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首页> 外文期刊>Analytica chimica acta >Orthogonal array design for the optimization of hollow fiber protected liquid-phase microextraction of salicylates from environmental waters
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Orthogonal array design for the optimization of hollow fiber protected liquid-phase microextraction of salicylates from environmental waters

机译:正交阵列设计优化中空纤维保护环境水杨酸的液相微萃取

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In the present study, a three phase-based hollow fiber protected liquid-phase microextraction (HF-LPME) method combined with high-performance liquid chromatography (HPLC) for the determination of salicylates in environmental waters was developed. The HF-LPME procedure was optimized by an L_(16)(4~5) orthogonal array experimental design (OAD) with five factors at four levels. Under the optimal extraction condition (pHs of donor and receiving phases of 3.0 and 6.2, respectively, extraction time of 45 min, stirring speed of 1000 rpm, and salt addition of 20% (w/v)), salicylates could be determined in a linear range from 0.025 to 1.0 μg mL~(-1) with a good correlation (r~2 >0.9930). The limits of detection (LODs) ranged between O.G ng mL~(-1) and 1.2 ng mL~(-1) for the target analytes. The relative standard deviations (RSDs) of intra-day and inter-day were in the range of 0.64-14.58% and 0.16-15.45%, respectively. This procedure afforded a convenient, sensitive, accurate and cost-saving operation with high extraction efficiency for the model analytes. The method was applied satisfactorily to the determination of salicylates in two environmental waters.
机译:在本研究中,开发了一种基于三相中空纤维保护的液相微萃取(HF-LPME)方法与高效液相色谱(HPLC)相结合的方法,用于测定环境水中的水杨酸酯。 HF-LPME程序通过L_(16)(4〜5)正交阵列实验设计(OAD)在四个级别上具有五个因素进行了优化。在最佳萃取条件下(供体和接收相的pH分别为3.0和6.2,萃取时间为45分钟,搅拌速度为1000 rpm,加盐量为20%(w / v)),可以在线性范围为0.025至1.0μgmL〜(-1),具有良好的相关性(r〜2> 0.9930)。目标分析物的检出限(LOD)在Ong ng mL〜(-1)和1.2 ng mL〜(-1)之间。日内和日间的相对标准偏差(RSD)分别在0.64-14.58%和0.16-15.45%的范围内。此过程为模型分析物提供了方便,灵敏,准确和节省成本的操作,并且提取效率很高。该方法可令人满意地用于两种环境水中水杨酸酯的测定。

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