Formation of carbon dioxide hydrate in soil and soil mineral suspensions with electrolytes
We have identified the effects of solid surface (soil, bentonite, kaolinite, nontronite, and pyrite) and electrolyte (NaCl, KCl, CaCl2, and MgCl2) types on the formation and dissociation of CO2 hydrate in this study. The hydrate formation experiments were conducted by injecting CO2 gas into the soil...
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AMER CHEMICAL SOC
2008
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Online Access: | http://hdl.handle.net/10203/7338 https://doi.org/10.1021/es702179p |
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ftkoasas:oai:koasas.kaist.ac.kr:10203/7338 2023-05-15T15:52:51+02:00 Formation of carbon dioxide hydrate in soil and soil mineral suspensions with electrolytes Lamorena, RB Lamorena, Rheo Baguio Lee, WJ Lee, Woo-Jin 200804 http://hdl.handle.net/10203/7338 https://doi.org/10.1021/es702179p ENG en_US eng AMER CHEMICAL SOC PHASE-EQUILIBRIUM; METHANE; WATER; SURFACE; DYNAMICS; SOLUBILITY; SIMULATION; SEDIMENTS; MODEL; CLAY ARTICLE A 2008 ftkoasas https://doi.org/10.1021/es702179p 2014-11-28T06:11:04Z We have identified the effects of solid surface (soil, bentonite, kaolinite, nontronite, and pyrite) and electrolyte (NaCl, KCl, CaCl2, and MgCl2) types on the formation and dissociation of CO2 hydrate in this study. The hydrate formation experiments were conducted by injecting CO2 gas into the soil suspensions with and without electrolytes in a 50 mL pressurized vessel. The formation of CO2 hydrate in deionized water was faster than that in aqueous electrolyte solutions. The addition of soil suspensions accelerated the formation of CO2 hydrate in the electrolyte solutions. The hydrate formation times in the solid suspensions without electrolytes were very similar to that in the deionized water. We did not observe any significant differences between the hydrate dissociation in the solid suspension and that in the deionized water. The pHs of clay mineral suspensions decreased significantly after CO2 hydrate formation and dissociation experiments, while the pH of the soil suspension slightly decreased by less than pH 1 and that of pyrite slightly increased due to the dissolution of CO2 forming carbonic acid. The results obtained from this research could be indirectly applied to the fate of CO2 sequestered into geological formations as well as its storage as a form of CO2 hydrate. This work was fully supported by grants from the Basic Research Program of the Korea Science and Engineering Foundation (Grant R01-2006-000-10727-0), the Korea Ministry of Construction and Transportation (Grant 07-UR-B04), and the Korea Research Foundation (Grant KRF-2007-211-C00045). Article in Journal/Newspaper Carbonic acid Korea Advanced Institute of Science and Technology: KOASAS - KAIST Open Access Self-Archiving System Environmental Science & Technology 42 8 2753 2759 |
institution |
Open Polar |
collection |
Korea Advanced Institute of Science and Technology: KOASAS - KAIST Open Access Self-Archiving System |
op_collection_id |
ftkoasas |
language |
English |
topic |
PHASE-EQUILIBRIUM; METHANE; WATER; SURFACE; DYNAMICS; SOLUBILITY; SIMULATION; SEDIMENTS; MODEL; CLAY |
spellingShingle |
PHASE-EQUILIBRIUM; METHANE; WATER; SURFACE; DYNAMICS; SOLUBILITY; SIMULATION; SEDIMENTS; MODEL; CLAY Lamorena, RB Lamorena, Rheo Baguio Lee, WJ Lee, Woo-Jin Formation of carbon dioxide hydrate in soil and soil mineral suspensions with electrolytes |
topic_facet |
PHASE-EQUILIBRIUM; METHANE; WATER; SURFACE; DYNAMICS; SOLUBILITY; SIMULATION; SEDIMENTS; MODEL; CLAY |
description |
We have identified the effects of solid surface (soil, bentonite, kaolinite, nontronite, and pyrite) and electrolyte (NaCl, KCl, CaCl2, and MgCl2) types on the formation and dissociation of CO2 hydrate in this study. The hydrate formation experiments were conducted by injecting CO2 gas into the soil suspensions with and without electrolytes in a 50 mL pressurized vessel. The formation of CO2 hydrate in deionized water was faster than that in aqueous electrolyte solutions. The addition of soil suspensions accelerated the formation of CO2 hydrate in the electrolyte solutions. The hydrate formation times in the solid suspensions without electrolytes were very similar to that in the deionized water. We did not observe any significant differences between the hydrate dissociation in the solid suspension and that in the deionized water. The pHs of clay mineral suspensions decreased significantly after CO2 hydrate formation and dissociation experiments, while the pH of the soil suspension slightly decreased by less than pH 1 and that of pyrite slightly increased due to the dissolution of CO2 forming carbonic acid. The results obtained from this research could be indirectly applied to the fate of CO2 sequestered into geological formations as well as its storage as a form of CO2 hydrate. This work was fully supported by grants from the Basic Research Program of the Korea Science and Engineering Foundation (Grant R01-2006-000-10727-0), the Korea Ministry of Construction and Transportation (Grant 07-UR-B04), and the Korea Research Foundation (Grant KRF-2007-211-C00045). |
format |
Article in Journal/Newspaper |
author |
Lamorena, RB Lamorena, Rheo Baguio Lee, WJ Lee, Woo-Jin |
author_facet |
Lamorena, RB Lamorena, Rheo Baguio Lee, WJ Lee, Woo-Jin |
author_sort |
Lamorena, RB Lamorena, Rheo Baguio |
title |
Formation of carbon dioxide hydrate in soil and soil mineral suspensions with electrolytes |
title_short |
Formation of carbon dioxide hydrate in soil and soil mineral suspensions with electrolytes |
title_full |
Formation of carbon dioxide hydrate in soil and soil mineral suspensions with electrolytes |
title_fullStr |
Formation of carbon dioxide hydrate in soil and soil mineral suspensions with electrolytes |
title_full_unstemmed |
Formation of carbon dioxide hydrate in soil and soil mineral suspensions with electrolytes |
title_sort |
formation of carbon dioxide hydrate in soil and soil mineral suspensions with electrolytes |
publisher |
AMER CHEMICAL SOC |
publishDate |
2008 |
url |
http://hdl.handle.net/10203/7338 https://doi.org/10.1021/es702179p |
genre |
Carbonic acid |
genre_facet |
Carbonic acid |
op_doi |
https://doi.org/10.1021/es702179p |
container_title |
Environmental Science & Technology |
container_volume |
42 |
container_issue |
8 |
container_start_page |
2753 |
op_container_end_page |
2759 |
_version_ |
1766387964103884800 |