COMPATIBILITY OF POLYETHER SULFONE AND POLYIMIDE DERIVED FROM ISOMERIZATION OF POLYISOIMIDE - AN APPROACH TO IN-SITU GENERATED RIGID-ROD MOLECULAR COMPOSITE
A. Mochizuki et al., COMPATIBILITY OF POLYETHER SULFONE AND POLYIMIDE DERIVED FROM ISOMERIZATION OF POLYISOIMIDE - AN APPROACH TO IN-SITU GENERATED RIGID-ROD MOLECULAR COMPOSITE, Polymer Journal, 29(4), 1997, pp. 339-345
An approach to in-situ generated rigid-rod molecular composites (RRMC)
was investigated. This method requires a coil-like aromatic polyisoim
ide (PII) which soluble and compatible with an amorphous matrix polyme
r and can undergoes thermal isomerization to the corresponding rigid-r
od polyimide CPI) in the solid composite state. PII was prepared by th
e ring-opening polyaddition of pyromellitic dianhydride (PMDA) and 2,2
',6,6'-tetramethylbenzidine (TMBZ) followed by treatment with trifluor
oacetic anhydride-triethylamine in NMP. A miscible solution blend of P
II and poly(oxy-1,4-phenylenesulfonyl- 1,4-phenylene) (PES) was obtain
ed. The compatibility of blend films was investigated by transmission
electron microscopy (TEM). The diameter of PI domain for the PI/PES, 4
/96 was found to be approximately 0.2 mu m, and the formation of an in
terpenetrating structure was confirmed by the elemental analysis on th
e domain part. Transparent composite films were obtained at PI content
of 2 to 10wt%.