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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
Main Authors: Rio, Javier Gomez del, Hayes, Douglas G., Urban, Volker S.
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cited_by cdi_FETCH-LOGICAL-c475t-362c37f8c00f6a406403edd79390e5e97bab98439058cce6a49fa9d7112395543
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creator Rio, Javier Gomez del
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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
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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. 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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. 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(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. 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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. 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[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>
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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
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-02T11%3A05%3A42IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_osti_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Partitioning%20behavior%20of%20an%20acid-cleavable,%201,3-dioxolane%20alkyl%20ethoxylate,%20surfactant%20in%20single%20and%20binary%20surfactant%20mixtures%20for%202-%20and%203-phase%20microemulsion%20systems%20according%20to%20ethoxylate%20head%20group%20size&rft.jtitle=Journal%20of%20colloid%20and%20interface%20science&rft.au=Rio,%20Javier%20Gomez%20del&rft.aucorp=Oak%20Ridge%20National%20Lab.%20(ORNL),%20Oak%20Ridge,%20TN%20(United%20States)&rft.date=2010-12-15&rft.volume=352&rft.issue=2&rft.spage=424&rft.epage=435&rft.pages=424-435&rft.issn=0021-9797&rft.eissn=1095-7103&rft.coden=JCISA5&rft_id=info:doi/10.1016/j.jcis.2010.08.076&rft_dat=%3Cproquest_osti_%3E869574120%3C/proquest_osti_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c475t-362c37f8c00f6a406403edd79390e5e97bab98439058cce6a49fa9d7112395543%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=759130160&rft_id=info:pmid/20880539&rfr_iscdi=true