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作 者:孙玉珍[1] 罗明标[1] 李建强[1] 郭国龙[1] 徐晶晶[1]
机构地区:[1]东华理工大学应用化学系,江西抚州344000
出 处:《现代农药》2008年第6期43-46,共4页MODERN AGROCHEMICALS
摘 要:研究了基于中空纤维的动态三相液相微萃取(LPME),并首次将其应用到稻谷、稻叶、田水和土壤中吡虫啉农药残留的快速分离富集。实验采用磷酸二氢钾作接受液,以高效液相色谱(HPLC)为检测手段,系统地优化了LPME技术的有机溶剂、搅拌速率和萃取时间等条件。最佳色谱条件为:SB-Phenyl C18(250mm×4.6mm,5μm)液相色谱柱,以甲醇–水–三乙胺(80∶20∶1,v/v)为流动相,流速0.8mL/min,270nm波长下检测。得到方法的线性范围0.001~10μg/mL,最低检出限为1ng/mL,加标回收率92.50%~110%,富集倍数19.2倍。结果表明该方法是一种简单、快速、准确、环境友好的农药残留检测方法。A novel method for fast separate and enrichment imidacloprid in paddy, leaf, water and soil was established by using high performance liquid chromatography (HPLC) coupled with a three-phase hollow fiber based liquid phase micro-extraction (TP-HF-LPME) technique for sample preparation. Parameters related to TP-HF-LPME (organic solvent, stirring speed, pH of donor and acceptor phase, extraction time) were also optimized experimentally. The method was developed using an SB-Phenyl C18(250mm×4.6mm,5μm) column, methanol - water - triethylamine (80:20:1, v/v) as mobile phase and detection at 270 nm. It has been demonstrated to be a very fast, effective and virtually ‘green' sample preparation technique, which provided a good linear range (0.001 to 10μg/mL) with r^2=0.9997 (standard working curves), a low detection limit (1ng/mL, S/N =3) and the addition recovery was obtained in the range of 92.50% to 110%. The proposed method integrates extraction, enrichment and clean-up into a single step, which is a simple, effective, veracious and environmental friendly method for detecting pesticide residue.
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