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Partitioning behavior of an acid-cleavable, 1,3-dioxolane alkyl ethoxylate, surfactant in single and binary surfactant mixtures for 2- and 3-phase microemulsion systems according to ethoxylate head group size
Partition coefficients for a 1,3-dioxolane alkyl ethoxylate surfactant in 2- and 3-phase microemulsion systems as a function of the ethoxylate size ( n): experimental data and thermodynamic model (curves). [Display omitted] ► Aerosol-OT and cyclic ketal alkyl ethoxylate form temperature-insensitive...
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Published in: | Journal of colloid and interface science 2010-12, Vol.352 (2), p.424-435 |
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container_title | Journal of colloid and interface science |
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creator | Rio, Javier Gomez del Hayes, Douglas G. Urban, Volker S. |
description | Partition coefficients for a 1,3-dioxolane alkyl ethoxylate surfactant in 2- and 3-phase microemulsion systems as a function of the ethoxylate size (
n): experimental data and thermodynamic model (curves).
[Display omitted]
► Aerosol-OT and cyclic ketal alkyl ethoxylate form temperature-insensitive microemulsions. ► HLB temperature for alkyl ethoxylate microemulsions predicted using partition coefficient data. ► Partitioning of cyclic ketal alkyl ethoxylates strongly affected by ethoxylate size. ► Tail region of cyclic ketal alkyl ethoxylates more polar than the that of fatty alcohol ethoxylates. ► Microemulsions in Winsor-III bottom phases formed by cyclic ketal alkyl ethoxylates (SANS).
Partition coefficients for a pH-degradable 1,3-dioxolane alkyl ethoxylate surfactant, 4-CH
3O (CH
2CH
2O)
5.6-CH
2, 2,2-(CH
2)
12CH
3, 2-(CH
2) CH
3, 1,3-dioxolane or “cyclic ketal” surfactant, CK-2,13-E
5.6,ave, between isooctane- and water-rich phases of 2- and 3-phase microemulsion systems (
K
n
) were determined as functions of the ethoxylate size,
n, and temperature for the neat surfactant and its binary surfactant mixtures, to understand the partitioning of alkyl ethoxylates possessing a broad distribution of ethoxylate size and to determine conditions required for formation of 3-phase microemulsion systems at an optimal temperature where phase separation occurs rapidly, important for protein purification
via proteins’ selective partitioning to the middle phase, driven by affinity to the second surfactant of the binary mixture. A semi-empirical thermodynamic mathematical model described the partitioning data well, provided optimal temperature values consistent with phase diagrams and theory, and demonstrated that the tail region of CK-2,13-E
5.6,ave is more polar than the hydrophobes of fatty alcohol ethoxylates. The addition of Aerosol-OT (AOT) removed the temperature sensitivity of CK-2,13-E
5.6,aves partitioning, producing 3-phase microemulsion systems between 20
°C and 40
°C. Analysis of the bottom phases of the 2- and 3-phase microemulsion systems formed by CK-2,13-E
5.6,ave via small-angle neutron scattering demonstrated the presence of spherical, monodisperse oil-in-water microemulsions. |
doi_str_mv | 10.1016/j.jcis.2010.08.076 |
format | article |
fullrecord | <record><control><sourceid>proquest_osti_</sourceid><recordid>TN_cdi_osti_scitechconnect_992111</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0021979710009926</els_id><sourcerecordid>869574120</sourcerecordid><originalsourceid>FETCH-LOGICAL-c475t-362c37f8c00f6a406403edd79390e5e97bab98439058cce6a49fa9d7112395543</originalsourceid><addsrcrecordid>eNqFks2OFCEUhStG44yjL-DC4MK4mWqhKIoicWMm_iWT6ELXhIJb07QUtEB1un1KH0nKbiezclYE7se5N-eeqnpO8Ipg0r3ZrDbaplWDywPuV5h3D6pzggWrOcH0YXWOcUNqwQU_q56ktMGYEMbE4-qswX2PGRXn1e-vKmabbfDW36AB1mpnQ0RhRMojpa2ptQO1U4ODS0QuaW1s2AenPCDlfhwcgrwO-4NTudTTHEels_IZWY9SUXQF8wYN1qt4uFuf7D7PERIaS7em_kvRertWCUpNxwDT7FIZC6VDyjClMowO0SxT5nCnK1qDMugmhnlbOv6Cp9WjUbkEz07nRfX9w_tvV5_q6y8fP1-9u651y1muaddoysdeYzx2qsVdiykYwwUVGBgIPqhB9G25sV5rKIgYlTCckIYKxlp6Ub086oaUrUzaZtBrHbwHnaUQDSGkMK-PzDaGnzOkLCebNLjFvjAnKcoW-8LSe8m-E4y3pMH3kpwJQovuQjZHsriZUoRRbqOdyh4kwXIJkNzIJUByCZDEvSwBKp9enOTnYQJz--VfYgrw6gSopJUbo_KLxi1HqWhExwv39shBWcLOQlw8Aq_B2LhYZIL93xx_AFvU5rI</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>759130160</pqid></control><display><type>article</type><title>Partitioning behavior of an acid-cleavable, 1,3-dioxolane alkyl ethoxylate, surfactant in single and binary surfactant mixtures for 2- and 3-phase microemulsion systems according to ethoxylate head group size</title><source>ScienceDirect Freedom Collection</source><creator>Rio, Javier Gomez del ; Hayes, Douglas G. ; Urban, Volker S.</creator><creatorcontrib>Rio, Javier Gomez del ; Hayes, Douglas G. ; Urban, Volker S. ; Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States) ; High Flux Isotope Reactor ; Center for Structural Molecular Biology</creatorcontrib><description>Partition coefficients for a 1,3-dioxolane alkyl ethoxylate surfactant in 2- and 3-phase microemulsion systems as a function of the ethoxylate size (
n): experimental data and thermodynamic model (curves).
[Display omitted]
► Aerosol-OT and cyclic ketal alkyl ethoxylate form temperature-insensitive microemulsions. ► HLB temperature for alkyl ethoxylate microemulsions predicted using partition coefficient data. ► Partitioning of cyclic ketal alkyl ethoxylates strongly affected by ethoxylate size. ► Tail region of cyclic ketal alkyl ethoxylates more polar than the that of fatty alcohol ethoxylates. ► Microemulsions in Winsor-III bottom phases formed by cyclic ketal alkyl ethoxylates (SANS).
Partition coefficients for a pH-degradable 1,3-dioxolane alkyl ethoxylate surfactant, 4-CH
3O (CH
2CH
2O)
5.6-CH
2, 2,2-(CH
2)
12CH
3, 2-(CH
2) CH
3, 1,3-dioxolane or “cyclic ketal” surfactant, CK-2,13-E
5.6,ave, between isooctane- and water-rich phases of 2- and 3-phase microemulsion systems (
K
n
) were determined as functions of the ethoxylate size,
n, and temperature for the neat surfactant and its binary surfactant mixtures, to understand the partitioning of alkyl ethoxylates possessing a broad distribution of ethoxylate size and to determine conditions required for formation of 3-phase microemulsion systems at an optimal temperature where phase separation occurs rapidly, important for protein purification
via proteins’ selective partitioning to the middle phase, driven by affinity to the second surfactant of the binary mixture. A semi-empirical thermodynamic mathematical model described the partitioning data well, provided optimal temperature values consistent with phase diagrams and theory, and demonstrated that the tail region of CK-2,13-E
5.6,ave is more polar than the hydrophobes of fatty alcohol ethoxylates. The addition of Aerosol-OT (AOT) removed the temperature sensitivity of CK-2,13-E
5.6,aves partitioning, producing 3-phase microemulsion systems between 20
°C and 40
°C. Analysis of the bottom phases of the 2- and 3-phase microemulsion systems formed by CK-2,13-E
5.6,ave via small-angle neutron scattering demonstrated the presence of spherical, monodisperse oil-in-water microemulsions.</description><identifier>ISSN: 0021-9797</identifier><identifier>EISSN: 1095-7103</identifier><identifier>DOI: 10.1016/j.jcis.2010.08.076</identifier><identifier>PMID: 20880539</identifier><identifier>CODEN: JCISA5</identifier><language>eng</language><publisher>Amsterdam: Elsevier Inc</publisher><subject>Acids - chemistry ; Aerosol-OT ; AFFINITY ; ALCOHOLS ; Alkyl ethoxylate surfactants ; Alkyl glucoside surfactant ; BASIC BIOLOGICAL SCIENCES ; BINARY MIXTURES ; Binary systems ; Chemistry ; Cleavable surfactants ; Colloidal state and disperse state ; Dioxolanes - chemistry ; DISTRIBUTION ; Emulsions - chemistry ; Emulsions. Microemulsions. Foams ; Ethylene Glycols - chemistry ; Exact sciences and technology ; GENERAL AND MISCELLANEOUS//MATHEMATICS, COMPUTING, AND INFORMATION SCIENCE ; General and physical chemistry ; HPLC analysis of surfactants ; Hydrogen-Ion Concentration ; MATHEMATICAL MODELS ; MICROEMULSIONS ; MIXTURES ; NEUTRONS ; Nonionic surfactants ; Octanes - chemistry ; Optimization ; Particle Size ; Partition coefficients ; Partitioning ; PHASE DIAGRAMS ; Phases ; Physical and chemical studies. Granulometry. Electrokinetic phenomena ; PHYSICS OF ELEMENTARY PARTICLES AND FIELDS ; PROTEINS ; PURIFICATION ; SCATTERING ; SENSITIVITY ; Small-angle neutron scattering ; Surface Properties ; Surface-Active Agents - chemical synthesis ; Surface-Active Agents - chemistry ; SURFACTANTS ; Thermodynamic model ; THERMODYNAMICS ; Water - chemistry</subject><ispartof>Journal of colloid and interface science, 2010-12, Vol.352 (2), p.424-435</ispartof><rights>2010 Elsevier Inc.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2010 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c475t-362c37f8c00f6a406403edd79390e5e97bab98439058cce6a49fa9d7112395543</citedby><cites>FETCH-LOGICAL-c475t-362c37f8c00f6a406403edd79390e5e97bab98439058cce6a49fa9d7112395543</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23392967$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20880539$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/992111$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Rio, Javier Gomez del</creatorcontrib><creatorcontrib>Hayes, Douglas G.</creatorcontrib><creatorcontrib>Urban, Volker S.</creatorcontrib><creatorcontrib>Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)</creatorcontrib><creatorcontrib>High Flux Isotope Reactor</creatorcontrib><creatorcontrib>Center for Structural Molecular Biology</creatorcontrib><title>Partitioning behavior of an acid-cleavable, 1,3-dioxolane alkyl ethoxylate, surfactant in single and binary surfactant mixtures for 2- and 3-phase microemulsion systems according to ethoxylate head group size</title><title>Journal of colloid and interface science</title><addtitle>J Colloid Interface Sci</addtitle><description>Partition coefficients for a 1,3-dioxolane alkyl ethoxylate surfactant in 2- and 3-phase microemulsion systems as a function of the ethoxylate size (
n): experimental data and thermodynamic model (curves).
[Display omitted]
► Aerosol-OT and cyclic ketal alkyl ethoxylate form temperature-insensitive microemulsions. ► HLB temperature for alkyl ethoxylate microemulsions predicted using partition coefficient data. ► Partitioning of cyclic ketal alkyl ethoxylates strongly affected by ethoxylate size. ► Tail region of cyclic ketal alkyl ethoxylates more polar than the that of fatty alcohol ethoxylates. ► Microemulsions in Winsor-III bottom phases formed by cyclic ketal alkyl ethoxylates (SANS).
Partition coefficients for a pH-degradable 1,3-dioxolane alkyl ethoxylate surfactant, 4-CH
3O (CH
2CH
2O)
5.6-CH
2, 2,2-(CH
2)
12CH
3, 2-(CH
2) CH
3, 1,3-dioxolane or “cyclic ketal” surfactant, CK-2,13-E
5.6,ave, between isooctane- and water-rich phases of 2- and 3-phase microemulsion systems (
K
n
) were determined as functions of the ethoxylate size,
n, and temperature for the neat surfactant and its binary surfactant mixtures, to understand the partitioning of alkyl ethoxylates possessing a broad distribution of ethoxylate size and to determine conditions required for formation of 3-phase microemulsion systems at an optimal temperature where phase separation occurs rapidly, important for protein purification
via proteins’ selective partitioning to the middle phase, driven by affinity to the second surfactant of the binary mixture. A semi-empirical thermodynamic mathematical model described the partitioning data well, provided optimal temperature values consistent with phase diagrams and theory, and demonstrated that the tail region of CK-2,13-E
5.6,ave is more polar than the hydrophobes of fatty alcohol ethoxylates. The addition of Aerosol-OT (AOT) removed the temperature sensitivity of CK-2,13-E
5.6,aves partitioning, producing 3-phase microemulsion systems between 20
°C and 40
°C. Analysis of the bottom phases of the 2- and 3-phase microemulsion systems formed by CK-2,13-E
5.6,ave via small-angle neutron scattering demonstrated the presence of spherical, monodisperse oil-in-water microemulsions.</description><subject>Acids - chemistry</subject><subject>Aerosol-OT</subject><subject>AFFINITY</subject><subject>ALCOHOLS</subject><subject>Alkyl ethoxylate surfactants</subject><subject>Alkyl glucoside surfactant</subject><subject>BASIC BIOLOGICAL SCIENCES</subject><subject>BINARY MIXTURES</subject><subject>Binary systems</subject><subject>Chemistry</subject><subject>Cleavable surfactants</subject><subject>Colloidal state and disperse state</subject><subject>Dioxolanes - chemistry</subject><subject>DISTRIBUTION</subject><subject>Emulsions - chemistry</subject><subject>Emulsions. Microemulsions. Foams</subject><subject>Ethylene Glycols - chemistry</subject><subject>Exact sciences and technology</subject><subject>GENERAL AND MISCELLANEOUS//MATHEMATICS, COMPUTING, AND INFORMATION SCIENCE</subject><subject>General and physical chemistry</subject><subject>HPLC analysis of surfactants</subject><subject>Hydrogen-Ion Concentration</subject><subject>MATHEMATICAL MODELS</subject><subject>MICROEMULSIONS</subject><subject>MIXTURES</subject><subject>NEUTRONS</subject><subject>Nonionic surfactants</subject><subject>Octanes - chemistry</subject><subject>Optimization</subject><subject>Particle Size</subject><subject>Partition coefficients</subject><subject>Partitioning</subject><subject>PHASE DIAGRAMS</subject><subject>Phases</subject><subject>Physical and chemical studies. Granulometry. Electrokinetic phenomena</subject><subject>PHYSICS OF ELEMENTARY PARTICLES AND FIELDS</subject><subject>PROTEINS</subject><subject>PURIFICATION</subject><subject>SCATTERING</subject><subject>SENSITIVITY</subject><subject>Small-angle neutron scattering</subject><subject>Surface Properties</subject><subject>Surface-Active Agents - chemical synthesis</subject><subject>Surface-Active Agents - chemistry</subject><subject>SURFACTANTS</subject><subject>Thermodynamic model</subject><subject>THERMODYNAMICS</subject><subject>Water - chemistry</subject><issn>0021-9797</issn><issn>1095-7103</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNqFks2OFCEUhStG44yjL-DC4MK4mWqhKIoicWMm_iWT6ELXhIJb07QUtEB1un1KH0nKbiezclYE7se5N-eeqnpO8Ipg0r3ZrDbaplWDywPuV5h3D6pzggWrOcH0YXWOcUNqwQU_q56ktMGYEMbE4-qswX2PGRXn1e-vKmabbfDW36AB1mpnQ0RhRMojpa2ptQO1U4ODS0QuaW1s2AenPCDlfhwcgrwO-4NTudTTHEels_IZWY9SUXQF8wYN1qt4uFuf7D7PERIaS7em_kvRertWCUpNxwDT7FIZC6VDyjClMowO0SxT5nCnK1qDMugmhnlbOv6Cp9WjUbkEz07nRfX9w_tvV5_q6y8fP1-9u651y1muaddoysdeYzx2qsVdiykYwwUVGBgIPqhB9G25sV5rKIgYlTCckIYKxlp6Ub086oaUrUzaZtBrHbwHnaUQDSGkMK-PzDaGnzOkLCebNLjFvjAnKcoW-8LSe8m-E4y3pMH3kpwJQovuQjZHsriZUoRRbqOdyh4kwXIJkNzIJUByCZDEvSwBKp9enOTnYQJz--VfYgrw6gSopJUbo_KLxi1HqWhExwv39shBWcLOQlw8Aq_B2LhYZIL93xx_AFvU5rI</recordid><startdate>20101215</startdate><enddate>20101215</enddate><creator>Rio, Javier Gomez del</creator><creator>Hayes, Douglas G.</creator><creator>Urban, Volker S.</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope><scope>OTOTI</scope></search><sort><creationdate>20101215</creationdate><title>Partitioning behavior of an acid-cleavable, 1,3-dioxolane alkyl ethoxylate, surfactant in single and binary surfactant mixtures for 2- and 3-phase microemulsion systems according to ethoxylate head group size</title><author>Rio, Javier Gomez del ; Hayes, Douglas G. ; Urban, Volker S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c475t-362c37f8c00f6a406403edd79390e5e97bab98439058cce6a49fa9d7112395543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Acids - chemistry</topic><topic>Aerosol-OT</topic><topic>AFFINITY</topic><topic>ALCOHOLS</topic><topic>Alkyl ethoxylate surfactants</topic><topic>Alkyl glucoside surfactant</topic><topic>BASIC BIOLOGICAL SCIENCES</topic><topic>BINARY MIXTURES</topic><topic>Binary systems</topic><topic>Chemistry</topic><topic>Cleavable surfactants</topic><topic>Colloidal state and disperse state</topic><topic>Dioxolanes - chemistry</topic><topic>DISTRIBUTION</topic><topic>Emulsions - chemistry</topic><topic>Emulsions. Microemulsions. Foams</topic><topic>Ethylene Glycols - chemistry</topic><topic>Exact sciences and technology</topic><topic>GENERAL AND MISCELLANEOUS//MATHEMATICS, COMPUTING, AND INFORMATION SCIENCE</topic><topic>General and physical chemistry</topic><topic>HPLC analysis of surfactants</topic><topic>Hydrogen-Ion Concentration</topic><topic>MATHEMATICAL MODELS</topic><topic>MICROEMULSIONS</topic><topic>MIXTURES</topic><topic>NEUTRONS</topic><topic>Nonionic surfactants</topic><topic>Octanes - chemistry</topic><topic>Optimization</topic><topic>Particle Size</topic><topic>Partition coefficients</topic><topic>Partitioning</topic><topic>PHASE DIAGRAMS</topic><topic>Phases</topic><topic>Physical and chemical studies. Granulometry. Electrokinetic phenomena</topic><topic>PHYSICS OF ELEMENTARY PARTICLES AND FIELDS</topic><topic>PROTEINS</topic><topic>PURIFICATION</topic><topic>SCATTERING</topic><topic>SENSITIVITY</topic><topic>Small-angle neutron scattering</topic><topic>Surface Properties</topic><topic>Surface-Active Agents - chemical synthesis</topic><topic>Surface-Active Agents - chemistry</topic><topic>SURFACTANTS</topic><topic>Thermodynamic model</topic><topic>THERMODYNAMICS</topic><topic>Water - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rio, Javier Gomez del</creatorcontrib><creatorcontrib>Hayes, Douglas G.</creatorcontrib><creatorcontrib>Urban, Volker S.</creatorcontrib><creatorcontrib>Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)</creatorcontrib><creatorcontrib>High Flux Isotope Reactor</creatorcontrib><creatorcontrib>Center for Structural Molecular Biology</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>OSTI.GOV</collection><jtitle>Journal of colloid and interface science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rio, Javier Gomez del</au><au>Hayes, Douglas G.</au><au>Urban, Volker S.</au><aucorp>Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)</aucorp><aucorp>High Flux Isotope Reactor</aucorp><aucorp>Center for Structural Molecular Biology</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Partitioning behavior of an acid-cleavable, 1,3-dioxolane alkyl ethoxylate, surfactant in single and binary surfactant mixtures for 2- and 3-phase microemulsion systems according to ethoxylate head group size</atitle><jtitle>Journal of colloid and interface science</jtitle><addtitle>J Colloid Interface Sci</addtitle><date>2010-12-15</date><risdate>2010</risdate><volume>352</volume><issue>2</issue><spage>424</spage><epage>435</epage><pages>424-435</pages><issn>0021-9797</issn><eissn>1095-7103</eissn><coden>JCISA5</coden><abstract>Partition coefficients for a 1,3-dioxolane alkyl ethoxylate surfactant in 2- and 3-phase microemulsion systems as a function of the ethoxylate size (
n): experimental data and thermodynamic model (curves).
[Display omitted]
► Aerosol-OT and cyclic ketal alkyl ethoxylate form temperature-insensitive microemulsions. ► HLB temperature for alkyl ethoxylate microemulsions predicted using partition coefficient data. ► Partitioning of cyclic ketal alkyl ethoxylates strongly affected by ethoxylate size. ► Tail region of cyclic ketal alkyl ethoxylates more polar than the that of fatty alcohol ethoxylates. ► Microemulsions in Winsor-III bottom phases formed by cyclic ketal alkyl ethoxylates (SANS).
Partition coefficients for a pH-degradable 1,3-dioxolane alkyl ethoxylate surfactant, 4-CH
3O (CH
2CH
2O)
5.6-CH
2, 2,2-(CH
2)
12CH
3, 2-(CH
2) CH
3, 1,3-dioxolane or “cyclic ketal” surfactant, CK-2,13-E
5.6,ave, between isooctane- and water-rich phases of 2- and 3-phase microemulsion systems (
K
n
) were determined as functions of the ethoxylate size,
n, and temperature for the neat surfactant and its binary surfactant mixtures, to understand the partitioning of alkyl ethoxylates possessing a broad distribution of ethoxylate size and to determine conditions required for formation of 3-phase microemulsion systems at an optimal temperature where phase separation occurs rapidly, important for protein purification
via proteins’ selective partitioning to the middle phase, driven by affinity to the second surfactant of the binary mixture. A semi-empirical thermodynamic mathematical model described the partitioning data well, provided optimal temperature values consistent with phase diagrams and theory, and demonstrated that the tail region of CK-2,13-E
5.6,ave is more polar than the hydrophobes of fatty alcohol ethoxylates. The addition of Aerosol-OT (AOT) removed the temperature sensitivity of CK-2,13-E
5.6,aves partitioning, producing 3-phase microemulsion systems between 20
°C and 40
°C. Analysis of the bottom phases of the 2- and 3-phase microemulsion systems formed by CK-2,13-E
5.6,ave via small-angle neutron scattering demonstrated the presence of spherical, monodisperse oil-in-water microemulsions.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><pmid>20880539</pmid><doi>10.1016/j.jcis.2010.08.076</doi><tpages>12</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0021-9797 |
ispartof | Journal of colloid and interface science, 2010-12, Vol.352 (2), p.424-435 |
issn | 0021-9797 1095-7103 |
language | eng |
recordid | cdi_osti_scitechconnect_992111 |
source | ScienceDirect Freedom Collection |
subjects | Acids - chemistry Aerosol-OT AFFINITY ALCOHOLS Alkyl ethoxylate surfactants Alkyl glucoside surfactant BASIC BIOLOGICAL SCIENCES BINARY MIXTURES Binary systems Chemistry Cleavable surfactants Colloidal state and disperse state Dioxolanes - chemistry DISTRIBUTION Emulsions - chemistry Emulsions. Microemulsions. Foams Ethylene Glycols - chemistry Exact sciences and technology GENERAL AND MISCELLANEOUS//MATHEMATICS, COMPUTING, AND INFORMATION SCIENCE General and physical chemistry HPLC analysis of surfactants Hydrogen-Ion Concentration MATHEMATICAL MODELS MICROEMULSIONS MIXTURES NEUTRONS Nonionic surfactants Octanes - chemistry Optimization Particle Size Partition coefficients Partitioning PHASE DIAGRAMS Phases Physical and chemical studies. Granulometry. Electrokinetic phenomena PHYSICS OF ELEMENTARY PARTICLES AND FIELDS PROTEINS PURIFICATION SCATTERING SENSITIVITY Small-angle neutron scattering Surface Properties Surface-Active Agents - chemical synthesis Surface-Active Agents - chemistry SURFACTANTS Thermodynamic model THERMODYNAMICS Water - chemistry |
title | Partitioning behavior of an acid-cleavable, 1,3-dioxolane alkyl ethoxylate, surfactant in single and binary surfactant mixtures for 2- and 3-phase microemulsion systems according to ethoxylate head group size |
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