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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Published in:Environmental Science & Technology
Main Authors: Lamorena, RB Lamorena, Rheo Baguio, Lee, WJ Lee, Woo-Jin
Format: Article in Journal/Newspaper
Language:English
Published: AMER CHEMICAL SOC 2008
Subjects:
Online Access:http://hdl.handle.net/10203/7338
https://doi.org/10.1021/es702179p
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spelling 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
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