Single-component coating having alkoxysilane-terminated N-substituted urea resins
US-9221942-B2 · Dec 29, 2015 · US
US2021309793A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2021309793-A1 |
| Application number | US-201917267524-A |
| Country | US |
| Kind code | A1 |
| Filing date | Aug 14, 2019 |
| Priority date | Aug 21, 2018 |
| Publication date | Oct 7, 2021 |
| Grant date | — |
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The invention relates to a polymer composition that can be produced by (a) reacting an NCO-reactive polymer having at least two NCO-reactive groups, with a polyisocyanate, the molar ratio of polyisocyanate molecules to NCO-reactive groups of the NCO-reactive polymer being at least 1.25:1; and (b) reacting the reaction product from step a) with an NCO-reactive silane. The invention also relates to a moisture-reactive composition containing the polymer composition and to methods for producing the polymer composition and the moisture-reactive composition. Finally, the invention relates to the use of the polymer composition as a drying agent for moisture-curing adhesives, sealants and coating agents.
Opening claim text (preview).
1 . A polymer composition produced by: a) reacting an NCO-reactive polymer having at least two NCO-reactive groups per molecule with a polyisocyanate, a molar ratio of the polyisocyanate molecules to the NCO-reactive groups of the NCO-reactive polymer being at least 1.25:1; and subsequently b) reacting remaining NCO groups in a reaction product from step a) with an NCO-reactive silane. 2 . The polymer composition as claimed in claim 1 , wherein the molar ratio of the polyisocyanate molecules to the NCO-reactive groups of the NCO-reactive polymer in (a) is 1.25:1 to 10:1. 3 . The polymer composition as claimed in claim 1 , wherein the NCO-reactive polymer has a number-average molecular weight of 2000 to 100 000 g/mol. 4 . The polymer composition as claimed in claim 1 , wherein the NCO-reactive polymer is a polyol. 5 . The polymer composition as claimed in claim 1 , wherein the polyisocyanate comprises 1,4-diisocyanatobutane, 1,5-diisocyanatopentane, hexamethylene 1,6-diisocyanate (HDI), 2-methyl-1,5-diisocyanatopentane, 1,5-diisocyanato-2,2-dimethylpentane, 2,2,4- and/or 2,4,4-trimethyl-1,6-diisocyanatohexane, 1,10-diisocyanatodecane, 1,3- and/or 1,4-diisocyanatocyclohexane, 1,4-diisocyanato-3,3,5-trimethylcyclohexane, 1,3-diisocyanato-2-methylcyclohexane, 1,3-diisocyanato-4-methylcyclohexane, 1-isocyanato-3,3,5-trimethyl-5-isocyanatomethylcyclohexane, 1-isocyanato-1-methyl-4(3)-isocyanatomethylcyclohexane, 2,4′- and/or 4,4′-diisocyanatodicyclohexylmethane, 1,3- and/or 1,4-bis(isocyanatomethyl)cyclohexane, bis(isocyanatomethyl)norbornane, 4,4′-diisocyanato-3,3′-dimethyldicyclohexylmethane, 4,4′-diisocyanato-3,3′,5,5′-tetramethyldicyclohexylmethane, 4,4′-diisocyanato-1,1′-bis(cyclohexyl), 4,4′-diisocyanato-3,3′-dimethyl-1,1′-bi(cyclohexyl), 4,4′-diisocyanato-2,2′,5,5′-tetramethyl-1,1′-bi(cyclohexyl), 1,8-diisocyanato-p-menthane, 1,3-diisocyanatoadamantane, 1,3-dimethyl-5,7-diisocyanatoadamantane, 1,3- and/or 1,4-bis(isocyanatomethyl)benzene, 1,3- and/or 1,4-bis(1-isocyanato-1-methylethyl)benzene, bis(4-(1-isocyanato-1-methylethyl)phenyl) carbonate, 2,4- and/or 2,6-diisocyanatotoluene, 2,4′- and/or 4,4′-diisocyanatodiphenylmethane, 1,5-diisocyanatonaphthalene, or a mixture thereof. 6 . The polymer composition as claimed in claim 1 , wherein the NCO-reactive silane is a compound of formula (I): R 1 3 Si(CH 2 ) n X (I), wherein R 1 each radical is in each case independently selected from C 1 -C 8 -alkyl, C 6 -C 20 -aryl, C 1 -C 8 -alkoxy, or C 1 -C 8 -acyloxy and at least one of the radicals R 1 is a C 1 -C 8 -alkoxy or C 1 -C 8 -acyloxy radical, n is an integer from 1 to 4, X is selected from —OH, —SH, and —NHR 2 , R 2 is selected from H, C 1 -C 20 -alkyl, —CH 2 CH 2 CN, and —CHR 3 CH 2 COOR 4 , R 3 is selected from H and —COOR 4 , and R 4 in each case is C 1 -C 20 -alkyl. 7 . A process for producing the polymer composition as claimed in claim 1 , comprising: a) reacting an NCO-reactive polymer having at least two NCO-reactive groups per molecule with a polyisocyanate, a molar ratio of the polyisocyanate molecules to the NCO-reactive groups of the NCO-reactive polymer being at least 1.25:1; and b) reacting a reaction product from step a) with an NCO-reactive silane. 8 . A moisture-curing composition comprising a polymer composition as claimed in claim 1 and at least one additive comprising one or more fillers, one or more crosslinking catalysts, one or more adhesion promoters, one or more plasticizers, or a combination thereof. 9 . The moisture-curing composition as claimed in claim 8 , wherein the moisture-curing composition has a water content, determined according to DIN EN ISO 15512:2017-03, method B2, of up to 0.1% by weight, based on a total weight of the moisture-curing composition. 10 . The moisture-curing composition as claimed in claim 8 , containing no further drying agents. 11 . The moisture-curing composition as claimed in claim 8 , comprising less than 1% by weight of vinyl group-containing silanes, based on a total weight of the moisture-curing composition. 12 . The moisture-curing composition as claimed in claim 8 , comprising 5% to 50% by weight of the polymer composition as claimed in claim 1 ; 10% to 70% by weight of at least one filler; up to 5% by weight of at least one adhesion promoter; 0.001% to 5% by weight of at least one crosslinking catalyst; and up to 50% by weight of at least one plasticizer, based in each case on a total weight of the moisture-curing composition. 13 . A process for producing the a moisture-curing composition, comprising mixing a polymer composition as claimed in claim 1 with at least one filler, at least one adhesion promoter, at least one crosslinking catalyst, at least one plasticizer, or a combination thereof. 14 . The process as claimed in claim 13 , wherein the polymer composition as claimed in claim 1 is mixed with at least one filler having a water content of up to 1% by weight, based on a total weight of the filler. 15 . The process as claimed in claim 13 , wherein at most 1% by weight of vinyl group-containing silanes are added to the moisture-curing composition. 16 . A drying agent for moisture-curing adhesives, sealants, or coating materials, comprising the polymer composition as claimed in claim 1 . 17 . A parquet adhesive containing the polymer composition as claimed in claim 1 .
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