LAPSE:2023.27290
Published Article

LAPSE:2023.27290
Enhanced Hydrate-Based Geological CO2 Capture and Sequestration as a Mitigation Strategy to Address Climate Change
April 4, 2023
Abstract
Geological sequestration of CO2-rich gas as a CO2 capture and storage technique has a lower technical and cost barrier compared to industrial scale-up. In this study, we have proposed CO2 capture and storage via hydrate in geological formation within the hydrate stability zone as a novel technique to contribute to global warming mitigation strategies, including carbon capture, utilization, and storage (CCUS) and to prevent vast methane release into the atmosphere caused by hydrate melting. We have attempted to enhance total gas uptake and CO2 capture efficiency in hydrate in the presence of kinetic promoters while using diluted CO2 gas (CO2-N2 mixture). Experiments are performed using unfrozen sands within hydrate stability zone condition and in the presence of low dosage surfactant and amino acids. Hydrate formation parameters, including sub-cooling temperature, induction time, total gas uptake, and split fraction, are calculated during the single-step formation and dissociation process. The effect of sands with varying particle sizes (160−630 µm, 1400−5000 µm), low dosage promoter (500−3000 ppm) and CO2 concentration in feed gas (20−30 mol%) on formation kinetic parameters was investigated. Enhanced formation kinetics are observed in the presence of surfactant (1000−3000 ppm) and hydrophobic amino acids (3000 ppm) at 120 bar and 1 ℃ experimental conditions. We report induction time in the range of 7−170 min and CO2 split fraction (0.60−0.90) in hydrate for 120 bar initial injection pressure. CO2 split fraction can be enhanced by reducing sand particle size or increasing the CO2 mol% in incoming feed gas at given injection pressure. This study also reports that formation kinetics in a porous medium are influenced by hydrate morphology. Hydrate morphology influences gas and water migration within sediments and controls pore space or particle surface correlation with the formation kinetics within coarse sediments. This investigation demonstrates the potential application of bio-friendly amino acids as promoters to enhance CO2 capture and storage within hydrate. Sufficient contact time at gas-liquid interface and higher CO2 separation efficiency is recorded in the presence of amino acids. The findings of this study could be useful in exploring the promoter-driven pore habitat of CO2-rich hydrates in sediments to address climate change.
Geological sequestration of CO2-rich gas as a CO2 capture and storage technique has a lower technical and cost barrier compared to industrial scale-up. In this study, we have proposed CO2 capture and storage via hydrate in geological formation within the hydrate stability zone as a novel technique to contribute to global warming mitigation strategies, including carbon capture, utilization, and storage (CCUS) and to prevent vast methane release into the atmosphere caused by hydrate melting. We have attempted to enhance total gas uptake and CO2 capture efficiency in hydrate in the presence of kinetic promoters while using diluted CO2 gas (CO2-N2 mixture). Experiments are performed using unfrozen sands within hydrate stability zone condition and in the presence of low dosage surfactant and amino acids. Hydrate formation parameters, including sub-cooling temperature, induction time, total gas uptake, and split fraction, are calculated during the single-step formation and dissociation process. The effect of sands with varying particle sizes (160−630 µm, 1400−5000 µm), low dosage promoter (500−3000 ppm) and CO2 concentration in feed gas (20−30 mol%) on formation kinetic parameters was investigated. Enhanced formation kinetics are observed in the presence of surfactant (1000−3000 ppm) and hydrophobic amino acids (3000 ppm) at 120 bar and 1 ℃ experimental conditions. We report induction time in the range of 7−170 min and CO2 split fraction (0.60−0.90) in hydrate for 120 bar initial injection pressure. CO2 split fraction can be enhanced by reducing sand particle size or increasing the CO2 mol% in incoming feed gas at given injection pressure. This study also reports that formation kinetics in a porous medium are influenced by hydrate morphology. Hydrate morphology influences gas and water migration within sediments and controls pore space or particle surface correlation with the formation kinetics within coarse sediments. This investigation demonstrates the potential application of bio-friendly amino acids as promoters to enhance CO2 capture and storage within hydrate. Sufficient contact time at gas-liquid interface and higher CO2 separation efficiency is recorded in the presence of amino acids. The findings of this study could be useful in exploring the promoter-driven pore habitat of CO2-rich hydrates in sediments to address climate change.
Record ID
Keywords
amino acids, climate change, CO2 capture and sequestration, formation kinetics, permafrost and marine sands
Subject
Suggested Citation
Pandey JS, Daas YJ, Karcz AP, von Solms N. Enhanced Hydrate-Based Geological CO2 Capture and Sequestration as a Mitigation Strategy to Address Climate Change. (2023). LAPSE:2023.27290
Author Affiliations
Pandey JS: Center for Energy Resource Engineering (CERE), Department of Chemical Engineering, Technical University of Denmark, 2800 Kgs. Lyngby, Denmark [ORCID]
Daas YJ: Center for Energy Resource Engineering (CERE), Department of Chemical Engineering, Technical University of Denmark, 2800 Kgs. Lyngby, Denmark
Karcz AP: PROSYS Research Centre, Department Chemical and Biochemical Engineering, Technical University of Denmark, 2800 Kgs. Lyngby, Denmark [ORCID]
von Solms N: Center for Energy Resource Engineering (CERE), Department of Chemical Engineering, Technical University of Denmark, 2800 Kgs. Lyngby, Denmark [ORCID]
Daas YJ: Center for Energy Resource Engineering (CERE), Department of Chemical Engineering, Technical University of Denmark, 2800 Kgs. Lyngby, Denmark
Karcz AP: PROSYS Research Centre, Department Chemical and Biochemical Engineering, Technical University of Denmark, 2800 Kgs. Lyngby, Denmark [ORCID]
von Solms N: Center for Energy Resource Engineering (CERE), Department of Chemical Engineering, Technical University of Denmark, 2800 Kgs. Lyngby, Denmark [ORCID]
Journal Name
Energies
Volume
13
Issue
21
Article Number
E5661
Year
2020
Publication Date
2020-10-29
ISSN
1996-1073
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Original Submission
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PII: en13215661, Publication Type: Journal Article
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LAPSE:2023.27290
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https://doi.org/10.3390/en13215661
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