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US4296208A Expired / Lapsed US ⏱️ 0.0 years remaining

Methods of preparing polyimides and polyimide precursors

Assignee: I M L Corp A CORP OF
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Filing: 1980-09-12
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Granted: 1981-10-20
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Expires: 2000-09-12
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Abstract

Abstract Methods of preparing polyimides and polyimide precursors from liquid resins containing tetracarboxylic acid esters and primary diamines which involve spray drying the resin.

Inventors

  • 👤 John Gagliani
  • 👤 Usman A. K. Sorathia

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-29 18:04
CPC Classifications
C; C08; C08J; C08J9/00; C08J9/02; B; B01; B01D; B01D1/00; B01D1/16; B01D1/18; B29; B29B; B29B9/00; B29B9/10; C08G; C08G73/00; C08G73/06; C08G73/10; C08G73/1003; C08G73/1007; C08G73/1028; C08G73/1046; C08G73/105; C08G73/1057; C08G73/1064; C08G73/1067; C08G73/1085; C08J2379/00; C08J2379/04; C08J2379/08

Claims Analysis

Total Claims: 20
Claim 1
Independent Claim 71 words
A method of preparing a dry, foamable, particulate precursor which can be converted into a polyimide by heating it, said method comprising the steps of: forming a primary diamine, 3,3',4,4'-benzophenonetetracarboxylic acid ester solution by dissolving one or more such diamines and the aforesaid acid or an anhydride thereof in a lower alkyl alcohol, atomizing said solution, and drying the droplets obtained by atomizing the diamine, ester solution with a heated gas.
Claim 2
Independent Claim 71 words
A method of preparing a dry, foamable, particulate precursor which can be converted into a polyimide by heating it, said method comprising the steps of: forming a primary diamine, 3,3',4,4'-benzophenonetetracarboxylic acid ester solution by dissolving one or more such diamines and the aforesaid acid or an anhydride thereof in a lower alkyl alcohol, atomizing said solution, and drying the droplets obtained by atomizing the diamine, ester solution with a heated gas.
Claim 3
Dependent Claim 66 words
A method of preparing a polyimide precursor as defined in claim 1 in which the atomized droplets of diamine, ester solution are dried in a chamber having an inlet and an outlet for a heated gas and in which the inlet temperature of said gas is maintained in the range of 100°-110° C. and the outlet temperature thereof is limited to a maximum of 80° C.
Claim 4
Dependent Claim 40 words
A method of preparing a polyimide precursor as defined in claim 1 wherein the outlet temperature of said gas is controlled by regulating the rate of feed of the diamine, ester solution to the chamber in which it is dried.
Claim 5
Dependent Claim 40 words
A method of preparing a polyimide precursor as defined in claim 1 wherein the gas with which the atomized droplets of the diamine, ester solution are dried is introduced into said chamber around, and in entraining relationship with, said droplets.
Claim 6
Dependent Claim 38 words
A method of preparing a polyimide precursor as defined in claim 1 wherein said diamine, ester solution is diluted with from 20 to 30 parts of alkyl alcohol per 100 parts of solution prior to atomizing said solution.
Claim 7
Dependent Claim 43 words
A method of preparing a polyimide precursor as defined in claim 1 wherein atomization of the diamine, ester solution is effected with a rotary type atomizer and wherein the atomizer is operated at a speed in the range of 32,000 to 35,000 rpm.
Claim 8
Dependent Claim 48 words
A method of preparing a polyimide precursor as defined in claim 1 wherein the dried particulate material is screened through a 24-48 mesh (Tyler) screen to generate a lump-free powder of sufficiently large particle size to be processable into a polyimide foam with a relatively homogeneous cellular structure.
Claim 9
Independent Claim 38 words
A method of preparing a polyimide which includes the steps of making a precursor by a process as defined in any of the preceding claims 1-7 and converting the precursor to a polyimide by the application of heat.
Claim 10
Independent Claim 68 words
A method of preparing a polyimide which includes the steps of: forming a half ester of 3,3',4,4'-benzophenonetetracarboxylic acid by reacting said acid or an anhydride thereof with a lower alkyl alcohol; dissolving one or more primary diamines in the half ester, alcohol solution; spray drying the material thus formed to convert it into a dry particulate polyimide precursor; and converting the precursor to a polyimide by heating it.
Claim 11
Independent Claim 68 words
A method of preparing a polyimide which includes the steps of: forming a half ester of 3,3',4,4'-benzophenonetetracarboxylic acid by reacting said acid or an anhydride thereof with a lower alkyl alcohol; dissolving one or more primary diamines in the half ester, alcohol solution; spray drying the material thus formed to convert it into a dry particulate polyimide precursor; and converting the precursor to a polyimide by heating it.
Claim 12
Dependent Claim 45 words
A method of preparing a polyimide foam as defined in claim 9 in which the diamine, ester solution also includes a surface active agent in an amount ranging from 0.01 to 1 percent based on the weight of the ester and diamine or diamines. PG,27
Claim 13
Dependent Claim 39 words
A method of preparing a polyimide foam as defined in claim 9 wherein the 3,3',4,4'-benzophenonetetracarboxylic acid ester and the diamine constituent are present in said diamine, ester solution in amounts such that the imide forming functionalities are substantially equimolar.
Claim 14
Dependent Claim 66 words
A method of preparing a polyimide foam as defined in claim 9 in which the diamine, ester solution contains a plurality of diamines, one of said diamines being heterocyclic and having nitrogen in the ring, another of said diamines being a para- or meta-substituted aromatic diamine which is free of aliphatic moieties, and any additional diamine being either a heterocyclic or an aromatic diamine as aforesaid.
Claim 15
Dependent Claim 37 words
A method of preparing a polyimide foam as defined in claim 12 wherein said heterocyclic diamine is present in said solution in a ratio of 0.4 to 0.6 mole of diamine per mole of 3,3',4,4'-benzophenonetetracarboxylic acid ester.
Claim 16
Dependent Claim 59 words
A method of preparing a polyimide foam as defined in claim 9 wherein the diamine, ester solution contains at least three diamines, one of said diamines being heterocyclic and having nitrogen in the ring, another of said diamines being a para- or meta-substituted aromatic diamine which is free of aliphatic moieties, and a third of said diamines being aliphatic.
Claim 17
Dependent Claim 42 words
A method of preparing a polyimide foam as defined in claim 14 in which the diamine, ester solution contains from 0.05 to 0.3 mole of aliphatic diamine and from 0.1 to 0.3 mole of heterocyclic diamine per mole of 3,3',4,4'-benzophenonetetracarboxylic acid ester.
Claim 18
Dependent Claim 27 words
A method of preparing a polyimide foam as defined in claim 14 wherein the aliphatic diamine in the diamine solution has from three to twelve carbon atoms.
Claim 19
Dependent Claim 33 words
A method of preparing a polyimide foam as defined in claim 14 wherein the aliphatic diamine in the diamine, ester solution has the formula ##STR3## where x is on the order of 2.6.
Claim 20
Independent Claim 53 words
A method of preparing a polyimide foam as defined in either of the preceding claims 12 or 14 wherein the heterocyclic and aromatic diamines are selected from the group consisting of: 2,6-diaminopyridine 3,5-diaminopyridine 3,3'-diaminodiphenyl sulfone 4,4'-diaminodiphenyl sulfone 4,4'-diaminodiphenyl sulfide 3,3'-diaminodiphenyl ether 4,4'-diaminodiphenyl ether meta-phenylene diamine para-phenylene diamine p,p'-methylene dianiline 2,6-diamino toluene 2,4-diamino toluene.

References Cited (Backward Citations)

US2187877A Cited
US2902223A Cited
US2880794A Cited
US3049174A Cited
US3489725A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1984-10-19 1985-04-20 1985-10-20 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1988-10-19 1989-04-20 1989-10-20 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1992-10-19 1993-04-20 1993-10-20 $7700.00 Window Closed / Lapsed

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