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Mesoporous carbon reinforced hollow fiber liquid-phase microextraction for the enrichment of phenylurea herbicides followed by their determination with high performance liquid chromatography

机译:介孔碳增强中空纤维液相微萃取富集苯脲类除草剂,然后用高效液相色谱法测定

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In this paper, a new sample preparation method based on mesoporous carbon reinforced hollow fiber liquid phase microextraction (MC-HF-LPME) was developed for the extraction of some phenylurea herbicides (chlortoluron, isoproturon, monolinuron and buturon) in river water and soil samples prior to high performance liquid chromatography-diode array detection. Mesoporous carbon was synthesized using MCM-41 as a template and sucrose as a carbon precursor. The as-prepared mesoporous carbon was characterized by SEM, TEM and nitrogen adsorption. Several important parameters that affect the extraction efficiencies, such as concentration of ordered porous carbon, fiber length, extraction time, sample solution pH, salt addition and stirring rate, were investigated and optimized. Under the optimum conditions, the linearity for buturon was in the range of 0.3a€“100.0 ng mLa?’1 and 5.0a€“300.0 ng ga?’1 for river water and soil samples, respectively. The linearity for the other three analytes was in the range of 0.2a€“100.0 ng mLa?’1 for the river water sample and 2.0a€“300.0 ng ga?’1 for the soil sample. The limits of detection (S/N = 3) of the method ranged from 0.05 to 0.1 ng mLa?’1 for the river water sample and 0.5 to 1.0 ng ga?’1 for the soil sample. The results indicated that the developed method is a simple, efficient and environmentally friendly method for the extraction and determination of phenylurea herbicides in river water and soil samples.
机译:本文开发了一种基于介孔碳增强中空纤维液相微萃取(MC-HF-LPME)的新样品制备方法,用于萃取河水和土壤样品中的某些苯脲类除草剂(氯甲苯,异丙隆,单亚麻隆和丁隆)。在进行高效液相色谱-二极管阵列检测之前。以MCM-41为模板,以蔗糖为碳前体合成介孔碳。制备的介孔碳通过SEM,TEM和氮吸附进行表征。研究和优化了影响萃取效率的几个重要参数,例如有序多孔碳的浓度,纤维长度,萃取时间,样品溶液的pH,盐的添加和搅拌速度。在最佳条件下,河水和土壤样品中丁隆的线性分别在0.3a€“ 100.0 ng mLa?1”和5.0a€“ 300.0 ng ga?1”的范围内。对于河水样品,其他三种分析物的线性范围为0.2a€” 100.0 ng mLa?” 1,对于土壤样品,线性范围为2.0a€” 300.0 ng ga?” 1。该方法的检出限(S / N = 3)在河水样品中为0.05到0.1 ng mLa?1,在土壤样品中为0.5到1.0 ng Ga?1。结果表明,该方法是一种简便,高效,环保的方法,用于河流水和土壤样品中苯脲类除草剂的提取和测定。

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