COMPARISON OF CHROMATOGRAPHIC BEHAVIOR OF OLIGOETHYLENE GLYCOL NONYLPHENYL ETHER NONIONIC AND ANIONIC SURFACTANTS IN REVERSED-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY
P. Jandera et J. Urbanek, COMPARISON OF CHROMATOGRAPHIC BEHAVIOR OF OLIGOETHYLENE GLYCOL NONYLPHENYL ETHER NONIONIC AND ANIONIC SURFACTANTS IN REVERSED-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY, Journal of chromatography, 689(2), 1995, pp. 255-267
A simple retention mechanism is proposed to describe the retention beh
aviour of oligomeric sulphated and non-sulphated surfactants of the ol
igoethylene glycol nonylphenyl ether type in reversed-phase systems co
ntaining ion-pairing reagents in aqueous-organic mobile phases. The eq
uations derived using this mechanism relate the capacity factors of th
e individual oligomers to the number of oxyethylene units and to the c
oncentrations of the organic solvent (2-propanol) and of the ion-pairi
ng reagent (cetyltrimethylammonium bromide) in the mobile phase. Most
capacity factors calculated using the best-fit parameters of these equ
ations agree with the experimental values with errors of less than +/-
5% relative. The capacity factors of the anionic surfactants with vari
ous degrees of polymerization on a C-18 column reach maximum values in
the mobile phases containing 0.02 mol/l cetyltrimethylammonium bromid
e, while the retention of the non-ionic surfactants decreases regularl
y with increasing concentration of the ion-pairing reagent. The concen
tration of propanol affects the retention of the anionic and non-ionic
surfactants in the same way, but the anionic surfactants are more str
ongly retained. The composition of the mobile phase can be optimized s
o that the sulphated and non-sulphated oligoethylene glycol nonylpheny
l ethers are distinguished into two groups of peaks and the separation
of the individual oligomers in the two groups is possible in a single
run.