Carbon capture and storage (CCS) is a developed technology to minimize CO2 emissions and reduce global climate change. Currently, shale gas formations are considered as a suitable target for CO2 sequestration projects predominantly due to their wide availability. Compared to conventional geological formations including saline aquifers and coal seams, depleted shale formations provide larger storage potential due to the high adsorption capacity of CO2 compared to methane in the shale formation. However, the injected CO2 causes possible geochemical interactions with the shale formation during storage applications and CO2 enhanced shale gas recovery (ESGR) processes. The CO2/shale interaction is a key factor for the efficiency of CO2 storage in shale formations, as it can significantly alter the shale properties. The formation of carbonic acid from CO2 dissolution is the main cause for the alterations in the physical, chemical and mechanical properties of the shale, which in return affects the storage capacity, pore properties, and fluid transport. Therefore, in this paper, the effect of CO2 exposure on shale properties is comprehensively reviewed, to gain an in-depth understanding of the impact of CO2/shale interaction on shale properties. This paper reviews the current knowledge of the CO2/shale interactions and describes the results achieved to date. The pore structure is one of the most affected properties by CO2/shale interactions; several scholars indicated that the differences in mineral composition for shales would result in wide variations in pore structure system. A noticeable reduction in specific surface area of shales was observed after CO2 treatment, which in the long-term could decrease CO2 adsorption capacity, affecting the CO2 storage efficiency. Other factors including shale sedimentary, pressure and temperature can also alter the pore system and decrease the shale “caprock” seal efficiency. Similarly, the alteration in shales’ surface chemistry and functional species after CO2 treatment may increase the adsorption capacity of CO2, impacting the overall storage potential in shales. Furthermore, the injection of CO2 into shales may also influence the wetting behavior. Surface wettability is mainly affected by the presented minerals in shale, and less affected by brine salinity, temperature, organic content, and thermal maturity. Mainly, shales have strong water-wetting behavior in the presence of hydrocarbons, however, the alteration in shale’s wettability towards CO2-wet will significantly minimize CO2 storage capacities, and affect the sealing efficiency of caprock. The CO2/shale interactions were also found to cause noticeable degradation in shales’ mechanical properties. CO2 injection can weaken shale, decrease its brittleness and increases its plasticity and toughness. Various reductions in tri-axial compressive strength, tensile strength, and the elastic modulus of shales were observed after CO2 injection, due to the dissolution effect and adsorption strain within the pores. Based on this review, we conclude that CO2/shale interaction is a significant factor for the efficiency of CCS. However, due to the heterogeneity of shales, further studies are needed to include various shale formations and identify how different shales’ mineralogy could affect the CO2 storage capacity in the long-term.

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To meet rising global demands for energy, the oil and gas industry continuously strives to develop innovative oilfield technologies. With the development of new enhanced oil recovery techniques, sandstone acidizing has been significantly developed to contribute to the petroleum industry. Different acid combinations have been applied to the formation, which result in minimizing the near wellbore damage and improving the well productivity. A combination of hydrofluoric acid and hydrochloric acid (HF:HCl) known as mud acid has gained attractiveness in improving the porosity and permeability of the reservoir formation. However, high-temperature matrix acidizing is now growing since most of the wells nowadays become deeper and hotter temperature reservoirs, with a temperature higher than 200°F. As a result, mud acid becomes corrosive, forms precipitates and reacts rapidly, which causes early consumption of acid, hence becoming less efficient due to high pH value. However, different acids have been developed to combat these problems where studies on retarded mud acids, organic-HF acids, emulsified acids, chelating agents have shown their effectiveness at different conditions. These acids proved to be alternative to mud acid in sandstone acidizing, but the reaction mechanism and experimental analysis have not yet been investigated. The paper critically reviews the sandstone acidizing mechanism with different acids, problems occurred during the application of different acids and explores the reasons when matrix stimulation is successful over fracturing. This paper also explores the future developing requirement for matrix acidizing treatments and new experimental techniques that can be useful for further development, particularly in developing new acids and acidizing techniques, which would provide better results and information of topology, morphology and mineral dissolution and the challenges associated with implementing these ''new'' technologies.