吸附
膨胀能力
自愈水凝胶
朗缪尔吸附模型
化学
双酚A
肿胀 的
乙二醇
缩水甘油醚
化学工程
核化学
高分子化学
聚合物
傅里叶变换红外光谱
环糊精
色谱法
有机化学
环氧树脂
工程类
作者
Hiroyuki Kono,Kenta Onishi,Taichi Nakamura
标识
DOI:10.1016/j.carbpol.2013.06.065
摘要
Novel hydrogel beads having molecular adsorption abilities were prepared from carboxymethylcellulose sodium salt (CMC) and β-cyclodextrin (β-CD) by suspension crosslinking, using ethylene glycol diglycidyl ether (EGDE) in basic medium as a crosslinking agent. FTIR and solid-state NMR spectroscopic analysis revealed that the amount of incorporated β-CD and crosslinking densities within the hydrogel bead structures are strongly dependent on the molar feed ratio of β-CD to CMC during preparation. The hydrogel beads showed water-swelling capacities of 70–200 mL/g-polymer, with decreases in capacity associated with increased amounts of β-CD incorporated in the gel structure. The hydrogel beads also showed a high adsorption capacity toward bisphenol A (BPA) in water. Batch BPA-adsorption experiments were analyzed employing Langmuir isotherm models; hydrogel bead adsorption isotherms for BPA could be fitted to the Langmuir model. The maximum BPA-adsorption among the prepared series of hydrogel beads amounted to 167 μmol g−1.
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