Separation and determination of cations in beverage products by capillary zone electrophoresis

被引:23
|
作者
Fung, YS [1 ]
Lau, KM [1 ]
机构
[1] Univ Hong Kong, Dept Chem, Hong Kong, Hong Kong, Peoples R China
关键词
capillary electrophoresis; cation determination; metal analysis; beverage drinks; orange juice; tea;
D O I
10.1016/j.chroma.2006.04.030
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Cation determination is important for quality control of beverage products. To determine a large group simultaneously, a capillary electrophoresis procedure is developed with indirect UV at 214 nm in a three-complex buffer system (10 mM N,N-dimethylbenzylamine (DBA), 8 mM lactic acid and 2 mM 18-crown-6) with good mobility matching with desired cations. Under optimized conditions with pH adjusted to 4.65, a baseline separation is achieved for 14 cations (Rb+, NH4+, K+, Ca2+, Na+, Mg2+, Mn2+, Co2+, Fe2+, Cd2+, Cr3+, Ni2+, Zn2+ and Cu2+) within 7 min using an uncoated silica column. To cover ng/l to mu g/l range, both hydrostatic and electrokinetic sampling are studied, showing working ranges within (0.05-50)/(0.005-2) mu g/l and detection limits (13-78)/(1.4-10) ng/l, respectively with satisfactory repeatability (RSD 0.31-0.47% for migration time, and 3.0-4.0% for peak height measurement). Agreeable results with established inductively coupled plasma-atomic emission spectrometry method have been obtained for orange juice and tea samples. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:144 / 150
页数:7
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