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...

Full description

Bibliographic Details
Main Authors: Meku Maruyama, Riku Matsuura, Ryo Ohmura
Format: Article
Language:English
Published: Nature Publishing Group 2021-05-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-90802-6
id doaj-873ca482b3a1489a9eaf7bdb0cb2c419
record_format Article
spelling 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 AT mekumaruyama crystalgrowthofclathratehydrateformedwithh2co2mixedgasandtetrahydropyran
AT rikumatsuura crystalgrowthofclathratehydrateformedwithh2co2mixedgasandtetrahydropyran
AT ryoohmura crystalgrowthofclathratehydrateformedwithh2co2mixedgasandtetrahydropyran
_version_ 1721393740003672064