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Title

NOM-Induced Dissolution of CrxFe1-x(OH)3Precipitates and Formation of Cr(III)-NOM-Fe Colloids under Oxic and Anoxic Conditions

Author
Corresponding AuthorLiao,Peng; Liu,Chongxuan
Publication Years
2022
DOI
Source Title
ISSN
2472-3452
EISSN
2472-3452
Abstract
Mixed Cr(III)-Fe(III) (hydr)oxides (CrxFe1-x(OH)3) are common reduction products of Cr(VI) that have long been considered as the sink of Cr in subsurface environments. While current field and laboratory studies have demonstrated that natural organic matter (NOMox) can dissolve CrxFe1-x(OH)3 under oxic conditions, much less is known regarding the dissolution of CrxFe1-x(OH)3 by reduced NOM (NOMred) and geochemical behaviors of released Cr(III) under anoxic conditions, which limited our ability to completely predict the cycle of Cr. This study provided new knowledge regarding the simultaneous dissolution of CrxFe1-x(OH)3 and formation of Cr(III)-NOM-Fe colloids by NOMox and NOMred under oxic and anoxic conditions. We showed that NOM dissolved CrxFe1-x(OH)3 via ligand-promoted dissolution under oxic conditions and reductive dissolution under anoxic conditions, releasing aqueous Cr(III) and Fe(III/II). Size fractionization results showed that the aqueous Cr(III) and Fe observed at high NOM concentration were Cr(III)-NOM-Fe colloids (ca. 3-450 nm). Dynamic light scattering results further revealed that the colloids had a particle size ranging from 79 to 167 nm and strongly negative surface charges (-40-17 mV). Cryogenic X-ray photoelectron spectroscopy and X-ray absorption fine structure measurements further indicated a close association of NOM with Cr and Fe within the particle structure. This study provides insights into the fate of CrxFe1-x(OH)3 in redox-dynamics and organic-rich environments, which is critical for evaluating the long-Term stability of Cr remediation sites.
Keywords
URL[Source Record]
Indexed By
Language
English
SUSTech Authorship
First ; Corresponding
Funding Project
[42177237] ; [2017ZT07Z479] ; [2022-217] ; [20214028]
WOS Research Area
Chemistry ; Geochemistry & Geophysics
WOS Subject
Chemistry, Multidisciplinary ; Geochemistry & Geophysics
WOS Accession No
WOS:000891585800001
Publisher
Scopus EID
2-s2.0-85143400425
Data Source
Scopus
Citation statistics
Cited Times [WOS]:0
Document TypeJournal Article
Identifierhttp://kc.sustech.edu.cn/handle/2SGJ60CL/416537
DepartmentSchool of Environmental Science and Engineering
Affiliation
1.State Environ. 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
2.State Key Laboratory of Environmental Geochemistry,Institute of Geochemistry,Chinese Academy of Sciences,Guiyang,550081,China
3.School of Environment,China University of Geosciences,Wuhan,388 Lumo Road,430074,China
First Author AffilicationSchool of Environmental Science and Engineering
Corresponding Author AffilicationSchool of Environmental Science and Engineering
First Author's First AffilicationSchool of Environmental Science and Engineering
Recommended Citation
GB/T 7714
Li,Binrui,Zhang,Shaojian,Liao,Peng,et al. NOM-Induced Dissolution of CrxFe1-x(OH)3Precipitates and Formation of Cr(III)-NOM-Fe Colloids under Oxic and Anoxic Conditions[J]. ACS Earth and Space Chemistry,2022.
APA
Li,Binrui,Zhang,Shaojian,Liao,Peng,Liu,Peng,Ye,Zhihang,&Liu,Chongxuan.(2022).NOM-Induced Dissolution of CrxFe1-x(OH)3Precipitates and Formation of Cr(III)-NOM-Fe Colloids under Oxic and Anoxic Conditions.ACS Earth and Space Chemistry.
MLA
Li,Binrui,et al."NOM-Induced Dissolution of CrxFe1-x(OH)3Precipitates and Formation of Cr(III)-NOM-Fe Colloids under Oxic and Anoxic Conditions".ACS Earth and Space Chemistry (2022).
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