A comprehensive review of remediation strategies for mitigating salt precipitation and enhancing CO2 injectivity during CO2 injection into saline aquifers.

Geological CO2 sequestration is a proven method for mitigating climate change by reducing atmospheric CO2 levels. However, CO2 injection often induces salt precipitation, leading to decreased formation permeability, which in turn limits CO2 injectivity and storage capacity. Conventional approaches, such as freshwater and low-salinity water injection, have been employed to mitigate salt precipitation. Despite their widespread use, these methods provide only temporary improvement and can be ineffective in some scenarios, resulting in long-term issues such as salt recrystallization and clay swelling. Given the complexity and significance of this issue, a comprehensive review of salt precipitation mechanisms and remediation techniques is essential. This paper critically examines the processes of salt precipitation during CO2 injection in saline aquifers and evaluates various remediation techniques aimed at improving CO2 injectivity. The paper reviews the influence of CO2 flow dynamics, geochemical reactions, and fluid properties on salt precipitation and pore throat accumulation, assessing the efficacy and limitations of existing mitigation methods. Additionally, the paper explores alternative techniques with potential for long-term CO2 sequestration, analyzing their advantages and drawbacks. Based on insights from the reviewed sources, the paper recommends exploring alternative treatment measures and the integration of hybrid solutions to enhance CO2 injectivity. The findings presented serve as a valuable reference for advancing research and practice in this critical area, offering a deeper understanding of the challenges and potential solutions for effective CO2 sequestration in saline aquifers.

Geochemical carbon dioxide removal potential of Spain.

Many countries have made pledges to reduce CO2 emissions over the upcoming decades to meet the Paris Agreement targets of limiting warming to no >1.5 °C, aiming for net zero by mid-century. To achieve national reduction targets, there is a further need for CO2 removal (CDR) approaches on a scale of millions of tonnes, necessitating a better understanding of feasible methods. One approach that is gaining attention is geochemical CDR, encompassing (1) in-situ injection of CO2-rich gases into Ca and Mg-rich rocks for geological storage by mineral carbonation, (2) ex-situ ocean alkalinity enhancement, enhanced weathering and mineral carbonation of alkaline-rich materials, and (3) electrochemical separation processes. In this context, Spain may host a notionally high geochemical CDR capacity thanks to its varied geological setting, including extensive mafic-ultramafic and carbonate rocks. However, pilot schemes and large-scale strategies for CDR implementation are presently absent in-country, partly due to gaps in current knowledge and lack of attention paid by regulatory bodies. Here, we identify possible materials, localities and avenues for future geochemical CDR research and implementation strategies within Spain. This study highlights the kilotonne to million tonne scale CDR options for Spain over the rest of the century, with attention paid to chemically and mineralogically appropriate materials, suitable implementation sites and potential strategies that could be followed. Mafic, ultramafic and carbonate rocks, mine tailings, fly ashes, slag by-products, desalination brines and ceramic wastes hosted and produced in Spain are of key interest, with industrial, agricultural and coastal areas providing opportunities to launch pilot schemes. Though there are obstacles to reaching the maximum CDR potential, this study helps to identify focused targets that will facilitate overcoming such barriers. The CDR potential of Spain warrants dedicated investigations to achieve the highest possible CDR to make valuable contributions to national reduction targets.

Compositional data analysis and geochemical modeling of CO2-water-rock interactions in three provinces of Korea.

The CO2-rich spring water (CSW) occurring naturally in three provinces, Kangwon (KW), Chungbuk (CB), and Gyeongbuk (GB) of South Korea was classified based on its hydrochemical properties using compositional data analysis. Additionally, the geochemical evolution pathways of various CSW were simulated via equilibrium phase modeling (EPM) incorporated in the PHREEQC code. Most of the CSW in the study areas grouped into the Ca-HCO3 water type, but some samples from the KW area were classified as Na-HCO3 water. Interaction with anorthite is likely to be more important than interaction with carbonate minerals for the hydrochemical properties of the CSW in the three areas, indicating that the CSW originated from interactions among magmatic CO2, deep groundwater, and bedrock-forming minerals. Based on the simulation results of PHREEQC EPM, the formation temperatures of the CSW within each area were estimated as 77.8 and 150 °C for the Ca-HCO3 and Na-HCO3 types of CSW, respectively, in the KW area; 138.9 °C for the CB CSW; and 93.0 °C for the GB CSW. Additionally, the mixing ratios between simulated carbonate water and shallow groundwater were adjusted to 1:9-9:1 for the CSW of the GB area and the Ca-HCO3-type CSW of the KW area, indicating that these CSWs were more affected by carbonate water than by shallow groundwater. On the other hand, mixing ratios of 1:9-5:5 and 1:9-3:7 were found for the Na-HCO3-type CSW of the KW area and for the CSW of the CB area, respectively, suggesting a relatively small contribution of carbonate water to these CSWs. This study proposes a systematic, but relatively simple, methodology to simulate the formation of carbonate water in deep environments and the geochemical evolution of CSW. Moreover, the proposed methodology could be applied to predict the behavior of CO2 after its geological storage and to estimate the stability and security of geologically stored CO2.