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1.
Sci Total Environ ; 946: 174406, 2024 Oct 10.
Artículo en Inglés | MEDLINE | ID: mdl-38964395

RESUMEN

The remediation of groundwater subject to in situ leaching (ISL) for uranium mining has raised extensive concerns in uranium mill and milling. This study conducted bioremediation through biostimulation and bioaugmentation to the groundwater in an area in northern China that was contaminated due to uranium mining using the CO2 + O2 neutral ISL (NISL) technology. It identified the dominant controlling factors and mechanisms driving bioremediation. Findings indicate that microorganisms can reduce the uranium concentration in groundwater subject to NISL uranium mining to its normal level. After 120 days of bioaugmentation, the uranium concentration in the contaminated groundwater fell to 0.36 mg/L, achieving a remediation efficiency of 91.26 %. Compared with biostimulation, bioaugmentation shortened the remediation timeframe by 30 to 60 days while maintaining roughly the same remediation efficiency. For groundwater remediation using indigenous microbial inoculants, initial uranium concentration and low temperatures (below 15 °C) emerge as the dominant factors influencing the bioremediation performance and duration. In settings with high carbonate concentrations, bioremediation involved the coupling of multiple processes including bioreduction, biotransformation, biomineralization, and biosorption, with bioreduction assuming a predominant role. Post-bioremediation, the relative abundances of reducing microbes Desulfosporosinus and Sulfurospirillum in groundwater increased significantly by 10.56 % and 6.91 %, respectively, offering a sustainable, stable biological foundation for further bioremediation of groundwater.


Asunto(s)
Biodegradación Ambiental , Agua Subterránea , Uranio , Contaminantes Radiactivos del Agua , Agua Subterránea/química , Uranio/metabolismo , China , Contaminantes Radiactivos del Agua/metabolismo , Contaminantes Radiactivos del Agua/análisis , Minería
2.
Environ Sci Technol ; 58(28): 12674-12684, 2024 Jul 16.
Artículo en Inglés | MEDLINE | ID: mdl-38965983

RESUMEN

Although natural attenuation is an economic remediation strategy for uranium (U) contamination, the role of organic molecules in driving U natural attenuation in postmining aquifers is not well-understood. Groundwaters were sampled to investigate the chemical, isotopic, and dissolved organic matter (DOM) compositions and their relationships to U natural attenuation from production wells and postmining wells in a typical U deposit (the Qianjiadian U deposit) mined by neutral in situ leaching. Results showed that Fe(II) concentrations and δ34SSO4 and δ18OSO4 values increased, but U concentrations decreased significantly from production wells to postmining wells, indicating that Fe(III) reduction and sulfate reduction were the predominant processes contributing to U natural attenuation. Microbial humic-like and protein-like components mediated the reduction of Fe(III) and sulfate, respectively. Organic molecules with H/C > 1.5 were conducive to microbe-mediated reduction of Fe(III) and sulfate and facilitated the natural attenuation of dissolved U. The average U attenuation rate was -1.07 mg/L/yr, with which the U-contaminated groundwater would be naturally attenuated in approximately 11.2 years. The study highlights the specific organic molecules regulating the natural attenuation of groundwater U via the reduction of Fe(III) and sulfate.


Asunto(s)
Agua Subterránea , Minería , Uranio , Contaminantes Radiactivos del Agua , Agua Subterránea/química , Contaminantes Radiactivos del Agua/análisis , Compuestos Orgánicos , Isótopos , Biodegradación Ambiental , Sulfatos
3.
J Environ Radioact ; 277: 107463, 2024 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-38815432

RESUMEN

Seepage of uranium tailings has become a focus of attention in the uranium mining and metallurgy industry, and in-situ microbial remediation is considered an effective way to treat uranium pollution. However, this method has the drawbacks of easy biomass loss and unstable remediation effect. To overcome these issues, spare red soil around the uranium mine was used to enhance the efficiency and stability of bioremediation. Furthermore, the bioremediation mechanism was revealed by employing XRD, FTIR, XPS, and 16S rRNA. The results showed that red soil, as a barrier material, had the adsorption potential of 8.21-148.00 mg U/kg soil, but the adsorption is accompanied by the release of certain acidic and oxidative substances. During the dynamic microbial remediation, red soil was used as a cover material to neutralize acidity, provide a higher reduction potential (<-200 mV), and increase the retention rate of microbial agent (19.06 mL/d) compared to the remediation group without red soil. In the presence of red soil, the anaerobic system could maintain the uranium concentration in the solution below 0.3 mg/L for more than 70 days. Moreover, the generation of new clay minerals driven by microorganisms was more conducive to the stability of uranium tailings. Through alcohol and amino acid metabolism of microorganisms, a reducing environment with reduced valence states of multiple elements (such as S2-, Fe2+, and U4+) was formed. At the same time, the relative abundance of functional microbial communities in uranium tailings improved in presence of red soil and Desulfovirobo, Desulfocapsa, Desulfosporosinus, and other active microbial communities reconstructed the anaerobic environment. The study provides a new two-in-one solution for treatment of uranium tailings and resource utilization of red soil through in-situ microbial remediation.


Asunto(s)
Biodegradación Ambiental , Minería , Microbiología del Suelo , Contaminantes Radiactivos del Suelo , Uranio , Uranio/metabolismo , Contaminantes Radiactivos del Suelo/metabolismo , Suelo/química , Restauración y Remediación Ambiental/métodos
4.
Water Res ; 233: 119778, 2023 Apr 15.
Artículo en Inglés | MEDLINE | ID: mdl-36871383

RESUMEN

Zerovalent iron [Fe(0)] can donate electron for bioprocess, but microbial uranium (VI) [U(VI)] reduction driven by Fe(0) is still poorly understood. In this study, Fe(0) supported U(VI) bio-reduction was steadily achieved in the 160-d continuous-flow biological column. The maximum removal efficiency and capacity of U(VI) were 100% and 46.4 ± 0.52 g/(m3·d) respectively, and the longevity of Fe(0) increased by 3.09 times. U(VI) was reduced to solid UO2, while Fe(0) was finally oxidized to Fe(III). Autotrophic Thiobacillus achieved U(VI) reduction coupled to Fe(0) oxidation, verified by pure culture. H2 produced from Fe(0) corrosion was consumed by autotrophic Clostridium for U(VI) reduction. The detected residual organic intermediates were biosynthesized with energy released from Fe(0) oxidation and utilized by heterotrophic Desulfomicrobium, Bacillus and Pseudomonas to reduce U(VI). Metagenomic analysis found the upregulated genes for U(VI) reduction (e.g., dsrA and dsrB) and Fe(II) oxidation (e.g., CYC1 and mtrA). These functional genes were also transcriptionally expressed. Cytochrome c and glutathione responsible for electron transfer also contributed to U(VI) reduction. This study reveals the independent and synergistic pathways for Fe(0)-dependent U(VI) bio-reduction, providing promising remediation strategy for U(VI)-polluted aquifers.


Asunto(s)
Hierro , Uranio , Hierro/metabolismo , Oxidación-Reducción , Transporte de Electrón , Citocromos c/metabolismo
5.
J Hazard Mater ; 165(1-3): 441-6, 2009 Jun 15.
Artículo en Inglés | MEDLINE | ID: mdl-19022579

RESUMEN

The effects of aquatic sediment concentrations, grain size distribution and hydrodynamic conditions on sorption behavior of phenanthrene (PHE) on sediments collected from Yangtze River (Wuhan catchment) were investigated. The results showed that the sorption behavior of PHE was mainly affected by the organic carbon in different phases, i.e. organic carbon contents (f(oc)) (w/w, organic carbon/dry weight sediment) in the sediments and dissolved organic carbon (DOC) in liquid phase. In this study, sediments were subjected to artificial resuspension under turbulent diffusion coefficients being 24.6, 29.5 and 46.2 cm(2)s(-1) corresponded to 0.4, 0.3 and 0.2 s cycle(-1) of the perforated grids, respectively, which were driven by variable speed motor with 150, 180 and 280 rotation per minute (rpm). The suspended particle concentration increased from 1.01 to 6.70 g L(-1) as the hydrodynamic strength increased from 150 to 280 rpm, whereas PHE concentration in liquid phase decreased from 0.56 to 0.34 microg mL(-1). The amount of DOC was supposed to play an important role in the partition of PHE under hydrodynamic conditions. Moreover, a sorption dynamic model was developed based on the linear isotherm expression and law of conservation of mass. The model was validated by PHE sorption behavior acquired with three different hydrodynamic conditions and the predicted values displayed satisfying accordance with experimental data.


Asunto(s)
Sedimentos Geológicos/análisis , Fenantrenos/análisis , Ríos/química , Adsorción , Carbono , China , Contaminantes Ambientales/análisis , Agua/análisis , Movimientos del Agua
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