Photochemical Formation and Transformation of Birnessite: Effects of Cations on Micromorphology and Crystal Structure
Journal Article
·
· Environmental Science and Technology
- Huazhong Agricultural Univ., Wuhan (China); Univ of Connecticut
- Huazhong Agricultural Univ., Wuhan (China)
- Univ. of Connecticut, Storrs, CT (United States)
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 Mn2+aq 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 Mn2+aq was oxidized to birnessite by superoxide radicals (O2•–) generated from the photolysis of NO3– 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. Finally, this study suggests that interlayer cations and Mn2+ play essential roles in the photochemical formation and transformation of birnessite in aqueous environments.
- Research Organization:
- Univ. of Connecticut, Storrs, CT (United States)
- Sponsoring Organization:
- Fok Ying-Tong Education Foundation; National Key Research and Development Program of China; National Natural Science Foundation of China (NNSFC); USDOE Office of Science (SC), Basic Energy Sciences (BES). Chemical Sciences, Geosciences & Biosciences Division
- Grant/Contract Number:
- FG02-86ER13622
- OSTI ID:
- 1598154
- Alternate ID(s):
- OSTI ID: 1539051
- Journal Information:
- Environmental Science and Technology, Journal Name: Environmental Science and Technology Journal Issue: 12 Vol. 52; ISSN 0013-936X
- Publisher:
- American Chemical Society (ACS)Copyright Statement
- Country of Publication:
- United States
- Language:
- English
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