One-component system based on coreactive latexes leading to coatings which are crosslikable at room temperature and post-crosslinkable by heat treatment, and their application in the field of coating

Abstract

The present invention relates to a one-component system based on coreactive latexes which is able to lead to coatings which are crosslinkable at room temperature and post-crosslinkable by heat treatment, the said system consisting of a mixture of two particle dispersions, (A) and (B), each obtained by aqueous emulsion polymerization of a monomer composition A and B, respectively, (a) at least one free-radically polymerizable ethylenically unsaturated monomer comprising a functional group ##STR1## where X represents O or S, which enters into the monomer composition A; and (b) at least one free-radically polymerizable ethylenically unsaturated monomer comprising a masked aldehyde functional group selected from acetal, mercaptal, mercaptol, dioxolane and dithiolane, which enters into the monomer composition B.

Description

FIELD OF THE INVENTION

The present invention relates to a one-component system based on a mixture of coreactive latexes, which leads to coatings which are crosslinkable at room temperature and post-crosslinkable by heat treatment.

BACKGROUND OF THE INVENTION

The coatings industry (paints, adhesives, paper, leather and textile coatings) employs latexes as binders in film-forming formulations which in some cases require post-crosslinking, this being intended to improve the properties of the coatings obtained, especially in terms of their solvent content and their mechanical properties, and to reduce the surface tack, thereby allowing a reduction in the soiling potential in the case of exterior paints.

This step of post-crosslinking must be adapted to the area of application and to the operating conditions (in the field of paints no heat treatment of the coating can be envisaged, whereas the textile industry currently employs processes of thermal crosslinking at temperatures of the order of 160.degree. C.).

Irrespective of the intended application, the objective is to obtain a system which is as reactive as possible at the lowest possible temperature whilst being a one-component system; in other words, one which is ready to use and is stable on storage, these two requirements very often being contradictory.

SUMMARY OF THE INVENTION

The Applicant Company has now discovered latex mixture has now been discovered which is able to meet all of these objectives, since it is stable on storage and leads to films which are crosslinkable at room temperature.

The two latexes which make up the mixture of the invention are functionalized, one by a group of the ureido type and the other by an aldehyde or masked aldehyde group. Following their synthesis, these latexes can be mixed without reaction between their respective abovementioned functions during storage, and in the course of or following coalescence at room temperature they lead to a crosslinked film having properties which are improved with respect to the base latexes, it being possible for the said crosslinking to be activated by a heat treatment.

The discovery of this combination of latexes is all the less obvious since it is not enough that the abovementioned functions react with one another merely during or after coalescence; it is also necessary that the crosslinking kinetics do not disrupt the coalescence of the particles and hence the formation of the film--too great a rate of crosslinking could in fact hamper the formation of the film and render a system unusable.

The American patent U.S. Pat. No. 5,468,800, the International Application WO 95/09896 and the German patent No. 4 439 457 describe the use of an ureido-functional monomer in the synthesis of latexes which lead to films which are crosslinked at room temperature by addition of a polyaldehyde or a polyacetal. Also referred to is the possibility of using copolymerizable aldehydes, such as (meth)acrolein, or masked aldehydes, such as diethoxypropyl acrylate or methacryloyloxypropyl-1,3-dioxolane or N-(1,1-dimethoxybut-4-yl)methacrylamide or acrylamidobutyraldehyde diethyl acetal, these monomers being combined with the ureido monomer in the course of the synthesis of the latex and not in the form of a mixture of the two latexes.

The American patent U.S. Pat. No. 4,918,139 and the European patent 514 654 disclose the use of monomers bearing an alcohol function and an acetal function, of the type CH.sub.2 .dbd.CH--CONH--CHOH--CH(OMe).sub.2, respectively in acrylic copolymers and copolymers comprising ethylene, with a view to obtaining a latex which leads to films which are heat-crosslinkable without releasing formaldehyde, these monomers here replacing the monomers of the N-alkylol(meth)acrylamide type.

In accordance with the present invention, the separate syntheses of the two functionalized latexes make it possible to preserve each of the functions optimally, the polymerization temperature generally being greater than room temperature, thereby permitting greater effectiveness in post-crosslinking during the coalescence of the film (interdiffusion of the chains, bringing about reaction between the functional groups): in effect, if the two functions are combined in the same latex, there would be precrosslinking, and hence little or no post-crosslinking and perhaps even coalescence problems.

Another advantage lies in the fact that the absence of small reactive molecules capable of diffusing into the particles ensures better stability on storage because, while in the latex state, the stabilizing system of the latex avoids particle contact and hence reaction between the two functions, ureido and aldehyde.

The present invention therefore firstly provides a one-component system based on coreactive latexes which is able to lead to coatings which are crosslinkable at room temperature and post-crosslinkable by heat treatment, the said system consisting essentially of the mixture of two particle dispersions (A) and (B), each obtained by aqueous emulsion polymerization of a monomer composition A and B, respectively,

(a) at least one free-radically polymerizable ethylenically unsaturated monomer comprising a functional group ##STR2## where X represents O or S, which enters into the monomer composition A; and (b) at least one free-radically polymerizable ethylenically unsaturated monomer comprising an aldehyde or masked aldehyde functional group selected from acetal, mercaptal, mercaptol, dioxolane and dithiolane, which enters into the monomer composition B.

The monomers (a) can be selected from those represented by the formulae (I) to (III) below: ##STR3## in which: X represents O or S;

R.sup.1 is a free-radically polymerizable ethylenically unsaturated group; R.sup.2 is a hydrogen atom or a C.sub.1 -C.sub.8 alkyl group; and A is an alkylene chain which has 2 or 3 carbon atoms and can be substituted by lower alkyl and/or hydroxyl and/or C.sub.1 -C.sub.4 alkoxy, and/or which can be interrupted by carbonyl.

The group R.sup.1 above can be selected from the groups: ##STR4## where: R.sup.3 represents hydrogen, 3-alkyloxy-2-hydroxypropyl, vinyl, methacryloyl, acryloyl or methacryloyloxyaceto;

A.sup.1 represents O, NH or NR.sup.4 ; R.sup.4 represents 3-allyloxy-2-hydroxypropyl when R.sup.3 represents 3-allyloxy-2-hydroxypropyl; Alk represents a C.sub.2 -C.sub.8 alkylene chain; and 2-(.beta.-carboxyacrylamido)ethyl.

Examples that may be mentioned of monomers (a) are N-(2-methacryloyloxyethyl)ethyleneurea, N-(2-acryloyloxyethyl)ethyleneurea, N-(methacrylamidomethylene)ethyleneurea, N-(acrylamidomethylene)ethyleneurea, N-(.beta.-methacrylamidoethyl)ethyleneurea, N-(.beta.-acrylamidoethyl)ethyleneurea, N-vinylethyleneurea, N-vinyloxyethylethyleneurea, N-[.beta.-(methacryloyloxyacetamido)ethyl]-N,N'-ethyleneurea, N-[.beta.-(acryloyloxyacetamido)ethyl]ethyleneurea, 1-[2-[[2-hydroxy-3-(2-propenyloxy)propyl]amino]ethyl]-2-imidazolidone, N-methacrylamidomethylurea, N-methacryloylurea, N-(3-[1,3-diazacyclohexan-2-one]propyl)methacrylamide, N-hydroxyethylethyleneurea, N-aminoethylethyleneurea, N-(3-allyloxy-2-hydroxypropyl)aminoethylethyleneurea, N-methacrylaminoethylethyleneurea, N-acrylaminoethylethyleneurea, N-methacryloxyacetoxyethylethyleneurea, N-methacryloxyacetaminoethylethyleneurea and N-di(3-allyloxy-2-hydroxypropyl)aminoethylethyleneurea, N-(2-acryloyloxyethyl)ethyleneurea, N-methacrylamidomethylurea and the allylalkylethyleneureas.

A particularly preferred monomer (a) is N-(2-methacryloyloxyethyl)ethyleneurea (1-(2-methacryloyloxyethyl)imidazolin-2-one).

As regards the monomers (b), they can be selected from aldehydes, such as acrolein, methacrolein, formylstyrene, crotonaldehyde and the aldehydes of the formula: ##STR5## and the masked aldehydes of the formula: ##STR6## in which formulae (IVa) and (IVb): R.sup.5 represents a hydrogen atom or a methyl radical;

R.sup.6 and R.sup.7 are identical and each represent a C.sub.1 -C.sub.8 -alkyl group or else together form a group --CH.sub.2 --CR.sup.8 R.sup.9 --(CH.sub.2).sub.n -- where n=0 or 1 and R.sup.8 and R.sup.9, which are identical or different, each represent a hydrogen atom or a methyl group; E represents O, NH or NR' (R'=C.sub.1 -C.sub.4 alkyl); G represents a C.sub.1 -C.sub.4 alkylene radical or a radical ##STR7## where R.sup.10 represents a hydrogen atom or a C.sub.1 -C.sub.4 alkyl radical.

The preferred monomers (b) can be selected from:

the N-(2,2-dialkoxy-1-hydroxyethyl)(meth)acrylamides and the N-(1,2,2-trialkoxyethyl)(meth)acrylamides, wherein the term alkoxy signifies C.sub.1 -C.sub.4 alkoxy, such as N-(2,2-dimethoxy-1-hydroxyethyl)acrylamide; N-(2,2-dimethoxy-1-hydroxyethyl)methacrylamide; N-(1,2,2-trimethoxyethyl)acrylamide; N-(1,2,2-trimethoxyethyl)methacrylamide; N-(2,2-dibutoxy-1-hydroxyethyl)acrylamide; N-(2,2-dibutoxy-1-hydroxyethyl)methacrylamide; N-(1,2,2-tributoxyethyl)acrylamide; N-(1,2,2-tributoxyethyl)methacrylamide; 4-acrylamidobutyraldehyde dimethyl or diethyl acetal; methacrylamidoacetaldehyde dimethyl acetal; diethoxypropyl acrylate; diethoxypropyl methacrylate; acryloyloxypropyl-1,3-dioxolane; methacryloyloxypropyl-1,3-dioxolane; and N-(1,1-dimethoxybut-4-yl)methacrylamide.

Preferably, the monomer or monomers (a) and (b) represent from 0.5 to 10% by weight, in particular from 1 to 5% by weight, of the monomer composition A and B respectively. The monomers (a) and (b) can be introduced homogeneously with the other monomers or in compositional gradients which make it possible to obtain products having different densities of functions.

The proportions of the two coreactive latexes according to the present invention are chosen such that the proportion of the polymer (A) is between 5 and 95% by weight, in particular between 25 and 75% by weight, of the polymers (A) and (B), and the proportion of the polymer (B) is between 95 and 5% by weight, in particular between 75 and 25% by weight, of the polymers (A) and (B), the nonvolatiles content of each of the dispersions generally being between 20 and 60% by weight.

In addition, the size of the particles of each of the dispersions (A) and (B) is, in particular, between 50 and 500 nm.

The monomers other than the monomers (a) and (b) of the two particle dispersions (A) and (B) of the invention are not critical provided that the glass transition temperatures (Tg) of the resulting copolymers have been adapted to the intended field of application. The combination of monomers capable of leading to homopolymers having different glass transition temperatures therefore makes it possible to control the glass transition temperature of each of the copolymers obtained, in other words by the combination of monomers leading to high Tg with monomers leading to low Tg, as is well known to the skilled worker.

Examples that may be mentioned of monomers capable of leading to homopolymers having a low Tg are ethyl acrylate, butyl acrylate, 2-ethylhexyl acrylate, nonyl acrylate, vinyl 2-ethylhexanoate, etc.

Examples that may be mentioned of monomers capable of leading to homopolymers having a high glass transition temperature are methyl methacrylate, vinyl acetate, styrene, acrylic acid, methacrylic acid, acrylamide, etc.

The two latexes of the invention are prepared by emulsion polymerization under conditions well known to the skilled worker. Thus the reaction is preferably conducted under an inert atmosphere in the presence of free-radical initiators. The initiator system employed may be a redox system, such as K.sub.2 S.sub.2 O.sub.8, (NH.sub.4).sub.2 S.sub.2 O.sub.8 /Na.sub.2 S.sub.2 O.sub.5, Na.sub.2 SO.sub.3, a thermal system, such as (NH.sub.4).sub.2 S.sub.2 O.sub.8, the amounts used being between 0.2 and 1.0% by weight relative to the total mass of the monomers, preferably between 0.25 and 0.5% by weight.

The emulsion polymerization reaction of the invention is carried out at a temperature which is between 65 and 85.degree. C. and which depends on the nature of the initiator system employed: 65-75.degree. C. for redox systems based on peroxodisulphate and metabisulphite, and 70-85.degree. C. for thermal systems based on peroxodisulphate alone.

The dispersions of the invention are preferably prepared by a semicontinuous process which makes it possible to limit the compositional derivatives which are a result of the differences in reactivity between the various monomers. The monomers are thus generally introduced in the form of a pre-emulsion with a portion of the water and surfactants over a period of time of from 3.5 to 5 hours. It is also useful, if not indispensable, to carry out seeding with from 1 to 15% of the monomers. The emulsifying systems employed in the emulsion polymerization process of the invention are chosen from the range of emulsifiers having an appropriate hydrophilic/lipophilic balance. The preferred systems consist of the combination of an anionic surfactant, such as sodium lauryl sulphate, ethoxylated nonylphenol sulphates incorporating in particular 20-25 moles of ethylene oxide, dodecylbenzenesulphonate and ethoxylated fatty alcohol sulphates, and a nonionic surfactant, such as ethoxylated nonylphenols incorporating in particular 10-40 moles of ethylene oxide, and ethoxylated fatty alcohols.

The total amount of emulsifier is generally within the range from 1 to 5% by weight and preferably from 2 to 4% by weight relative to the monomers.

The mixtures of dispersions (A) and (B) of the invention are realized at room temperature.

The films obtained from the latex mixtures of the invention were analysed as obtained after drying at room temperature and then after an additional heat treatment of 15 minutes at 160.degree. C.

The film properties that were evaluated are the solvent resistance, which is determined by measuring the percentage of insolubles in samples immersed in acetone at room temperature for 24 h and the percentage of acetone absorbed by these samples, also referred to as "swelling index", and the mechanical properties of the film, by way of a tensile test (determination of the breaking stress and elongation at break).

The degree of crosslinking of the films--which determines very good performance properties--is characterized by as high as possible an insolubles content, as low as possible a swelling index, and a breaking stress and elongation at break which are as high as possible.

The existence of crosslinking at room temperature of the film in the course of coalescence is demonstrated by a film obtained from the mixture leading to properties superior to those of the initial latexes, while the existence of thermal crosslinking of the film is demonstrated by comparing the properties before and after heat treatment.

Under these conditions, it was observed that the mixtures of coreactive latexes of the invention lead to films which crosslink at room temperature and thus exhibit improved properties.

The good stability on storage of the latex mixtures, in other words the possibility of producing one-component (one-pack) systems, is verified by determining the properties of a film obtained from a mixture which has been stored for 10 days at 60.degree. C. and comparing these properties with the properties of a film obtained from a freshly prepared mixture. The stability of the latexes is also verified by monitoring the basic characteristics of the latex, i.e. the particle size, viscosity, etc.

The properties of films obtained from the mixtures of the invention before and after heat treatment for 15 minutes at 160.degree. C. are equal irrespective of the treatment undergone by the latex mixtures (fresh mixture or mixture treated for 10 days at 60.degree. C.), thereby demonstrating the good stability on storage of the mixtures.

The present invention likewise provides for the use of the one-component system based on coreactive latexes, as defined above, as a binder in compositions intended for producing a crosslinkable coating, such as a paint in the architectural field, a varnish or a finish for leather, a finish for textiles, a protective varnish for wood, or in compositions for the coating of paper; as a binder and/or impregnating agent for various woven or nonwoven textile materials, paper, cardboard, fibre webs; and as an adhesive, especially in the woodworking industry.

The examples which follow illustrate the present invention without, however, limiting its scope. In these examples, the parts and percentages are by weight unless indicated otherwise. In Example 1, the quantities of the ingredients in the formulations and of the monomers are expressed in parts of active substance.

EXAMPLE 1

Synthesis of a Latex A and a Latex B

General Procedure

A 3 l reactor equipped with hot water circulation in the jacket, a central stirrer and a condenser is charged with an initial charge formulated as follows:

Water . . . 54.00 parts Sodium ethoxylated fatty alcohol sulphate, 32% in water . . . 0.25 parts Ethoxylated fatty alcohol, 65% in water . . . 0.05 parts

This initial charge is homogenized and brought to 75.degree. C.

When the temperature of the initial charge reaches 75.degree. C., the pre-emulsion and initiator solution, formulated as shown below, are run in over the course of four hours:

Pre-emulsion Water . . . 62.00 parts Sodium ethoxylated fatty alcohol sulphate, 32% in water . . . 2.25 parts Ethoxylated fatty alcohol, 65% in water . . . 0.45 parts Monomers . . . 100.00 parts Initiator Solution Water . . . 6.00 parts Sodium persulphate . . . 0.30 parts

The mixture is left to react for one hour more at 75.degree. C.

It is then cooled to room temperature and filtered through a 100 .mu.m mesh.

Preparation of the Latexes A and B

The latexes A and B were synthesized from monomers A and B, respectively, as indicated in Table 1, which also shows the characteristics of the latexes obtained.

TABLE 1______________________________________ A B______________________________________Monomers.cndot. Ethyl acrylate 90 98.cndot. 1-(2-Methacryloyloxyethyl) imidazolin-2-one in solution at a concentrationof 50% in methyl methacrylate, soldby the company "ELF ATOCHEM" underthe name "NORSOCRYL 1.04".cndot. N-(2,2-Dimethoxy-1-hydroxyethyl)- 10 2acrylamide (CH.sub.2 .dbd.CH--CONH--CHOH--CH(OMe).sub.2)in aqueous solution at a concentra-tion of 50%LatexNonvolatiles content (%) 45.3 43.8pH 1.6 3.2Diameter (nm) 141 149______________________________________

EXAMPLE 2

Crosslinking and Crosslinkability of Films Obtained from the Latexes A and B

The degree of pre-crosslinking of a film obtained from the latex A and a film obtained from the latex B by drying at 23.degree. C. and 50% relative humidity was determined on samples measuring 10.times.25 mm and with a thickness of between 1 and 2 mm after immersion for 24 hours in acetone at room temperature (measurement of the resistance to the acetone solvent) by measuring the percentage of acetone absorbed (swelling index) and the insolubles content. The results (in each case the mean of three measurements) are reported in Table 2.

Similarly, the degree of thermal post-crosslinking was determined on films obtained from the latexes A and B, respectively, dried as before and then subjected to heat treatment for 15 minutes at 160.degree. C. The results are likewise indicated in Table 2.

TABLE 2______________________________________Film obtained from the latex A B______________________________________Swelling index (23.degree. C.) (%) 10.9 .infin.Swelling index (160.degree. C.) (%) 8.3 6.8% insolubles (23.degree. C.) 72.3 0% insolubles (160.degree. C.) 90.5 95.1______________________________________

The film of latex A presents a certain degree of pre-crosslinking and slight thermal post-crosslinkability, whereas the film of latex B is not pre-crosslinked at all but exhibits an excellent heat-crosslinkability.

EXAMPLE 3

Mixtures of Coreactive Latexes

The latexes A and B were mixed at room temperature in various proportions. The characteristics of the films originating from these mixtures were examined as in Example 2: after drying at 23.degree. C., 50% RH, then after heat treatment for 15 minutes at 160.degree. C.

The results are reported in Table 3, which for purposes of comparison also repeats the data of Table 2.

TABLE 3______________________________________Latex Swelling Swelling %or index index insolub- % insolu-mixture Latex A Latex B (23.degree. C.) (160.degree. C.) bles blesNo. (%) (%) (%) (%) (23.degree. C.) (160.degree. C.)______________________________________1 100 0 10.9 8.3 72.3 90.52 75 25 8.8 6.4 85.3 91.13 50 50 10.3 5.6 86.0 92.94 25 75 11.6 7.0 86.3 92.95 0 100 .infin. 6.8 0 95.1______________________________________

The films obtained from mixtures of the latexes A and B show a greater degree of crosslinking than the films obtained from the base latexes A and B, showing the existence of crosslinking at room temperature. This crosslinking can be increased by heat treatment.

EXAMPLE 4

Mechanical Properties

The mechanical properties of the film obtained from the mixture No. 3 are compared with the mechanical properties of the films obtained from the latexes A and B by means of a tensile test carried out in accordance with the standard ISO 527. The results are presented in Table 4.

TABLE 4______________________________________ Elongation Elongation Elongation at breakFilm obtained at break Breaking at break (%) (MPa)from the (%) drying stress (MPa) tempering temperinglatex 23.degree. C. drying 23.degree. C. 160.degree. C. 160.degree. C.______________________________________A 488 1.15 440 0.64B 1100 1.2 442 1.22Mixture No. 3 400 2.85 416 2.63______________________________________

The breaking stress of the film obtained from the mixture is much greater than that of the base latexes, demonstrating a crosslinking reaction at low temperature.

EXAMPLE 5

Stability on Storage

Mixture No. 3 is stored for 10 days at 60.degree. C. and then cooled to room temperature. A new film is then prepared as above by drying the latex at 23.degree. C. The acetone resistance of the film before and after heat treatment is compared with that of the film obtained from the fresh mixture, the results being presented in Table 5.

TABLE 5______________________________________ Swelling Swelling % % index index insolubles insolublesFilm (23.degree. C.) (%) (160.degree. C.) (%) (23.degree. C.) (160.degree. C.)______________________________________Mixture No. 3 10.3 5.6 86.0 92.9Mixture No. 3 7.4 5.9 90.2 93.0(10d 60.degree. C.)______________________________________

The properties of the film after accelerated aging of the latex for 10 days at 60.degree. C. are largely the same as those of the film obtained with the fresh latex.

The entire disclosure of all applications, patents and publications, cited above and below, and of corresponding French application No. 97 05269, filed Apr. 29, 1997, is hereby incorporated by reference.

The preceding examples can be repeated with similar success by substituting the generically or specifically described reactants and/or operating conditions of this invention for those used in the preceding examples.

From the foregoing description, one skilled in the art can easily ascertain the essential characteristics of this invention and, without departing from the spirit and scope thereof, can make various changes and modifications of the invention to adapt it to various usages and conditions.

Claims

1. A one-component system based on coreactive latexes which is able to lead to coatings which are crosslinkable at room temperature and post-crosslinkable by heat treatment, the said system consisting essentially of the mixture of two separately prepared particle dispersions (A) and (B), each obtained by aqueous emulsion polymerization of a monomer composition A and B, respectively,

(a) at least one free-radically polymerizable ethylenically unsaturated monomer comprising a functional group ##STR8## where X represents O or S, which enters into the monomer composition A; and

(b) at least one free-radically polymerizable ethylenically unsaturated monomer comprising an aldehyde or masked aldehyde functional group selected from acetal, mercaptal, mercaptol, dioxolane and dithiolane, which enters into the monomer composition B, the proportions and members of (A) and (B) providing said mixture with the capability of yielding a film having a higher degree of cross-linking at 23.degree. C. and a higher breaking stress than either (A) or (B) alone.

2. A system according to claim 1, characterized in that the monomer or monomers (a) are selected from those represented by the formulae (I) to (III) below: ##STR9## in which: X represents O or S;

R.sup.1 is a free-radically polymerizable ethylenically unsaturated group;

R.sup.2 is a hydrogen atom or a C.sub.1 -C.sub.8 alkyl group; and

A is an alkylene chain which has 2 or 3 carbon atoms and can be substituted by lower alkyl and/or hydroxyl and/or C.sub.1 -C.sub.4 alkoxy, and/or which can be interrupted by carbonyl.

3. A system according to claim 2, characterized in that R.sup.1 is selected from the groups: ##STR10## where: R.sup.3 represents hydrogen, 3-alkyloxy-2-hydroxypropyl, vinyl, methacryloyl, acryloyl or methacryloyloxyaceto;

A.sup.1 represents O, NH or NR.sup.4 ;

R.sup.4 represents 3-allyloxy-2-hydroxypropyl when R.sup.3 represents 3-allyloxy-2-hydroxypropyl;

Alk represents a C.sub.2 -C.sub.8 alkylene chain; and

2-(.beta.-carboxyacrylamido)ethyl.

4. A system according to claim 1, characterized in that the monomer or monomers (a) are selected from N-(2-methacryloyloxyethyl)ethyleneurea, N-(2-acryloyloxyethyl)ethyleneurea, N-(methacrylamidomethylene)ethyleneurea, N-(acrylamidomethylene)ethyleneurea, N-(.beta.-methacrylamidoethyl)ethyleneurea, N-(.beta.-acrylamidoethyl)ethyleneurea, N-vinylethyleneurea, N-vinyloxyethylethyleneurea, N-[.beta.-(methacryloyloxyacetamido)ethyl]-N,N'-ethyleneurea, N-[.beta.-(acryloyloxyacetamido)ethyl]ethyleneurea, 1-[2-[[2-hydroxy-3-(2-propenyloxy)propyl]amino]ethyl]-2-imidazolidone, N-methacrylamidomethylurea, N-methacryloylurea, N-(3-[1,3-diazacyclohexan-2-one]propyl)methacrylamide, N-hydroxyethylethyleneurea, N-aminoethylethyleneurea, N-(3-allyloxy-2-hydroxypropyl)aminoethylethyleneurea, N-methacrylaminoethylethyleneurea, N-acrylaminoethylethyleneurea, N-methacryloxyacetoxyethylethyleneurea, N-methacryloxyacetaminoethylethyleneurea and N-di(3-allyloxy-2-hydroxypropyl)aminoethylethyleneurea, N-(2-acryloyloxyethyl)ethyleneurea, N-methacrylamidomethylurea and the allylalkylethyleneureas.

5. A system according to claim 1, characterized in that the monomer (a) is N-(2-methacryloyloxyethyl)ethyleneurea(1-(2-methacryloyloxyethyl)imidazolin-2-one).

6. A system according to claim 1, characterized in that the monomer or monomers (b), are the masked aldehydes of the formula: ##STR11## in which formulae (IVa) and (IVb): R.sup.5 represents a hydrogen atom or a methyl radical;

R.sup.6 and R.sup.7 are identical and each represent a C.sub.1 -C.sub.8 -alkyl group or else together form a group --CH.sub.2 --CR.sup.8 R.sup.9 --(CH.sub.2).sub.n -- where n=0 or 1 and R.sup.8 and R.sup.9, which are identical or different, each represent a hydrogen atom or a methyl group;

E represents O, NH or NR' (R'=C.sub.1 -C.sub.4 alkyl);

G represents a C.sub.1 -C.sub.4 alkylene radical or a radical ##STR12## where R.sup.10 represents a hydrogen atom or a C.sub.1 -C.sub.4 alkyl radical.

7. A system according to claim 1, characterized in that the monomer (b) is selected from:

the N-(2,2-dialkoxy-1-hydroxyethyl)(meth)acrylamides and the N-(1,2,2-trialkoxyethyl)(meth)acrylamides, wherein the term alkoxy signifies C.sub.1 -C.sub.4 alkoxy,

4-acrylamidobutyraldehyde dimethyl or diethyl acetal;

methacrylamidoacetaldehyde dimethyl acetal;

diethoxypropyl acrylate;

diethoxypropyl methacrylate;

acryloyloxypropyl-1,3-dioxolane;

methacryloyloxypropyl-1,3-dioxolane; and

N-(1,1-dimethoxybut-4-yl)methacrylamide.

8. A system according to claim 1, characterized in that the monomer or monomers (a) and (b) represent from 0.5 to 10% by weight of the monomer composition A and B respectively.

9. A system according to claim 1, characterized in that the proportions of the two coreactive latexes are chosen such that the proportion of the polymer (A) is between 5 and 95% by weight, of the polymers (A) and (B), and the proportion of the polymer (B) is between 95 and 5% by weight, of the polymers (A) and (B), the nonvolatiles content of each of the dispersions being between 20 and 60% by weight.

10. A system according to claim 1, characterized in that the size of the particles of each of the dispersions (A) and (B) is between 50 and 500 nm.

11. A system according to claim 8, characterized in that monomers other than the monomers (a) and (b) of the two particle dispersions (A) and (B) are chosen so that the glass transition temperatures (Tg) of the resulting copolymers are adapted to the intended field of application, by the combination of monomers capable of leading to homopolymers having a high Tg with monomers capable of leading to homopolymers having a low Tg.

12. A system according to claim 11, characterized in that the monomers capable of leading to homopolymers having a low Tg are selected from ethyl acrylate, butyl acrylate, 2-ethylhexyl acrylate, nonyl acrylate and vinyl 2-ethylhexanoate; and the monomers capable of leading to homopolymers having a high Tg are selected from methyl methacrylate, vinyl acetate, styrene, acrylic acid, methacrylic acid and acrylamide.

13. A composition comprising a one-component system of coreactive latexes, as defined in claim 1, said composition being a binder intended for producing a crosslinkable coating, a paint in the architectural field, a varnish or a finish for leather, a finish for textiles, a protective varnish for wood, or a composition for the coating of paper; a binder and/or impregnating agent for woven or nonwoven textile materials, paper, cardboard, fiber webs; or as an adhesive composition for wood.

14. A system according to claim 1, characterized in that the monomer or monomer s(b), are aldehydes selected from, methacrolein, formylstyrene, crotonaldehyde and the aldehydes of the formula: ##STR13## and the masked aldehydes of the formula: ##STR14## in which formulae (IVa) and (IVb): R.sup.5 represents a hydrogen atom or methyl radical;

R.sup.6 and R.sup.7 are identical and each represent a C.sub.1 -C.sub.8 -alkyl group or else together form a group --CH.sub.2 --CR.sup.8 R.sup.9 --(CH.sub.2).sub.n -- where n=0 or 1 and R.sup.8 and R.sup.9, which are identical or different, each represent hydrogen atom or a methyl group;

E represents O, NH or NR', (R'=C.sub.1 -C.sub.4 -alkyl);

G represents a C.sub.1 -C.sub.4 -alkylene radical or a radical ##STR15## where R.sup.10 represents a a hydrogen atom or a C.sub.1 -C.sub.4 -alkyl radical.

15. A system according to claim 4, characterized in that the monomer (b) is selected from:

the N-(2,2-dialkoxy-1-hydroxyethyl)(meth)acrylamides and the N-(1,2,2-trialkoxyethyl)(meth)acrylamides, wherein the term alkoxy signifies C.sub.1 -C.sub.4 -alkoxy;

4-acrylamidobutyraldehyde dimethyl or diethyl acetal;

methacrylamidoacetaldehyde dimethyl acetal;

diethoxypropyl acrylate;

diethoxyporpyl methacrylate;

acryloyloxypropyl-1,3-dioxolane;

methacryloyloxypropyl-1,3-dioxolane; and

N-(1,1-dimethoxybut-4-yl)methacrylamide.

16. A partially crosslinked film produced by applying the system of claim 1 to a substrate.

17. A crosslinked film obtained by heating the film of claim 16, the crosslinking being augmented thereby.

18. A system according to claim 14, characterized in that the monomer or monomer s(a) and (b) represent from 0.5 to 10% by weight of the monomer composition A and B, respectively.

19. A system according to claim 18, characterized in that the size of the particles of each of the dispersions (A) and (B) is between 50 and 500 nm.

20. A system according to claim 15, wherein the monomers (a) and (b) represent from 0.5 to 10% by weight of the monomers in composition A and B, respectively; the proportion of the polymer (A) is between 5 and 95% by weight, of the polymer s(A) and (B), and the proportion of the polymer (B) is between 95 and 5% by weight, of the polymer s(A) and (B), the nonvolatiles content of each of the dispersions being between 20 and 60% by weight; and the size of the particles of each of the dispersions (A) and (B) is between 50 and 500 nm.

21. A one-component system based on coreactive latexes which is able to lead to coatings which are crosslinkable at room temperature and post-crosslinkable by heat treatment, the said system consisting of the mixture of two particle dispersions (A) and (B), each obtained by aqueous emulsion polymerization of a monomer composition A and B, respectively,

(a) at least one free-radically polymerizable ethylenically unsaturated monomer comprising a functional group ##STR16## where X represents O or S, which enters into the monomer composition A; and

(b) at least one free-radically polymerizable ethylenically unsaturated monomer which enters into the monomer composition (B) said monomer entering into the composition (B) being selected from the group consisting of the N-(2,2-dialkoxy-1-hydroxyethyl) (meth)acrylamides and the N-(1,2,2-trialkoxyethyl)(meth)acrylamides, wherein the term alkoxy signifies C.sub.1 -C.sub.4 alkoxy, 4-acrylamidobutyraldehyde dimethyl or diethyl acetal; methacrylamidoacetaldehyde dimethyl acetal; diethoxypropyl acrylate; diethoxypropyl methacrylate; acryloyloxypropyl-1,3-dioxolane; methacryloyloxypropyl-1,3-dioxolane; and N-(1,1-dimethoxybut-4-yl) methacrylamide.

22. A system according to claim 21, characterized in that the monomer or monomers (a) are selected from N-(2-methacryloyloxyethyl)ethyleneurea, N-(2-acryloyloxyethyl)ethyleneurea, N-(methacrylamidomethylene)ethyleneurea, N-(acrylamidomethylene)ethyleneurea, N-(.beta.-methacrylamidoethyl)ethyleneurea, N-(.beta.-acrylamidoethyl)ethyleneurea, N-vinylethyleneurea, N-vinyloxyethylethyleneurea, N-[.beta.-(methacryloyloxyacetamido)ethyl]-N,N'-ethyleneurea, N-[.beta.-(acryloyloxyacetamide)ethyl]ethyleneurea, 1-[2-[[2-hydroxy-3-(2-propenyloxy)propyl]amino]ethyl]-2-imidazolidone, N-methacrylamidomethylurea, N-methacryloylurea, N-(3-[1,3-diazacyclohexan-2-one]propyl)methacrylamide, N-hydroxyethylethyleneurea, N-aminoethylethyleneurea, N-(3-allyloxy-2-hydroxypropyl)aminoethylethyleneurea, N-methacrylaminoethylethyleneurea, N-acrylaminoethylethyleneurea, N-acrylaminoethylethyleneurea, N-methacryloxyacetoxyethylethyleneurea, N-methacryloxyacetaminoethylethyleneurea and N-di(3-allyoxy-2-hydroxypropyl)aminoethylethyleneurea, N-(2-acryloyloxyethyl)ethyleneurea, N-methacrylamidomethylurea and the allylalkylethyleneureas.

23. A system according to claim 21, wherein said monomer (B) is selected from the group consisting of:

N-(2,2-dimethoxy-1-hydroxyethyl)acrylamide;

N-(2,2-dimethoxy-1-hydroxyethyl)methacrylamide;

N-(1,2,2-trimethoxyethyl)acrylamide;

N-(1,2,2-trimethoxyethyl)methacrylamide;

N-(2,2-dibutoxy-1-hydroxyethyl)acrylamide;

N-(2,2-dibutoxy-1-hydroxyethyl)methacrylamide;

N-(1,2,2-tributoxyethyl)acrylamide; and

N-(1,2,2-tributoxyethyl)methacrylamide.

24. A system according to claim 22, wherein said monomer (B) is selected from the group consisting of:

N-(2,2-dimethoxy-1-hydroxyethyl)acrylamide;

N-(2,2-dimethoxy-1-hydroxyethyl)methacrylamide;

N-(1,2,2-trimethoxyethyl)acrylamide;

N-(1,2,2-trimethoxyethyl)methacrylamide;

N-(2,2-dibutoxy-1-hydroxyethyl)acrylamide;

N-(2,2-dibutoxy-1-hydroxyethyl)methacrylamide;

N-(1,2,2-tributoxyethyl)acrylamide; and

N-(1,2,2-tributoxyethyl)methacrylamide.

25. A system according to claim 1, and the proportion of the polymer (A) is between 25 and 75% by weight of the polymers (A) and (B) and the proportion of the polymer (B) is between 75 and 25% by weight of the polymers (A) and (B).

26. A method of increasing the room temperature cross-linking and breaking stress of films produced from latices, said method comprising mixing in sufficient proportions, separately prepared particle dispersions (A) and (B), each obtained by aqueous emulsion polymerization of a monomer composition A and B, respectively,

(a) at least one free-radically polymerizable ethylenically unsaturated monomer comprising a functional group ##STR17## where X represents O or S, which enters into the monomer composition A; and

(b) at least one free-radically polymerizable ethylenically unsaturated monomer which enters into the monomer composition (B) said monomer entering into the composition (B) being selected from the group consisting of the N-(2,2-dialkoxy-1-hydroxyethyl) (meth)acrylamides and the N-(1,2,2-trialkoxyethyl)(meth)acrylamides, wherein the term alkoxy signifies C.sub.1 -C.sub.4 alkoxy, 4-acrylamidobutyraldehyde dimethyl or diethyl acetal; methacrylamidoacetaldehyde dimethyl acetal; diethoxypropyl acrylate; diethoxypropyl methacrylate; acryloyloxypropyl-1,3-dioxolane; methacryloyloxypropyl-1,3-dioxolane; and N-(1,1-dimethoxybut-4-yl) methacrylamide;

and forming a film from said mixture.

27. A composition according to claim 1, wherein ethyl acrylate constitutes a predominant proportion of the monomers in both latex (A) and latex (B).

28. A process according to claim 26, wherein the ethyl acrylate constitutes a predominant proportions of the monomers in both latex (A) and latex (B).