Browse > Article

Novel Method for Polystyrene Reactions at Low Temperature  

Katsuhiko Saido (College of Pharmacy, Nihon University)
Hiroyuki Taguchi (College of Pharmacy, Nihon University)
Yoichi Kodera (AIST)
Yumiko Ishihara (Polymer Decomposition Laboratory Co. Ltd.)
Ryu, In-Jae (College of Engineering, Chonnam National University)
Chung, Seon-yong (College of Engineering, Chonnam National University)
Publication Information
Macromolecular Research / v.11, no.2, 2003 , pp. 87-91 More about this Journal
Abstract
Thermal decomposition reactions of polystyrene using a new heating medium were carried out by a batch system at 190-280 $^{\circ}C$ to clarify the manner in which decomposition is initiated. Polystyrene obtained from a commercial source and low molecular weight compounds obtained from the thermal decomposition were analyzed by GC, GPC, IR, $^{13}$ C-NMR and GC-MS. The main chain underwent virtually no change by heat application. Polystyrene underwent decomposition below its molding temperature and the major decomposition products were 2,4,6-triphenyl-1-hexene (trimer), 2,4-diphenyl-1-butene(dimer) and styrene (monomer). Ethylbenzene, propylbenzene, naphthalene, benzaldehyde, biphenyl and 1,3-diphenylpropane were detected as minor products. This paper presents a new method for examining the decomposition of polystyrene at low temperature into volatile low molecular weight compounds.
Keywords
polystyrene; 2,4-diphenyl-1-butene (styrene dimer); 2,4,6-triphenyl-1-hexene (strene trimer); endocrine disrupter; low temperature decomposition;
Citations & Related Records

Times Cited By Web Of Science : 1  (Related Records In Web of Science)
Times Cited By SCOPUS : 4
연도 인용수 순위
1 /
[ H. Hishizaki ] / Nikka
2 /
[ T. Watabe;A. Jiratsuka ] / Eisei Kagaku   DOI
3 /
[ A. V. Krishnau;P. Starhis;S. F. Permuth;L. Tokes;D. Feldman ] / Endocrinology   DOI   ScienceOn
4 /
[ K. D. Henry;J. P. Quinu;F. D. Mclafferty ] / J. Am. Chem. Soc.   DOI
5 /
[ Y. Kawamura;K. Nishi;H. Sasaki;T. Yamada ] / Shokueishi
6 /
[ Shih-Tse Cai;D. C. Locke ] / J. Chromatog.   DOI
7 /
[ A. R. Singh;W. H. Lawrence;J. Autian ] / Toxicol. Appl. Pharmacol.   DOI   ScienceOn
8 /
[ Editor's ] / Plastics
9 /
[ M. A. Markielob;E. I. Siemiensenko ] / Plast. Massy
10 /
[ A. R. Singh;W. H. Lawrence;J. Autian ] / J. Pent. Res.
11 /
[ G. Madras;J. M. Smith;B. J. McCoy ] / Polym. Degrad. Stab.   DOI
12 /
[ N. Grassie;N. A. Weir ] / J. Appl. Polym. Sci.   DOI
13 /
[ S. Sato;T. Murakata;S. Baba;Y. Saito;S. Watanabe ] / J. Appl. Polym. Sci.   DOI
14 /
[ T. Yamada ] / YGKKAE
15 /
[ J. H. Kahn;E. G. Laroe;H. A. Couner ] / J. Food Sci.   DOI
16 /
[ J. R. Withey ] / Environ. Health Persp.   DOI
17 /
[ R. S. Lehrle;D. J. Atkinson Bate;P. A. Gardner;M. R. Grimbley;S. A. Groves;E. J. Place;R. J. Williams ] / Polym. Degrad. Stab.   DOI   ScienceOn
18 /
[ R. J. Kociba;D. G. Keys;J. E. Beyer;R. M. Carreon;C. E. Qada;D. A. Dittenber;R. P. Kalnins;L. E. Frauson;C. N. Park;S. D. Barnard;R. A. Hummel;C. G. Humiston ] / Toxicol. Appl. Pharmacol.   DOI   ScienceOn
19 /
[ H. W. Lawrence;M. Malik;J. E. Turner;J. Autian ] / J. Pharm. Sci.   DOI