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超高效液相色谱/串联质谱分析生活饮用水中莠去津和灭草松 被引量:21

Determination of atrazine and bentazone in drinking water by UPLC-ESI-MS/MS
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摘要 目的:建立超高效液相色谱-电喷雾串联四极杆质谱快速测定生活饮用水中莠去津、灭草松的方法。方法:水样经WatersOasisHLB固相萃取净化,应用超高效液相色谱/电喷雾串联四极杆质谱仪多离子反应监测(MRM)定量法检测莠去津、灭草松,建立了定量检测生活饮用水中莠去津、灭草松的快速、准确、高灵敏度的方法。结果:经方法学验证。该方法对莠去津、灭草松的最低检出限LOD分别为0.08、0.8μg/L(进样量10μl),最低定量限LOQ分别是0.1、1.0μg/L。在1.0~100.0μg/L的线性范围中,相关系数r〉0.9999,回收率:87.6%~103.0%。结论:方法灵敏度高、操作简单、定量准确、测定浓度范围宽阔,是环境水质样品中莠去津、灭草松含量检测的理想方法。 Objective: A UPLC - ESI - MS/MS method was developed for the determination of atrazine and bentazone in drinking water. Methods: For clean- up and concentration solid phase extraction (SPE) with OASIS HLB cartridges were used, or membrane filter was used to remove dirties. UPLC analysis was performed on a Waters ACQUITY UPLC BEH C18 1.0 × 50 mm column, water and acidified acetonitrile was used as mobile phase. The 2 agents were determined by UPLC - ESI - MS/MS and quantified with multiple reaction monitoring (MRM) mode. Results:The detection limits (LOD) for atrazine and bentazone were 0. 08,0. 8μg/L,respectively. The limits of quantification (LOQ) were 0. 1,1.0μg/L, respectively. The linear ranges were 1.0 100. 0μg/L with correlation coefficients above O. 9999. The mean recoveries were between 87.6% and 103.0%. Conclusion:This method can be applied for the determination of atrazine and bentazone in drinking water for its high sensitivity and high selectivity.
出处 《中国卫生检验杂志》 CAS 2008年第4期590-592,625,共4页 Chinese Journal of Health Laboratory Technology
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