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碳酸氢根、钙和pH值对五价砷和六价铀混合物反应活性的影响。

Effect of Bicarbonate, Calcium, and pH on the Reactivity of As(V) and U(VI) Mixtures.

作者信息

Gonzalez-Estrella Jorge, Meza Isabel, Burns Annie Jane, Ali Abdul-Mehdi S, Lezama-Pacheco Juan S, Lichtner Peter, Shaikh Nabil, Fendorf Scott, Cerrato José M

机构信息

Department of Civil, Construction and Environmental Engineering, University of New Mexico, MSC01 1070, Albuquerque, New Mexico 87131, United States.

Center for Water and the Environment, University of New Mexico, Albuquerque, New Mexico 87131, United States.

出版信息

Environ Sci Technol. 2020 Apr 7;54(7):3979-3987. doi: 10.1021/acs.est.9b06063. Epub 2020 Mar 23.

Abstract

Natural or anthropogenic processes can increase the concentration of uranium (U) and arsenic (As) above the maximum contaminant levels in water sources. Bicarbonate and calcium (Ca) can have major impacts on U speciation and can affect the reactivity between U and As. We therefore investigated the reactivity of aqueous U and As mixtures with bicarbonate and Ca for acidic and neutral pH conditions. In experiments performed with 1 mM U and As mixtures, 10 mM Ca, and without added bicarbonate (pCO = 3.5), aqueous U decreased to <0.25 mM at pH 3 and 7. Aqueous As decreased the most at pH 3 (∼0.125 mM). Experiments initiated with 0.005 mM As and U showed similar trends. X-ray spectroscopy (i.e., XAS and EDX) and diffraction indicated that U-As-Ca- and U-Ca-bearing solids resemble uranospinite [Ca(UO)(AsO)·10HO] and becquerelite [Ca(UO)O(OH)·8(HO)]. These findings suggest that U-As-Ca-bearing solids formed in mixed solutions are stable at pH 3. However, the dissolution of U-As-Ca and U-Ca-bearing solids at pH 7 was observed in reactors containing 10 mM bicarbonate and Ca, suggesting a kinetic reaction of aqueous uranyl-calcium-carbonate complexation. Our study provides new insights regarding U and As mobilization for risk assessment and remediation strategies.

摘要

自然或人为过程会使水源中铀(U)和砷(As)的浓度升高至超过最大污染物水平。碳酸氢根和钙(Ca)会对铀的形态产生重大影响,并能影响铀与砷之间的反应活性。因此,我们研究了在酸性和中性pH条件下,含铀和砷的水溶液混合物与碳酸氢根和钙的反应活性。在用1 mM铀和砷混合物、10 mM钙且未添加碳酸氢根(pCO = 3.5)进行的实验中,在pH 3和7时,水溶液中的铀降至<0.25 mM。水溶液中的砷在pH 3时下降最多(约0.125 mM)。以0.005 mM砷和铀开始的实验显示出类似趋势。X射线光谱法(即XAS和EDX)及衍射表明,含U-As-Ca和U-Ca的固体类似于水砷铀矿[Ca(UO₂)(AsO₄)·10H₂O]和板铅铀矿[Ca(UO₂)₂O(OH)₂·8(H₂O)]。这些发现表明,混合溶液中形成的含U-As-Ca的固体在pH 3时是稳定的。然而,在含有10 mM碳酸氢根和钙的反应器中,观察到含U-As-Ca和U-Ca的固体在pH 7时溶解,这表明存在水合铀酰-钙-碳酸络合的动力学反应。我们的研究为铀和砷的迁移在风险评估和修复策略方面提供了新的见解。

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