...
【24h】

Bionanocomposites based on poly(ε-caprolactone)-grafted cellulose nanocrystals by ring-opening polymerization

机译:通过开环聚合制备基于聚(ε-己内酯)接枝的纤维素纳米晶体的Bionanocomposites

获取原文
获取原文并翻译 | 示例
           

摘要

A 'grafting from' approach was used to graft poly(s-caprolactone) (PCL) polymers to cellulose nanocrystals by Sn(Oct)2-catalyzed ring-opening polymerization (ROP). The grafting efficiency was evidenced by the long-term stability of suspension of PCL-grafted cellulose nanocrystals in toluene. These observations were confirmed by Fourier Transform Infrared Spectroscopy (FT-IR) and Time-of-Flight Secondary Ion Mass Spectrometry (TOF-SIMS). Extracted nanohybrids were characterized by Differential Scanning Calorimetry (DSC), X-ray photoelectron spectroscopy (XPS), and contact angle measurements. The morphology and crystalline structure of the PCL-grafted cellulose nanocrystals was examined by transmission electron microscopy (TEM) and X-Ray diffraction, respectively. Results showed that cellulose nanocrystals kept their initial morphological integrity and their native crystallinity. Nanocomposites with high content of cellulose nanocrystals were prepared using either neat cellulose nanocrystals or PCL-grafted cellulose nanocrystals and high molecular weight PCL as matrix using a casting/evaporation technique. Thermo-mechanical properties of processed nanocomposites were studied by DSC, dynamical mechanical analyses (DMA) and tensile tests. A significant improvement in terms of Young's modulus and storage modulus was obtained.
机译:通过从Sn(Oct)2催化的开环聚合(ROP),采用“接枝”方法将聚(s-己内酯)(PCL)聚合物接枝到纤维素纳米晶体上。 PCL接枝的纤维素纳米晶体在甲苯中悬浮液的长期稳定性证明了接枝效率。这些观察结果通过傅里叶变换红外光谱(FT-IR)和飞行时间二次离子质谱(TOF-SIMS)得以证实。通过差示扫描量热法(DSC),X射线光电子能谱(XPS)和接触角测量来表征提取的纳米杂化物。通过透射电子显微镜(TEM)和X射线衍射分别检查了PCL接枝的纤维素纳米晶体的形态和晶体结构。结果表明,纤维素纳米晶体保持其初始形态完整性和天然结晶度。使用流延/蒸发技术,使用纯纤维素纳米晶体或PCL接枝的纤维素纳米晶体和高分子量PCL作为基质,制备具有高含量纤维素纳米晶体的纳米复合材料。通过DSC,动态力学分析(DMA)和拉伸试验研究了加工后的纳米复合材料的热机械性能。获得了杨氏模量和储能模量的显着改善。

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