{"title":"Molecular-level elucidation of residual hydrocarbon effects on hydrogen adsorption and distribution in geological minerals","authors":"Temoor Muther, Amirmasoud Kalantari Dahaghi","doi":"10.1016/j.molliq.2025.127422","DOIUrl":null,"url":null,"abstract":"<div><div>The presence of hydrogen within depleted geological formations is gaining significant interest due to its enormous capacity to hold hydrogen underground for storage and withdrawal. However, the adsorption and distribution of hydrogen in depleted geological pores concentrated with residual hydrocarbons remain unclear. To evaluate these physical characteristics under different geological minerals and varying thermodynamic conditions, we conducted a series of Grand Canonical Monte Carlo (GCMC) simulations. In this study, decane was introduced as a residual hydrocarbon component to represent long-chain heavy alkanes commonly found in depleted hydrocarbon formations. Furthermore, in our analysis, we considered minerals, including hydroxylated quartz, calcite, kaolinite, K-illite, and Na-montmorillonite, representative of common rock types found in geological formations, such as sandstones, shales, and carbonates, relevant to hydrogen geo-storage and production. Initially, we examined pure hydrogen adsorption on these minerals to understand the fundamental interactions. Decane was then incrementally introduced to the system, enabling a study of hydrogen interactions in the presence of residual hydrocarbons. To increase the system’s complexity, CO<sub>2</sub> was introduced, allowing a detailed analysis of hydrogen distribution and interaction potentials within this multi-component environment. The findings revealed that hydrogen uptake showed negligible variation among the selected minerals in the absence of decane and CO<sub>2</sub>. However, incrementally introducing decane led to a linear reduction in hydrogen uptakes, ranging from 3% to 51%, depending on the mineral type. Additionally, the presence of ions caused significant shifts in the hydrogen surface adsorption peaks. The introduction of CO<sub>2</sub> further decreased hydrogen uptake by 56 to 92% compared to the pure hydrogen uptakes by occupying the mineral surfaces, thereby reducing the availability of hydrogen near the surface. These results contribute to our understanding of hydrogen distribution in multi-component systems within depleted geological formations.</div></div>","PeriodicalId":371,"journal":{"name":"Journal of Molecular Liquids","volume":"427 ","pages":"Article 127422"},"PeriodicalIF":5.3000,"publicationDate":"2025-03-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Molecular Liquids","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0167732225005896","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
The presence of hydrogen within depleted geological formations is gaining significant interest due to its enormous capacity to hold hydrogen underground for storage and withdrawal. However, the adsorption and distribution of hydrogen in depleted geological pores concentrated with residual hydrocarbons remain unclear. To evaluate these physical characteristics under different geological minerals and varying thermodynamic conditions, we conducted a series of Grand Canonical Monte Carlo (GCMC) simulations. In this study, decane was introduced as a residual hydrocarbon component to represent long-chain heavy alkanes commonly found in depleted hydrocarbon formations. Furthermore, in our analysis, we considered minerals, including hydroxylated quartz, calcite, kaolinite, K-illite, and Na-montmorillonite, representative of common rock types found in geological formations, such as sandstones, shales, and carbonates, relevant to hydrogen geo-storage and production. Initially, we examined pure hydrogen adsorption on these minerals to understand the fundamental interactions. Decane was then incrementally introduced to the system, enabling a study of hydrogen interactions in the presence of residual hydrocarbons. To increase the system’s complexity, CO2 was introduced, allowing a detailed analysis of hydrogen distribution and interaction potentials within this multi-component environment. The findings revealed that hydrogen uptake showed negligible variation among the selected minerals in the absence of decane and CO2. However, incrementally introducing decane led to a linear reduction in hydrogen uptakes, ranging from 3% to 51%, depending on the mineral type. Additionally, the presence of ions caused significant shifts in the hydrogen surface adsorption peaks. The introduction of CO2 further decreased hydrogen uptake by 56 to 92% compared to the pure hydrogen uptakes by occupying the mineral surfaces, thereby reducing the availability of hydrogen near the surface. These results contribute to our understanding of hydrogen distribution in multi-component systems within depleted geological formations.
期刊介绍:
The journal includes papers in the following areas:
– Simple organic liquids and mixtures
– Ionic liquids
– Surfactant solutions (including micelles and vesicles) and liquid interfaces
– Colloidal solutions and nanoparticles
– Thermotropic and lyotropic liquid crystals
– Ferrofluids
– Water, aqueous solutions and other hydrogen-bonded liquids
– Lubricants, polymer solutions and melts
– Molten metals and salts
– Phase transitions and critical phenomena in liquids and confined fluids
– Self assembly in complex liquids.– Biomolecules in solution
The emphasis is on the molecular (or microscopic) understanding of particular liquids or liquid systems, especially concerning structure, dynamics and intermolecular forces. The experimental techniques used may include:
– Conventional spectroscopy (mid-IR and far-IR, Raman, NMR, etc.)
– Non-linear optics and time resolved spectroscopy (psec, fsec, asec, ISRS, etc.)
– Light scattering (Rayleigh, Brillouin, PCS, etc.)
– Dielectric relaxation
– X-ray and neutron scattering and diffraction.
Experimental studies, computer simulations (MD or MC) and analytical theory will be considered for publication; papers just reporting experimental results that do not contribute to the understanding of the fundamentals of molecular and ionic liquids will not be accepted. Only papers of a non-routine nature and advancing the field will be considered for publication.