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Transfer of the tetraethylammonium cation across a phosphatidic acid layer adsorbed at a water/1,2-dichloroethane interface: The effect of electric polarization of the interface - Electrochemically controlled ion exchange

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    SYSNO ASEP0341186
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleTransfer of the tetraethylammonium cation across a phosphatidic acid layer adsorbed at a water/1,2-dichloroethane interface: The effect of electric polarization of the interface - Electrochemically controlled ion exchange
    Author(s) Jänchenová, Hana (UFCH-W)
    Štulík, K. (CZ)
    Maeda, K. (JP)
    Mareček, Vladimír (UFCH-W) RID
    Source TitleJournal of Electroanalytical Chemistry. - : Elsevier - ISSN 1572-6657
    Roč. 632, 1-2 (2009), s. 55-58
    Number of pages4 s.
    Languageeng - English
    CountryCH - Switzerland
    Keywordsliquid-liquid interface ; phospholipid layers ; phosphatidic acid (DPPA)
    Subject RIVCF - Physical ; Theoretical Chemistry
    R&D ProjectsIAA400400806 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
    CEZAV0Z40400503 - UFCH-W (2005-2011)
    UT WOS000267432300008
    DOI10.1016/j.jelechem.2009.03.015
    AnnotationThe transfer of the tetraethylammonium (TEA) cations across the interface between an aqueous phase and an organic phase of 1,2-dichloroethane, with a layer of dipalmitoyl phosphaticlic acid (DPPA) adsorbed at the interface, was studied by cyclic voltammetry. It has been shown that the passage of the TEA(+) cations into the organic phase is permitted by ion exchange of the TEA(+) cations for protons contained in the DPPA molecules, followed by re-exchange permitting the release of the TEA(+) cations into the organic phase. The principal steps of the reaction mechanism are the transport of the TEA(+) cations through the layers of adsorbed DPPA and the slow re-exchange in the adsorbed layer. The cyclic voltammetry experiments permit semiquantitative estimation of the appropriate kinetic and thermodynamic constants describing the process.
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2010
Number of the records: 1  

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