From Ionic Liquid to Electrolyte Solution: Dynamics of 1-N-Butyl-3-N-methylimidazolium Tetrafluoroborate/Dichloromethane Mixtures

2008 ◽  
Vol 112 (41) ◽  
pp. 12913-12919 ◽  
Author(s):  
Johannes Hunger ◽  
Alexander Stoppa ◽  
Richard Buchner ◽  
Glenn Hefter
2018 ◽  
Vol 260 ◽  
pp. 640-647 ◽  
Author(s):  
Ximei Gao ◽  
Yuanlei Ding ◽  
Qunting Qu ◽  
Gao Liu ◽  
Vincent S. Battaglia ◽  
...  

2018 ◽  
Vol 3 (2) ◽  
pp. 85-92
Author(s):  
Wipsar Sunu Brams Dwandaru ◽  
Oktiana Lusi Priyani ◽  
Bagas Prakoso ◽  
Rhyko Irawan Wisnuwijaya ◽  
Iman Santoso

An optical absorbance study using Ultraviolet-Visible (UV-Vis) spectrophotometer device has been conducted on graphene oxide (GO) in copper (Cu) ionic liquid using electrochemical exfoliation combined with a direct current (DC) electrical circuit of copper coil given inside the electrolyte solution. The electrolyte solutions used are sulfuric acid (H2SO4) and chloride acid (HCl). The UV-Vis spectrum of the samples shows absorbance peaks at around 214 nm to 218 nm and shouldering peaks around 245 nm to 249 nm. The first peak corresponds to the existence of copper (Cu) ionic liquid in the solution, whereas the shouldering peak is related to the occurrence of GO material. A comparison between UV-Vis spectral of graphite in dimethylformamide (DMF) and GO in Cu ionic liquid in DMF resulted in the existence of a blue shift which signifies the production of Cu ionic liquid from the Cu coils inside the electrolyte solution. Increasing the concentration of the solution increases the absorbance peaks. Furthermore, raising the number of loops yields in the increase of the absorbance value at the first peaks that show Cu ionic liquid, but tends to decrease the absorbance value of the shouldering peaks of the GO material.


2020 ◽  
Vol 22 (18) ◽  
pp. 6127-6136
Author(s):  
Jonas Winters ◽  
Wim Dehaen ◽  
Koen Binnemans

Aromatic polyamides can be dissolved and processed in an organic electrolyte solution, where the ionic liquid and γ-valerolactone interact with the polymer through hydrogen bonding and dispersion forces, respectively.


2009 ◽  
Vol 81 (8) ◽  
pp. 1473-1488 ◽  
Author(s):  
Zdenĕk Samec ◽  
Jan Langmaier ◽  
Takashi Kakiuchi

This article provides a brief review of theoretical and methodological concepts in the area of the charge-transfer processes at the interface between a hydrophobic ionic liquid (IL) and an electrolyte solution in water (W). Electrochemical methods of study of the W|IL interfaces are described, current experimental problems are indicated, and the most important experimental results are summarized. The relevance of electrochemistry at the W|IL interfaces to the extraction behavior of ILs is outlined.


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