Patent US3951902A successfully refreshed from Google Patents.
US3951902A
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Polyimide sealant composition
Assignee: Northrop Grumman Space and Mission Systems Corp
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Filing: 1974-11-18
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Granted: 1976-04-20
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Expires: 1994-11-18
Abstract
Abstract A compliant polyimide having superior thermal-mechanical properties can be produced by reacting an aromatic bis(furfurylimide) with an aliphatic ether bis(maleimide) via a Diels-Alder reaction. These polyimides display a long-term thermal-oxidative stability and a high percent recoverable elongation to break, and they are suitable for use as films, fibers, coatings, adhesives, structures, and sealants.
Inventors
- 👤 Robert J. Jones
- 👤 Howard N. Cassey
- 👤 Howard E. Green
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-07 14:42
CPC Classifications
C; C08; C08G; C08G73/00; C08G73/06; C08G73/10; C08G73/12; C08G73/121; C08G73/122
Claims Analysis
Total Claims: 9
Claim 1
Independent Claim
95 words
A method for making a compliant polyimide comprising polymerizing: an aromatic bis furfurylimide prepared by reacting (A) one equivalent of an aromatic dianhydride with (B) one molecular weight of furfurylamine with an aliphatic ether bis(maleimide) prepared by reacting (C) one equivalent weight of functionally terminated aliphatic ether selected from the group consisting of diisocyanate terminated aliphatic ethers and diamine terminated ethers with (D) one molecular weight of maleic anhydride in a temperature range of from 20°C to 60°C; and curing said imide polymer by heating in a temperature range of from 150°C to approximately 240°C.
Claim 2
Independent Claim
95 words
A method for making a compliant polyimide comprising polymerizing: an aromatic bis furfurylimide prepared by reacting (A) one equivalent of an aromatic dianhydride with (B) one molecular weight of furfurylamine with an aliphatic ether bis(maleimide) prepared by reacting (C) one equivalent weight of functionally terminated aliphatic ether selected from the group consisting of diisocyanate terminated aliphatic ethers and diamine terminated ethers with (D) one molecular weight of maleic anhydride in a temperature range of from 20°C to 60°C; and curing said imide polymer by heating in a temperature range of from 150°C to approximately 240°C.
Claim 3
Dependent Claim
56 words
A method according to claim 1 wherein: said dianhydride has the structure: ##EQU3## wherein R is a tetrafunctional radical selected from the group consisting of ##SPC6## wherein X is selected from the group consisting of --O--, --S--, --SO 2 --, --CO--, --CH 2 --, --C 2 H 4 --, --C 3 H 6 --, and ##SPC7##
Claim 4
Dependent Claim
88 words
A method according to claim 1 wherein: said functionally terminated aliphatic ethers have the structure: Z(OA).sub.y Z wherein Z is a monovalent radical selected from the group consisting of --N=C=O and --NH 2 ; A is an aliphatic radical consisting of alkylene groups having one to six carbon atoms, alkylidene groups having one to six carbon atoms, haloalkylene groups having one to six carbon atoms; and wherein y is an integer from 4 to 50 to yield a difunctional compound having a molecular weight of at least 400.
Claim 5
Independent Claim
109 words
A method for making a compliant polyimide sealant comprising polymerizing: an aromatic bis furfurylimide prepared by reacting (A) one equivalent of an aromatic dianhydride with (B) one molecular weight of furfurylamine with an aliphatic ether bis(maleimide) prepared by reacting (C) one equivalent weight of functionally terminated aliphatic ether selected from the group consisting of diisocyanate terminated aliphatic ethers and diamine terminated ethers with (D) one molecular weight of maleic anhydride in a temperature range of from 20°C to 60°C, said bis (furfurylimide) and bis(maleimide) homogeneously admixed with a solid inert filler; and curing said filled imide polymer by heating in a temperature range of from 150°C to approximately 240°C.
Claim 6
Independent Claim
109 words
A method for making a compliant polyimide sealant comprising polymerizing: an aromatic bis furfurylimide prepared by reacting (A) one equivalent of an aromatic dianhydride with (B) one molecular weight of furfurylamine with an aliphatic ether bis(maleimide) prepared by reacting (C) one equivalent weight of functionally terminated aliphatic ether selected from the group consisting of diisocyanate terminated aliphatic ethers and diamine terminated ethers with (D) one molecular weight of maleic anhydride in a temperature range of from 20°C to 60°C, said bis (furfurylimide) and bis(maleimide) homogeneously admixed with a solid inert filler; and curing said filled imide polymer by heating in a temperature range of from 150°C to approximately 240°C.
Claim 7
Dependent Claim
56 words
A method according to claim 4 wherein: said dianhydride has the structure: ##EQU4## wherein R is a tetrafunctional radical selected from the group consisting of ##SPC8## wherein X is selected from the group consisting of --O--, --S--, --SO 2 --, --CO--, --CH 2 --, --C 2 H 4 --, --C 3 H 6 --, and ##SPC9##
Claim 8
Dependent Claim
90 words
A method according to claim 4 wherein: said functionally terminated aliphatic ethers have the structure: Z(AO).sub.y Z (22) wherein Z is a monovalent radical selected from the group consisting of --N=C=O and --NH 2 ; A is an aliphatic radical consisting of alkylene groups having one to six carbon atoms, haloalkylene groups having one to six carbon atoms, and oxyalkylene groups having one to six carbon atoms; and wherein y is an integer from 4 to 50 to yield a difunctional compound having a molecular weight of at least 400.
Claim 9
Dependent Claim
31 words
A method according to claim 4 wherein: said solid inert filler is selected from the group consisting of silicon dioxide, calcium oxide, titanium dioxide, molecular sieves, diatomaceous earth, and aluminum oxide.
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) | 1979-04-20 | 1979-10-20 | 1980-04-20 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1983-04-20 | 1983-10-20 | 1984-04-20 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1987-04-20 | 1987-10-20 | 1988-04-20 | $7700.00 | Window Closed / Lapsed |