文献类型：期刊文献

英文题名：Recognition properties of poly(vinylidene fluoride) hollow-fiber membranes modified by Levofloxacin-Imprinted polymers

作者：Bing, Nai-Ci[1]; Xu, Zhen-Liang[1]; Wang, Xue-Jun[1]; Yang, Zuo-Guo[1]; Yang, Hu[1]

机构：[1]E China Univ Sci & Technol, Chem Engn Res Ctr, Shanghai 200237, Peoples R China

年份：2007

卷号：106

期号：1

起止页码：71

外文期刊名：JOURNAL OF APPLIED POLYMER SCIENCE

收录：;EI(收录号：20073710808955);WOS:【SCI-EXPANDED(收录号:WOS:000248609900009)】；

语种：英文

外文关键词：chiral; membranes; separation techniques

摘要：Through the use of thermal polymerization, polv(vinylidene fluoride) (PVDF) hollow-fiber membranes mo dified by a thin laver of molecularly imprinted polymers (MIPs) were developed for the selective separation of levofloxacin. To demonstrate the changes induced by thermal polymerization, PVDF hollow-fiber membranes with different modification degrees by repeated polymerization were weighed. The total weight of the imprinted membranes increased by 14 mu g/cm(2) after a five-cycle polymerization. An increase in the membrane weight indicated the deposition of an MIP laver on the external surface of PVDF hollow-fiber membranes during each polymerization cycle, which was also characterized by scanning electron microscopy. MIP membranes with different degrees of surface modification provided highly selective binding of levofloxacin. Both hollow-fiber MIP membranes and nonimprinted membranes showed enhanced adsorption of levofloxacin and ofloxacin gradually with an increase in the modification degrees of PVDF hollow-fiber membranes to a maximum value followed by a decrease. These results indicate that thermal polymerization indeed produces an MIP layer on the external surface of PVDF hollow-fiber membranes and that it is feasible to control the permeability by repeated polymerization cycles. Different solvent systems in the permeation experiments were used to understand the hydrophobic interaction as one of the results of the binding specificity of MIP membranes. Selective separation was obtained by multisite binding to the template via ionic, hydrogen-bond, and hydrophobic interactions. (c) 2007 Wiley Periodicals, Inc.