首页> 外文期刊>Polymer: The International Journal for the Science and Technology of Polymers >Influence of soft segment molecular weight on the mechanical hysteresis and set behavior of silicone-urea copolymers with low hard segment contents
【24h】

Influence of soft segment molecular weight on the mechanical hysteresis and set behavior of silicone-urea copolymers with low hard segment contents

机译:软链段分子量对低硬链段含量的有机硅-脲共聚物的机械迟滞和固化行为的影响

获取原文
获取原文并翻译 | 示例
       

摘要

Effect of polydimethylsiloxane (PDMS) soft segment molecular weight (M _n = 3200, 10,800 and 31,500 g/mol) and urea hard segment content (2.0-11.4% by weight) on the hysteresis and permanent set behavior of segmented silicone-urea (TPSU) copolymers were investigated. In spite of very low hard segment contents, all copolymers formed self-supporting films and displayed good mechanical properties. When the mechanical hysteresis and set behavior of the silicone-urea copolymers with similar hard segment contents (around 7.5% by weight) but based on PDMS-3K, PDMS-11K and PDMS-32K were compared, it was very clear that as the PDMS molecular weight increased, hysteresis and instantaneous set values decreased significantly. Copolymers based on the same silicone soft segment (PDMS-11K or PDMS-32K) but with different hard segment contents showed a linear increase in hysteresis and a slight decrease in the instantaneous set as a function of hard segment content. Constant initial stress creep experiments also showed lower creep as the PDMS segment molecular weight increased for copolymers with similar urea contents. Since the critical entanglement molecular weight (M_e) of PDMS is stated to be 24,500 g/mol, our results tend to suggest important contribution of chain entanglements on the hysteresis and instantaneous set of these silicone-urea copolymers.
机译:聚二甲基硅氧烷(PDMS)软链段分子量(M _n = 3200、10,800和31,500 g / mol)和尿素硬链段含量(2.0-11.4%(重量))对链段有机硅-脲(TPSU)的滞后和永久凝固行为的影响)进行了研究。尽管硬链段含量非常低,但所有共聚物仍会形成自支撑膜并显示出良好的机械性能。当比较具有类似硬链段含量(约7.5%重量)但基于PDMS-3K,PDMS-11K和PDMS-32K的有机硅-脲共聚物的机械滞后性和固化性能时,很显然,作为PDMS分子量增加,磁滞和瞬时设定值明显降低。基于相同的有机硅软链段(PDMS-11K或PDMS-32K)但硬链段含量不同的共聚物显示,磁滞线性增加,瞬时变形随硬链段含量的变化而略有下降。恒定初始应力蠕变实验还表明,对于具有相似尿素含量的共聚物,随着PDMS链段分子量的增加,蠕变降低。由于PDMS的临界缠结分子量(M_e)据称为24,500 g / mol,因此我们的结果倾向于表明链缠结对这些硅酮-脲共聚物的滞后性和瞬时形变的重要贡献。

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