首页 | 本学科首页   官方微博 | 高级检索  
     检索      


Synthesis and characterization of polyhedral oligomeric silsesquioxane hybrid co‐crosslinked poly(N‐isopropylacrylamide‐co‐dimethylaminoethyl methacrylate) hydrogels
Authors:Yi Chen  Yuanqin Xiong  Chang Peng  Wenyong Liu  Yue Peng  Weijian Xu
Institution:1. Institute of Polymer Research, College of Chemistry and Chemical Engineering, Hunan University, , Changsha, 410082 People's Republic of China;2. Key Laboratory of Advanced Materials and Technology for Packaging, Hunan University of Technology, , Zhuzhou, 421007 People's Republic of China
Abstract:Polyhedral oligomeric silsesquioxane hybrid temperature and pH double‐responsive hydrogels with organic–inorganic co‐crosslinked networks are synthesized by in situ, free‐radical polymerization of N‐isopropylacrylamide and dimethylaminoethyl methacrylate in the presence of both organic crosslinker N,N′‐methylenebis(acrylamide) (BIS) and inorganic crosslinker octavinyl polyhedral oligomeric silsesquioxane (OvPOSS) in tetrahydrofuran media. The resulting hydrogels (OR‐OvP gels) display obvious temperature and pH double responsiveness, OvPOSS particles dispersed in polymer make a dominant effect on the properties of gels. With the increase of OvPOSS, the aggregation of particles on nano‐ or microscale happens and causes a considerable change on the properties of gels, such as the lower critical solution temperature and better compression strength. Specially, the interconnected microporous structure of gels ascribed to the microphase separation results in faster deswelling rate, which makes the gel become attractive. Besides, the crosslink by BIS intensifies the heterogeneity of gels significantly, which could also be used to adjust the properties of gels. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2013 , 51, 1494–1504
Keywords:co‐crosslink  double stimulus responsiveness  gels  hydrogels  nanocomposites  nanostructures  NIPA  DMAEMA  organic‐inorganic hybrid composites  polyhedral oligomeric silsesquioxane
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号