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作 者:曹玉华[1] 张欣[1] 方禹之[1] 叶建农[1]
出 处:《高等学校化学学报》2001年第12期2011-2013,共3页Chemical Journal of Chinese Universities
基 金:中国科学院长春应用化学研究所电分析化学实验室资助
摘 要:A simultaneous determination of (-) epictechin, (+) catechin, gentisic acid, ferulic acid, quercetin and gallic acid in red wine by capillary zone electrophoresis with electrochemical detection(CE ED) was reported. The effects of potential of working electrode, pH and concentration of running buffer, separation voltage and injection time on CE ED were investigated. Under the optimum conditions, these six analytes could be separated in a 100 mmol/L borate buffer(pH=9 24) within 30 min. A 300 μm diameter carbon disk electrode has a good response at +0 85 V( vs . SCE) for all analytes. The responses were linear over two orders of magnitude with detection limit( S/N =3) ranged from 7×10 -8 g/mL to 1 4×10 -7 g/mL for all six analytes. This method has been used for the determination of these analytes in red wine without enrichment, and the assay result was satisfactory.A simultaneous determination of (-) epictechin, (+) catechin, gentisic acid, ferulic acid, quercetin and gallic acid in red wine by capillary zone electrophoresis with electrochemical detection(CE ED) was reported. The effects of potential of working electrode, pH and concentration of running buffer, separation voltage and injection time on CE ED were investigated. Under the optimum conditions, these six analytes could be separated in a 100 mmol/L borate buffer(pH=9 24) within 30 min. A 300 μm diameter carbon disk electrode has a good response at +0 85 V( vs . SCE) for all analytes. The responses were linear over two orders of magnitude with detection limit( S/N =3) ranged from 7×10 -8 g/mL to 1 4×10 -7 g/mL for all six analytes. This method has been used for the determination of these analytes in red wine without enrichment, and the assay result was satisfactory.
分 类 号:TS262.6[轻工技术与工程—发酵工程] TS261.7[轻工技术与工程—食品科学与工程]
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