"Investigation of microwave irradiation as an energy source in polymeri" by Xiaomei Fang

Investigation of microwave irradiation as an energy source in polymerization reactions

Date of Completion

January 1999

Keywords

Chemistry, Polymer|Plastics Technology

Degree

Ph.D.

Abstract

Variable frequency microwaves were investigated as an energy source to cure unidirectional carbon fiber reinforced phenylethynyl-terminated polyimide composites, and to synthesize the poly( 3 -caprolactam), poly( 3 -caprolactone) and copoly(amide-ester) via ring opening polmerization. ^ The mechanism of the thermal and microwave cure reactions of a phenylethynyl-terminated imide model compound, 3,4-bis[(4-phenylethynyl)phthalimido]diphenyl ether (PEPA-3,4-ODA) and a phenylethynyl-terminated imide oligomer PETI-5 (Mn ∼ 5000 g/mol) was studied by kinetics and solid-state 13C nuclear magnetic resonance (NMR) spectroscopy. Both the model compound and PETI-5 exhibited much lower activation energies and higher rate constants by the microwave cure process than by the thermal cure process. Solid-state 13C-NMR studies revealed that the major cure reaction in both the model compound and PETI-5 resin is an ethynyl to ethynyl addition reaction, with a minor reaction to further form carbon-carbon single bonded structures.^ Microwave energy was successfully applied to fabricate carbon fiber reinforced phenylethynyl-terminated polyimide composites, PETI-5/IM7, with higher glass transition temperatures (by 11° to 16°C) and enhanced mechanical properties at both room temperature and 177°C and in one-half the time, compared to the standard thermal process. Equivalent physical and mechanical properties were obtained from microwave synthesized nylon-6 and poly( 3 -caprolactone) in reduced time relative to the commercially produced thermal products. Anionic copolymerization of 3 -caprolactam with 3 -caprolactone via microwave irradiation produced poly( 3 -caprolactam-co- 3 -caprolactone) with higher yield, higher amide content, and higher Tg's relative to the thermally produced copolymer. ^

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