INVESTIGATION OF CHROMATOGRAPHIC BEHAVIOR OF ETHOXYLATED ALCOHOL SURFACTANTS IN NORMAL-PHASE AND REVERSED-PHASE SYSTEMS USING HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY MASS-SPECTROMETRY
P. Jandera et al., INVESTIGATION OF CHROMATOGRAPHIC BEHAVIOR OF ETHOXYLATED ALCOHOL SURFACTANTS IN NORMAL-PHASE AND REVERSED-PHASE SYSTEMS USING HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY MASS-SPECTROMETRY, Journal of chromatography, 813(2), 1998, pp. 299-311
Citations number
53
Categorie Soggetti
Chemistry Analytical","Biochemical Research Methods
Retention behaviour of ethoxylated alcohols was investigated on octade
cyl silica, unmodified silica and aminosilica columns. Good separation
according to the alcoholic alkyl length is achieved in reversed-phase
systems. The elution order of the oligomers with different numbers of
oxyethylene groups depends on the type of the organic solvent (methan
ol or acetonitrile) and on its concentration in the mobile phase. Diff
erent retention behaviour of lower and higher oligomers was observed.
The distribution of the oligomers according to the number of oxyethyle
ne units is suppressed, but it overlaps with the peak distribution acc
ording to the alkyl length in mobile phases containing high concentrat
ions of acetonitrile. In normal-phase systems, the alkyl length affect
s the retention much less than the number of oxyethylene units. Better
separation than on unmodified silica gel columns can be achieved on a
chemically bonded aminosilica column in 2-propanol-n-hexane and espec
ially in acetonitrile-water-dichloromethane mobile phases. Possible re
tention mechanisms in the systems studied are discussed. The retention
is strongly affected by solvation of the oxyethylene groups by the mo
bile phase. The retention factors of higher oligomers with bimodal mas
s distribution can be described using a simple equation. HPLC-MS with
atmospheric pressure chemical ionization allows sensitive detection, e
asy identification and reconstruction of the chromatographic peaks in
chromatograms of complex mixtures of oligomers with different numbers
of methylene and oxyethylene groups. (C) 1998 Elsevier Science B.V. Al
l rights reserved.