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钴的生物地球化学循环研究:低温水条件下钴硫化纳米颗粒的沉淀和转化。

Insights into the Biogeochemical Cycling of Cobalt: Precipitation and Transformation of Cobalt Sulfide Nanoparticles under Low-Temperature Aqueous Conditions.

机构信息

Department of Geological Sciences, The University of Texas at El Paso, El Paso, Texas 79968, United States.

Virginia Tech National Center for Earth and Environmental Nanotechnology (NanoEarth), Blacksburg, Virginia 24061, United States.

出版信息

Environ Sci Technol. 2020 May 5;54(9):5598-5607. doi: 10.1021/acs.est.0c01363. Epub 2020 Apr 14.

DOI:10.1021/acs.est.0c01363
PMID:32243750
Abstract

Cobalt sulfide precipitates, key phases in the natural biogeochemistry of cobalt and in relevant remediation and resource recovery processes, are poorly defined under low-temperature aqueous conditions. Here, we systematically studied Co (Fe) sulfides precipitated and aged in environmentally relevant solutions, defined by different combinations of pH, initial cobalt to iron ratios ([Co]/[Fe]), with/without S, and the presence/absence of sulfate-reducing bacteria. The initial abiogenic precipitates were composed exclusively of amorphous Co sulfide nanoparticles (CoS·HO) that were stable in anoxic solution for 2 months, with estimated log values 1-5 orders of magnitude higher than that previously reported for Co sulfides. The addition of S, in combination with acidic pH and elevated temperature (60 °C), resulted in recrystallization of the amorphous precipitates into nanocrystalline jaipurite (hexagonal CoS) within 1 month. In the presence of Fe(II), the abiogenic precipitates were composed of more crystalline Co sulfides and/or Co-rich mackinawite, the exact phase being dependent on the [Co]/[Fe] value. The biogenic precipitates displayed higher crystallinity for Co sulfides (up to the formation of nanocrystalline cobalt pentlandite, CoS) and lower crystallinity for Co-rich mackinawite, suggestive of mineral-specific bacterial interaction. The revealed precipitation and transformation pathways of Co (Fe) sulfides in this study allows for a better constraint of Co biogeochemistry in various natural and engineered environments.

摘要

硫化钴沉淀是钴的自然生物地球化学以及相关修复和资源回收过程中的关键相,但在低温水相条件下其定义还不够明确。在这里,我们系统地研究了在环境相关溶液中沉淀和老化的 Co(Fe)硫化物,这些溶液由不同 pH 值、初始钴铁比([Co]/[Fe])、有无硫以及是否存在硫酸盐还原菌的组合来定义。最初的非生物沉淀仅由非晶态 Co 硫化物纳米颗粒(CoS·HO)组成,这些纳米颗粒在缺氧溶液中稳定 2 个月,其 log 值比以前报道的 Co 硫化物高 1-5 个数量级。在添加 S 的情况下,与酸性 pH 值和高温(60°C)结合,可在 1 个月内使非晶态沉淀物重新结晶成纳米晶方钴矿(六方 CoS)。在存在 Fe(II)的情况下,非生物沉淀由更具结晶度的 Co 硫化物和/或 Co 富型磁黄铁矿组成,具体相取决于[Co]/[Fe]值。生物沉淀的 Co 硫化物具有更高的结晶度(高达形成纳米晶的钴镍黄铁矿 CoS),而 Co 富型磁黄铁矿的结晶度较低,表明存在特定于矿物的细菌相互作用。本研究揭示的 Co(Fe)硫化物的沉淀和转化途径,可以更好地约束各种自然和工程环境中的钴生物地球化学。

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