Tannic acid-based adsorbent with superior selectivity for lead(II) capture: Adsorption site and selective mechanism

选择性 吸附 化学 单宁酸 无机化学 铅(地质) 选择性吸附 机制(生物学) 组合化学 有机化学 催化作用 化学工程 地质学 哲学 工程类 地貌学 认识论
作者
Liezhao Zou,Penghui Shao,Kai Zhang,Liming Yang,Deng You,Hui Shi,Spyros G. Pavlostathis,Weiqiang Lai,Dahao Liang,Xubiao Luo
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:364: 160-166 被引量:109
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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