摘要
将γ-环糊精(γ-CD)和3种不同长度烷基(Cn,n为12,16,18)分别按照一定的接枝率接枝于聚丙烯酸链上,利用环糊精与疏水烷基链之间的包合作用,成功制备了大分子自组装网络,并利用流变学手段对影响高分子网络结构的因素进行了系统研究。结果表明:γ-CD与Cn之间的包合作用主要以1∶2的量化模式进行,即1个γ环糊精空腔可以同时穿入2条烷基链。当聚合物的质量分数较低时(w≤1.7%),聚合物之间以包合作用交联为主;随着聚合物质量分数的增加并超过临界浓度,疏水缔合作用产生且迅速增大,并最终超过包合作用。单体γ-CD及表面活性剂十二烷基硫酸钠(SDS)的加入可以调节聚合物的网络结构,从而对自组装体系的黏度起到调控作用。
γ-Cyclodextrin(γ-CD) and three alkyl groups(C12,C16,C18) with different lengths were grafted onto poly(acrylic acid)(PAA).Polymer networks were prepared by mixing γ-CD and Cn(n=12,16,18) modified PAA based on the inclusion associations between alkyl and γ-CD grafts.Rheological method was employed to study the properties of polymer networks.The γ-CD/alkyl inclusion compounds were formed at a stoichiometric ratio of 1∶2,i.e.two alkyl groups entered into one γ-CD cavity.At low polymer concentration(w≤1.7%),the inclusion associations between γ-CD and alkyl grafts were dominated while the hydrophobic associations among the hydrophobic alkyl groups became stronger upon increasing polymer concentration.Viscosity of polymer solutions could be modulated by addition of γ-CD and surfactant SDS and thus regulating the structure of polymer networks.
出处
《华东理工大学学报(自然科学版)》
CAS
CSCD
北大核心
2011年第3期268-273,共6页
Journal of East China University of Science and Technology
基金
国家自然科学基金(20774030)
上海市浦江人才计划(08PJ14036)