Multi-Isotope Geochemical Baseline Study of the Carbon Management Canada Research Institutes CCS Field Research Station (Alberta, Canada), Prior to CO2 Injection

R. Utley, Emma Martin-Roberts, N. Utting, G. Johnson, D. Györe, M. Żurakowska, F. Stuart, A. Boyce, T. Darrah, P. Gulliver, R. Haszeldine, D. Lawton, S. Gilfillan
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Abstract

Carbon capture and storage (CCS) is an industrial scale mitigation strategy for reducing anthropogenic CO2 from entering the atmosphere. However, for CCS to be routinely deployed, it is critical that the security of the stored CO2 can be verified and that unplanned migration from a storage site can be identified. A number of geochemical monitoring tools have been developed for this purpose, however, their effectiveness critically depends on robust geochemical baselines being established prior to CO2 injection. Here we present the first multi-well gas and groundwater characterisation of the geochemical baseline at the Carbon Management Canada Research Institutes Field Research Station. We find that all gases exhibit CO2 concentrations that are below 1%, implying that bulk gas monitoring may be an effective first step to identify CO2 migration. However, we also find that predominantly biogenic CH4 (∼90%–99%) is pervasive in both groundwater and gases within the shallow succession, which contain numerous coal seams. Hence, it is probable that any upwardly migrating CO2 could be absorbed onto the coal seams, displacing CH4. Importantly, 4He concentrations in all gas samples lie on a mixing line between the atmosphere and the elevated 4He concentration present in a hydrocarbon well sampled from a reservoir located below the Field Research Station (FRS) implying a diffusive or advective crustal flux of 4He at the site. In contrast, the measured 4He concentrations in shallow groundwaters at the site are much lower and may be explained by gas loss from the system or in situ production generated by radioactive decay of U and Th within the host rocks. Additionally, the injected CO2 is low in He, Ne and Ar concentrations, yet enriched in 84Kr and 132Xe relative to 36Ar, highlighting that inherent noble gas isotopic fingerprints could be effective as a distinct geochemical tracer of injected CO2 at the FRS.
加拿大碳管理研究所CCS野外研究站(加拿大阿尔伯塔)二氧化碳注入前的多同位素地球化学基线研究
碳捕集与封存(CCS)是一种工业规模的减缓战略,旨在减少人为排放的二氧化碳进入大气。然而,对于CCS的常规部署,至关重要的是可以验证存储的二氧化碳的安全性,并且可以识别存储地点的计划外迁移。为此目的已经开发了许多地球化学监测工具,然而,它们的有效性在很大程度上取决于在注入二氧化碳之前建立的牢固的地球化学基线。在这里,我们展示了加拿大碳管理研究所野外研究站地球化学基线的第一个多井天然气和地下水特征。我们发现,所有气体的二氧化碳浓度都低于1%,这意味着大宗气体监测可能是识别二氧化碳迁移的有效第一步。然而,我们还发现,在含有大量煤层的浅层演替中,地下水和气体中普遍存在以生物成因为主的CH4(~ 90%-99%)。因此,任何向上迁移的CO2都可能被煤层吸收,取代CH4。重要的是,所有气体样品中的4He浓度都位于大气和从位于野外研究站(FRS)下方的储层中取样的碳氢化合物井中出现的升高的4He浓度之间的混合线上,这意味着该地点的4He存在扩散或平流的地壳通量。相比之下,该站点浅层地下水中测量到的4He浓度要低得多,这可能是由于系统中的气体损失或宿主岩石中U和Th的放射性衰变产生的原位生产。此外,注入CO2的He、Ne和Ar浓度较低,而84Kr和132Xe相对于36Ar富集,表明固有稀有气体同位素指纹可以作为注入CO2的独特地球化学示踪剂在FRS中有效。
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