1994
DOI: 10.1021/ac00092a025
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Selectivity in Micellar Reversed-Phase Liquid Chromatography: C-18 and C-8 Alkyl Bonded Phases

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Cited by 30 publications
(13 citation statements)
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“…The alkyl tail of negatively charged surfactants such as SDS interact with the bonded groups leaving their charged head groups orientated at the stationary phase surface, forming a hydrophilic layer. Conversely, the head groups of positively charged surfactants interact with the bonded phases leaving their alkyl tails uppermost, retaining the hydrophobicity of the stationary phase [27].…”
Section: Effect Of Surfactant Type and Concentrationmentioning
confidence: 99%
“…The alkyl tail of negatively charged surfactants such as SDS interact with the bonded groups leaving their charged head groups orientated at the stationary phase surface, forming a hydrophilic layer. Conversely, the head groups of positively charged surfactants interact with the bonded phases leaving their alkyl tails uppermost, retaining the hydrophobicity of the stationary phase [27].…”
Section: Effect Of Surfactant Type and Concentrationmentioning
confidence: 99%
“…Retention in MLC has been shown to be correlated to surfactant type and the concentration of surfactant in the mobile phase. [11,15] Solute retention in MLC generally decreases with increasing surfactant concentration, but the rate of decrease can vary considerably from one solute to another.…”
Section: Micellar Liquid Chromatographymentioning
confidence: 99%
“…Ž The same was proposed to occur in micellar liquid chromatography Gonzalez et al, . 1992;Lavine et al, 1994 . The reduced affinity for ODS in the presence of adsorbed surfactants can be explained by the observation that the hydrophobicity of aliphatic Ž moieties is reduced by ionic groups in their vicinity Noordman et al, 1993;Hol et al, .…”
Section: Adsorbed Rhamnolipid Reduces the Affinity Of Fluorene And Phmentioning
confidence: 99%