Electrochemical monitoring of the co-extraction of water with hydrated ions into an organic solvent
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F18%3A00486652" target="_blank" >RIV/61388955:_____/18:00486652 - isvavai.cz</a>
Výsledek na webu
<a href="http://dx.doi.org/10.1016/j.elecom.2018.01.017" target="_blank" >http://dx.doi.org/10.1016/j.elecom.2018.01.017</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.elecom.2018.01.017" target="_blank" >10.1016/j.elecom.2018.01.017</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Electrochemical monitoring of the co-extraction of water with hydrated ions into an organic solvent
Popis výsledku v původním jazyce
An electrochemical cell based on the interface between two immiscible electrolyte solutions (ITIES) was designed and used to study the co-extraction of water with hydrated chloride ions from the aqueous to the organic solvent phase. The interfacial potential was controlled by the distribution of a common tetralkylammonium (TAA+) ion. Transfer of hydrated chloride ions is accompanied by the transfer of TAA+, decreasing its concentration on the aqueous side of the interface. Changes in the TAA+ concentration at the interface were monitored by measuring the open circuit potential (OCP). The proposed mechanism of TAACl transport involves a follow-up reaction with the co-extracted water molecules, leading to the formation of clusters of water containing TAACl in the organic phase.
Název v anglickém jazyce
Electrochemical monitoring of the co-extraction of water with hydrated ions into an organic solvent
Popis výsledku anglicky
An electrochemical cell based on the interface between two immiscible electrolyte solutions (ITIES) was designed and used to study the co-extraction of water with hydrated chloride ions from the aqueous to the organic solvent phase. The interfacial potential was controlled by the distribution of a common tetralkylammonium (TAA+) ion. Transfer of hydrated chloride ions is accompanied by the transfer of TAA+, decreasing its concentration on the aqueous side of the interface. Changes in the TAA+ concentration at the interface were monitored by measuring the open circuit potential (OCP). The proposed mechanism of TAACl transport involves a follow-up reaction with the co-extracted water molecules, leading to the formation of clusters of water containing TAACl in the organic phase.
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/GA17-09980S" target="_blank" >GA17-09980S: Biomimetická elektrochemie emulzních mikrokapek na polarizovaném rozhraní dvou nemísitelných roztoků elektrolytů</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2018
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Electrochemistry Communications
ISSN
1388-2481
e-ISSN
—
Svazek periodika
88
Číslo periodika v rámci svazku
MAR 2018
Stát vydavatele periodika
NL - Nizozemsko
Počet stran výsledku
4
Strana od-do
57-60
Kód UT WoS článku
000426512900013
EID výsledku v databázi Scopus
2-s2.0-85041483665