VLE measurement of binary systems containing imidazolium ionic liquids and water or ethanol

2022 ◽  
pp. 113400
Author(s):  
Elena Graczová ◽  
Pavol Steltenpohl
Keyword(s):  
Ionic Liquids ◽  
Binary Systems ◽  
Imidazolium Ionic Liquids

scholarly journals Carbon dioxide capture using water-imidazolium ionic liquids-amines ternary systems

2021 ◽  
Vol 105 ◽  
pp. 103210
Author(s):  
Mariusz Zalewski ◽  
Tomasz Krawczyk ◽  
Agnieszka Siewniak ◽  
Aleksander Sobolewski
Keyword(s):  
Carbon Dioxide ◽  
Ionic Liquids ◽  
Carbon Dioxide Capture ◽  
Ternary Systems ◽  
Imidazolium Ionic Liquids

Degradation of imidazolium ionic liquids in a thermally activated persulfate system

2021 ◽  
Vol 412 ◽  
pp. 128624
Author(s):  
Tian-Lin Ren ◽  
Xi-Wen Ma ◽  
Xiao-Qiong Wu ◽  
Li Yuan ◽  
Yang-Li Lai ◽  
...  
Keyword(s):  
Ionic Liquids ◽  
Imidazolium Ionic Liquids ◽  
Thermally Activated ◽  
Activated Persulfate

α−Fe2O3/rGO cooperated with tri-alkyl-substituted-imidazolium ionic liquids for enhancing oxygen sensing

2021 ◽  
Vol 341 ◽  
pp. 130029
Author(s):  
Wenyan Yin ◽  
Khaled Tawfik Alali ◽  
Milin Zhang ◽  
Jingyuan Liu ◽  
Dalei Song ◽  
...  
Keyword(s):  
Ionic Liquids ◽  
Oxygen Sensing ◽  
Imidazolium Ionic Liquids

Self-organization of imidazolium ionic liquids in aqueous solution

2008 ◽  
Vol 329 (3) ◽  
pp. 125-133 ◽  
Author(s):  
Justyna Łuczak ◽  
Jan Hupka ◽  
Jorg Thöming ◽  
Christian Jungnickel
Keyword(s):  
Aqueous Solution ◽  
Ionic Liquids ◽  
Self Organization ◽  
Imidazolium Ionic Liquids

scholarly journals Reaction of allene esters with Selectfluor/TMSX (X = I, Br, Cl) and Selectfluor/NH4SCN: Competing oxidative/electrophilic dihalogenation and nucleophilic/conjugate addition

2015 ◽  
Vol 11 ◽  
pp. 1641-1648 ◽  
Author(s):  
A Srinivas Reddy ◽  
Kenneth K Laali
Keyword(s):  
Ionic Liquids ◽  
Conjugate Addition ◽  
Nucleophilic Additions ◽  
Product Analysis ◽  
Imidazolium Ionic Liquids ◽  
Presence And Absence ◽  
Competing Pathways

Reaction of benzyl and ethyl allenoates with TMSX (X = I, Br, Cl) and with NH4SCN were investigated in MeCN, DMF, and in imidazolium ionic liquids [BMIM][NTf2] and [BMIM][PF6] as solvent, in the presence and absence of Selectfluor. Comparative product analysis studies demonstrate that the ability of Selectflour to promote oxidative/electrophilic dihalogenation/dithiocyanation with TMSX/NH4SCN (as observed previously for 1-arylallenes) is diminished in allenoates, most significantly in reactions with TMSCl, and essentially disappearing in reactions with NH4SCN, in favor of nucleophilic/conjugate addition. The study underscores the contrasting reactivity patterns in 1-arylallenes and allenoates toward electrophilic and nucleophilic additions in halofunctionalization with TMSX/Selectfluor and thiocyanation reactions with NH4SCN/Selectfluor. These competing pathways are influenced by the nature of the anion, allene structure, and the choice of solvent.

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