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腐殖酸在缺氧条件下对钠锰矿的结构转化。

Structural Transformation of Birnessite by Fulvic Acid under Anoxic Conditions.

机构信息

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

出版信息

Environ Sci Technol. 2018 Feb 20;52(4):1844-1853. doi: 10.1021/acs.est.7b04379. Epub 2018 Feb 7.

Abstract

The structure and Mn(III) concentration of birnessite dictate its reactivity and can be changed by birnessite partial reduction, but effects of pH and reductant/birnessite ratios on the changes by reduction remain unclear. We found that the two factors strongly affect the structure of birnessite (δ-MnO) and its Mn(III) content during its reduction by fulvic acid (FA) at pH 4-8 and FA/solid mass ratios of 0.01-10 under anoxic conditions over 600 h. During the reduction, the structure of δ-MnO is increasingly accumulated with both Mn(III) and Mn(II) but much more with Mn(III) at pH 8, whereas the accumulated Mn is mainly Mn(II) with little Mn(III) at pH 4 and 6. Mn(III) accumulation, either in layers or over vacancies, is stronger at higher FA/solid ratios. At FA/solid ratios ≥1 and pH 6 and 8, additional hausmannite and MnOOH phases form. The altered birnessite favorably adsorbs FA because of the structural accumulation of Mn(II, III). Like during microbially mediated oxidative precipitation of birnessite, the dynamic changes during its reduction are ascribed to the birnessite-Mn(II) redox reactions. Our work suggests low reactivity of birnessite coexisting with organic matter and severe decline of its reactivity by partial reduction in alkaline environment.

摘要

钠锰矿的结构和 Mn(III)浓度决定了其反应活性,并且可以通过钠锰矿的部分还原来改变,但还原过程中 pH 和还原剂/钠锰矿比例对结构变化的影响仍不清楚。我们发现,在缺氧条件下,pH 值为 4-8,FA/固体质量比为 0.01-10 时,这两个因素强烈影响了腐殖酸(FA)还原钠锰矿(δ-MnO)时的结构及其 Mn(III)含量,反应时间超过 600 h。在还原过程中,δ-MnO 的结构随着 Mn(III)和 Mn(II)的积累而增加,但在 pH 值为 8 时,随着 Mn(III)的积累更多,而在 pH 值为 4 和 6 时,积累的 Mn 主要是 Mn(II),只有少量的 Mn(III)。在较高的 FA/固体质量比下,Mn(III)在层间或空位处的积累更强。在 FA/固体质量比≥1 和 pH 值为 6 和 8 时,会形成水钠锰矿和 MnOOH 相。由于 Mn(II, III)的结构积累,改性钠锰矿有利于 FA 的吸附。与微生物介导的钠锰矿氧化沉淀过程相似,还原过程中的动态变化归因于钠锰矿-Mn(II)的氧化还原反应。我们的工作表明,在碱性环境中,与有机物共存的钠锰矿反应活性较低,部分还原会导致其反应活性严重下降。

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