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Structure and Properties of Novel Asymmetric Biphenyl Type Polyimides. Homo- and Copolymers and Blends

Asymmetric biphenyl type polyimides (PI) were prepared by thermal imidization of polyamic acids (PAA) derived from 2,3,3‘,4‘-biphenyltetracarboxylic dianhydride (a-BPDA) and p-phenylenediamine (PDA) or 4,4‘-oxydianiline (ODA). The dynamic mechanical properties of these PIs were compared with those o...

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Published in:Macromolecules 1999-01, Vol.32 (2), p.387-396
Main Authors: Hasegawa, Masatoshi, Sensui, Nobuyuki, Shindo, Yoichi, Yokota, Rikio
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cited_by cdi_FETCH-LOGICAL-a390t-6c4183b649cf88b1c24955f8e2b8482749b8dde1d3f6ad774df5bac2a6bf72543
cites cdi_FETCH-LOGICAL-a390t-6c4183b649cf88b1c24955f8e2b8482749b8dde1d3f6ad774df5bac2a6bf72543
container_end_page 396
container_issue 2
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container_title Macromolecules
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creator Hasegawa, Masatoshi
Sensui, Nobuyuki
Shindo, Yoichi
Yokota, Rikio
description Asymmetric biphenyl type polyimides (PI) were prepared by thermal imidization of polyamic acids (PAA) derived from 2,3,3‘,4‘-biphenyltetracarboxylic dianhydride (a-BPDA) and p-phenylenediamine (PDA) or 4,4‘-oxydianiline (ODA). The dynamic mechanical properties of these PIs were compared with those of the isomeric PIs derived from symmetric 3,4,3‘,4‘-biphenyltetracarboxylic dianhydride (s-BPDA). a-BPDA/PDA polyimide has a considerably bent chain structure compared to semirigid s-BPDA/PDA. Nevertheless, the a-BPDA/PDA film annealed at 350 °C showed a higher T g than the s-BPDA/PDA film prepared under the same conditions. When these PIs were annealed at 400 °C, a-BPDA/PDA exhibited an abrupt E‘ decrease at the T g (=410 °C) as well as the counterpart annealed at 350 °C, whereas s-BPDA/PDA showed no distinct T g in the E‘ curve. Similar annealing effects were also observed for the ODA systems. The unexpectedly higher T g's of a-BPDA-based PIs could be explained in terms of the more restricted conformational change through the crank shaft-like motion. The difference between the extents of the E‘ decrease at the T g for a- and s-BPDA-based PIs is attributed to the difference of the intensity of intermolecular interactions. The blends of s-BPDA/PDA with a-BPDA-based PI (80/20) and the corresponding copolyimide improved the insufficient thermal processability of homo s-BPDA/PDA without causing a decrease in T g. The results revealed that, for semirigid s-BPDA/PDA, a-BPDA-based PIs are better matrix polymers than s-BPDA/ODA.
doi_str_mv 10.1021/ma9808629
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When these PIs were annealed at 400 °C, a-BPDA/PDA exhibited an abrupt E‘ decrease at the T g (=410 °C) as well as the counterpart annealed at 350 °C, whereas s-BPDA/PDA showed no distinct T g in the E‘ curve. Similar annealing effects were also observed for the ODA systems. The unexpectedly higher T g's of a-BPDA-based PIs could be explained in terms of the more restricted conformational change through the crank shaft-like motion. The difference between the extents of the E‘ decrease at the T g for a- and s-BPDA-based PIs is attributed to the difference of the intensity of intermolecular interactions. The blends of s-BPDA/PDA with a-BPDA-based PI (80/20) and the corresponding copolyimide improved the insufficient thermal processability of homo s-BPDA/PDA without causing a decrease in T g. 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source American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)
subjects Applied sciences
Exact sciences and technology
Organic polymers
Physicochemistry of polymers
Properties and characterization
Rheology and viscoelasticity
title Structure and Properties of Novel Asymmetric Biphenyl Type Polyimides. Homo- and Copolymers and Blends
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