US4210702A
Expired / Lapsed
US
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Process for the manufacture of soluble copolymers which contain hydroxyl groups and which copolymers can be crosslinked with organic polyisocyanates
Assignee: Hoechst AG
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Filing: 1978-08-18
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Granted: 1980-07-01
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Expires: 1998-08-18
Abstract
Abstract The present invention relates to a process for the manufacture of soluble copolymers, which contain hydroxyl groups, can be crosslinked with organic polyisocyanates and are based on mixtures of styrene, methyl methacrylate, hydroxyethyl methacrylate, acrylic acid and glycidyl esters of α-alkylalkanemonocarboxylic acids and/or α,α-dialkylalkanemonocarboxylic acids, by heating in inert organic solvents in the presence of polymerization initiators and optionally chain stoppers, simultaneous esterification and polymerization taking place.
Inventors
- 👤 Horst Dalibor
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-31 17:08
CPC Classifications
C; C08; C08G; C08G18/00; C08G18/06; C08G18/28; C08G18/40; C08G18/62; C08G18/6216; C08G18/625; C08G18/6258; C08F; C08F220/00; C08F220/02; C08F220/10; C08F220/20; Y; Y10; Y10T; Y10T428/00; Y10T428/31504; Y10T428/31511; Y10T428/31529; Y10T428/31678; Y10T428/31692; Y10T428/31699; Y10T428/31855; Y10T428/3188; Y10T428/31895; Y10T428/31906
Claims Analysis
Total Claims: 24
Claim 1
Independent Claim
239 words
A process for the manufacture of coatings from polyhydroxy compounds, which are based on copolymers, which contain hydroxyl groups and are reaction products of mixtures of styrene, methyl methacrylate, hydroxyethyl methacrylate, acrylic acid and glycidyl esters of α-alkylalkanemonocarboxylic acids and/or α,α-dialkylalkanemonocarboxylic acids, and from organic polyisocyanates in solvents which have no active hydrogen atoms, which comprises mixing A. a copolymer, which contains hydroxyl groups and consists of components (a) 26-28% by weight of styrene, (b) 20-22% by weight of methyl methacrylate, (c) 18-20% by weight of hydroxyethyl methacrylate, (d and e) 32.5-35.5% by weight of a reaction product of acrylic acid and glycidyl esters of acids selected from the group consisting of α-alkylalkanemonocarboxylic acids and α,α-dialkylalkanemonocarboxylic acids, having the empirical formula C 13 H 24 O 3 , which reaction product has the formula ##STR9## wherein R is the radical of an α-alkylalkanemonocarboxyl acid or an α,α-dialkylalkanemonocarboxylic acid and the radical has the empirical formula C 10 H 19 O 2 , and in which the incorporated components (a), (b), (c), (d) and (e) add up to 100% by weight, dissolved in solvents which do not contain active hydrogen atoms, is reacted with (B) an organic polyisocyanate, the amounts of the copolymer (A) and the polyisocyanate (B) in the mixture adding up to 100 percent by weight, and applying this mixture to a substrate to be coated, and then removing the solvent in order to obtain the finished coating.
Claim 2
Dependent Claim
239 words
A process for the manufacture of coatings from polyhydroxy compounds, which are based on copolymers, which contain hydroxyl groups and are reaction products of mixtures of styrene, methyl methacrylate, hydroxyethyl methacrylate, acrylic acid and glycidyl esters of α-alkylalkanemonocarboxylic acids and/or α,α-dialkylalkanemonocarboxylic acids, and from organic polyisocyanates in solvents which have no active hydrogen atoms, which comprises mixing A. a copolymer, which contains hydroxyl groups and consists of components (a) 26-28% by weight of styrene, (b) 20-22% by weight of methyl methacrylate, (c) 18-20% by weight of hydroxyethyl methacrylate, (d and e) 32.5-35.5% by weight of a reaction product of acrylic acid and glycidyl esters of acids selected from the group consisting of α-alkylalkanemonocarboxylic acids and α,α-dialkylalkanemonocarboxylic acids, having the empirical formula C 13 H 24 O 3 , which reaction product has the formula ##STR9## wherein R is the radical of an α-alkylalkanemonocarboxyl acid or an α,α-dialkylalkanemonocarboxylic acid and the radical has the empirical formula C 10 H 19 O 2 , and in which the incorporated components (a), (b), (c), (d) and (e) add up to 100% by weight, dissolved in solvents which do not contain active hydrogen atoms, is reacted with (B) an organic polyisocyanate, the amounts of the copolymer (A) and the polyisocyanate (B) in the mixture adding up to 100 percent by weight, and applying this mixture to a substrate to be coated, and then removing the solvent in order to obtain the finished coating.
Claim 3
Dependent Claim
49 words
A process according to claim 1, characterised in that 60-80% by weight of component (A) is dissolved in a solvent which does not contain active hydrogen atoms, and 20-40% by weight of (B) are mixed therewith, the amounts of components (A) and (B) adding up to 100% by weight.
Claim 4
Dependent Claim
63 words
A process according to claim 1, which is further characterised in that component (A) is employed in an amount of 60-70% by weight, component (B) is employed in an amount of 20-40% by weight, and an additional component (C), which is a mixture of at least one of a monomethylol-pentamethoxymethylmelamine and dimethylol-tetramethoxymethylmelamine with trimethyloltrimethoxymethylmelamine, is employed in an amount of 1-10% by weight.
Claim 5
Dependent Claim
55 words
A process according to claim 1, characterised in that component (A) is employed in an amount of 63-68% by weight and the organic polyisocyanate component (B) is employed in an amount of 32-37% by weight and the organic polyisocyanate component (B) is a reaction product of 3 mols of hexamethylenediisocyanate and 1 mol of water.
Claim 6
Dependent Claim
62 words
A process according to claim 1, characterised in that the component (A) is employed in an amount of 63-68% by weight and the organic polyiscyanate component (B), which contains biuret groups, has a NCO content of 16.0-17% and is a reaction product obtained from 3 mols of hexamethylenediisocyanate and 1 mol of water, is employed in an amount of 32-37% by weight.
Claim 7
Dependent Claim
46 words
A process according to claim 1, characterised in that the component (A) polymer is one which contains hydroxyl groups and has a hydroxyl numer of 4 to 5% by weight, based on the weight of the starting monomers, and an acid number between 6 and 12.
Claim 8
Dependent Claim
54 words
A process according to claim 1, characterised in that the copolymer of component (A) is one which contains hydroxyl groups and, after removal of the solvent, has a melting range of 60° to 80° C., the start and end of the melting point range of said copolymer being separated by at most 3° C.
Claim 9
Dependent Claim
36 words
A process according to claim 1, characterised in that the mixture of the component (A) containing hydroxyl groups and the component (B) organic polyisocyanate is such that there are 0.7-1.2 NCO groups per hydroxyl group therein.
Claim 10
Dependent Claim
38 words
A process according to claim 8, wherein the reaction of the component (A) copolymer with the component (B) organic polyisocyanate is carried out using amounts such that there are from 0.9 to 1.1 NCO groups per hydroxyl group.
Claim 11
Dependent Claim
46 words
A lacquer composition comprising a solution of the hydroxyl-containing copolymer component (A) and an organic polyisocyanate component (B) in a solvent which has no active hydrogen atoms, prepared according to the process recited in claim 1, before it is applied to the substrate to be coated.
Claim 12
Dependent Claim
39 words
A lacquer composition according to claim 10, which further includes a melamine derivative component (C) which is a mixture of at least one monomethylol-pentamethoxymethylmelamine and dimethylol-tetramethoxymethylmelamine with trimethyloltrimethoxymethylmelamine, employed in the amount of 1 to 10 percent, by weight.
Claim 13
Dependent Claim
27 words
A lacquer composition according to claim 10, wherein the organic polyisocyanate component (B) is a reaction product of 3 mols of hexamethylene-diisocyanate and 1 mol of water.
Claim 14
Dependent Claim
80 words
A lacquer composition according to claim 10, wherein the component (A) is employed in the amount of from 63 to 68 percent by weight and the organic polyisocyanate component (B) is one which contains biuret groups, has an NCO content of 16 to 17 percent and is the reaction product obtained from 3 mols of hexamethylene diisocyanate and 1 mol of water, and said organic polyisocyanate component is employed in an amount of from 32 to 37 percent by weight.
Claim 15
Dependent Claim
47 words
A lacquer composition according to claim 10, wherein the component (A) polymer is one which contains a hydroxyl group and has a hydroxyl number of from 4 to 5 by weight, based on the weight of the starting monomers, and an acid number between 6 and 12.
Claim 16
Dependent Claim
33 words
A lacquer composition according to claim 10, which contains the component (A) copolymer and component (B) organic polyisocyanate in amounts such that there are 0.7 to 1.2 NCO groups per hydroxyl groups therein.
Claim 17
Dependent Claim
10 words
An article coated according to the process of claim 1.
Claim 18
Dependent Claim
10 words
An article coated according to the process of claim 2.
Claim 19
Dependent Claim
10 words
An article coated according to the process of claim 3.
Claim 20
Dependent Claim
10 words
An article coated according to the process of claim 4.
Claim 21
Dependent Claim
10 words
An article coated according to the process of claim 5.
Claim 22
Dependent Claim
10 words
An article coated according to the process of claim 6.
Claim 23
Dependent Claim
10 words
An article coated according to the process of claim 7.
Claim 24
Dependent Claim
10 words
An article coated according to the process of claim 8.
References Cited (Backward Citations)
US3330814A
Cited
US3442873A
Cited
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1983-07-01 | 1983-12-31 | 1984-07-01 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1987-07-01 | 1987-12-31 | 1988-07-01 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1991-07-01 | 1991-12-31 | 1992-07-01 | $7700.00 | Window Closed / Lapsed |