US4360633A
Expired / Lapsed
US
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Coating solution of polyetherimide oligomers
Assignee: Von Roll Isola USA Inc
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Filing: 1981-07-27
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Granted: 1982-11-23
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Expires: 2001-07-27
Abstract
Abstract Disclosed is a coating solution including an oligomeric polyetherimide component, an oligomeric diamine component, a solvent system and optionally water which may be coated on a substrate and polymerized to form high quality polyetherimide coatings and a process for preparing the solution.
Inventors
- 👤 Donald A. Bolon
- 👤 Thomas B. Gorczyca
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-03 01:59
CPC Classifications
C; C08; C08G; C08G73/00; C08G73/06; C08G73/10; C08G73/1003; C08G73/1007; C08G73/101; C08G73/1014; C08G73/1046; C08G73/1053; C08G73/1057; C08G73/1064; C08G73/1067; C08G73/1071; C08L; C08L79/00; C08L79/04; C08L79/08; Y; Y10; Y10S; Y10S525/00; Y10S525/928; Y10T; Y10T428/00; Y10T428/29; Y10T428/2913; Y10T428/2933; Y10T428/294
Claims Analysis
Total Claims: 11
Claim 1
Independent Claim
278 words
A coating solution including oligomeric polyetherimides formed by: (a) reacting at least one aromatic bis(ether anhydride) of the formula: ##STR10## with less than a stoichometric amount of at least one diamine of the general formula: H.sub.2 N--R.sup.1 --NH.sub.2 in a suitable solvent to form oligomeric polyetheramic acids containing terminal anhydride groups; (b) heating the solution of (a) to a temperature between 80° C. and 250° C. to form oligomeric polyetherimide anhydrides; (c) hydrolizing the oligomeric anhydrides of (b) to form the free acids of the formula: ##STR11## (d) adding to the oligomer solution of (c) more of the same or different diamine, and optionally more solvent and water, where R is a member selected from the class consisting of (A) divalent organic radicals having the following formulas: ##STR12## and (B) divalent organic radicals of the general formula: ##STR13## where m is 0 or 1 and X is a member selected from the class consisting of divalent radicals of the formulas, ##STR14## where y is an integer from 1 to 4; R 1 is a divalent organic radical selected from the class consisting of (a) aromatic hydrocarbon radicals having from 6 to about 20 carbon atoms and haloginated derivatives thereof, (b) alkylene radicals having from 2 to about 20 carbon atoms, and cycloalkylene radicals having from 3 to about 30 carbon atoms, (c) from C 2 to about C 8 alkylene terminated polydiorganosiloxane, and (d) divalent radicals of the general formula: ##STR15## where m is as previously defined and Q is a member selected from the class consisting of ##STR16## where x is an integer from 1 to 5 inclusive; and n is an integer from 0 to 100.
Claim 2
Dependent Claim
278 words
A coating solution including oligomeric polyetherimides formed by: (a) reacting at least one aromatic bis(ether anhydride) of the formula: ##STR10## with less than a stoichometric amount of at least one diamine of the general formula: H.sub.2 N--R.sup.1 --NH.sub.2 in a suitable solvent to form oligomeric polyetheramic acids containing terminal anhydride groups; (b) heating the solution of (a) to a temperature between 80° C. and 250° C. to form oligomeric polyetherimide anhydrides; (c) hydrolizing the oligomeric anhydrides of (b) to form the free acids of the formula: ##STR11## (d) adding to the oligomer solution of (c) more of the same or different diamine, and optionally more solvent and water, where R is a member selected from the class consisting of (A) divalent organic radicals having the following formulas: ##STR12## and (B) divalent organic radicals of the general formula: ##STR13## where m is 0 or 1 and X is a member selected from the class consisting of divalent radicals of the formulas, ##STR14## where y is an integer from 1 to 4; R 1 is a divalent organic radical selected from the class consisting of (a) aromatic hydrocarbon radicals having from 6 to about 20 carbon atoms and haloginated derivatives thereof, (b) alkylene radicals having from 2 to about 20 carbon atoms, and cycloalkylene radicals having from 3 to about 30 carbon atoms, (c) from C 2 to about C 8 alkylene terminated polydiorganosiloxane, and (d) divalent radicals of the general formula: ##STR15## where m is as previously defined and Q is a member selected from the class consisting of ##STR16## where x is an integer from 1 to 5 inclusive; and n is an integer from 0 to 100.
Claim 3
Dependent Claim
25 words
The coating solution of claim 1 wherein the diamine is used in a ratio of between 0.5 and 0.2 moles diamine per mole of dianhydride.
Claim 4
Dependent Claim
25 words
The coating solution of claim 1 wherein the diamine is used in a ratio of between 1.0 and 1.2 moles diamine per mole of dianhydride.
Claim 5
Dependent Claim
25 words
The coating solution of claim 1 where the aromatic bis(ether anhydride) is ##STR17## where R 2 is ##STR18## and Q 1 is selected from ##STR19##
Claim 6
Dependent Claim
25 words
The coating solution of claim 1 where the aromatic bis(ether anhydride) is ##STR20## where R 2 is ##STR21## and Q 1 is selected from ##STR22##
Claim 7
Dependent Claim
13 words
The coating solution of claim 1 where the organic diamine is methylene dianiline.
Claim 8
Dependent Claim
12 words
The coating solution of claim 1 where the organic diamine is oxydianiline.
Claim 9
Dependent Claim
20 words
The coating solution of claim 1, where the aromatic bis(ether anhydride) is 2,2-bis[4-3(3,4-dicarboxyphenoxy)phenyl]propane dianhydride and the organic diamine is 4,4'-methylenedianiline.
Claim 10
Dependent Claim
282 words
A process for preparing a coating solution which includes oligomeric polyetherimides comprising: (a) reacting at least one aromatic bis(ether anhydride) of the formula: ##STR23## with less than a stoichometric amount of at least one diamine of the general formula: H.sub.2 N--R.sup.1 --NH.sub.2 in a suitable solvent to form oligomeric polyetheramic acids containing terminal anhydride groups (b) heating the solution of (a) to a temperature between 80° C. and 250° C. to form oligomeric polyetherimide anhydrides (c) hydrolizing the oligomeric anhydrides of (b) to form the free acids of the formula: ##STR24## (d) adding to the oligomer solution of (c) more of the same or different diamine, and optionally more solvent and water, where R is a member selected from the class consisting of (A) divalent organic radicals having the following formulas: ##STR25## and (B) divalent organic radicals of the general formula: ##STR26## where m is 0 or 1 and X is a member selected from the class consisting of divalent radicals of the formulas, ##STR27## where y is an integer from 1 to 4; R 1 is a divalent organic radical selected from the class consisting of (a) aromatic hydrocarbon radicals having from 6 to about 20 carbon atoms and haloginated derivatives thereof, (b) alkylene radicals having from 2 to about 20 carbon atoms, and cycloalkylene radicals having from 3 to about 30 carbon atoms, (c) from C 2 to about C 8 alkylene terminated polydiorganosiloxane, and (d) divalent radicals of the general formula: ##STR28## where m is as previously defined and Q is a member selected from the class consisting of ##STR29## where x is an integer from 1 to 5 inclusive, and n is an integer from 0 to 100.
Claim 11
Dependent Claim
282 words
A process for preparing a coating solution which includes oligomeric polyetherimides comprising: (a) reacting at least one aromatic bis(ether anhydride) of the formula: ##STR23## with less than a stoichometric amount of at least one diamine of the general formula: H.sub.2 N--R.sup.1 --NH.sub.2 in a suitable solvent to form oligomeric polyetheramic acids containing terminal anhydride groups (b) heating the solution of (a) to a temperature between 80° C. and 250° C. to form oligomeric polyetherimide anhydrides (c) hydrolizing the oligomeric anhydrides of (b) to form the free acids of the formula: ##STR24## (d) adding to the oligomer solution of (c) more of the same or different diamine, and optionally more solvent and water, where R is a member selected from the class consisting of (A) divalent organic radicals having the following formulas: ##STR25## and (B) divalent organic radicals of the general formula: ##STR26## where m is 0 or 1 and X is a member selected from the class consisting of divalent radicals of the formulas, ##STR27## where y is an integer from 1 to 4; R 1 is a divalent organic radical selected from the class consisting of (a) aromatic hydrocarbon radicals having from 6 to about 20 carbon atoms and haloginated derivatives thereof, (b) alkylene radicals having from 2 to about 20 carbon atoms, and cycloalkylene radicals having from 3 to about 30 carbon atoms, (c) from C 2 to about C 8 alkylene terminated polydiorganosiloxane, and (d) divalent radicals of the general formula: ##STR28## where m is as previously defined and Q is a member selected from the class consisting of ##STR29## where x is an integer from 1 to 5 inclusive, and n is an integer from 0 to 100.
References Cited (Backward Citations)
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1985-11-22 | 1986-05-24 | 1986-11-23 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1989-11-22 | 1990-05-24 | 1990-11-23 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1993-11-22 | 1994-05-24 | 1994-11-23 | $7700.00 | Window Closed / Lapsed |