大分子单体
自愈水凝胶
高分子化学
丙烯酸
自由基聚合
材料科学
单体
丙烯酰氯
傅里叶变换红外光谱
肿胀 的
化学
化学工程
聚合物
丙烯酸酯
复合材料
工程类
作者
Hongliang Liu,Mingzhu Liu,Liwei Ma,Jun Chen
标识
DOI:10.1016/j.eurpolymj.2009.03.019
摘要
Poly(N,N-diethylacrylamide) with a terminal hydroxyl end group (PDEA-CH) was synthesized by radical telomerization of N,N-diethylacrylamide (DEA) monomer using 2-hydroxy-ethanethiol as a chain transfer agent. Macromonomer of thermo-sensitive PDEA was synthesized by condensation reaction of PDEA-OH with acryloyl chloride. The macromonomer was characterized by FTIR and (1)H NMR, and the molecular weight was determined by GPC. Thermo- and pH-sensitive comb-type grafted poly(N,N-diethylacrylamide-co-acrylic acid) (PDEA-co-AA) hydrogels (GHs) were successfully prepared by grafting PDEA chains with freely mobile ends onto the backbone of a cross-linked (PDEA-co-AA) network. The results showed that the deswelling behavior of the hydrogels was dependent on the test temperature. At 45 degrees C (beneath the VPTT of the hydrogels), both the normal-type hydrogels (NHs) and comb-type grafted P(DEA-co-AA) hydrogels had lower deswelling rates. While at 60 degrees C (far beyond the VPTT of the hydrogels), the deswelling rates of the GHs were faster than that of the NHs. Furthermore, pulsatile stimuli-responsive studies indicated that the GHs had excellent thermo-reversibility and were superior to the NHs in the magnitude of their swelling ratios to temperature changes. However, the reversibility to pH changes was poor for both the NHs and the GHs. (C) 2009 Elsevier Ltd. All rights reserved.
科研通智能强力驱动
Strongly Powered by AbleSci AI