Surface Aggregate Phase Transition
A surface aggregate phase transition is described. Atomic force microscopy has been used to image the equilibrium association of sodium dodecyl sulfate (SDS) and 1-dodecanol molecules at the interface between graphite and aqueous solutions. In pure SDS solutions, the molecules associate into long, p...
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Veröffentlicht in: | Langmuir 1997-08, Vol.13 (16), p.4223-4228 |
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description | A surface aggregate phase transition is described. Atomic force microscopy has been used to image the equilibrium association of sodium dodecyl sulfate (SDS) and 1-dodecanol molecules at the interface between graphite and aqueous solutions. In pure SDS solutions, the molecules associate into long, parallel hemicylindrical surface aggregates over a concentration range from about one-third to at least 10 times the critical micelle concentration (cmc). Above the cmc, dodecanol has little influence on the surface aggregate structure, probably because dodecanol is partitioned into the bulk micelles. Below the cmc, dodecanol causes a transition from hemicylindrical aggregates to a two-phase mixture in which flat sheets coexist with swollen hemicylindrical aggregates. In this mixture, the hemicylindrical aggregates are preferentially located at and parallel to steps on the underlying graphite substrate. Under conditions where hemicylinders and flat sheets coexist, an increase in bulk dodecanol concentration results in an increase in surface coverage by flat sheets. No bulk solution changes were detected by NMR in the region where the surface phase transition was observed. |
doi_str_mv | 10.1021/la970146k |
format | Article |
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Atomic force microscopy has been used to image the equilibrium association of sodium dodecyl sulfate (SDS) and 1-dodecanol molecules at the interface between graphite and aqueous solutions. In pure SDS solutions, the molecules associate into long, parallel hemicylindrical surface aggregates over a concentration range from about one-third to at least 10 times the critical micelle concentration (cmc). Above the cmc, dodecanol has little influence on the surface aggregate structure, probably because dodecanol is partitioned into the bulk micelles. Below the cmc, dodecanol causes a transition from hemicylindrical aggregates to a two-phase mixture in which flat sheets coexist with swollen hemicylindrical aggregates. In this mixture, the hemicylindrical aggregates are preferentially located at and parallel to steps on the underlying graphite substrate. Under conditions where hemicylinders and flat sheets coexist, an increase in bulk dodecanol concentration results in an increase in surface coverage by flat sheets. No bulk solution changes were detected by NMR in the region where the surface phase transition was observed.</description><identifier>ISSN: 0743-7463</identifier><identifier>EISSN: 1520-5827</identifier><identifier>DOI: 10.1021/la970146k</identifier><identifier>CODEN: LANGD5</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Chemistry ; Colloidal state and disperse state ; Exact sciences and technology ; General and physical chemistry ; Micelles. Thin films</subject><ispartof>Langmuir, 1997-08, Vol.13 (16), p.4223-4228</ispartof><rights>Copyright © 1997 American Chemical Society</rights><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a324t-fe25311f9d2f63403d27413c2e0166e8ff4375d092cd9fddf5f283f116f7fea83</citedby><cites>FETCH-LOGICAL-a324t-fe25311f9d2f63403d27413c2e0166e8ff4375d092cd9fddf5f283f116f7fea83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/la970146k$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/la970146k$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2751,27055,27903,27904,56717,56767</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2791507$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Wanless, Erica J</creatorcontrib><creatorcontrib>Davey, Tim W</creatorcontrib><creatorcontrib>Ducker, William A</creatorcontrib><title>Surface Aggregate Phase Transition</title><title>Langmuir</title><addtitle>Langmuir</addtitle><description>A surface aggregate phase transition is described. Atomic force microscopy has been used to image the equilibrium association of sodium dodecyl sulfate (SDS) and 1-dodecanol molecules at the interface between graphite and aqueous solutions. In pure SDS solutions, the molecules associate into long, parallel hemicylindrical surface aggregates over a concentration range from about one-third to at least 10 times the critical micelle concentration (cmc). Above the cmc, dodecanol has little influence on the surface aggregate structure, probably because dodecanol is partitioned into the bulk micelles. Below the cmc, dodecanol causes a transition from hemicylindrical aggregates to a two-phase mixture in which flat sheets coexist with swollen hemicylindrical aggregates. In this mixture, the hemicylindrical aggregates are preferentially located at and parallel to steps on the underlying graphite substrate. Under conditions where hemicylinders and flat sheets coexist, an increase in bulk dodecanol concentration results in an increase in surface coverage by flat sheets. No bulk solution changes were detected by NMR in the region where the surface phase transition was observed.</description><subject>Chemistry</subject><subject>Colloidal state and disperse state</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Micelles. Thin films</subject><issn>0743-7463</issn><issn>1520-5827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><recordid>eNptj8FKAzEQhoMoWKsH36CIHjysziTZZHMspVWhaLEVvIWQzdRta7ckW9C3d2WlJ09zmO-f-T_GLhHuEDjeb5zRgFKtj1gPcw5ZXnB9zHqgpci0VOKUnaW0AgAjpOmxq_k-kvNhMFwuY1i6JgxmHy6FwSK6baqaqt6esxNymxQu_mafvU3Gi9FjNn15eBoNp5kTXDYZBZ4LRDIlJyUkiJJricLzAKhUKIik0HkJhvvSUFlSTrwQhKhIU3CF6LPb7q6PdUoxkN3F6tPFb4tgf-XsQa5lrzt255J3G2rL-iodAlwbzEG3WNZhVWrC12Ht4toq3baxi9nc4vPsdVK8awstf9Pxzie7qvdx2wr_8_4Hrrdn9Q</recordid><startdate>19970806</startdate><enddate>19970806</enddate><creator>Wanless, Erica J</creator><creator>Davey, Tim W</creator><creator>Ducker, William A</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19970806</creationdate><title>Surface Aggregate Phase Transition</title><author>Wanless, Erica J ; Davey, Tim W ; Ducker, William A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a324t-fe25311f9d2f63403d27413c2e0166e8ff4375d092cd9fddf5f283f116f7fea83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Chemistry</topic><topic>Colloidal state and disperse state</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>Micelles. Thin films</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wanless, Erica J</creatorcontrib><creatorcontrib>Davey, Tim W</creatorcontrib><creatorcontrib>Ducker, William A</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Langmuir</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wanless, Erica J</au><au>Davey, Tim W</au><au>Ducker, William A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Surface Aggregate Phase Transition</atitle><jtitle>Langmuir</jtitle><addtitle>Langmuir</addtitle><date>1997-08-06</date><risdate>1997</risdate><volume>13</volume><issue>16</issue><spage>4223</spage><epage>4228</epage><pages>4223-4228</pages><issn>0743-7463</issn><eissn>1520-5827</eissn><coden>LANGD5</coden><abstract>A surface aggregate phase transition is described. Atomic force microscopy has been used to image the equilibrium association of sodium dodecyl sulfate (SDS) and 1-dodecanol molecules at the interface between graphite and aqueous solutions. In pure SDS solutions, the molecules associate into long, parallel hemicylindrical surface aggregates over a concentration range from about one-third to at least 10 times the critical micelle concentration (cmc). Above the cmc, dodecanol has little influence on the surface aggregate structure, probably because dodecanol is partitioned into the bulk micelles. Below the cmc, dodecanol causes a transition from hemicylindrical aggregates to a two-phase mixture in which flat sheets coexist with swollen hemicylindrical aggregates. In this mixture, the hemicylindrical aggregates are preferentially located at and parallel to steps on the underlying graphite substrate. Under conditions where hemicylinders and flat sheets coexist, an increase in bulk dodecanol concentration results in an increase in surface coverage by flat sheets. No bulk solution changes were detected by NMR in the region where the surface phase transition was observed.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/la970146k</doi><tpages>6</tpages></addata></record> |
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subjects | Chemistry Colloidal state and disperse state Exact sciences and technology General and physical chemistry Micelles. Thin films |
title | Surface Aggregate Phase Transition |
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