首页> 外文期刊>Journal of separation science. >Determination of 3,5,6-trichloro-2-pyridinol, phoxim and chlorpyrifos-methyl in water samples using a new pretreatment method coupled with high-performance liquid chromatography
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Determination of 3,5,6-trichloro-2-pyridinol, phoxim and chlorpyrifos-methyl in water samples using a new pretreatment method coupled with high-performance liquid chromatography

机译:新型前处理方法-高效液相色谱法测定水样中的3,5,6-三氯-2-吡啶醇,毒死im和甲基毒死os

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摘要

A novel low-density solvent-based vortex-assisted surfactant-enhanced-emulsification liquid-liquid microextraction with the solidification of floating organic droplet method coupled with high-performance liquid chromatography was developed for the determination of 3,5,6-trichloro-2-pyridinol, phoxim and chlorpyrifos-methyl in water samples. In this method, the addition of a surfactant could enhance the speed of the mass transfer from the sample solution into the extraction solvent. The extraction solvent could be dispersed into the aqueous by the vortex process. The main parameters affecting the extraction efficiency were investigated and the optimum conditions were established as follows: 80 mu L 1-undecanol as extraction solvent, 0.2 mmol/L of Triton X-114 selected as the surfactant, the vortex time was fixed at 60 s with the vortex agitator set at 3000 rpm, the concentration of acetic acid in sample solution was 0.4% v/v and 1.0 g addition of NaCl. Under the optimum conditions, the enrichment factors were from 172 to 186 for the three analytes. The linear ranges were from 0.5 to 500 mu g/L with a coefficient of determination (r(2)) of between 0.9991 and 0.9995. Limits of detections were varied between 0.05 and 0.12 mu g/L. The relative standard deviations (n = 6) ranged from 0.26 to 2.62%.
机译:开发了一种新型的低密度溶剂型涡旋表面活性剂增强乳化液-液微萃取-漂浮有机液滴固化法-高效液相色谱法测定3,5,6-三氯-2 -吡啶醇,辛硫磷和毒死rif甲基。在这种方法中,添加表面活性剂可以提高从样品溶液到萃取溶剂的质量转移速度。萃取溶剂可通过涡旋过程分散到水溶液中。研究了影响萃取效率的主要参数,确定了最佳条件:以80μL1-十一烷醇为萃取溶剂,选用0.2 mmol / L Triton X-114作为表面活性剂,涡旋时间固定为60 s。在涡旋搅拌器设置为3000 rpm的情况下,样品溶液中乙酸的浓度为0.4%v / v,并添加1.0 g NaCl。在最佳条件下,三种分析物的富集系数为172至186。线性范围为0.5至500μg / L,测定系数(r(2))在0.9991至0.9995之间。检出限在0.05和0.12μg / L之间变化。相对标准偏差(n = 6)为0.26%至2.62%。

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