US4389504A
Expired / Lapsed
US
⏱️ 0.0 years remaining
Elastomer toughened polyimide adhesives
Assignee: National Aeronautics and Space Administration
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Filing: 1981-10-02
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Granted: 1983-06-21
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Expires: 2001-10-02
Abstract
Abstract A rubber-toughened addition-type polyimide composition having excellent high temperature bonding characteristics in the fully cured state and improved peel strength and adhesive fracture resistance physical property characteristics is disclosed. The process for making the improved adhesive involves preparing the rubber-containing amic acid prepolymer by chemically reacting an amine-terminated elastomer and an aromatic diamine with an aromatic dianhydride with which a reactive chain stopper anhydride has been mixed, and utilizing solvent or mixture of solvents for the reaction.
Inventors
- 👤 Anne K. St. Clair
- 👤 Terry L. St. Clair
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-03 11:35
CPC Classifications
C; C08; C08G; C08G73/00; C08G73/06; C08G73/10; C08G73/1003; C08G73/1007; C08G73/101; C08G73/1028; C08G73/12; C08G73/121; C08G73/122; C08L; C08L79/00; C08L79/04; C08L79/08
Claims Analysis
Total Claims: 7
Claim 1
Independent Claim
147 words
A method for preparing a high temperature elastomer-containing addition polyamic acid adhesive in a solvent solution which comprises: chemically reacting an aromatic diamine and an aromatic amine-terminated butadiene/acrylonitrile (AATBN) or an aromatic amine-terminated silicone (AATS) with an aromatic dianhydide selected from the group consisting of: 3,3',4,4'-benzophenone tetracarboxylic acid dianhydride, 4,4'-oxydiphthalic anhydride, 2,2-bis(3-4-dicarboxyphenyl) hexafluoropropane dianhydride, bis(3,4-dicarboxyphenyl) sulfone dianhydride, and bis-(4-(3',4'-dicarboxyphenoxy) diphenyl sulfone dianhydride, each member of said group of dianhydrides being mixed with a reactive endcapping agent; all ingredients being dissolved and reacted in a solvent or mixture of solvents, at least one of which is selected from the group consisting of: N,N'-dimethylformamide, N,N'-dimethylacetamide, N-methyl-2-pyrrolidone, and dimethylsulfoxide, to yield an addition polyamic acid adhesive solution having the inherent physical property characteristic of being converted to a fully crosslinked polyimide matrix with rubbery inclusions when applied to substrate surfaces and heated in the range of 250°-300° C. under pressure.
Claim 2
Independent Claim
147 words
A method for preparing a high temperature elastomer-containing addition polyamic acid adhesive in a solvent solution which comprises: chemically reacting an aromatic diamine and an aromatic amine-terminated butadiene/acrylonitrile (AATBN) or an aromatic amine-terminated silicone (AATS) with an aromatic dianhydide selected from the group consisting of: 3,3',4,4'-benzophenone tetracarboxylic acid dianhydride, 4,4'-oxydiphthalic anhydride, 2,2-bis(3-4-dicarboxyphenyl) hexafluoropropane dianhydride, bis(3,4-dicarboxyphenyl) sulfone dianhydride, and bis-(4-(3',4'-dicarboxyphenoxy) diphenyl sulfone dianhydride, each member of said group of dianhydrides being mixed with a reactive endcapping agent; all ingredients being dissolved and reacted in a solvent or mixture of solvents, at least one of which is selected from the group consisting of: N,N'-dimethylformamide, N,N'-dimethylacetamide, N-methyl-2-pyrrolidone, and dimethylsulfoxide, to yield an addition polyamic acid adhesive solution having the inherent physical property characteristic of being converted to a fully crosslinked polyimide matrix with rubbery inclusions when applied to substrate surfaces and heated in the range of 250°-300° C. under pressure.
Claim 3
Dependent Claim
36 words
The method of claim 1 wherein the aromatic diamine is selected from the group of diamines consisting of: 3,3'-methylenedianiline; 3,4'-methylenedianiline; 4,4'-methylenedianiline; 3,3'-diaminobenzophenone; 3,4'-diaminobenzophenone; 4,4'-diaminobenzophenon m-phenylenediamine; p-phenylenediamine; 3,3'-diaminodiphenyl sulfone; 3,4'-diaminodiphenyl sulfone; 4,4'-diaminodiphenyl sulfone; 2,4'-oxydianiline; 3,3'-oxydianiline; and, 4,4'-oxydianiline.
Claim 4
Dependent Claim
24 words
The method of claim 1 wherein said reactive endcapping agent is selected from the group consisting of: 5-norbornene-2,3-dicarboxylic anhydride, 4-vinylphthalic anhydride, and 4-ethynylphthalic anhydride.
Claim 5
Dependent Claim
93 words
The method of claim 1 including the further steps of applying the elastomer-containing adhesive to substrate surfaces; removing some or all of the solvent and converting the elastomer/amic acid to the imide prepolymer by heating in the range of 180°-200° C.; assembling together the treated surfaces with or without an adhesive carrier cloth and heating the elastomer/imide prepolymer in the range of 250°-300° C. with pressure in the range of 345-380 kPa to remove all solvent and convert the prepolymer to a thermally resistant, fully crosslinked polyimide containing a finely dispersed elastomer phase.
Claim 6
Dependent Claim
22 words
The method of claim 1 wherein the aromatic amine-terminated elastomer is: ##STR4## where x and y are repeat units and x=75-99% y=25-1%.
Claim 7
Dependent Claim
38 words
The method of claim 1 wherein the aromatic amine-terminated elastomer is: ##STR5## where n is approximately 100, and R is an aliphatic moiety selected from the group consisting of: --CH.sub.2 --; --(CH.sub.2).sub.2 --; --(CH.sub.2).sub.3 --; and, --(CH.sub.2).sub.4 --.
References Cited (Backward Citations)
US3440203A
Cited
US4030948A
Cited
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1986-06-20 | 1986-12-20 | 1987-06-21 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1990-06-20 | 1990-12-20 | 1991-06-21 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1994-06-20 | 1994-12-20 | 1995-06-21 | $7700.00 | Window Closed / Lapsed |