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US4137389A Expired / Lapsed US ⏱️ 0.0 years remaining

Low-molecular weight acrylate resins and a process for their production

Assignee: Bayer AG
•
Filing: 1978-01-23
•
Granted: 1979-01-30
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Expires: 1998-01-23
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Abstract

Abstract A process for the production of a crosslinkable low-molecular weight acrylic resin containing hydroxyl-groups and having a low-molecular consistency factor by the radical bulk copolymerization of (A) 0 to 30 parts by weight of a hydroxyalkyl ester of acrylic acid or methacrylic acid or mixtures thereof; (B) 0 to 60 parts by wt. of styrene or a substituted styrene or methyl methacrylate or mixtures thereof; (C) 10 to 90 parts by weight of an acrylic acid ester or of a methacrylic acid ester with 2 to 12 carbon atoms in the alcohol radical or mixtures thereof; (D) 0 to 30 parts by weight of an α,β-monoolefinically saturated mono- or di-carboxylic acid with 3 to 5 carbon atoms or of a maleic acid semiester or mixtures thereof or reaction products thereof with a monoglycidyl compound, in the presence of 10 to 70 parts by weight of a monoallyl ether of an at least trihydric alcohol, The sum of the parts by weight of all the monomers A - E amounting to 100, Wherein the indicated quantity of monomer E is initially introduced and, at temperatures above 100° C, monomers A to D together with 0.5 to 6% by weight, based on A to D, of an initiator with a half-life period at 100 to 160° C of 0.01 to 100 minutes, are introduced over a period of 1 to 6 hours and polymerized, at least 98% by weight of the monomers A to D and from 36 to 95% by weight of monomer E being converted. Acrylate resins of this type are eminently suitable for the production of readily processible binder mixtures which although low in viscosity, have a very high solids content.

Inventors

  • 👤 Frank Wingler
  • 👤 Josef Pedain
  • 👤 Walter Uerdingen

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-03 06:42
CPC Classifications
C; C08; C08J; C08J3/00; C08J3/02; C08J3/09; C08J3/091; C08J3/095; C08F; C08F2/00; C08F2/02; C08F220/00; C08F220/02; C08F220/10; C08F220/12; C08F220/16; C08F220/18; C08F220/1804; C08K; C08K5/00; C08K5/04; C08K5/06; C08J2333/00; C08J2333/04; C08J2333/06

Claims Analysis

Total Claims: 3
Claim 1
Independent Claim 285 words
A process for the production of an acrylic resin, which comprises the radical bulk copolymerisation of (A) 0 to 30 parts by weight of at least one hydroxyalkyl ester of acrylic acid or methacrylic acid with 2 to 4 carbon atoms in the hydroxyalkyl radical, or a mixture thereof; (B) 0 to 60 parts by weight of styrene, α-methyl styrene, o-chlorostyrene, p-chlorostyrene, o-, m- or p-methyl styrene, p-tert.-butyl styrene or methyl methacrylate, or a mixture thereof; (C) 10 to 90 parts by weight of at least one acrylic acid ester with 1 to 12 carbon atoms in the alcohol radical or of at least one methacrylic acid ester with 2 to 12 carbon atoms in the alcohol radical, or a mixture thereof; (D) 0 to 30 parts by weight of at least one α,β-monoolefinically saturated mono- or di-carboxylic acid with 3 to 5 carbon atoms or of at least one maleic acid semiester with 2 to 14 carbon atoms in the alcohol radical, or a mixture thereof or a reaction product thereof with a monoglycidyl compound, in the presence of (E) 10 to 70 parts by weight of at least one monoallyl ether of an at least trihydric alcohol, the sum of the parts by weight of all the monomers A-E amounting to 100, wherein the indicated quantity of monomer E is initially introduced and, at a temperature above 100° C., monomers A to D together with 0.5 to 6% by weight, based on A to D, of an initiator, are introduced over a period of 1 to 6 hours and polymerised, at least 98% by weight of the monomers A to D and from 36 to 95% by weight of monomer E being converted.
Claim 2
Dependent Claim 285 words
A process for the production of an acrylic resin, which comprises the radical bulk copolymerisation of (A) 0 to 30 parts by weight of at least one hydroxyalkyl ester of acrylic acid or methacrylic acid with 2 to 4 carbon atoms in the hydroxyalkyl radical, or a mixture thereof; (B) 0 to 60 parts by weight of styrene, α-methyl styrene, o-chlorostyrene, p-chlorostyrene, o-, m- or p-methyl styrene, p-tert.-butyl styrene or methyl methacrylate, or a mixture thereof; (C) 10 to 90 parts by weight of at least one acrylic acid ester with 1 to 12 carbon atoms in the alcohol radical or of at least one methacrylic acid ester with 2 to 12 carbon atoms in the alcohol radical, or a mixture thereof; (D) 0 to 30 parts by weight of at least one α,β-monoolefinically saturated mono- or di-carboxylic acid with 3 to 5 carbon atoms or of at least one maleic acid semiester with 2 to 14 carbon atoms in the alcohol radical, or a mixture thereof or a reaction product thereof with a monoglycidyl compound, in the presence of (E) 10 to 70 parts by weight of at least one monoallyl ether of an at least trihydric alcohol, the sum of the parts by weight of all the monomers A-E amounting to 100, wherein the indicated quantity of monomer E is initially introduced and, at a temperature above 100° C., monomers A to D together with 0.5 to 6% by weight, based on A to D, of an initiator, are introduced over a period of 1 to 6 hours and polymerised, at least 98% by weight of the monomers A to D and from 36 to 95% by weight of monomer E being converted.
Claim 3
Dependent Claim 24 words
A process as claimed in claim 1, wherein monomers A-D and the initiator are introduced at a temperature of from 130° to 160° C.

References Cited (Backward Citations)

US3028367A Cited
US3753958A Cited
US3865904A Cited
US3935173A Cited
US3957741A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1982-01-29 1982-07-31 1983-01-30 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1986-01-29 1986-07-31 1987-01-30 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1990-01-29 1990-07-31 1991-01-30 $7700.00 Window Closed / Lapsed

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