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电化学方法控制可变氧化还原电位下吸附的 Pb(II)在氧化石墨烯上的命运。

Fate of adsorbed Pb(II) on graphene oxide under variable redox potential controlled by electrochemical method.

机构信息

Shaanxi Key Laboratory of Environmental Engineering, Xi'an University of Architecture and Technology, Xi'an 710055, People's Republic of China; Key Laboratory of Northwest Water Resource, Environment and Ecology, MOE, Xi'an University of Architecture and Technology, Xi'an 710055, People's Republic of China.

Shaanxi Key Laboratory of Environmental Engineering, Xi'an University of Architecture and Technology, Xi'an 710055, People's Republic of China; Key Laboratory of Northwest Water Resource, Environment and Ecology, MOE, Xi'an University of Architecture and Technology, Xi'an 710055, People's Republic of China.

出版信息

J Hazard Mater. 2019 Apr 5;367:152-159. doi: 10.1016/j.jhazmat.2018.12.073. Epub 2018 Dec 21.

Abstract

Lead removal using graphene oxide (GO) and GO based adsorbents has attracted increasing attention worldwide, whereas the potential release of previously adsorbed Pb(II) from GO surfaces induced by exposure to variable redox conditions is presently underappreciated. The current study revealed that reduction of GO to r-GO (the reduced form) was coupled with a decrease of oxygen-containing groups (OCGs) under reductive potential, and the maximum adsorption capacity of GO for Pb(II) decreased from 931.66 to 714.78 mg g after electrochemical reduction. The release of adsorbed Pb(II) from GO-Pb(II) increased gradually when the potential dropped from 0 to -600 mV. The content of released Pb(II) decreased when the potential reached -700 mV because of the reduction of Pb(II) to insoluble Pb(0). Cyclic voltammetry (CV) analysis demonstrated that there are three reductive potentials, e.g. -760, -400, and -120 mV, related to the reduction of OCGs. X-ray photoelectron spectroscopy indicated that the reducing sequence of three OCGs, namely C-O, CO and OCO groups, depended on the applied potential. This application of an electrochemical method to investigate adsorbed Pb(II) from spent GO absorbent provides valuable information about heavy metal transportation in environments containing GO under varying redox conditions.

摘要

使用氧化石墨烯 (GO) 和基于 GO 的吸附剂去除铅已引起全球越来越多的关注,然而,目前人们对 GO 表面先前吸附的 Pb(II) 在暴露于可变氧化还原条件下释放的潜在风险认识不足。本研究表明,在还原电位下,GO 还原为 r-GO(还原形式)伴随着含氧基团(OCGs)的减少,电化学还原后,GO 对 Pb(II) 的最大吸附容量从 931.66 降至 714.78 mg/g。当电位从 0 降至-600 mV 时,GO-Pb(II) 中吸附的 Pb(II) 逐渐释放。当电位达到-700 mV 时,由于 Pb(II) 还原为不溶性 Pb(0),释放的 Pb(II) 含量减少。循环伏安法 (CV) 分析表明,与 OCGs 的还原有关的三个还原电位分别为-760、-400 和-120 mV。X 射线光电子能谱表明,三种 OCGs(即 C-O、CO 和 OCO 基团)的还原顺序取决于施加的电位。电化学方法在研究废弃 GO 吸附剂中吸附的 Pb(II) 的应用为在不同氧化还原条件下含有 GO 的环境中重金属迁移提供了有价值的信息。

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