CAJ | 학술논문

本文采用有机溶剂萃取的提取方法，利用气相色谱一质谱选择离子检测，建立了海水及水产品中莠去津的检测方法。该方法在0．001-0．5μg/L的范围内具有良好的线性范围，线性相关系数为0．9996；在海水和水产品中的检出限（S／N=3）分别为0．001μg/L和0．001mg／kg；在加标回收率试验中，海水中莠去津回收率为95．8％-113．2％，水产品中莠去津回收率为83．1％～92．6％；相对标准偏差（n=6）均小于4．4％。
본문채용유궤용제췌취적제취방법，이용기상색보일질보선택리자검측，건립료해수급수산품중유거진적검측방법。해방법재0．001-0．5μg/L적범위내구유량호적선성범위，선성상관계수위0．9996；재해수화수산품중적검출한（S／N=3）분별위0．001μg/L화0．001mg／kg；재가표회수솔시험중，해수중유거진회수솔위95．8％-113．2％，수산품중유거진회수솔위83．1％～92．6％；상대표준편차（n=6）균소우4．4％。
A gas chromatohraph - mass spectrum method was established for determination of atrazine in sea- water and sea food. The pretreatment and chromatographic conditions were optimized. The total of 50 mL di- chloromethane was chosen in the process of organic solvent - seawater extract with liquid - liquid extraction technique. Florisil SPE column and hexane mixed with ethyl acetate were used to clean up the sea food sample so as to reduce continuum organic interference in Ionization mode (EI) using select ion monitori obtained for atrazine in the range of 0. 001 -0. ng 5 GC -MS detection. Identification was achieved by Electron (SIM). Under the optimal conditions, good linearities were μg/L. The quantification was performed with internal stand- ards. The recoveries of atrazine in seawater and sea food were in the range of 95.8% - 113.2% and 83.1% -92.6% respectively. The relative standard deviations (RSD) were less than 4.4%. The limits of detection were 0. 001 μg/L for atrazine in seawater, and 0 successfully applied to determination of atrazine in an accident 001 mg/kg for atrazine in sea food. The method has been seawater and sea food in sea area of Fujian province during