Redox Reactions between Mn(II) and Hexagonal Birnessite Change Its Layer Symmetry

• Published in: Environmental science & technology Vol. 50; no. 4; pp. 1750 - 1758
• Main Authors: Zhao, Huaiyan, Zhu, Mengqiang, Li, Wei, Elzinga, Evert J, Villalobos, Mario, Liu, Fan, Zhang, Jing, Feng, Xionghan, Sparks, Donald L
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 16-02-2016; American Chemical Society (ACS)
• Subjects: Adsorption; Manganese - chemistry; Minerals; Oxidation; Oxidation-Reduction; Oxides - chemistry; Sorption; Symmetry; Water - chemistry
• ISSN: 0013-936X; 1520-5851
• DOI: 10.1021/acs.est.5b04436

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.