首页> 外文期刊>Journal of Applied Polymer Science >Thermal degradations of chlorinated natural rubber from latex and chlorinated natural rubber from solution
【24h】

Thermal degradations of chlorinated natural rubber from latex and chlorinated natural rubber from solution

机译:胶乳对氯化天然橡胶的热降解和溶液对氯化天然橡胶的热降解

获取原文
获取原文并翻译 | 示例
           

摘要

The thermal degradations of chlorinated natural rubbers from latex (CNR-L) and from solution (CNR-S) under nitrogen atmosphere were studied with thermogravimetric analysis (TGA). The thermal degradations of CNR-L and CNR-S are one-step reaction. The shapes of the thermogravimetric and derivative thermogravimetric curves are similar. The degradation temperatures of CNR-L and CNRS increase linearly with the increment of heating rates. The heating rate hardly affects the thermal degradation rates of CNR-L and CNR-S at the various degradation stages. The thermal degradations of CNR-S and CNR-L are dehydrochlonation reactions. The reaction activation energy (E) of CNR, at the first stage, is around 100 kJ/mol. After that, E remains relatively steady (80-140 kJ/mol). At the last stage, E rises rapidly (130-270 kJ/mol). The variation tendency of frequency factor (A) is similar to that of E. As the initial degradation temperature To of CNR-L is 10.9'C lower than that of CNR-S, the thermal stability of CNR-S is better than that of CNR-L, which may be caused by the difference of molecular structure between CNR-L and CNR-S, as FTIR results indicate that there are more -OH, -C=O and -COOgroups in the CNR-L molecular chains. (c) 2007 Wiley Periodicals, Inc.
机译:用热重分析(TGA)研究了乳胶(CNR-L)和溶液(CNR-S)在氮气气氛下对氯化天然橡胶的热降解。 CNR-L和CNR-S的热降解是一步反应。热重曲线和导数热重曲线的形状相似。 CNR-L和CNRS的降解温度随​​着加热速率的增加而线性增加。在各个降解阶段,加热速率几乎不影响CNR-L和CNR-S的热降解速率。 CNR-S和CNR-L的热降解是脱氢氯化反应。在第一阶段,CNR的反应活化能(E)约为100 kJ / mol。之后,E保持相对稳定(80-140 kJ / mol)。在最后阶段,E迅速升高(130-270 kJ / mol)。频率因子(A)的变化趋势与E相似。由于CNR-L的初始降解温度To比CNR-S低10.9'C,因此CNR-S的热稳定性要好于由于FTIR结果表明CNR-L分子链中存在更多的-OH,-C = O和-COO基团,这可能是由于CNR-L和CNR-S之间的分子结构差异引起的CNR-L。 (c)2007年Wiley Periodicals,Inc.

著录项

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