Skip to main content

Research Repository

Advanced Search

Surface thermodynamics of hydrocarbon vapors and carbon dioxide adsorption on shales

Tang, Xu

Surface thermodynamics of hydrocarbon vapors and carbon dioxide adsorption on shales Thumbnail


Authors

Xu Tang



Abstract

Understanding hydrocarbon vapors and carbon dioxide adsorption mechanism on shales lays the foundation for in situ hydrocarbon resource estimation and enhanced hydrocarbon recovery via carbon dioxide injection. However, surface thermodynamic potentials of hydrocarbon vapor and carbon dioxide adsorption on shales have rarely been reported. This work develops a rigorous framework for direct description of hydrocarbon vapors and carbon dioxide adsorption isotherms on shales and for straightforward calculation of the intrinsic thermodynamic potentials by considering non-ideal gas behavior. On the basis of the Langmuir adsorption model, the maximum adsorption capacity of methane, ethane, propane, n-butane, iso-butane and carbon dioxide adsorption on shales positively correlates to each gas’ molecular mass. Carbon dioxide adsorption capacity is higher than methane and ethane but is lower than propane, n-butane and iso-butane. According to the generalized multilayer adsorption model, the monolayer adsorption capacity of n-hexane is slightly higher than that of n-heptane due to the small molecular diameter of n-hexane. The temperature-dependent behavior of isosteric enthalpy and entropy for these vapors is attributed to their non-ideal gas behavior and the temperature-dependent adsorption uptakes. Isosteric enthalpy and entropy in general positively correlate to the molecular mass of vapors. Isosteric enthalpy and entropy of carbon dioxide and propane are almost identical in behavior given that their molecular masses are very close. Isosteric enthalpy and entropy of iso-butane are lower than that of n-butane due to their molecule polarity difference. The shale selectivity of propane, n-butane and iso-butane is higher than carbon dioxide while the shale selectivity of methane and ethane is lower than carbon dioxide. These surface thermodynamic characteristics therefore provide new perspectives on understanding the interaction of hydrocarbon vapors/carbon dioxide and shales for enhanced hydrocarbon recovery via carbon dioxide injection.

Citation

Tang, X. (2019). Surface thermodynamics of hydrocarbon vapors and carbon dioxide adsorption on shales. Fuel, 238, 402-411. https://doi.org/10.1016/j.fuel.2018.10.034

Journal Article Type Article
Acceptance Date Oct 4, 2018
Online Publication Date Nov 1, 2018
Publication Date Feb 15, 2019
Deposit Date Nov 2, 2018
Publicly Available Date Nov 2, 2019
Journal Fuel
Print ISSN 0016-2361
Electronic ISSN 1873-7153
Publisher Elsevier
Peer Reviewed Peer Reviewed
Volume 238
Pages 402-411
DOI https://doi.org/10.1016/j.fuel.2018.10.034
Keywords Shale; Hydrocarbon vapor; Adsorption; Enthalpy; Entropy
Public URL https://nottingham-repository.worktribe.com/output/1219763
Publisher URL https://www.sciencedirect.com/science/article/pii/S0016236118317472?via%3Dihub
Additional Information This article is maintained by: Elsevier; Article Title: Surface thermodynamics of hydrocarbon vapors and carbon dioxide adsorption on shales; Journal Title: Fuel; CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.fuel.2018.10.034; Content Type: article; Copyright: Crown Copyright © 2018 Published by Elsevier Ltd. All rights reserved.

Files




Downloadable Citations