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Interfacial instability associated with the transfer of non-adsorbing ions across the polarized water/1,2-dichloroethane interface

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F18%3A00489822" target="_blank" >RIV/61388955:_____/18:00489822 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1016/j.jelechem.2017.09.011" target="_blank" >http://dx.doi.org/10.1016/j.jelechem.2017.09.011</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.jelechem.2017.09.011" target="_blank" >10.1016/j.jelechem.2017.09.011</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Interfacial instability associated with the transfer of non-adsorbing ions across the polarized water/1,2-dichloroethane interface

  • Original language description

    Polarography with the electrolyte dropping electrode is used to study the transfer of several non-adsorbing ions including Na+, H+, Cl-, tetrabutylammonium+ (TBA+) and tetraethylammonium+ (TEA+) across the water/1,2-dichloroethane interface. The transfer of Na+, H+, Cl- and TBA+ in the thermodynamically favored direction is accompanied by the interfacial instability, which is manifested by the substantial faradaic current amplification (polarographic current maximum). No such amplification is observed in case of the transfer of TEA+ in either direction. The potential range of the interfacial instability, as well as of its absence, is correctly predicted by the linear instability analysis developed by Aogaki et al. (Electrochim. Acta 23 (1978) 867). The analysis also provides an explanation for the experimentally observed decrease of the interfacial tension in the potential range of the instability. Two remarkable effects of the interfacial instability are demonstrated, specifically the irregularly repeated swapping of the faradaic current and the interfacial tension occurring close to the electrocapillary maximum between the amplified current/low interfacial tension and diffusion current/high interfacial tension levels, and the mechanical oscillation of the electrolyte drop in the former state.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10405 - Electrochemistry (dry cells, batteries, fuel cells, corrosion metals, electrolysis)

Result continuities

  • Project

    <a href="/en/project/GA17-09980S" target="_blank" >GA17-09980S: Biomimetic electrochemistry of emulsion micro-droplets at the polarised interface between two immiscible electrolyte solutions</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2018

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Journal of Electroanalytical Chemistry

  • ISSN

    1572-6657

  • e-ISSN

  • Volume of the periodical

    819

  • Issue of the periodical within the volume

    JUN 2018

  • Country of publishing house

    CH - SWITZERLAND

  • Number of pages

    6

  • Pages from-to

    95-100

  • UT code for WoS article

    000435619700013

  • EID of the result in the Scopus database

    2-s2.0-85029420128