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Process for preparing polyimide solution

Assignee: Ube Corp
•
Filing: 1979-11-08
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Granted: 1981-09-22
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Expires: 1999-11-08
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Abstract

Abstract A polyimide solution is prepared by a process wherein a tetracarboxylic acid ingredient containing at least about 80% by mole of 3,3',4,4'-biphenyltetracarboxylic acid or its functional derivative and an aromatic diamine ingredient containing at least about 50% by mole of 4,4'-diaminodiphenyl ether are polymerized at from about 100 DEG to 300 DEG C. in phenol or a halogenated phenolic compound; the amount of the acid and diamine ingredients being approximately equimolar to each other; whereby polymerization of the tetracarboxylic acid ingredient and the aromatic diamine ingredient is effected while being accompanied by imidation. Preferably, the polymerization accompanied by imidation is effected in a manner such that at least a second half of the polymerization is carried out in a closed reaction system. The resulting polyimide solution is suitable for making therefrom shaped articles, such as films, possessing excellent mechanical properties.

Inventors

  • 👤 Yoshikazu Sasaki
  • 👤 Hiroshi Inoue
  • 👤 Ichiro Sasaki
  • 👤 Hiroshi Itatani
  • 👤 Mikito Kashima

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-29 15:41
CPC Classifications
C; C08; C08G; C08G73/00; C08G73/06; C08G73/10; C08G73/1003; C08G73/1007; C08G73/1028

Claims Analysis

Total Claims: 12
Claim 1
Independent Claim 194 words
A process for preparing a polyimide solution, which comprises the step of polymerizing ingredients consisting essentially of: (A) a tetracarboxylic acid ingredient consisting of, based on the tetracarboxylic acid ingredient, (a) approximately 80 to 100% by mole of 3,3',4,4'-biphenyltetracarboxylic acid or its functional derivative and (b) 0 to 20% by mole of at least one compound selected from the group consisting of 2,3,3',4'-biphenyltetracarboxylic acid, 2,2',3,3'-biphenyltetracarboxylic acid, 3,3',4,4'-benzophenonetetracarboxylic acid, bis(3,4-dicarboxyphenyl) methane, 2,2-bis-(3,4-dicarboxyphenyl) propane, bis(3,4-dicarboxyphenyl) ether, bis(3,4-dicarboxyphenyl)thioether, bis(3,4-dicarboxyphenyl) sulfone, 2,3,6,7-naphthalenetetracarboxylic acid, pyromellitic acid and functional derivatives thereof, and (B) an aromatic diamine ingredient containing at least approximately 50% by mole, based on the aromatic diamine ingredient, of 4,4'-diaminodiphenyl ether, at a temperature of from approximately 100° to 300° C. in phenol or a halogenated phenolic compound; the amounts of the tetracarboxylic acid ingredient and the aromatic diamine ingredient being approximately equimolar to each other; whereby the tetracarboxylic acid ingredient and the aromatic diamine ingredient are polymerized, while being accompanied by imidation, to produce a homogeneous polyimide solution containing a polyimide having a logarithmic viscosity of from 0.7 to 6, as measured at 50° C., on a solution of 0.5 g polymer in 100 ml of p-chlorophenol.
Claim 2
Dependent Claim 194 words
A process for preparing a polyimide solution, which comprises the step of polymerizing ingredients consisting essentially of: (A) a tetracarboxylic acid ingredient consisting of, based on the tetracarboxylic acid ingredient, (a) approximately 80 to 100% by mole of 3,3',4,4'-biphenyltetracarboxylic acid or its functional derivative and (b) 0 to 20% by mole of at least one compound selected from the group consisting of 2,3,3',4'-biphenyltetracarboxylic acid, 2,2',3,3'-biphenyltetracarboxylic acid, 3,3',4,4'-benzophenonetetracarboxylic acid, bis(3,4-dicarboxyphenyl) methane, 2,2-bis-(3,4-dicarboxyphenyl) propane, bis(3,4-dicarboxyphenyl) ether, bis(3,4-dicarboxyphenyl)thioether, bis(3,4-dicarboxyphenyl) sulfone, 2,3,6,7-naphthalenetetracarboxylic acid, pyromellitic acid and functional derivatives thereof, and (B) an aromatic diamine ingredient containing at least approximately 50% by mole, based on the aromatic diamine ingredient, of 4,4'-diaminodiphenyl ether, at a temperature of from approximately 100° to 300° C. in phenol or a halogenated phenolic compound; the amounts of the tetracarboxylic acid ingredient and the aromatic diamine ingredient being approximately equimolar to each other; whereby the tetracarboxylic acid ingredient and the aromatic diamine ingredient are polymerized, while being accompanied by imidation, to produce a homogeneous polyimide solution containing a polyimide having a logarithmic viscosity of from 0.7 to 6, as measured at 50° C., on a solution of 0.5 g polymer in 100 ml of p-chlorophenol.
Claim 3
Dependent Claim 142 words
A process according to claim 1 wherein the polymerization of the tetracarboxylic acid ingredient and the aromatic diamine ingredient, accompanied by imidation, is effected in two half stages: p1 in the first half stage, the tetracarboxylic acid ingredient and the aromatic diamine ingredient are heated in phenol or a halogenated phenolic compound to a temperature of from approximately 100° to 200° C. thereby to obtain a homogeneous polyimide solution having a rotation viscosity of not more than 50 poises as measured at 140° C., and; then, in the second half stage, the reaction mixture obtained in the first half stage is polymerized at a temperature of from approximately 100° to 300° C. in a closed reaction system at least until both the partial pressure of steam in the reaction system and the content of water in the liquid reaction mixture become constant.
Claim 4
Dependent Claim 37 words
A process according to claim 2 wherein prior to or at the beginning of the second half stage, not more than approximately 0.8 g of water per g of the polyimide is added to the reaction mixture.
Claim 5
Dependent Claim 28 words
A process according to claim 2 wherein the first half stage is conducted in the closed reaction system, and both the first and second stages are incessantly continued.
Claim 6
Dependent Claim 43 words
A process according to claim 4 wherein prior to or during the first and second half stages, not more than approximately 0.8 g of water per g of the polyimide to be finally produced is added to the reaction mixture to be polymerized.
Claim 7
Dependent Claim 19 words
A process according to claim 1, 2 or 4 wherein said tetracarboxylic acid ingredient is comprised of 3,3'4,4'-biphenyltetracarboxylic dianhydride.
Claim 8
Dependent Claim 33 words
A process according to claim 1, 2 or 4 wherein the ratio of the tetracarboxylic acid ingredient to the aromatic diamine ingredient is in the range of from 0.9 to 1.1 by mole.
Claim 9
Dependent Claim 74 words
A process according to claim 1, 2 or 4 wherein the halogenated phenolic compound has a melting point not higher than approximately 100° C. and a boiling point at normal pressure not higher than 300° C. and is expressed by the formula: ##STR3## wherein X is a halogen selected from the group consisting of chlorine, bromine, iodine and fluorine and R is a hydrogen or an alkyl group having 1 to 4 carbon atoms.
Claim 10
Dependent Claim 52 words
A process according to claim 1, 2 or 4 wherein the total amount of the tetracarboxylic acid ingredient and the aromatic diamine ingredient is from 2 to 30% by weight based on the total amount of the tetracarboxylic acid ingredient, the aromatic diamine ingredient and the phenol or the halogenated phenolic compound.
Claim 11
Dependent Claim 79 words
A polyimide solution which has a rotation viscosity of 1 to 50,000 poise as measured at 140° C. and contains from 5 to 30% by weight of polyimide having a logarithmic viscosity of from approximately 0.7 to 6 as measured at 50° C. on a solution of 0.5 g polymer in 100 ml of p-chlorophenol and exhibiting a degree of imidation of at least 90%, said solution being prepared by a process defined in claim 1, 2 or 4.
Claim 12
Dependent Claim 28 words
The process of claim 1 wherein said tetracarboxylic acid ingredient contains 90 to 100% by mole, based on the tetracarboxylic ingredient, of 3,3',4,4'-biphenyltetracarboxylic acid or its functional derivative.

References Cited (Backward Citations)

US3179630A Cited
US3933745A Cited
US4075171A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1984-09-21 1985-03-23 1985-09-22 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1988-09-21 1989-03-23 1989-09-22 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1992-09-21 1993-03-23 1993-09-22 $7700.00 Window Closed / Lapsed

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