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铊吸附于锰氧化物。

Thallium Sorption onto Manganese Oxides.

机构信息

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

Institute of Biogeochemistry and Pollutant Dynamics , ETH Zürich , CH-8092 Zürich , Switzerland.

出版信息

Environ Sci Technol. 2019 Nov 19;53(22):13168-13178. doi: 10.1021/acs.est.9b04454. Epub 2019 Nov 1.

DOI:10.1021/acs.est.9b04454
PMID:31674774
Abstract

The sorption of thallium (Tl) onto manganese (Mn) oxides critically influences its environmental fate and geochemical cycling and is also of interest in water treatment. Combined quantitative and mechanistic understanding of Tl sorption onto Mn oxides, however, is limited. We investigated the uptake of dissolved Tl(I) by environmentally relevant phyllo- and tectomanganates and used X-ray absorption spectroscopy to determine the oxidation state and local coordination of sorbed Tl. We show that extremely strong sorption of Tl onto vacancy-containing layered δ-MnO at low dissolved Tl(I) concentrations (log ≥ 7.4 for ≤10 M Tl(I); in (L/kg)) is due to oxidative uptake of Tl and that less specific nonoxidative Tl uptake only becomes dominant at very high Tl(I) concentrations (>10 M). Partial reduction of δ-MnO induces phase changes that result in inhibited oxidative Tl uptake and lower Tl sorption affinity (log 6.2-6.4 at 10 M Tl(I)) and capacity. Triclinic birnessite, which features no vacancy sites, and todorokite, a 3 × 3 tectomanganate, bind Tl with lower sorption affinity than δ-MnO, mainly as hydrated Tl in interlayers (triclinic birnessite; log 5.5 at 10 M Tl(I)) or tunnels (todorokite). In cryptomelane, a 2 × 2 tectomanganate, dehydrated Tl replaces structural K. The new quantitative and mechanistic insights from this study contribute to an improved understanding of the uptake of Tl by key Mn oxides and its relevance in natural and engineered systems.

摘要

铊(Tl)在锰(Mn)氧化物上的吸附对其环境归宿和地球化学循环具有重要影响,在水处理中也具有重要意义。然而,对于 Mn 氧化物上 Tl 吸附的综合定量和机理理解是有限的。我们研究了环境相关的层状和隧道状锰酸盐对溶解态 Tl(I)的吸收,并使用 X 射线吸收光谱确定了吸附 Tl 的氧化态和局部配位。结果表明,在低溶解态 Tl(I)浓度(≤10 M Tl(I)时,log ≥ 7.4;在 (L/kg))下,空位层状 δ-MnO 对 Tl 的极强吸附是由于 Tl 的氧化吸收,而在非常高的 Tl(I)浓度(>10 M)下,非氧化 Tl 的吸收才变得更为重要。δ-MnO 的部分还原会导致相变化,从而抑制氧化 Tl 的吸收,并降低 Tl 的吸附亲和力(在 10 M Tl(I)时,log 6.2-6.4)和容量。没有空位的三方晶系钠锰矿和 3 × 3 隧道状锰矿对 Tl 的吸附亲和力低于 δ-MnO,主要是作为层间(三方晶系钠锰矿;在 10 M Tl(I)时,log 5.5)或隧道(隧道状锰矿)中的水化 Tl 进行吸附。在 2 × 2 隧道状锰矿中,脱水 Tl 取代了结构中的 K。本研究的新的定量和机理见解有助于更好地理解关键 Mn 氧化物对 Tl 的吸收及其在自然和工程系统中的相关性。

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