene glycol monomethyl ether, diethylene glycol monoethyl ether and monomethyl ether, and aromatic alcohols, in particular aromatic monoalcohols such as benzyl alcohol, phenoxyethanol, and mixtures thereof. The organic solvents may be present in a total amount of between 0.01 and 60% by weight, preferably between 0.05 and 50% by weight and more preferably inclusively between 0.1 and 45% by weight relative to the total weight of composition C. Additives The composition CÇ used in the context of the process according to the invention may contain any adjuvant or additive usually used. Among the additives that may be contained in the composition, mention may be made of reducing agents, softeners, anti-foaming agents, moisturizing agents, UV filters, peptizers, perfumes, anionic, cationic, non-ionic or amphoteric surfactants, proteins, vitamins, polymers other than the polymers previously described, preservatives, silicones, oils, waxes other than silicones in wax form, and mixtures thereof. The composition CÇ used in the context of the process according to the invention may be in particular in the form of a suspension, dispersion, gel, emulsion, in particular oil-in-water (O / W) or water-in-oil (W / O) emulsion, or multiple (W / O / W or polyol / O / W or O / W / O), in the form of a cream, mousse, stick, dispersion of vesicles in particular of ionic or non-ionic lipids, two-phase or multi-phase lotion. A person skilled in the art will be able to choose the appropriate galenic form, as well as its method of preparation, on the basis of his general knowledge, taking into account on the one hand the nature of the constituents used, in particular their solubility in the support, and on the other hand the application envisaged for the composition. Application of composition D The hair coloring process according to the invention may further comprise the application to the hair of a composition D comprising at least one silicone compound comprising at least one carboxylic group. Preferably, the silicone compound comprising at least one carboxylic group is a silicone compound different from the silicone acrylic copolymer as described previously. “Carboxylic group” means a COOH or functional group COO-, the counterion of the COO- group being able to be chosen from alkali metals, alkaline earth metals, quaternary ammoniums. The silicones that may be used may be soluble or insoluble in composition D; they may be in the form of oil, wax, resin or gum; silicone oils and gums are preferred. Silicones are described in detail in Walter NOLL's book “Chemistry and Technology of Silicones” (1968), Academie Press. Preferably, the silicone compound(s) comprising at least one carboxylic group are chosen from the organosiloxanes of the following formula (XXVII): (XXVID R4 8 3 M T1 81 [nt 4 1 4 Fi È and 1 to fa—6—04- 81008 Li 0 ufr Ri (BA |} R2 4 LAt 3, | na "has in which: - Rl independently represent an alkyl group having from 1 to 20 carbon atoms, preferably from 1 to 10 carbon atoms; a hydroxy group; an alkoxy group having from 1 to 20 carbon atoms or an aryl group having from 6 to 12 carbon atoms; - R2 independently represents a group R4-COOM with R4 representing a linear or branched alkylene group, having from 1 to 20 carbon atoms, preferably from 4 to 16 carbon atoms, optionally interrupted by at least one heteroatom chosen from the sulfur atom, the nitrogen atom, the oxygen atom and their mixtures, and M representing a hydrogen atom; an alkali or alkaline-earth metal or a quaternary ammonium NR'3, with R° identical or different, representing H or alkyl having from 1 to 4 carbon atoms; a pyrrolidone radical comprising a carboxylic group COOH or a group Ra-(ORb)x-COOM with Ra representing a linear or branched alkylene group, having from 1 to 4 carbon atoms, Rb representing an alkyl group having from 1 to 4 carbon atoms, x being an integer ranging from 1 to 200;and M representing a hydrogen atom, an alkali or alkaline earth metal or a quaternary ammonium NR',, with R', identical or different, representing H or an alkyl having from 1 to 4 carbon atoms; ; - R3 independently represent an alkyl group having from 1 to 20 carbon atoms; a hydroxy group; an R4-COOM group with R4 representing a linear or branched alkylene group, having from 1 to 20 carbon atoms, preferably from 4 to 16 carbon atoms, optionally interrupted by at least one heteroatom chosen from the sulfur atom, the nitrogen atom, the oxygen atom and their mixtures, and M representing a hydrogen atom; an alkali or alkaline-earth metal or a quaternary ammonium NR'3, with R° identical or different, representing H or alkyl having from 1 to 4 carbon atoms; an alkoxy group having from 1 to 20 carbon atoms; an aryl group having from 6 to 12 carbon atoms or a group R,-(OR;), - COOM with R, representing a linear or branched alkylene group, having from 1 to 4 carbon atoms, R, representing an alkyl group having from 1 to 4 carbon atoms, x being an integer ranging from 1 to 200; and M representing a hydrogen atom, an alkali or alkaline earth metal or a quaternary ammonium NR°;, with R° identical or different, representing H or an alkyl having from 1 to 4 carbon atoms; - n denotes an integer ranging from 1 to 1000; - p designated an integer ranging from 0 to 1000; it being understood that at least one of the radicals R2 and / or R3 comprises a carboxylic group COOH or COOM with M representing an alkali or alkaline-earth metal or a quaternary ammonium NR°3, with R', identical or different, representing H or an alkyl having from 1 to 4 carbon atoms. In particular, the silicone compound(s) comprising at least one carboxylic group may be chosen from the organosiloxanes of the following formula (XXVIII): (XX VIT, R1 Rti 1 BR l 4 1 { J: MOOC + Re Er ce —R4—COoM R4—Si o 5 0-81 R4-—0 t 3 4 15 8 da Às There in which: - R1 independently represents a linear or branched alkyl group having from 1 to 20 carbon atoms, preferably from 1 to 10 carbon atoms, even better from 1 to 6 carbon atoms; preferably methyl; - R4 independently represents a linear or branched alkylene group, having from 1 to 20 carbon atoms, preferably from 4 to 16 carbon atoms, optionally interrupted by at least one heteroatom chosen from the sulfur atom, the nitrogen atom, the oxygen atom and their mixtures; or a divalent group R,-(OR,),- with R, representing a linear or branched alkylene group, having from 1 to 4 carbon atoms, R, representing an alkylene group having from 1 to 4 carbon atoms, and x being an integer ranging from 1 to 200; - M independently represents a hydrogen atom, an alkali or alkaline earth metal or a quaternary ammonium NR°,, with R° identical or different, representing H or an alkyl having from 1 to 4 carbon atoms; - n denotes an integer ranging from 1 to 1000; - organosiloxanes of the following formula (XXIX): (XXIX). Rt 1 3 (em TT TM OUTRE Riom 0 + $ + aff a acc 1° FE # +. 1 | i + J Ft J Ri IR Ré À R1 1st = To, | Coom di in which: - RI independently represents an alkyl group having from 1 to 10 carbon atoms, preferably from 1 to 6 carbon atoms, more preferably a methyl - R4 represents a linear or branched, saturated or unsaturated alkylene group having from 1 to 20 carbon atoms, preferably from 4 to 16 carbon atoms, optionally interrupted by at least one heteroatom chosen from the sulfur atom, the nitrogen atom, the oxygen atom and their mixtures; or a divalent group R,-(OR,),- with R, representing a linear or branched alkylene group having from 1 to 4 carbon atoms, Rs representing an alkylene group having from 1 to 4 carbon atoms, and x being an integer ranging from 1 to 200; - M represents a hydrogen atom; an alkali or alkaline earth metal or a quaternary ammonium NR';, with R° identical or different, representing H or an alkyl having from 1 to 4 carbon atoms; - p denotes an integer ranging from 1 to 1000; - n denotes an integer ranging from 1 to 1000; - organosiloxanes of the following formula (XXX): Yours vs (XXX) R1 TM CE Mt +} RE come Bio Q———êt-——00 cafe ve ee COOM R4 hs da There in which: - R1 independently represents an alkyl group having from 1 to 20 carbon atoms, preferably from 1 to 10 carbon atoms, even better from 1 to 6 carbon atoms; preferably methyl; - R4 represents a linear or branched alkylene group, having from 1 to 20 carbon atoms, preferably from 4 to 16 carbon atoms, optionally interrupted by at least one heteroatom chosen from the sulfur atom, the nitrogen atom, the oxygen atom and their mixtures; or a divalent group R,-(OR;),- with R, representing a linear or branched alkylene group, having from 1 to 4 carbon atoms, R » representing an alkylene group having from 1 to 4 carbon atoms, and x being an integer ranging from 1 to 200: - R3 represents an alkyl group having from 1 to 20 carbon atoms; an alkoxy group having from 1 to 20 carbon atoms or an aryl group having from 6 to 12 carbon atoms; - M independently represents a hydrogen atom, an alkali or alkaline earth metal or a quaternary ammonium NR°4, with R° identical or different, representing H or an alkyl having from 1 to 4 carbon atoms; - n denotes an integer ranging from 1 to 1000; - organosiloxanes of the following formula (XXXI): (XXXT) ct [ok [eh CR | cs He—si—o —g—0 He—0|—s— 0H t JA TI DJ t | ) OH, | CH; |e | | se JLf* H&——Rs ee — 4 4 NS YH in which: - R8 represents an alkyl group having from 1 to 6 carbon atoms, preferably a methyl group; - m denotes an integer ranging from 1 to 1000; - n denotes an integer ranging from 1 to 1000. -and their mixtures. Among the organosiloxanes of formula (XXVIIT), we can cite polydimethyl- carboxy-terminated siloxane (PDMS) such as the compounds sold by the company Momentive under the trade name SILFORM INX (INCI name: Bis-Carboxydecyl dimethicone). Among the organosiloxanes of formula (XXIX), mention may be made of polydimethylsiloxane (PDMS) with a carboxy pendant function such as the compounds sold by the company Shin Etsu under the trade name X-22-3701E. Among the organosiloxanes of formula (XXX), mention may be made of polydimethylsiloxane (PDMS) with a carboxy terminal function such as the compounds sold by the company Shin Etsu under the trade name X-22-3710. Among the organosiloxanes of formula (XXXI), we can cite the compounds sold by the company Grant Industries under the trade name Grandsil SiW-PCA-10 (INCI name: Dimethicone (and) PCA Dimethicone (and) Butylene Glycol (and) Decyl Glucoside). The silicone compounds comprising a carboxylic group may, for example, correspond to the compounds described in patent application EP186507 in the name of Chisso Corporation introduced here by reference. Preferably, the silicone compound(s) comprising at least one carboxylic group are chosen from organopolysiloxanes of formula (XXVIII), organopolysiloxanes of formula (XXIX) and mixtures thereof. More preferably, the silicone compound(s) comprising at least one carboxylic group are chosen from organopolysiloxanes of the following formula (XXVIII): (XXVITD nor TR Ri | | $ 4 MOOC— Rd $8-——D je Stoe—0 = Juan move Re COHOM t To q 10 Ra ge êt L da in which: - R1 independently represents a linear or branched alkyl group having from 1 to 20 carbon atoms, preferably from 1 to 10 carbon atoms, even better from 1 to 6 carbon atoms; preferably methyl; - R4 independently represents a linear or branched alkylene group, having from | to 20 carbon atoms, preferably from 4 to 16 carbon atoms, optionally interrupted by at least one heteroatom chosen from the sulfur atom, the nitrogen atom, the oxygen atom and their mixtures; or a divalent group R,(OR;),- with R, representing a linear or branched alkylene group, having from 1 to 4 carbon atoms, R, representing an alkylene group having from 1 to 4 carbon atoms, and x being an integer ranging from 1 to 200: - M independently represents a hydrogen atom, an alkali or alkaline earth metal or a quaternary ammonium NR°4, with R° identical or different, representing H or an alkyl having from 1 to 4 carbon atoms; - n denotes an integer ranging from 1 to 1000. Advantageously, the total quantity of silicone compound(s) comprising at least one carboxylic group ranges from 0.01 to 20% by weight, preferably from 0.1 to 15% by weight, more preferably from 0.5 to 10% by weight, better still from 1 to 5% by weight relative to the total weight of composition D. Oils Composition D may comprise one or more oil(s) different from the silicone compounds comprising at least one carboxylic group previously described. Preferably, composition D comprises one or more oil(s). More preferably, composition D comprises one or more oil(s) chosen from alkanes. The term "oil" means a fatty substance that is liquid at room temperature (25°C) and atmospheric pressure (760 mm Hg or 1.013 105 Pa). Oil can be volatile or non-volatile. "Volatile oil" means an oil that is capable of evaporating upon contact with the skin in less than one hour at room temperature and atmospheric pressure. Volatile oil is a volatile cosmetic oil that is liquid at room temperature. More specifically, a volatile oil has an evaporation rate of between 0.01 and 200 mg / cm? / min, inclusive. By "non-volatile oil" we mean an oil remaining on the skin or keratin fiber at room temperature and atmospheric pressure. More precisely, a non-volatile oil has an evaporation rate strictly less than 0.01 mg / cm2 / min. Preferably, the composition comprises one or more oil(s) chosen from C1-C5 alkanes and / or mixtures thereof. As for Cs-Cs alkanes, these can be linear, branched, possibly cyclic. Examples include branched Cs-C,5 alkanes such as isoalkanes (also called isoparaffins) in Cs-C5, isododecane, isodecane, isohexadecane and for example oils sold under the trade names Isopars or Permetyls, and their mixtures. We can also cite linear alkanes, preferably of plant origin, comprising from 7 to 15 carbon atoms, in particular from 9 to 14 carbon atoms, and more particularly from 11 to 13 carbon atoms. Examples of linear alkane suitable for the invention include n-heptane (C7), n-octane (C8), n-nonane (C9), n-decane (C10), n-undecane (C11), n-dodecane (C12), n-tridecane (C13), n-tetradecane (C14), -pentadecane (C15), and mixtures thereof, and in particular the mixture of n-undecane (C11) and n-tridecane (C13) described in example 1 of application WO2008 / 155059 from Cognis. We can also mention n-dodecane (C12) and n-tetradecane (C14) sold by Sasol respectively under the references PARAFOL 12-97 and PARAFOL 14-97, as well as their mixtures. As examples of alkanes suitable for the invention, mention may be made of the alkanes described in patent applications WO 2007 / 068371 and WO2008 / 155059. These alkanes are obtained from fatty alcohols, themselves obtained from copra or palm oil. According to a particular embodiment, the composition comprises isododecane. Such a compound is, for example, isododecane sold under the reference ISO-DODECANE by INEOS. Preferably, composition D comprises one or more oil(s) chosen from Cs-Cy5 alkanes, more preferably from isododecane, isohexadecane, tetradecane and / or mixtures thereof. More preferably, composition D comprises isododecane. Composition D may comprise one or more oils different from the silicone compounds comprising at least one carboxylic group present in a total amount of between 30% and 99% by weight, preferably between 50% and 99% by weight, better still between 70% and 99% by weight relative to the total weight of composition D. Composition D may comprise at least one coloring agent chosen from pigments, direct dyes, and their mixtures as described previously. Protocol The treatment with composition T comprising at least one alkaline agent as defined above can be carried out on dry or damp hair, as well as on all types of hair, light or dark, natural or colored, permed, bleached or straightened. According to a particular embodiment of the invention, the hair is rinsed with water or washed after treatment with an alkaline agent as defined above. Preferably, a washing or rinsing, spinning or drying step is carried out after the treatment with a composition T comprising at least one alkaline agent as defined previously. More preferably, a drying step is implemented after the treatment. with an alkaline agent as defined above. Treatment with an alkaline agent as defined above can be carried out at room temperature (between 15 and 25°C). After treatment with an alkaline agent as defined above, one can wait between 1 minute and 6 hours, in particular between 1 minute and 2 hours, more particularly between 1 minute and 1 hour, more preferably between 1 minute and 30 minutes, before applying composition C to the hair. Preferably, the exposure time is between 1 minute and 20 minutes before applying composition C to the hair. Composition Ç and possible composition D described above can be used on dry or damp hair, as well as on all types of hair, light or dark, natural or colored, permed, bleached or straightened. According to a preferred embodiment, composition C and optional composition D are applied simultaneously to the hair, According to another preferred embodiment, composition D is applied to the hair after the application of composition C to the hair. According to another preferred embodiment, composition D is applied to the hair before applying composition C to the hair. More preferably, composition D is applied to the hair after applying composition C to the hair. Preferably, a rinsing, wringing and / or drying step is carried out after the application of composition C to the hair and before the application of composition D to the hair. More preferably, a drying step is carried out after the application of composition C to the hair and before the application of any composition D to the hair. Application to hair can be carried out by any conventional means, in particular by means of a comb, brush, sponge or fingers. The application of composition C and possible composition D to the hair is generally carried out at room temperature (between 15 and 25°C). After applying composition C to the hair, one can wait between 1 minute and 6 hours, in particular between 1 minute and 2 hours, more particularly between 1 minute and 1 hour, more preferably between 1 minute and 30 minutes, before for example applying composition D to the hair or for example a drying step. Preferably, there is no exposure time after applying composition C to the hair and before applying any composition D to the hair. After applying composition C and any composition D, the hair can be left to dry or dried, for example at a temperature greater than or equal to 30°C. The method according to the invention can thus comprise a step of applying heat to the keratin fibers using a heating tool. The heat application step of the method of the invention can be carried out using a helmet, a hair dryer, a straightening or curling iron, a climazon, Preferably, the heat application step of the method of the invention is carried out using a hair dryer. When the method of the invention implements a step of applying heat to the hair, the step of applying heat to the hair takes place after the application of composition C and optional composition D to the hair. During the heat application stage on the hair, a mechanical action on the strands can be exerted such as combing, brushing, or passing the fingers through. When the step of applying heat to the hair is carried out using a helmet or a hair dryer, the temperature is preferably between 30 and 110°C, preferably between 50 and 90°C. When the step of applying heat to the hair is carried out using a straightening iron, the temperature is preferably between 110 and 220°C, preferably between 140 and 200°C. In a particular variant, the method of the invention implements a step (cl) of applying heat using a helmet, a hair dryer or a climazon, preferably a hair dryer and a step (c2) of applying heat using a straightening or curling iron, preferably a straightening iron. Step (c!) can be done before step (c2). During step (cl), also called the drying step, the hair may be dried, for example at a temperature greater than or equal to 30°C. According to a particular embodiment, this temperature is greater than 40°C. According to a particular embodiment, this temperature is greater than 45°C and less than 110°C. Preferably, if the hair is dried, it is dried with airflow in addition to heat. This airflow during drying helps improve the individualization of the sheathing. During drying, mechanical action can be applied to the strands, such as combing, brushing, or passing the fingers through them. During step (c2), the passage of the straightening or curling iron, preferably the straightening iron, can be carried out at a temperature ranging from 110 to 220°C, preferably between 140 and 200°C. After the heating step, a shaping step can be carried out with, for example, a hair straightener, the temperature for the shaping step is between 110 and 220°C, preferably between 140 and 200°C. Preferably, the invention is a hair coloring process comprising the following steps: (i) a step consisting of treating the hair with a composition T comprising at least one alkaline agent as defined previously, then (ii) optionally a time for leaving said composition T on the hair which may range from 1 minute to 30 minutes, preferably from 1 to 20 minutes; then (iii) a step consisting of applying to the hair at least one coloring composition C comprising: 1. at least one (poly)carbodiimide compound as defined previously; 2, at least one coloring agent as defined previously. (iv) optionally a time for leaving said composition C on the hair of 1 minute to 30 minutes, preferably 1 to 20 minutes; then (v) optionally a step of washing, rinsing, wringing and / or drying said hair, then (vi) optionally the application to the hair of at least one composition D comprising at least one silicone compound comprising at least one carboxylic group as described previously; then (vit) optionally a time for leaving said composition D on the hair of 1 minute to 30 minutes, preferably 1 to 20 minutes; then (viii) optionally a step of washing, rinsing, wringing and / or drying the hair. More preferably, the invention is a hair coloring process comprising the following steps: (i) a step consisting of treating the hair with a composition T comprising at least one alkaline agent as defined previously, then (ii) optionally a time for leaving said composition T on the hair which may range from 1 minute to 30 minutes, preferably from 1 to 20 minutes; then (ii) optionally a step of washing, rinsing, wringing and / or drying said hair; then (iii) a step consisting of applying to the hair at least one coloring composition C comprising: 1. at least one (poly)carbodiimide compound as defined previously; 2 at least one coloring agent as defined previously. (iv) optionally a time for leaving said composition C on the hair of 1 minute to 30 minutes, preferably 1 to 20 minutes; then (v) optionally a step of washing, rinsing, wringing and / or drying said hair, then (vi) optionally the application to the hair of at least one composition D comprising at least one silicone compound comprising at least one carboxylic group as described previously; then (vii) optionally a time for leaving said composition D on the hair of 1 minute to 30 minutes, preferably 1 to 20 minutes; then (viii) optionally a step of washing, rinsing, wringing and / or drying the hair. Preferably, composition C further comprises at least one compound having at least one carboxylic function, as described previously. Advantageously, the coloring process comprises step (vi) of applying to the hair a composition D comprising at least one silicone compound comprising at least one carboxylic group as described previously. Preferably, the step of applying composition C to the hair is repeated several times. Advantageously, in the coloring process according to the invention, step (ii) consists of mixing extemporaneously at the time of use at least two compositions A and B to obtain a composition C and applying composition C to the hair, with: - composition A comprising (1) at least one (poly)carbodiimide compound as defined previously; - composition B comprising (2) at least one coloring agent as defined previously. According to a preferred embodiment, the coloring process according to the invention is a hair coloring process comprising: (i) a step consisting of treating the hair with a composition T comprising at least one alkaline agent as defined previously, then (it) a step consisting of mixing extemporaneously at the time of use at least two compositions A and B to obtain a composition C and applying composition C to the hair, with: - composition A comprising (1) at least one (poly)carbodiimide compound as defined previously; - composition B comprising (2) at least one coloring agent as defined previously; composition A and / or composition B optionally comprising at least one compound having at least one carboxylic function, as described previously. Advantageously, the coloring process further comprises the application to the hair of at least one composition D comprising at least one silicone compound comprising at least one carboxylic group as described above, said composition D being applied to the hair before and / or after the application of composition C to the hair, preferably said composition D being applied after the application of composition C to the hair. Preferably, composition A does not comprise a coloring agent as defined previously. According to this embodiment, compositions A and B are preferably mixed less than 15 minutes before application to the hair, more preferably less than 10 minutes before application, better still less than 5 minutes before application. The weight ratio between composition A and composition B preferably ranges from 0.1 to 10, preferably from 0.2 to 5, better still from 0.5 to 2, or even from 0.6 to 1.5. In a particular embodiment, the weight ratio between composition A and composition B is equal to 1. According to a particular embodiment, the coloring process according to the invention is a hair coloring process comprising: (i) a step consisting of treating the hair with a composition T comprising at least one alkaline agent as defined previously, then (ii) a step consisting of extemporaneously mixing at the time of use at least two compositions A and B to obtain a composition C and applying composition C to the hair, with: - composition A comprising (1) at least one (poly)carbodiimide compound as defined previously; - composition B comprising (2) at least one coloring agent as defined previously; composition A and / or composition B optionally comprising at least one compound having at least one carboxylic function, as described previously, and - the application to the hair of at least one composition D comprising at least one silicone compound comprising at least one carboxylic group as described previously, said composition D being applied to the hair before and / or after the application of composition C to the hair. The total amount of the (poly)carbodiimide compound(s) preferably ranges from 0.01 to 40% by weight, more preferably from 0.1 to 30% by weight, better still from 0.5 to 20% by weight, even more preferably from 1 to 15% by weight relative to the total weight of composition A. The total amount of the compound(s) having at least one carboxylic function preferably ranges from 0.2 to 60% by weight, more preferably from 1 to 40% by weight, better still from 1 to 30% by weight, and even more preferably from 2 to 25% by weight. weight relative to the total weight of composition B. The total quantity of the aqueous dispersion(s) of polymer particles chosen from polyurethanes, acrylic polymers, and their mixtures preferably ranges from 0.2 to 60% by weight, more preferably from 1 to 50% by weight, better still from 1 to 40% by weight, and even more preferably from 2 to 30% by weight relative to the total weight of composition B. According to a particular embodiment, the total quantity of the aqueous dispersion(s) of acrylic polymer particles preferably ranges from 0.2 to 60% by weight, more preferably from 1 to 50% by weight, better still from 1 to 40% by weight, and even more preferably from 2 to 30% by weight relative to the total weight of composition B. Multi-compartment device (kit) The present invention also relates to a device for coloring hair comprising several compartments containing: * in a first compartment, a composition T comprising at least one alkaline agent as defined previously, and #* in a second compartment, a composition C comprising: (1) at least one (poly)carbodiimide compound as defined above, (2) at least one coloring agent as defined above, and * optionally, in a third compartment, a composition D comprising at least one silicone compound comprising at least one carboxylic group as described previously. The present invention also relates to a device for coloring hair comprising several compartments containing: * in a first compartment, a composition T comprising at least one alkaline agent as defined previously, # in a second compartment, a composition A comprising at least one (poly)carbodiimide compound as defined previously, # in a third compartment, a composition B comprising at least one coloring agent as defined previously, and # optionally, in a fourth compartment, a composition D comprising at least one silicone compound comprising at least one carboxylic group as described previously. Composition A and / or composition B, preferably composition B, may optionally further comprise at least one compound having at least one carboxylic function, as described previously. The present invention will now be described more specifically by way of examples, which are in no way limiting of the scope of the invention. However The examples are provided to support specific features, variations, and preferred embodiments of the invention. EXAMPLES The (poly)carbodiimide(s) of the invention are accessible by synthesis methods known to those skilled in the art from commercial products or reagents that can be synthesized according to chemical reactions also known to those skilled in the art. Examples include the work Sciences of Synthesis — Houben — Weyl Methods of Molecular Transformations, 2005, Georg Thiem Verlag Kg, Rudigerstrasse 14, D-70469 Stuttgart, or American patent US 4,284,730 or Canadian application CA 2,509,861. More particularly, the process for preparing the (poly)carbodiimides of the invention uses, in a first step, a diisocyanate reagent (1): O=C=NL,-N=C=0 (1), formula (1) in which L, is as defined above which reacts in the presence of a carboimidation catalyst (2) such as those described in US 4,284,730 in particular phosphorus catalysts particularly chosen from phospholene oxides and phospholene sulfoxides, diaza and oxazaphospholanes, preferably under an inert atmosphere (nitrogen or Argon), and in particular in a polar solvent, preferably aprotic, such as THF, glyme, diglyme, 1,4-dioxane, and DMF, at a temperature between room temperature and solvent reflux, preferably around 140°C; to yield the carbodiimide diisocyanate compound (3): O=C=EN-L,-{N=C=NL,),-N=C=0 (3), formula (3) in which Ly and n are as defined above. Halogenated benzoyl such as benzoyl chloride may be added to deactivate the catalyst. To obtain “symmetrical” (poly)carbodiimides, during the second step of the preparation process, compound (3) reacts with 1 molar equivalent (1 eq) of nucleophilic reagent R,-X,-H, then 0.5 eq. of HEH reagent with R,, X, and E as defined previously, to lead to the “symmetrical” compound according to the invention (4): [R,-X,-C(0)-NH-L,-(N=C=NL;),-NH-C(O)]--E (4), formula (4) in which R;, X;, L;, n, and E are as defined previously. According to a variant to obtain compound (4) from (3) it is possible to first add 0.5 eq. of HEH reagent, then 1 eq. of R,-X,-H reagent. To obtain “asymmetric” (poly)carbodiimides, during the second step of the preparation process, compound (3) reacts with 1 molar equivalent (1 eq) of nucleophilic reagent R,-X,-H then 1 eq. of HEH reagent with R,, X, and E as defined previously, to lead to compound (5): R,-X,-C(0)-NH-L,-(N=C=NL,),-_NH-C(O)-EH (5), formula (5) in which R,, X,, L;, n, and E are as defined previously. According to a variant to obtain compound (5) from (3) it is possible to first add 1 eq. of reagent R,-X,-H, then 0.5 eq. of reagent HEH. In a third step, compound {5) reacts with 1 eq. of compound (6) R2-X,-C(O)-NH-L,-(N=C=NL,),-N=C=0 (6), said compound (6) is prepared beforehand from compound (3°): O=C=EN-L,-{N=C=NL,),-N=C=0 (3). formula (3”) in which L, and z are as defined previously which reacts with 1 eq of nucleophilic reagent R,-X,-H with L;, Ra, X, and z as defined previously, to lead to the asymmetric compound (7): Ry-X,-C(O)-NH-L,-(N=C=NL,),-NH-C(O)-EC(O)-NH-L,--(N=C=NL,) NH-C(O) -X,-R> (7), Formula (7) in which R,, X,, L;, Ra, X2, N, Z and E are as defined previously. It is also possible to react 1 molar equivalent of compound O=C=NL, - (N=C=NL;),-N=C=0 (3°) with 1 / w molar equivalent of HEH, then 1 eq. of nucleophilic reagent R,-X;-H to lead to compound (8): H-[EC(O)-NH-L,-(N=C=EN-L;),]|,-NH-C(O)-X--R (8), formula (8) in which L;, Ra, X2, Z and E are as defined previously, and w is an integer between | to 3, more preferably w = 1. This last compound (8) can then react with the eq of compound (4): Ry-X,-C(O)-NH-L,-(N=C=NL;),-N=C=0 (4°), (said compound (4') can be synthesized by reaction of 0.5 eq. of nucleophilic reagent R,-X,-H with 1 equivalent of compound (3)), to lead to the (poly)carbodiimide of the invention (9): Ry-X1-C(0)-NH-L;-(N=C=NL,),-NH-C(O)-[EC(O)-NH-L,-(N=C=N-L1):]y-NH C(O)-X,-R, (9), formula (9) in which L;, R:, X1, Ra, X2, N, Z, wW, and E are as defined previously. The (poly)carbodiimide compounds as well as all reaction intermediates and reagents can be purified with conventional methods known to those skilled in the art, such as extraction with water and water-immiscible organic solvent, precipitation, centrifugation, filtration, and / or chromatography. Example 1: Process for the synthesis of the compound (poly)carbodiimide In a 500 mL three-necked flask equipped with a thermometer, a stirrer and a reflux tube, 50 g of dicyclohexylmethane 4,4"-diisocyanate and 0.5 g of 4,5-dihydro-3-methyl-1-phenyl-1H-phosphole 1-oxide were introduced with stirring. The reaction medium was heated to 140°C under nitrogen for 4 hours, following the reaction by infrared spectroscopy through the absorption of the isocyanate functions. between 2200 and 2300 cmr!, then cooled to 120°C. A mixture of 5.3 g of polyethylene glycol monomethyl ether and 1.2 g of 1,4-butanediol is introduced into the reaction medium with stirring. The temperature of 120°C is maintained until the isocyanate functions have completely disappeared, monitored by infrared spectroscopy at 2200-2300°C, and then cooled to room temperature. After cooling to room temperature, the reaction medium is poured dropwise with vigorous stirring into a 500 mL glass beaker containing 85 g of distilled water to yield the desired product in the form of a translucent yellow liquid. Example 2 Compositions A and B as described below were prepared: the quantities are expressed in g of raw material as is / 100g, unless otherwise stated. [Tables 1] 0.75 Compositions ja Polycarbodiimide '> 14 pre (and) Trideceth-5 (and) |s Amodimethicone (and) Trideceth-10 Preservatives _Jo75 Water —|asp 1 qsp 100 1. synthesized according to the synthesis process described in example 1 (at 40% material active in cau), 2. sold by the company WACKER under the name BELSIL ADM LOG 1 (at 15% active ingredient) [Tables 2] 0.35 Composition Acrylates copolymer Red iron oxide (CI 77491) Amodimethicone (and) Trideceth-5 (and) Amodimethicone (and) Trideceth-10 @ Preservatives Water qsp 100 l sold by the company DAITO KASEI KOGYO under the name com- commercial DAITOSOL 3000SLPN-PE1 (aqueous dispersion with 30% material active) Composition A was then mixed with composition B at a mass ratio of 50 / 50 to obtain a composition C according to the invention. Then, composition D as described below was prepared: the quantities are expressed in g of raw material as is / 100g. [Tables 3] Jp 8 Organopolysiloxane composition with carboxylic group '9 Isododecane qsp 100 1. Silform INX sold by the company Momentive Performance Materials Pre-treatment with a composition comprising an alkaline agent: Before applying any other composition, certain strands are pre-treated with one of the alkaline agents below: the quantities are expressed in g of raw material as is / 100g. unless otherwise stated. [Tables 4] (m2 Compositions re m2 Diguanidinium carbonate © |1 | Hydroxylamine 6 - | [Water qsp 100 qsp 100 l. sold by the company Borealis (CAS: 593-85-1) 2. sold by the company Sigma-Aldrich under the reference 255580 (CAS: 5470-11-1) Protocol When a treatment step with a composition T comprising at least one alkaline agent as defined previously is carried out, the following protocol was applied: a treatment with a composition T comprising at least one alkaline agent as defined above is carried out on locks of 90% white natural hair, at a rate of 2 g of composition per gram of lock. The treatment is left to act for a period of 15 minutes, at a temperature of 35°C. Then the locks are rinsed with water before being dried with a hairdryer. Composition C is then applied to the treated strands, at a rate of 0.5 g of composition per gram of strand. The hair strands are then dried with a hairdryer. Then, composition D was applied to the strands of hair previously treated with the alkaline agent and composition Ç, at a rate of 0.5 g of composition per gram of strand. Then, the strands of hair are dried with a hair dryer. The hair strands were then stored at room temperature for 24 hours. Three processes 1 to 3 were applied and were summarized in Table 5 below: [Tables 5] [Processes 1 2 3 (invention) |(invention) (comparative) [Treatment with a YES YES NO |T1 +C+D T2 +C+D |c+D Treatment with an alkaline agent Application of the compositions Thus, the locks of hair treated with compositions TI or T2 then C and D are treated by methods 1 and 2 according to the invention. The hair strands treated with compositions C and D only are treated with comparative process 3. The locks of hair treated by processes 1 to 3 were then subjected to a test of several repeated shampoos in order to evaluate the tenacity (the persistence) of the coloring obtained from the shampoos. Results The color persistence of the highlights was evaluated in the CIE L*a*b* system, using a Minolta CM3610A spectrophotometer (illuminant D65, angle 10°, specular component included). In this L*a*b* system, L* represents the color intensity, a* indicates the green / red color axis, and b* the blue / yellow color axis. Color persistence is assessed by the color difference AE,émanenceé between the colored strands before shampooing, then after undergoing 15 shampoos. The lower the value of AE,émanence €St, the more the color persists after shampooing. The value of AEremanence€St calculated according to the following equation: # 62 412 AE emanation = ((L*-Lo*) + (a*-a0*)"+ (b°-bo*) In this equation, L*, a* and b* represent the values ​​measured after hair coloring and after shampooing, and Lo*, ao* and bo* represent the values ​​measured after hair coloring but before shampooing. [Tables 6] |Processes [Number of |L+ [a | 1 (invention) Number of |L* Eu [b* [AE shampoos Jo 33.04 [25.57 |19.66 [17.15 15 46.68 |15.97 |15.69 [2 (invention) po 32.26 25.87 |19.83 16.00 [15 43.91 |16.65 |13.89 | |3 (comparative) |o [83.91 [25.98 [20.1 [26.59 [15 [53.88 [9.28 |14.68 | The hair strands treated with the methods | and 2 according to the invention and washed with fifteen shampoos have a higher persistence than that of the hair strands treated with the comparative method 3. Thus, the colored coating obtained with the methods according to the invention has improved persistence to shampooing.

Claims

Claims

1. A method of coloring hair comprising: (1) a step of treating the hair with a composition T comprising at least one alkaline agent chosen from alkaline agents minerals, which are chosen from alkali metal phosphates or alkaline earth, mineral hydroxides, silicates or meta- alkali or alkaline earth metal silicates, hydroxylamine, ammonia and their mineral and / or organic salts; agents organic alkalis, their mineral and / or organic salts, and their mixes, then (ii) a step of applying to the hair at least one com- coloring position C including: at least one (poly)carbodiimide compound; and 2. at least one coloring agent chosen from pigments, direct dyes and their mixtures.

2. Method according to claim !, characterized in that the agent(s) alkali(s) are chosen from sodium hydroxide, sodium hydroxide calcium, hydroxylamine, hydroxylamine hydrochloride, guanidine, 1,1,3,3-tetramethylguanidine, digua carbonate- nidinium, guanidinium hydroxide, and mixtures thereof, more preferably- partly among sodium hydroxide, calcium hydroxide, hydroxylamine, hydroxylamine hydrochloride, di-carbonate guanidinium, guanidinium hydroxide, and mixtures thereof.

3. A method according to claim | or 2, characterized in that the alkaline agent(s) are present in a content of 0.05% to 15% by weight, preferably from 0.05% to 10% by weight, more preferably from 0.1% at 10% by weight, better from 0.1% to 7% by weight, even better from 0.5% to 5% by weight relative to the total weight of composition T.

4. Method according to any one of the preceding claims, ca- characterized in that the (poly)carbodiimide compound(s) is (are) chosen from the compounds of formula (I) following: (D 9% THERE Re XF pa sCroeN oATSN DXa—Ra in which: - X, and X; represent, independently, an oxygen atom O, a sulfur atom S or an NH group; - R, and R, independently represent a group chosen from a hydrocarbon radical, preferably alkyl, optionally interrupted by one or more heteroatom(s), a group chosen from alkoxysilyl, hydroxysilyl, acetoxysilyl, vinylsilyl, acrylalkylsilyl, methacrylalkylsilyl, crotonylalkylsilyl, carboxyanhydridoalkylsilyl, carboxyalkylsilyl, hydroxyalkylsilyl, aldehydoalkylsilyl, mercaptoalkylsilyl, norbornenylsilyl, acylpentadienylalkylsilyl, maleimidoalkylsilyl, sulphonylalkylsilyl, (meth)acrylalkyl, crotonylalkyl, alkylepoxide such as propylepoxide or butylepoxide, and azacyclopropane, and a hydrocarbon radical, preferably alkyl, optionally interrupted by one or more heteroatom(s) and by one or more groups chosen from alkoxysilyl, hydroxysilyl, acetoxysilyl, vinylsilyl, acrylalkylsilyl, methacrylaalkylsilyl, crotonylalkylsilyl, carboxyanhydridoalkylsilyl, carboxyalkylsilyl groups,hydroxyalkylsilyl, aldehydoalkylsilyl, mercaptoalkylsilyl, norbornenylsilyl, acylpentadienylalkylsilyl, maleimidoalkylsilyl, sulphonylalkylsilyl, (meth)acrylalkyl, crotonylalkyl, alkylepoxide such as propylepoxide or butylepoxide, and azacyclopropane; - n denotes an integer ranging from 1 to 1000; and, - A is a monomer chosen from the compounds below: L * *.j sf 4 .f * > , 4, ena d SÉR ESS f=t-dD 'it-ta6 tr-tog L + x father . 8 RELL A CA = + see st a resumé ap” ss Bridge * eds Re LT UN me ; ; - ADS Se, OS ESS VTT CT; ; RS TS; CUT TS Ï % Serves art rt 7 Fc dead sat LD Ÿ y Ÿ Se Sais AS Sa” Ksr NL Ka ti fi CT A Le ; t SF tt ia Pi , TN CD CUT CO SLaF KP RP NI TT É PS [Claim Method according to any one of claims 1 to 3, characterized in what the (poly)carbodiimide compound(s) is (are) chosen among the compounds of formula (II) following: e among the compounds of formula (II) following: 8 Fe AN CR ph 5 za; 3 at 5 Vu 8 HA 25% 29 F NF % Li % tr À Ry (year in which: - X, and X» represent, independently, an oxygen atom O, a sulfur atom S or an NH group; - R, and R independently represent a hydrocarbon radical, even- permanently interrupted by one or more heteroatom(s); - net z denote an integer ranging from 1] to 20, with n+z > 2 and w denotes a centicr number ranging from 1 to 3; - L, independently represents an aliphatic hydrocarbon radical divalent C,-C;;, A C7-C;s cycloalkylene radical, a group C;-C; heterocycloalkylene, or a C5-C;4 arylene group, and their mixtures; - E independently represents a group chosen from: -OR--O-; -S-R4-S-; -Rs-N(R6)-R4-N(Rç)-Rs-, in which R; and R4 independently represent a hy- radical divalent carbon possibly interrupted by one or more he- teratom(s); - Rs independently represents a covalent bond or a hy- radical divalent saturated carbon, possibly interrupted by one or several heteroatom(s); - Rs independently represents a hydrogen atom, or a radical hydrocarbon possibly interrupted by one or more he- teratom(s).

6. Method according to claim 5, characterized in that the (poly)carbodiimide compound(s) is (are) chosen from compounds of formula (II) in which: - X, and X, independently represent an oxygen atom; - R, and R,, are independently chosen from dialkylaminoalcohols, hydroxycarboxylic acid alkyl esters and monoalkyl ethers (poly)alkylene glycol alkyls, in which a hydroxy group was removed, and their mixtures; -netz denotes an integer from 1 to 20, with n+z > 2 and w is equal to 1; - LI] is chosen from a divalent aliphatic hydrocarbon radical in C; -Cys, a C7-C cycloalkylene radical;«, a heterocy- group C1-C3 alkylene, OR a Ce-Cy;4 arylene group, and their mixtures; - E independently represents a group chosen from: - -OR,-0-; -S-R4-S-; -Rs-N(R6)-R4-N(R5)-Rs-; in which R3 and R4 are independently chosen from a radical Cs-C;4 arylene, A C4-C;2 cycloalkylene radical, a radical linear or branched C,-Cys alkylene, optionally interrupted by a or more heteroatom(s), and mixtures thereof; - when Rs is not a covalent bond, Rs is chosen from a Cs-C,4 arylene radical, A C;-C;2 cycloalkylene radical, A radical linear or branched C,-C,3 alkylene, optionally interrupted by a or more heteroatom(s), and mixtures thereof; and - R, is chosen from a Cs-Cs arylene radical;4, A cy- radical C-C alkylene A linear or branched C,-C alkylene radical;8, possibly interrupted by one or more heteroatom(s), and their mixtures.

7. Method according to claim 5 or 6, characterized in that the (poly)carbodiimide compound(s) is (are) chosen from compounds of formula (IT) in which: - X, and X, independently represent an oxygen atom; - R, and R, are independently monoalkyl ethers of (poly)alkylene glycol, in which a hydroxy group has been removed; - net z denote an integer ranging from 1] to 20, with n+z = 2 and w is equal to 1; - L, is a C3-C15 cycloalkylene radical; - E independently represents a group chosen from: -O-R4,-0-; -SR,-S-; -Rs-N(R5)-R4-N(R5)-Rs-: in which R; and R4 are independently chosen from a radical C;-C;4 arylene, A C+-C,, cycloalkylene radical, a radical linear or branched C,-C; alkylene, optionally interrupted by a or more heteroatom(s), and mixtures thereof; - when Rs is not a covalent bond, Rs; is chosen from a C5-C4 arylene radical, A Cz-C2 cycloalkylene radical, a radical linear or branched C,-C; alkylene, optionally interrupted by a or more heteroatom(s), and mixtures thereof; and - R, is chosen from a Ce-C arylene radical;4, A cy- radical C1-C13 alkylene radical, linear or branched, possibly interrupted by one or more heteroatom(s), and their mixtures.

8. Method according to any one of claims 5 to 7, characterized in what the (poly)carbodiimide compound(s) is (are) chosen among the compounds of formula (II) in which: - X, and X, independently represent an oxygen atom; - R, and R>, independently represent the compound of formula (VI) next: R1>-[O-CH-C(H(R14)la VD, in which R;; represents a C,-C, alkyl group, or a phenyl, preferably a C1-C10 alkyl group, more preferably a methyl, R,4 represents a hydrogen atom or a C,-alkyl group C4, preferably a hydrogen atom and q denotes an integer ranging from 4 to 30; - net z denotes an integer ranging from 1 to 20, with n+z ranging from 4 to 10 and west equal to 1; - L, is a C;-Cy5 cycloalkylene radical such as cyclopentylene, cyclo- heptylene, cyclohexylene and 4,4-dicyclohexylene methane, and - E represents a group -OR,-O- in which R; is chosen from a Cs-C;4 arylene radical, a C;-C;> cycloalkylene radical, a linear or branched C,-C;3 alkylene radical, optionally in- interrupted by one or more heteroatom(s), and mixtures thereof.

9. Method according to any one of claims 5 to 8, characterized in what the (poly)carbodiimide compound(s) is (are) chosen among the compounds of formula (IT) in which: - X, and X» independently represent an oxygen atom; - R, and R,, independently represent the compound of formula (VI) next: R13-[O-CH,-C(H(R;4)]e- (VD, in which R;; represents a C,-C, alkyl group, or a phenyl, preferably a C1-C10 alkyl group, more preferably a methyl, R,; represents a hydrogen atom or a C alkyl group 1-C4, preferably a hydrogen atom and q denotes an integer ranging from 4 to 30; -netz denotes an integer ranging from 1 to 20, with n+z ranging from 4 to 10, and w is equal to 1; - L, is a Cz-Cs cycloalkylene radical such as cyclopentylene, cycloheptylene, cyclohexylene and 4,4-dicyclohexylene methane, preferably 4,4-dicyclohexylene methane; and - E represents a group -O-R3-O- in which R; represents a linear or branched C;-C; alkylene radical; such as methylene, propylene, butylene, ethylene, possibly interrupted by one or several heteroatom(s).

10. Method according to any one of claims 5 to 9, characterized in what the (poly)carbodiimide compound(s) is (are) chosen among the compounds of formula (XII) following: spé * ox Sat, NH se draws e NF ut 2 Sn The NH a pa ao À SN * mo 5 Hu THE F0 $ > (XI), in which L, is 4,4-dicyclohexylene methane, n and z denote a integer ranging from | to 20, with n+z ranging from 4 to 10, E represents a group- -OR;-O- in which R; represents an alkylene radical linear or branched C,-C;; such as methylene, propylene, butylene ethylene, possibly interrupted by one or more heteroatom(s), etret s denote an integer ranging from 4 to 30.

11. | A method according to any preceding claim, ca- characterized in that the total quantity of the compound(s) (poly)carbodiimide(s) ranges from 0.01 to 20% by weight, preferably from 0.1 to 15% by weight, more preferably from 0.2 to 10% by weight, still more preferably from 0.5 to 8% by weight, better still from 1 to 6% by weight relative to the total weight of composition C.

12. A method according to any preceding claim, ca- characterized in that the total quantity of coloring agent(s) ranges from 0.001 at 20% by weight, preferably from 0.005 to 15% by weight relative to the total weight of composition C, preferably the coloring agent(s) are chosen from among the pigments.

13. A method according to any preceding claim, ca- characterized in that it further comprises a step of application on the hair of a composition D comprising at least one compound silicone comprising at least one carboxylic group.

14. Method according to claim 13, characterized in that the quantity total in silicone compound(s) comprising at least one group carboxylic acid ranges from 0.01 to 20% by weight, preferably from 0.1 to 15% by weight. weight, more preferably from 0.5 to 10% by weight, better from | to 5% by weight relative to the total weight of composition D.

15. A method according to any one of claims 1 to 10, 13 and 14 ca- characterized in that step (ii) consists of extemporaneously mixing with at the time of use at least two compositions A and B to obtain a composition C and to apply the composition C on the hair, with - composition A comprising (1) at least one compound (poly)carbodiimide as defined in any one of the claims let4to10; - composition B comprising (2) at least one coloring agent such as defined in claim 1.

16. Device for coloring hair comprising several com- compartments containing: - in a first compartment, a composition T comprising at least less than one alkaline agent as defined in any one of claims 1 to 3, - in a second compartment, a composition A comprising at least one (poly)carbodiimide compound as defined in any one of claims 1 and 4 to 10, - in a third compartment, a composition B comprising at least one coloring agent as defined in claim 1, and - optionally, in a fourth compartment, a composition D comprising at least one silicone compound comprising at least one carboxylic group as defined in claim 13 or 14.