Department of Chemistry, Colorado State University , 1872 Campus Delivery, Fort Collins, Colorado 80523, United States.
Environ Sci Technol. 2014 Dec 16;48(24):14326-34. doi: 10.1021/es5037496. Epub 2014 Nov 24.
Uranium (U) and arsenic (As) often occur together naturally and, as a result, can be co-contaminants at sites of uranium mining and processing, yet few studies have examined the simultaneous redox dynamics of U and As. This study examines the influence of arsenate (As(V)) on the reduction of uranyl (U(VI)) by the redox-active mineral mackinawite (FeS). As(V) was added to systems containing 47 or 470 μM U(VI) at concentrations ranging from 0 to 640 μM. In the absence of As(V), U was completely removed from solution and fully reduced to nano-uraninite (nano-UO2). While the addition of As(V) did not reduce U uptake, at As(V) concentrations above 320 μM, the reduction of U(VI) was limited due to the formation of a trögerite-like uranyl arsenate precipitate. The presence of U also significantly inhibited As(V) reduction. While less U(VI) reduction to nano-UO2 may take place in systems with high As(V) concentrations, formation of trögerite-like mineral phases may be an acceptable reclamation end point due to their high stability under oxic conditions.
铀 (U) 和砷 (As) 通常在自然界中同时存在,因此可能是铀矿开采和加工地点的共同污染物,但很少有研究同时考察 U 和 As 的氧化还原动力学。本研究考察了砷酸盐 (As(V)) 对还原性矿物黄铁矿 (FeS)还原铀酰 (U(VI)) 的影响。在含有 47 或 470 μM U(VI)的体系中添加 As(V),浓度范围为 0 至 640 μM。在没有 As(V)的情况下,U 完全从溶液中去除并完全还原为纳米铀矿 (nano-UO2)。虽然添加 As(V)并没有减少 U 的摄取量,但当 As(V)浓度高于 320 μM 时,由于形成类似于 Troegerite 的铀砷酸盐沉淀物,U(VI)的还原受到限制。U 的存在也显著抑制了 As(V)的还原。虽然在高 As(V)浓度的系统中,U(VI)还原为纳米-UO2 的量可能会减少,但形成类似于 Troegerite 的矿物相可能是一种可接受的复垦终点,因为它们在氧化条件下具有很高的稳定性。