Facilitated Transfer of Alkali-Metal Cations by Dibenzo-18-crown-6 across the Electrochemically Polarized Interface between an Aqueous Solution and a Hydrophobic Room-Temperature Ionic Liquid

2006 ◽  
Vol 78 (16) ◽  
pp. 5805-5812 ◽  
Author(s):  
Naoya Nishi ◽  
Hiroshi Murakami ◽  
Seiichi Imakura ◽  
Takashi Kakiuchi
1967 ◽  
Vol 45 (20) ◽  
pp. 2411-2418 ◽  
Author(s):  
R. W. Chlebek ◽  
M. W. Lister

The rates of the reaction of ferrocyanide and persulfate ions, in the presence of various concentrations of different alkali metal cations, have been measured at various temperatures and ionic strengths. The results are interpreted in terms of ion pairs and support the view that the actual reacting species are MFe(CN)6−3 and MS2O8−, where M is an alkali metal. This is similar to the situation found earlier for potassium salts of these ions. The rate constants obtained on this assumption increase gradually from lithium to cesium. Values are also obtained for the apparent activation energies of these reactions.


2015 ◽  
Vol 51 (31) ◽  
pp. 6851-6853 ◽  
Author(s):  
Justyna Jedraszko ◽  
Wojciech Nogala ◽  
Wojciech Adamiak ◽  
Saustin Dongmo ◽  
Gunther Wittstock ◽  
...  

H2O2 is produced at the interface between a room-temperature ionic liquid with decamethylferrocene as an electron donor and an acidic aqueous solution. The electron donor can be regenerated electrochemically.


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