首页> 外文期刊>Polymer Degradation and Stability >Pyrolysis mechanism of Poly(lactic acid) for giving lactide under the catalysis of tin
【24h】

Pyrolysis mechanism of Poly(lactic acid) for giving lactide under the catalysis of tin

机译:锡催化下聚乳酸热解生成丙交酯的机理

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

In order to obtain the mechanisms of the pyrolysis reaction that poly (lactic acid) (PLA) gives lactide in the presence of Sn, the four types of low molecular weight PLAs (L-PLA) with different end-groups were prepared, including HO-L-PLA-COOH, R-L-PLA-OH, R-L-PLA-COOH, and R-L-PLA-R, and depolymerized by thermogravimetry at different heating rates. As for the pyrolysis reactions of the L-PLAs, their activation energy (E-a) were estimated by the several isoconversional model-free methods and their kinetic models were also explored by the Malek method. The random degradation behavior of L-PLAs was determined by the plots of ln{-ln[1 - (1 - w)(0.5)]} vs. 1/T for experimental data from TG for L-PLAs and model reactions. The experimental results showed that the E-a values and the possible kinetic models for the pyrolysis reactions of the L-PLAs were different due to the different end-groups and thereof the mechanisms for the pyrolysis reactions of PLA that give lactide were proposed under the catalysis of Sn. The pyrolysis reactions of R-L-PLA-OH and R-L-PLA-R trend to be controlled by a single kinetic model. The pyrolysis reactions of HO-L-PLA-COOH and R-L-PLA-COOH are more complex and controlled by not less than two kinetic processes. The pyrolysis reaction of PLA selectively produces lactide through the unzipping and intramolecular transesterification reactions, including the backbiting reaction caused by the Sn-carboxylate and Sn-alkoxide chain ends, which are directly formed from the hydroxyl and carboxyl end-groups of PLA, and the lactide selective elimination at the random position of the polymeric backbone. (C) 2018 Elsevier Ltd. All rights reserved.
机译:为了获得在锡存在下聚乳酸(PLA)产生丙交酯的热解反应机理,制备了四种具有不同端基的低分子量PLA(L-PLA),包括HO -L-PLA-COOH,RL-PLA-OH,RL-PLA-COOH和RL-PLA-R,并通过热重法在不同的加热速率下解聚。至于L-PLA的热解反应,通过几种无等转化模型的方法估算了它们的活化能(E-a),还通过Malek方法探索了其动力学模型。 L-PLA的随机降解行为由ln {-ln [1-(1- w)(0.5)]}对1 / T的图确定,其中TG用于L-PLA的实验数据和模型反应。实验结果表明,由于不同的端基不同,L-PLAs的热解反应的Ea值和可能的动力学模型有所不同,并提出了在L-PLA催化下生成丙交酯的PLA热解反应机理。锡R-L-PLA-OH和R-L-PLA-R的热解反应趋于由单一动力学模型控制。 HO-L-PLA-COOH和R-L-PLA-COOH的热解反应更为复杂,并且受不少于两个动力学过程的控制。 PLA的热解反应通过解链和分子内酯交换反应(包括由PLA的羟基和羧基端基直接形成的Sn-羧酸盐和Sn-醇盐链端引起的回咬反应)选择性地产生丙交酯。丙交酯在聚合物主链的随机位置上选择性消除。 (C)2018 Elsevier Ltd.保留所有权利。

著录项

  • 来源
    《Polymer Degradation and Stability》 |2018年第11期|212-223|共12页
  • 作者单位

    Chinese Acad Sci, Changchun Inst Appl Chem, Key Lab Polymer Ecomat, Changchun 130022, Jilin, Peoples R China;

    Jilin Univ, Coll Chem, Changchun 130012, Jilin, Peoples R China;

    Chinese Acad Sci, Changchun Inst Appl Chem, Key Lab Polymer Ecomat, Changchun 130022, Jilin, Peoples R China;

    Chinese Acad Sci, Changchun Inst Appl Chem, Key Lab Polymer Ecomat, Changchun 130022, Jilin, Peoples R China;

    Chinese Acad Sci, Changchun Inst Appl Chem, Key Lab Polymer Ecomat, Changchun 130022, Jilin, Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Poly(lactic acid); Lactide; Pyrolysis mechanism; Thermal degradation; Thermogravimetry;

    机译:聚乳酸;丙交酯;热解机理;热降解;热重法;

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号