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Enhanced Removal of Uranium(VI) by Nanoscale Zerovalent Iron Supported on Na-Bentonite and an Investigation of Mechanism  ( SCI-EXPANDED收录 EI收录)   被引量:106

文献类型:期刊文献

英文题名:Enhanced Removal of Uranium(VI) by Nanoscale Zerovalent Iron Supported on Na-Bentonite and an Investigation of Mechanism

作者:Sheng, Gudong[1];Shao, Xiaoyu[1];Li, Yimin[1];Li, Jianfa[1];Dong, Huaping[1];Cheng, Wei[1];Gao, Xing[2];Huang, Yuying[2]

机构:[1]Shaoxing Univ, Coll Chem & Chem Engn, Shaoxing 312000, Zhejiang, Peoples R China;[2]Chinese Acad Sci, SSRF, Shanghai Inst Appl Phys, Shanghai 201204, Peoples R China

年份:2014

卷号:118

期号:16

起止页码:2952

外文期刊名:JOURNAL OF PHYSICAL CHEMISTRY A

收录:SCI-EXPANDED(收录号:WOS:000335114000010)、、EI(收录号:20141917690015)、Scopus(收录号:2-s2.0-84899545110)、WOS

基金:This work was supported by the National Natural Science Foundation of China (21177088 and 201207092).

语种:英文

外文关键词:Bentonite - Efficiency - Mass transfer - Nanotechnology - Reusability - Sodium compounds - Uranium compounds - X ray absorption

外文摘要:The reductive removal of U(VI) by nanoscale zerovalent iron (NZVI) was enhanced by using Na+-saturated bentonite (Na-bent) as the support, and the mechanism for the enhanced removal were investigated comprehensively. Under the same experimental conditions, NZVI supported on the negatively charged Na-bent showed much higher removal efficiency (99.2%) of cationic U(VI) than either bare NZVI (48.3%) or NZVI supported on the positively charged bentonite (Al-bent) did. Subsequent experimental investigations revealed the unique roles of bentonite on enhancing the reactivity and reusability of NZVI. First, Na-bent can buffer the pH in reaction media, besides preventing NZVI from aggregation. Second, Na-bent promoted the mass transfer of U(VI) from solution to NZVI surface, leading to the enhanced removal efficiency. Third, the bentonite may transfer some insoluble reduction products away from the iron surface according to X-ray absorption fine structure (XAFS) study. Finally, Na-bent as the adsorbent to Fe(II) makes it more reactive with U(VI), which enhanced stoichiometrically the reduction capacity of NZVI besides accelerating the reaction rate.

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