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Study on depolymerization of polycarbonate in supercritical ethanol

机译:聚碳酸酯在超临界乙醇中的解聚研究

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The characteristics of depolymerization of PC in supercritical ethanol were investigated in the range of 483-563 K by using a high-pressure batch autoclave reactor. Based on the qualitative and quantitative analyses of the products, a depolymerization-reaction model was proposed to explain the reaction mechanism, i.e. random scission and ester exchange reaction occurred simultaneously during the process of depolymerizaition of PC. It was suggested that the process of depolymerization consisted of subcritical region, transitional region and supercritical region. It was indicated that PC degraded with slow decrease of molecular weight determined by GPC and with the conversion of 7.5% at 513 K in subcritical region. While in the supercritical region, the molecular weight of PC decreased quickly and degraded completely in 30 min at 563 K. Continuous-distribution kinetics could be used to describe the mechanism of polymer degradation and the energy of activation for the random scission of PC in the supercritical region was 97.2 kJ/mol. Moreover, PC could be degraded completely into diethyl carbonate (DEC) and bisphenol A (BPA) with the yields of 89% and 90%, respectively, in supercritical region. (c) 2006 Elsevier Ltd. All rights reserved.
机译:通过使用高压间歇高压釜反应器,研究了PC在483-563 K范围内在超临界乙醇中的解聚特性。在对产品进行定性和定量分析的基础上,提出了一种解聚反应模型来解释反应机理,即在PC解聚过程中同时发生无规断裂和酯交换反应。提出解聚过程由亚临界区,过渡区和超临界区组成。结果表明,PC降解的程度是由GPC确定的,分子量的缓慢降低和亚临界区在513 K处的7.5%转化率。在超临界区,PC的分子量迅速下降并在563 K下30分钟内完全降解。连续分布动力学可用于描述PC随机断裂时聚合物降解的机理和活化能。超临界区为97.2kJ / mol。此外,在超临界区,PC可以完全降解为碳酸二乙酯(DEC)和双酚A(BPA),产率分别为89%和90%。 (c)2006 Elsevier Ltd.保留所有权利。

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