马红枣,潘立刚,李安,张志勇.气相色谱-质谱法测定水体中乙酰甲胺磷和 甲胺磷残留量[J].食品安全质量检测学报,2017,8(2):481-485
气相色谱-质谱法测定水体中乙酰甲胺磷和 甲胺磷残留量
Determination of acephate and methamidophos residues by gas chromatography-mass spectrometry
投稿时间:2016-11-25  修订日期:2017-02-18
DOI:
中文关键词:  乙酰甲胺磷  甲胺磷  气相色谱质谱联用  条件优化
英文关键词:Supported by Beijing Academy of Agriculture and Forestry Special Plan for Technical Innovation (KJCX20150408) and the Project of Risk Assessment of Quality and Safety of Nation Agro-Products (GJFP201601402)
基金项目:北京市农林科学院科技创新能力建设专项 (KJCX20150408)、国家农产品质量安全风险评估项(GJFP201601402)
作者单位
马红枣 北京农学院植物科学技术学院, 农业应用新技术北京市重点实验室, 北京农业质量标准与 检测技术研究中心, 农业部农产品质量安全风险评估实验室(北京) 
潘立刚 北京农学院植物科学技术学院, 农业应用新技术北京市重点实验室 
李安 北京农业质量标准与 检测技术研究中心, 农业部农产品质量安全风险评估实验室(北京) 
张志勇 北京农学院植物科学技术学院, 农业应用新技术北京市重点实验室 
AuthorInstitution
MA Hong-Zao Beijing Key Laboratory of New Technology in Agricultural Application, College of Plant Science and Technology, Beijing University of Agriculture, Beijing Research Center for Agricultural Standards and Testing, Risk Assessment Lab for Agro-products (Beijing), Ministry of Agriculture 
PAN Li-Gang Beijing Key Laboratory of New Technology in Agricultural Application, College of Plant Science and Technology, Beijing University of Agriculture 
LI An Beijing Key Laboratory of New Technology in Agricultural Application, College of Plant Science and Technology, Beijing University of Agriculture 
ZHANG Zhi-Yong Beijing Key Laboratory of New Technology in Agricultural Application, College of Plant Science and Technology, Beijing University of Agriculture 
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中文摘要:
      目的 建立气相色谱-质谱法(gas chromatography-mass spectrometry, GC-MS)同时检测乙酰甲胺磷和甲胺磷的残留量。方法 通过正交试验优化并确定升温程序参数, 利用液液萃取方法从水中提取乙酰甲胺磷及甲胺磷后, 采用基质匹配标准溶液对两种农药的回收率进行校准。结果 升温程序应采用一阶程序升温, 初始温度为95 ℃, 升温速度为10 ℃/min, 末温为280 ℃; 进样口采用惰性衬管; 添加水平为0.1~1 mg/L时, 回收率在80.3%~110.5%之间, 相对标准偏差在5.5%~6.5%之间。乙酰甲胺磷和甲胺磷在用纯溶剂(丙酮)和空白基质配制0.01~0.5 mg/L浓度范围内线性关系良好(r2>0.999), 乙酰甲胺磷和甲胺磷的检出限分别为0.02 mg/L、0.008 mg/L, 定量检测分别为0.066 mg/L、0.027 mg/L。结论 该方法的精密性、重复性和稳定性良好, 可适用于乙酰甲胺磷和甲胺磷残留量的检测。
英文摘要:
      Objective To establish a method for detection of acephate and methamidophos by gas chromatography-mass spectrometry (GC-MS). Methods The temperature program of GC was optimized and determined by orthogonal experiment, and pesticides were extracted from aqueous solution by liquid-liquid extraction. In addition, the recovery rates of extraction from aqueous solution were corrected by matrix-matched standard calibration. Results The temperature program used first order temperature programming as follows: the temperature of column was from 95 ℃ to 280 ℃ at a speed of 10 ℃/min,. The inert liner was inert. Under the optimized conditions, the average recoveries of the method ranged from 80.3% to 110.5% at the spiked levels of 0.1~1 mg/L with the relative standard deviations of 5.5%~6.5%. Acephate and methamidophos had good linear relationship in the range of 0.01~0.5 mg/L (r2>0.999), the limits of detection (LODs) were 0.02 mg/L and 0.008 mg/L, and the limits of quantitation (LOQs) were 0.066 mg/L and 0.027 mg/L for acephate and methamidophos, respectively. Conclusion The established method had good precision, repeatability and stability, which can be applied to the detection of acephate and methamidophos.
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