吸附
活性炭
化学
阳离子聚合
疏水效应
化学工程
离子强度
碳纤维
离子
离子键合
色谱法
环境化学
粉末活性炭处理
表面张力
氯化物
自来水
水处理
吸附
无机化学
水溶液
膜
静电相互作用
离子交换
作者
Yi Zhang,Cheng‐Shiuan Lee,Duning Li,Size Zheng,Benjamin S. Hsiao,Arjun K. Venkatesan
标识
DOI:10.1021/acs.est.5c03457
摘要
) by 23-96%. The changes in sorption capacities were hypothesized to result from the altered physicochemical properties of the formed ion pair complex, thereby affecting its uptake on GAC. Both the linear free energy relationship (LFER) calculation and molecular dynamic (MD) simulation suggested that short-chain PFAS sorption was improved via enhanced hydrophobicity of formed ion pairs with a low self-assembly tendency, while long-chain PFAS sorption was inhibited due to the formation of large complexes with a high self-assembly tendency. Rapid small-scale column tests were performed for tap water spiked with an equal mass of perfluorobutanoate (PFBA), perfluorobutanesulfonate (PFBS), and perfluorooctanesulfonate (PFOS). The bed volume for 50% breakthrough was improved by 350% and 230% for PFBA and PFBS, respectively, in the presence of CTAC and PFOS.
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