选择性
吸附
化学
单宁酸
无机化学
离子交换
选择性吸附
X射线光电子能谱
水溶液中的金属离子
金属
离子
有机化学
催化作用
化学工程
工程类
作者
Liezhao Zou,Ping Shao,Kai Zhang,Liming Yang,Deng You,Hui Shi,Spyros G. Pavlostathis,Weiqiang Lai,Dahao Liang,Xubiao Luo
标识
DOI:10.1016/j.cej.2019.01.160
摘要
Rational design and directed synthesis of an adsorbent with superior selectivity is challenging but of utmost importance for the remediation of heavy metal-laden actual wastewater. In this work, a novel tannic acid (TA)-based adsorbent ([email protected]) was synthesized by a simple coordination reaction. Adsorption isotherm experiments exhibited the [email protected] had a high capacity for Pb2+ capture. Impressively, an outstanding selectivity with extremely high selective coefficient (40–170) can be achieved by the [email protected] With decrease of Zr precursor, the selectivity of as-synthesized [email protected] remained unchanged, implying that the Zr species played a negligible role in the selectivity of [email protected] Even the Zr species were completely replaced by Ti precursor, the resultant adsorbent still possessed a remarkable selectivity. All these results revealed that it was the TA, rather than the Zr species, made a substantial contribution to the selectivity of [email protected] Further, based on the results of XPS, DFT and batch adsorption experiments, it can be deduced that the phenolic hydroxyl groups on TA functioned as the dominant adsorption sites in which the hydroxyl groups’ oxygen atoms coordinated with Pb2+ while hydrogen atoms of hydroxyl groups were replaced and released as hydrogen ions, thus extending a proton exchange mechanism for the selective adsorption of Pb2+ ions.
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