Adsorption of U(VI) on bentonite in simulation environmental conditions
文献类型:期刊论文
作者 | Wang, Jiaquan1; Chen, Zhi1; Shao, Dadong2; Li, Yuying3; Xu, Zimu1; Cheng, Cheng2; Asiri, Abdullah M.4; Marwani, Hadi M.4; Hu, Shuheng1 |
刊名 | JOURNAL OF MOLECULAR LIQUIDS
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出版日期 | 2017-09-01 |
卷号 | 242期号:无页码:678-684 |
关键词 | u(Vi) Bentonite Ha Radioactive Waste Management Adsorption |
DOI | 10.1016/j.molliq.2017.07.048 |
文献子类 | Review |
英文摘要 | The bentonite derived from Huangshan County was used as adsorbent for the adsorption of uranium (U(VI)). The effect of environmental factors, such as contact time, pH, ionic strength, HA and reaction temperature, on U(VI) adsorption on bentonite surface was investigated in detail. The adsorption capability of bentonite for U(VI) is obviously rest with pH value and ionic strength. The presence of HA in solution strongly enhance and reduce the adsorption of U(VI) on bentonite at low and high pH, respectively. The Langmuir and Freundlich models were applied to simulate the adsorption isotherms of U(VI) at three different temperatures of 298 +/- 1, 318 +/- 1 and 338 +/- 1 K, respectively. The thermodynamic parameters (Delta H-0, Delta G(0) and Delta S-0) calculated from the temperature-dependence adsorption isotherms indicates that U(VI) adsorption on bentonite is an endothermic and spontaneous process. At pH < 7, the adsorption of U(VI) was dominated by the outer-sphere surface complexation and ion exchange with H+/Na+ on bentonite surfaces; At pH > 7, the inner-sphere surface complexation was the main adsorption mechanism. Based on the experimental analysis results, bentonite is an appropriate material for the enrichment and solidification of U(VI) ions. The results are important for the radioactive waste management. (C) 2017 Published by Elsevier B.V. |
WOS关键词 | HUMIC-ACID ; AQUEOUS-SOLUTIONS ; IONIC-STRENGTH ; SORPTION BEHAVIOR ; ENHANCED REMOVAL ; FACILE SYNTHESIS ; NUCLEAR-ENERGY ; PH ; CLAY ; TEMPERATURE |
WOS研究方向 | Chemistry ; Physics |
语种 | 英语 |
WOS记录号 | WOS:000412607300074 |
资助机构 | NSAF(U1530131) ; NSAF(U1530131) ; NSAF(U1530131) ; NSAF(U1530131) ; NSAF(U1530131) ; NSAF(U1530131) ; NSAF(U1530131) ; NSAF(U1530131) ; National Natural Science Foundation of China(11675210) ; National Natural Science Foundation of China(11675210) ; National Natural Science Foundation of China(11675210) ; National Natural Science Foundation of China(11675210) ; National Natural Science Foundation of China(11675210) ; National Natural Science Foundation of China(11675210) ; National Natural Science Foundation of China(11675210) ; National Natural Science Foundation of China(11675210) ; China Postdoctoral Science Foundation(2015M582769X13 ; China Postdoctoral Science Foundation(2015M582769X13 ; China Postdoctoral Science Foundation(2015M582769X13 ; China Postdoctoral Science Foundation(2015M582769X13 ; China Postdoctoral Science Foundation(2015M582769X13 ; China Postdoctoral Science Foundation(2015M582769X13 ; China Postdoctoral Science Foundation(2015M582769X13 ; China Postdoctoral Science Foundation(2015M582769X13 ; 2016T90872) ; 2016T90872) ; 2016T90872) ; 2016T90872) ; 2016T90872) ; 2016T90872) ; 2016T90872) ; 2016T90872) ; NSAF(U1530131) ; NSAF(U1530131) ; NSAF(U1530131) ; NSAF(U1530131) ; NSAF(U1530131) ; NSAF(U1530131) ; NSAF(U1530131) ; NSAF(U1530131) ; National Natural Science Foundation of China(11675210) ; National Natural Science Foundation of China(11675210) ; National Natural Science Foundation of China(11675210) ; National Natural Science Foundation of China(11675210) ; National Natural Science Foundation of China(11675210) ; National Natural Science Foundation of China(11675210) ; National Natural Science Foundation of China(11675210) ; National Natural Science Foundation of China(11675210) ; China Postdoctoral Science Foundation(2015M582769X13 ; China Postdoctoral Science Foundation(2015M582769X13 ; China Postdoctoral Science Foundation(2015M582769X13 ; China Postdoctoral Science Foundation(2015M582769X13 ; China Postdoctoral Science Foundation(2015M582769X13 ; China Postdoctoral Science Foundation(2015M582769X13 ; China Postdoctoral Science Foundation(2015M582769X13 ; China Postdoctoral Science Foundation(2015M582769X13 ; 2016T90872) ; 2016T90872) ; 2016T90872) ; 2016T90872) ; 2016T90872) ; 2016T90872) ; 2016T90872) ; 2016T90872) |
源URL | [http://ir.hfcas.ac.cn:8080/handle/334002/33779] ![]() |
专题 | 合肥物质科学研究院_中科院等离子体物理研究所 |
作者单位 | 1.Hefei Univ Technol, Sch Resources & Environm Engn, Hefei 230009, Anhui, Peoples R China 2.Chinese Acad Sci, Inst Plasma Phys, Hefei 230031, Anhui, Peoples R China 3.Wuyi Univ, Sch Chem & Environm Engn, Jiangmen 529020, Peoples R China 4.King Abdulaziz Univ, Chem Dept, Fac Sci, Jeddah 21589, Saudi Arabia |
推荐引用方式 GB/T 7714 | Wang, Jiaquan,Chen, Zhi,Shao, Dadong,et al. Adsorption of U(VI) on bentonite in simulation environmental conditions[J]. JOURNAL OF MOLECULAR LIQUIDS,2017,242(无):678-684. |
APA | Wang, Jiaquan.,Chen, Zhi.,Shao, Dadong.,Li, Yuying.,Xu, Zimu.,...&Hu, Shuheng.(2017).Adsorption of U(VI) on bentonite in simulation environmental conditions.JOURNAL OF MOLECULAR LIQUIDS,242(无),678-684. |
MLA | Wang, Jiaquan,et al."Adsorption of U(VI) on bentonite in simulation environmental conditions".JOURNAL OF MOLECULAR LIQUIDS 242.无(2017):678-684. |
入库方式: OAI收割
来源:合肥物质科学研究院
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