Polyimides with improved compression moldability

Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – From phenol – phenol ether – or inorganic phenolate

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528128, 528170, 528172, 528173, 528176, 528183, 528185, 528188, 528220, 528229, 528350, 528351, 528353, 4284735, C08G 802, C08G 7310, C08G 6926

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active

052122760

ABSTRACT:
The semicrystalline polyimide prepared by reaction of 3,3',4,4'-benzophenonetetracarboxylic dianhydride (BTDA) and 1,3-bis(4-aminophenoxy-4'-benzoyl)benzene (1,3-BABB) is modified so that it can be more readily processed to form adhesive bonds, moldings and composites. The stoichiometric ratio of the two monomers, BTDA and 1,3-BABB is controlled so that the intermediate polyamide acid is of a calculated molecular weight. A polyamide acid with excess anhydride groups is then reacted with the stoichiometrically required amount of monofunctional aromatic or aliphatic amine required for complete endcapping. A polyamide acid with excess amino groups is reacted with the stoichiometrically required amount of monofunctional aromatic anhydride required for complete endcapping. The stoichiometrically offset, endcapped polyimide is processed at lower temperatures and pressures than the unmodified high molecular weight polyimide with the same repeat unit, and exhibits an improved melt stability.

REFERENCES:
patent: 4713438 (1987-12-01), Harris et al.
patent: 4820791 (1989-04-01), Hergenrother et al.
CA: 107: 7716z, Hergenrother, et al.
CA: 109: 150528m, Hergenrother, et al.
CA: 111: 39986m, Hergenrother, et al.
"Polyimides Containing Carbonyl & Ether Connecting Groups II," (1989) Journ. Poly. Sci.: Part A: Polym. Chem., vol. 27, pp. 1161-1174, Hergenrother, et al.
"Polyimides Containing Carbonyl & Ether Connecting Groups", Hergenrother, et al., Journ. Poly. Sci.: Part A: Poly. Chem., vol. 25, (1987) pp. 1093-1103.

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