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Modeling the potential impacts of CO\u3csub\u3e2\u3c/sub\u3e sequestration on shallow groundwater: The fate of trace metals and organic compounds before and after leakage stops

机译:模拟CO

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摘要

Large-scale deployment of CO2 geological sequestration requires understanding and assessing the risks of such an operation. One of these risks is the potential contamination of groundwater by CO2/brine leakage into shallow aquifers. Although our understanding of this issue has improved significantly over the last decade, several questions still need to be better addressed, including the fate of organic constituents, the dominant source of trace metals (are they mainly coming from aquifer sediments, or leaking brine), and whether the trace metals released during the leakage phase recover to background levels if the leakage were to be detected and stopped. In this paper, reactive transport simulations that model the behavior of trace metals and organic compounds in response to the leakage of CO2 and brine into a shallow aquifer are presented to address these questions. Model results show that the metals and organic compounds brought by the leaking brine form a plume at the bottom of the aquifer because the density of the brine is higher than that of groundwater. In contrast, metals are mobilized by CO2 over a larger vertical extent because of the spreading of gaseous CO2 by buoyancy. The concentration of organic contaminants is strongly attenuated by adsorption and degradation, with degradation playing the major role in the modeled scenarios. Although the leaking brine is assumed to contain elevated concentrations of As, Pb, Cd, and Ba, it does not contribute significantly to the contamination of the modeled shallow aquifer by these elements. Once the leakage stops, mobilized organic compounds that undergo degradation vanish, while less degradable compounds linger for a longer time; the dissolved concentrations of trace metals decrease significantly, as a result of re-sorption and reversal of processes leading to Ca-driven cation exchange.
机译:大规模部署二氧化碳地质隔离技术需要了解并评估这种操作的风险。这些风险之一是二氧化碳/盐水渗入浅层含水层可能对地下水造成污染。尽管在过去十年中,我们对这个问题的理解有了很大的提高,但是仍然需要更好地解决一些问题,包括有机成分的命运,微量金属的主要来源(它们主要来自含水层沉积物或盐水泄漏),如果要检测并阻止泄漏,则泄漏阶段释放的痕量金属是否恢复到背景水平。在本文中,提出了反应性输运模拟,以模拟痕量金属和有机化合物的行为,以响应于CO2和盐水向浅层含水层的泄漏,以解决这些问题。模型结果表明,由于盐水的密度高于地下水的密度,因此泄漏的盐水带来的金属和有机化合物在含水层的底部形成了羽状流。相反,由于浮力使气态二氧化碳扩散,金属在较大的垂直范围内被二氧化碳带动。有机污染物的浓度会因吸附和降解而大大减弱,而降解在模拟场景中起主要作用。尽管假定泄漏的盐水中As,Pb,Cd和Ba的浓度较高,但是它们对这些浅层含水层的污染没有明显贡献。一旦泄漏停止,经过降解的迁移的有机化合物就会消失,而难降解的化合物会停留更长的时间。由于重吸收和逆转导致Ca驱动的阳离子交换的过程,因此痕量金属的溶解浓度显着降低。

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