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机构地区:[1]山东轻工业学院化工系
出 处:《色谱》1997年第1期65-66,共2页Chinese Journal of Chromatography
基 金:山东省自然科学基金
摘 要:以自制毛细管电泳-电化学检测系统对VC,VB1和VB6的毛细管区带电泳和胶束电动色谱的分离与检测情况进行了初探。结果表明,在0.01mol/LNH3-NH4Cl介质中,检测电势定于510~540mV(对SCE)时,三种维生素均有较好的CZE图,对VC的分离效率达468800块理论板。使用十二烷基硫酸钠时。In this paper, separation of water soluble vitamins C(VC),B 1 (VB 1) and B 6 (VB 6) has been studied preliminarily by capillary zone electrophoresis (CZE) and micellar electrokinetic capillary chromatography (MECC) with a home made amperometric electrochemical detector at the working electrode carbon fiber(5μm o.d.) potential of 510 540mV (vs.SCE). It has been shown that each of the three vitamins has more than one peak in NH 3 NH 4Cl (pH 9.0) which were mainly caused by the decomposition products in weak base medium and by heat except those from impurities.The electrochemical detector has better performance for the three vitamins from CZE and MECC. They can be separated either by CZE or by MECC. The separation by CZE is better than that by MECC with sodium dodecyl sulfate(SDS). SDS and buffer acidity can influence the retention time, peak sequence and height. The separation efficiency of CZE in 0 01mol/L NH 3 NH 4Cl was 468 800 theoretical plates for VC.
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