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Effect of hydrogen donor on the thermal degradation of poly(vinyl acetate) in solution
Author(s) -
Madras Giridhar,
Chattopadhyay Sujay
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.1631
Subject(s) - diphenylamine , vinyl acetate , polymer chemistry , polystyrene , hydrogen atom abstraction , molar mass distribution , chemistry , activation energy , polymer , thermal decomposition , degradation (telecommunications) , decomposition , materials science , hydrogen , copolymer , organic chemistry , telecommunications , computer science
The thermal decomposition of poly(vinyl acetate) (PVAc) in solution was investigated both in the presence and absence of a hydrogen donor (H‐donor). Thermal degradation experiments at 220–250°C were conducted in a batch reactor by dissolving PVAc in diphenylether. The molecular weight distributions were measured as a function of reaction time. Experimental data indicated that the polymer degrades by random chain scission. The random scission degradation rate coefficient was between 9.01 × 10 −4 and 6.12 × 10 −3 min −1 . The activation energy, determined from the temperature dependence of the rate coefficient, was 31.5 kcal/mol. The effect of an H‐donor, diphenylamine, was also investigated by varying the concentration from 0 to 0.472 mol/L. The data indicated that the presence of diphenylamine increases the PVAc degradation rate from 3.67 × 10 −3 to 4.59 × 10 −3 min −1 at 240°C. This is in contrast to the reduction in the degradation rate of polystyrene in the presence of diphenylamine. Continuous distribution models have been developed by treating molecular weight as a continuous variable. The experimentally observed variation of the degradation rates with H‐donor concentration is satisfactorily explained by a continuous distribution model based on the radical mechanism that involves the elementary reactions including the hydrogen abstraction steps. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 81: 1996–2000, 2001

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