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硝酸盐对地下生物还原区铀稳定性的影响。

Effects of nitrate on the stability of uranium in a bioreduced region of the subsurface.

机构信息

Department of Civil and Environmental Engineering, Stanford University, Stanford, California 94305, USA.

出版信息

Environ Sci Technol. 2010 Jul 1;44(13):5104-11. doi: 10.1021/es1000837.

Abstract

The effects of nitrate on the stability of reduced, immobilized uranium were evaluated in field experiments at a U.S. Department of Energy site in Oak Ridge, TN. Nitrate (2.0 mM) was injected into a reduced region of the subsurface containing high levels of previously immobilized U(IV). The nitrate was reduced to nitrite, ammonium, and nitrogen gas; sulfide levels decreased; and Fe(II) levels increased then deceased. Uranium remobilization occurred concomitant with nitrite formation, suggesting nitrate-dependent, iron-accelerated oxidation of U(IV). Bromide tracer results indicated changes in subsurface flowpaths likely due to gas formation and/or precipitate. Desorption-adsorption of uranium by the iron-rich sediment impacted uranium mobilization and sequestration. After rereduction of the subsurface through ethanol additions, background groundwater containing high levels of nitrate was allowed to enter the reduced test zone. Aqueous uranium concentrations increased then decreased. Clone library analyses of sediment samples revealed the presence of denitrifying bacteria that can oxidize elemental sulfur, H(2)S, Fe(II), and U(IV) (e.g., Thiobacillus spp.), and a decrease in relative abundance of bacteria that can reduce Fe(III) and sulfate. XANES analyses of sediment samples confirmed changes in uranium oxidation state. Addition of ethanol restored reduced conditions and triggered a short-term increase in Fe(II) and aqueous uranium, likely due to reductive dissolution of Fe(III) oxides and release of sorbed U(VI). After two months of intermittent ethanol addition, sulfide levels increased, and aqueous uranium concentrations gradually decreased to <0.1 microM.

摘要

在美国田纳西州橡树岭能源部的一个场地进行的现场实验中,评估了硝酸盐对还原态固定铀的稳定性的影响。将硝酸盐(2.0 mM)注入含有先前固定化 U(IV)的地下还原区。硝酸盐被还原为亚硝酸盐、铵和氮气;硫化物水平下降;Fe(II) 水平先增加后减少。铀的再迁移伴随着亚硝酸盐的形成,表明 U(IV)的硝酸盐依赖、铁加速氧化。溴化物示踪剂结果表明,由于气体形成和/或沉淀物,地下水流路径发生了变化。富铁沉积物对铀的解吸-吸附影响了铀的迁移和固定。通过添加乙醇使地下再次还原后,允许含有高浓度硝酸盐的背景地下水进入还原测试区。水相铀浓度先增加后减少。沉积物样品的克隆文库分析表明,存在能够氧化元素硫、H(2)S、Fe(II)和 U(IV)(例如硫杆菌属)的反硝化细菌,以及能够还原 Fe(III)和硫酸盐的细菌相对丰度减少。沉积物样品的 XANES 分析证实了铀氧化态的变化。添加乙醇恢复了还原条件,并引发了 Fe(II)和水相铀的短期增加,这可能是由于 Fe(III)氧化物的还原溶解和吸附的 U(VI)的释放。在间歇性添加乙醇两个月后,硫化物水平增加,水相铀浓度逐渐降至<0.1 microM。

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