摘要
提出了气相色谱-串联质谱法测定稻米中毒死蜱及其代谢物3,5,6-三氯-2-羟基吡啶(TCP)含量的方法。样品经含体积分数为1%盐酸的乙腈提取,盐析并浓缩至近干后,残渣用乙酸乙酯溶解TCP用N-甲基-N-叔丁基二甲基硅基三氟乙酰胺衍生化,用气相色谱-串联质谱法测定,外标法定量。毒死蜱及TCP的质量浓度与峰面积均在0.02~0.4mg.L-1范围呈线性关系,测定下限(10S/N)依次为0.5,0.2μg.kg-1。在3个浓度水平下进行了回收和精密度试验,毒死蜱和TCP的回收率分别在94.3%~111.9%和95.1%~109.6%范围内,相对标准偏差(n=5)分别在1.7%~4.0%和3.1%~11.6%范围内。
GC MS/MS was applied to the determination of chlorpyrifos and its metabolite 3,5,6-trichloro-2- hydroxy pyridine (TCP) in rice. Samples were extracted with acetonitrile which contained (φ) 1% HC1. The extract was treated by salting out and evaporated to near-dryness and the residue and dissolved with ethyl acetate. TCP was derivatized with N-methybN tert-butyl trimethylsilyl trifluoroacetamide, and the derivatized product and chlorpyrifos were determined by GC- MS/MS. External standard calibration was adopted in the determination. I.inear relationships between peak areas and mass concentrations of chlorpyrifos and TCP were obtained in the same range of 0.02-0.4mg·L^-1. Values of lower limit of determination (lOS/N)were0.5,0.2μg·kg^-1 for chlorpyrifos and 0. 2 /xg ~ kg i for TCP. Tests for recovery and precision were made by standard addition method at 3 different concentration levels, values of recovery found were in the ranges of94.3%-111.9% and 95.1%-109.6%with values of RSD's (n=5) in the ranges of 1.7%-4.0% and 3.1%-11.6% for chlorpyrifos and TCP respectively.
出处
《理化检验(化学分册)》
CAS
CSCD
北大核心
2012年第6期667-670,共4页
Physical Testing and Chemical Analysis(Part B:Chemical Analysis)
基金
浙江省重大科技专项(2011C12024)