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Reliable electrophoretic mobilities free from Joule heating effects using CE.

Reliable electrophoretic mobilities free from Joule heating effects using CE. Research Abstract Details 

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  • Reliable electrophoretic mobilities free from Joule heating effects using CE. Abstract Text:

    christopher j evenhuisChristopher J Evenhuis,vlastimil hruskaVlastimil Hruska,rosanne m guijtRosanne M Guijt,miroslav mackaMiroslav Macka,bohuslav gasBohuslav Gas,philip j marriottPhilip J Marriott,paul r haddadPaul R Haddad,christopher j evenhuisChristopher J Evenhuis,vlastimil hruskaVlastimil Hruska,rosanne m guijtRosanne M Guijt,miroslav mackaMiroslav Macka,bohuslav gasBohuslav Gas,philip j marriottPhilip J Marriott,paul r haddadPaul R Haddad,

    Ionic electrophoretic mobilities determined by means of CE experiments are sometimes different when compared to generally accepted values based on limiting ionic conductance measurements. While the effect of ionic strength on electrophoretic mobility has been long understood, the increase in the mobility that results from Joule heating (the resistive heating that occurs when a current passes through an electrolyte) has been largely overlooked. In this work, a simple method for obtaining reliable and reproducible values of electrophoretic mobility is described. The electrophoretic mobility is measured over a range of driving powers and the extrapolation to zero power dissipation is employed to eliminate the effect of Joule heating. These extrapolated values of electrophoretic mobility can then be used to calculate limiting ionic mobilities by making a correction for ionic strength; this somewhat complicated calculation is conveniently performed by using the freeware program PeakMaster 5. These straightforward procedures improve the agreement between experimentally determined and literature values of limiting ionic mobility by at least one order of magnitude. Using Tris-chromate BGE with a value of conductivity 0.34 S/m and ionic strength 59 mM at a modest dissipated power per unit length of 2.0 W/m, values of mobility for inorganic anions were increased by an average of 12.6% relative to their values free from the effects of Joule heating. These increases were accompanied by a reduction in mobilities due to the ionic strength effect, which was 11% for univalent and 28% for divalent inorganic ions compared to their limiting ionic mobilities. Additionally, it was possible to determine the limiting ionic mobility for a number of aromatic anions by using PeakMaster 5 to perform an ionic strength correction. A major significance of this work is in being able to use CE to obtain reliable and accurate values of electrophoretic mobilities with all its benefits, including understanding and interpretation of physicochemical phenomena and the ability to model and simulate such phenomena accurately.

    Reliable electrophoretic mobilities free from Joule heating effects using CE. Publishing Authors By Initials

    cj evenhuisCJ Evenhuis,v hruskaV Hruska,rm guijtRM Guijt,m mackaM Macka,b gasB Gas,pj marriottPJ Marriott,pr haddadPR Haddad,cj evenhuisCJ Evenhuis,v hruskaV Hruska,rm guijtRM Guijt,m mackaM Macka,b gasB Gas,pj marriottPJ Marriott,pr haddadPR Haddad,

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    Reliable electrophoretic mobilities free from Joule heating effects using CE. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Electrophoresis

    VOLUME: 28

    Page Numbers: 3759-66

    Journal Abbreviation: Electrophoresis

    ISSN: 0173-0835

    DAY: 23

    MONTH: Oct

    YEAR: 2007

    Reliable electrophoretic mobilities free from Joule heating effects using CE. Information

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    LANGUAGE: eng

    NlmUniqueID: 8204476

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    Grant and Affiliation Information for Reliable electrophoretic mobilities free from Joule heating effects using CE.

    AFFILIATION: Australian Centre for Research on Separation Science, University of Tasmania, School of Chemistry, Hobart, Tasmania, Australia.

    Country: Germany

    Germany Research PublicationGermany Research Publication

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    MEDLINETA: Electrophoresis

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