TY - JOUR
T1 - Synthesis and characterization of polyimides based on 3,6-diphenylpyromellitic dianhydride
AU - Harris, Frank W.
AU - Hsu, Steve L.C.
PY - 1989
Y1 - 1989
N2 - Due to their insolubility and high glass transition temperatures (Tg's), aromatic polyimides have traditionally been processed in the form of their poly(amic acid) precursors. Considerable research over the past decade has led to several systems that can be melt and/or solution processed. The objective of this research was the preparation of a series of soluble, aromatic polyimides that would display high moduli. In particular, 3,6-diphenylpyromellitic dianhydride was to be synthesized and polymerized with a series of aromatic diamines. It was postulated that the phenyl groups would afford solubility while the pyromellitic moiety would maintain chain rigidity.
AB - Due to their insolubility and high glass transition temperatures (Tg's), aromatic polyimides have traditionally been processed in the form of their poly(amic acid) precursors. Considerable research over the past decade has led to several systems that can be melt and/or solution processed. The objective of this research was the preparation of a series of soluble, aromatic polyimides that would display high moduli. In particular, 3,6-diphenylpyromellitic dianhydride was to be synthesized and polymerized with a series of aromatic diamines. It was postulated that the phenyl groups would afford solubility while the pyromellitic moiety would maintain chain rigidity.
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M3 - Conference article
AN - SCOPUS:0024868517
SN - 0743-0515
VL - 60
SP - 206
EP - 210
JO - Polymeric Materials Science and Engineering, Proceedings of the ACS Division of Polymeric Materials Science and Engineering
JF - Polymeric Materials Science and Engineering, Proceedings of the ACS Division of Polymeric Materials Science and Engineering
ER -