US4603061A
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Process for preparing highly optically transparent/colorless aromatic polyimide film
Assignee: National Aeronautics and Space Administration
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Filing: 1984-08-23
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Granted: 1986-07-29
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Expires: 2004-08-23
Abstract
Abstract An aromatic condensation polyimide film that is approximately 90% transparent at 500 nm, useful for thermal protective coatings and the like and the process for preparing same are disclosed. An essential feature of the invention for achieving maximum optical transparency films requires utilizing recrystallized and/or sublimated specific aromatic diamines and dianhydride monomers and introducing bulky electron-withdrawing groups and separator groups into the polymer molecular structure. The incorporation of bulky electron-withdrawing groups in the diamine portion of the polymer structure serves to reduce the formation of inter-chain and intra-chain charge transfer complexes which normally cause large absorptions in the UV-visible range. Incorporation of separator atoms into either the diamine or dianhydride monomers serves to reduce the amount of conjugation and inter-and intra-chain electronic interactions and thereby lessen charge transfer complex formation.
Inventors
- 👤 Anne K. St. Clair
- 👤 Terry L. St. Clair
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-31 15:43
CPC Classifications
C; C08; C08J; C08J5/00; C08J5/18; C08J2379/00; C08J2379/04; C08J2379/08; Y; Y10; Y10T; Y10T428/00; Y10T428/26; Y10T428/263; Y10T428/264; Y10T428/265; Y10T428/31504; Y10T428/31721
Claims Analysis
Total Claims: 16
Claim 1
Independent Claim
112 words
A method for preparing a high temperature, highly optically transparent-to-colorless aromatic polyimide film comprising: chemically reacting equimolar quantities of (1) a highly purified aromatic diamine and (2) a highly purified aromatic dianhydride, in a solvent medium to form a high molecular weight polyamic acid solution, at least one of the highly purified, aromatic diamine and the highly purified aromatic dianhydride containing a bulky electron-withdrawing group in the monomer molecular structure, applying a desired thickness film layer of the polyamic acid solution onto a surface, thermally curing the applied film in the temperature range of 250° C. to 300° C. for at least one hour to yield an optically transparent polyimide film layer.
Claim 2
Independent Claim
112 words
A method for preparing a high temperature, highly optically transparent-to-colorless aromatic polyimide film comprising: chemically reacting equimolar quantities of (1) a highly purified aromatic diamine and (2) a highly purified aromatic dianhydride, in a solvent medium to form a high molecular weight polyamic acid solution, at least one of the highly purified, aromatic diamine and the highly purified aromatic dianhydride containing a bulky electron-withdrawing group in the monomer molecular structure, applying a desired thickness film layer of the polyamic acid solution onto a surface, thermally curing the applied film in the temperature range of 250° C. to 300° C. for at least one hour to yield an optically transparent polyimide film layer.
Claim 3
Dependent Claim
22 words
The method of claim 1 wherein the highly purified aromatic diamine is selected from the group consisting of recrystallized: 3,3'-diaminodiphenylsulfone, and 2,2-bis[4-(4-aminophenoxy)phenyl]hexafluoropropane.
Claim 4
Dependent Claim
31 words
The method of claim 1 wherein the highly purified aromatic dianhydride is selected from the group consisting of recrystallized and/or sublimed: 2,2-bis(3,4-dicarboxyphenyl)hexafluoropropane dianhydride, 4,4'-bis(3,4-dicarboxyphenoxy)diphenyl sulfide dianhydride, 4,4'-oxydiphthalic anhydride, and pyromellitic dianhydride.
Claim 5
Dependent Claim
30 words
The method of claim 1 wherein the solvent is distilled prior to use and is selected from one or more of the group consisting of: N,N-dimethylacetamide, N,N'-dimethylformamide, N-methyl-2-pyrrolidone, and dimethylsulfoxide.
Claim 6
Dependent Claim
33 words
The method of claim 1 wherein the applied polyamic film layer is cast onto a glass plate and the recovered cured optically transparent polyimide film is stripped from the glass for use thereof.
Claim 7
Dependent Claim
41 words
The method of claim 1 wherein the applied polyamic acid film layer is approximately 15% w/w solids and is applied by brush coating onto a surface and the cured optically transparent polyimide film layer serves as thermal protection for the surface.
Claim 8
Dependent Claim
66 words
The method of claim 1 wherein the polyamic acid solution is 15% w/w solids and including the further step of diluting the polyamic acid solution by adding additional solvent thereto prior to applying a film layer thereof onto a surface and wherein the applied film layer is sprayed onto the surface and the cured resulting transparent polyimide serves as a thermal protection layer for the surface.
Claim 9
Independent Claim
108 words
A method for preparing a high temperature, highly optically transparent-to-colorless aromatic polyimide film comprising: chemically reacting equimolar quantities of (1) a highly purified aromatic diamine, and (2) a highly purified aromatic dianhydride in a solvent medium to form a high molecular weight polyamic acid solution, at least one of the reacted diamine and the dianhydride containing separator linking atoms in the monomer molecular structure, applying a controlled thickness film layer of the polyamic acid solution onto a surface, and thermally curing the applied film layer in the temperature range of 250° C. to 300° C. for at least one hour to yield the optically transparent polyimide film layer.
Claim 10
Independent Claim
108 words
A method for preparing a high temperature, highly optically transparent-to-colorless aromatic polyimide film comprising: chemically reacting equimolar quantities of (1) a highly purified aromatic diamine, and (2) a highly purified aromatic dianhydride in a solvent medium to form a high molecular weight polyamic acid solution, at least one of the reacted diamine and the dianhydride containing separator linking atoms in the monomer molecular structure, applying a controlled thickness film layer of the polyamic acid solution onto a surface, and thermally curing the applied film layer in the temperature range of 250° C. to 300° C. for at least one hour to yield the optically transparent polyimide film layer.
Claim 11
Dependent Claim
27 words
The method of claim 8 wherein the highly purified aromatic diamine has a formulation of: H.sub.2 N--Ar--NH.sub.2 where Ar is selected from the group consisting of: ##STR57##
Claim 12
Dependent Claim
26 words
The method of claim 8 wherein the highly purified aromatic dianhydride has a formulation of: ##STR58## where R is selected from the group consisting of: ##STR59##
Claim 13
Dependent Claim
36 words
An aromatic condensation polyimide film having the inherent physical property characteristics of being essentially colorless-to-totally colorless and providing approximately 90% transparency at 500 nm when prepared in the film thickness range of 0.2 to 1.0 mil.
Claim 14
Dependent Claim
36 words
An aromatic condensation polyimide film having the inherent physical property characteristics of being essentially colorless-to-totally colorless and providing approximately 90% transparency at 500 nm when prepared in the film thickness range of 0.2 to 1.0 mil.
Claim 15
Dependent Claim
26 words
A highly optically transparent-to-colorless aromatic polyimide film having a film thickness range of 0.2 to 1.0 mil and prepared according to the process of claim 1.
Claim 16
Dependent Claim
26 words
A highly optically transparent-to-colorless aromatic polyimide film having a film thickness range of 0.2 to 1.0 mil and prepared according to the process of claim 8.
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) | 1989-07-28 | 1990-01-27 | 1990-07-29 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1993-07-28 | 1994-01-27 | 1994-07-29 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1997-07-28 | 1998-01-27 | 1998-07-29 | $7700.00 | Window Closed / Lapsed |