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六方纤锌矿矿型水钠锰矿与铊(I)反应的转化:水钠锰矿结晶度、pH 值和铊浓度的影响。

Transformation of Hexagonal Birnessite upon Reaction with Thallium(I): Effects of Birnessite Crystallinity, pH, and Thallium Concentration.

机构信息

Molecular Environmental Geochemistry Laboratory, Laboratorio Nacional de Geoquímica y Mineralogía (LANGEM), Institute of Geology, Universidad Nacional Autónoma de México (UNAM), 04510 Mexico City, México.

Eawag, Swiss Federal Institute of Aquatic Science and Technology, Überlandstrasse 133, CH-8600 Dübendorf, Switzerland.

出版信息

Environ Sci Technol. 2021 Apr 20;55(8):4862-4870. doi: 10.1021/acs.est.0c07886. Epub 2021 Mar 25.

DOI:10.1021/acs.est.0c07886
PMID:33764067
Abstract

We examined the uptake of Tl(I) by two hexagonal birnessites and related phase transformations in laboratory experiments over 12 sequential additions of 0.01 M Tl(I)/Mn at pH 4.0, 6.0, and 8.0. The Tl-reacted Mn oxides were characterized for their structure, Tl binding, and morphology using X-ray diffraction, X-ray photoelectron and X-ray absorption spectroscopies, and transmission electron microscopy. Very limited Tl oxidation was observed in contrast to previous works, where equal Tl(I)/Mn was added in a single step. Instead, both birnessites transformed into a 2 × 2 tunneled phase with dehydrated Tl(I) in its tunnels at pH 4, but only partially at pH 6, and at pH 8.0 they remained layered. The first four to nine sequential Tl(I)/Mn additions resulted in lower residual dissolved Tl concentrations than when the same amounts of Tl(I)/Mn were added in single steps. This study thus shows that the repeated reaction of hexagonal birnessites with smaller Tl(I)/Mn at ambient temperature triggers a complete phase conversion with Tl(I) as the sole reacting cation. The novel pathway found may be more relevant for contaminated environments and may help explain the formation of minerals like thalliomelane [Tl(MnCu)O]; it also points to the possibility that other reducing species trigger similar Mn oxide transformation reactions.

摘要

我们在实验室实验中研究了 Tl(I) 在两种六方纤锌矿和相关相转变中的吸收,在 pH 值为 4.0、6.0 和 8.0 下,连续添加 0.01 M Tl(I)/Mn 共 12 次。使用 X 射线衍射、X 射线光电子能谱和 X 射线吸收光谱以及透射电子显微镜对 Tl 反应的 Mn 氧化物的结构、Tl 结合和形态进行了表征。与之前的工作相比,观察到的 Tl 氧化非常有限,在之前的工作中,以单一步骤添加等量的 Tl(I)/Mn。相反,两种纤锌矿在 pH 值为 4 时都转化为具有脱水 Tl(I)的 2×2 隧道相,但在 pH 值为 6 时仅部分转化,而在 pH 值为 8 时它们仍保持层状。在前四次至第九次连续添加 Tl(I)/Mn 后,残留的溶解 Tl 浓度低于以单次步骤添加相同量的 Tl(I)/Mn 时的浓度。因此,这项研究表明,在环境温度下,六方纤锌矿与较小的 Tl(I)/Mn 的重复反应会引发完全的相转化,其中 Tl(I)是唯一的反应阳离子。发现的新途径可能与污染环境更相关,并可能有助于解释 thalliomelane [Tl(MnCu)O]等矿物的形成;它还表明其他还原物种可能引发类似的 Mn 氧化物转化反应。

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