X射线吸收光谱法
针铁矿
鳞片岩
扩展X射线吸收精细结构
化学
砷
无机化学
内球面电子转移
八面体
氧化还原
协调球
X射线吸收精细结构
吸收光谱法
结晶学
吸附
物理化学
晶体结构
光谱学
离子
有机化学
物理
量子力学
作者
Sophie Thoral,Jérôme Rose,Jérémie Garnier,Alexander van Geen,Philippe Refait,A. Traverse,Emiliano Fonda,D. Nahon,Jean-Yves Bottero
摘要
The speciation of As and Fe was studied during the oxidation of Fe(II)-As(III) solutions by combining XAS analysis at both the Fe and As K-edges. Fe(II) and As(III) were first hydrolyzed to pH 7 under anoxic conditions; the precipitate was then allowed to oxidize in ambient air for 33 h under vigorous stirring. EXAFS analysis at the As K-edge shows clear evidence of formation of inner-sphere complexes between As(III) and Fe(II), i.e., before any oxidation. Inner-sphere complexes were also observed when Fe became sufficiently oxidized, in the form of edge-sharing and double-corner linkages between AsIIIO3 pyramids and FeIIIO6 octahedra. XAS analyses at the Fe K-edge reveal that the presence of As(III) in the solution limits the polymerization of Fe(II) and the formation of green rust and inhibits the formation of goethite and lepidocrocite. Indeed, As(III) accelerates the Fe(II) oxidation kinetics and leads to the formation of nanosized Fe-As subunits of amorphous aggregates. These observations, rather than a presumed weaker affinity of As(III) for iron oxyhydroxides, might explain why As(III) is more difficult to remove than As(V) by aerating reducing groundwater.
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