Loading…
Quantitative Study of Concentration Overload, Peak Asymmetry, and Efficiency Loss in Micellar Electrokinetic Chromatography
An equation is derived for the velocity of a thin zone of specific analyte concentration in micellar electrokinetic chromatography. The velocity varies with analyte concentration, because micellar solubilization changes electrical conductivity, micellar electrophoretic mobility, and the partitioning...
Saved in:
Published in: | Analytical chemistry (Washington) 2002-12, Vol.74 (23), p.5969-5981 |
---|---|
Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-a406t-42dbf8de9ac0afe41569faf3ad2b62deeb7b9f848360f458cc09b1cde3a34953 |
---|---|
cites | cdi_FETCH-LOGICAL-a406t-42dbf8de9ac0afe41569faf3ad2b62deeb7b9f848360f458cc09b1cde3a34953 |
container_end_page | 5981 |
container_issue | 23 |
container_start_page | 5969 |
container_title | Analytical chemistry (Washington) |
container_volume | 74 |
creator | Smith, Keith W Davis, Joe M |
description | An equation is derived for the velocity of a thin zone of specific analyte concentration in micellar electrokinetic chromatography. The velocity varies with analyte concentration, because micellar solubilization changes electrical conductivity, micellar electrophoretic mobility, and the partitioning of analyte between mobile and micellar phases. Two studies based on a weakly and a strongly retained neutral analyte are made to test a limiting form of the equation in which the first two changes are ignored. In the first study, peak asymmetries are characterized and plate numbers are measured in two types of experiments: one of fixed surfactant concentration and variable analyte concentration and one of fixed analyte concentration and variable surfactant concentration. In the second study, the isotherm describing both experiment types is measured and interpreted by the Langmuir model to evaluate the velocity equation. The equation of continuity is solved numerically for the peak profiles governed by the velocity equation. In all but one case, a good agreement is found between theoretical and experimental peak asymmetries and plate numbers in both experiment types. An equation is derived for the relative change of analyte velocity caused by the Langmuir isotherm. The change depends on the relative migration time, micellar saturation, and retardation factor. The predicted velocity changes correlate well with peak asymmetries and efficiency losses. |
doi_str_mv | 10.1021/ac020376q |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_72794458</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>260038971</sourcerecordid><originalsourceid>FETCH-LOGICAL-a406t-42dbf8de9ac0afe41569faf3ad2b62deeb7b9f848360f458cc09b1cde3a34953</originalsourceid><addsrcrecordid>eNpl0V1rFDEUBuAgil2rF_4BCYKC0KlJ5jOX7bq1lpWudO_DmUxi051JtkmmOPjnTd2lC3oVSJ4c3nMOQm8pOaWE0c8gCSN5Xd0_QzNaMpJVTcOeoxkhJM9YTcgRehXCHSGUElq9REeUFbyhnM3Q7x8j2GgiRPOg8E0cuwk7jefOSmWjT9fO4usH5XsH3QleKdjgszANg4p-OsFgO7zQ2kijrJzw0oWAjcXfjVR9Dx4veiWjdxtjVTQSz2-9GyC6nx62t9Nr9EJDH9Sb_XmM1heL9fwyW15__TY_W2ZQkCpmBeta3XSKpzZBq4KWFdegc-hYW7FOqbZuuW6KJq-ILspGSsJbKjuVQ17wMj9GH3dlt97djypEMZjwN59VbgyiZjUv0r8E3_8D79zobYomGK2b5GiV0Kcdkj4165UWW28G8JOgRDxuQzxtI9l3-4JjO6juIPfjT-DDHkCQ0GsPVppwcEXDOCePybKdMyGqX0_v4DeiqvO6FOvVjbj8Qsvzi9WVOD_UBRkOTfwf8A-pta7C</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>217872716</pqid></control><display><type>article</type><title>Quantitative Study of Concentration Overload, Peak Asymmetry, and Efficiency Loss in Micellar Electrokinetic Chromatography</title><source>American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)</source><creator>Smith, Keith W ; Davis, Joe M</creator><creatorcontrib>Smith, Keith W ; Davis, Joe M</creatorcontrib><description>An equation is derived for the velocity of a thin zone of specific analyte concentration in micellar electrokinetic chromatography. The velocity varies with analyte concentration, because micellar solubilization changes electrical conductivity, micellar electrophoretic mobility, and the partitioning of analyte between mobile and micellar phases. Two studies based on a weakly and a strongly retained neutral analyte are made to test a limiting form of the equation in which the first two changes are ignored. In the first study, peak asymmetries are characterized and plate numbers are measured in two types of experiments: one of fixed surfactant concentration and variable analyte concentration and one of fixed analyte concentration and variable surfactant concentration. In the second study, the isotherm describing both experiment types is measured and interpreted by the Langmuir model to evaluate the velocity equation. The equation of continuity is solved numerically for the peak profiles governed by the velocity equation. In all but one case, a good agreement is found between theoretical and experimental peak asymmetries and plate numbers in both experiment types. An equation is derived for the relative change of analyte velocity caused by the Langmuir isotherm. The change depends on the relative migration time, micellar saturation, and retardation factor. The predicted velocity changes correlate well with peak asymmetries and efficiency losses.</description><identifier>ISSN: 0003-2700</identifier><identifier>EISSN: 1520-6882</identifier><identifier>DOI: 10.1021/ac020376q</identifier><identifier>PMID: 12498192</identifier><identifier>CODEN: ANCHAM</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Analytical chemistry ; Chemistry ; Chromatographic methods and physical methods associated with chromatography ; Chromatography ; Chromatography, Micellar Electrokinetic Capillary ; Exact sciences and technology ; Models, Chemical ; Motion ; Other chromatographic methods ; Surface-Active Agents ; Velocity</subject><ispartof>Analytical chemistry (Washington), 2002-12, Vol.74 (23), p.5969-5981</ispartof><rights>Copyright © 2002 American Chemical Society</rights><rights>2003 INIST-CNRS</rights><rights>Copyright American Chemical Society Dec 1, 2002</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a406t-42dbf8de9ac0afe41569faf3ad2b62deeb7b9f848360f458cc09b1cde3a34953</citedby><cites>FETCH-LOGICAL-a406t-42dbf8de9ac0afe41569faf3ad2b62deeb7b9f848360f458cc09b1cde3a34953</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=14829908$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12498192$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Smith, Keith W</creatorcontrib><creatorcontrib>Davis, Joe M</creatorcontrib><title>Quantitative Study of Concentration Overload, Peak Asymmetry, and Efficiency Loss in Micellar Electrokinetic Chromatography</title><title>Analytical chemistry (Washington)</title><addtitle>Anal. Chem</addtitle><description>An equation is derived for the velocity of a thin zone of specific analyte concentration in micellar electrokinetic chromatography. The velocity varies with analyte concentration, because micellar solubilization changes electrical conductivity, micellar electrophoretic mobility, and the partitioning of analyte between mobile and micellar phases. Two studies based on a weakly and a strongly retained neutral analyte are made to test a limiting form of the equation in which the first two changes are ignored. In the first study, peak asymmetries are characterized and plate numbers are measured in two types of experiments: one of fixed surfactant concentration and variable analyte concentration and one of fixed analyte concentration and variable surfactant concentration. In the second study, the isotherm describing both experiment types is measured and interpreted by the Langmuir model to evaluate the velocity equation. The equation of continuity is solved numerically for the peak profiles governed by the velocity equation. In all but one case, a good agreement is found between theoretical and experimental peak asymmetries and plate numbers in both experiment types. An equation is derived for the relative change of analyte velocity caused by the Langmuir isotherm. The change depends on the relative migration time, micellar saturation, and retardation factor. The predicted velocity changes correlate well with peak asymmetries and efficiency losses.</description><subject>Analytical chemistry</subject><subject>Chemistry</subject><subject>Chromatographic methods and physical methods associated with chromatography</subject><subject>Chromatography</subject><subject>Chromatography, Micellar Electrokinetic Capillary</subject><subject>Exact sciences and technology</subject><subject>Models, Chemical</subject><subject>Motion</subject><subject>Other chromatographic methods</subject><subject>Surface-Active Agents</subject><subject>Velocity</subject><issn>0003-2700</issn><issn>1520-6882</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNpl0V1rFDEUBuAgil2rF_4BCYKC0KlJ5jOX7bq1lpWudO_DmUxi051JtkmmOPjnTd2lC3oVSJ4c3nMOQm8pOaWE0c8gCSN5Xd0_QzNaMpJVTcOeoxkhJM9YTcgRehXCHSGUElq9REeUFbyhnM3Q7x8j2GgiRPOg8E0cuwk7jefOSmWjT9fO4usH5XsH3QleKdjgszANg4p-OsFgO7zQ2kijrJzw0oWAjcXfjVR9Dx4veiWjdxtjVTQSz2-9GyC6nx62t9Nr9EJDH9Sb_XmM1heL9fwyW15__TY_W2ZQkCpmBeta3XSKpzZBq4KWFdegc-hYW7FOqbZuuW6KJq-ILspGSsJbKjuVQ17wMj9GH3dlt97djypEMZjwN59VbgyiZjUv0r8E3_8D79zobYomGK2b5GiV0Kcdkj4165UWW28G8JOgRDxuQzxtI9l3-4JjO6juIPfjT-DDHkCQ0GsPVppwcEXDOCePybKdMyGqX0_v4DeiqvO6FOvVjbj8Qsvzi9WVOD_UBRkOTfwf8A-pta7C</recordid><startdate>20021201</startdate><enddate>20021201</enddate><creator>Smith, Keith W</creator><creator>Davis, Joe M</creator><general>American Chemical Society</general><scope>BSCLL</scope><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>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7TA</scope><scope>7TB</scope><scope>7TM</scope><scope>7U5</scope><scope>7U7</scope><scope>7U9</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>H94</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20021201</creationdate><title>Quantitative Study of Concentration Overload, Peak Asymmetry, and Efficiency Loss in Micellar Electrokinetic Chromatography</title><author>Smith, Keith W ; Davis, Joe M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a406t-42dbf8de9ac0afe41569faf3ad2b62deeb7b9f848360f458cc09b1cde3a34953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Analytical chemistry</topic><topic>Chemistry</topic><topic>Chromatographic methods and physical methods associated with chromatography</topic><topic>Chromatography</topic><topic>Chromatography, Micellar Electrokinetic Capillary</topic><topic>Exact sciences and technology</topic><topic>Models, Chemical</topic><topic>Motion</topic><topic>Other chromatographic methods</topic><topic>Surface-Active Agents</topic><topic>Velocity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Smith, Keith W</creatorcontrib><creatorcontrib>Davis, Joe M</creatorcontrib><collection>Istex</collection><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>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Materials Business File</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Analytical chemistry (Washington)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Smith, Keith W</au><au>Davis, Joe M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quantitative Study of Concentration Overload, Peak Asymmetry, and Efficiency Loss in Micellar Electrokinetic Chromatography</atitle><jtitle>Analytical chemistry (Washington)</jtitle><addtitle>Anal. Chem</addtitle><date>2002-12-01</date><risdate>2002</risdate><volume>74</volume><issue>23</issue><spage>5969</spage><epage>5981</epage><pages>5969-5981</pages><issn>0003-2700</issn><eissn>1520-6882</eissn><coden>ANCHAM</coden><abstract>An equation is derived for the velocity of a thin zone of specific analyte concentration in micellar electrokinetic chromatography. The velocity varies with analyte concentration, because micellar solubilization changes electrical conductivity, micellar electrophoretic mobility, and the partitioning of analyte between mobile and micellar phases. Two studies based on a weakly and a strongly retained neutral analyte are made to test a limiting form of the equation in which the first two changes are ignored. In the first study, peak asymmetries are characterized and plate numbers are measured in two types of experiments: one of fixed surfactant concentration and variable analyte concentration and one of fixed analyte concentration and variable surfactant concentration. In the second study, the isotherm describing both experiment types is measured and interpreted by the Langmuir model to evaluate the velocity equation. The equation of continuity is solved numerically for the peak profiles governed by the velocity equation. In all but one case, a good agreement is found between theoretical and experimental peak asymmetries and plate numbers in both experiment types. An equation is derived for the relative change of analyte velocity caused by the Langmuir isotherm. The change depends on the relative migration time, micellar saturation, and retardation factor. The predicted velocity changes correlate well with peak asymmetries and efficiency losses.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>12498192</pmid><doi>10.1021/ac020376q</doi><tpages>13</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0003-2700 |
ispartof | Analytical chemistry (Washington), 2002-12, Vol.74 (23), p.5969-5981 |
issn | 0003-2700 1520-6882 |
language | eng |
recordid | cdi_proquest_miscellaneous_72794458 |
source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
subjects | Analytical chemistry Chemistry Chromatographic methods and physical methods associated with chromatography Chromatography Chromatography, Micellar Electrokinetic Capillary Exact sciences and technology Models, Chemical Motion Other chromatographic methods Surface-Active Agents Velocity |
title | Quantitative Study of Concentration Overload, Peak Asymmetry, and Efficiency Loss in Micellar Electrokinetic Chromatography |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T14%3A01%3A17IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Quantitative%20Study%20of%20Concentration%20Overload,%20Peak%20Asymmetry,%20and%20Efficiency%20Loss%20in%20Micellar%20Electrokinetic%20Chromatography&rft.jtitle=Analytical%20chemistry%20(Washington)&rft.au=Smith,%20Keith%20W&rft.date=2002-12-01&rft.volume=74&rft.issue=23&rft.spage=5969&rft.epage=5981&rft.pages=5969-5981&rft.issn=0003-2700&rft.eissn=1520-6882&rft.coden=ANCHAM&rft_id=info:doi/10.1021/ac020376q&rft_dat=%3Cproquest_cross%3E260038971%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-a406t-42dbf8de9ac0afe41569faf3ad2b62deeb7b9f848360f458cc09b1cde3a34953%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=217872716&rft_id=info:pmid/12498192&rfr_iscdi=true |