Luo Wensui, Gu Baohua
Environmental Sciences Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, USA.
Environ Sci Technol. 2009 Jan 1;43(1):152-6. doi: 10.1021/es8013979.
Biological reduction and precipitation of uranium (U) has been proposed as a remedial option for immobilizing uranium at contaminated sites, but the long-term stability and mobility of uranium remain a concern because the uranium is neither removed nor destroyed. In this study, the dissolution and mobilization of reduced and oxidized forms of uranium [U(IV) and U(VI)] by natural humic substances were investigated in batch and column-flow systems using a bioreduced sediment containing both U(IV) and U(VI). The addition of humic substances significantly increased the dissolution of U(IV) under anaerobic conditions. Humic acid (HA) was found to be more effective than fulvic acid (FA) in dissolving U(IV) in 1 mM KCl or KHCO3 background solution. However, more U(VI) was dissolved in 1 mM KHCO3 than in 1 mM KCl background electrolyte. HA also was found to be more effective than FA in mobilizing uranium under reducing and column-flow conditions, although the cumulative amount of eluted U(VI) and U(IV) was relatively low (<60 microg) after leaching with approximately 97 pore volumes of the humic solution in 1 mM KHCO3. These observations suggestthat natural humic substances could potentially influence the long-term stability of bioreduced U(IV) even under strongly reducing environments.
生物还原和沉淀铀(U)已被提议作为在受污染场地固定铀的一种补救选择,但铀的长期稳定性和迁移性仍然是一个问题,因为铀既未被去除也未被销毁。在本研究中,使用含有U(IV)和U(VI)的生物还原沉积物,在间歇式和柱流系统中研究了天然腐殖质对还原态和氧化态铀[U(IV)和U(VI)]的溶解和迁移作用。在厌氧条件下,添加腐殖质显著增加了U(IV)的溶解。发现在1 mM KCl或KHCO3背景溶液中,腐殖酸(HA)比富里酸(FA)在溶解U(IV)方面更有效。然而,在1 mM KHCO3中溶解的U(VI)比在1 mM KCl背景电解质中更多。在还原和柱流条件下,HA在迁移铀方面也比FA更有效,尽管在用1 mM KHCO3中的腐殖质溶液以约97个孔隙体积淋洗后,洗脱的U(VI)和U(IV)的累积量相对较低(<60微克)。这些观察结果表明,即使在强还原环境下,天然腐殖质也可能潜在地影响生物还原U(IV)的长期稳定性。