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The role of natural Fe(II)-bearing minerals in chemoautotrophic chromium (VI) bio-reduction in groundwater
被引:78
|作者:
Lu, Jianping
[1
]
Zhang, Baogang
[1
]
He, Chao
[1
]
Borthwick, Alistair G. L.
[2
,3
]
机构:
[1] China Univ Geosci Beijing, Sch Water Resources & Environm, MOE Key Lab Groundwater Circulat & Environm Evolu, Beijing 100083, Peoples R China
[2] St Edmund Hall,Queens Lane, Oxford OX1 4AR, England
[3] Univ Edinburgh, Sch Engn, Kings Bldg, Edinburgh EH9 3JL, Midlothian, Scotland
基金:
中国国家自然科学基金;
关键词:
Chromium (VI);
Bio-reduction;
Fe(II)-bearing minerals;
Mackinawite;
HEXAVALENT CHROMIUM;
ELECTRON-TRANSFER;
CR(VI) REMOVAL;
PYRITE;
OXIDATION;
MACKINAWITE;
CHROMATE;
BACTERIA;
CARBON;
MICROORGANISMS;
D O I:
10.1016/j.jhazmat.2019.121911
中图分类号:
X [环境科学、安全科学];
学科分类号:
08 ;
0830 ;
摘要:
To date, comparatively little is known about the role of natural Fe(II)-bearing minerals in bioremediation of chromium (VI) contaminated aquifers subject to chemoautotrophic conditions. This work employed four kinds of Fe(II)-bearing minerals (pyrite, mackinawite, wustite, and magnetite) as inorganic electron donors to support Cr (VI) bio-reduction. In batch experiments, mackinawite (FeS) performed best, with Cr(VI) removal efficiency of 98.1 +/- 1.21 % in 96 h. Continuous column experiments lasting 180 d implied that groundwater chemistry and hydrodynamics influenced the Cr(VI) removal process. A breakthrough study suggested that biotic and abiotic contributions to Cr(VI) reduction were 76.0 +/- 1.12 % and 24.1 +/- 1.43 %, respectively. Cr(VI) was reduced to insoluble Cr(III), whereas Fe(II) and S(-II) in mackinawite were finally oxidized to Fe(III) and sulfate. Mackinawite evolved progressively into pyrrhotite. High-throughput 16S rRNA gene sequencing indicated that mackinawite-driven Cr(VI) reduction was mediated through synergistic interactions of microbial consortia; i.e. autotrophs as Acidovorax synthesized volatile fatty acids as metabolic intermediates, which were consumed by Cr(VI) reducers as Geobacter. Genes encoding enzymes for S oxidation (soxB) and Cr(VI) reduction (chrA, yieF) were upregulated. Cytochrome c participating in Fe(II) oxidation increased significantly. This work advances the development of sustainable techniques for Cr(VI) polluted groundwater remediation.
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