Enrichment of gas storage in clathrate hydrates by optimizing the molar liquid water-gas ratio

Natural gas (NG) is considered a modern source of energy. Gas hydrates are anticipated to be an alternative method for gas storage and transportation applications. The process must be handy, rapid, and proficient for scale-up. In the present study, methane (CH 4 ) and carbon dioxide (CO 2 ) hydrates...

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Bibliographic Details
Published in:RSC advances Vol. 12; no. 4; pp. 274 - 282
Main Authors: Burla, Sai Kiran, Pinnelli, S. R. Prasad
Format: Journal Article
Language:English
Published: England Royal Society of Chemistry 12-01-2022
The Royal Society of Chemistry
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Summary:Natural gas (NG) is considered a modern source of energy. Gas hydrates are anticipated to be an alternative method for gas storage and transportation applications. The process must be handy, rapid, and proficient for scale-up. In the present study, methane (CH 4 ) and carbon dioxide (CO 2 ) hydrates are synthesized by varying the guest (gas) to host (water) volume. The experiments are performed in a non-stirred system. The results specify that the maximum storage capacity is achieved when the molar liquid water-gas ratio is about 4.08 and 8.25 for CH 4 and CO 2 hydrates. At the optimal water-gas ratios, the total CH 4 and CO 2 gas uptake capacity is about 14.3 ± 0.4 and 9.1 ± 0.4 liters at standard temperature and pressure (STP) conditions. The gas uptake gradually increases with the solution volume and abruptly falls after a threshold point. The hydrate grows across the reactor's metal surface; when the process fully covers the surface, the growth continues horizontally (increase in thickness). With varying the liquid water-gas ratio (low to high), the formation kinetics ( t 90 ) is delayed. The hydrate growth rate gradually decreases and does not significantly influence the hydrate formation temperatures. Optimizing the molar liquid water-gas ratio yields a high gas storage capacity and faster process kinetics. Methane and carbon dioxide storage in hydrate form.
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ISSN:2046-2069
2046-2069
DOI:10.1039/d1ra07585c