Solid State Transitions of Asymmetric Catanionic Surfactants
A series of asymmetric surfactants were prepared from cationic surfactant, hexadecyltrimethylammonium bromide, and anionic surfactant, sodium alkyl sulfate (the number of carbon atoms per chain being 10, 12, or 14). The influence of the alkyl chain asymmetry on the thermal properties of formed hexad...
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Veröffentlicht in: | Journal of colloid and interface science 1999-07, Vol.215 (2), p.280-289 |
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description | A series of asymmetric surfactants were prepared from cationic surfactant, hexadecyltrimethylammonium bromide, and anionic surfactant, sodium alkyl sulfate (the number of carbon atoms per chain being 10, 12, or 14). The influence of the alkyl chain asymmetry on the thermal properties of formed hexadecyltrimethylammonium alkyl sulfates was investigated by means of polarizing microscopy, differential scanning calorimetry, and X-ray diffraction. Asymmetric catanionic surfactants exhibited a complex polymorphism and thermotropic mesomorphism from the stable crystalline form to the isotropic phase. On heating, successive phase transitions (several solid crystalline–solid crystalline, solid crystalline–liquid crystalline, and liquid crystalline–isotropic liquid) were observed. The number of polymorphs, in all of the bilayered structure, depended on the asymmetry between the lengths of surfactant tails. The basic lamellar thickness varied linearly with the increase of alkyl sulfate chain length. An increase of the basic lamellar thickness with temperature was determined. Polarizing microscopy revealed a characteristic texture of the smectic phase. On cooling, all compounds underwent reversibly the isotropic liquid–liquid crystalline transitions, while crystallization from melted samples was kinetically controlled. |
doi_str_mv | 10.1006/jcis.1999.6234 |
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The influence of the alkyl chain asymmetry on the thermal properties of formed hexadecyltrimethylammonium alkyl sulfates was investigated by means of polarizing microscopy, differential scanning calorimetry, and X-ray diffraction. Asymmetric catanionic surfactants exhibited a complex polymorphism and thermotropic mesomorphism from the stable crystalline form to the isotropic phase. On heating, successive phase transitions (several solid crystalline–solid crystalline, solid crystalline–liquid crystalline, and liquid crystalline–isotropic liquid) were observed. The number of polymorphs, in all of the bilayered structure, depended on the asymmetry between the lengths of surfactant tails. The basic lamellar thickness varied linearly with the increase of alkyl sulfate chain length. An increase of the basic lamellar thickness with temperature was determined. Polarizing microscopy revealed a characteristic texture of the smectic phase. 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The influence of the alkyl chain asymmetry on the thermal properties of formed hexadecyltrimethylammonium alkyl sulfates was investigated by means of polarizing microscopy, differential scanning calorimetry, and X-ray diffraction. Asymmetric catanionic surfactants exhibited a complex polymorphism and thermotropic mesomorphism from the stable crystalline form to the isotropic phase. On heating, successive phase transitions (several solid crystalline–solid crystalline, solid crystalline–liquid crystalline, and liquid crystalline–isotropic liquid) were observed. The number of polymorphs, in all of the bilayered structure, depended on the asymmetry between the lengths of surfactant tails. The basic lamellar thickness varied linearly with the increase of alkyl sulfate chain length. An increase of the basic lamellar thickness with temperature was determined. Polarizing microscopy revealed a characteristic texture of the smectic phase. On cooling, all compounds underwent reversibly the isotropic liquid–liquid crystalline transitions, while crystallization from melted samples was kinetically controlled.</description><subject>catanionic surfactants</subject><subject>Chemistry</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>liquid crystals</subject><subject>phase transitions</subject><subject>polymorphism</subject><subject>Surface physical chemistry</subject><subject>Surface-active agents: properties</subject><subject>thermal analysis</subject><issn>0021-9797</issn><issn>1095-7103</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNp1kMtrGzEQh0VoaRy31xzDHnrIZd2Z3dULejGmaQqGHuyehTyrBZl9JJIc8H9fLTYll57mwTc_ho-xe4QVAohvR_JxhVrrlajq5oYtEDQvJUL9gS0AKiy11PKW3cV4BEDkXH9itwgNaiGqBfu-m3rfFrtkkyv2wY7RJz-NsZi6Yh3Pw-BS8FRsbLJj3ud2dwqdpTym-Jl97Gwf3ZdrXbI_Tz_2m-dy-_vnr816W1ItMZW2ahURCdE0B8m1AmjUgYTq0FJrBbdO1hqBUB0aDVJpxUlS3eYRKlm39ZI9XnJfwvR6cjGZwUdyfW9HN52iQcV1jaB4ldHVBaUwxRhcZ16CH2w4GwQzGzOzMTMbM7OxfPBwzT4dBte-wy-KMvD1CthItu-yoznhH6cEVxXPmLpgLot48y6YSN6N5FofHCXTTv5_L_wFuqaGKw</recordid><startdate>19990715</startdate><enddate>19990715</enddate><creator>TOMASIC, V</creator><creator>POPOVIC, S</creator><creator>FILIPOVIC-VINCEKOVIC, N</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19990715</creationdate><title>Solid State Transitions of Asymmetric Catanionic Surfactants</title><author>TOMASIC, V ; POPOVIC, S ; FILIPOVIC-VINCEKOVIC, N</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c371t-a2d8ccc6644b75980048bc68f1acda65ae73910c18b49078985c7c3d8b40273d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>catanionic surfactants</topic><topic>Chemistry</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>liquid crystals</topic><topic>phase transitions</topic><topic>polymorphism</topic><topic>Surface physical chemistry</topic><topic>Surface-active agents: properties</topic><topic>thermal analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>TOMASIC, V</creatorcontrib><creatorcontrib>POPOVIC, S</creatorcontrib><creatorcontrib>FILIPOVIC-VINCEKOVIC, N</creatorcontrib><collection>Pascal-Francis</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of colloid and interface science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>TOMASIC, V</au><au>POPOVIC, S</au><au>FILIPOVIC-VINCEKOVIC, N</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Solid State Transitions of Asymmetric Catanionic Surfactants</atitle><jtitle>Journal of colloid and interface science</jtitle><addtitle>J Colloid Interface Sci</addtitle><date>1999-07-15</date><risdate>1999</risdate><volume>215</volume><issue>2</issue><spage>280</spage><epage>289</epage><pages>280-289</pages><issn>0021-9797</issn><eissn>1095-7103</eissn><coden>JCISA5</coden><abstract>A series of asymmetric surfactants were prepared from cationic surfactant, hexadecyltrimethylammonium bromide, and anionic surfactant, sodium alkyl sulfate (the number of carbon atoms per chain being 10, 12, or 14). The influence of the alkyl chain asymmetry on the thermal properties of formed hexadecyltrimethylammonium alkyl sulfates was investigated by means of polarizing microscopy, differential scanning calorimetry, and X-ray diffraction. Asymmetric catanionic surfactants exhibited a complex polymorphism and thermotropic mesomorphism from the stable crystalline form to the isotropic phase. On heating, successive phase transitions (several solid crystalline–solid crystalline, solid crystalline–liquid crystalline, and liquid crystalline–isotropic liquid) were observed. The number of polymorphs, in all of the bilayered structure, depended on the asymmetry between the lengths of surfactant tails. The basic lamellar thickness varied linearly with the increase of alkyl sulfate chain length. An increase of the basic lamellar thickness with temperature was determined. Polarizing microscopy revealed a characteristic texture of the smectic phase. On cooling, all compounds underwent reversibly the isotropic liquid–liquid crystalline transitions, while crystallization from melted samples was kinetically controlled.</abstract><cop>San Diego, CA</cop><pub>Elsevier Inc</pub><pmid>10419662</pmid><doi>10.1006/jcis.1999.6234</doi><tpages>10</tpages></addata></record> |
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subjects | catanionic surfactants Chemistry Exact sciences and technology General and physical chemistry liquid crystals phase transitions polymorphism Surface physical chemistry Surface-active agents: properties thermal analysis |
title | Solid State Transitions of Asymmetric Catanionic Surfactants |
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