乙烯醇
自愈水凝胶
聚乙烯吡咯烷酮
材料科学
高分子化学
化学工程
纳米颗粒
傅里叶变换红外光谱
肿胀 的
纳米复合材料
透射电子显微镜
扫描电子显微镜
聚合
自由基聚合
聚丙烯酰胺
聚合物
纳米技术
复合材料
工程类
作者
Qing-Bo Wie,Yan‐Ling Luo,Feng Fu,Loujun Gao,Song Yan-wei
标识
DOI:10.1134/s1061933x13010146
摘要
Polyacrylamide grafted poly(vinyl alcohol)/polyvinylpyrrolidone (PAM-g-PVA/PVP) semi-interpenetrating network (semi-IPN) hydrogels were designed and prepared via a simple free radical polymerization reaction process initiated by a PVA-(NH4)2Ce(NO3)6 redox system. The structure of the PAM-g-PVA/PVP semi-IPNs was characterized by a Fourier transform infrared spectroscopy. The morphologies of PAM-g-PVA/PVP hydrogels and PAM-g-PVA/PVP/Ag nanocomposite hydrogels were examined by scanning electron microscopy and transmission electron microscopy (TEM). The experimental results indicated that the PAM, PVA or PVP chains can efficiently act as stabilizing agents for Ag nanoparticles. TEM investigation of sample morphology showed the presence of nearly spherical-, square- or rectangular-shaped Ag nanoparticles with diameters ranging from 10 to 60 nm. The characteristic surface plasmon resonance band appeared at 390–400 run as a result of the immobilization of Ag nanoparticles within the hydrogel matrices. The self-assembly of Ag nanoparticles and the swelling behavior of the resulting nanocomposites can be controlled and modulated by altering the mole fraction of PVP in the PAM-g-PVA/PVP semi-IPNs.
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