Abstract
In this work three 1-alkyl-3-ethylimidazolium bromide ionic liquids (alkyl=ethyl, hexyl and octyl) were synthesized applying both, conventional and microwave assisted synthetic paths. The phase diagrams for aqueous solutions of 1-alkyl-3-ethylimidazolium bromide ionic liquids as novel extractants combined with phosphate-based salts are reported and discussed in terms of aqueous biphasic system (ABS) formation. Merchuk equation was applied in order to correlate the experimental binodal data. The liquidliquid equilibrium data (tie-line compositions and tie-line length) were also experimentally determined by a gravimetric method. The influence of the alkyl chain length on ABS formation ability was investigated. It was found that ability to form ABS increases with the increase of the alkyl chain length on the imidazolium cation. Also, it was found that ionic liquids with ethyl group in the N-3 position better form ABS compared to those with methyl substituent. This was discussed in terms of increasing ionic liquid hydrophobicity and poor affinity for water. In order to better understand the impact of the alkyl side chain of the imidazolium ion and the efficiency of ABS formation, computer simulations were performed using investigated ionic liquids with the ethyl group in the position N-3 of the cation and different alkyl substituents in the position N-1. Also, extraction of selected organic dyes was performed to demonstrate application of studied ionic liquids as novel extractants.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.