Extracellular polymeric substances altered ferrihydrite (trans)formation and induced arsenic mobilization

铁酸盐 磁铁矿 麦金纳维 化学 胞外聚合物 环境化学 无机化学 化学工程 矿物学 有机化学 材料科学 地质学 冶金 吸附 古生物学 工程类 细菌 黄铁矿 生物膜
作者
Kun Gao,Shuai Wang,Wenjing Zhou,Bowei Zhang,Zhi Dang,Chongxuan Liu
出处
期刊:Journal of Hazardous Materials [Elsevier BV]
卷期号:473: 134434-134434 被引量:18
标识
DOI:10.1016/j.jhazmat.2024.134434
摘要

The behavior of As is closely related to trans(formation) of ferrihydrite , which often coprecipitates with extracellular polymeric substances (EPS), forming EPS-mineral aggregates in natural environments. While the effect of EPS on ferrihydrite properity, mineralogy reductive transformation, and associated As fate in sulfate-reducing bacteria (SRB)-rich environments remains unclear. In this research, ferrihydrite-EPS aggregates were synthesized and batch experiments combined with spectroscopic, microscopic, and geochemical analyses were conducted to address these knowledge gaps. Results indicated that EPS blocked micropores in ferrihydrite, and altered mineral surface area and susceptibility. Although EPS enhanced Fe(III) reduction, it retarded ferrihydrite transformation to magnetite by inhibiting Fe atom exchange in systems with low SO 4 2- . As a result, 16% of the ferrihydrite was converted into magnetite in the Fh-0.3 treatment, and no ferrihydrite transformation occurred in the Fh-EPS-0.3 treatment. In systems with high SO 4 2- , however, EPS promoted mackinawite formation and increased As mobilization into the solution. Additionally, the coprecipitated EPS facilitated As(V) reduction to more mobilized As(III) and decreased conversion of As into the residual phase, enhancing the potential risk of As contamination. These findings advance our understanding on biogeochemistry of elements Fe, S, and As and are helpful for accurate prediction of As behavior.
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