Bioremediation of Uranium- and Nitrate-Contaminated Groundwater after the In Situ Leach Mining of Uranium
Uranium and nitrate are common groundwater pollutants near in situ leach uranium mines. However, we still lack techniques that can simultaneously immobilize uranium and reduce nitrate using a single bacterial species. In this study, the potential of simultaneous uranium immobilization and nitrate re...
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oai:doaj.org-article:ad09cd8e12e44fb686dcd6df201c4c682021-11-25T19:15:18ZBioremediation of Uranium- and Nitrate-Contaminated Groundwater after the In Situ Leach Mining of Uranium10.3390/w132231882073-4441https://doaj.org/article/ad09cd8e12e44fb686dcd6df201c4c682021-11-01T00:00:00Zhttps://www.mdpi.com/2073-4441/13/22/3188https://doaj.org/toc/2073-4441Uranium and nitrate are common groundwater pollutants near in situ leach uranium mines. However, we still lack techniques that can simultaneously immobilize uranium and reduce nitrate using a single bacterial species. In this study, the potential of simultaneous uranium immobilization and nitrate reduction by a single AFODN (anaerobic Fe(II) oxidizing denitrifier), <i>Clostridium</i> sp. PXL2, was investigated. <i>Clostridium</i> sp. PXL2 showed tolerance to U(VI) concentrations varying from 4.2 µM to 42 µM. The U(VI) immobilization and nitrate reduction rates in groundwater samples inoculated with this bacterium reached up to 75.1% and 55.7%, respectively, under neutral conditions. Exposure to oxidation conditions led to further U(VI) removal but did not show any noticeable effect on nitrate reduction. The U(VI) immobilization rate reached up to 85% with an increased Fe(II) initial concentration, but this inhibited nitrate reduction. SEM (scanning electron microscopy) coupled with EDS (energy dispersive spectroscopy) showed that the U(VI) immobilization was mainly due to sorption to amorphous ferric oxides. U(VI) and nitrate bioremediation by AFODNs, including <i>Clostridium</i> sp. PXL2, may provide a promising method for the treatment of uranium- and nitrate-contaminated groundwater after the in situ leach mining of uranium.Rehemanjiang WufuerJia DuoWenfeng LiJinglong FanXiangliang PanMDPI AGarticle<i>Clostridium</i> sp. PXL2immobilizationreductionHydraulic engineeringTC1-978Water supply for domestic and industrial purposesTD201-500ENWater, Vol 13, Iss 3188, p 3188 (2021) |
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<i>Clostridium</i> sp. PXL2 immobilization reduction Hydraulic engineering TC1-978 Water supply for domestic and industrial purposes TD201-500 |
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<i>Clostridium</i> sp. PXL2 immobilization reduction Hydraulic engineering TC1-978 Water supply for domestic and industrial purposes TD201-500 Rehemanjiang Wufuer Jia Duo Wenfeng Li Jinglong Fan Xiangliang Pan Bioremediation of Uranium- and Nitrate-Contaminated Groundwater after the In Situ Leach Mining of Uranium |
description |
Uranium and nitrate are common groundwater pollutants near in situ leach uranium mines. However, we still lack techniques that can simultaneously immobilize uranium and reduce nitrate using a single bacterial species. In this study, the potential of simultaneous uranium immobilization and nitrate reduction by a single AFODN (anaerobic Fe(II) oxidizing denitrifier), <i>Clostridium</i> sp. PXL2, was investigated. <i>Clostridium</i> sp. PXL2 showed tolerance to U(VI) concentrations varying from 4.2 µM to 42 µM. The U(VI) immobilization and nitrate reduction rates in groundwater samples inoculated with this bacterium reached up to 75.1% and 55.7%, respectively, under neutral conditions. Exposure to oxidation conditions led to further U(VI) removal but did not show any noticeable effect on nitrate reduction. The U(VI) immobilization rate reached up to 85% with an increased Fe(II) initial concentration, but this inhibited nitrate reduction. SEM (scanning electron microscopy) coupled with EDS (energy dispersive spectroscopy) showed that the U(VI) immobilization was mainly due to sorption to amorphous ferric oxides. U(VI) and nitrate bioremediation by AFODNs, including <i>Clostridium</i> sp. PXL2, may provide a promising method for the treatment of uranium- and nitrate-contaminated groundwater after the in situ leach mining of uranium. |
format |
article |
author |
Rehemanjiang Wufuer Jia Duo Wenfeng Li Jinglong Fan Xiangliang Pan |
author_facet |
Rehemanjiang Wufuer Jia Duo Wenfeng Li Jinglong Fan Xiangliang Pan |
author_sort |
Rehemanjiang Wufuer |
title |
Bioremediation of Uranium- and Nitrate-Contaminated Groundwater after the In Situ Leach Mining of Uranium |
title_short |
Bioremediation of Uranium- and Nitrate-Contaminated Groundwater after the In Situ Leach Mining of Uranium |
title_full |
Bioremediation of Uranium- and Nitrate-Contaminated Groundwater after the In Situ Leach Mining of Uranium |
title_fullStr |
Bioremediation of Uranium- and Nitrate-Contaminated Groundwater after the In Situ Leach Mining of Uranium |
title_full_unstemmed |
Bioremediation of Uranium- and Nitrate-Contaminated Groundwater after the In Situ Leach Mining of Uranium |
title_sort |
bioremediation of uranium- and nitrate-contaminated groundwater after the in situ leach mining of uranium |
publisher |
MDPI AG |
publishDate |
2021 |
url |
https://doaj.org/article/ad09cd8e12e44fb686dcd6df201c4c68 |
work_keys_str_mv |
AT rehemanjiangwufuer bioremediationofuraniumandnitratecontaminatedgroundwateraftertheinsituleachminingofuranium AT jiaduo bioremediationofuraniumandnitratecontaminatedgroundwateraftertheinsituleachminingofuranium AT wenfengli bioremediationofuraniumandnitratecontaminatedgroundwateraftertheinsituleachminingofuranium AT jinglongfan bioremediationofuraniumandnitratecontaminatedgroundwateraftertheinsituleachminingofuranium AT xiangliangpan bioremediationofuraniumandnitratecontaminatedgroundwateraftertheinsituleachminingofuranium |
_version_ |
1718410115207397376 |