Reverse micelle chromatography for evaluation of partition of organic solutes to micellar pseudophases
[Display omitted] •A chromatographic method is proposed for determining solute partition constants.•The method is applicable without interferences from UV-absorption of the medium.•The specific properties of confined water are confirmed under some conditions. The evaluation of solute partition from...
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Published in | Journal of colloid and interface science Vol. 577; pp. 191 - 198 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Elsevier Inc
01.10.2020
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Subjects | |
Online Access | Get full text |
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Summary: | [Display omitted]
•A chromatographic method is proposed for determining solute partition constants.•The method is applicable without interferences from UV-absorption of the medium.•The specific properties of confined water are confirmed under some conditions.
The evaluation of solute partition from an organic solvent to a reverse micelle (RM) is critical for designing effective reaction systems and for synthesizing functional materials using the nano water-phase in the RM. Although spectroscopic methods have been extensively employed for determining the partition constants of solutes in the RM systems, their applications are limited to the case, in which the background absorption is low and the spectroscopic features of the solute are effectively varied by its partitioning to RMs. This paper proposes a novel chromatographic method to overcome this limitation of conventional methods. In the present system, a size-exclusion chromatographic column is used with RM solutions as mobile phases. The RM is excluded from the stationary phase and, therefore, is eluted first. A solute is eluted with the retention volume determined by its affinities to the stationary phase and the RM. The elution volumes of a solute measured by varying the concentrations of RM in the mobile phase allow us to determine its partition constant to the RM. The partition of phenols in hexadecyltrimethylammonium chloride and bromide RMs in chloroform is successfully evaluated without interferences from the UV-absorption of the media. The larger partition constant is confirmed for a smaller water/surfactant molar ratio (w) and for chloride than bromide as the RM counterion. This suggests that the nature of water is more strongly influenced by confinement in the RM cores for smaller w and the chloride counterion because water molecules are strongly imbibed by the interface. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0021-9797 1095-7103 |
DOI: | 10.1016/j.jcis.2020.05.074 |