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US4293661A Expired / Lapsed US ⏱️ 0.0 years remaining

Low molecular weight acrylate resins containing hydroxyl and tertiary amino groups

Assignee: Bayer AG
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Filing: 1979-12-31
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Granted: 1981-10-06
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Expires: 1999-12-31
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Abstract

Abstract A reaction product of an acrylate resin containing glycidyl groups and secondary mono-amines containing hydroxyl groups, obtained by reacting of said acrylate resin of copolymerized, statistically distributed units of (A) 3 to 30% by weight of the glycidyl ester of (meth)acrylic acid and/or of vinyl glycidyl ether; (B) 0 to 20% by weight of at least a hydroxy C 2 -C 4 alkyl ester of (meth)acrylic acid; (C) 5 to 80% by weight of at least an optionally substituted styrene, methyl methacrylate, (meth)acrylonitrile or any mixture thereof; (D) 5 to 70% by weight of an acrylic acid C 1 -C 12 -alkyl-or of a methacrylic acid C 2 -C 12 -alkyl ester or any mixture thereof; and (E) 0 to 10% by weight of an α,β-mono-olefinically unsaturated monocarboxylic or dicarboxylic acid containing from 3 to 5 carbon atoms or of a maleic acid C 2 -C 14 -mono ester or any mixture thereof, with at least one secondary mono-amine containing at least one secondary hydroxyl group. The reaction products are useful for crosslinking polyisocyanates.

Inventors

  • 👤 Joachim Probst
  • 👤 Michael Sonntag
  • 👤 Gunter Kolb

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-25 20:09
CPC Classifications
C; C08; C08G; C08G18/00; C08G18/06; C08G18/28; C08G18/40; C08G18/62; C08G18/6216; C08G18/622; C08G18/6237; C08F; C08F8/00; C08F8/30; C08F8/32; C08F2800/00; C08F2800/20

Claims Analysis

Total Claims: 2
Claim 1
Independent Claim 346 words
A composition comprising a compound which contains or is capable of forming more than one isocyanate group and; as a crosslinking component a reaction product of an acrylate resin containing glycidyl groups and a secondary mono-amine containing hydroxyl groups, obtained by reaction of said acrylate resin of copolymerised, statistically distributed units of (A) 3 to 30% by weight of the glycidyl ester of acrylic acid or methacrylic acid or of vinyl glycidyl ether, or any mixture thereof; (B) 0 to 20% by weight of a hydroxyalkyl ester of acrylic acid or methacrylic acid containing from 2 to 4 carbon atoms in the hydroxyalkyl radical, or any mixture thereof; (C) 5 to 80% by weight of styrene, α-methyl styrene, o-chlorostyrene, p-chlorostyrene o-, m- or p-methyl styrene, p-tert.-butyl styrene, methyl methacrylate, acrylonitrile or methacrylonitrile, or any mixture thereof; (D) 5 to 70% by weight of an acrylic acid ester containing from 1 to 12 carbon atoms in the alcohol radical or of a methacrylic acid ester containing from 2 to 12 carbon atoms in the alcohol radical, or any mixture thereof; and (E) 0 to 10% by weight of an α,β-mono-olefinically unsaturated monocarboxylic or dicarboxylic acid containing from 3 to 5 carbon atoms or of a maleic acid mono-ester containing from 2 to 14 carbon atoms in the alcohol radical, or any mixture thereof, with at least one amine containing hydroxyl groups corresponding to the formula: ##STR7## in which n=1 to 4, R=a single bond or an alkylene group containing from 1 to 4 carbon atoms, R'=alkyl containing from 1 to 4 carbon atoms, R"=alkyl containing from 1 to 4 carbon atoms or ##STR8## or in which R and R' together with ##STR9## represent an alicyclic 5- or 6-membered ring ##STR10## or R' and R" together with ##STR11## represent a pyrrolidine or piperidine ring, at a temperature of from 50° to 200° C. in such a ratio that one epoxide equivalent of the acrylate resin has been reacted with from 0.7 to 1 NH equivalent of the amine containing hydroxyl groups with the OH function remaining largely intact.
Claim 2
Dependent Claim 346 words
A composition comprising a compound which contains or is capable of forming more than one isocyanate group and; as a crosslinking component a reaction product of an acrylate resin containing glycidyl groups and a secondary mono-amine containing hydroxyl groups, obtained by reaction of said acrylate resin of copolymerised, statistically distributed units of (A) 3 to 30% by weight of the glycidyl ester of acrylic acid or methacrylic acid or of vinyl glycidyl ether, or any mixture thereof; (B) 0 to 20% by weight of a hydroxyalkyl ester of acrylic acid or methacrylic acid containing from 2 to 4 carbon atoms in the hydroxyalkyl radical, or any mixture thereof; (C) 5 to 80% by weight of styrene, α-methyl styrene, o-chlorostyrene, p-chlorostyrene o-, m- or p-methyl styrene, p-tert.-butyl styrene, methyl methacrylate, acrylonitrile or methacrylonitrile, or any mixture thereof; (D) 5 to 70% by weight of an acrylic acid ester containing from 1 to 12 carbon atoms in the alcohol radical or of a methacrylic acid ester containing from 2 to 12 carbon atoms in the alcohol radical, or any mixture thereof; and (E) 0 to 10% by weight of an α,β-mono-olefinically unsaturated monocarboxylic or dicarboxylic acid containing from 3 to 5 carbon atoms or of a maleic acid mono-ester containing from 2 to 14 carbon atoms in the alcohol radical, or any mixture thereof, with at least one amine containing hydroxyl groups corresponding to the formula: ##STR7## in which n=1 to 4, R=a single bond or an alkylene group containing from 1 to 4 carbon atoms, R'=alkyl containing from 1 to 4 carbon atoms, R"=alkyl containing from 1 to 4 carbon atoms or ##STR8## or in which R and R' together with ##STR9## represent an alicyclic 5- or 6-membered ring ##STR10## or R' and R" together with ##STR11## represent a pyrrolidine or piperidine ring, at a temperature of from 50° to 200° C. in such a ratio that one epoxide equivalent of the acrylate resin has been reacted with from 0.7 to 1 NH equivalent of the amine containing hydroxyl groups with the OH function remaining largely intact.

References Cited (Backward Citations)

US2949445A Cited
US3959237A Cited
US4049607A Cited
US3969327A Cited
US4205148A Cited
US4215029A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1984-10-05 1985-04-06 1985-10-06 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1988-10-05 1989-04-06 1989-10-06 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1992-10-05 1993-04-06 1993-10-06 $7700.00 Window Closed / Lapsed

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