0000000000485329
AUTHOR
G. P. Hellmann
showing 2 related works from this author
Phenylene motion in polycarbonate and polycarbonate/additive mixtures
1987
Pulsed deuteron NMR line shapes have been analysed to characterize type and time scale of the phenylene group motion in glassy bisphenol-A polycarbonate. The motional mechanism involvesπ-flips about theC1C4 axis augmented by small angle fulctuations about the same axis, reaching a rms amplitude of ±35‡ at 380 K. The distribution of correlation times for theπ-flips is heterogeneous in nature and can be described either by a log-Gaussian or an asymmetric distribution with a more rapid decay at high correlation times comparable to the Williams-Watts distribution. From both distributions essentailly the same mean activation energy of 37 kJ/mol is obtained, whereas the temperature dependent widt…
Fragmentation of polycarbonate macroinitiators in solution and in the bulk state
1990
The diphenylethane initiator 3,4-diethyl-3,4-(p-methoxyphenyl)-hexane (T–OCH3) was synthesized. By cocondensation of bisphenol A or C and the bisphenol derivative (“T”) of T–OCH3 with phosgene, polycarbonate macroinitiators PC(TxA1-x) and PC(TxC1-x) with different compositions x were made. The thermal fragmentation of T–OCH3 and the copolycarbonates was investigated with and without a radical scavenger both in solution and in the bulk state. The primary dissociation of T–OCH3 is a monomolecular Arrhenius process with a characteristic temperature of T* (τ = 1h) = 140°C (τ: average life time of the intact molecule). When the radicals are not intercepted, the dissociation is excessively revert…