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三价锑和五价锑在富铝相上的吸附:水合氧化铝和粘土矿物高岭石 KGa-1b 以及氧化和还原型钠水辉石 NAt-1。

Sb(III) and Sb(V) sorption onto Al-rich phases: hydrous Al oxide and the clay minerals kaolinite KGa-1b and oxidized and reduced nontronite NAu-1.

机构信息

Department of Chemistry and Biochemistry, University of Alaska Fairbanks, P.O. Box 756160, 900 Yukon Drive, Room 194, Fairbanks, Alaska 99775-6160, United States.

出版信息

Environ Sci Technol. 2012 Jan 17;46(2):843-51. doi: 10.1021/es203027v. Epub 2011 Dec 21.

DOI:10.1021/es203027v
PMID:22136137
Abstract

We have studied the immobilization of Sb(III) and Sb(V) by Al-rich phases - hydrous Al oxide (HAO), kaolinite (KGa-1b), and oxidized and reduced nontronite (NAu-1) - using batch experiments to determine the uptake capacity and the kinetics of adsorption and Extended X-ray Absorption Fine Structure (EXAFS) Spectroscopy to characterize the molecular environment of adsorbed Sb. Both Sb(III) and Sb(V) are adsorbed in an inner-sphere mode on the surfaces of the studied substrates. The observed adsorption geometry is mostly bidentate corner-sharing, with some monodentate complexes. The kinetics of adsorption is relatively slow (on the order of days), and equilibrium adsorption isotherms are best fit using the Freundlich model. The oxidation state of the structural Fe within nontronite affects the adsorption capacity: if the clay is reduced, the adsorption capacity of Sb(III) is slightly decreased, while Sb(V) uptake is increased significantly. This may be a result of the presence of dissolved Fe(II) in the reduced nontronite suspensions or associated with the structural rearrangements in nontronite due to reduction. These research findings indicate that Sb can be effectively immobilized by Al-rich phases. The increase in Sb(V) uptake in response to reducing structural Fe in clay can be important in natural settings since Fe-rich clays commonly go through oxidation-reduction cycles in response to changing redox conditions.

摘要

我们通过批量实验研究了富铝相——水合氧化铝(HAO)、高岭石(KGa-1b)和氧化还原型钠蒙脱石(NAu-1)对 Sb(III)和 Sb(V)的固定化作用,以确定其吸附容量和吸附动力学,并采用扩展 X 射线吸收精细结构(EXAFS)光谱来表征吸附 Sb 的分子环境。Sb(III)和 Sb(V)均以内圈络合的方式被吸附在研究基质的表面上。观察到的吸附几何形状主要是双齿顶角共享,有些是单齿络合物。吸附动力学相对较慢(约几天),平衡吸附等温线最适合用 Freundlich 模型拟合。非蒙脱石中结构 Fe 的氧化态影响吸附容量:如果粘土被还原,Sb(III)的吸附容量略有降低,而 Sb(V)的吸附量则显著增加。这可能是由于还原型非蒙脱石悬浮液中存在溶解的 Fe(II),或者与还原导致的非蒙脱石结构重排有关。这些研究结果表明,Sb 可以被富铝相有效地固定化。粘土中结构 Fe 的还原导致 Sb(V)的吸收增加,这在自然环境中可能很重要,因为富含 Fe 的粘土通常会随着氧化还原条件的变化而经历氧化还原循环。

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