Ultra-high arsenic adsorption by graphene oxide iron nanohybrid: Removal mechanisms and potential applications

石墨烯 吸附 氧化物 氧化铁 纳米颗粒 无机化学 化学工程 水溶液 材料科学 氧化铁纳米粒子 化学 纳米技术 冶金 有机化学 工程类
作者
Tonoy K. Das,Tamil S. Sakthivel,Aadithya Jeyaranjan,Sudipta Seal,Achintya N. Bezbaruah
出处
期刊:Chemosphere [Elsevier BV]
卷期号:253: 126702-126702 被引量:104
标识
DOI:10.1016/j.chemosphere.2020.126702
摘要

Iron (Fe)-based adsorbents have been promoted for aqueous arsenic adsorption because of their low cost and potential ease of scale-up in production. However, their field application is, so far, limited because of their low Fe use efficiency (i.e., not all available Fe is used), slow adsorption kinetics, and low adsorption capacity. In this study, we synthesized graphene oxide iron nanohybrid (GFeN) by decorating iron/iron oxide (Fe/FexOy) core-shell structured iron nanoparticles (FeNPs) on the surface of graphene oxide (GO) via a sol-gel process. The deposition of FeNPs on GO for the nanohybrid (GFeN) improves Fe use efficiency and arsenic mobility in the nanohybrid, thereby improving the arsenic removal capacity and kinetics. We achieved removal capacities of 306 mg/g for As(III) and 431 mg/g for As(V) using GFeN. Rapid reduction (>99% in <10 min) of As(III) and As(V) (initial concentration, C0 = 100 μg/L) was achieved with the nanohybrid (250 mg/L). There were no significant interferences by the coexisting anions and organic matters at environmentally relevant concentrations. Based on the experimental data, we have proposed that both electrostatic interaction and surface complexation contributed to ultra-high arsenic removal by GFeN. The GO sheets acted as the reservoirs for the electrons released during surface corrosion of the FeNPs and the electrons were transferred back to the FeNPs to rejuvenate the oxidized surface. The rejuvenated FeNP surface layer helped in additional arsenic removal.
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