Adsorption behavior and mechanism of arsenate at Fe-Mn binary oxide/water interface
Zhang, Gaosheng1,2; Liu, Huijuan1; Liu, Ruiping1; Qu, Jiuhui1
发表期刊JOURNAL OF HAZARDOUS MATERIALS
ISSN0304-3894
2009-09-15
卷号168期号:2-3页码:820-825
关键词Fe-mn Binary Oxide Arsenate Adsorption Mechanism Specific Adsorption
产权排序Chinese Acad Sci, State Key Lab Environm Aquat Chem, Ecoenvironm Sci Res Ctr;Chinese Acad Sci, Yantai Inst Coastal Zone Res Sustainable Dev
通讯作者Qu, JH, Chinese Acad Sci, State Key Lab Environm Aquat Chem, Ecoenvironm Sci Res Ctr, POB 2871, Beijing 100085, Peoples R China
作者部门污染过程与控制实验室
英文摘要Preliminary study revealed that a prepared Fe-Mn binary oxide adsorbent with a Fe:Mn molar ratio of 3:1 was more effective for As(V) removal than pure amorphous FeOOH, which MS unanticipated. In this paper, the As(V) adsorption capacities of Fe-Mn binary oxide and amorphous FeOOH were compared in detail. Furthermore, the adsorption behaviors as well as adsorption mechanism of As(V) at the Fe-Mn binary oxide/water interface were investigated. The higher uptake of As(V) by the Fe-Mn binary oxide may be due to its higher surface area (265 m(2)/g) and pore volume (0.47 cm(3)/g) than those of amorphous FeOOH. The As(V) adsorption process on the Fe-Mn binary oxide is endothermic and the increase of temperature is favoring its adsorption. A slight increase in the As(V) adsorption was observed with increasing ionic strength of the solution, which indicated that As(V)anions might form inner-sphere surface complexes at the oxide/water interface. The Zeta potential along with FTIR analysis confirmed further the formation of inner-sphere surface complexes between As(V) anions and the surface of Fe-Mn binary oxide. In addition, the influences of coexisting ions such as phosphate, bicarbonate, silicate, sulfate, chloride, calcium and magnesium which are generally present in groundwater on As(V) adsorption were examined. Among the tested anions, chloride and sulfate had no significant effect on As(V) removal, silicate decreased obviously the As(V) removal, while phosphate caused the greatest percentage decrease in As(V) adsorption. On the contrary, the presence of cations of Ca(2+) and Mg(2+) enhanced the adsorption of As(V). (C) 2009 Elsevier B.V. All rights reserved.
文章类型Article
资助机构Funds for Creative Research Groups of China [50621804]; National Natural Science Foundation of China [20577063]
收录类别SCI
语种英语
关键词[WOS]OXIDE ADSORBENT ; SURFACE-CHEMISTRY ; NATURAL-WATERS ; REMOVAL ; ARSENITE ; SORPTION ; HYDROXIDE ; ANIONS
研究领域[WOS]Engineering ; Environmental Sciences & Ecology
WOS记录号WOS:000268200700035
引用统计
被引频次:186[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符http://ir.yic.ac.cn/handle/133337/3514
专题中国科学院海岸带环境过程与生态修复重点实验室_污染过程与控制实验室
作者单位1.Chinese Acad Sci, State Key Lab Environm Aquat Chem, Ecoenvironm Sci Res Ctr, Beijing 100085, Peoples R China
2.Chinese Acad Sci, Yantai Inst Coastal Zone Res Sustainable Dev, Yantai 264003, Shandong, Peoples R China
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GB/T 7714
Zhang, Gaosheng,Liu, Huijuan,Liu, Ruiping,et al. Adsorption behavior and mechanism of arsenate at Fe-Mn binary oxide/water interface[J]. JOURNAL OF HAZARDOUS MATERIALS,2009,168(2-3):820-825.
APA Zhang, Gaosheng,Liu, Huijuan,Liu, Ruiping,&Qu, Jiuhui.(2009).Adsorption behavior and mechanism of arsenate at Fe-Mn binary oxide/water interface.JOURNAL OF HAZARDOUS MATERIALS,168(2-3),820-825.
MLA Zhang, Gaosheng,et al."Adsorption behavior and mechanism of arsenate at Fe-Mn binary oxide/water interface".JOURNAL OF HAZARDOUS MATERIALS 168.2-3(2009):820-825.
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