LAPSE:2023.20946
Published Article

LAPSE:2023.20946
Hydrate Stability and Methane Recovery from Gas Hydrate through CH4−CO2 Replacement in Different Mass Transfer Scenarios
March 21, 2023
Abstract
CH4−CO2 replacement is a carbon-negative, safer gas production technique to produce methane gas from natural gas hydrate reservoirs by injecting pure CO2 or other gas mixtures containing CO2. Laboratory-scale experiments show that this technique produces low methane volume and has a slow replacement rate due to the mass transfer barrier created due to impermeable CO2 hydrate layer formation, thus making the process commercially unattractive. This mass-transfer barrier can be reduced through pressure reduction techniques and chemical techniques; however, very few studies have focused on depressurization-assisted and chemical-assisted CH4−CO2 replacement to lower mass-transfer barriers and there are many unknowns. In this work, we qualitatively and quantitatively investigated the effect of the pressure reduction and presence of a hydrate promoter on mixed hydrate stability, CH4 recovery, and risk of water production during CH4−CO2 exchange. Exchange experiments were carried out using the 500 ppm sodium dodecyl sulfate (SDS) solution inside a high-pressure stirred reactor. Our results indicated that mixed hydrate stability and methane recovery depends on the degree of pressure reduction, type, and composition of injected gas. Final selection between CO2 and CO2 + N2 gas depends on the tradeoff between mixed hydrate stability pressure and methane recovery. Hydrate morphology studies suggest that production of water during the CH4−CO2 exchange is a stochastic phenomenon that is dependent on many parameters.
CH4−CO2 replacement is a carbon-negative, safer gas production technique to produce methane gas from natural gas hydrate reservoirs by injecting pure CO2 or other gas mixtures containing CO2. Laboratory-scale experiments show that this technique produces low methane volume and has a slow replacement rate due to the mass transfer barrier created due to impermeable CO2 hydrate layer formation, thus making the process commercially unattractive. This mass-transfer barrier can be reduced through pressure reduction techniques and chemical techniques; however, very few studies have focused on depressurization-assisted and chemical-assisted CH4−CO2 replacement to lower mass-transfer barriers and there are many unknowns. In this work, we qualitatively and quantitatively investigated the effect of the pressure reduction and presence of a hydrate promoter on mixed hydrate stability, CH4 recovery, and risk of water production during CH4−CO2 exchange. Exchange experiments were carried out using the 500 ppm sodium dodecyl sulfate (SDS) solution inside a high-pressure stirred reactor. Our results indicated that mixed hydrate stability and methane recovery depends on the degree of pressure reduction, type, and composition of injected gas. Final selection between CO2 and CO2 + N2 gas depends on the tradeoff between mixed hydrate stability pressure and methane recovery. Hydrate morphology studies suggest that production of water during the CH4−CO2 exchange is a stochastic phenomenon that is dependent on many parameters.
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Keywords
CO2 + N2 injection, hydrate stability, mass transfer, methane recovery, morphology studies, sodium dodecyl sulfate
Subject
Suggested Citation
Pandey JS, Solms NV. Hydrate Stability and Methane Recovery from Gas Hydrate through CH4−CO2 Replacement in Different Mass Transfer Scenarios. (2023). LAPSE:2023.20946
Author Affiliations
Pandey JS: Center for Energy Resource Engineering (CERE), Department of Chemical Engineering, Technical University of Denmark, Lyngby 2800, Denmark [ORCID]
Solms NV: Center for Energy Resource Engineering (CERE), Department of Chemical Engineering, Technical University of Denmark, Lyngby 2800, Denmark
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Solms NV: Center for Energy Resource Engineering (CERE), Department of Chemical Engineering, Technical University of Denmark, Lyngby 2800, Denmark
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Journal Name
Energies
Volume
12
Issue
12
Article Number
E2309
Year
2019
Publication Date
2019-06-17
ISSN
1996-1073
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Original Submission
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PII: en12122309, Publication Type: Journal Article
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LAPSE:2023.20946
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https://doi.org/10.3390/en12122309
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Mar 21, 2023
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