Manipulation of separation selectivity of inorganic anions in electrostatic ion chromatography by the use of mixed cationic-zwitterionic micelles as the column coating solution

被引:13
|
作者
Hu, W [1 ]
Haddad, PR
Cook, H
Yamamoto, H
Hasebe, K
Tanaka, K
Fritz, JS
机构
[1] Hokkaido Univ, Grad Sch Sci, Div Chem, Sapporo, Hokkaido 0600810, Japan
[2] Univ Tasmania, Sch Chem, Hobart, Tas 7001, Australia
[3] Hokkaido Univ, Grad Sch Environm Earth Sci, Div Sci Mat, Sapporo, Hokkaido 0600810, Japan
[4] Natl Ind Res Inst Nagoya, Nagoya, Aichi 4628510, Japan
[5] Iowa State Univ, Ames Lab, USDOE, Ames, IA USA
[6] Iowa State Univ, Dept Chem, Ames, IA USA
关键词
micelles; electrostatic ion chromatography; ion chromatography; stationary phases; LC; selectivity; coated columns; inorganic anions;
D O I
10.1016/S0021-9673(01)00534-9
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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)propane (Zwittergent-3-14) and the cationic surfactant was tetradecyl-trimethylammonium (TTA). Using a reversed-phase C-18 column (250 x 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-< HPO42- < Cl- < SO42- < NO2- < Br- < NO3-. 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- < HPO42- < SO42- < Cl- < NO2- < Br- < NO3-. 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 mul) were 0.11, 0.12, 0.12, 0.18, 0.49, 0.49, 0.52 muM, respectively. (C) 2001 Elsevier Science B;V. All rights reserved.
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页码:95 / 100
页数:6
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