...
首页> 外文期刊>Journal of Macromolecular Science. Physics >Rheological behavior of poly(vinylpyrrolidone)/fullerene C-60 complexes in aqueous medium
【24h】

Rheological behavior of poly(vinylpyrrolidone)/fullerene C-60 complexes in aqueous medium

机译:聚乙烯吡咯烷酮/富勒烯C-60配合物在水性介质中的流变行为

获取原文
获取原文并翻译 | 示例

摘要

Aqueous solutions of complexes formed between poly(vinylpyrrolidone) (PVP), as a matrix polymer, and fullerene C-60 were investigated. The effect of the external hydrodynamic field on the supermolecular assemblies formed by the complexes was analyzed. Despite the low content in the complexes (1.5 mass%), fullerene significantly modified the viscosity of aqueous PVP. Thus, the dynamic viscosity of the PVP/C-60 complexes grew faster than that of the pure PVP upon increasing the PVP/C-60 concentration. The difference in viscosities is especially pronounced for semidilute solutions. As a possible explanation, it is assumed that fullerenes act as crosslinks, in addition to the physical entanglements of the PVP macromolecules, which appear in the vicinity of the crossover concentration. Shear flow corresponding to the high shear rates destroyed fullerene-induced intermolecular crosslinks in PVP/C-60 solutions.
机译:研究了作为基质聚合物的聚乙烯吡咯烷酮(PVP)与富勒烯C-60之间形成的络合物的水溶液。分析了外部流体动力场对由配合物形成的超分子组装体的影响。尽管配合物中的含量低(1.5质量%),但富勒烯显着改变了水性PVP的粘度。因此,随着PVP / C-60浓度的增加,PVP / C-60配合物的动态粘度增长快于纯PVP。对于半稀释溶液,粘度差异尤为明显。作为可能的解释,假定富勒烯除了在交叉浓度附近出现的PVP大分子的物理缠结外,还充当交联键。对应于高剪切速率的剪切流破坏了PVP / C-60溶液中富勒烯诱导的分子间交联。

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