New leading electrolyte for the direct determination of chloride and other anions in analytical isotachophoresis

被引:20
作者
Meissner, T
Eisenbeiss, F
Jastorff, B
机构
[1] Merck KGaA, SLP, D-64271 Darmstadt, Germany
[2] J&M, D-73431 Aalen, Germany
[3] Univ Bremen, Zentrum Umweltforsch & Umwelttechnol, D-28334 Bremen, Germany
关键词
isotachophoresis; water analysis; environmental analysis; buffer composition; chloride; organic acids; inorganic anions;
D O I
10.1016/S0021-9673(98)00968-6
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In a number of experiments it was shown that the dithionate ion possesses a higher effective mobility than the chloride ion in aqueous solution, thus enabling the direct and simultaneous isotachophoretic determination of chloride and other anions. Using an acid-base titration, we found only one pK(a) value for dithionic acid, which is in contrast to the two pK(a) values stated in the literature. Based on this pK(a) value, theoretical calculations and the experimentally observed effective mobility of the dithionate ion indicate a higher effective mobility compared to the chloride ion from pH 3. Taking into account the physico-chemical properties of the dithionate, its unrestricted use as isotachophoretic leading ion was confirmed. Based on the dithionate ion, new electrolyte systems for the determination of chloride were used. One system was optimised for the determination of chloride and other low-molecular-mass anions and applied to the analysis of waste water and drinking water. The water samples were analysed in parallel by ion chromatography and compared with the isotachophoretic results. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:81 / 88
页数:8
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