Mechanism of arsenate coprecipitation at the solid/liquid interface of ferrihydrite: A perspective review

被引:28
|
作者
Tokoro, Chiharu [1 ]
Kadokura, Masakazu [2 ]
Kato, Tatsuya [2 ]
机构
[1] Waseda Univ, Fac Sci & Engn, Shinjuku Ku, 3-4-1 Okubo, Tokyo 1698555, Japan
[2] Waseda Univ, Grad Sch Creat Sci & Engn, Shinjuku Ku, 3-4-1 Okubo, Tokyo 1698555, Japan
关键词
XAFS; EXAFS; Tetrahedral structure; Octahedral structure; Local structure; SURFACE COMPLEXATION; AQUEOUS-SOLUTION; SORPTION MECHANISMS; ALUMINUM-HYDROXIDE; FERRIC ARSENATE; ADSORPTION; IRON; OXIDE; REMOVAL; WATER;
D O I
10.1016/j.apt.2019.12.004
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Arsenate (As(V)) is a toxic element in acid mine drainage and has to be removed during the neutralization process. Coprecipitation with ferrihydrite is the main mechanism for As(V) removal from acid mine drainage. To improve treatment efficiency, a quantitative understanding of the coprecipitation mechanism is required. Coprecipitation can incorporate more As(V) into ferrihydrite than adsorption. The results of XRD (X-ray Diffraction) and XANES (X-ray Adsorption Near Edge Structure) analysis confirmed that the formation of poorly crystalline ferric arsenate increased when the initial As/Fe molar ratio increased in the coprecipitation with ferrihydrite. EXAFS (Extended X-ray Adsorption Fine Structure) analysis at the iron K-edge showed that the proportion of octahedral structures in ferrihydrite increased when the initial As/Fe molar ratio increased. Moreover, EXAFS analysis at the arsenic K-edge, assuming three kinds of surface complexes for the AsAFe bond, revealed that the coordination number for AsAFe with an atomic distance of 2.85 x 10(-10) m increased and that for As-Fe with an atomic distance of 3.24 x 10(-10) m decreased as the initial As/Fe molar ratio increased. Thus, for more efficient wastewater treatment, active control of coprecipitation phenomena according to mechanistic details is essential. (C) 2019 The Society of Powder Technology Japan. Published by Elsevier B.V. and The Society of Powder Technology Japan. All rights reserved.
引用
收藏
页码:859 / 866
页数:8
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