Immobilization of uranium into magnetite from aqueous solution by electrodepositing approach

被引:72
作者
Lu, Bing-qing [1 ]
Li, Mi [1 ,2 ]
Zhang, Xiao-wen [1 ,2 ]
Huang, Chun-mei [1 ]
Wu, Xiao-yan [1 ,2 ]
Fang, Qi [1 ,2 ]
机构
[1] Univ South China, Sch Environm Protect & Safety Engn, Hengyang 421001, Peoples R China
[2] Univ South China, Key Lab Radioact Waste Treatment & Disposal, Hengyang 421001, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Uranium; Electrodeposition; Magnetite; Iron; Incorporation; ZERO-VALENT IRON; ELECTRIC DOUBLE-LAYER; EFFICIENT REMOVAL; URANYL IONS; WASTE-WATER; RECOVERY; NANOPARTICLES; ADSORPTION; SURFACE; FE3O4;
D O I
10.1016/j.jhazmat.2017.09.037
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Immobilization of uranium into magnetite (Fe3O4), which was generated from metallic iron by electrochemical method, was proposed to rapidly remove uranium from aqueous solution. The effects of electrochemical parameters such as electrode materials, voltage, electrode gap, reaction time and pH value on the crystallization of Fe3O4 and uranium removal efficiencies were investigated. More than 90% uranium in the solution was precipitated with Fe3O4 under laboratory conditions when uranium concentration range from 0.5 mg/L to 10 mg/L. The Fe3O4 crystallization mechanism and immobilization of uranium was proved by XPS, XRD, TEM, FTIR and VSM methods. The results indicated that the cationic (including Fe2+, Fe3+ and U(VI)) migrate to cathode side under the electric field and the uranium was incorporated or adsorbed by Fe3O4 which was generated at cathode while the pH ranges between 2-7. The uranium-containing precipitate of Fe3O4 can exist stably at the acid concentration below 60 g/L. Furthermore, the precipitate may be used as valuable resources for uranium or iron recycling, which resulted in no secondary pollution in the removal of uranium from aqueous solution. (C) 2017 Published by Elsevier B.V.
引用
收藏
页码:255 / 265
页数:11
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