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Brønsted acidity in deep eutectic solvents and ionic liquids.

journal contribution
posted on 2018-04-17, 14:19 authored by Andrew P. Abbott, Sahar S. M. Alabdullah, Azhar Y. M. Al-Murshedi, Karl S. Ryder
Despite the importance of ionic liquids in a variety of fields, little is understood about the behaviour of protons in these media. The main difficulty arises due to the unknown activity of protons in non-aqueous solvents. This study presents acid dissociation constants for nine organic acids in deep eutectic solvents (DESs) using standard pH indicator solutes. The pKInvalue for bromophenol blue was found by titrating the DES with triflic acid. The experimental method was developed to understand the acid-base properties of deep eutectic solvents, and through this study it was found that the organic acids studied were slightly less dissociated in the DES than in water with pKavalues between 0.2 and 0.5 higher. pKInvalues were also determined for two ionic liquids, [Bmim][BF4] and [Emim][acetate]. The anion of the ionic liquid changes the pH of the solution by acting as a buffer. [Emim][acetate] was found to be more basic than water. It is also shown that water significantly affects the pH of ionic liquids. This is thought to arise because aqueous mixtures with ionic liquids form heterogeneous solutions and the proton partitions into the aqueous phase. This study also attempted to develop an electrochemical pH sensor. It was shown that a linear response of cell potential vs. ln aH+could be obtained but the slope for the correlation was less than that obtained in aqueous solutions. Finally it was shown that the liquid junction potential between two reference electrodes immersed in different DESs was dependent upon the pH difference between the liquids.

History

Citation

Faraday Discussions, 2018, 206, pp. 365-377

Author affiliation

/Organisation/COLLEGE OF SCIENCE AND ENGINEERING/Department of Chemistry

Version

  • AM (Accepted Manuscript)

Published in

Faraday Discussions

Publisher

Royal Society of Chemistry

issn

1359-6640

eissn

1364-5498

Acceptance date

2017-05-23

Copyright date

2017

Available date

2018-09-19

Publisher version

http://pubs.rsc.org/en/Content/ArticleLanding/2018/FD/C7FD00153C#!divAbstract

Notes

The file associated with this record is under embargo until 12 months after publication, in accordance with the publisher's self-archiving policy. The full text may be available through the publisher links provided above.

Language

en

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