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Effect of water solubility in organic solvents on the standard Gibbs energy of ion transfer across a water/organic solvent interface

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F23%3A00570455" target="_blank" >RIV/61388955:_____/23:00570455 - isvavai.cz</a>

  • Result on the web

    <a href="https://hdl.handle.net/11104/0341746" target="_blank" >https://hdl.handle.net/11104/0341746</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.electacta.2023.142222" target="_blank" >10.1016/j.electacta.2023.142222</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Effect of water solubility in organic solvents on the standard Gibbs energy of ion transfer across a water/organic solvent interface

  • Original language description

    Ion transfer voltammetry is used to study the transfer of alkali metal and proton cations and the Cl- anion from the aqueous solution of MCl (M+ = H+, Li+, Na+, K+, Rb+, Cs+) to the solution of bis(triphenylphosphor-anylidene)ammonium tetrakis(pentafluorophenyl)borate in alpha,alpha.alpha-trifluorotoluene (TFT) or 1,2-dichloroethane (DCE). The scale of the applied potentials is converted to the scale of the Galvani potential differences on the basis of the voltammetric measurements of the standard ion transfer potential for the tetraethylammonium (TEA+) ion used as a reference ion in situ. The interfacial tension measurements at the water/TFT interface yield the zero-charge potential difference, which is close to the expected zero value. The standard Gibbs energies of ion transfer Delta owG0i are evaluated from the voltammetric data on considering both the effect of the association between the transferred ion and the counter-ion of the organic solvent phase, and the effect of the ion migration in the aqueous phase. The values of Delta owG0i for the ion transfer to TFT are found to be considerably higher than those obtained for the ion transfer to DCE. This difference is proposed to be related to the significantly lower solubility of water in TFT, possibly requiring the removal of the ion hydration shell in the course of the ion transfer from water to TFT. Such conclusion is supported by the calculations of Delta owG0i by using an advanced Born-type model of ion solvation.

  • 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/GA22-32631S" target="_blank" >GA22-32631S: Anomalous salt extraction from water to polar organic solvents: A novel mechanism of the spontaneous emulsification and practical application</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2023

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Electrochimica acta

  • ISSN

    0013-4686

  • e-ISSN

    1873-3859

  • Volume of the periodical

    449

  • Issue of the periodical within the volume

    MAY 2023

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    8

  • Pages from-to

    142222

  • UT code for WoS article

    000955300400001

  • EID of the result in the Scopus database

    2-s2.0-85150270464