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Oppositely charged dye surfactant interactions: Extent and selectivity of ion pair formation
Interactions of oppositely charged dye (eosin yellow) and surfactant (Cetyltrimethylammonium bromide) were investigated using conductometric and spectrophotometric studies. The conductometric investigations showed a negligible change in critical micellar concentration of Cetyltrimethylammonium bromi...
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Published in: | Journal of molecular liquids 2018-09, Vol.266, p.591-596 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Interactions of oppositely charged dye (eosin yellow) and surfactant (Cetyltrimethylammonium bromide) were investigated using conductometric and spectrophotometric studies. The conductometric investigations showed a negligible change in critical micellar concentration of Cetyltrimethylammonium bromide at the point of the ion pair formation which was found to be 1 × 10−3 M. Spectroscopic studies revealed the formation of ion pair by a bathochromic shift of 10 nm in the original spectra by using yellow (517 nm) after the addition of cetyltrimethylammonium bromide (527 nm). The investigations were further confirmed the phenomenon by monitoring the effect of electrolyte, and calculating the values of thermodynamic parameters. Furthermore, the metal effect on dye and in dye-surfactant ion pair was studied and the noticeable change on the interactions were found. At the terminal part of the study the selectivity of dye-surfactant ion pair was observed. The system was found to be selective towards the eosin yellow among studied dyes.
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•Interaction of CTAB and EY is spontaneous and exothermic at all temperatures.•The ion pair formation of CTAB-EY was thermodynamically spontaneous and exothermic•Pb and Cr produce a shift in the spectra due to different interaction species.•The ion pair formation of CTAB-EY is selective in the presence of different dyes. |
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ISSN: | 0167-7322 1873-3166 |
DOI: | 10.1016/j.molliq.2018.06.108 |