乙烯醇
肿胀 的
聚乙烯醇
蒸馏水
丙烯酸
差示扫描量热法
高分子化学
自愈水凝胶
水溶液
材料科学
核化学
壳聚糖
傅里叶变换红外光谱
互穿聚合物网络
膨胀能力
聚电解质
共聚物
扫描电子显微镜
化学工程
聚合物
化学
有机化学
复合材料
色谱法
工程类
物理
热力学
作者
Jianghua Liu,Yian Zheng,Wenbo Wang,Aiqin Wang
摘要
Abstract The phosphorylated poly(vinyl alcohol) (P‐PVA) samples with various substitution degrees were prepared through the esterification reaction of PVA and phosphoric acid. By using chitosan (CTS), acrylic acid (AA) and P‐PVA as raw materials, ammonium persulphate (APS) as an initiator and N,N ‐methylenebisacrylamide as a crosslinker, the CTS‐ g ‐PAA/P‐PVA semi‐interpenetrated polymer network (IPN) ssuperabsorbent hydrogel was prepared in aqueous solution by the graft copolymerization of CTS and AA and followed by an interpenetrating and crosslinking of P‐PVA chains. The hydrogel was characterized by Fourier transform infrared (FTIR), scanning electron microscopy (SEM), and differential scanning calorimetry (DSC) techniques, and the influence of reaction variables, such as the substitution degree and content of P‐PVA on water absorbency were also investigated. FTIR and DSC results confirmed that PAA had been grafted onto CTS backbone and revealed the existence of phase separation and the formation of semi‐IPN network structure. SEM observations indicate that the incorporation of P‐PVA induced highly porous structure, and P‐PVA was uniformly dispersed in the polymeric network. Swelling results showed that CTS‐ g ‐PAA/P‐PVA semi‐IPN superabsorbent hydrogel exhibited improved swelling capability (421 g·g −1 in distilled water and 55 g·g −1 in 0.9 wt % NaCl solution) and swelling rate compared with CTS‐ g ‐PAA/PVA hydrogel (301 g·g −1 in distilled water and 47 g·g −1 in 0.9 wt % NaCl solution) due to the phosphorylation of PVA. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009
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