首页> 外文期刊>Polymer: The International Journal for the Science and Technology of Polymers >Thermogravimetric analysis of poly(#epsilon#-caprolactam) and poly[(#epsilon#-caprolactam)-co-(#epsilon#-caprolactone)] polymers
【24h】

Thermogravimetric analysis of poly(#epsilon#-caprolactam) and poly[(#epsilon#-caprolactam)-co-(#epsilon#-caprolactone)] polymers

机译:聚(ε-己内酰胺)和聚[(ε-己内酰胺)-共-(ε-己内酯)]聚合物的热重分析

获取原文
获取原文并翻译 | 示例
           

摘要

The thennal degradation of poly(#epsilon#-caprolactam) and its copolymers with e-caprolactone has been studied by high-resolution thenno- gravimetric analysis (TGA), followed by the analysis of evolved gas via a simultaneous coupling to Fourier transfonn infrared spectrometry (FfIR) and mass spectrometry (MS). Poly(#epsilon#-caprolactam) and poly(#epsilon#-caprolactone) polymers are, respectively, degraded at different temperatures, rendering this study to be particularly useful in detennining the structure of their copolymers, i.e. random or blocky-like copolymers. The poly[(#epsilon#-caprolactam)-co-(#epsilon#-caprolactone)] polymers have been synthesized in bulk by anionic ring-opening copolymer- ization promoted by e-caprolactammagnesium bromide in a temperature range from120 to 180degC. A multi-step degradation was observed by TGA, and characterization of the evolved gas byFTIR and MS gives credit to some blocky-like enchainment of the comonomers. This assignation has been further confinned by TGA directly perfonned on blends of poly(e-caprolactam) and poly(#epsilon#-caprolactone) as obtained by solvent casting.
机译:通过高分辨率的重量分析法(TGA)研究了聚ε-己内酰胺及其共聚物与ε-己内酰胺的热降解,然后通过同时耦合至傅立叶透射红外光谱法分析了析出的气体(FfIR)和质谱(MS)。聚(ε-己内酰胺)和聚(ε-己内酯)聚合物分别在不同温度下降解,这使得该研究在确定其共聚物(即无规或嵌段状共聚物)的结构中特别有用。聚[(εε-己内酰胺)-共-(εε-己内酯)]聚合物是通过在120-180℃的温度范围内,由ε-己内酰胺溴化镁促进的阴离子开环共聚反应合成的。通过TGA观察到多步降解,并且通过FTIR和MS表征放出的气体归因于共聚单体的一些块状链状。通过直接用溶剂浇铸法得到的聚(ε-己内酰胺)和聚(ε-己内酯)的共混物的TGA进一步限定了这种分配。

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