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作 者:慕卫[1] 刘峰[1] 孙作洋[1] 魏光[1] 杨连来[1]
机构地区:[1]山东农业大学植物保护学院,山东泰安271018
出 处:《农药科学与管理》2005年第7期1-3,共3页Pesticide Science and Administration
摘 要:采用气相色谱法和液相色谱法2种方法分别对戊唑醇、丙环唑和三唑酮进行定性定量分析,气相色谱法中都以邻苯二甲酸二戊酯为内标物,色谱柱都采用3%OV-101chromosorbAWDMCS150 ̄177μm1m×3mm玻璃柱,柱温为200~205℃,汽化温度和检测温度均为230℃,戊唑醇、丙环唑和三唑酮的回收率分别为99.1%~100.3%,98.5%~99.8%和99.3% ̄100.7%;方法变异系数分别为0.34%,0.51%和0.37%。高效液相色谱法中使用Nova-PaKC18250mm×4.6mm色谱柱,以甲醇+水=85+15为流动相,检测波长为225nm。戊唑醇、丙环唑和三唑酮的回收率分别为99.1%~100.7%,98.9% ̄99.6%和99.9%~101.2%;方法变异系数分别为0.74%,0.43%和0.58%。The quantitative analysis of tebuconazole, propiconazole and triadimefon by GC and HPLC were studied.The operation conditions of gas chromatographic method were: 3%OV-101 on Chromosorb AW DMCS, 1m×3mm (i.d.) glass column at column temperature of 200-205℃ and detector temperature of 230℃.The internal standard was disoamyl phthalate.The recoveries were 99.1%-100.3%, 98.5%-99.8% and 99.3%-100.7%, their coefficients of variation were 0.34%,0.51% and 0.37% respectively. The operation conditions of HPLC were: C18 column (250mm×4.6mm) , methanol +water=85 +15 (V/V) as mobile phase, UV detector at 225 nm.The recoveries of this method were 99.1%-100.7%, 98.9%-99.6% and 99.9%-101.2%.The coefficients of variation were 0.74% , 0.43% and 0.58% for tebuconazole, propiconazole and triadimefon respectively.
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