Zhang Y, Huang Z Q, Li Y J
Hunan Entry-Exit Inspection and Quarantine Bureau of the People's Republic of China, Changsha 410007, China.
Se Pu. 2001 May;19(3):273-5.
An efficient gas chromatographic method for the determination of 14 organophosphorus pesticide residues in tea by gas chromatography using micro-chemical and solid phase extraction technique has been established. The organophosphorus pesticides were extracted from tea samples with ethyl acetate and mixture of ethyl acetate-hexane(1:1, V/V). The extracts were cleaned up with a column of 3 mL Supelclean Envl-carb by GILSON ASPEC XL. The 14 organophosphorus pesticides were separated from each other through SPB-1701 capillary column(30 m x 0.53 mm i.d. x 1.0 micron) and determined by flame photometric detector. The recoveries ranged 70.8%-120% when the added levels were from 0.100 mg/kg to 1.00 mg/kg, the RSD was 2%-7% and the limits of detection were 0.01 mg/kg-0.08 mg/kg. This method is rapid, sensitive and suitable for the analysis of pesticide residues. It can also be applied to the determination of organophosphorus pesticide multi-residues in other plant samples such as vegetables, fruits and so on.
建立了一种高效气相色谱法,采用微化学和固相萃取技术,通过气相色谱测定茶叶中14种有机磷农药残留。用乙酸乙酯和乙酸乙酯 - 己烷混合液(1:1,V/V)从茶叶样品中提取有机磷农药。提取物通过GILSON ASPEC XL用3 mL Supelclean Envl-carb柱进行净化。14种有机磷农药通过SPB-1701毛细管柱(30 m×0.53 mm内径×1.0微米)彼此分离,并由火焰光度检测器测定。当添加水平为0.100 mg/kg至1.00 mg/kg时,回收率在70.8% - 120%之间,相对标准偏差为2% - 7%,检测限为0.01 mg/kg - 0.08 mg/kg。该方法快速、灵敏,适用于农药残留分析。它也可用于测定其他植物样品如蔬菜、水果等中的有机磷农药多残留。