Adsorption Characteristics of CO2/CH4/H2S Mixtures in Calcite Nanopores with the Implications for CO2 Sequestration

被引:0
|
作者
Rui, Zhenhua [1 ,2 ,3 ,4 ]
Qian, Cheng [1 ,2 ]
Liu, Yueliang [1 ,2 ,3 ]
Zhao, Yang [1 ,2 ,3 ]
Li, Huazhou Andy [5 ]
Afanasyev, Andrey [6 ]
Torabi, Farshid [7 ]
机构
[1] China Univ Petr, Natl Key Lab Petr Resources & Engn, Beijing, Peoples R China
[2] China Univ Petr, Coll Petr Engn, Beijing, Peoples R China
[3] China Univ Petr, Coll Carbon Neutral Future Technol, Beijing, Peoples R China
[4] China Univ Petr, Coll Petr, Beijing, Peoples R China
[5] Univ Alberta, Civil & Environm Engn Dept, Edmonton, AB, Canada
[6] Moscow MV Lomonosov State Univ, Inst Mech, Moscow, Russia
[7] Univ Regina, Petr Syst Engn, Regina, SK, Canada
来源
SPE JOURNAL | 2024年 / 29卷 / 05期
基金
中国国家自然科学基金;
关键词
COMPASS FORCE-FIELD; SELECTIVE ADSORPTION; CARBON-DIOXIDE; BINARY-MIXTURE; GAS; STORAGE; H2S; SALINITY; OIL; VALIDATION;
D O I
10.2118/219463-PA
中图分类号
TE [石油、天然气工业];
学科分类号
0820 ;
摘要
Injecting CO2 into reservoirs for storage and enhanced oil recovery (EOR) is a practical and cost-effective strategy for reducing carbon emissions. Commonly, CO2-rich industrial waste gas is used as the CO2 source, whereas contaminants such as H2S may severely impact carbon storage and EOR via competitive adsorption. Hence, the adsorption behavior of CH4, CO2, and H2S in calcite (CaCO3) micropores and the impact of H2S on CO2 sequestration and methane recovery are specifically investigated. The Grand Canonical Monte Carlo (GCMC) simulations were applied to study the adsorption characteristics of pure CO2, CH4, and H2S, and their multicomponent mixtures were also investigated in CaCO3 nanopores to reveal the impact of H2S on CO2 storage. The effects of pressure (0-20 MPa), temperature (293.15-383.15 K), pore width, buried depth, and gas mole fraction on the adsorption behaviors are simulated. Molecular dynamics (MD) simulations were performed to explore the diffusion characteristics of the three gases and their mixes. The amount of adsorbed CH4, CO2, and H2S enhances with rising pressure and declines with rising temperature. The order of adsorption quantity in CaCO3 nanopores is H2S > CO2 > CH4 based on the adsorption isotherm. At 10 MPa and 323.15 K, the interaction energies of CaCO3 with CO2, H2S, and CH4 are -2166.40 kcal/mol, -2076.93 kcal/mol, and -174.57 kcal/mol, respectively, which implies that the order of adsorption strength between the three gases and CaCO3 is CO2 > H2S > CH4. The CH4-CaCO3 and H2S-CaCO3 interaction energies are determined by van der Waals energy, whereas electrostatic energy predominates in the CO2-CaCO3 system. The adsorption loading of CH4 and CO2 are lowered by approximately 59.47% and 24.82% when the mole fraction of H2S is 20% at 323.15 K, reflecting the weakening of CH4 and CO2 adsorption by H2S due to competitive adsorption. The diffusivities of three pure gases in CaCO3 nanopore are listed in the following order: CH4 > H2S approximate to CO2. The presence of H2S in the ternary mixtures will limit diffusion and outflow of the system and each single gas, with CH4 being the gas most affected by H2S. Concerning carbon storage in CaCO3 nanopores, the CO2/CH4 binary mixture is suitable for burial in shallower formations (around 1000 m) to maximize the storage amount, while the CO2/CH4/H2S ternary mixture should be buried as deep as possible to minimize the adverse effects of H2S. The effects of H2S on CO2 sequestration and CH4 recovery in CaCO3 nanopores are clarified, which provides theoretical assistance for CO2 storage and EOR projects in carbonate formation.
引用
收藏
页码:2748 / 2762
页数:15
相关论文
共 50 条
  • [41] Mechanism and Characteristics of CH4/CO2/H2O Adsorption in Lignite Molecules
    Wen, Zhihui
    Yang, Yunpeng
    Wang, Qi
    Yao, Banghua
    GEOFLUIDS, 2021, 2021
  • [42] Far infrared measurements of absorptions by CH4 + CO2 and H2 + CO2 mixtures and implications for greenhouse warming on early Mars
    Turbet, Martin
    Tran, Ha
    Pirali, Olivier
    Forget, Francois
    Boulet, Christian
    Hartmann, Jean-Michel
    ICARUS, 2019, 321 : 189 - 199
  • [43] Cross second virial coefficients and dilute gas transport properties of the (CH4 + CO2), (CH4 + H2S), and (H2S + CO2) systems from accurate intermolecular potential energy surfaces
    Hellmann, Robert
    Bich, Eckard
    Vesovic, Velisa
    JOURNAL OF CHEMICAL THERMODYNAMICS, 2016, 102 : 429 - 441
  • [44] Investigation of adsorption kinetics of CH4 and CO2 on shale exposure to supercritical CO2
    Qin, Chao
    Jiang, Yongdong
    Zuo, Shuangying
    Chen, Shiwan
    Xiao, Siyou
    Liu, Zhengjie
    ENERGY, 2021, 236
  • [45] Molecular simulations of hybrid cross-linked membranes for H2S gas separation at very high temperatures and pressure: Binary 90%/10% N2/H2S and CH4/H2S, ternary 90%/9%/1% N2/CO2/H2S and CH4/CO2/H2S mixtures
    Neyertz, Sylvie
    Benes, Nieck E.
    Brown, David
    JOURNAL OF MEMBRANE SCIENCE, 2023, 687
  • [46] Molecular simulation on CO2/H2S co-adsorption in organic and inorganic shale nanopores
    Zhang, Mingshan
    Liu, Zaobao
    Pan, Bin
    Iglauer, Stefan
    Jin, Zhehui
    APPLIED SURFACE SCIENCE, 2023, 624
  • [47] CO2/CH4, CH4/H2 and CO2/CH4/H2 separations at high pressures using Mg2(dobdc)
    Herm, Zoey R.
    Krishna, Rajamani
    Long, Jeffrey R.
    MICROPOROUS AND MESOPOROUS MATERIALS, 2012, 151 : 481 - 487
  • [48] H2S Removal and CO2/CH4 Separation of Ternary Mixtures Using Polyimide Hollow Fiber Membrane
    Park, Bo-Ryoung
    Kim, Dae-Hoon
    Jo, Hang-Dae
    Seo, Yong-Seog
    Hwang, Taek-Sung
    Lee, Hyung-Keun
    KOREAN CHEMICAL ENGINEERING RESEARCH, 2011, 49 (02): : 250 - 255
  • [49] Thermodynamic and molecular insights into the absorption of H2S, CO2, and CH4 in choline chloride plus urea mixtures
    Liu, Fujian
    Chen, Wei
    Mi, Jinxing
    Zhang, Jia-Yin
    Kan, Xun
    Zhong, Fu-Yu
    Huang, Kuan
    Zheng, An-Min
    Jiang, Lilong
    AICHE JOURNAL, 2019, 65 (05)
  • [50] Computational screening of covalent organic frameworks for CH4/H2, CO2/H2 and CO2/CH4 separations
    Tong, Minman
    Yang, Qingyuan
    Zhong, Chongli
    MICROPOROUS AND MESOPOROUS MATERIALS, 2015, 210 : 142 - 148