Crystal growth of clathrate hydrate formed with H2 + CO2 mixed gas and tetrahydropyran
Abstract Hydrate-based gas separation technology is applicable to the CO2 capture and storage from synthesis gas mixture generated through gasification of fuel sources including biomass. This paper reports visual observations of crystal growth dynamics and crystal morphology of hydrate formed in the...
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2021-05-01
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Online Access: | https://doi.org/10.1038/s41598-021-90802-6 |
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doaj-873ca482b3a1489a9eaf7bdb0cb2c4192021-06-06T11:39:26ZengNature Publishing GroupScientific Reports2045-23222021-05-011111910.1038/s41598-021-90802-6Crystal growth of clathrate hydrate formed with H2 + CO2 mixed gas and tetrahydropyranMeku Maruyama0Riku Matsuura1Ryo Ohmura2Department of Mechanical Engineering, Keio UniversityDepartment of Mechanical Engineering, Keio UniversityDepartment of Mechanical Engineering, Keio UniversityAbstract Hydrate-based gas separation technology is applicable to the CO2 capture and storage from synthesis gas mixture generated through gasification of fuel sources including biomass. This paper reports visual observations of crystal growth dynamics and crystal morphology of hydrate formed in the H2 + CO2 + tetrahydropyran (THP) + water system with a target for developing the hydrate-based CO2 separation process design. Experiments were conducted at a temperature range of 279.5–284.9 K under the pressure of 4.9–5.3 MPa. To simulate the synthesis gas, gas composition in the gas phase was maintained around H2:CO2 = 0.6:0.4 in mole fraction. Hydrate crystals were formed and extended along the THP/water interface. After the complete coverage of the interface to shape a polycrystalline shell, hydrate crystals continued to grow further into the bulk of liquid water. The individual crystals were identified as hexagonal, tetragonal and other polygonal-shaped formations. The crystal growth rate and the crystal size varied depending on thermodynamic conditions. Implications from the obtained results for the arrangement of operating conditions at the hydrate formation-, transportation-, and dissociation processes are discussed.https://doi.org/10.1038/s41598-021-90802-6 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Meku Maruyama Riku Matsuura Ryo Ohmura |
spellingShingle |
Meku Maruyama Riku Matsuura Ryo Ohmura Crystal growth of clathrate hydrate formed with H2 + CO2 mixed gas and tetrahydropyran Scientific Reports |
author_facet |
Meku Maruyama Riku Matsuura Ryo Ohmura |
author_sort |
Meku Maruyama |
title |
Crystal growth of clathrate hydrate formed with H2 + CO2 mixed gas and tetrahydropyran |
title_short |
Crystal growth of clathrate hydrate formed with H2 + CO2 mixed gas and tetrahydropyran |
title_full |
Crystal growth of clathrate hydrate formed with H2 + CO2 mixed gas and tetrahydropyran |
title_fullStr |
Crystal growth of clathrate hydrate formed with H2 + CO2 mixed gas and tetrahydropyran |
title_full_unstemmed |
Crystal growth of clathrate hydrate formed with H2 + CO2 mixed gas and tetrahydropyran |
title_sort |
crystal growth of clathrate hydrate formed with h2 + co2 mixed gas and tetrahydropyran |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2021-05-01 |
description |
Abstract Hydrate-based gas separation technology is applicable to the CO2 capture and storage from synthesis gas mixture generated through gasification of fuel sources including biomass. This paper reports visual observations of crystal growth dynamics and crystal morphology of hydrate formed in the H2 + CO2 + tetrahydropyran (THP) + water system with a target for developing the hydrate-based CO2 separation process design. Experiments were conducted at a temperature range of 279.5–284.9 K under the pressure of 4.9–5.3 MPa. To simulate the synthesis gas, gas composition in the gas phase was maintained around H2:CO2 = 0.6:0.4 in mole fraction. Hydrate crystals were formed and extended along the THP/water interface. After the complete coverage of the interface to shape a polycrystalline shell, hydrate crystals continued to grow further into the bulk of liquid water. The individual crystals were identified as hexagonal, tetragonal and other polygonal-shaped formations. The crystal growth rate and the crystal size varied depending on thermodynamic conditions. Implications from the obtained results for the arrangement of operating conditions at the hydrate formation-, transportation-, and dissociation processes are discussed. |
url |
https://doi.org/10.1038/s41598-021-90802-6 |
work_keys_str_mv |
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