4.8 Article

Photochemical Formation and Transformation of Birnessite: Effects of Cations on Micromorphology and Crystal Structure

Journal

ENVIRONMENTAL SCIENCE & TECHNOLOGY
Volume 52, Issue 12, Pages 6864-6871

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.7b06592

Keywords

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Funding

  1. National Natural Science Foundation of China [41571228, 41425006]
  2. National Key Research and Development Program of China [2017YFD0801000]
  3. Fok Ying-Tong Education Foundation [141024]
  4. Fundamental Research Funds for the Central Universities [2662018JC055, 2662015JQ002]
  5. US Department of Energy, Office of Basic Energy Sciences, Division of Chemical, Biological and Geological Sciences [DE-FG02-86ER13622.A000]

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As important components with excellent oxidation and adsorption activity in soils and sediments, manganese oxides affect the transportation and fate of nutrients and pollutants in natural environments. In this work, birnessite was formed by photocatalytic oxidation of Mn-aq(2+) in the presence of nitrate under solar irradiation. The effects of concentrations and species of interlayer cations (Na+, Mg2+, and K+) on birnessite crystal structure and micromorphology were investigated. The roles of adsorbed Mn2+ and pH in the transformation of the photosynthetic birnessite were further studied. The results indicated that Mn-aq(2+) was oxidized to birnessite by superoxide radicals (0(2)center dot-)generated from the photolysis of N0(3)- under UV irradiation. The particle size and thickness of birnessite decreased with increasing cation concentration. The birnessite showed a plate-like morphology in the presence of K+, while exhibited a rumpled sheet-like morphology when Na+ or Mg2+ was used. The different micromorphologies of birnessites could be ascribed to the position of cations in the interlayer. The adsorbed Mn2+ and high pH facilitated the reduction of birnessite to low-valence manganese oxides including hausmannite, feitknechtite(;) and manganite. This study suggests that interlayer cations and Mn2+ play essential roles in the photochemical formation and transformation of birnessite in aqueous environments.

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