EP3762438A1

EP3762438A1 - Biocidal coating material and associated production process

Info

Publication number: EP3762438A1
Application number: EP19708111.0A
Authority: EP
Inventors: Karim El Kudsi
Original assignee: Individual
Current assignee: Individual
Priority date: 2018-03-06
Filing date: 2019-03-05
Publication date: 2021-01-13
Also published as: EP3536725A1; WO2019170653A1

Abstract

The invention relates to a biocidal coating material and an associated production process. The process comprises the steps of: (i) providing a ureamine component obtainable by reaction of a) an aliphatic or araliphatic di- or triisocyanate with b) a mixture of a first amine having a primary or secondary amine group and one or more second amines having 2 or more primary or secondary amine groups, wherein a ratio of the sum of the primary and secondary amine groups to the isocyanate groups is 10:1 to 2:1; (ii) providing an epoxide component which comprises one or more aliphatic polyfunctional glycidyl ethers; and (iii) reacting the ureamine component with the epoxide component, wherein a ratio of the epoxide groups of the epoxide component to the amine groups of the ureamine component is 0.25:1 to 1:0.25.

Description

Biocidal coating material and associated manufacturing process

The invention relates to a biocidal coating material and an associated production method.

Technological background

Coatings based on epoxides are widely used. These are based essentially on bisphenol A diglycidyl ether, bisphenol F diglycidyl ether, bisphenol diglycidyl ether, novolak epoxy systems and various amines as Hartem, z. Diethylenetriamine, dipropylenetriamine, isophoronediamine, 2,2,4- / 2,4,4-trimethylhexanediamine, etc. A biocidal effect, i. H. the prevention of the formation of biofilms on the surface of the coating and the subsequent growth of bacteria, algae, microfungi or marine organisms is usually achieved by additives. Such additives may include metals such as copper, tin or silver in various forms, organic chloro and sulfur compounds such as carbendazim or 2-methylthio-4-ferf-butylamino-6-cyclopropylamino-s-triazine, propioconazole, 3- (3,4 Dichlorophenyl) -1, 1-dimethylurea (diuron), 2-octylisothiazol-3 (2H) on (octhilinone), or metal compounds such as bis (tributyltin) oxide, triphenyltin hydroxide, and triphenyltin chloride. The active principle of all these compounds is based on the fact that small amounts are continuously released into the environment, but there can not be degraded due to their properties and accumulate.

Alternative solutions consist in the coating with wax, silicones or other hydrophobic materials, which are intended to prevent the attachment of microorganisms. The use of polyfluorinated compounds, which were traded as a possible alternative, has been prohibited by law, at least in Germany. Other hydrophobic compounds are under observation as potentially harmful to the environment.

The approaches mentioned primarily relate to coatings in the maritime area and for floors as well as those with contact for food or children. Bisphenol-A, S, F may no longer be used in the food and water sectors. This also applies to internal pipe coatings for service and drinking water.

Furthermore, it has been proposed coatings of cement-based systems or ceramic-like materials, see, for. WO 2007/1 15649 A1 or WO 2011/000339 A1. In newer technical solutions are mainly nanoparticles of different structure, nanoscale or hollow microspheres with biocides as content or nanoscale metals such as zinc or copper described, see, for. For example, US Pat. No. 7,201,790 B1.

Another technical solution, WO 2014/008264 A1, describes antimicrobial compositions based on polyhaloolefin polymers and cationic antimicrobial reagents as well as a carrier with plasticizer and heat stabilizer, wherein the antimicrobial compound is incorporated into the polymer structure.

According to the technical teaching of DE 10 2009 042 1 18 A1, algae-resistant threads with algicides, which are firmly incorporated into the polymer matrix and thus permanently prevent algae attack, are described. These are z. B. Alkylbenzyldimethylammoniumchloride or N, N-Dialkylharnstoffderivate alone or in combination added to the plastic granules prior to extrusion. This technical solution involves a coalescence of polymer and algicide and not a chemical reaction to build up the polymer.

Furthermore, it is known that certain nanoscale, modified clays have biocidal properties, see, for. G.J. Houben, Applied Geochemistry 18, Issue 6, 941-954 (2003). For oxonium ions on the surface of the particles, this effect should be particularly pronounced.

The preparation of antifouling coatings using amino-terminated oligourea compounds is described in WO 2012/095105 A1, wherein the oligourea compounds are dispersed in glycols and / or polyether alcohols. Polyurethane urea coatings based on this have inherently biocidal activity. These oligourea compounds are due to the content of diols / polyols as hardener components for epoxy resins less or not suitable, especially in coatings in which the leaching of ingredients of the coating is to be avoided in contact with water.

There is consequently a need for coating materials having an adjustable curing rate and barrier properties to water or gases which, in particular, do not contain any environmentally harmful additives and, if possible, retain their biocidal activity in the long term. Summary of the invention

One or more of the described disadvantages of the prior art can be solved or at least reduced by means of the method according to the invention for producing a biocidal coating material. For this purpose, the method comprises the steps:

(i) providing a urea amine component, obtainable by reaction

a) an aliphatic or araliphatic di- or triisocyanate

With

b) a mixture of a first amine having a primary or secondary amine group and one or more second amine (s) having 2 or more primary or secondary amine groups,

wherein a ratio of the sum of the primary and secondary amine groups to the isocyanate groups is 10: 1 to 2: 1;

(ii) providing an epoxy component comprising one or more aliphatic polyfunctional glycidyl ethers; and

(iii) reacting the urea amine component with the epoxy component,

wherein a ratio of the epoxy groups of the epoxy component to the amine groups of the urea amine component is 0.25: 1 to 1: 0.25, preferably 0.5: 1 to 1: 0.5.

Surprisingly, it has now been found that the oligoureaamines obtainable by the process according to the invention based on mixtures of monoamines and di- and / or polyamines which have been partially reacted with one or more di- or triisocyanates can form layers or films in their further reaction with epoxide compounds which have inherent biocidal activity. These layers or films also have high water, oxygen and / or carbon dioxide blocking capability.

In step (i) of the process, an oligourea composite is first formed by an addition reaction of isocyanates and various amines. The latter is then reacted in step (iii) with polyfunctional glycidyl ethers to form a novel, crosslinked coating material.

To produce the urea amine component, two different types are used in step (i) used by amines, which differ by the number of existing primary or secondary amine groups. A first amine has only a single primary or secondary amine group, while the second amine has 2 or more of these functionalities and may optionally include a tertiary amino group. Subsequent reaction with polyfunctional isocyanates produces a complex mixture of oligoureas still having free amine groups and one or more amines.

The first amine is preferably a C 3 -C 15 -cycloamine or a compound of the formula (1)

R ¹ -NHR ² (1)

With

R ¹ selected from the group consisting of C ¹ -C 15 alkyl, C ₃ -C 10 cycloalkyl and C ₃ -C 10 heterocycloalkyl and

R ² selected from the group comprising hydrogen, C 1 -C 15 alkyl, C 3 -C 10 cycloalkyl and C 3 -C 10 heterocycloalkyl.

The second amine is preferably a C 3 -C 15 -cycloamine or a compound of the formula (2)

R ¹ (-NHR ² ) ^a (-NHR ³ ) ^b (2)

With

R ² and R ^{3 are} independently selected from the group comprising hydrogen, C1 - C15 alkyl, C3-C10 cycloalkyl, and C ₃ -C ₀ heterocycloalkyl. The two amine groups (-NH ₂ ) ^a and (-NH ₂ ) ^b are bonded to the radical R ¹ directly or via alkylene, in particular methylene bridges. The alkyl groups of the diamines may also be linked by an optionally substituted amino group, such as in bis-N, N- (3-aminopropyl) -N-methylamine.

By an aliphatic di- or triisocyanate is meant an acyclic or cyclic, saturated or unsaturated carbon compound having two or three isocyanate groups. Preference is given to diisocyanates of the formula (3)

R ¹ (-NCO) ^a (-NCO) ^b (3) With

R ¹ selected from the group consisting of C ¹ -C 15 alkyl, C ₃ -C 10 cycloalkyl and C ₃ -C 10 heterocycloalkyl. The two isocyanate groups (-NCO) ^a and (-NCO) ^b are bonded directly to the radical R ¹ .

An araliphatic di- or triisocyanate is understood as meaning a carbon compound in which the two or three isocyanate groups are bonded directly to one or more aliphatic side chains of an aryl group. Preference is given to araliphatic diisocyanates of the formula (4)

wherein R ¹ and R ^{2 are} independently selected from hydrogen or C 1 -C 5 alkyl and n = 1 - 10.

Alternatively, the isocyanate components may be prepolymers (prepolymers or quasi-prepolymers) of di- and / or triols and diisocyanates, diamines and diisocyanates, or triisocyanates obtained by symmetrical or asymmetric trimerization of aliphatic and / or cycloaliphatic diisocyanates. In this case, preferably short-chain diols such as butane-1, 4-diol, dipropylene glycol, tripropylene glycol, diethylene glycol, polytetrahydrofurans of molecular weight 200 to 2000, ethylene oxide-propylene oxide copolymers of molecular weight 1000 to 4000 or polycarbonate diols of molecular weight 500 to 2000 used. The ratio of the isocyanate groups to the hydroxyl groups is preferably between 2.1: 1 and 5: 1, in particular between 2.1: 1 and 2.8: 1.

In a particular embodiment, prepolymers are formed from a diol and a diisocyanate in a ratio of 2.1: 1 to 3.5: 1 and added immediately after their preparation in a mixture of mono- and diamines and split therein again with urea formation and release of the diol , Suitable diols for this variant of the method according to the invention are, for. As ethylene glycol, diethylene glycol, propane-1, 3-diol, butane-1, 4-diol, Dipropylene glycol, hexane-1, 6-diol, and 2-ethyl-1,3-hexanediol.

By C1-C15 alkyl is meant a linear or branched alkyl radical having the general formula C _n H _{2n + i} , where n = 1 to 15. C 1 -C 5 alkyl includes, for example, methyl, ethyl, n-propyl, 1-methylethyl, n-butyl, 1-methylpropyl, 2-methylpropyl, 1, 1-dimethylethyl, n-pentyl, 1-methylbutyl, 2-methylbutyl, 3 Methylbutyl, 1, 1-dimethylpropyl,

1, 2-dimethylpropyl, 2,2-dimethylpropyl and 1-ethylpropyl. Examples of alkyl radicals with n> 6 include n-hexane, n-heptane, n-octane, n-nonane, n-decane, 1-methylpentyl, 1-methylhexyl, 1-methylheptyl, 1-methyloctyl, 1-methylnonyl, 1 Methyldecanyl, 1-ethylbutyl, 1-ethylpentyl, 1-ethylhexyl, 1-ethylheptyl, 1-ethyl octyl, 1-ethylnonyl, 1-ethyldecanyl, 2-methylpentyl, 2-methylhexyl, 2-methylheptyl, 2-methyloctyl, 2-methylnonyl, 2-methyldecanyl, 2-ethylpropyl, 2-ethylbutyl, 2-ethylpentyl, 2-ethylhexyl, 2-ethylheptyl, 2-ethyloctyl, 2-ethylnonyl, 2-ethyldecanyl, 1, 1-dimethylbutyl, 1, 1-dimethylpentyl, 1, 1-dimethylhexyl, 1, 1-dimethylheptyl,

1,1-dimethyloctyl, 1,1-dimethylnonyl, 1,1-dimethyldecanyl, 1,2-dimethylbutyl, 1,2-dimethylpentyl, 1,2-dimethylhexyl, 1,2-dimethylheptyl, 1,2-dimethyloctyl, 1, 2- dimethylnonyl,

1,2-Dimethyldecanyl, 2-ethyl-1-methylbutyl, 2-ethyl-1-methylpentyl, 2-ethyl-1-methylhexyl, 2-ethyl-1-methylheptyl, 2-ethyl-1-methyloctyl, 2-ethyl-1 methylnonyl, 2-ethyl-1-methyldecanyl, 1-ethyl-2-methylpropyl, 1-ethyl-2-methylbutyl, 1-ethyl-2-methylpentyl, 1-ethyl-2-methylhexyl,

1-ethyl-2-methylheptyl, 1-ethyl-2-methyloctyl, 1-ethyl-2-methylnonyl and 1-ethyl-2-methyldecanyl.

By C 3 -C 10 cycloalkyl is meant a monocyclic or bicyclic cycloalkyl radical having 3 to 15 carbon atoms. Examples include cycloalkyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl and cycloheptyl. The cycloalkyl radicals may in turn be monosubstituted or polysubstituted by C 1 -C 5 -alkyl radicals of the meaning given above. Examples of such substituted cycloalkyl radicals include 1-methyl-1-cyclopropyl, 1-methyl-1-cyclobutyl, 1-methyl-1-cyclopentyl, 1-methyl-1-cyclohexyl, 1-methyl-1-cycloheptyl,

2-methyl-1-cyclopropyl, 2-methyl-1-cyclobutyl, 2-methyl-1-cyclopentyl, 2-methyl-1-cyclohexyl, 2-methyl-1-cycloheptyl, 3-methyl-1-cyclobutyl, 3 Methyl-1-cyclopentyl, 3-methyl-1-cyclohexyl, 3-methyl-1-cycloheptyl, 4-methyl-1-cyclohexyl, 4-methyl-1-cycloheptyl, 1, 2-dimethyl-1-cyclopropyl, 2, 2-Dimethyl-1-cyclopropyl, 2, 3-dimethyl-1-cyclopropyl, 1, 2-dimethyl-1-cyclobutyl, 1, 3-dimethyl-1-cyclobutyl, 2, 2-dimethyl-1-cyclobutyl, 2, 3-Dimethyl-1-cyclobutyl, 2,4-dimethyl-1-cyclobutyl, 3, 3-dimethyl-1-cyclobutyl, 1, 2-dimethyl-1-cyclopentyl,

1,3-dimethyl-1-cyclopentyl, 2, 2-dimethyl-1-cyclopentyl, 2, 3-dimethyl-1-cyclopentyl, 2,4-dimethyl-1-cyclopentyl, 2, 5-dimethyl-1-cyclopentyl, 3, 3-dimethyl-1-cyclopentyl, 3,4- Dimethyl-1-cyclopentyl, 1, 2-dimethyl-1-cyclohexyl, 1, 3-dimethyl-1-cyclohexyl, 1, 4-dimethyl-1-cyclohexyl, 1, 5-dimethyl-1-cyclohexyl, 1, 6 Dimethyl 1-cyclohexyl, 2,2-dimethyl-1-cyclohexyl, 2,3-dimethyl-1-cyclohexyl, 2,4-dimethyl-1-cyclohexyl, 2,5-dimethyl-1-cyclohexyl, 2,6- Dimethyl 1-cyclohexyl, 3,3-dimethyl-1-cyclohexyl, 3,4-dimethyl-1-cyclohexyl, 3,5-dimethyl-1-cyclohexyl, 3,6-dimethyl-1-cyclohexyl, 4,4- Dimethyl-1-cyclohexyl, 1, 2,2-trimethyl-1-cyclopropyl, 1, 2,3-trimethyl-1-cyclopropyl, 1, 2,2-trimethyl-1-cyclobutyl, 1,3,3-trimethyl 1-cyclobutyl, 1, 2,3-trimethyl-1-cyclobutyl, 2,2,3-trimethyl-1-cyclobutyl, 2,2,4-trimethyl-1-cyclobutyl, 1, 2,2-trimethyl-1 - Cyclopentyl, 1, 2,3-trimethyl-1-cyclopentyl, 1, 2,4-trimethyl-1-cyclopentyl, 1, 2,5-trimethyl-1-cyclopentyl, 1,3,3-trimethyl-1-cyclopentyl, 1, 3,4-trimethyl-1-cyclopentyl, 1, 3,5-trimethyl-1-cyclopentyl, 2,2,3-trimethyl-1-cyclopentyl, 2,2,4-trimethyl-1-cyclopentyl, 2, 2,5-trimethyl-1-cyclopentyl, 2,3,3-trimethyl-1-C cyclopentyl, 2,3,4-trimethyl-1-cyclopentyl, 2,3,5-trimethyl-1-cyclopentyl, 2,3,3-trimethyl-1-cyclopentyl, 2,4,4-trimethyl-1-cyclopentyl, 2,4,5-trimethyl-1-cyclopentyl, 2,5,5-trimethyl-1-cyclopentyl, 3,3,4-trimethyl-1-cyclopentyl, 3,3,5-trimethyl-1-cyclopentyl, 3, 4,5-trimethyl-1-cyclopentyl, 3,4,4-trimethyl-1-cyclopentyl, 1,2,2-trimethyl-1-cyclohexyl, 1, 2,3-trimethyl-1-cyclohexyl, 1, 2, 4-trimethyl-1-cyclohexyl, 1, 2,5-trimethyl-1-cyclohexyl, 1, 2,6-trimethyl-1-cyclohexyl, 1,3,3-trimethyl-1-cyclohexyl, 1, 3,4- Trimethyl-1-cyclohexyl, 1, 3,5-trimethyl-1-cyclohexyl, 1, 3,6-trimethyl-1-cyclohexyl, 1,4,4-trimethyl-1-cyclohexyl, 2,2,3-trimethyl 1-cyclohexyl, 2,2,4-trimethyl-1-cyclohexyl, 2,2,5-trimethyl-1-cyclohexyl, 2,2,6-trimethyl-1-cyclohexyl, 2,3,3-trimethyl-1 Cyclohexyl, 2,3,4-trimethyl-1-cyclohexyl, 2,3,5-trimethyl-1-cyclohexyl, 2,3,6-trimethyl-1-cyclohexyl, 2,4,4-trimethyl-1-cyclohexyl, 2,4,5-trimethyl-1-cyclohexyl, 2,4,6-trimethyl-1-cyclohexyl, 2,5,5-trimethyl-1-cyclohexy 1, 2,5,6-trimethyl-1-cyclohexyl, 2,6,6-trimethyl-1-cyclohexyl, 3,3,4-trimethyl-1-cyclohexyl, 3,3,5-trimethyl-1-cyclohexyl, 3,3,6-trimethyl-1-cyclohexyl, 3,4,4-trimethyl-1-cyclohexyl, 3,4,5-trimethyl-1-cyclohexyl, 3,4,6-trimethyl-1-cyclohexyl, 3, 5,6-trimethyl-1-cyclohexyl, 1, 2,3,3-tetramethyl-1-cyclopropyl, 2,2,3,3-tetramethyl-1-cyclopropyl, 1, 2,2,3-tetramethyl-1 - Cyclopropyl, 1, 2,2,3-tetramethyl-1-cyclobutyl, 1, 2,3,3-tetramethyl-1-cyclobutyl, 2,2,3,3-tetramethyl-1

Cyclobutyl, 2,3,3,4-tetramethyl-1-cyclobutyl, 1, 2,2,3-tetramethyl-1-cyclopentyl, 1, 2,2,4-tetramethyl-1-cyclopentyl, 1, 2,2, 5-tetramethyl-1-cyclopentyl, 1, 2,3,3-tetramethylm-

Cyclopentyl, 1, 2,3,4-tetramethyl-1-cyclopentyl, 1,2,3,5-tetramethyl-1-cyclopentyl, 1, 2,5,5-tetramethyl-1-cyclopentyl, 2,2,3, 3-tetramethyl-1-cyclopentyl, 2,2,3,3-tetramethyl-1

Cyclohexyl, 2,2,4,4-tetramethyl-1-cyclohexyl, 2,2,5,5-tetramethylM-cyclohexyl, 3,3,4,4-tetramethyl-1-cyclohexyl, 3,3,5,5- Tetramethyl-1-cyclohexyl, 1-ethyl-1-cyclopropyl, 1-ethyl 1-cyclobutyl, 1-ethyl-1-cyclopentyl, 1-ethyl-1-cyclohexyl), 1-ethyl-1-cycloheptyl, 2-ethyl-1-cyclopropyl, 2-ethyl-1-cyclobutyl, 2-ethyl-1 Cyclopentyl, 2-ethyl-1-cyclohexyl, 2-ethyl-1-cycloheptyl, 3-ethyl-1-cyclobutyl, 3-ethyl-1-cyclopentyl, 3-ethyl-1-cyclohexyl, 3-ethyl-1-cycloheptyl , 4-ethyl-1-cyclohexyl and 4-ethyl-1-cycloheptyl.

By C -C heterocycloalkyl is meant a monocyclic or bicyclic cycloalkyl radical having 3 to 15 carbon atoms, in which at least one carbon atom of the ring is replaced by a heteroatom selected from the group consisting of N, O, P and S. The cycloalkyl radicals may in turn be monosubstituted or polysubstituted by C 1 -C 5 -alkyl radicals of the meaning given above.

By C -C cycloamine is meant a monocyclic or bicyclic cycloalkyl compound of 3 to 15 carbon atoms in which at least one carbon atom of the ring is replaced by an NH group. Further carbon atoms of the ring can be replaced by a heteroatom selected from the group N, O, P and S. Examples include aziridine, azetidine, pyrrolidine, and piperidine. The cycloamines can be monosubstituted or polysubstituted by C 1 -C 5 -alkyl radicals of the meaning given above.

As used herein, the term "first amine" refers to both individual compounds and mixtures thereof. In other words, the first amine may comprise two or more individual compounds (amines having a primary or secondary amine group). The same applies analogously to the term "second amine".

Preferably, the first amine has a secondary amine group. The first amine is particularly preferably a compound or a mixture of compounds which are selected from the group comprising di-n-butylamine, butylamine, piperidine, cyclohexylamine, N-ethyl-N-cyclohexylamine, 2-aminoethanol, dimethylamine, N-methyl N-cyclohexylamine, N-propyl-N-cyclohexylamine, N-butyl-N-cyclohexylamine, N, N-dicyclohexylamine and aziridine.

It is further preferred if the second amine has two amine groups. The second amine is preferably a compound or mixture of compounds selected from the group consisting of 1-amino-3-aminomethyl-3,5,5-trimethylcyclohexane (isophoronediamine), 1, 3-benzenedimethaneamine, bis (4- aminocyclohexyl) methane, 1, 4-diaminobutane, 1, 6-diaminohexane, 2-methyl-1,5-diaminopentane, 1,6-diamino-2,2,4-trimethylhexane, 1,6-diamino-2,4, 4-trimethylhexane, cyclohexane-1,4-diamine, 2-ethylimidazolidine, 1,5-pentanediamine, piperazine, ethylenediamine, N, N-bis (3-aminopropyl) -N-methylamine, 4,4'-methylenebis (cyclohexylamine), 1, 3-phenylenediamine, 2,2- Bis (aminoethoxy) propane, 1,3-cyclohexane bis (methylamine), 1,9-diaminononane, 4,9-dioxa-1, 12-dodecanediamine, 2,2 '- (ethylenedioxy) bis (ethylamine), 4,7, 10-trioxa-1, 13-tridecanediamine, tris (2-aminoethyl) amine, p-xylylenediamine, adipoguanamine, isoadipoguanamine, 2-methylglutaroguanamine and caprinoguanamine. Alternatively, for example, polyamines, such as N, N-dipropylenetriamine, N ² -methyl-dipropylenetriamine, N, N-diethylenetriamine, tripropylenetetramine, triethylenetetramine, dicyandiamide, 2,4,6-triamino-1, 3,5-triamine, and hexamethylenetetramine used become.

Furthermore, specific heterocyclic di- and / or polyamines can be used alone or mixed or as a solution in one or more of the abovementioned amines, for example 2,4-diamino-6-phenyl-1,3,5-triazine, 2 , 4-diamino-6-capryl-1, 3,5-triazine and 2,4-diamino-6-undecyl-1,3,5-triazine. These compounds can be used as well as those mentioned above in combination with dycandiamide.

Preferably, a molar ratio of the first amine to the second amine is in the range of 1.5: 1 to 1: 5.

According to a further preferred embodiment, one or more guanamines selected from the group consisting of adipoguanamine, isoadipoguanamine, 2-methylglutaroguanamine and caprinoguanamine are added to the urea-amine component provided in step (i). Preferably, the weight fraction of guanamines in the total weight of the provided urea amine component and the guanamines is 5 to 35 wt.%.

It is further preferred if the di- or triisocyanate is a compound or a mixture of compounds which are selected from the group comprising isophorone diisocyanate (IPDI), 1,4-cyclohexane diisocyanate, 1, 3

Bis (isocyanatomethyl) cyclohexane, 1,5-diisocyanato-2-methylpentane, 1,8-diisocyanato-octane, 4,4'-methylene-bis (cyclohexylisocyanate), 2,2,4-trimethyl-1,6-diisocyanatohexane, 2, 4,4-trimethyl-1,6-diisocyanatohexane, 1,12-diisocyanatododecane, 2-ethylbutane-1,4-diisocyanate, hexamethylene diisocyanate (HDI), octadecyl diisocyanate, tricyclodecanediisocyanate, biuret of hexamethylene diisocyanate, trimers of hexamethylene diisocyanate, trimers of isophorone diisocyanate, xylylene diisocyanates (1, 2, 1, 3, 1, 4 isomer or mixtures thereof, in particular 1, 3-xylylene diisocyanate, (XDI)) and tetramethylxylylene diisocyanates (1, 2, 1, 3, 1, 4-isomers or Mixtures thereof, in particular 1, 3-tetramethylxylylene diisocyanate, (TMXDI)). Particularly preferred is 1, 3-tetramethylxylylene diisocyanate. As used herein, reference is to di- or tri-isocyanate, as used herein to mean both individual compounds and mixtures thereof. In other words, two or more individual compounds may be provided as a mixture in step (ii) and reacted in step (iii). In place of the monomeric diisocyanates prepolymers can be used (see above).

Step (i) is preferably carried out at temperatures in the range of 10 to 180 ° C. The reaction may preferably be carried out in such a way that a solution or a dispersion of the urea amine component is present in the excess amine.

The reaction of the amines with the isocyanate or the prepolymer is carried out either in bulk or in the presence of solvents.

In the reaction in mass, the amines are preferably initially charged and the isocyanate or prepolymer slowly added dropwise at a temperature below or equal to 45 ° C, if the amines are still liquid. The reaction temperature should not exceed 120 ° C.

In the reaction in the presence of solvents, the amount of solvent between 1% and 90%, each based on the total mixture adjusted. Preference is given to the lowest possible amounts of solvent, for example 5 to 25% based on the total mixture. The solvents used are preferably N-methylpyrrolidone, dimethylformamide, dimethylacetamide, dimethyl sulfoxide, hexamethylphosphonamide, and tetrahydrofuran.

In the reaction of the amines with prepolymers, it is preferable to work without further solvents. The prepolymer is added to the amine mixture at a temperature between 30 and 150 ° C. After completion of the addition, the mixture is reacted for a further 10 minutes to 8 hours, preferably 1 to 4 hours, at temperatures between 150 and 250 ° C, preferably 180 to 200 ° C, whereby the urethane groups of the prepolymer are split and converted to urea groups.

As used herein, the term 'glycidyl ether' means both individual compounds and mixtures thereof. In other words, the glycidyl ether may include two or more individual compounds (aliphatic polyfunctional glycidyl ethers).

As polyfunctional glycidyl ethers are preferably mono-, di-, tri- or Tetraglycidether used. In particular, the polyfunctional glycidyl ether is a compound or a mixture of compounds which are selected from the group consisting of ethylene glycol diglycidyl ether, diethylene glycol diglycidyl ether, diethylene glycol diglycidyl ether, butanediol-1,4 diglycidyl ether, hexanediol 1,6-diglycidyl ether, octanediol -1, 8-diglycidyl ether, dodecane-1, 12-diglycidether, isosorbide diglycidyl ether, glycerol monoglycidyl ether, glycerol diglycidyl ether, glycerol triglycidyl ether, trimethylolpropane triglycidyl ether, pentaerythritol monoglycidyl ether, pentaerythritol diglycidyl ether, pentaerythritol triglycidyl ether, pentaerythritol tetraglycidyl ether , Diglycerol tetraglycidyl ether, dipentaerythritol hexaglycidyl ether, dipentaerythritol tetraglycidyl ether. The polyfunctional glycidyl ether is particularly preferably a mixture of trimethylolpropane monoglycidyl ether, trimethylolpropane diglycidyl ether and trimethylolpropane triglycidyl ether.

Furthermore, glycidol esters of dicarboxylic acids can be used, for example cyclohexane-1,2-dicarboxylic acid diglycidyl ester or terephthalic acid diglycidyl ester.

Particularly preferred embodiments comprise the following combinations:

• 1, 3-tetramethylxylylene diisocyanate, isophoronediamine and bis-N, N- (3-aminopropyl) -N-methylamine for the preparation of the urea amine component;

M-xylylene diisocyanate, isophoronediamine and bis-N, N- (3-aminopropyl) -N-methylamine for the preparation of the urea amine component;

• 1, 3-tetramethylxylylene diisocyanate, isophoronediamine and N-ethyl-N-cyclohexylamine for the preparation of the urea amine component;

1, 3-tetramethylxylylene diisocyanate, isophoronediamine and bis-N, N- (3-aminopropyl) -N-methylamine for the preparation of the urea amine component and a mixture of trimethylolpropane monoglycidyl ether, trimethylolpropane diglycidyl ether and trimethylolpropane triglycidyl ether as epoxide Component;

M-xylylene diisocyanate, isophoronediamine and bis-N, N- (3-aminopropyl) -N-methylamine for the preparation of the urea amine component and a mixture of

Trimethylolpropane monoglycidyl ether, trimethylolpropane diglycidyl ether and trimethylolpropane triglycidyl ether as epoxide component; and

• 1, 3-tetramethylxylylene diisocyanate, isophorone diamine and N-ethyl-N-cyclohexylamine for the preparation of the urea amine component and a mixture of

Trimethylolpropane monoglycidyl ether, trimethylolpropane diglycidyl ether and trimethylolpropane triglycidyl ether as epoxide component. One or more additives may be added to the urea amine component and / or the epoxy component.

Nanosized metal oxides, metal hydroxides, metal oxide hydroxides, semimetal oxides, silicates, layer silicates, surface-modified layer silicates, graphene, surface-modified graphenes, carbon hollow fibers and modified carbon hollow fibers can be used in particular as additives. Particular preference is given to nanoscale, partially exfoliated phyllosilicates, such as cloisites, montmorillonites (about 1 nm thick aluminosilicate layers with metal cations optionally substituted on the surface) or montmorillonites surface-modified with onium ions as layers, cages or tubes. Also suitable are silicates such as albite, also calcite (calcium carbonate) or dolomite (calcium magnesium carbonate).

Other additives may include dyes, pigments, solid or liquid flame retardants, dispersing aids, compatibilizers, leveling agents and thixotropic agents. In particular, as solid pigments iron oxides, carbon black, titanium dioxide, hematite, etc., are used as thixotropic agent, in particular silica (fumed silica) having a specific surface area of 90 to 380 m ² / g.

Both in the epoxy component and in the urea amine component, the solid and / or liquid additives can be incorporated. When using solid additives z. As mixtures of a thixotropic agent, such as fumed silica, pigments, such as iron oxides, and a nanoscale sheet silicate, such as a montmorillonite surface-modified with onium ions are used. The respective proportions can vary within a wide range, for example:

Pyrogenic silica 1 to 10 wt .-% based on the total mixture, in particular 1 to 5 wt .-%;

Iron black pigment 0.1 to 10% by weight, based on the total mixture, in particular 0.5 to 2.5%; and

Nanoscale sheet silicate 0.001 to 20 wt .-% based on the total mixture, in particular 0.01 to 5 wt .-%.

Another aspect of the invention relates to a biocidal coating material prepared by the above-described method.

The biocidal coating material is preferably used to prepare a coating for Ship walls, ship interior, ship deck, ramps, propellers, wind power blades, wind turbine housings, floors (for example, in hypermarkets or cold stores) and pipes, in particular for the production of an inner pipe coating of hot water, hot water or drinking water pipes used.

To prepare the coatings or films, the epoxy component and the urea amine component can be intimately mixed at a temperature of 5 to 45 ° C with each other. About the used amines, additives and the ratio of the epoxy groups to the amine groups, the reaction time of the systems and their curing behavior can be controlled so that, for example, reaction times of 3 minutes to 90 minutes are possible. The reacting mixture is processed after a time of 1 minute to 1 hour by means of a doctor blade, draw knife, patting or by entering into a pipe system with subsequent smoothing by a pig to the coatings according to the invention. For certain surfaces, the application of a primer is possible before the coating according to the invention.

The mixture of the two components can be done manually or mechanically with 2-component mixing machines. Thus, the components mixed by means of 2-component mixing machines can be entered into tubes through which tubes a compressed air is pressed by means of compressed air, so that tube inner coatings of 20 to 500 μm are produced on the inner wall.

Further preferred embodiments of the invention will become apparent from the following embodiments.

Detailed description of the invention

example 1

(a) Preparation of the urea amine component

173 g of isophoronediamine and 63 g of N-ethyl-N-cyclohexylamine are introduced into a heatable 750 ml glass reactor with magnetic stirrer, condenser, thermocouple and dropping funnel and the stirrer is started at 20 ° C. With rapid stirring (4000 min ¹ ) are added dropwise 37 g of hexamethylene diisocyanate within 90 minutes, whereby the temperature of the mixture to 85 ° C increases. A clear solution of the urea amine in the amine mixture is obtained, the amine number is 245 mg KOH / g, the viscosity 860 mPas (25 ° C). Amine number means the amount of KOH in mg, which is equated to the amine content of 1 g of substance. According to DIN 53176, the amine number is determined by potentiometric titration. The viscosity of liquids is measured with a viscometer z. B. measured according to EN ISO 3219.

(b) Preparation of a coating according to the invention

The epoxide component is prepared from 52.5 g of trimethylolpropane triglycidyl ether, 5.5 g of butane-1, 4-diol diglycidyl ether, 3.5 g of fumed silica (trade name Aerosil 380 from Evonik AG), 0.5 g of iron oxide black (Particle size 12 - 56 pm) and 0.5 g of a modified montmorillonite (trade name Nanocor I.30E).

12.5 g of the epoxy component is mixed intensively at 30.degree. C. with 7.55 g of the urea amine and spread on a laboratory streak table with integrated dryer (LabCater from Mathis) to a 200 .mu.m film by means of a knife blade. The pot life is 12 minutes. The film is cured at 55 ° C for 30 minutes.

This gives a black film with the glass transition temperature (DSC) 79 ° C.

Growing tests were carried out with 20 x 20 cm films on the experimental stations in Wilhelmshaven (Jade) and Berlin-Wendenschloss (Dahme) under the given environmental conditions. The films were regularly checked for fouling. The results:

Wilhelmshaven: no fouling or growth detectable after 90 days

Turning lock: no growth or growth detectable after 1 to 10 days

Example 2

(a) Preparation of the urea amine component

In a heatable 750 ml glass reactor with magnetic stirrer, condenser, thermocouple and dropping funnel, 158 g of a mixture of 2,2,4- and 2,4,4-trimethylhexane-1,6-diamine and 63 g of N-ethyl-N- cyclohexylamine and the agitator started at 20 ° C. With rapid stirring (4000 min ¹ ) are added dropwise 42 g of hexamethylene diisocyanate within 90 minutes, whereby the temperature of the mixture to 79 ° C increases. A clear solution of the urea amine in the amine mixture is obtained, the amine number is 267 mg KOH / g, the viscosity 1240 mPas (25 ° C).

(b) Preparation of a coating according to the invention The epoxide component is prepared from 52.5 g of trimethylolpropane triglycidyl ether, 5.5 g of hexane-1, 6-diol diglycidyl ether, 3.5 g of fumed silica (trade name Aerosil R208 from Evonik AG), 0.5 g of iron oxide black (Particle size 12-56 pm) and 0.8 g of a modified montmorillonite (trade name Nanocor I.30E).

12.5 g of the epoxy component is mixed intensively at 30.degree. C. with 7.75 g of the urea amine and spread on a laboratory streak table with integrated dryer (LabCater from Mathis) to a 200 .mu.m film by means of a knife blade. The pot life is 6 minutes. The film is cured at 55 ° C for 30 minutes.

This gives a black film with the glass transition temperature (DSC) 42 ° C.

Wilhelmshaven: no fouling or growth detectable after 90 days

Turning lock: no growth or growth detectable after 100 days

Example 3

(a) Preparation of the urea amine component

173 g of isophoronediamine and 63 g of N-ethyl-N-cyclohexylamine are introduced into a heatable 750 ml glass reactor with magnetic stirrer, condenser, thermocouple and dropping funnel and the stirrer is started at 20 ° C. With rapid stirring (4000 min ¹ ) are added dropwise 22 g of hexamethylene diisocyanate within 90 minutes, whereby the temperature of the mixture to 85 ° C increases. A clear solution of the urea amine in the amine mixture is obtained, the amine number is 168 mg KOH / g, the viscosity 647 mPas (25 ° C).

(b) Preparation of a coating according to the invention

The epoxide component is prepared from 49.7 g of pentaerythritol tetraglycidyl ether and triglycidyl ether (mixture about 1: 1), 7.5 g of butane-1, 4-diol diglycidyl ether, 3.5 g of fumed silica (trade name Aerosil 380 from Evonik AG), 0.5 g of iron oxide black (particle size 12-56 μm) and 0.25 g of a modified montmorillonite (trade name Nanocor I.30E).

12.5 g of the epoxy component is at 30 ° C with 6.35 g of urea amine intensive mixed and spread on a laboratory blending table with integrated dryer (LabCoater Mathis) to a 200 pm film using knife blade. The pot life is 9 minutes. The film is cured at 55 ° C for 30 minutes.

This gives a black film with the glass transition temperature (DSC) 99 ° C.

Wilhelmshaven: no fouling or growth detectable after 60 days

Turning lock: no growth or growth detectable after 90 days

Example 4

(a) Preparation of the urea amine component

173 g of isophoronediamine and 63 g of N-ethyl-N-cyclohexylamine are introduced into a heatable 750 ml glass reactor with magnetic stirrer, condenser, thermocouple and dropping funnel and the stirrer is started at 20 ° C. With rapid stirring (4000 min ¹ ) is added dropwise, a mixture of 37 g of hexamethylene diisocyanate and 1 10g dimethyl sulfoxide within 60 minutes, whereby the temperature of the mixture to 76 ° C increases. A clear solution of the urea amine in the amine mixture is obtained. The amine number is 278 mg KOH / g and the viscosity 743 mPas (25 ° C).

(b) Preparation of a coating according to the invention

12.5 g of the epoxy component is mixed intensively at 30.degree. C. with 7.75 g of the urea amine and spread on a laboratory streak table with integrated dryer (LabCater from Mathis) to a 200 .mu.m film by means of a knife blade. The pot life is 16 minutes. The film is cured at 55 ° C for 30 minutes.

This gives a black film with the glass transition temperature (DSC) 86 ° C. Growing tests were carried out with 20 x 20 cm films on the experimental stations in Wilhelmshaven (Jade) and Berlin-Wendenschloss (Dahme) under the given environmental conditions. The films were regularly checked for fouling. The results:

Wilhelmshaven: no fouling or growth detectable after 60 days

Turning lock: no growth or growth detectable after 90 days

Example 5

(a) Preparation of the urea amine component

In a heatable 750 ml glass reactor with magnetic stirrer, condenser, thermocouple and dropping funnel, 158 g of trimethylhexane-1,6-diamine (mixture of 2,2,4- and 2,4,4-isomers) and 35 g of N-ethyl- Added N-cyclohexylamine and the agitator started at 20 ° C. With rapid stirring (4000 min ¹ ), a mixture of 33 g of hexamethylene diisocyanate and 20 g of dimethylacetamide is added dropwise within 100 minutes, whereby the temperature of the mixture rises to 71 ° C. A solution of the urea amine in the amine mixture is obtained, the amine number is 222 mg KOH / g, the viscosity 682 mPas (25 ° C).

(b) Preparation of a coating according to the invention

This gives a black film with the glass transition temperature (DSC) 45 ° C.

Wilhelmshaven: no fouling or growth detectable after 60 days Turning lock: no growth or growth detectable after 75 days

Example 6

(a) Preparation of the urea amine component

173 g of isophoronediamine and 63 g of N-ethyl-N-cyclohexylamine are introduced into a heatable 750 ml glass reactor with magnetic stirrer, condenser, thermocouple and dropping funnel and the stirrer is started at 20 ° C. With rapid stirring (4000 min ¹ ) is added dropwise a mixture of 37 g of hexamethylene diisocyanate and 37 g of dimethyl sulfoxide within 60 minutes, whereby the temperature of the mixture to 81 ° C increases. After completion of the addition, the temperature is slowly increased to 1 15 ° C and stirred for 15 minutes at this temperature. A clear solution of the urea amine in the amine mixture is obtained, the amine number is 243 mg KOH / g, the viscosity of 1 127 mPas (25 ° C).

(b) Preparation of a coating according to the invention

12.5 g of the epoxy component is mixed intensively at 30.degree. C. with 7.4 g of the urea amine and spread on a laboratory streak table with integrated dryer (LabCater from Mathis) to a 200 .mu.m film by means of a knife blade. The pot life is 10 minutes. The film is cured at 55 ° C for 30 minutes.

This gives a black film with the glass transition temperature (DSC) 77 ° C.

Wilhelmshaven: no growth or growth detectable after 45 days

Turning lock: no growth or growth detectable after 45 days

Example 7 (a) Preparation of the urea amine component

In a heatable 2 l glass reactor with magnetic stirrer, condenser, thermocouple and dropping funnel, 735 g of isophoronediamine, 466 g of 4,4'-methylenebis (cyclohexylamine) and 342 g of N-ethyl-piperazine are added and the stirrer is started at 20 ° C. With rapid stirring (4000 min ¹ ), a mixture of 121 g of hexamethylene diisocyanate and 83 g of isophorone diisocyanate is added dropwise within 240 minutes, whereby the temperature of the mixture rises to 96 ° C. After completion of the addition, the temperature is slowly increased to 130 ° C and stirred for 45 minutes at this temperature. A clear solution of the urea amine in the amine mixture is obtained, the amine number is 188 mg KOH / g, the viscosity 1455 mPas (25 ° C).

(b) Preparation of a coating according to the invention

The epoxide component is prepared from 500 g pentaerythritol tetraglycidyl ether, 125 g dipentaerythritol pentaglycidyl ether, 12.5 g micronized titanium dioxide, 12.5 g iron oxide black (particle size 12-56 pm) and 1.5 g of a modified montmorillonite (trade name Nanocor I. 30E).

The epoxy component is mixed by means of a static mixer at 30 ° C. by means of a mixing machine from Hilger & Kern in a ratio of 1.33: 1 and spread onto the screed of a concrete floor by means of a doctor, so that a coating of on average 400 μm was formed. The pot life was 20 minutes, the tack-free time 56 minutes, the curing time 12 hours. This gives a black film with the glass transition temperature (DSC) 176 ° C, a tear strength of 22 N / mm ² , a Shore D hardness of 62 and an elongation at break of 5.8%.

On a concrete test plate of 40 x 40 cm, this coating was also applied and overcoated with a water sample from a nearby body of water. After 30 days, the supernatant water was removed and the layer checked. After rinsing with 0.5 at water, the layer was completely clean.

Example 8

(a) Preparation of the urea amine component

In a heatable 2 l glass reactor with magnetic stirrer, condenser, thermocouple and dropping funnel, 466 g of 4,4'-methylenebis (cyclohexylamine), 355 g of 2,2- Add bis (aminoethoxy) propane and 165 g of N-ethyl-N-cyclohexylamine and start the agitator at 20 ° C. With rapid stirring (4000 min ¹ ) is added dropwise a mixture of 121 g of hexamethylene diisocyanate and 52 g of 1, 3-bis (isocyanatomethyl) cyclohexane within 180 minutes, whereby the temperature of the mixture rises to 106 ° C. After completion of the addition, the temperature is slowly increased to 125 ° C and stirred for 30 minutes at this temperature. A clear solution of the urea amine in the amine mixture is obtained, the amine number is 205 mg KOH / g, the viscosity 1086 mPas (25 ° C).

(b) Preparation of a coating according to the invention

The epoxide component is prepared from 525 g of trimethylolpropane triglycidyl ether, 75 g of pentaerythritol triglycidyl ether, 35 g of fumed silica (trade name Aerosil R208 from Evonik AG), 7 g of iron oxide black (particle size 12-56 μm) and 4 g of a modified montmorillonite ( Trade name Nanocor I.30E).

The epoxy component is mixed with the urea amine component by means of a static mixer at 30 ° C by means of a mixing machine from Hilger & Kern in the ratio 1, 48: 1 and placed in a HDPE pipe of 14 mm internal diameter. Thereafter, a 13 mm pig is guided through the tube by means of compressed air, so that a coating of an average of 300 pm was formed on the tube inner wall. The pot life was 20 minutes, the tack-free time 56 minutes, the curing time 12 hours. This gives a black film with the glass transition temperature (DSC) 81 ° C, a Shore A hardness of 85, an elongation at break of 8.4% and a tear strength of 18 N / mm ² .

A sample of the internally coated tube of 30 cm in length was treated with a drinking water sample which additionally contained 1000 germs per ml of Listeria. After 7 days at 25 ° C, the water was rechecked for its germ count. A value of 678 germs per ml was determined.

Example 9

(a) Preparation of the urea amine component

(a1) Preparation of an isocyanate prepolymer

1 1 1, 1 g of isophorone diisocyanate and 92.5 g of polytetrahydrofuran molecular weight 250 are placed in a 350 ml glass reactor and the mixture stirred at 45 ° C. When the addition is complete, the mixture is stirred at 60 ° C. for a further hour. It turns a colorless, clear low viscous prepolymer with 14.3% isocyanate.

(a2) Preparation of the urea amine component

In a heatable 200 ml glass reactor 34.06 g of isophoronediamine, 6.36 g of N-ethyl-N-cyclohexylamine, 8.67 g of hexatrane 100 are introduced and 4.46 g of the prepolymer slowly under nitrogen blanket at 50 ° C. after the addition is heated to 160 ° C and stirred for 1 h at this temperature. Then it is cooled. The urea amine has the following properties:

Amine number: 603.4 mg KOH / g

P ₂₅ -c = 41 mPas

(b) Preparation of a coating according to the invention

12.5 g of the epoxide component from a mixture of glycerol diglycidyl ether and glycerol triglycidyl ether with the epoxide equivalent of 143 g / mol is mixed intensively at 30.degree. C. with 8.13 g of the urea amine and placed on a laboratory streak table with integrated dryer (LabCoater der Company Mathis) to a 200 pm film by means of a knife blade. The pot life is 23 minutes. The film is cured at 55 ° C for 30 minutes.

This gives a crystal-clear film with the glass transition temperature (DSC) 59 ° C.

Growing tests were carried out with 20 x 20 cm films on a test station under the environmental conditions given there. The films were regularly checked for fouling. After 45 days, no fouling was detected. A control sample prepared by curing alone with isophorone diamine had a significant (green) algae growth after 21 days.

Example 10

(a) Preparation of the urea amine component

(a1) Preparation of an isocyanate prepolymer

1 1 1, 1 g of isophorone diisocyanate and 92.5 g of polytetrahydrofuran molecular weight 250 are placed in a 350 ml glass reactor and the mixture stirred at 45 ° C. When the addition is complete, the mixture is stirred at 60 ° C. for a further hour. There is obtained a colorless, clear, low viscosity prepolymer with 14.3% isocyanate. (a2) Preparation of the urea amine component

A heatable 750 ml glass reactor is charged with 341 g of isophoronediamine, 25 g of N-ethyl-N-cyclohexylamine and 145 g of N, N-bis (3-aminopropyl) -N-methylamine and 56 g of the prepolymer are added slowly under nitrogen blanketing gas Add 50 ° C, whereby the temperature rises to 75 ° C; after the addition is heated to 100 ° C and stirred for 1 h at this temperature. Thereafter, it is heated to 185 ° C for three hours with stirring and cooled. The urea amine has the following properties:

Amine number: 686 mg KOH / g

P ₂₅ ° C = 67 mPas

(b) Preparation of a coating according to the invention

14.5 g of the epoxy component from a mixture of glycerol and glycerol triglycidyl ether with the epoxide equivalent 143 g / mol is mixed intensively at 30 ° C with 8.2 g of urea and on a laboratory table with integrated dryers (LabCoater the Company Mathis) to a 200 pm film by means of a knife blade. The pot life is 7 minutes. The film is cured at 55 ° C for 30 minutes.

This gives a crystal-clear film with the glass transition temperature (DSC) 45 ° C.

Screening tests were carried out with 20 x 20 cm films on a test station under the given environmental conditions in November 2017. The films were regularly checked for fouling. No fouling was detected after 35 days. A control sample prepared by curing alone with isophorone diamine had a significant (green) algae growth after 21 days.

Example 1 1

(a) Preparation of the urea amine component

(a1) Preparation of an isocyanate prepolymer

1 1 1, 1 g of isophorone diisocyanate and 90 g of polytetrahydrofuran molecular weight 250 are placed in a 350 ml glass reactor and the mixture stirred at 45 ° C. When the addition is complete, the mixture is stirred at 60 ° C. for a further hour. A colorless, clear, low viscosity, 14.45% isocyanate prepolymer is obtained. (a2) Preparation of the urea amine component

In a 750 ml heatable glass reactor 15 g of N-ethyl-N-cyclohexylamine, 272.5 g of isophoronediamine and 63.5 g of N, N-bis (3-aminopropyl) -N-methylamine presented and 98 g of the prepolymer slowly under Add nitrogen blanket at 50 ° C, raising the temperature to 65 ° C; after the addition is heated to 100 ° C and stirred for 1 h at this temperature. Thereafter, it is heated to 190 ° C for three hours with stirring and cooled. The urea amine has the following properties:

Amine number: 451 mg KOH / g

P 25 ° c = 521 mPas

(b) Preparation of a coating according to the invention

14.5 g of the epoxy component from a mixture of glycerol and glycerol triglycidyl ether with the epoxide equivalent of 143 g / mol is mixed intensively at 30 ° C with 6.3 g of urea and on a laboratory table with integrated dryers (LabCoater the Company Mathis) to a 200 pm film by means of a knife blade. The pot life is 23 minutes. The film is cured at 60 ° C for 60 minutes.

This gives a crystal-clear film with the glass transition temperature (DSC) 69 ° C.

Example 12

(a) Preparation of the urea amine component

(a1) Preparation of an isocyanate prepolymer

In a 750 ml heatable glass reactor, 63.5 g of N-ethyl-N-cyclohexylamine, 255 g of isophorone diamine and 32.5 g of diethylenetriamine are introduced and 96 g of the prepolymer slowly under nitrogen blanket at 45 ° C, whereby the temperature on Rises 75 ° C; after the addition is heated to 120 ° C and stirred for 1 h at this temperature. Thereafter, it is heated to 190 ° C for three hours with stirring and cooled. The urea amine has the following properties:

Amine number: 467 mg KOH / g

P 25 ° C ⁼ 143 mPas

(b) Preparation of a coating according to the invention

14.5 g of the epoxide component from a mixture of glycerol and glycerol triglycidyl ether with the epoxide equivalent of 143 g / mol is mixed intensively at 30 ° C with 6.0 g of urea and on a laboratory Streichisch with integrated dryer (LabCoater the Company Mathis) to a 200 pm film by means of a knife blade. The pot life is 26 minutes. The film is cured at 60 ° C for 60 minutes.

This gives a crystal-clear film with the glass transition temperature (DSC) 71 ° C.

Example 13

(a) Preparation of the urea amine component

(a1) Preparation of an isocyanate prepolymer

In a heated 750 ml glass reactor, 45 g of N-ethyl-N-cyclohexylamine, 258.5 g of isophoronediamine and 25 g of dicyandiamide are introduced and 98 g of the prepolymer slowly under nitrogen blanket at 60 ° C, whereby the temperature to 75 ° C increases; after the addition is heated to 130 ° C and stirred for 1 h at this temperature. Thereafter, it is heated to 210 ° C for three hours with stirring and cooled. The urea amine has the following properties:

Amine number: 389.5 mg KOH / g

P ₂₅ ° C = 4900 mPas

(b) Preparation of a coating according to the invention

14.5 g of the epoxy component of a mixture of glycerol and glycerol triglycidyl ether with the epoxide equivalent of 143 g / mol is mixed intensively at 30 ° C with 7.35 g of urea and on a laboratory table with integrated dryers (LabCoater the Company Mathis) to a 200 pm film by means of a knife blade. The pot life is 44 minutes. The film is cured at 60 ° C for 60 minutes.

This gives a crystal-clear film with the glass transition temperature (DSC) 76 ° C.

Example 14

(a) Preparation of the urea amine component

In a heatable 2 l glass reactor with magnetic stirrer, condenser, thermocouple and dropping funnel, 1020 g of IPDA, 191 g of N-ethyl-N-cyclohexylamine (NECHA), 260 g of trisaminomethylhexane are added and heated to 60 ° C. with rapid stirring , In this mixture, 134 g of a prepolymer of 533.5 g of isophorone diisocyanate and 90.5 g of butane-1, 4-diol are added with rapid stirring such that the temperature does not exceed 75 ° C. Subsequently, the temperature is slowly increased to 175 ° C and stirring hold at this temperature for one hour. The reaction product has an amine value of 603.4 mg KOH / g and a viscosity of G | ₂₅ ° c = 2160 mPas.

(b) Preparation of a coating according to the invention

The epoxy component is mixed by means of a static mixer at 30 ° C. by means of a mixing machine from Hilger & Kern in a ratio of 1.75: 1 and introduced into an HDPE pipe of 14 mm internal diameter. Thereafter, a 13 mm pig was passed through the tube by means of compressed air, so that a coating of on average 300 pm was formed on the tube inner wall. The pot life was 40 minutes, the tack-free time 250 minutes, the curing time 18 hours. This gives a black film with the glass transition temperature (DSC) 72 ° C, a Shore A hardness of 82, an elongation at break of 16.5% and a tensile strength of 33 N / mm ² .

A sample of the internally coated tube of 30 cm in length was treated with a drinking water sample which additionally contained 1000 germs per ml of Listeria. After 7 days at 25 ° C, the water was rechecked for its germ count. A value of 82 germs per ml was determined.

Example 15

(a) Preparation of the urea amine component

In a heatable 2 l glass reactor with magnetic stirrer, condenser, thermocouple and dropping funnel, 1010 g of IPDA, 75 g of N-ethyl-N-cyclohexylamine (NECHA), 435 g of N ² -methyl-dipropylenetriamine are added and the mixture is heated to 50 ° C. with rapid stirring heated. In this mixture, 167 g of a prepolymer of 533.5 g of isophorone diisocyanate and 92.0 g of butane-1, 4-diol are added with rapid stirring such that the temperature does not exceed 75 ° C. Subsequently, the temperature is slowly increased to 175 ° C and keep stirring for one hour at this temperature. The reaction product has an amine value of 608.7 mg KOH / g and a viscosity of G | ₂₅ ° c = 2740 mPas.

(b) Preparation of a coating according to the invention The epoxide component is prepared from 525 g of trimethylolpropane triglycidyl ether, 75 g of pentaerythritol triglycidyl ether, 35 g of fumed silica (trade name Aerosil R208 from Evonik AG), 7 g of iron oxide black (particle size 12-56 μm) and 4 g of a modified montmorillonite ( Trade name Nanocor I.30E).

The epoxy component is mixed by means of a static mixer at 30 ° C. by means of a mixing machine from Hilger & Kern in a ratio of 1.75: 1 and introduced into an HDPE pipe of 14 mm internal diameter. Thereafter, a 13 mm pig was passed through the tube by means of compressed air, so that a coating of on average 300 pm was formed on the tube inner wall. The pot life was 27 minutes, the tack-free time 130 minutes, the curing time 1 1 hours. This gives a black film with the glass transition temperature (DSC) 78 ° C, a Shore A hardness of 76, an elongation at break of 12% and a tensile strength of 21 N / mm ² .

A sample of the internally coated tube of 30 cm in length was treated with a drinking water sample which additionally contained 1000 germs per ml of Listeria. After 7 days at 25 ° C, the water was rechecked for its germ count. A value of 255 germs per ml was determined.

Example 16

(a) Preparation of the urea amine component

In a 750 ml heatable glass reactor with intensive stirrer, condenser, thermocouple and dropping funnel, 238.5 g of isophoronediamine and 203 g of bis-N, N- (3-aminopropyl) -N-methylamine are placed under nitrogen blanketing. A solution of 26.2 g of m-xylylene diisocyanate in 17.5 g of dimethyl sulfoxide is added dropwise with stirring in such a way that the temperature does not exceed 50 ° C in the mixture. After completion of the addition, the temperature is raised to 180 ° C and stirred at this temperature for two hours. A clear, yellowish Oligoharnstofflösung in excess amine.

The properties of the urea amine hardener:

Amine number: 762 mg KOH / g

Viscosity (25 ° C): 19 mPas

(b) Preparation of the coating according to the invention The epoxy component is a mixture of 29% by weight of trimethylolpropane monoglycidyl ether, 30% by weight of trimethylolpropane diglycidyl ether and 41% by weight of trimethylolpropane triglycidyl ether.

143 g of the glycidyl ether mixture are mixed at ambient temperature with 38.9 g of the hardener component for 5 minutes and then spread on silkonisiertem release paper on a laboratory Streichisch with integrated dryer (LabCoater® Mathis) to a 200 pm film using knife blade. The pot life is 18 minutes. The film is cured at 60 ° C for 300 minutes.

This gives a pale yellowish film with the glass transition temperature (DSC) 77 ° C.

Wilhelmshaven: no fouling, growth or discoloration after 90 days detectable

Turning lock: no growth, growth or discoloration detectable after 100 days

Example 17

(a) Preparation of the urea amine component

In a 750 ml heatable glass reactor with intensive stirrer, condenser, thermocouple and dropping funnel, 238.4 g of isophoronediamine and 203 g of bis-N, N- (3-aminopropyl) -N-methylamine are initially charged with nitrogen. A solution of 38.5 g of m-tetramethylxylylene diisocyanate in 17.5 g of dimethyl sulfoxide is added dropwise with stirring to the mixture so that the temperature does not exceed 50 ° C. After completion of the addition, the temperature is raised to 180 ° C and stirred at this temperature for two hours. A clear, yellowish Oligoharnstofflösung in excess amine.

The properties of the urea amine hardener:

Amine number: 735 mg KOH / g

Viscosity (25 ° C): 35 mPas

(b) Preparation of a coating according to the invention

The epoxy component is a mixture of 29% by weight of trimethylolpropane monoglycidyl ether, 30% by weight of trimethylolpropane diglycidyl ether and 41% by weight of trimethylolpropane triglycidyl ether. 143 g of the glycidyl ether mixture are mixed at ambient temperature with 40.3 g of the hardener component for 5 minutes and then spread on silkonisiertem release paper on a laboratory Streichisch with integrated dryer (LabCoater® Mathis) to a 200 pm film by knife blade. The pot life is 18 minutes. The film is cured at 60 ° C for 300 minutes.

This gives a pale yellowish film with the glass transition temperature (DSC) 79 ° C.

Wilhelmshaven: no fouling, growth or discoloration after 90 days detectable

Turning lock: no growth, growth or discoloration detectable after 100 days

Example 18

(a) Preparation of the urea amine component

In a heatable 750 ml glass reactor with high-performance stirrer, condenser, thermocouple and dropping funnel, 238.6 g of isophoronediamine and 147 g of bis-N, N- (3-aminopropyl) -N-methylamine are initially charged with nitrogen. A solution of 29.05 g of m-xylylene diisocyanate in 17.5 g of dimethyl sulfoxide is added dropwise with stirring in such a way that the temperature does not exceed 50 ° C in the mixture. After completion of the addition, the temperature is raised to 180 ° C and stirred at this temperature for two hours. A clear, yellowish Oligoharnstofflösung in excess amine.

The properties of the urea amine hardener:

Amine number: 686 mg KOH / g

Viscosity (25 ° C): 21700 mPas

(b) Preparation of a coating according to the invention

The epoxy component is a mixture of 29% by weight of trimethylolpropane monoglycidyl ether, 30% by weight of trimethylolpropane diglycidyl ether and 41% by weight of trimethylolpropane triglycidyl ether.

143 g of the Glycidethergemisches be at ambient temperature with 43.2 g of Hardener component mixed for 5 minutes and then spread on a siliconized release paper on a laboratory table with integrated dryers (LabCoater® Mathis) to a 200 pm film by knife blade. The pot life is 18 minutes. The film is cured at 60 ° C for 300 minutes.

This gives a pale yellowish film with the glass transition temperature (DSC) 72 ° C.

Wilhelmshaven: no fouling, growth or discoloration after 90 days detectable

Turning lock: no growth, growth or discoloration detectable after 100 days

Example 19

(a) Preparation of the urea amine component

In a heatable 750 ml glass reactor with high-performance stirrer, condenser, thermocouple and dropping funnel, 308.5 g of isophoronediamine and 48 g of N-ethyl-N-cyclohexylamine are initially charged with nitrogen. 60.05 g of m-tetramethylxylylene diisocyanate are added dropwise with stirring in such a way that the temperature does not exceed 50 ° C. After completion of the addition, the temperature is raised to 180 ° C and stirred at this temperature for two hours. This gives a clear, almost colorless Oligoharnstofflösung in excess amine.

The properties of the urea amine hardener:

Amine number: 475 mg KOH / g

Viscosity (25 ° C): 3420 mPas

(b) Preparation of a coating according to the invention

143 g of the Glycidethergemisches are mixed at ambient temperature with 1 18 g of the curing agent component for 5 minutes and then on silkonisiertem release paper on a laboratory Streichisch with integrated dryer (LabCoater® Mathis) to a 200 pm Film passed by knife blade. The pot life is 18 minutes. The film is cured at 60 ° C for 300 minutes.

This gives an almost colorless film with the following properties:

Shore D hardness (24 hours 60 ° C): 85

Tensile strength (24 hours 60 ° C) (MPa): 71, 7

Elongation at break (24 hours 60 ° C) (%): 4.3

E-train module (24 hours 60 ° C) (MPa): 1830

Glass transition temperature (DSC): 81 ° C

Water absorption (24 hours 60 ° C): 4.2% after 24 hours storage

Oxygen permeability to water (24 hours 40 ° C): 82 ppb (ISO 17455: 2005)

Wilhelmshaven: no fouling, growth or discoloration after 180 days detectable

Turning lock: no growth, growth or discoloration after 210 days detectable

Example 20

(a) Preparation of the urea amine component

In a heatable 750 ml glass reactor with high-performance stirrer, condenser, thermocouple and dropping funnel, 303 g of isophoronediamine and 25.3 g of N-ethyl-N-cyclohexylamine are initially charged with nitrogen. 71.7 g of m-tetramethylxylylene diisocyanate are added dropwise with stirring to the mixture in such a way that the temperature does not exceed 50.degree. After completion of the addition, the temperature is raised to 180 ° C and stirred at this temperature for two hours. This gives a clear, almost colorless Oligoharnstofflösung in excess amine.

The properties of the urea amine hardener:

Amine number: 430 mg KOH / g

Viscosity (25 ° C): 2310 mPas Laser light scattering: peaks at 0.85 and 13.2 nm

(b) Preparation of a coating according to the invention

The epoxy component is a mixture of 29% by weight of trimethylolpropane monoglycidyl ether, 30% by weight of trimethylolpropane diglycidyl ether and 41% by weight of trimethylolpropane triglycidyl ether. 143 g of Glycidethergemisches be at ambient temperature with 130.5 g of

Hardener component mixed for 5 minutes and then spread on a siliconized release paper on a laboratory table with integrated dryers (LabCoater® Mathis) to a 200 pm film by knife blade. The pot life is 18 minutes. The film is cured at 60 ° C for 300 minutes.

This gives an almost colorless film with the following properties:

Shore D hardness (24 hours 60 ° C): 86

Tensile strength (24 hours 60 ° C) (MPa): 84.3

Elongation at break (24 hours 60 ° C) (%): 3.9

E-train module (24 hours 60 ° C) (MPa): 1990

Glass transition temperature (DSC): 84 ° C

Water absorption (24 hours 60 ° C): 4.1% after 24 hours storage

Oxygen permeability to water (24 hours 40 ° C): 80 ppb (ISO 17455: 2005)

Wilhelmshaven: no fouling, growth or discoloration detectable after 120 days

Turning lock: no growth, growth or discoloration detectable after 120 days

Claims

claims

A process for producing a biocidal coating material comprising the steps of:

(i) providing a urea amine component obtainable by reacting a) an aliphatic or araliphatic di- or triisocyanate with

(iii) reacting the urea amine component with the epoxy component,

wherein a ratio of the epoxy groups of the epoxy component to the amine groups of the urea amine component is 0.25: 1 to 1: 0.25.

2. The method of claim 1, wherein a molar ratio of the first amine to the second amine in the range of 1, 5: 1 to 1: 3.

A process according to any one of the preceding claims wherein the first amine has a secondary amine group.

4. The method of claim 3, wherein the first amine is a compound or a mixture of compounds which are selected from the group comprising di-n-butylamine, butylamine, piperidine, cyclohexylamine, N-ethyl-N-cyclohexylamine, 2 Aminoethanol, dimethylamine, N-methyl-N-cyclohexylamine, N-propyl-N- cyclohexylamine, N-butyl-N-cyclohexylamine, N, N-dicyclohexylamine and aziridine.

5. The method according to any one of the preceding claims, wherein the second amine has two amine groups.

The process of claim 5 wherein the second amine is a compound or mixture of compounds selected from the group consisting of 1-amino-3-aminomethyl-3,5,5-trimethylcyclohexane (isophoronediamine), 1,3 - benzenedimethanamine, bis (4-aminocyclohexyl) methane, 1, 4-diaminobutane, 1, 6-diaminohexane, 2-methyl-1,5-diaminopentane, 1, 6-diamino-2,2,4-trimethylhexane, 1, 6-diamino-2,4,4-trimethylhexane, cyclohexane-1,4-diamine, 2-ethyl-imidazolidine, 1,5-pentanediamine, piperazine, ethylenediamine, 4,4'-methylenebis (cyclohexylamine), 1, 3 Phenylenediamine, 2,2-bis (aminoethoxy) propane, 1,3-cyclohexanebis (methylamine), 1,9-diaminononane, 4,9-dioxa-1,12-dodecanediamine, 2,2 '- (ethylenedioxy) bis (ethylamine ), 4,7,10-trioxa-1, 13-tridecanediamine, tris (2-aminoethyl) amine, p-xylylenediamine, adipoguanamine, isoadipoguanamine, 2-methylglutaroguanamine and caprinoguanamine.

7. The method according to any one of the preceding claims, wherein the di- or triisocyanate is a compound or a mixture of compounds which are selected from the group comprising isophorone diisocyanate (IPDI), 1, 4- cyclohexane diisocyanate, 1, 3-bis (isocyanatomethyl ) cyclohexane, 1, 5-diisocyanato-2-methylpentane, 1, 8-diisocyanato-octane, 4,4'-methylene bis (cyclohexyl isocyanate), 2,2,4-trimethyl-1,6-diisocyanatohexane, 2,4,4-trimethyl -1, 6-diisocyanatohexane, 1, 12-diisocyanatododecanes, 2-ethylbutane-1,4-diisocyanate, hexamethylene diisocyanate (HDI), octadecyl diisocyanate, tricyclodecanediisocyanate, biuret of hexamethylene diisocyanate, trimers of hexamethylene diisocyanate, trimers of isophorone diisocyanate, xylylene diisocyanates and tetramethylxylylene diisocyanates.

8. The method according to any one of the preceding claims, wherein the polyfunctional glycidyl ether is a di-, tri- or Tetraglycidether.

9. The process of claim 8, wherein the polyfunctional glycidyl ether is a mixture of trimethylolpropane monoglycidyl ether, trimethylolpropane diglycidyl ether and trimethylolpropane triglycidyl ether.

10. The method according to any one of the preceding claims, wherein the polyfunctional

Glycidyl ether is a compound or a mixture of compounds which are selected from the group comprising ethylene glycol diglycidyl ether,

Diethylene glycol diglycidyl ether, triethylene glycol diglycidyl ether, butanediol-1, 4-diglycidyl ether, hexanediol-1, 6-diglycidyl ether, octanediol-1, 8-diglycidyl ether, dodecane-1, 12-diglycidyl ether, isosorbide diglycidyl ether, glycerol monoglycidyl ether, glycerol diglycidyl ether, glycerol triglycidyl ether, trimethylolpropane triglycidyl ether, pentaerythritol monoglycidyl ether, pentaerythritol diglycidyl ether, pentaerythritol triglycidyl ether,

Pentaerythritol tetraglycidyl ether, diglycerol tetraglycidyl ether, dipentaerythritol hexaglycidyl ether, and dipentaerythritol tetraglycidyl ether.

1 1. A method according to any one of the preceding claims, wherein the urea amine component and / or the epoxy component one or more additives are added.

12. The method according to any one of the preceding claims, wherein the urea amine component one or more guanamines selected from the group adipoguanamine, isoadipoguanamine, 2-methylglutaroguanamine and caprinoguanamine are added.

13. biocidal coating material prepared by a process of the preceding claims.

14. Use of the biocidal coating material according to claim 13 for the production of a coating for ship walls, ship interior, ship deck, ramps, propellers, wind power blades, wind turbine housings, floors and Pipes.

15. Use of the biocidal coating material according to claim 14 for the production of a tube inner coating.