检验检疫学刊
檢驗檢疫學刊
검험검역학간
INSPECTION AND QUARANTINE SCIENCE
2012年
5期
29-32
,共4页
楼成杰%任莹%陈丽%严颖鹏%涂俊%方群
樓成傑%任瑩%陳麗%嚴穎鵬%塗俊%方群
루성걸%임형%진려%엄영붕%도준%방군
气相色谱-质谱法%负化学电离源%茶叶%氟乐灵%三唑酮%溴丙磷
氣相色譜-質譜法%負化學電離源%茶葉%氟樂靈%三唑酮%溴丙燐
기상색보-질보법%부화학전리원%다협%불악령%삼서동%추병린
Gas Chromatography-Mass Spectrometry(GC-MS)%Negative Chemical Ionization(NCI)%Tea%Trifluralin%Triadimefon%Profenofos
采用有机溶剂液液萃取的方式,以气相色谱-质谱联用仪负化学电离源法同时检测茶叶中氟乐灵、三唑酮和溴丙磷的残留量。茶叶加水浸泡后用丙酮:正己烷=1:1(V/V)的混合溶液高速均质提取,TPT柱净化后,用气相色谱-质谱联用仪进行测定和确认,外标法定量。该方法对茶叶中氟乐灵、三唑酮、溴丙磷的定量限均为0.01 mg/kg,方法在0.01-0.2mg/kg质量浓度范围内具有良好的线性关系。
採用有機溶劑液液萃取的方式,以氣相色譜-質譜聯用儀負化學電離源法同時檢測茶葉中氟樂靈、三唑酮和溴丙燐的殘留量。茶葉加水浸泡後用丙酮:正己烷=1:1(V/V)的混閤溶液高速均質提取,TPT柱淨化後,用氣相色譜-質譜聯用儀進行測定和確認,外標法定量。該方法對茶葉中氟樂靈、三唑酮、溴丙燐的定量限均為0.01 mg/kg,方法在0.01-0.2mg/kg質量濃度範圍內具有良好的線性關繫。
채용유궤용제액액췌취적방식,이기상색보-질보련용의부화학전리원법동시검측다협중불악령、삼서동화추병린적잔류량。다협가수침포후용병동:정기완=1:1(V/V)적혼합용액고속균질제취,TPT주정화후,용기상색보-질보련용의진행측정화학인,외표법정량。해방법대다협중불악령、삼서동、추병린적정량한균위0.01 mg/kg,방법재0.01-0.2mg/kg질량농도범위내구유량호적선성관계。
A gas chromatography-mass spectrometry method using negative chemical ionization(NCI) was presented for the determination of trifluralin,triadimefon and profenofos residues in tea.In the method,the tea sample was soaked by water and then extracted with acetone: hexane =1:1(V/V) mixed solvent twice,cleaned up on a TPT solid-phase extraction column.After purification,using gas chromatography-mass spectrometry for the determination and confirmation,and the quantification was performed by external standard method.The quantitation limit of this method is 0.01mg/kg for trifluralin,triadimefon and profenofos.The concentration exhibited a good linearity over the range of 0.01 to 0.2 mg/kg.