首页> 外文期刊>Applied Geochemistry: Journal of the International Association of Geochemistry and Cosmochemistry >Reactive transport modeling of an aquifer storage and recovery (ASR) pilot to assess long-term water quality improvements and potential solutions
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Reactive transport modeling of an aquifer storage and recovery (ASR) pilot to assess long-term water quality improvements and potential solutions

机译:含水层存储和回收(ASR)试点的反应运输模型,以评估长期水质改善和潜在解决方案

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This reactive transport modeling study presents a follow up to the mass balance-based identification and quantification of the main hydrogeochemical processes that occurred during an aquifer storage and recovery (ASR) trial in an anoxic sandy aquifer (Herten, the Netherlands). Kinetic rate expressions were used to simulate oxidation of pyrite, soil organic matter (SOM), and ferrous iron, and dissolution of calcite and Mn-siderite. Cation exchange, precipitation of Fe- and Mn-(hydr)oxides, and surface complexation were treated as equilibrium processes. The PHREEQC model was automatically calibrated with PEST to observations from the first ASR cycle, and was then allowed to run for all 14 cycles to evaluate its long term performance. A sensitivity analysis was conducted to find the most controlling model parameters. Pyrite was ranked as the most important reductant, followed by SOM, whereas Fe(II) was least important. Moreover, the pH and oxygen gradients were found to enhance the rate of pyrite over SOM oxidation with distance away from the ASR well. The increasing sorption capacity of precipitating Fe-hydroxides was reflected by the decreasing Fe(II) concentrations with subsequent cycles whereas Mn(II) showed a tendency to mobilize during recovery and remain above standards. Oxidation and dissolution rates were found to depend on travel time and injection rate as well as on the presence or absence of flow. Oxygen enrichment of the injection water increased oxidation rates and therefore accelerated the aquifer's leaching from its reactive species. We specifically focused on impeding the release of Mn(II) to the groundwater, a process that acted as a restraining factor for the feasibility of ASR application at this site. The undesirable side-effects of oxygen enrichment as well as the Mn(II) issues were found to be partly suppressed by enriching the source water with pH buffers according to scenario simulations.
机译:这项反应性运输模型研究为基于缺氧砂质含水层(荷兰赫尔滕)的含水层存储和回收(ASR)试验期间发生的主要水文地球化学过程提供了基于质量平衡的识别和量化的后续措施。动力学速率表达式用于模拟黄铁矿,土壤有机质(SOM)和亚铁的氧化以及方解石和锰铁矿的溶解。阳离子交换,Fe-和Mn-(氢氧化)氧化物的沉淀以及表面络合被视为平衡过程。 PHREEQC模型通过PEST自动校准为第一个ASR周期的观测值,然后允许运行所有14个周期以评估其长期性能。进行了敏感性分析以找到最可控制的模型参数。黄铁矿是最重要的还原剂,其次是SOM,而Fe(II)最不重要。此外,发现pH和氧梯度在远离ASR井的距离上会提高黄铁矿的速率,使其超过SOM氧化。 Fe(II)浓度随随后的循环而降低,反映出沉淀的氢氧化铁吸附能力的提高,而Mn(II)在回收期间表现出动员的趋势,并保持在标准以上。发现氧化和溶解速率取决于行程时间和注入速率以及是否存在流动。注入水的富氧增加了氧化速率,因此加速了含水层从其反应性物种中的浸出。我们特别关注阻止Mn(II)释放到地下水中,这一过程是限制该地点进行ASR可行性的一个因素。根据方案模拟,发现通过用pH缓冲液富集源水可以部分抑制氧富集以及Mn(II)问题的不良副作用。

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