The environmental mobility of antimony (Sb) is controlled by interactions with iron (Fe) oxides, such as ferrihydrite. Under near-neutral pH conditions, Fe(II) catalyzes the transformation of ferrihydrite to more stable phases, thereby potentially altering the partitioning and speciation of associated Sb. Although largely unexplored, Sb itself may also influence ferrihydrite transformation pathways. Here, we investigated the impact of Sb on the Fe(II)-induced transformation of ferrihydrite at pH 7 across a range of Sb(V) loadings (Sb:Fe(III) molar ratios of 0, 0.003, 0.016, and 0.08). At low and medium Sb loadings, Fe(II) induced rapid transformation of ferrihydrite to goethite, with some lepidocrocite forming as an intermediate phase. In contrast, the highest Sb:Fe(III) ratio inhibited lepidocrocite formation, decreased the extent of goethite formation, and instead resulted in substantial formation of feroxyhyte, a rarely reported FeOOH polymorph. At all Sb loadings, the transformation of ferrihydrite was paralleled by a decrease in aqueous and phosphate-extractable Sb concentrations. Extended X-ray absorption fine structure spectroscopy showed that this Sb immobilization was attributable to incorporation of Sb into Fe(III) octahedral sites of the neo-formed minerals. Our results suggest that Fe oxide transformation pathways in Sb-contaminated systems may strongly differ from the well-known pathways under Sb-free conditions.
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http://dx.doi.org/10.1021/acs.est.0c08660 | DOI Listing |
Sci Total Environ
January 2025
School of Environment and Energy, South China University of Technology, Guangzhou 510006, China.
The efficacy of ferrihydrite in remediating Cd-contaminated soil is tightly regulated by Fe(II)-induced mineralogical transformations. Despite the common coexistence of iron minerals such as goethite and lepidocrocite, which can act as templates for secondary mineral formation, the impact of these minerals on Fe(II)-induced ferrihydrite transformation and the associated Cd fate have yet to be elucidated. Herein, we investigated the simultaneous evolution of secondary minerals and Cd speciation during Fe(II)-induced ferrihydrite transformation in the presence of goethite versus lepidocrocite.
View Article and Find Full Text PDFJ Environ Manage
January 2025
School of Environmental Science and Engineering, Guangdong University of Technology, Guangzhou 510006, China. Electronic address:
Naturally widespread ferrihydrite is unstable and often coexists with complex ions, such as the heavy metal ion Pb(II). Ferrihydrite could fix Pb(II) by precipitation and hydroxyl adsorption, but release Pb(II) with mineral aging. Gallic acid plays an important role in influencing the geochemical behavior of ferrihydrite-Pb, and anoxia is one of the factors influencing the transformation of mineral.
View Article and Find Full Text PDFSci Total Environ
December 2024
State Environmental Protection Key Laboratory of Environmental Risk Assessment and Control on Chemical Process, School of Resource and Environmental Engineering, East China University of Science and Technology, Shanghai 200237, China.
Nanoplastics (NPs) have been found in natural environments. However, the sequestration of NPs and natural organic matter (NOM) coupled with the Fe(III) hydrolysis and subsequent iron oxides transformation remains unclear. Here, we investigated the behaviors of NPs during the dynamic transformation process of iron oxides in the presence of humic acids (HA).
View Article and Find Full Text PDFEnviron Pollut
December 2024
Key Laboratory of Arable Land Conservation (Middle and Lower Reaches of Yangtse River), Ministry of Agriculture and Rural Affairs, College of Resources and Environment, Huazhong Agricultural University, Wuhan, 430070, China; Hubei Key Laboratory of Soil Environment and Pollution Remediation, College of Resources and Environment, Wuhan, 430070, China. Electronic address:
Organoarsenicals are toxic pollutants of global concern, and their environmental geochemical behavior might be greatly controlled by iron (Fe) (hydr)oxides through coprecipitation, which is rarely investigated. Here, the effects of the incorporation of dimethylarsenate (DMAs(V)), a typical organoarsenical, into the ferrihydrite (Fh) structure on the mineral physicochemical properties and Fe(II)-induced phase transformation of DMAs(V)-Fh coprecipitates with As/Fe molar ratios up to 0.0876 ± 0.
View Article and Find Full Text PDFEnviron Pollut
December 2024
State Environmental Protection Key Laboratory of Integrated Surface Water-Groundwater Pollution Control, School of Environmental Science and Engineering, Southern University of Science and Technology, Shenzhen, 518055, China.
The sulfate-reducing bacteria (SRB)-induced ferrihydrite transformation is an important cause for arsenic (As) contamination in the aquifer near mining area. Calcium carbonate (CaCO) is widespread and has the potential of regulating As fate directly or indirectly. However, the influence of CaCO on ferrihydrite transformation and the associated As mobilization/redistribution in SRB-containing environments remains unclear.
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