Affiliation: | a Division of Chemistry, Graduate School of Science, Hokkaido University, Sapporo 060-0810, Japan b School of Chemistry, University of Tasmania, GPO Box 252-75, Hobart 7001, Tasmania, Australia c Division of Material Science, Graduate School of Environmental Earth Science, Hokkaido University, Sapporo 060-0810, Japan d National Industrial Research Institute of Nagoya, Nagoya 462-8510, Japan e Ames Laboratory, U.S.D.O.E. and Department of Chemistry, Iowa State University, Ames, IA, USA |
Abstract: | This paper describes an electrostatic ion chromatographic system in which the separation selectivity for inorganic anions, especially for sulfate and phosphate, could be manipulated by altering the molar ratio of the zwitterionic and cationic surfactants in the column coating solution used to prepare the stationary phase. The zwitterionic surfactant used for this study was 3-(N,N-dimethyltetradecylammonio)propanesulfonate (Zwittergent-3-14) and the cationic surfactant was tetradecyltrimethylammonium (TTA). Using a reversed-phase C18 column (250×4.6 mm I.D.) coated with 10/10 (mM/mM) of TTA/Zwittergent-3-14 mixed micelles as the stationary phase and either NaHCO3 or Na2CO3 aqueous solution as the eluent, together with suppressed conductivity detection, baseline separation of seven model inorganic anions was obtained. The elution order for those anions was found to be F−42−−42−2− −3−. Under the same conditions but using 1/10 (mM/mM) of TTA/Zwittergent-3-14 mixed micelles as the column coating solution, the elution order for these model ions was F−42−42−−2− −3−. The early elution of phosphate and sulfate is a unique attribute of this system. Detection limits for F−, HPO42−, Cl−, SO42−, NO2−, Br− and NO3− (S/N=3, sample injection volume 100 μl) were 0.11, 0.12, 0.12, 0.18, 0.49, 0.49, 0.52 μM, respectively. |