Electrostatic Ion Chromatography of Common Anions and Cations with a Zwitterionic Surfactant-Modified Silica-C18 Column Using Water Eluent

被引:4
|
作者
Masuda, Wakako [1 ]
Kozaki, Daisuke [1 ]
Nakatani, Nobutake [1 ]
Goto, Ryozo [1 ]
Mori, Masanobu [2 ]
Fugetsu, Bunshi [3 ]
Tanaka, Kazuhiko [1 ]
机构
[1] Hiroshima Univ, Grad Sch Int Dev & Cooperat, Higashihiroshima, Hiroshima 7398529, Japan
[2] Gunma Univ, Grad Sch Engn, Kiryu, Gunma 3768515, Japan
[3] Hokkaido Univ, Grad Sch Environm Earth Sci, Kita Ku, Sapporo, Hokkaido 0600810, Japan
关键词
electrostatic ion chromatography; ion-pairing; CHAPS; water eluent; river water; MOBILE-PHASE;
D O I
10.2116/bunsekikagaku.58.311
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Electrostatic ion chromatography (EIC) of anions and cations with water eluent has been investigated for the development of water-monitoring systems in developing countries, which have the nature of simple, lower running cost, and non-chemical waste. For selecting the separation column, sulfobetaine-type zwitterionic surfactant (CHAPS)-modified silica C-18 and silica C-30 columns, and a zwitterionic stationary phased column HILIC were compared for anion separations. The retention order of the analyte anions was SO42- < Cl- < NO3- < I- < ClO4- without regard to the types of the columns, depending on the nature of EIC separation. However, the resolutions were different, because the anion separations by EIC were strongly affected by the hydrophobicity of the stationary phase. As a result, the CHAPS-rnodified silica C-18 column was the most suitable as a separation column in EIC in terms of the peak resolution and the retention time. In contrast, cation separations using the CHAPS-modified silica C-18 column with a water eluent were in the order of monovalent cations (Li+, Na+, K+ and NH4+) < divalent cations (Mg2+ and Ca2+). This fact means that the sulfobetain-type zwitterionic stationary phase has much higher selectivity for anions than for cations. Moreover, a pre-column (cation-exchange resin in the Li+-form for anion separations, and anion-exchange resin in the Cl--form for cation separations) was connected in tandem before the separation column, in order to make uniform the counter ion for analyte ions and to apply this method to real water samples. Under the optimized conditions, the linearity of the calibration graph, the detection limit, and the reproducibility for the common anions were tested, and satisfactory results was obtained for all common anions. The potentiality of EIC was demonstrated in practical applications to the determination of common anions (SO42-, Cl-, NO3- and HCO3-) and hardness in river water.
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页码:311 / 315
页数:5
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