Analytical study of highly condensed non ionic surfactants. Separation on cation exchangers |
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Authors: | B. Desmazières F. Portet P. -L. Desbène |
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Affiliation: | (1) Laboratoire de Chimie Organique Structurale, Université P. et M. Curie, Bât. F, 4, Place Jussieu, 75005 Paris, France;(2) Institut Européen des Peptides, 76000 Rouen, France;(3) U.A. 455, L.A.S.O.C., Université de Rouen, I.U.T., 43, rue Saint-Germain, 27000 Evreux, France |
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Abstract: | Summary This study was aimed at optimizing the separation of non-ionic surfactants, resulting from the condensation of ethylene oxide with natural fatty alcohols in the C16 and C18 range (saturated and unsaturated), and presenting a high degree of condensation, i.e. 20 and 25 ethylene oxide units (Brij 99 and KM 25). The cation exchange stationary phase is a partially ionized silica, conditioned in different ways. We have studied the influence of the nature of cations on the separation selectivity. Cations studied included alkali metals (Li+, Na+, K+, Rb+, Cs+), alkaline earth metals (Mg2+, Ca2+, Sr2+, Ba2+), transition metals (Zn2+, Cd2+, Hg2+, Pb2+, Cu2+), and quaternary ammonium (NH4+, NMe4+) ions as well as a proton (acetic acid). The influences of ionic strength, pH and addition of cosolvent were examined. A study of the influence of temperature on the system selectivity evidenced a strong interdependance of these two parameters. The optimized conditions [mobile phase: CH3CN/H2O (92/8), pH 7.4, sodium acetate 5.10–3 M; temperature gradient between 25 and 50°C] allowed for the first time the distributions of Brij 99 and KM 25 to be obtained. |
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Keywords: | Complexion chromatography Silica ion exchanger Polyoxyethylenic surfactants |
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