A Review-Dissolution and Mineralization Storage of CO2 Geological Storage in Saline Aquifers

Bo Wang, Xiangzen Wang, Yiming Chen, Quansheng Liang, F. Zeng
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Abstract

Saline aquifer has become the preferred storage location of carbon capture, and storage (CCS) technology because of its wide distribution, large storage capacity and high safety factor. According to IPCC statistics, the storage capacity of saline aquifers worldwide is 400 – 10000 Gt, which is dozens of times that of oil and gas reservoirs and hundreds of times that of coal seams. Therefore, the carbon storage in saline aquifer has the most potential for CO2 storage. Carbon sequestration in saline aquifers includes four trapping mechanisms: short-term geological and hydrodynamic capture and long-term geochemical (solubility and mineral) capture. Moreover, the solubility of CO2 in saline aquifer and the mechanism of mineral capture (salt precipitation) depends on the injected CO2 and the water-rock characteristics of saline aquifer. However, current knowledge on geochemical capture is still at an early stage compared to other capture theories. Recent researches indicate that although temperature, pressure, salinity of formation water and mineral composition of formation rocks are important factors affecting mineral storage, other reservoir parameters, such as reservoir thickness, dip angle, anisotropy, and bedding distribution, may also significantly affect salt precipitation, mineral storage, and geo-chemical storage. In this paper, we would like to present a comprehensive review on the solubility model of CO2 in saline aquifers, the phase permeability change of CO2 and saline aquifers, the mechanism of CO2-water -rock interaction, the dissolution and precipitation model of inorganic salt minerals, and the influencing factors for CO2 sequestration in saline aquifers. We believe that this review lays a foundation for future study of carbon storage technology in saline aquifer.
含盐含水层CO2地质封存的溶解与矿化研究进展
咸水含水层因其分布广、储存容量大、安全系数高而成为碳捕集与封存(CCS)技术的首选储存地点。据IPCC统计,全世界咸水含水层的储存量为400 - 10000 Gt,是油气藏的几十倍,煤层的数百倍。因此,含盐含水层的碳储量具有最大的CO2储量潜力。含盐含水层中的碳固存包括四种捕获机制:短期地质和水动力捕获和长期地球化学(溶解度和矿物)捕获。此外,CO2在咸水含水层中的溶解度和矿物捕获(盐沉淀)机制取决于注入的CO2和咸水含水层的水岩特征。然而,与其他捕获理论相比,目前对地球化学捕获的认识仍处于初级阶段。近年来的研究表明,虽然地层水的温度、压力、盐度和地层岩石的矿物组成是影响矿物储存的重要因素,但储层厚度、倾角、各向异性和层理分布等其他储集参数也可能对盐降水、矿物储存和地球化学储存产生显著影响。本文就CO2在含盐含水层中的溶解度模型、CO2与含盐含水层的相渗变化、CO2-水-岩相互作用机理、无机盐矿物的溶解与沉淀模型、含盐含水层中CO2固存的影响因素等方面进行了综述。本文的研究为今后盐碱层碳储存技术的研究奠定了基础。
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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