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页岩气藏有机组分的水吸附特性及机理

Water Adsorption Characteristics and Mechanisms in the Organic Components of Shale Gas Reservoirs.

作者信息

Xie Weidong, Fu Xiaofei, Wang Haixue, Sun Yu, Gan Huajun, Wang Hua, Vandeginste Veerle, Jiang Fei

机构信息

School of Earth Sciences, Northeast Petroleum University, Daqing 163318, China.

Key Laboratory of Tectonics and Petroleum Resources of Ministry of Education, China University of Geosciences, Wuhan 430074, China.

出版信息

Langmuir. 2025 Aug 5;41(30):20259-20271. doi: 10.1021/acs.langmuir.5c02538. Epub 2025 Jul 23.

Abstract

To reveal the adsorption characteristics and mechanisms of water vapor in the organic matter (OM) of shale gas reservoirs, OM was isolated from the Longmaxi shale and used in water adsorption experiments. The primary, secondary, and entire adsorption behaviors of OM were compared with those of montmorillonite, kaolinite, illite, and intact shale to characterize its contribution to the water adsorption capacity of shale gas reservoirs. Thermodynamic parameters of Gibbs free energy change (Δ), enthalpy change (Δ), entropy change (Δ), and isosteric heat () were calculated and compared among all adsorption carriers to discuss their differences in adsorption intensity, spontaneous nature, and driving factor. Moreover, the water vapor adsorption mechanisms were identified from the perspectives of composition, chemical structure, and pore structure of the adsorbent. The results indicate that (i) the adsorption amount on montmorillonite is the largest and, thus, greater than that on OM, kaolinite, illite, and intact shale. (ii) The primary adsorption intensity of clay minerals is significantly higher than that of OM due to their strong hydrophilicity, whereas the secondary adsorption intensity of OM is slightly higher, caused by the superimposition of the adsorption potential in its extensively developed nanopores. (iii) Montmorillonite is expandable and characterized by large interlayer space, cation exchange capacity (CEC), and pore structure parameters. Although OM is composed mainly of hydrophobic aromatic structures, with low hydrophilic polarity and alkaline functional group content, the multilayer adsorption and capillary condensation in its widely developed pore structures are significant. (iv) The water adsorption capacity of OM is greater than that of kaolinite and illite, and the adsorption amount is mainly influenced by accumulation spaces and adsorption sites rather than the adsorption intensity.

摘要

为揭示页岩气储层有机质(OM)中水蒸气的吸附特性及机理,从龙马溪页岩中分离出OM并用于水吸附实验。将OM的一次、二次及整体吸附行为与蒙脱石、高岭石、伊利石和完整页岩的吸附行为进行比较,以表征其对页岩气储层水吸附能力的贡献。计算并比较了所有吸附载体的吉布斯自由能变化(Δ)、焓变(Δ)、熵变(Δ)和等量吸附热()等热力学参数,以探讨它们在吸附强度、自发性质和驱动因素方面的差异。此外,还从吸附剂的组成、化学结构和孔隙结构角度确定了水蒸气吸附机理。结果表明:(i)蒙脱石上的吸附量最大,因此大于OM、高岭石、伊利石和完整页岩上的吸附量。(ii)由于黏土矿物的强亲水性,其一次吸附强度明显高于OM,而OM的二次吸附强度略高,这是由于其广泛发育的纳米孔中吸附势的叠加所致。(iii)蒙脱石具有可膨胀性,其层间空间、阳离子交换容量(CEC)和孔隙结构参数较大。虽然OM主要由疏水芳香结构组成,亲水极性和碱性官能团含量较低,但其广泛发育的孔隙结构中的多层吸附和毛细管凝聚作用显著。(iv)OM的水吸附能力大于高岭石和伊利石,吸附量主要受堆积空间和吸附位点的影响,而非吸附强度。

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