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Origin of chronoamperometric responses associated with impacts of single electrolyte droplets at a polarized liquid/liquid interface

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F20%3A00531040" target="_blank" >RIV/61388955:_____/20:00531040 - isvavai.cz</a>

  • Výsledek na webu

    <a href="http://hdl.handle.net/11104/0309797" target="_blank" >http://hdl.handle.net/11104/0309797</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.electacta.2020.136653" target="_blank" >10.1016/j.electacta.2020.136653</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Origin of chronoamperometric responses associated with impacts of single electrolyte droplets at a polarized liquid/liquid interface

  • Popis výsledku v původním jazyce

    Chronoamperometric measurements at a constant potential are used to study the single impacts of the water-in-DCE emulsion droplets containing an electrolyte (tetrapropylammonium chloride, TPrACl) at a polarized water(W)/1,2-dichloroethane (DCE) interface. The impacts give rise to the spike-like current transients, which are characterized by the initial current step (time constant less than 2 ms) followed by a slower exponential current decay with a time constant in tens of milliseconds. It is shown that the theoretical treatment of the current spikes can be based on a modification of the bulk electrolysis model including (1) the droplet collision at the W/DCE interface, (2) a partial coalescence (fusion) of the droplet with the impacted interface, (3) a reorganization of the electric double layer leading to the propagation of the interfacial potential difference from the impacted interface to the surface of the droplet, and (4) stripping (bulk electrolysis) of TPrA+ from the droplet to the DCE phase accompanied by the chloride depletion into the bulk water phase. On assuming that the stripping of TPrA+ is the rate-determining step of the impact event, the theoretical relationships for the current transient are derived, which are confirmed by the experimental data. An analysis of the current transients yields the charge corresponding to the ionic content of the droplets, which is used to evaluate the droplet diameter. Droplet size distribution with the droplet diameter of around 8 μm is verified by an analysis of the microscopic images of the W-in-DCE emulsion, and in part also by the dynamic laser scattering measurements. It is shown that the frequency of the droplet collisions with the W/DCE interface (1–10 Hz) is controlled by migration of the negatively charged droplets towards the interface.

  • Název v anglickém jazyce

    Origin of chronoamperometric responses associated with impacts of single electrolyte droplets at a polarized liquid/liquid interface

  • Popis výsledku anglicky

    Chronoamperometric measurements at a constant potential are used to study the single impacts of the water-in-DCE emulsion droplets containing an electrolyte (tetrapropylammonium chloride, TPrACl) at a polarized water(W)/1,2-dichloroethane (DCE) interface. The impacts give rise to the spike-like current transients, which are characterized by the initial current step (time constant less than 2 ms) followed by a slower exponential current decay with a time constant in tens of milliseconds. It is shown that the theoretical treatment of the current spikes can be based on a modification of the bulk electrolysis model including (1) the droplet collision at the W/DCE interface, (2) a partial coalescence (fusion) of the droplet with the impacted interface, (3) a reorganization of the electric double layer leading to the propagation of the interfacial potential difference from the impacted interface to the surface of the droplet, and (4) stripping (bulk electrolysis) of TPrA+ from the droplet to the DCE phase accompanied by the chloride depletion into the bulk water phase. On assuming that the stripping of TPrA+ is the rate-determining step of the impact event, the theoretical relationships for the current transient are derived, which are confirmed by the experimental data. An analysis of the current transients yields the charge corresponding to the ionic content of the droplets, which is used to evaluate the droplet diameter. Droplet size distribution with the droplet diameter of around 8 μm is verified by an analysis of the microscopic images of the W-in-DCE emulsion, and in part also by the dynamic laser scattering measurements. It is shown that the frequency of the droplet collisions with the W/DCE interface (1–10 Hz) is controlled by migration of the negatively charged droplets towards the interface.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

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

Návaznosti výsledku

  • Projekt

    <a href="/cs/project/GA20-01589S" target="_blank" >GA20-01589S: Nové strategie pro zlepšení senzorových vlastností nových elektrodových materiálů prostřednictvím jejich předúpravy či modifikace povrchu</a><br>

  • Návaznosti

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Ostatní

  • Rok uplatnění

    2020

  • Kód důvěrnosti údajů

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

Údaje specifické pro druh výsledku

  • Název periodika

    Electrochimica acta

  • ISSN

    0013-4686

  • e-ISSN

  • Svazek periodika

    354

  • Číslo periodika v rámci svazku

    SEP 2020

  • Stát vydavatele periodika

    GB - Spojené království Velké Británie a Severního Irska

  • Počet stran výsledku

    8

  • Strana od-do

    136653

  • Kód UT WoS článku

    000569140400006

  • EID výsledku v databázi Scopus

    2-s2.0-85086891141