## Abstract Polystyrene with one or two terminal hydroxyl groups was obtained in a high yield (88β90%) from polyurethaneβpolystyrene block copolymers (PUβPS). The block copolymers were prepared by radical polymerization of styrene with a polyurethaneβtype macroazo initiator, and then the urethane b
Preparation of telechelic oligomers by thermal degradation of propylene copolymers
β Scribed by Daisuke Sasaki; Yoshihiro Suzuki; Hagiwara Toshiki; Shoichiro Yano; Takashi Sawaguchi
- Publisher
- Elsevier Science
- Year
- 2007
- Tongue
- English
- Weight
- 453 KB
- Volume
- 80
- Category
- Article
- ISSN
- 0165-2370
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β¦ Synopsis
The reactive end groups of nonvolatile oligomers obtained by controlled thermal degradation of poly(propylene-ran-ethylene) and poly(propylene-ran-1-butene) were determined by 1 H and 13 C NMR spectroscopy. The molar ratio of unsaturated to saturated end groups was found to be about 9:1. The average number of unsaturated end groups per molecule was between 1.6 and 1.8, indicating that 60-80 mol% of the oligomer molecules were telechelic, having two terminal unsaturated end groups. These oligomers had a lower polydispersity than the raw material, despite their lower molecular weight and melting temperature. Although the end groups resulting from each monomer unit could be detected by 13 C NMR, the end group composition differed from that of the main chains of the raw materials. The end group composition was satisfactorily explained by the differences in bond dissociation energy and activation energy of elementary reactions that occurred during thermal degradation, based on the monomer composition of the raw materials.
π SIMILAR VOLUMES
A newly designed experimental apparatus has been developed to effectively depress the secondary reactions of volatiles, which are the primary products of thermal degradation of polymers. In this communication, we report that controlled thermal degradation of polystyrenes and polypropylenes leads to