Nanoscaled zero valent iron/graphene composite as an efficient adsorbent for Co(II) removal from aqueous solution

被引:99
|
作者
Xing, Min [1 ]
Wang, Jianlong [1 ,2 ]
机构
[1] Tsinghua Univ, INET, Collaborat Innovat Ctr Adv Nucl Energy Technol, Beijing 100084, Peoples R China
[2] Tsinghua Univ, Beijing Key Lab Radioact Waste Treatment, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
Graphene; Zero valent iron; Magnetic graphene; Co(II); Adsorption; LEPIDOCROCITE GAMMA-FEOOH; HEAVY-METAL IONS; GRAPHENE OXIDE; ADSORPTION PROPERTIES; ARSENATE ADSORPTION; IRON NANOPARTICLES; GRAPHITE OXIDE; WASTE-WATER; CO2+; BIOSORPTION;
D O I
10.1016/j.jcis.2016.04.031
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A magnetic graphene, i.e., nanoscaled zero valent iron/graphene (0FG) composite, was prepared, characterized and applied for the removal of Co(II) from aqueous solution. The magnetic graphene (0FG) was synthesized through reduction of graphene oxide (GO) and ferrous ions by potassium borohydride. The kinetics and isotherms of Co(II) adsorption onto 0FG were investigated. The mechanism for Co(II) removal was proposed based on the Fourier transform infrared (FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS) and the X-ray absorption fine structure (XAFS) analysis. The results showed that pseudo second-order models and the Freundlich isotherm model fitted well with the data obtained. The adsorption capacity of 0FG was calculated from the Langmuir isotherm, which was 65.58, 101.60 and 134.27 mg/g at 10, 20 and 30 degrees C, respectively. Thermodynamic parameters suggested that the adsorption process was endothermic and spontaneous. Co2+ was stabilized by gamma-FeOOH/gamma-Fe2O3/Fe3O4 on the surface of graphene sheets, forming CoFe2O4-like nanocrystals. The coordination numbers and interatomic distances indicated that Co2+ mainly occupied the octahedral site, while pseudo tetrahedral coordination may occur by dehydroxylation of Co(O,OH)(6). Magnetic graphene is a potential adsorbent for Co2+ removal. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:119 / 128
页数:10
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