US4456740A
Expired / Lapsed
US
⏱️ 0.0 years remaining
Coating composition comprising chain-extendable crosslinkable polyol and diblocked diisocyanate diurethane oligomer
Assignee: EIDP Inc
•
Filing: 1983-01-05
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Granted: 1984-06-26
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Expires: 2003-01-05
Abstract
Abstract Resin composition suitable for high-solids solvent-based coating composition comprises chain-extendable, crosslinkable polyol of molecular weight from about 200 to 1000, having at least three hydroxyl groups, chain-extendable diblocked diisocyanate diurethane oligomer of molecular weight between about 300 to 1500, crosslinking agent reactive with the hydroxy functionality of the polyol and substantially unreactive with de-blocked isocyanate functionality of the diblocked diisocyanate diurethane oligomer, and, preferably, catalyst(s). The composition cures at elevated temperature to provide a coating on a substrate, such as steel, which coating is highly resistant to corrosion, humidity and solvents and provides corrosion protection for the substrate. The diblocked diisocyanate diurethane oligomer is preferably the reaction product of a diol with a half-blocked diisocyanate, wherein the half-blocked diisocyanate is preferably the reaction product of an organic diisocyanate with monofunctional blocking agent. The polyol is preferably the reaction product of a diol of molecular weight about 60 to 500 with a diepoxide of molecular weight about 100 to 1000 such as bisphenol. A epichlorohydrin epoxy resin, hydantoin epoxy resin and the like.
Inventors
- 👤 Joseph W. Holubka
- 👤 Ray A. Dickie
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-03 23:25
CPC Classifications
C; C08; C08G; C08G18/00; C08G18/06; C08G18/70; C08G18/72; C08G18/80; C08G18/8061; C08G18/28; C08G18/40; C08G18/48; C08G18/487; C08G18/4879; C08G18/64; C08G18/8003; C08G18/8006; C08L; C08L75/00; C08L75/04
Claims Analysis
Total Claims: 10
Claim 1
Independent Claim
187 words
A resin composition comprising: chain-extendable, crosslinking polyol of molecular weight about 200 to about 1000, having at least three hydroxyl groups, selected from polyhydroxy functional straight or branched chain saturated or unsaturated hydrocarbons, optionally comprising one or more oxy or ester moieties and optionally comprising one or more heterocyclic atoms, aromatic and/or heterocyclic rings, the heterocyclic atom(s) being selected from N, O and S, wherein said chain-extendable crosslinkable polyol is the reaction product of a diepoxide of molecular weight about 100 to 1000 with a diol of molecular weight about 60 to 500; chain-extendable, diblocked diisocyanate diurethane oligomer reaction product of diol with a half-blocked diisocyanate in molar ration of about 1:2, respectively, said oligomer being of molecular weight about 300 to about 1500, the blocking group of which oligomer has a de-blocking temperature of about 100° C. to about 190° C.; and crosslinking agent reactive with the hydroxy functionality of said polyol and substantially unreactive with de-blocked isocyanate functionality of said diblocked diisocyanate diurethane oligomer, wherein said crosslinking agent and said polyol are present in a molar equivalent ratio of about 1:1 to about 1:15, respectively.
Claim 2
Dependent Claim
187 words
A resin composition comprising: chain-extendable, crosslinking polyol of molecular weight about 200 to about 1000, having at least three hydroxyl groups, selected from polyhydroxy functional straight or branched chain saturated or unsaturated hydrocarbons, optionally comprising one or more oxy or ester moieties and optionally comprising one or more heterocyclic atoms, aromatic and/or heterocyclic rings, the heterocyclic atom(s) being selected from N, O and S, wherein said chain-extendable crosslinkable polyol is the reaction product of a diepoxide of molecular weight about 100 to 1000 with a diol of molecular weight about 60 to 500; chain-extendable, diblocked diisocyanate diurethane oligomer reaction product of diol with a half-blocked diisocyanate in molar ration of about 1:2, respectively, said oligomer being of molecular weight about 300 to about 1500, the blocking group of which oligomer has a de-blocking temperature of about 100° C. to about 190° C.; and crosslinking agent reactive with the hydroxy functionality of said polyol and substantially unreactive with de-blocked isocyanate functionality of said diblocked diisocyanate diurethane oligomer, wherein said crosslinking agent and said polyol are present in a molar equivalent ratio of about 1:1 to about 1:15, respectively.
Claim 3
Dependent Claim
18 words
The resin composition of claim 1, wherein said diepoxide has a molecular weight of about 100 to 700.
Claim 4
Dependent Claim
14 words
The resin composition of claim 1, wherein said diepoxide bears two terminal epoxide functionality.
Claim 5
Dependent Claim
36 words
The resin composition of claim 1, wherein said diepoxide is selected from the group consisting of Bisphenol A epichlorohydrin epoxy resin, hydantoin epoxy resin, cyclic or acyclic aliphatic diepoxide and a mixture of any of them.
Claim 6
Dependent Claim
17 words
The resin composition of claim 1, wherein said diol has molecular weight of about 60 and 200.
Claim 7
Dependent Claim
31 words
The resin composition of claim 1, wherein said diol is selected from the group consistion of alkyl substituted or unsubstituted propanediol, butanediol, pentanediol, hexanediol, and a mixture of any of them.
Claim 8
Dependent Claim
14 words
The resin composition of claim 1, wherein said diol bears two terminal hydroxy functionality.
Claim 9
Dependent Claim
47 words
The resin composition of claim 1, wherein said diol comprises aromatic diol wherein each hydroxyl group is substituted on the same benzene ring or on different benzene rings linked through a covalent bond or through one or more carbons of a one to seven carbon aliphatic moiety.
Claim 10
Dependent Claim
28 words
The resin composition of claim 8, wherein said diol is selected from the group consistion of Bisphenol A, Bisphenol B, catechol and a mixture of any of them.
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USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1987-06-26 | 1987-12-26 | 1988-06-26 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1991-06-26 | 1991-12-26 | 1992-06-26 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1995-06-26 | 1995-12-26 | 1996-06-26 | $7700.00 | Window Closed / Lapsed |