Removal of cesium from liquid radioactive waste by in situ electrochemical synthesis of cesium zinc ferrocyanide

被引:9
|
作者
Yang, Xing [1 ]
Jiang, Li [1 ]
Peng, Shiming [1 ]
Zhang, Lehua [1 ]
Huang, Guangtuan [1 ]
机构
[1] East China Univ Sci & Technol, Sch Resources & Environm Engn, Natl Engn Lab Ind Wastewater Treatment, State Environm Protect Key Lab Environm Risk Asse, Shanghai 200237, Peoples R China
关键词
Cesium zinc ferrocyanide; In situ electrochemical synthesis; Liquid  radioactive waste; Cesium; AQUEOUS-SOLUTION; ADSORPTION; NICKEL; IONS; NANOCOMPOSITES; BIOSORBENTS; EXCHANGER; COBALT;
D O I
10.1016/j.colsurfa.2021.127050
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
Cesium ion in the simulated liquid radioactive waste was treated with cesium zinc ferrocyanide (CsZnFC) precipitate synthesized by in situ electrochemical synthesis method (ISESM) in this study. The best removal rate of Cs+ was 99.42%, and the residual Cs+ in the effluent was 29.13 mu g L-1 under the optimal experimental conditions of initial pH (pHint) of 7.0, reaction temperature (T) of 35 degrees C, current density (J) of 0.7 mA cm-2, electrolytic time (t) of 30 min, and molar ratio of [Fe(CN)6]4- to Cs (RFCN/Cs) of 1.0. The synthesized precipitate was characterized by SEM-EDS, XRD and FT-IR. The precipitated particles are cubic with a particle size of around 190 nm. The XRD pattern shows that the phase composition of the synthesized compound is Cs2Zn[Fe(CN)6], and the absorption peaks of O-H bonds, C-N bonds, and C-Fe bonds appear in IR spectrum. The method of in situ electrochemical synthesis of CsZnFC is promising for the treatment of liquid radioactive wastes.
引用
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页数:7
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