posted on 2016-01-08, 00:00authored byHuaiyan Zhao, Mengqiang Zhu, Wei Li, Evert J. Elzinga, Mario Villalobos, Fan Liu, Jing Zhang, Xionghan Feng, Donald L. Sparks
Birnessite, a phyllomanganate and
the most common type of Mn oxide,
affects the fate and transport of numerous contaminants and nutrients
in nature. Birnessite exhibits hexagonal (HexLayBir) or orthogonal
(OrthLayBir) layer symmetry. The two types of birnessite contain contrasting
content of layer vacancies and Mn(III), and accordingly have different
sorption and oxidation abilities. OrthLayBir can transform to HexLayBir,
but it is still vaguely understood if and how the reverse transformation
occurs. Here, we show that HexLayBir (e.g., δ-MnO2 and acid birnessite) transforms to OrthLayBir after reaction with
aqueous Mn(II) at low Mn(II)/Mn (in HexLayBir) molar ratios (5–24%)
and pH ≥ 8. The transformation is promoted by higher pH values,
as well as smaller particle size, and/or greater stacking disorder
of HexLayBir. The transformation is ascribed to Mn(III) formation
via the comproportionation reaction between Mn(II) adsorbed on vacant
sites and the surrounding layer Mn(IV), and the subsequent migration
of the Mn(III) into the vacancies with an ordered distribution in
the birnessite layers. This study indicates that aqueous Mn(II) and
pH are critical environmental factors controlling birnessite layer
structure and reactivity in the environment.