The zero-order kinetics of acetaldehyde thermal generation from polyethylene terephthalate

G. W. Halek
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引用次数: 7

Abstract

The thermal decomposition of polyethylene terephthalale has been examined by healing isothermally in a high-mass reaction chamber and collecting the evolved acetaldehyde on a GC column for quantization. Kinetics were determined at lime intervals up to 1 h for temperatures 225°C, 240°C, 250°C, 260°C, 265°C, 270°C, 280°C, and 300°C. The rate of acetaldehyde evolution was found to be directly proportional to time of reaction at each temperature, thus fitting a zero-order reaction. The Arrhenius plot of the data yielded a straight line above the melting point with a slope different from the straight line for reaction rates below the melting point. The change in slopes occurred around the crystalline melting point. The following thermodynamic values were found above and below the melting point, respectively: EA, 37.5 and 8.2 kcal/mol; ΔSA, + 1.5 and −54 e.u.; A, 0.68 × 1014 and 0.43 × 102 sec−1. Possible mechanistic implications are discussed.

聚对苯二甲酸乙二醇酯热生成乙醛的零级动力学
通过在高质量反应室中等温愈合并在气相色谱柱上收集进化的乙醛进行量化,研究了聚对苯二甲酸乙二醇酯的热分解。在225°C、240°C、250°C、260°C、265°C、270°C、280°C和300°C的温度下,以长达1小时的石灰间隔测定动力学。在每个温度下,乙醛的演化速率与反应时间成正比,因此符合零级反应。数据的阿伦尼乌斯图在熔点以上得到一条直线,其斜率与熔点以下反应速率的直线不同。斜率的变化发生在晶体熔点附近。熔点以上和熔点以下的热力学值分别为EA、37.5和8.2 kcal/mol;ΔSA, + 1.5和- 54 e.u.;A, 0.68 × 1014和0.43 × 102秒−1。讨论了可能的机制含义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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