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高效液相色谱法同时测定香兰素与邻位香兰素
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作者单位
金海涛,马健瑜,王晓珣,陈星,任丽艳,关瑾,李云 沈阳化工大学应用化学学院 
基金项目:辽宁省自然基金资助项目(20090655),辽宁省教育厅2008年度科研计划项目(2008S184)
中文摘要:建立了同时测定香兰素和邻位香兰素的高效液相色谱法。考察了流动相组成、柱温等因素对分析效率的影响。在流动相为5% 乙酸-乙腈(60∶40,体积比),流速10 mL/min,柱温25 ℃的优化条件下,香兰素和邻位香兰素可在5 min内实现分离。测定结果表明,香兰素和邻位香兰素在10~240 mg/L范围内线性关系良好,相关系数均为0999 7;方法的检出限(S/N=3)分别为006、002 mg/L;样品的加标回收率为99%~102%,相对标准偏差为02%~06%。该方法操作简单、快速,用于实际样品的分析,结果满意。
中文关键词:高效液相色谱法  香兰素  邻位香兰素  同分异构体
 
Simultaneous Determination of Vanillin and o Vanillin by High Performance Liquid Chromatography
Abstract:A high performance liquid chromatographic method was developed for the simultaneous separation and determination of vanillin and o vanillin. Influences of mobile phase composition and column temperature on the separation were investigated. Under the condition of 5% acetic acid-acetonitrile (60∶40,by volume) as mobile phase at a flow rate of 10 mL/min and 25 ℃,the vanillin and o vanillin were separated in less than 5 min. The calibration curves of vanillin and o vanillin showed good linearities in the range of 10-240 mg/L with both correlation coefficients of 0999 7. The limits of detection(S/N=3) for vanillin and o vanillin were 006 mg/L and 002 mg/L,respectively. The average recoveries at three spiked levels were in the range of 99% -102% with relative standard deviations of 02% - 06%. The method was successfully used for the determination of vanillin and o vanillin in real samples with satisfactory results.
Key Words:high performance liquid chromatography  vanillin  o vanillin  isomers
引用本文:金海涛,马健瑜,王晓珣,陈星,任丽艳,关瑾,李云.高效液相色谱法同时测定香兰素与邻位香兰素[J].分析测试学报,2011,30(2):222-224.
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