DE19816528A1 - Aqueous dispersion comprising a carbodiimide substituted polyurethane - Google Patents

Abstract

An aqueous dispersion (I) contains a polyurethane having carbodiimide structural units of formula -N=C=N- (1). Also claimed are: (i) a process for the coating of articles (II) of metal, plastic, paper, textiles, leather or wood by the application of a film of (I) and drying the dispersion. (ii) a process for the bonding of articles (II) by the application of a film of (I) and contacting with another article before or after drying the dispersion. (iii) a process for the impregnation of textile, leather or paper articles by immersing them in (I) followed by drying. (iv) the resulting coated, bonded or impregnated articles.

Description

The present invention relates to aqueous dispersions containing a polyurethane which contains carbodiimide structural units of the formula (I)

-N = C = N- (I)

contains.

The invention further relates to methods for coating, Bonding and impregnation of objects different materials with these dispersions as well as the coated, glued and impregnated with these dispersions objects.

The use of aqueous dispersions, the polyurethanes contain (short: PUR dispersions), for coating substrates ten such as textile or leather has been known for a long time. Because of your excellent mechanical properties are preferred PUR dispersions based on polyesterols are used.

In WO 94/06852 it is recommended to coat any gene substrates, preferably leather, aqueous dispersions use an ionomeric polyurethane and a foam stabilizer included. If necessary, this dispersion with be mixed with another polymer dispersion and others Auxiliaries and additives such as dyes, leveling and wetting agents, Contain anti-glue, plasticizers and matting agents. The Application of the dispersion as a coating agent is carried out by they are mechanically foamed, applied to the substrate and the Foam dries.

From EP-A-276482 aqueous dispersions for the production of coated textiles. The essential components are: a polyurethane dispersion film-forming below 70 ° C and one below 70 ° C non-film-forming dispersion of a polymer with a Melting point <70 ° C, for example an acrylonitrile-styrene copoly mer.  

The textiles known from the prior art are suitable however only to a limited extent for use in building protection and especially as roofing membranes.

Roofing membranes have to meet a complex requirement profile; The following combination of properties is often required:

• - high mechanical strength and elasticity both in the Cold as well as warm, as roofs are seasonal are subject to strong temperature fluctuations
• - high water resistance
• - good water vapor permeability
• - If necessary, classification as high as possible Fire protection class and
• - Absence of chlorinated products as part of the Public products avoided from chlorinated polymers because he gave the impression that they were questionable for ecological reasons.
• - No noticeable loss in the aforementioned properties over a period of several years under usage conditions, especially under the influence of a humid-warm atmosphere.

From US 4 113 676 it is known that aqueous PU dispersions by the addition of monocarbodiimides, which are no other wear functional groups against hydrolytic degradation can be protected. However, a disadvantage of these systems is the presence of the low molecular weight carbodiimides, the migrate from the coating, for example, and thus to can cause hygienic problems. Another disadvantage is that those formed by reaction of the CDI with carboxyl groups Acrylic ureas in amide and the one underlying carbodiimide Cleave isocyanate (Williams &Ibrahim; Chem. Rev. 81, 603 (1981), that can also migrate and cause problems.

WO 96/08 524, EP-A-207 414 and DE-A-4 039 193 describe aqueous dispersions of acrylic urea-containing polyisocyanate Addition products. Carbo diimide-containing polyurethanes or prepolymers and the Carbodiimide groups before dispersing the polyurethanes  Carboxylic acids such as stearic acid to the acylurea groups implemented.

It was therefore the task to find PUR dispersions that the Not have disadvantages of the prior art and from which coatings and films can be produced during storage no loss of mechanical properties under warm and humid conditions Properties, especially their tensile strength, suffer. These dispersions are also intended for the production of coated textiles that can be used as roofing membranes are suitable.

Accordingly, the above-mentioned dispersions, processes for the production of coatings, bonds and impregnation stanchions as well as the coated, glued and coated Found objects.

The dispersions according to the invention contain the carbodiimide structural units of the formula (I) preferably in amounts of 5 to 200, particularly preferably in amounts of 5 to 150 and whole particularly preferably in amounts of 10 to 100 mmol per kg Polyurethane.

The carbodiimide structural units are particularly simple of formula (I) in the aqueous polyurethane according to the invention incorporate dispersion by building the polyurethane Diisocyanates (a1.1) used or co-used in the statistical agents 1 to 10, preferably 1 to 4 structural units of the Have formula (I).

Suitable diisocyanatocarbodiimides (a1.1) are, for example, those of the general formula (Ia1.1)

OCN- (R ¹ -N = C = N) _m -R ¹ -NCO (Ia1)

in R ¹ for a divalent hydrocarbon radical, optionally containing urethane, ester and / or ether groups, such as that obtained by removing the isocyanate groups from a simple organic isocyanate or a urethane group and optionally containing ether or ester groups, the terminal isocyanate groups carries, is obtained, where there are several radicals R ¹ in the same molecule, different radicals R ¹ corresponding to the definition mentioned can also be present and
m stands for a whole or (on statistical average) fractional number from 1 to 10, preferably from 1 to 4.

The residues R1 are preferably derived by abstraction of the Isocyanate groups from monomers (a1), which are the Diisocyanates, which is usually used in polyurethane chemistry be used.

Particularly worth mentioning as monomers (a1) are diisocyanates X (NCO) ₂ , where X represents an aliphatic hydrocarbon radical having 4 to 12 carbon atoms, a cycloaliphatic or aromatic hydrocarbon radical having 6 to 15 carbon atoms or an araliphatic hydrocarbon radical having 7 to 15 carbon atoms. Examples of such diisocyanates are tetramethylene diisocyanate, hexamethylene diisocyanate, dodeca methylene diisocyanate, 1,4-diisocyanatocyclohexane, 1-iso cyanato-3,5,5-trimethyl-5-isocyanatomethylcyclohexane (IPDI), 2,2-bis (4-isocyanatocyclohexyl) propane , Trimethylhexanediiso cyanate, 1,4-diisocyanatobenzene, 2,4-diisocyanatotoluene, 2,6-diisocyanatotoluene, 4,4'-diisocyanato-diphenylmethane, 2,4'-diisocyanato-diphenylmethane, p-xylylene diisocyanate, tetra methylxylylene diisocyanate (TMXDI), the isomers of bis (4-iso cyanatocyclohexyl) methane (HMDI) such as the trans / trans, the cis / cis and the cis / trans isomer and mixtures consisting of these compounds.

Mixtures of these are, in particular, mixtures of these isocyanates respective structural isomers of diisocyanatotoluene and diisocya nato-diphenylmethane is important, especially the mixture from 80 mol% 2,4-diisocyanatotoluene and 20 mol% 2,6-diiso suitable for cyanatotoluene. Furthermore, the mixtures of aromatic isocyanates such as 2,4 diisocyanatotoluene and / or 2,6-diisocyanatotoluene with aliphatic or cycloaliphatic Isocyanates such as hexamethylene diisocyanate, HMDI or IPDI in particular advantageous, the preferred mixing ratio of the alipha tables to aromatic isocyanates 4: 1 to 1: 4.

The radicals R ¹ , which are formed by abstraction of the isocyanate groups from a urethane group, optionally ether or ester groups and prepolymer having terminal isocyanate groups, are preferably those which consist of the diols (b1) and the diisocyanates (a1.2) are built up.

The preparation of the monomers (a1.1) is known per se and is e.g. B. in US 2 840 589, 2 941 966, EP-A-628 541 and by P.W. Campbell and K.C. Smeltz in Journal of Organic Chemistry, 28, 2069 (1963). Particularly gentle and free of  By-products can also be diisocyanatocarbodiimides heterogeneous catalysis according to the German disclosure specification Manufacture 2 504 400 and 2 552 350. Carbodiimidization of Diisocyanates in the presence of very small amounts of phospholine oxide with subsequent blocking of the catalyst Acid chlorides are described in DE-OS 26 53 120.

In general, the diisoocyanates (a1.2) except for the manufacture the diisocyanates (a1.1) are also used directly to build up the polyure thane contained in polyurethane dispersions according to the invention are used because there is often more to build the polyurethanes Isocyanate is needed as to introduce the carbodiimide Groups is required.

For the structure of the polyurethanes, one can use compounds (a1.2) in addition to the aforementioned also use isocyanates which in addition to free isocyanate groups further blocked isocyanate groups, e.g. Wear uretdione groups.

With regard to good film formation and elasticity come as diols (b1) primarily higher molecular weight diols (b1.1) into consideration, the a molecular weight of about 500 to 5000, preferably about Have 1000 to 3000 g / mol.

The diols (b1.1) are, in particular, polyester polyols which, for. B. from Ullmann's Encyclopedia of Industrial Chemistry, 4th Edition, Volume 19, pp 62 to 65 are known. Polyester polyols are preferably used, which are obtained by reacting dihydric alcohols with dihydric carboxylic acids. Instead of the free polycarboxylic acids, the corresponding polycarboxylic acid anhydrides or corresponding polycarboxylic acid esters of lower alcohols or their mixtures can also be used to prepare the polyester polyols. The polycarboxylic acids can be aliphatic, cycloaliphatic, araliphatic, aromatic or heterocyclic and, if necessary, z. B. by halogen atoms, substituted and / or unsaturated. Examples include: suberic acid, azelaic acid, phthalic acid, isophthalic acid, terephthalic acid, phthalic anhydride, tetrahydrophthalic anhydride, hexahydro phthalic anhydride, tetrachlorophthalic anhydride, endomethylene tetrahydrophthalic anhydride, glutaric acid anhydride, glutaric acid anhydride, glutaric acid fatty acid, malutanic acid anhydride, glutaric acid anhydride, fumaric acid anhydride, malutaric acid anhydride. Preferred are dicarboxylic acids of the general formula HOOC- (CH ₂ ) _y -COOH, where y is a number from 1 to 20, preferably an even number from 2 to 20, e.g. B. succinic acid, adipic acid, sebacic acid and dodecanedicarboxylic acid.

As polyhydric alcohols such. B. ethylene glycol, propane-1,2-diol, propane-1,3-diol, butane-1,3-diol, butene-1,4-diol, butyne-1,4-diol, pentane-1,5- diol, neopentyl glycol, bis (hydroxy methyl) cyclohexanes such as 1,4-bis (hydroxymethyl) cyclohexane, 2-methyl propane-1,3-diol, methyl pentanediols, also diethylene glycol, triethylene glycol, tetraethylene glycol, polyethylene glycol, dipropylene glycol, Polypropylene glycol, dibutylene glycol and poly butylene glycols into consideration. Alcohols of the general formula HO- (CH ₂ ) _x -OH are preferred, where x is a number from 1 to 20, preferably an even number from 2 to 20. Examples include ethylene glycol, butane-1,4-diol, hexane-1,6-diol, octane-1,8-diol and dodecane-1,12-diol. Neopentyl glycol and 1,5-pentanediol are further preferred.

Also come polycarbonate diols, such as z. B. by Implementation of phosgene with an excess of that as a build-up components for the low molecular weight polyester polyols Alcohols can be obtained.

Lactone-based polyester diols are also suitable, these being homopolymers or copolymers of lactones, preferably addition products of lactones with terminal hydroxyl groups onto suitable difunctional starter molecules. Suitable lactones are preferably those which are derived from compounds of the general formula HO- (CH ₂ ) _z -COOH, where z is a number from 1 to 20 and an H atom of a methylene unit also by a C ₁ - to C ₄ -alkyl radical may be substituted. Examples are ε-caprolactone, β-propiolactone, γ-butyrolactone and / or methyl-ε-caprolactone and mixtures thereof. Suitable starter components are e.g. B. the above-mentioned as a structural component for the polyester polyols low molecular weight dihydric alcohols. The corresponding polymers of ε-caprolactone are particularly preferred. Lower polyester diols or polyether diols can also be used as starters for the preparation of the lactone polymers. Instead of the polymers of lactones, the corresponding chemically equivalent polycondensates of the hydroxycarboxylic acids corresponding to the lactones can also be used.

In addition, polyether diols are suitable as monomers (b1.1). They are in particular by polymerization of ethylene oxide, propylene oxide, butylene oxide, tetrahydrofuran, styrene oxide or epichlorohydrin with themselves, for. B. in the presence of BF ₃ or by addition of these compounds, optionally in a mixture or in succession, to starting components with reactive hydrogen atoms, such as alcohols or amines, for. B. water, ethylene glycol, propane-1,2-diol, propane-1,3-diol, 1,2-bis (4-hydroxydi phenyl) propane or aniline available. Polytetrahydrofuran with a molecular weight of 240 to 5000, and especially 500 to 4500, is particularly preferred.

Polyhydroxyolefins are also suitable, preferably those with 2 terminal hydroxyl groups, e.g. B. α, -ω-dihydroxypolybutadiene, α, -ω-Dihydroxypolymethacrylester or α, -ω-Dihydroxypolyacryl esters as monomers (c1). Such connections are, for example known from EP-A-0622378. Other suitable polyols are Polyacetals, polysiloxanes and alkyd resins.

The polyols can also be used as mixtures in a ratio of 0.1: 1 to 1: 9 can be used.

The hardness and elastic modulus of the polyurethanes can be increase if as diols (b1) in addition to the diols (b1.1) low molecular weight diols (b1.2) with a molecular weight of about 62 to 500, preferably from 62 to 200 g / mol, are used.

Above all, the structural components of the for the production of polyester polyols called short-chain Alkanediols used, the unbranched diols with 2 to 12 carbon atoms and an even number of carbon atoms and pentane-1,5-diol and neopentyl glycol are preferred.

The proportion of the diols (b1.1) is preferably based on the Total amount of diols (b1) 10 to 100 mol% and the proportion of Monomers (b1.2), based on the total amount of diols (b1) 0 to 90 mol%. The ratio of the diols is particularly preferably (b1.1) to the monomers (b1.2) 0.1: 1 to 5: 1, especially before increases 0.2: 1 to 2: 1.

In order to achieve the water dispersibility of the polyurethanes, are the polyurethanes in addition to components (a1), (b1) and (d1) from monomers different from components (a1), (b1) and (d1) ren (c1), the at least one isocyanate group or at least a group reactive toward isocyanate groups and beyond at least one hydrophilic group or a group that is in can transfer a hydrophilic group, wear, built. in the following text is the term "hydrophilic groups or potentially hydrophilic groups "with N (potentially) hydrophilic Groups ". The (potentially) hydrophilic groups react with isocyanates much more slowly than that functional groups of the monomers that are used to build the Main polymer chain serve.  

The proportion of components with (potentially) hydrophilic groups on the total amount of components (a1), (b1), (c1), (d1) and (e1) is generally dimensioned so that the molar amount of (po tentiell) hydrophilic groups, based on the amount by weight of all monomers (a1) to (e1), 30 to 1000, preferably 50 to 500 and is particularly preferably 80 to 300 mmol / kg.

The (potentially) hydrophilic groups can be non-ionic or preferably around (potentially) ionic hydrophilic Trade groups.

Hydrophilic polyalky come as nonionic hydrophilic groups lenoxide residues, especially polyethylene glycol ether from preference example 5 to 100, preferably 10 to 80 ethylene oxide repetition units into consideration. The content of polyethylene oxide units is generally 0 to 10% by weight, preferably 0 to 6% by weight, based on the weight of all monomers (a1) to (e1).

Preferred monomers with nonionic hydrophilic groups are hydrophilic polyalkylene oxides, polyethylene oxide monools and the Reaction products from a polyethylene glycol and a diiso cyanate, which is a terminally etherified polyethylene glycol residue carry. Such isocyanates and processes for their preparation are given in US Pat. Nos. 3,905,929 and 3,920,598 ben.

Ionic hydrophilic groups are mainly anionic groups such as the sulfonate, carboxylate and phosphate groups in the form their alkali metal or ammonium salts and cationic groups such as ammonium groups, especially protonated tertiary Amino groups or quaternary ammonium groups.

Potentially ionic hydrophilic groups are primarily those that by simple neutralization, hydrolysis or quaterni sation reactions in the above-mentioned ionic hydrophilic Have groups transferred, e.g. B. carboxylic acid groups or tertiary amino groups.

(Potentially) ionic monomers (c1) are e.g. B. in Ullmanns Encyclopedia of Technical Chemistry, 4th Edition, Volume 19, Pp. 311-313 and for example in DE-A 1 495 745 in detail described.

Above all, (potential) cationic monomers (c1) are Monomers with tertiary amino groups of particularly practical Meaning, for example: tris (hydroxyalkyl) amines, N, N'-bis (hydroxyalkyl) alkylamines, N-hydroxyalkyl dialkylamines,  Tris (aminoalkyl) amines, N, N'-bis (aminoalkyl) alkylamines, N-ami noalkyl-dialkylamine, the alkyl radicals and alkanediyl unit th of these tertiary amines independently of one another from 1 to 6 Carbon atoms exist. There are also tertiary nitrogen atom-containing polyethers with preferably two terminals Hydroxyl groups, such as. B. by alkoxylation of two Amines containing amine nitrogen-bonded hydrogen atoms, e.g. B. Methylamine, aniline or N, N'-dimethylhydrazine, in itself are accessible in the usual way. Such polyethers generally have a value between 500 and 6000 g / mol Molecular weight on.

These tertiary amines are either with acids, preferably strong mineral acids such as phosphoric acid, sulfuric acid, halogenic acids or strong organic acids or by reaction with suitable quaternizing agents such as C ₁ - to C ₆ -alkyl halides or benzyl halides, for. As bromides or chlorides, converted into the ammonium salts.

Suitable monomers with (potentially) anionic groups are usually aliphatic, cycloaliphatic, araliphatic or aromatic carboxylic acids and sulfonic acids which carry at least one alcoholic hydroxyl group or at least one primary or secondary amino group. Dihydroxyalkylcarboxylic acids are preferred, especially those with 3 to 10 carbon atoms, as are also described in US Pat. No. 3,412,054. In particular, compounds of the general formula (d1)

in which R ¹ and R ^{2 is} a C ₁ - to C ₄ -alkanediyl unit and R ^{3 is} a C ₁ - to C ₄ -alkyl unit and especially dimethylol propionic acid (DMPA) is preferred.

Corresponding dihydroxysulfonic acids and Dihydroxyphosphonic acids such as 2,3-dihydroxypropanephosphonic acid.

Otherwise, dihydroxyl compounds with one molecule are suitable Lar weight over 500 to 10,000 g / mol with at least 2 carboxylate groups known from DE-A 3 911 827. you are through Implementation of dihydroxyl compounds with tetracarboxylic acid di anhydrides such as pyromellitic dianhydride or cyclopentantetra carboxylic acid dianhydride in a molar ratio of 2: 1 to 1.05: 1 in  a polyaddition reaction available. As a dihydroxyver bindings are especially those as chain extenders Monomers listed (b1.2) and the diols (b1.1) are suitable.

As monomers (c1) with amino groups reactive towards isocyanates Pen come aminocarboxylic acids such as lysine, β-alanine or those in the DE-A-2034479 adducts of aliphatic diprimary di amines on α, β-unsaturated carboxylic or sulfonic acids into consideration.

Such compounds obey, for example, the formula (d2)

H ₂ NR ⁴ -NH-R ⁵ -X (d2)

in the

• - R ⁴ and R ⁵ independently of one another for a C ₁ - to C ₆ -alkanediyl unit, preferably ethylene
  and x represents COOH or SO ₃ H.

Particularly preferred compounds of formula (d2) are N- (2-aminoethyl) -2-aminoethane carboxylic acid and the N- (2-amino ethyl) -2-aminoethanesulfonic acid or the corresponding Alkali salts, Na being particularly preferred as the counter ion.

The adducts of the abovementioned are also particularly preferred aliphatic diprimary diamines on 2-acrylamido-2-methylpropane sulfonic acid as z. B. in DE patent 1 954 090 are described.

If monomers with potentially ionic groups are used can be converted into the ionic form before, during, but preferably after the isocyanate polyaddition, because the ionic monomers in the reaction mixture often only difficult to solve. The sulfonate or Carboxylate groups in the form of their salts with an alkali ion or an ammonium ion as a counter ion.

The monomers (d1) which are from the monomers (a1) to (c1) are generally used for networking or Chain extension. They are generally more than two-valued non-phenolic alcohols, amines with 2 or more primary and / or secondary amino groups and compounds which in addition to a or more alcoholic hydroxyl groups one or more wear primary and / or secondary amino groups.  

Alcohols with a higher valence than 2, for adjustment a certain degree of branching or networking can, for. B. trimethylolpropane, glycerin or sugar.

Also suitable are monoalcohols which, in addition to the hydroxyl Group carry another isocyanate-reactive group such as monoalcohols with one or more primary and / or secondary amino groups, e.g. monoethanolamine.

Polyamines with 2 or more primary and / or secondary amino groups pen are mainly used when the chain extension or crosslinking should take place in the presence of water, since Amines are generally faster than using alcohols or water Isocyanates react. This is often necessary when aqueous dispersions of cross-linked polyurethanes or polyures thanen with a high molecular weight are desired. In such cases the procedure is such that prepolymers with isocyanate groups manufactures, quickly dispersed in water and then by adding compounds with more than isocyanates reactive amino groups chain-extended or cross-linked.

Suitable amines are generally polyfunctional amines of the molecular weight range from 32 to 500 g / mol, preferably from 60 to 300 g / mol, which selected at least two amino groups from the group of primary and secondary amino groups, contain. Examples include diamines such as diaminoethane, Diaminopropanes, diaminobutanes, diaminohexanes, piperazine, 2,5-dimethylpiperazine, amino-3-aminomethyl-3,5,5-trimethyl-cyclo hexane (isophoronediamine, IPDA), 4,4'-diaminodicyclohexylmethane, 1,4-diaminocyclohexane, aminoethylethanolamine, hydrazine, hydrazine hydrate or triamines such as diethylenetriamine or 1,8-diamino-4-aminomethyloctane.

The amines can also be in blocked form, e.g. B. in the form of ent speaking ketimines (see e.g. CA-A-1 129 128), ketazines (cf. e.g. B. US-A 4 269 748) or amine salts (see US-A 4 292 226) be used. Also oxazolidines, as for example in of US-A 4 192 937 are capped polyamines represents the production of the polyurethanes of the invention can be used to extend the chain of the prepolymers. When using such capped polyamines, they become generally with the prepolymers in the absence of water mixed and then this mixture with the Dis persion water or part of the dispersion water mixed, so that the corresponding polyamines are released hydrolytically the.  

Mixtures of di- and triamines are preferably used, mixtures of isophoronediamine (IPDA) and Diethylene triamine (DETA).

The polyurethanes preferably contain 0 to 30, especially preferably 4 to 25 mol%, based on the total amount of the compo nenten (b1) and (d1) of a polyamine with at least 2 opposite Isocyanate-reactive amino groups as monomers (d1).

For the same purpose, monomers (d1) can also be higher than divalent isocyanates are used. Commercial Compounds are, for example, isocyanurate or biuret of hexamethylene diisocyanate.

Monomers (e1), which may also be used, are mono isocyanates, monoalcohols and monoprimary and monosecondary amines. In general, their proportion is at most 10 mol%, based on the total molar amount of the monomers. These monofunctional Compounds usually carry further functional groups such as olefinic groups or carbonyl groups and are used for Introduction of functional groups in the polyurethane that the Dispersion or crosslinking or other polymer-analog Enable implementation of the polyurethane. Come into consideration here for monomers such as isopropenyl-α, α-dimethylbenzyl isocyanate (TMI) and esters of acrylic or methacrylic acid such as hydroxyethyl acrylate or hydroxyethyl methacrylate.

Coatings with a particularly good property profile are obtained especially when essentially only as monomers (a1) aliphatic diisocyanates, in particular the proportion of HMDI is at least 33 mol%, cycloaliphatic diisocyanates or TMXDI and essentially only a polyester as monomer (b1.1) diol, built up from the aliphatic diols and diacid mentioned ren, are used.

This combination of monomers is excellently supplemented as Component (c1) by diaminosulfonic acid alkali salts; all especially through the N- (2-aminoethyl) -2-aminoethanesulfonic acid or their corresponding alkali salts, the Na salt being best is suitable, and a mixture of DETA / IPDA as component (d1).

In the field of polyurethane chemistry, it is well known how the molecular weight of the polyurethanes by choosing the proportions of the mutually reactive monomers and the arithmetic mean the number of reactive functional groups per molecule can be put.  

Components (a1) to (e1) and their respective molar amounts are normally chosen so that the ratio A: B with

• A) the molar amount of isocyanate groups and
• B) the sum of the molar amount of the hydroxyl groups and the mol amount of functional groups with isocyanates in one Can react addition reaction.

0.5: 1 to 2: 1, preferably 0.8: 1 to 1.5, particularly preferably 0.9: 1 to 1.2: 1. That is very particularly preferred Ratio A: B as close as possible to 1: 1.

The monomers (a1) to (e1) used bear on average usually 1.5 to 2.5, preferably 1.9 to 2.1, particularly preferably 2.0 isocyanate groups or functional groups with Isocyanates can react in an addition reaction.

The polyurethanes contained in the dispersion according to the invention preferably do not contain effective amounts of acylurea group pen, which is implemented in the polyurethanes contained carbodiimide groups of the formula (I) with carboxylic acids, especially those of the formula RCOOH, in which R is sown for one saturated or unsaturated hydrocarbon radical is obtained to let.

At least the ratio of acyl groups to groups is Formula (I) less than 4: 1, preferably less than 1: 1, particularly preferably less than 0.2: 1.

The polyaddition of components (a1) to (e1) takes place in generally at reaction temperatures of 20 to 180 ° C, preferred 50 to 150 ° C under normal pressure or under autogenous pressure.

The required response times can be a few minutes extend to a few hours. It is in the field of Polyurethane chemistry is known as the reaction time through a Variety of parameters such as temperature, concentration of the Monomers, reactivity of the monomers is affected.

To accelerate the reaction of the isocyanates, the usual catalysts, such as dibutyltin dilaurate, stannous octoate or diazabicyclo- (2,2,2) octane.  

Stirred tanks are suitable as polymerization apparatus especially when using solvents ensures low viscosity and good heat dissipation is.

Preferred solvents are infinitely miscible with water, have a boiling point at normal pressure of 40 to 100 ° C and do not react or react only slowly with the monomers. If necessary, others can be proportionate, with water unlimited miscible solvents with a boiling point at normal pressure <100 ° C can be used. Examples include N-methylpyrroli don, dimethylformamide or dimethylacetamide.

These high-boiling solvents can be in the dispersion remain. However, they should not be in quantities greater than 10% by weight, on dispersion. Most often the dispersions are made according to one of the following Process made:

After the "acetone process" is in a miscible with water and at normal pressure below 100 ° C boiling solvent from the Components (a1) to (c1) made an ionic polyurethane. So much water is added until a dispersion forms, in which water is the coherent phase.

The "prepolymer mixing process" differs from the acetonever drive in that not a fully reacted (potentially) ionic Polyurethane but first a prepolymer is made which carries isocyanate groups. The components are like this chosen that the definition ratio A: B greater than 1.0 to 3, preferably 1.05 to 1.5. The prepolymer is first in Dispersed water and then optionally by reaction of the isocyanate groups with amines that are more than 2 opposite Wear isocyanate-reactive amino groups, crosslinked or with amino NEN which carry 2 amino groups reactive towards isocyanates, chain extended. A chain extension also takes place if no amine is added. In this case, isocyanate groups hydrolyzed to amino groups, with those still remaining Isocyanate groups of the prepolymers with chain extension react.

Usually, if in the manufacture of the polyurethane a solvent was used, most of the Solvent removed from the dispersion, for example by Distillation under reduced pressure. Preferably, the Dispersions have a solvent content of less than 10% by weight and are particularly preferably free of solvents.  

The dispersions generally have a solids content of 10 to 75, preferably 20 to 65% by weight and a viscosity of 10 to 500 m Pas (measured at a temperature of 20 ° C. and a shear rate of 250 s ^-1 ).

Hydrophobic aids that can be difficult to homogenize to be distributed in the finished dispersion, for example Phenol condensation resins made from aldehydes and phenol or phenol derivatives or epoxy resins and other z. B. in DE-A-39 03 538, 43 09 079 and 40 24 567 polymers mentioned in polyurethane dispersions serve, for example, as adhesion improvers, can be described according to the two fonts mentioned above The methods already mentioned are the polyurethane or the prepolymer be added to the dispersion.

Preparations containing the polyurethane dis according to the invention persion (1), commercially available auxiliaries and additives such as further polymers (b1) in dispersed form, blowing agents, Defoamers, emulsifiers, thickeners and thixotropic agents medium, contain colorants such as dyes and pigments.

The polymers (B) which the dispersion according to the invention contains can be, for example, a polyurethane (2) which is usually composed of

• a2) Diisocyanates that do not contain carbodiimide groups
• b2) diols, of which
  • b2.1) 0 to 100 mol%, based on the total amount of diols (b2), have a molecular weight of 500 to 5000, and
    b2.2) 0 to 90 mol%, based on the total amount of diols (b2), have a molecular weight of 60 to 500 g / mol,
• c2) with monomers different from monomers (a2) and (b1) at least one isocyanate group or at least one ge compared to isocyanate groups reactive group that from at least one hydrophilic group or one potentially wear hydrophilic group, causing water dispersion availability of the polyurethanes is effected,
• ed2) optionally further of the monomers (a2) to (c2) various multivalent compounds with reactive group pen, which are alcoholic hydroxyl groups, pri  mary or secondary amino groups or isocyanate groups acts and
• e2) optionally different from the monomers (a2) to (d2) monovalent compounds with a reactive group in which it is an alcoholic hydroxyl group, a primary one or secondary amino group or an isocyanate group delt.

The same monomers come as (a2), (b2), (c2), (d2), (e2) Monomers into consideration as monomers (a1.2), (b1), (c1), (d1), (e1) can be used. Aside from the fact that they do not contain carbodiimide groups, the same applies to them as for the polyurethanes (1), d. H. otherwise they generally indicate mean the same properties and can in principle can be produced in the same way as the polyurethanes (1).

Polymers (polymer 3) prepared by radical-initiated polymerization are also suitable as polymers (B). These are usually made up of

• a3) 30 to 100 parts by weight of at least one monomer from the group comprising C ₁ to C ₂₀ alkyl (meth) acrylates, vinyl esters, carboxylic acids having up to 20 C atoms, ethylenically unsaturated nitriles, vinyl aromatics with up to 20 C atoms, vinyl halides and aliphatic hydrocarbons with 2 to 8 C atoms and 1 or 2 double bonds (monomers a3) and
• b3) 0 to 70 parts by weight of other, at least one ethylenically compounds I having unsaturated group (monomers b3).

(Meth) acrylic is a shortening for methacrylic or acrylic.

As monomers (a3) are z. B. (meth) acrylic acid alkyl ester with a C ₁ -C ₁₀ alkyl radical, such as methyl methacrylate, methyl acrylate, n-butyl acrylate, ethyl acrylate and 2-ethylhexyl acrylate.

In particular, mixtures of the (meth) acrylic acid alkyl esters suitable.

Vinyl esters of carboxylic acids with 1 to 20 carbon atoms are e.g. B. Vinyl laurate, stearate, vinyl propionate and vinyl acetate.  

Suitable vinyl aromatic compounds are vinyl toluene, α- and p-methylstyrene, α-butylstyrene, 4-n-butylstyrene, 4-n-decylstyrene and preferably styrene.

Examples of nitriles are acrylonitrile and methacrylonitrile.

The vinyl halides are substituted with chlorine, fluorine or bromine ethylenically unsaturated compounds, preferably vinyl chloride and Vinylidene chloride. However, vinyl halides are not preferred.

As non-aromatic hydrocarbons with 2 to 8 carbon atoms and one or two olefinic double bonds are butadiene, iso pren and chloroprene, as well as ethylene, propylene and isobutylene called.

The main monomers are also preferably mixed set.

Vinyl aromatic compounds such as styrene are e.g. B. often mixed with C ₁ -C ₂₀ alkyl (meth) acrylates, in particular with C ₁ -C ₈ alkyl (meth) acrylates, or non-aromatic hydrocarbons such as isoprene or preferably butadiene.

As monomers (b3) come, for. B. into consideration: esters of acrylic and Methacrylic acid of alcohols with 1 to 20 carbon atoms, which besides that Oxygen atom in the alcohol group at least one more Contain heteroatom and / or an aliphatic or aroma table ring contain, such as 2-ethoxyethyl acrylate, 2-butoxy ethyl (meth) acrylate, dimethylaminoethyl (meth) acrylate, diethyl aminoethyl (meth) acrylate, (meth) acrylic acid aryl, alkaryl or Cycloalkyl esters, such as cyclohexyl (meth) acrylate, phenyl ethyl (meth) acrylate, phenylpropyl (meth) acrylate or acrylic acid esters of heterocyclic alcohols such as furfuryl (meth) acrylate.

In addition, monomers with amino or amide groups such as (meth) acrylamide and their derivatives substituted on the nitrogen with C ₁ -C ₄ -alkyl are also suitable.

Of particular importance are hydroxy-functional monomers, e.g. B. (meth) acrylic acid-C ₁ -C ₁₅ alkyl esters which are substituted by one or two hydroxyl groups. Of particular importance as hydroxy-functional comonomers are (meth) acrylic acid C ₂ -C ₈ hydroxy alkyl esters, such as n-hydroxyethyl, n-hydroxypropyl or n-hydroxybutyl (meth) acrylate.

It is often advisable to use monomers with carbon acid or carboxylic anhydride groups, e.g. B. acrylic acid, meth acrylic acid, itaconic acid, maleic or fumaric anhydride; these monomers are preferably in amounts of 0 to 10, be particularly preferably from 0.1 to 3% by weight, based on the copoly merisat, used.

The copolymer A) is prepared by free radicals Polymerization. Suitable polymerization methods, such as substance, Solution, suspension or emulsion polymerization are that Known specialist.

The copolymer is preferably obtained by solution polymerization with subsequent dispersion in water or especially preferably produced by emulsion polymerization.

The comonomers can be used as usual in emulsion polymerization in the presence of a water-soluble initiator and one Emulsifier can be polymerized at preferably 30 to 95 ° C.

Suitable initiators are e.g. B. sodium, potassium and ammonium persulfate, peroxides such as B. tert-butyl hydroperoxide, water-soluble azo compounds or redox initiators.

As emulsifiers z. B. Long chain alkali salts Fatty acids, alkyl sulfates, alkyl sulfonates, alkylated aryl sulfonates or alkylated biphenyl ether sulfonates. Furthermore come as emulsifiers reaction products of alkylene oxides, especially ethylene or propylene oxide with fatty alcohols or acids or phenol or alkylphenols into consideration.

In the case of aqueous secondary dispersions, the copolymer first by solution polymerization in an organic Solvent produced and then with the addition of Salt formers, e.g. B. of ammonia, ent to carboxylic acid groups holding copolymers in water without using a Emulsifier or dispersing agent dispersed. The organic solvents can be distilled off. The The preparation of aqueous secondary dispersions is known to the person skilled in the art known and z. B. described in DE-A-37 20 860.

To adjust the molecular weight in the polymer sation controller can be used. Are suitable for. B. -SH groups containing compounds such as mercaptoethanol, mercaptopropanol, Thiophenol, thioglycerin, thioglycolic acid ethyl ester, thioglycol acid methyl ester and tert-dodecyl mercaptan. You can e.g. B. in  Quantities from 0 to 0.5% by weight, based on the copolymer, be used.

The type and amount of the comonomers are preferably chosen so that that the copolymer obtained has a glass transition temperature between -60 to + 140 ° C, preferably -60 to + 100 ° C. The Glass transition temperature of the copolymer is determined by Differential thermal analysis or differential scanning calorimetry determined according to ASTM 3418/82.

The number average molecular weight M _n is preferably 10 ³ to 5.10 ⁶ , particularly preferably 10 ⁵ to 2.10 ⁶ g / mol (determined by gel permeation chromatography with polystyrene as standard).

Aqueous dispersions which are suitable for the production of coated textiles, which are mainly used in building protection and in particular as roofing membranes, preferably have the following composition:

• A) 10 to 100 wt .-% of a polyurethane (1) which is hydrophilic Groups that increase the water dispersibility of the polyure enable thans
• B) optionally 5 to 90% by weight of a polymer (B)
• C) optionally 0.1 to 10% by weight of an emulsifier
• D) optionally 0.1 to 10 wt .-% of an aminoplast or Phenolic resin
• E) optionally 1 to 30% by weight of a flame retardant and
• F) optionally 1 to 70% by weight of a filler.
• G) optionally 1 to 30% by weight of an oleophobicizing agent.

Components (B) to (G) are commercially available. What materia lien are particularly suitable, for example, in the DE-A-196 09 311 explained in more detail. In this script there is also a Process for the production of coated textiles are particularly suitable for building protection and under Made using other aqueous dispersions are described, which also applies to the invention Preparation containing component (A) and optionally further of components (B) to (G) is applicable.  

The aqueous dispersion according to the invention contains, for example, higher alkyl sulfates, alkylbenzenesulfonates, dialkylsulfosuccinates, polyoxyethylene alkylphenyl ethers or fatty acids as emulsifiers in the form of their alkali metal or ammonium salts. A mixture of alkali n-octadecyl sulfonate and alkali (C ₉ -C ₁₄ -alkyl) sulfosuccinate is preferably used as the emulsifier, the mixing ratio being 0.5: 1 to 1: 1.

Suitable aminoplast or phenolic resins (component D) are generally known commercial products (cf. Ullmanns Encyclopedia of Technical Chemistry, Volume 7, 4th edition, 1974, Pages 403 to 422 and Ullmann's encyclopedia of industrial chemistry, volume A19, 5th edition, 1991, pages 371 to 384.

The melamine-formaldehyde resins are preferred, with up to 20 mol% of melamine can be replaced by equivalent amounts of urea can. Methylolated melamine, e.g. B. bi-, Tri- and / or tetramethylolmelamine.

The melamine formaldehyde resins are usually in powder form or used in the form of their concentrated aqueous solutions, whose solids content is 40 to 70 wt .-%.

Suitable flame retardants (component E) are, for example, antimony trioxide Sb ₂ O ₃ , antimony pentoxide Sb ₂ O ₃ , aluminum oxide hydrate Al ₂ O ₃ .3H ₂ O, zinc borate Zn (BO ₂ ) ₂ .2H ₂ O or 2ZnO (B ₂ O ₃ ) _3. (H ₂ O) _3.5 , ammonium orthophosphate or polyphosphate NH ₄ H ₂ PO ₄ or (NH ₄ PO ₃ ) _n , melamine, melamine cyanurate and chlorinated paraffins.

The melamine is suspended in the aqueous dispersion Form before. The average particle diameter is preferably 5 up to 100 µm, particularly preferably 10 to 50 µm. It becomes more convenient as a powder of the particle size mentioned used.

The phosphonic acid esters are particularly preferred, in particular 5-ethyl-2-methyl-1,3,2-dioxaphosphorinan-5-yl) methylphosphonate P-oxide and bis (5-ethyl-2-methyl-1,3,2-dioxaphosphorinan-5-yl) -me thymethylphosphonate-P, P'-dioxide.

For the fillers (component F), which are the aqueous Containing dispersions are common types available commercially suitable.

The average particle diameter is preferably 0.1 to 10 µm.  

Suitable fillers (component F) are, for example, CaCO ₃ BaSO ₄ , TiO ₂ , ZnO and talc.

Kaolins are particularly preferred.

Suitable oleophobicizing agents (component G) are examples wise fluorocarbons, optionally in aqueous emuls sion.

The aqueous dispersions according to the invention are used moderately if necessary with the help of thickening average to a viscosity of 500 to 3000 mPa.s (measured at Room temperature). Are suitable as thickeners usual thickeners such as polyacrylic acids, polyvinyl pyrrolidones or cellulose derivatives such as methyl cellulose.

The pH of the aqueous dispersions according to the invention is usually 3 to 10, preferably 8 to 10 and her Solids content generally 20 to 70, preferably 30 to 60.

The aqueous dispersion according to the invention is suitable as a coating agent for coating woven, knitted or fleece-like textile carrier materials for their waterproof, vapor-permeable and flame-retardant finish. Carrier materials made of synthetic fibers are preferably used. Examples of these are polyethylene, polypropylene, polyester, polyamide, polyacrylonitrile and glass fibers. Raw nonwovens, in particular spunbonded nonwovens, made from the synthetic fibers mentioned and having a basis weight of 50 to 300 g / m ² are particularly preferred.

To produce the coated textiles, the aqueous dispersions according to the invention by customary processes directly or indirectly (transfer coating) on the textile Carrier materials applied, e.g. B. by knife or brush, and then the coated carrier material is dried.

The procedure is preferably as follows:
The coating agent is applied in foam form to the carrier material, as this significantly improves the vapor permeability. For this purpose, the coating agent is mechanically foamed after adding the foam stabilizer and, if appropriate, thickener and other additives. This can be done in a foam mixer with high shear forces. Another possibility is to foam up in a foam generator by blowing in compressed air. Foaming is preferably carried out by means of a foam generator.

The foamed coating composition is then applied to the carrier material using conventional coating devices, for example a doctor blade or other foam application device. The order can be made on one or both sides; it is preferably carried out on both sides. The application quantity per side is from 20 to 150 g / m ² , in particular 50 to 90 g / m ² . At quantities below 20 g / m ² , good vapor permeability is obtained at low costs, but insufficient flame protection and poor water resistance. At quantities above 150 g / m ² , crack formation occurs during drying.

After application, the foam is in the air with little air Drying tunnel, for example by infrared heating, with a Temperature gradients from 60 to 180 ° C, preferably 60 to 130 ° C dried.

In order to improve the flame retardant effect preferred embodiment of the foam on both sides in one Layer thickness of 0.3 to 1.0 mm applied. Particularly preferred the foam is applied to the two in different layer thicknesses Sides of the carrier material applied. With the latter The foam is on the bottom of the embodiment Carrier material in a thin layer of maximum 0.4 mm Layer thickness, preferably applied with a knife knife, that it is as deep as possible in the cavities of the fleece between the Fibers penetrates. The foam on the top becomes an improvement waterproofing, preferably with a splitting knife, especially in a layer of 0.3 to 1.0 mm layer thickness, applied.

In a particularly preferred embodiment, in order to improve the abrasion resistance, the flame-retardant effect and the watertightness, the foam layer can be compressed after drying and partially pressed into the fleece. The compression can take place, for example, by calendering in a temperature range from 20 to 180 ° C. and at a line pressure of 50 to 3000 N / cm, it being advantageous to hot calender between two smooth rollers, one made of steel and one made of a softer material, for example polyamide or rubber. In particular, only the foam layer on the top of the textile carrier material is compressed. If necessary, a further coating, preferably in an amount of 5 to 30 g / m ² , with unfoamed dispersion can be carried out to improve the water resistance and the abrasion resistance.

It is also possible to ensure the waterproofness of the coated To improve textiles by using a fluorocarbon, e.g. B. as an aqueous emulsion, and then drying.

With the procedure according to the invention, in the preferred foam coating, for example of polyester nonwovens (PET), materials with very high water resistance (DIN 53 886: <300 mm water column), with very high water vapor permeability (DIN 53 122/1: <350 g) are obtained / m ² / d) and an excellent flame retardancy, which corresponds to the classification according to DIN 4102 B2.

Those with the preparation containing components (A) to (G), coated textile substrates are suitable for Use in building protection as roofing membranes or sealing membranes, for example under roof tiles or wooden facade walls. she are also suitable for use as protective tarpaulins for devices and Materials and for use in the geotextile sector.

Objects made of metal, plastic, paper, leather or wood can also be used with other objects, preferably the the aforementioned objects, glue by the aqueous dispersion according to the invention in the form of a film applies one of these items and applies it before or after Drying the film together with another item.

Objects made of textile, leather or paper can be used with the Impregnate dispersions according to the invention by this Soak objects with the aqueous dispersion and then dries.

Generally used to manufacture the coated textiles or Fleeces as well as the glued objects the preparations, containing the aqueous dispersion (1) according to the invention applied conventional methods, e.g. B. by knife or brush and then the coated carrier material is dried. The Process and other components of the preparations described in the preparation has its generally known function, depend on the respective area of application.

Experimental part Abbreviations

DETA = diethylene triamine
HMDI = bis (4-isocyanatocyclohexyl) methane
IPDA = isophoronediamine
DBTL = dibutyltin dilaurate
TMXDI = tetramethylxylylene diisocyanate
IPDI = 1-isocyanato-3,5,5-trimethyl-5-isocyanatomethylcyclohexane
CDI = carbodiimide.

A. Starting products Example 1 (CDI-containing PUD) Dispersion D1

400 g (0.200 mol) of a polyesterol from adipic acid, neopentyl glycol and hexanediol of OH number 56 and 2.5 g (0.003 mol) of one Carbodiimids from TMXDI with an NCO content of 10.0% by weight and a CDI content of 14.2% by weight was added in a stirred kettle 50 ° C submitted. To this were added 35.4 g (0.1594 mol) IPDI, 42.9 g (0.1624 mol) HMDI and 80 g acetone added. After 60 min. stir 0.15 g of DBTL were added at 90 ° C. and the mixture was stirred for a further 120 min. The mixture was then diluted with 500 g of acetone and at the same time at 50 ° C. chilled. The NCO content of the solution was 0.97% (calc. 0.94%). After adding 22.5 g (0.0534 mol) of a 50% aqueous solution of the Na salt of aminoethylaminoethanesulfonic acid was by 800 g of water are added within 5 minutes. dispersed. After at the end of the dispersion, a solution of 3.9 g (0.0379 mol) DETA and 1.8 g (0.0106 mol) IPDA in 50 g water were added. After distilling the acetone, a fine particle size resulted aqueous PUR dispersion with approx. 40% solids content.

Carbodiimide content: 17.2 mmol / kg.

Example 2 (CDI-containing PUD) Dispersion D2

400 g (0.200 mol) of a polyesterol from adipic acid, neopentyl glycol and hexanediol of OH number 56 and 5.0 g (0.006 mol) of one Carbodiimids from TMXDI with an NCO content of 10.0% by weight and a CDI content of 14.2% by weight was added in a stirred kettle 50 ° C submitted. For this purpose, 34.8 g (0.1565 mol) IPDI, 42.9 g (0.1624 mol) HMDI and 80 g acetone added. After stirring for 60 min 90 ° C., 0.15 g of DBTL were added and the mixture was stirred for a further 120 min. Then was diluted with 500 g acetone and simultaneously cooled to 50 ° C. The NCO content of the solution was 0.99% (calc. 0.94%). After encore of 22.5 g (0.0534 mol) of a 50% aqueous solution of Na-Sal The aminoethylaminoethanesulfonic acid was removed by adding  800 g of water dispersed within 5 minutes. After the end of the Dispersion was a solution of 3.9 g (0.0379 mol) DETA and 1.8 g (0.0106 mol) of IPDA in 50 g of water were added. After Distillation of the acetone resulted in a finely divided aqueous solution PUR dispersion with approx. 40% solids content.

Carbodiimide content: 35.5 mmol / kg.

Comparative Example 1 (without carbodiimide) Dispersion D3

400 g (0.200 mol) of a polyesterol from adipic acid, neopentyl Glycol and hexanediol with OH number 56 were in a stirred kettle submitted at 50 ° C. To this were added 36.1 g (0.1624 mol) IPDI, 42.9 g (0.1624 mol) HMDI and 80 g acetone added. After stirring for 60 min 90 ° C., 0.15 g of DBTL were added and the mixture was stirred for a further 120 min. Then was diluted with 500 g acetone and simultaneously cooled to 50 ° C. The NCO content of the solution was 0.99% (calc. 0.94%). After encore of 22.5 g (0.0534 mol) of a 50% aqueous solution of Na-Sal The aminoethylaminoethanesulfonic acid was removed by adding 800 g of water dispersed within 5 minutes. After the end of the Dispersion was a solution of 3.9 g (0.0379 mol) DETA and 1.8 g (0.0106 mol) of IPDA in 50 g of water were added. After Distillation of the acetone resulted in a finely divided aqueous solution PUR dispersion with approx. 40% solids content.

Comparative Example 2 (carbodiimide added to the dispersion) Dispersion D4

5.6 g were added to 500 g of the dispersion from comparative example 1 one prepared according to Example 3 of EP 628 541 water soluble carbodiimide containing carbodiimide of 1250 mmol / kg added.

Carbodiimide content: 35.0 mmol / kg.

exam

For testing, the dispersions were films with a thickness of approximately 1 mm poured and allowed to dry for 3 days at 23 ° C. Immediately after their manufacture and after 7 days of storage at 70 ° C and Their tensile strength was 90% relative humidity according to DIN 53 504 measured.

The test results are shown in Table 1.  

Table 1

It is surprising that the tensile strength due to the wet-warm Storage not only does not decrease, but even increases.

Examples of use PUR mixing dispersion (CDI-free) Dispersion D5

400 g (0.200 mol) of a polyesterol from adipic acid, neopentyl Glycol and hexanediol with OH number 56 were in a stirred kettle submitted at 50 ° C. 110.0 g (0.4948 mol) of IPDI, 129.9 g, were added (0.4917 mol) HMDI and 100 g acetone added. After stirring for 60 min at 90 ° C 0.15 g DBTL and 54.0 g (0.600 mol) 1,4-butanediol added and stirred for a further 120 min. Then with 640 g of acetone diluted and cooled to 50 ° C at the same time. The NCO content of the Solution was 0.97% (calc. 1.02%). After adding 25.3 g (0.060 mol) of a 50% aqueous solution of the Na salt of aminoethyl aminoethanesulfonic acid was internal by adding 850 g of water dispersed half of 5 min. After the end of the dispersion was a solution of 6.5 g (0.0631 mol) DETA and 2.4 g (0.0141 mol) IPDA added in 50 g of water. After distilling the acetone resulted in a fine-particle aqueous PU dispersion with approx. 40% Fixed salary.

B. Preparation of the coating agent Example B1

46 g of dispersion D1 were introduced and 12 g with stirring Dispersion D5 added. Then 14.2 g of water and 0.85 g of ammonia (25%) was added. With further stirring then 2.5 g of 35% ammonium stearate (from Bärlocher) and 0.4 g of one Disodium n-octadecylsulfosuccinamate (Aerosol® 18, Cytec)  and 0.2 g of a sodium alkyl sulfate (Empimin® LR 28, Albright & Wilson) added. Furthermore, 0.75 g of brown pigment (Helizarin® Braun TT conc., From BASF), 10 g melamine (<40 µm, from. BASF) and 13 g of kaolin (China Clay SPS, Bassermann) added. Then 1.1 g of melamine resin (Saduren® 163, from BASF) and 3.2 g of a flame retardant (Amgart CT®, Albright & Wilson) added. This approach then becomes 0.8 g Polyacrylic acid thickener (Latekoll® D, BASF) on a Viscosity of 1800-2000 mPas (Haake VT 02, spindle 1) thickened.

Example B2

46 g of dispersion D1 were introduced and 12 g of dis persion D5 added. Then 14.2 g of water and 0.85 g Ammonia (25%) added. Then, with further stirring 2.5 g of 35% ammonium stearate (from Bärlocher) and 0.4 g of a dina trium-n-octadecylsulfosuccinamate (Aerosol® 18, Cytec) and 0.2 g of a sodium alkyl sulfate (Empimin® LR 28, Albright & Wilson) added. 0.75 g of brown pigment (Helizarin® Braun TT conc., From BASF), 5 g melamine cyanurate (Budit 315 approx. 2 µm, Chem. Fabrik, Budenheim) and 13 g kaolin (China Clay SPS, Bassermann) admitted. Then 1.1 g of melamine resin (Saduren® 163, from BASF) and 3.2 g of a flame retardant (Am gart CT®, Albright & Wilson) added. This approach will then with 0.8 g of a polyacrylic acid thickener (Latekoll® D, Fa. BASF) to a viscosity of 1800-2000 mPas (Haake VT 02, Spin del 1) thickened.

Example B3

28.5 g of dispersion D1 were initially introduced and 28.5 g with stirring Dispersion D5 added. Then 13.8 g of water and 0.85 g of ammonia (25%) was added. With further stirring then 3.2 g of 35% ammonium stearate (from Bärlocher) and 0.5 g of one Disodium n-octadecylsulfosuccinamate (Aerosol® 18, Cytec) and 0.3 g of a sodium alkyl sulfate (Empimin® LR 28, Albright & Wilson) added. Next, 0.63 g of brown pigment (Helizarin® Braun TT conc., From BASF) and 5.3 g of melamine cyanurate (Budit 314, approx. 8 µm, from Chem. Fabrik, Budenheim) and 12.7 g Kaolin (China Clay SPS, Fa. Bassermann) added. After that still 1.1 g of melamine resin (Saduren® 163, from BASF) and 3.2 g of one Flame retardant (Amgart CT®, Albright & Wilson) added puts. This batch is then mixed with 1.4 g of a polyacrylic acid Thickeners (Latekoll® D, BASF) to a viscosity of 2400 m.Pas (Haake VT 02, spindle 1) thickened.  

Example B4

28.5 g of dispersion D1 were initially introduced and 28.5 g with stirring Dispersion D5 added. Then 13.8 g of water and 0.85 g of ammonia (25%) was added. With further stirring then 3.2 g of 35% ammonium stearate (from Bärlocher) and 0.5 g of one Disodium n-octadecylsulfosuccinamate (Aerosol® 18, Cytec) and 0.3 g of a sodium alkyl sulfate (Empimin® LR 28, Fa. Albright & Wilson) added. Next, 0.63 g of brown pigment (Helizarin® Braun TT conc., From BASF) and 5.3 g of melamine cyanurate (Budit 315, approx. 2 µm, from Chem. Fabrik, Budenheim) and 12.7 g Kaolin (China Clay SPS, Fa. Bassermann) added. After that 1.1 g of Melaminhar® (Saduren® 163, from BASF) and 3.2 g of one Flame retardant (Amgart CT®, Albright & Wilson) added puts. This batch is then mixed with 1.3 g of a polyacrylic acid Thickeners (Latekoll® D, BASF) to a viscosity of 2300 mPas (Haake VT 02, spindle 1) thickened.

Example B5

40 g of dispersion 1 were introduced and 20 g of Acronal® with stirring S 560, 40 g Vinofan® V 800 and 200 g water added. Under 22.5 g of yellow seal chalk (from Norway Talc) added. 6 g of brown pigment (Helizarin® Brown TT conc., From BASF) added. Then 2.5 g of melamine resin (Saduren® 163, from BASF) added. This approach then with 0.1 g of an acrylic acid / acrylamide thickener (Streocoll® BL, BASF) and 12.5 g of a polyacrylic acid thickener (Lutexal® TX 4623X, from BASF) to a viscosity of 9500 m.Pas (Haake VT 02, Spindle 1) thickened.

Example B6

60 g of dispersion 1 were introduced and 40 g of Vinofan with stirring V 800 and 180 g of water were added. With further stirring then 22.5 g of yellow seal chalk (from Norway Talk) were added. 6 g of brown pigment (Helizarin® Braun TT conc., Fa. BASF) added. Then 2.5 g of melamine resin (Saduren® 163, BASF) added. This approach is then 0.1 g Acrylic acid / acrylamide thickener (Streocoll® BL, from BASF) and 12.5 g of a polyacrylic acid thickener (Lutexal® TX 4623X, Fa. BASF) to a viscosity of 8500 m.Pas (Haake VT 02, spindle 1) thickened.  

C. Manufacture of the fleece coating Examples V1-V4

The coating compositions according to Examples B1-B4 were mechanically foamed using a stork mixer (foam density 250 g / l) and spunbonded on a polyester gauze weighing approx. 130 g / m ² by means of a splitting knife (Monforts) on one side of the fleece surface (foam height: 1 mm). The coated fleece was then pre-dried in a forced-air drying cabinet at 100 ° C. The foam layer was calendered with a line pressure of 80 KN / 60 cm at approx. 20 ° C and then oleophobicized with 40 g / l Persistol O (fluorocarbon). The crosslinking took place at 2 min. at 160 ° C.

Examples V5-V6

The coating compositions according to Examples B5-B6 were knife-coated onto a "Supermatt" transfer paper (from Warren & Co, Belgium) using a splitting knife (0.15 mm) and left for approx. 3 min. predried at 100 ° C in a circulating air dryer. Subsequently, this coating coat (top coat) with the coating agent according to Example 5-6 with a doctor blade (0.2 mm) is knife-coated (laminating coat) and the carrier fleece (PET, approx. 115 g / m ² ) is laminated with a defined pressure and 4 min. pre-dried at 100 ° C in a circulating air dryer. The coated sample was then separated from the paper, oleophobicized and 2 min. Networked at 170 ° C in a circulating air dryer.

D. Application test

The coated nonwovens produced according to Examples V1-V6 have been tested for water resistance, water vapor permeability and Flame retardancy tested. The test results are in Table 2 reproduced.

For comparison, a Roofing membrane manufactured according to Example 1 from the DE-A-196 09 311 (comparative example 3) checked.  

Table 2

Claims (13)

1. Aqueous dispersions containing a polyurethane (1) which contains carbodiimide structural units of the formula (I)
-N = C = N- (I)
contains. 2. Aqueous dispersions according to claim 1, wherein the content of Carbodiimide structural units, based on the polyurethane, 5 to 200 mmol / kg. 3. Aqueous dispersions according to claim 1 or 2, wherein the Carbodiimide structural units of formula (I) in the poly urethane are introduced via polyisocyanates (a1.1), containing one or more of the carbodiimide structural units ten of formula (I). 4. Aqueous dispersions according to claim 3, wherein it is the polyisocyanates (a1.1) around tetramethylxylylene diisocyanate (TMXDI) acts. 5. Aqueous dispersions according to claims 1 to 4, built up from

• a1) diisocyanates, the
  • a1.1) contain structural units of the formula (I) and, if appropriate,
  • a1.2) which are free from structural units of the formula (I),
• b1) diols, of which
  • b1.1) 0 to 100 mol%, based on the total amount of diols (b1), have a molecular weight of 500 to 5000, and
  • b1.2) 0 to 90 mol%, based on the total amount of diols (b1), have a molecular weight of 62 to 500 g / mol,
• c1) monomers different from the monomers (a1) and (b1) with at least one isocyanate group or at least one group which is reactive toward isocyanate groups and which, moreover, carry at least one hydrophilic group or a potentially hydrophilic group, where the water-dispersibility of the polyurethanes results in
• d1) optionally further polyvalent compounds with reactive groups different from the monomers (a1) to (c1), which are alcoholic hydroxyl groups, primary or secondary amino groups or isocyanate groups and
• e1) if appropriate from the monomers (a1) to (d1) different monovalent compounds having a reactive group which is an alcoholic hydroxyl group, a primary or secondary amino group or an isocyanate group.

6. Aqueous dispersions according to claim 5, wherein it is in the Diols (b1.1) are polyesterols. 7. Aqueous dispersions which are suitable for the production of coated textiles containing, based on the solids content

• A) 10 to 100 wt .-% of a polyurethane (1) which carries hydrophilic groups which enable the water dispersibility of the polyurethane
• B) optionally 5 to 90% by weight of a polymer (B), which is
  • B1) a polyurethane (2) which is different from the polyurethane (1) and is constructed
    • a2) Diisocyanates that do not contain carbodiimide groups
    • b2) diols, of which
      • b2.1) 10 to 100 mol%, based on the total amount of diols (b1), have a molecular weight of 500 to 5000, and
      • b2.2) 0 to 90 mol%, based on the total amount of the diols (b2), have a molecular weight of 60 to 500 g / mol,
    • c2) monomers different from the monomers (a2) and (b2) with at least one isocyanate group or at least one group which is reactive toward isocyanate groups and which, moreover, carry at least one hydrophilic group or a potentially hydrophilic group, thereby causing the water-dispersibility of the polyurethanes,
    • d2) optionally further from the monomers (a2) to (c1) different polyvalent compounds with reactive groups which are alcoholic hydroxyl groups, primary or secondary amino groups or isocyanate groups and
    • e2) optionally of the monomers (a2) to (d2) which monovalent compounds having a reactive group which is an alcoholic hydroxyl group, a primary or secondary amino group or an isocyanate group, or
  • B2) is a polymer (polymer 3) produced by radical-initiated polymerization, which is built up from
    • a3) 30 to 100 parts by weight of at least one monomer from the group comprising C ₁ - to C ₂₀ -alkyl (meth) acrylates, vinyl esters, of up to 20 carbon atoms having carboxylic acids, ethylenically unsaturated nitriles, vinyl aromatics with bis to 20 carbon atoms, vinyl halides and aliphatic hydrocarbons with 2 to 8 carbon atoms and 1 or 2 double bonds (monomers a3) and
    • b3) 0 to 70 parts by weight of other compounds I having at least one ethylenically unsaturated group (monomers b3)
• C) optionally 0.1 to 5% by weight of an emulsifier
• D) optionally 0.1 to 10% by weight of an aminoplast or phenolic resin
• E) optionally 1 to 30% by weight of a flame retardant and
• F) optionally 1 to 70% by weight of a kaolin.
• G) optionally 1 to 30% by weight of an oleophobicizing agent.

8. Process for coating metal objects, Plastic, paper, textile, leather or wood, characterized thereby records that an aqueous dispersion according to the Claims 1 to 7 in the form of a film on these items applies and the dispersion dries. 9. Process for gluing objects made of metal, art fabric, paper, textile, leather or wood, characterized by net that an aqueous dispersion according to the claims 1 to 7 in the form of a film on one of these objects and before and after drying the film another object. 10. Process for impregnating textile articles, Leather or paper, characterized in that one Objects with the aqueous dispersion according to the claims Soak 1 to 7 and then dry. 11. Process for the production of coated textiles, characterized in that

• I. an aqueous dispersion according to claims 1 to 7 thickened to a paste or mechanically foams to a foam,
• II. The foam or the paste is applied directly or indirectly (transfer) to the textile backing material and dries and
• III.
• optionally compressed the dried foam.

12. Objects with the aqueous dispersion according to the Claims 1 to 7 coated, glued or impregnated are. 13. Use of the coated according to claim 11 Textiles in building protection as roofing membranes or waterproofing membranes.