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Microscopic observations of clathrate-hydrate films formed at liquid/liquid interfaces. I. Morphology of hydrate films
This study aims to obtain cross-sectional views of clathrate-hydrate films each formed at the interface between a liquid-water phase and a hydrophobic hydrate-former phase. For this purpose, an experimental scheme was devised which permitted us to observe, through a high-resolution microscope, cross...
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Published in: | Chemical engineering science 2001-07, Vol.56 (14), p.4331-4338 |
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creator | Kobayashi, Izushi Ito, Yusuke Mori, Yasuhiko H. |
description | This study aims to obtain cross-sectional views of clathrate-hydrate films each formed at the interface between a liquid-water phase and a hydrophobic hydrate-former phase. For this purpose, an experimental scheme was devised which permitted us to observe, through a high-resolution microscope, cross sections of a ring-shaped hydrate film formed over the surface of each discoid drop of HCFC-141b (CH
3CCl
2F) held stationary in a narrow space between two transparent plates filled with flowing, or quiescent, water. We found that the hydrate films, once exposed to a shear flow of water and then held in a quiescent medium of water, continued to thicken at a much higher rate than the films which had been held exclusively in a quiescent water medium since their formation. The former films kept their surface/internal texture much coarser, in the course of their thickening, than the latter films which showed very fine texture throughout. When continuously exposed to a steady water flow, the hydrate films kept their thickness constant. The steady-state thickness thus recognized showed a negative dependency on the flow velocity. A temperature rise, slightly exceeding the thermodynamic stability limit for the hydrate, caused each hydrate film once grown at a lower temperature to undergo crystal dissociation simultaneously throughout its thickness, in which numerous HCFC-141b droplets, a few micrometers in diameter, were evolved and migrated into the adjacent water phase. |
doi_str_mv | 10.1016/S0009-2509(00)00544-3 |
format | article |
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3CCl
2F) held stationary in a narrow space between two transparent plates filled with flowing, or quiescent, water. We found that the hydrate films, once exposed to a shear flow of water and then held in a quiescent medium of water, continued to thicken at a much higher rate than the films which had been held exclusively in a quiescent water medium since their formation. The former films kept their surface/internal texture much coarser, in the course of their thickening, than the latter films which showed very fine texture throughout. When continuously exposed to a steady water flow, the hydrate films kept their thickness constant. The steady-state thickness thus recognized showed a negative dependency on the flow velocity. A temperature rise, slightly exceeding the thermodynamic stability limit for the hydrate, caused each hydrate film once grown at a lower temperature to undergo crystal dissociation simultaneously throughout its thickness, in which numerous HCFC-141b droplets, a few micrometers in diameter, were evolved and migrated into the adjacent water phase.</description><identifier>ISSN: 0009-2509</identifier><identifier>EISSN: 1873-4405</identifier><identifier>DOI: 10.1016/S0009-2509(00)00544-3</identifier><identifier>CODEN: CESCAC</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Chemistry ; Clathrate hydrate ; Convective transport ; Crystallization ; Exact sciences and technology ; Gas hydrate ; Gas-liquid interface and liquid-liquid interface ; General and physical chemistry ; Mass transfer ; Morphology ; Surface physical chemistry</subject><ispartof>Chemical engineering science, 2001-07, Vol.56 (14), p.4331-4338</ispartof><rights>2001 Elsevier Science Ltd</rights><rights>2001 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c464t-a150b53fe601af086d4ece4db6c4a7a175e4d8a65a7bbb9abfc4b9f62e4f82353</citedby><cites>FETCH-LOGICAL-c464t-a150b53fe601af086d4ece4db6c4a7a175e4d8a65a7bbb9abfc4b9f62e4f82353</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1109825$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Kobayashi, Izushi</creatorcontrib><creatorcontrib>Ito, Yusuke</creatorcontrib><creatorcontrib>Mori, Yasuhiko H.</creatorcontrib><title>Microscopic observations of clathrate-hydrate films formed at liquid/liquid interfaces. I. Morphology of hydrate films</title><title>Chemical engineering science</title><description>This study aims to obtain cross-sectional views of clathrate-hydrate films each formed at the interface between a liquid-water phase and a hydrophobic hydrate-former phase. For this purpose, an experimental scheme was devised which permitted us to observe, through a high-resolution microscope, cross sections of a ring-shaped hydrate film formed over the surface of each discoid drop of HCFC-141b (CH
3CCl
2F) held stationary in a narrow space between two transparent plates filled with flowing, or quiescent, water. We found that the hydrate films, once exposed to a shear flow of water and then held in a quiescent medium of water, continued to thicken at a much higher rate than the films which had been held exclusively in a quiescent water medium since their formation. The former films kept their surface/internal texture much coarser, in the course of their thickening, than the latter films which showed very fine texture throughout. When continuously exposed to a steady water flow, the hydrate films kept their thickness constant. The steady-state thickness thus recognized showed a negative dependency on the flow velocity. A temperature rise, slightly exceeding the thermodynamic stability limit for the hydrate, caused each hydrate film once grown at a lower temperature to undergo crystal dissociation simultaneously throughout its thickness, in which numerous HCFC-141b droplets, a few micrometers in diameter, were evolved and migrated into the adjacent water phase.</description><subject>Chemistry</subject><subject>Clathrate hydrate</subject><subject>Convective transport</subject><subject>Crystallization</subject><subject>Exact sciences and technology</subject><subject>Gas hydrate</subject><subject>Gas-liquid interface and liquid-liquid interface</subject><subject>General and physical chemistry</subject><subject>Mass transfer</subject><subject>Morphology</subject><subject>Surface physical chemistry</subject><issn>0009-2509</issn><issn>1873-4405</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNqFkU9r20AQxZfSQF2nH6Gwh1Kag-xZaXclnUox-QcxOaQ9L6PVbL1F1jq7ssHfPlIcGnLK6THwmzfDe4x9FbAQIPTyAQDqLFdQ_wC4AFBSZsUHNhNVWWRSgvrIZv-RT-xzSv_GsSwFzNhh7W0MyYadtzw0ieIBBx_6xIPjtsNhE3GgbHNsJ-XOd9vEXYhbajkOvPOPe98uT8J9P1B0aCkt-O2Cr0PcbUIX_h4nszcW5-zMYZfoy4vO2Z-ry9-rm-zu_vp29esus1LLIUOhoFGFIw0CHVS6lWRJto22EksUpRqHCrXCsmmaGhtnZVM7nZN0VV6oYs6-n3x3MTzuKQ1m65OlrsOewj6ZXJdVDkX9LigqUZd6ROdMncApthTJmV30W4xHI8BMdZjnOsyUtQEwz3WYYtz79nIAk8XOReytT6_LAuoqnx7-ecJoTOXgKZpkPfWWWh_JDqYN_p1DTxV9oSI</recordid><startdate>20010701</startdate><enddate>20010701</enddate><creator>Kobayashi, Izushi</creator><creator>Ito, Yusuke</creator><creator>Mori, Yasuhiko H.</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QH</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope></search><sort><creationdate>20010701</creationdate><title>Microscopic observations of clathrate-hydrate films formed at liquid/liquid interfaces. I. Morphology of hydrate films</title><author>Kobayashi, Izushi ; Ito, Yusuke ; Mori, Yasuhiko H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c464t-a150b53fe601af086d4ece4db6c4a7a175e4d8a65a7bbb9abfc4b9f62e4f82353</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Chemistry</topic><topic>Clathrate hydrate</topic><topic>Convective transport</topic><topic>Crystallization</topic><topic>Exact sciences and technology</topic><topic>Gas hydrate</topic><topic>Gas-liquid interface and liquid-liquid interface</topic><topic>General and physical chemistry</topic><topic>Mass transfer</topic><topic>Morphology</topic><topic>Surface physical chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kobayashi, Izushi</creatorcontrib><creatorcontrib>Ito, Yusuke</creatorcontrib><creatorcontrib>Mori, Yasuhiko H.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Aqualine</collection><collection>Technology Research Database</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><jtitle>Chemical engineering science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kobayashi, Izushi</au><au>Ito, Yusuke</au><au>Mori, Yasuhiko H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Microscopic observations of clathrate-hydrate films formed at liquid/liquid interfaces. I. Morphology of hydrate films</atitle><jtitle>Chemical engineering science</jtitle><date>2001-07-01</date><risdate>2001</risdate><volume>56</volume><issue>14</issue><spage>4331</spage><epage>4338</epage><pages>4331-4338</pages><issn>0009-2509</issn><eissn>1873-4405</eissn><coden>CESCAC</coden><abstract>This study aims to obtain cross-sectional views of clathrate-hydrate films each formed at the interface between a liquid-water phase and a hydrophobic hydrate-former phase. For this purpose, an experimental scheme was devised which permitted us to observe, through a high-resolution microscope, cross sections of a ring-shaped hydrate film formed over the surface of each discoid drop of HCFC-141b (CH
3CCl
2F) held stationary in a narrow space between two transparent plates filled with flowing, or quiescent, water. We found that the hydrate films, once exposed to a shear flow of water and then held in a quiescent medium of water, continued to thicken at a much higher rate than the films which had been held exclusively in a quiescent water medium since their formation. The former films kept their surface/internal texture much coarser, in the course of their thickening, than the latter films which showed very fine texture throughout. When continuously exposed to a steady water flow, the hydrate films kept their thickness constant. The steady-state thickness thus recognized showed a negative dependency on the flow velocity. A temperature rise, slightly exceeding the thermodynamic stability limit for the hydrate, caused each hydrate film once grown at a lower temperature to undergo crystal dissociation simultaneously throughout its thickness, in which numerous HCFC-141b droplets, a few micrometers in diameter, were evolved and migrated into the adjacent water phase.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><doi>10.1016/S0009-2509(00)00544-3</doi><tpages>8</tpages></addata></record> |
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subjects | Chemistry Clathrate hydrate Convective transport Crystallization Exact sciences and technology Gas hydrate Gas-liquid interface and liquid-liquid interface General and physical chemistry Mass transfer Morphology Surface physical chemistry |
title | Microscopic observations of clathrate-hydrate films formed at liquid/liquid interfaces. I. Morphology of hydrate films |
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