NCGRT, Flinders University, Adelaide, SA 5001, Australia.
Environ Sci Technol. 2010 Jul 1;44(13):5035-41. doi: 10.1021/es100463q.
Managed Aquifer Recharge (MAR) is promoted as an attractive technique to meet growing water demands. An impediment to MAR applications, where oxygenated water is recharged into anoxic aquifers, is the potential mobilization of trace metals (e.g., arsenic). While conceptual models for arsenic transport under such circumstances exist, they are generally not rigorously evaluated through numerical modeling, especially at field-scale. In this work, geochemical data from an injection experiment in The Netherlands, where the introduction of oxygenated water into an anoxic aquifer mobilized arsenic, was used to develop and evaluate conceptual and numerical models of arsenic release and attenuation under field-scale conditions. Initially, a groundwater flow and nonreactive transport model was developed. Subsequent reactive transport simulations focused on the description of the temporal and spatial evolution of the redox zonation. The calibrated model was then used to study and quantify the transport of arsenic. In the model that best reproduced field observations, the fate of arsenic was simulated by (i) release via codissolution of arsenopyrite, stoichiometrically linked to pyrite oxidation, (ii) kinetically controlled oxidation of dissolved As(III) to As(V), and (iii) As adsorption via surface complexation on neo-precipitated iron oxides.
含水层人工补给(MAR)作为一种满足日益增长的用水需求的有吸引力的技术而受到推崇。在含氧水被注入缺氧含水层的情况下,MAR 应用的一个障碍是痕量金属(例如砷)的潜在迁移。虽然在这种情况下存在砷运移的概念模型,但它们通常没有通过数值模拟进行严格评估,尤其是在现场尺度上。在这项工作中,利用来自荷兰一项注入实验的地球化学数据,其中含氧水引入缺氧含水层会使砷迁移,开发并评估了砷释放和衰减的概念和数值模型,以适应现场尺度条件。最初,开发了一个地下水流动和非反应性传输模型。随后的反应性传输模拟侧重于描述氧化还原分区的时空演化。然后使用经过校准的模型来研究和量化砷的迁移。在所模拟的最能重现现场观测结果的模型中,砷的命运是通过(i)与黄铁矿氧化化学计量相关的毒砂共溶解而释放,(ii)通过动力学控制溶解的 As(III)氧化为 As(V),以及(iii)通过新沉淀的氧化铁表面络合吸附来模拟。