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• W2059358466 abstract "It is well known that As(III) has a higher mobility compared to As(V) in the environment. This fact is explained by the high reversibility of As(III) adsorption on minerals such as Al (hydr)oxides. Nevertheless, experimental results pointed out that adsorption of As(III) leads to inner-sphere complexes, which appears to be in conflict with the high mobility of these species as inner-sphere complexes should be strongly attached. In this work we used density functional methods and cluster models to study two different mechanisms for the H3AsO3 adsorption on gibbsite-γ-Al(OH)3, one of the most abundant aluminum hydroxide minerals. Our results show that, differently from the As(V) case, As(III) is not adsorbed via an acid/base, but by a non-dissociative mechanism in which O–H bonds are not being broken. This non-dissociative mechanism also conciliates the high remobilization of As(III) with the apparently inconsistent formation of inner-sphere adsorption complexes." @default.
• W2059358466 created "2016-06-24" @default.
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• W2059358466 date "2006-04-01" @default.
• W2059358466 modified "2023-09-27" @default.
• W2059358466 title "Structural model of arsenic(III) adsorbed on gibbsite based on DFT calculations" @default.
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• W2059358466 doi "https://doi.org/10.1016/j.theochem.2005.08.038" @default.
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