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Process for the preparation of copolymers

Assignee: Hoechst AG
•
Filing: 1980-02-25
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Granted: 1981-09-15
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Expires: 2000-02-25
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Abstract

Abstract A process for the preparation of copolymers in which in a first step an olefinically unsaturated dicarboxylic acid is reacted with a polyhydric alcohol to yield a hemi-ester having free hydroxyl groups, which in a second step is reacted with a monoepoxy compound to yield an olefinically unsaturated diester containing hydroxyl groups, wherein the diester is copolymerized in at least one further step with at least one unsaturated monomer having no free carboxyl groups, and the hardenable reaction product thus obtained is either isolated or hardened with a hardening agent, and coating and adhesive compositions containing a copolymer thus obtained.

Inventors

  • 👤 Jurgen Ritz
  • 👤 Hermann Hotze
  • 👤 Hans-Dieter Mummenthey

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-30 05:42
CPC Classifications
C; C08; C08G; C08G18/00; C08G18/06; C08G18/28; C08G18/40; C08G18/62; C08G18/6216; C08G18/622; C08G18/6241; C08F; C08F222/00; C08F222/10; C08F222/12; C08F222/20; C09; C09D; C09D135/00; Y; Y10; Y10T; Y10T428/00; Y10T428/31504; Y10T428/31855

Claims Analysis

Total Claims: 11
Claim 1
Independent Claim 176 words
In a process for the manufacture of copolymers reacting in a first step an olefinically unsaturated dicarboxylic acid with a polyhydric alcohol to yield a hemi-ester having free hydroxyl groups, reacting said hemi-ester in a second step with a monoepoxy compound to yield an olefinically unsaturated diester containing hydroxyl groups and copolymerizing said diester with at least one unsaturated monomer having no free carboxyl groups, the improvement which comprises reacting the hemiester having no ether groups in a second step with an equivalent amount of a monoepoxide compound, based on the hydroxyl groups of the hemi-ester, selected from the group consisting of glycidol, a glycidylether of a phenol and glycidylester of saturated carboxylic acids at a temperature between 100° and 170° C. to yield a reaction product having a molecular weight between 250 and 1500 and an OH-number between 175 and 550 and then copolymerizing the diester having 2 hydroxyalkyl radicals at a temperature between 80° and 220° C. and wherein the hardenable reaction product thus obtained is either isolated or hardened with a hardening agent.
Claim 2
Dependent Claim 176 words
In a process for the manufacture of copolymers reacting in a first step an olefinically unsaturated dicarboxylic acid with a polyhydric alcohol to yield a hemi-ester having free hydroxyl groups, reacting said hemi-ester in a second step with a monoepoxy compound to yield an olefinically unsaturated diester containing hydroxyl groups and copolymerizing said diester with at least one unsaturated monomer having no free carboxyl groups, the improvement which comprises reacting the hemiester having no ether groups in a second step with an equivalent amount of a monoepoxide compound, based on the hydroxyl groups of the hemi-ester, selected from the group consisting of glycidol, a glycidylether of a phenol and glycidylester of saturated carboxylic acids at a temperature between 100° and 170° C. to yield a reaction product having a molecular weight between 250 and 1500 and an OH-number between 175 and 550 and then copolymerizing the diester having 2 hydroxyalkyl radicals at a temperature between 80° and 220° C. and wherein the hardenable reaction product thus obtained is either isolated or hardened with a hardening agent.
Claim 3
Dependent Claim 38 words
A process according to claim 1 wherein the copolymerization is carried out with a monomer mixture containing at least about 50 mol % of at least one aromatic vinyl compound and at most about 20% of hydroxyalkyl esters.
Claim 4
Dependent Claim 36 words
A process according to claim 1 wherein the copolymerization is carried out with a monomer mixture containing at least about 50 mol% of at least one aromatic vinyl compound but being free from hydroxy alkyl ester.
Claim 5
Dependent Claim 28 words
A process according to claim 1 wherein the copolymerization is carried out at least in part in the presence of a free radical catalyst and in two steps.
Claim 6
Dependent Claim 23 words
A process according to claim 1 wherein the copolymerization is carried out at a temperature in the range from 80° to 220° C.
Claim 7
Dependent Claim 88 words
A process according to claim 1 wherein the reaction of the hemi-ester in the second stage is carried out at a temperature in the range from about 120° to 155° C. with an equivalent amount of epoxy compound, based on the hydroxyl groups of the diester, to yield a product having a molecular weight from about 400 to 1250 and an OH-number in the range from about 280 to 450 and wherein the copolymerization is carried out at a temperature in the range from 130° to 170° C.
Claim 8
Dependent Claim 26 words
A process according to claim 1 wherein the copolymerization is carried out until the solids content of the copolymer is about 60 to 80% by weight.
Claim 9
Dependent Claim 37 words
A process according to claim 1 wherein the copolymer is hardened by reaction with a compound selected from the group consisting of free and masked polyisocyanates, polycarboxylic acids and the anhydrides thereof, amino resins and phenolic resins.
Claim 10
Dependent Claim 30 words
A process according to claim 8, wherein the hardening is carried out in the presence of a catalyst selected from the group consisting of organometallic compounds, amines and combinations thereof.
Claim 11
Dependent Claim 24 words
A binding composition comprising a copolymer prepared by a process as claimed in claim 1 and suitable as a coating or an adhesive composition.

References Cited (Backward Citations)

US3221043A Cited
US3270088A Cited
US3367992A Cited
US3414635A Cited
US3406221A Cited
US4166893A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1984-09-14 1985-03-16 1985-09-15 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1988-09-14 1989-03-16 1989-09-15 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1992-09-14 1993-03-16 1993-09-15 $7700.00 Window Closed / Lapsed

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