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作 者:张杰[1] 谷淑波[2] 林琎[1,3] 慕卫[1,3]
机构地区:[1]山东农业大学农药环境毒理研究中心,山东泰安271018 [2]山东农业大学农学院,山东泰安271018 [3]山东农业大学植物保护学院,山东泰安271018
出 处:《农药》2016年第12期896-897,926,共3页Agrochemicals
摘 要:【目的】采用高效液相色谱仪,建立25%灭·喹·氟磺胺微乳剂3种有效成分同时测定的分析方法。【方法】该方法选用乙腈-0.5%磷酸水溶液为流动相,215nm为检测波长,可同时对灭草松、精喹禾灵、氟磺胺草醚含量进行测定。【结果】在质量浓度0.1-50mg/L范围内,灭草松、精喹禾灵、氟磺胺草醚的线性相关系数分别为1.0000、1.0000、0.9999,回收率分别为87.29%。94.96%、88.13%-95.12%、81.72%-92.83%,相对标准偏差分别为1.70%、1.35%、2.35%,仪器最低检出限分别为2.2、8.3、10.0μg/L。【结论】该方法可用于这3种成分的复配制剂含量标定,也可用于3种成分的残留量测定。[Aims] The aims were to establish a quantitative analysis method for bentazone- quizalofop, fomesafen 25% ME. [Methods] The simultaneous determination of three active ingredients in the pesticide formulation was conducted by HPLC with the mix,re of acetonitrile and 0.5% phosphoric acid aqueous solution as mobile phase at 215 rim. [Results] When the concentration was in the range of 0.1-50 mg/L, the linear correlation coefficients for bentazone, quizalofop and fomesafen were 1.0000, 1.0000 and 0.9999, the average recoveries were 87.29-94.96, 88.13-95.12 and 81.72-92.83%, the variation coefficients were 1.70, 1.35 and 2.35%, and the limit of determination were 2.2, 8.3 and 10.0 μg/L, respectively. [Conclusions] The method can be used for the determination of the contents of the 3 compound comnonents, and also can be used for the determination of the residues of the 3 comr-onents.
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