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作 者:王淑菊[1] 于彦彬[2] 谭培功 苗在京[2] 魏亦山[2]
机构地区:[1]中国海洋大学,山东青岛266003 [2]农业部农产品质量安全监督检验测试中心(青岛),山东青岛266109 [3]青岛市环境监测中心站,山东青岛266003
出 处:《色谱》2007年第2期226-229,共4页Chinese Journal of Chromatography
摘 要:采用硅镁吸附剂和硅胶作吸附剂,建立了固相萃取-高效液相色谱法同时测定苹果中残留的克菌丹和灭菌丹的分析方法。研究了甲醇-乙腈-水(含0.1mmol/L乙酸-乙酸钠缓冲溶液(pH3.80))三元体系下克菌丹和灭菌丹的最佳分离条件,在波长210nm下检测,克菌丹和灭菌丹的线性范围为0.40-8.00mg/kg,线性相关系数均大于0.999 9;最低检出限克菌丹为0.27mg/kg、灭菌丹为0.20mg/kg;保留时间的相对标准偏差(RSD)≤0.60%。苹果样品中3个添加水平的平均加标回收率为克菌丹69.3%-106%,RSD为3.7%-4.7%;灭菌丹101%-108%,RSD为1.3%-5.4%。A method for the simultaneous determination of captan and folpet pesticide residues in apples was developed by solid-phase extraction and high performance liquid chromatography. The sample was extracted with acetonitrile and cleaned-up by a mixture of homemade sorbent and silica gel with hexane-dichloromethane-acetonitrile (50: 49: 1, v/v) as the eluent. The cleaned effects by using Florisil column, amino column, the mixed sorbent were compared, and the effect of the mixed sorbent was the best. The optimal analytical conditions were follow as: an methanol-acetonitrile-water (50: 5: 45, v/v) containing 0. 1 mmol/L acetic-acetate buffer (pH 3.80) as the mobile phase, detection at 210 nm. The method had a good linear relationship in the range of 0.40 - 8.00 mg/kg for captan and folpet ( r 〉 0. 999 9 ). The detection limits of captan and folpet were 0.27 mg/kg and 0.20 mg/kg, respectively. The relative standard deviations (RSDs) of retention time were no more than 0.60%. The average recoveries of captan and folpet from the apples spiked at three levels ranged from 69.3% - 106% and 101% - 108%, with RSD of 3.7% - 4.7% and 1.3% - 5.4%, respectively.
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