Assessment of the in situ biomethanation potential of a deep aquifer used for natural gas storage

Magali Ranchou-Peyruse, Marion Guignard, Pierre Chiquet, Pierre Cézac, Anthony Ranchou-Peyruse
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Abstract

In response to the challenges of sustainable development and the H 2 sector, it is foreseeable that H 2 will be stored into geological storage, such as deep aquifers. However, CO 2 evolves in deep aquifers because it may be naturally present there; it may also be a constituent of the stored gas mix, or could even be voluntarily stored in the context of the fight against global warming. Autochthonous microorganisms can consume them as sources of energy and carbon (methanogens, (homo)-acetogens and sulfate-reducers). This was already demonstrated in a previous experiment (Haddad 2022) and under operating conditions (Lobodice, Czech Republic ; Smigan 1990). Understanding these mechanisms and quantifying them appear necessary to assess the modifications generated by this type of microorganisms on the properties of the gas. The methanogenesis reaction (CO 2 gas + 4H 2 gas → CH 4 gas + 2H 2 O liquid ) induces a lowering of pressure, since 5 gas molecules are transformed into a single gas molecule: CH 4 (water being condensed at subsurface conditions). In situ biomethanation technique could represent a potential on several scales larger than conventional catalytic or biological methanation reactors, due to the very large reservoir volumes involved. Biomethanation in geological reservoirs would enable us to reduce our consumption of fossil fuels, so as not to emit more CO 2 , while meeting the growing energy needs of a region and ensuring its independence from hydrocarbon-producing countries. A deep aquifer already used as UGS was selected for this study. Formation waters from 17 control wells in this aquifer (Fig. 1) were sampled to assess the potential activity of indigenous methanogenic populations, as well as sulfate-reducers. Despite relatively low sulfate concentrations for a deep aquifer (0.025-1.35 mM), sulfate reducers were found at all sites targeting and quantifying the dsrB gene, which is characteristic of this metabolic group (between 1.8∙10 1 ±2.0x10 0 and 1.3∙10 4 ±2.0∙10 3 dsrB gene copy numbers.mL -1 ). In contrast, methanogenic archaea based on the mcrA gene quantification were detected at only 10 of the 17 sites (up to 4.3∙10 2 ±8.3∙10 1 mcrA gene copy numbers.mL -1 ). The choice was made to focus the rest of the study on 7 of these 10 sites. The potential for methanogenesis was assessed on cultural tests with formation water alone or supplemented with calcite (CaCO 3 ), a mineral present in the formation. Results indicate that initial times and controls are controlled by the sulfate variable, since the latter was not consumed by sulfate-reducers. Biotic trials in the presence of calcite and H 2 /CO 2 (abiotic controls and final times) are logically characterized by higher concentrations of calcite, bicarbonate and calcium, but this is not the case for trials in the presence of H 2 alone. We therefore deduce that methanogenesis took place mainly via gaseous CO 2 , but that without the latter, calcite was a source of carbon for lithoautotrophs. Cultures incubated with H 2 as the sole gas phase have the highest methane concentrations, logically associated with the lowest sulfate concentrations (consumed by sulfate-reducers), the lowest Eh (probably due to the presence of sulfides) and more alkaline pH values up to 10 (which may have led to precipitation of carbonate and calcium ions). All the sites studied showed sulfate consumption and methane production. Analysis of taxonomic diversity (MiSeq; 16S rRNA gene V4-V5) showed the dominance of three genera of sulfate-reducers with Thermodesulfovibrio-Desulfovibrio-Desulfotomaculum and methanogenic populations belonging to the Methanobacterium genus. These initial results show a strong potential of in situ biomethanation for the deep aquifer studied. All these experiments were carried out at near-atmospheric pressure, and the results still need to be confirmed and refined in the laboratory under conditions that simulate real-life conditions as closely as possible (rock, pressure, nature of gases).
用于天然气储存的深层含水层的原位生物甲烷化潜力评估
为了应对可持续发展和氢部门的挑战,可以预见的是,氢将被储存在地质储存中,如深层含水层。然而,二氧化碳在深层含水层中进化,因为它可能自然存在于那里;它也可能是储存气体混合物的一个组成部分,或者甚至可以在对抗全球变暖的背景下自愿储存。本地微生物可以将它们作为能量和碳的来源(产甲烷菌、(同质)产氧菌和硫酸盐还原剂)来消耗。这已经在之前的实验(Haddad 2022)和操作条件(Lobodice,捷克共和国;Smigan 1990)。了解这些机制并对其进行量化,对于评估这类微生物对气体性质产生的改变似乎是必要的。甲烷生成反应(co2气体+ 4h2气体→ch4气体+ 2h2o液体)导致压力降低,因为5个气体分子转化为单个气体分子:ch4(水在地下条件下凝结)。由于涉及的储层容量非常大,原位生物甲烷化技术在几个规模上可能比传统的催化或生物甲烷化反应器具有更大的潜力。地质储层中的生物甲烷化将使我们能够减少化石燃料的消耗,从而不排放更多的二氧化碳,同时满足一个地区日益增长的能源需求,并确保其独立于碳氢化合物生产国。本研究选择了一个已经用作UGS的深层含水层。从该含水层的17口对照井的地层水中取样(图1),以评估本地产甲烷种群的潜在活动,以及硫酸盐还原剂。尽管深层含水层的硫酸盐浓度相对较低(0.025-1.35 mM),但在所有定位和量化dsrB基因的位点都发现了硫酸盐还原物,这是该代谢组(在1.8∙10 1±2.0 × 10 0和1.3∙10 4±2.0∙10 3之间)的特征。mL -1)。相比之下,基于mcrA基因定量的产甲烷古菌在17个位点中仅检测到10个(高达4.3∙10 2±8.3∙10 1 mcrA基因拷贝数)。mL -1)。我们选择将剩下的研究集中在这10个地点中的7个。通过单独使用地层水或添加方解石(caco3)(地层中存在的一种矿物)进行培养试验,评估了甲烷生成的潜力。结果表明,初始时间和控制是由硫酸盐变量控制的,因为硫酸盐不被硫酸盐还原剂消耗。在方解石和h2 /CO 2存在下的生物试验(非生物对照和最终时间)在逻辑上以方解石、碳酸氢盐和钙的浓度较高为特征,但在单独存在h2的试验中情况并非如此。因此,我们推断甲烷生成主要通过气态CO 2发生,但如果没有后者,方解石是岩石自养生物的碳源。以h2作为唯一气相培养的培养物具有最高的甲烷浓度,逻辑上与最低的硫酸盐浓度(被硫酸盐还原剂消耗),最低的Eh(可能由于硫化物的存在)和更高的碱性pH值高达10(这可能导致碳酸盐和钙离子的沉淀)相关。所有研究地点均显示硫酸盐消耗和甲烷生产。分类多样性分析(MiSeq;16S rRNA基因V4-V5)显示3个硫酸盐还原剂属占优势,其中Thermodesulfovibrio-Desulfovibrio-Desulfotomaculum和产甲烷菌属的产甲烷菌群。这些初步结果表明,所研究的深层含水层具有很强的原位生物甲烷化潜力。所有这些实验都是在接近大气的压力下进行的,结果仍然需要在实验室中尽可能接近模拟现实条件(岩石、压力、气体性质)的条件下进行确认和完善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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