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在潜在 CO2 泄漏过程中,从储存 CO2 的储层与上覆含水层之间的碳酸盐岩中迁移和固定元素。

Element mobilization and immobilization from carbonate rocks between CO storage reservoirs and the overlying aquifers during a potential CO leakage.

机构信息

Pacific Northwest National Laboratory (PNNL), 902 Battelle Boulevard, Richland, WA 99352, USA.

Pacific Northwest National Laboratory (PNNL), 902 Battelle Boulevard, Richland, WA 99352, USA.

出版信息

Chemosphere. 2018 Apr;197:399-410. doi: 10.1016/j.chemosphere.2017.12.199. Epub 2018 Jan 4.

Abstract

Despite the numerous studies on changes within the reservoir following CO injection and the effects of CO release into overlying aquifers, little or no literature is available on the effect of CO release on rock between the storage reservoirs and subsurface. This is important, because the interactions that occur in this zone between the CO storage reservoir and the subsurface may have a significant impact on risk analysis for CO storage projects. To address this knowledge gap, relevant rock materials, temperatures and pressures were used to study mineralogical and elemental changes in this intermediate zone. After rocks reacted with CO-acidified 0.01 M NaCl, liquid analysis showed an increase of major elements (e.g., Ca and Mg) and variable concentrations of potential contaminants (e.g., Sr and Ba); lower aqueous concentrations of these elements were observed in N control experiments, likely due to differences in pH between the CO and N experiments. In experiments with As/Cd and/or organic spikes, representing potential contaminants in the CO plume originating in the storage reservoir, most or all of these contaminants were removed from the aqueous phase. SEM and Mössbauer spectroscopy results showed the formation of new minerals and Fe oxides in some CO-reacted samples, indicating potential for contaminant removal through mineral incorporation or adsorption onto Fe oxides. These experiments show the interactions between the CO-laden plume and the rock between storage reservoirs and overlying aquifers have the potential to affect the level of risk to overlying groundwater, and should be considered during site selection and risk evaluation.

摘要

尽管有大量关于 CO 注入后储层内部变化以及 CO 释放到上覆含水层影响的研究,但关于 CO 释放对储层与地下之间岩石影响的文献却很少。这很重要,因为在 CO 储层和地下之间的这个区域中发生的相互作用可能会对 CO 储存项目的风险分析产生重大影响。为了解决这一知识空白,使用相关的岩石材料、温度和压力来研究这个中间带的矿物学和元素变化。在岩石与 CO-酸化的 0.01 M NaCl 反应后,液体分析表明主要元素(如 Ca 和 Mg)和潜在污染物(如 Sr 和 Ba)的浓度增加;在 N 对照实验中观察到这些元素的水相浓度较低,这可能是由于 CO 和 N 实验之间的 pH 值差异所致。在含有 As/Cd 和/或有机尖峰的实验中,这些尖峰代表了源自储层的 CO 羽流中的潜在污染物,大部分或所有这些污染物都从水相中去除。SEM 和 Mössbauer 光谱结果表明,在一些 CO 反应样品中形成了新的矿物和 Fe 氧化物,表明通过矿物掺入或 Fe 氧化物吸附去除污染物的潜力。这些实验表明,富含 CO 的羽流与储层与上覆含水层之间的岩石之间的相互作用有可能影响上覆地下水的风险水平,因此在选址和风险评估过程中应加以考虑。

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