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

机译:Mn(Ⅱ)与六方水钠锰矿之间的氧化还原反应改变其层对称性

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摘要

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-MnO_2 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.
机译:水钠锰矿,一种页锰锰酸盐,也是最常见的Mn氧化物类型,会影响自然界中许多污染物和营养物的命运和运输。水钠锰矿表现出六边形(HexLayBir)或正交(OrthLayBir)层对称性。两种类型的水钠锰矿具有相反的层空位含量和Mn(Ⅲ)含量,因此具有不同的吸附和氧化能力。 OrthLayBir可以转换为HexLayBir,但仍不清楚是否以及如何进行反向转换。在这里,我们显示了在低Mn(Ⅱ)/ Mn(HexLayBir)摩尔比(5-24%)和pH≥pH≥ 8.较高的pH值,较小的粒径和/或更大的HexLayBir堆积异常促进了转化。该转变归因于吸附在空位上的Mn(Ⅱ)与周围层Mn(Ⅳ)之间的相称反应形成Mn(Ⅲ),随后Mn(Ⅲ)迁移到空位中并有序分布水钠锰矿层。研究表明,Mn(Ⅱ)水溶液和pH是控制水钠锰矿层结构和环境反应性的关键环境因素。

著录项

  • 来源
    《Environmental Science & Technology》 |2016年第4期|1750-1758|共9页
  • 作者单位

    Key Laboratory of Arable Land Conservation (Middle and Lower Reaches of Yangtse River), Ministry of Agriculture, College of Resources and Environment, Huazhong Agricultural University, Wuhan 430070, China;

    Department of Ecosystem Science and Management, University of Wyoming, Laramie, Wyoming 82071, United States;

    Key Laboratory of Surficial Geochemistry, Ministry of Education, School of Earth Sciences and Engineering, Nanjing University, Nanjing 210093, China,Environmental Soil Chemistry Group, Delaware Environmental Institute and Department of Plant and Soil Sciences, University of Delaware, Newark, Delaware 19716, United States;

    Department of Earth & Environmental Sciences, Rutgers University, Newark, New Jersey 07102, United States;

    Geochemistry Department, Geology Institute, Universidad Nacional Autonoma de Mexico (UNAM), Mexico, D.F. 04510, Mexico;

    Key Laboratory of Arable Land Conservation (Middle and Lower Reaches of Yangtse River), Ministry of Agriculture, College of Resources and Environment, Huazhong Agricultural University, Wuhan 430070, China;

    Beijing Synchrotron Radiation Facility, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100039, China;

    Key Laboratory of Arable Land Conservation (Middle and Lower Reaches of Yangtse River), Ministry of Agriculture, College of Resources and Environment, Huazhong Agricultural University, Wuhan 430070, China,Environmental Soil Chemistry Group, Delaware Environmental Institute and Department of Plant and Soil Sciences, University of Delaware, Newark, Delaware 19716, United States;

    Environmental Soil Chemistry Group, Delaware Environmental Institute and Department of Plant and Soil Sciences, University of Delaware, Newark, Delaware 19716, United States;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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  • 入库时间 2022-08-17 13:58:42

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