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High‐resolution thermogravimetry of poly(phenylene sulfide) film under four atmospheres
Author(s) -
Li XinGui,
Huang MeiRong,
Bai He
Publication year - 2001
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.10120
Subject(s) - thermogravimetry , argon , nitrogen , helium , analytical chemistry (journal) , reaction rate constant , materials science , char , sulfide , activation energy , thermal decomposition , chemistry , kinetics , pyrolysis , inorganic chemistry , organic chemistry , metallurgy , physics , quantum mechanics
The thermal degradation of poly(phenylene sulfide) (PPS) film is investigated in air, nitrogen, helium, and argon with different physical and reactive characteristics at room temperature to 790°C as ascertained by high‐resolution thermogravimetry (TG) at a variable heating rate in response to the changes in the sample's weight‐loss rate. Only a one‐step degradation process of the PPS is observed in nitrogen and argon, but a two‐step degradation process of PPS is found in helium. A four‐step degradation process of the PPS, which is hardly ever revealed by traditional TG, is found in this investigation, especially in air. The initial thermal degradation temperature and temperature at the first maximum weight‐loss rate of the PPS increase in the following order: helium < nitrogen < argon < air. The first maximum weight‐loss rate also increases with the variation of the atmosphere in the order nitrogen < air < argon < helium. The char yield at 700°C increases in the order air < helium < nitrogen < argon. The activation energy of the major degradation process of PPS, as calculated based on the high‐resolution TG data, is very high and increases in the order nitrogen < argon < helium < air. The thermal decomposition parameters of the PPS determined by the high‐resolution TG are systematically compared with those by traditional TG at a constant heating rate. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 1940–1946, 2002