摘要
建立了一种测定食用菌中八氯二丙醚(S-2)残留量的气相色谱方法。样品中的八氯二丙醚经丙酮-正己烷混合溶剂提取,浓硫酸液-液分配磺化法进行净化,以气相色谱法(GC-ECD)测定,外标法定量。实验结果表明:样品中加入0.005~0.05mg/kg浓度水平的S-2,回收率在72.4%~104.4%之间,相对标准偏差小于7.86%(RSD,n=6)。本方法快速、准确,可用于食用菌类样品的日常检测和质量监控。
The method was established for the determination of octachlorodipropyl ether(S-2) residue in edible fungi by GC.The samples were extracted with acetone and hexane,and purified by liquid-liquid partition sulfonation with H2SO4.The external standard method was adopted for the determination by μECD.Tests of recovery were made by addition of standard S-2 to the edible fungi samples at the concentration levels in the range of 0.005~0.05 mg/kg,and the recoveries were between 72.4% and 104.4%,with RSDs less than 7.86%.The results indicated the method had the advantages of rapidness and accuracy,and can be used for routine analysis and quality control in fungi samples.
出处
《广州化工》
CAS
2011年第7期115-116,149,共3页
GuangZhou Chemical Industry
关键词
气相色谱
八氯二丙醚
残留量
食用菌
gas chromatography
octachlorodipropyl ether
residue
edible fungi