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Effect of sample matrix on the determination of total petroleum hydrocarbons (TPH) in soil by gas chromatography-flame ionization detection

机译:样品基质对气相色谱-火焰电离检测法测定土壤中总石油烃的影响

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Research papers in different fields of analytics indicate that the effect of matrix-induced chromatographic response enhancement (matrix effect) is a commonly encountered problem in gas chromatography applications. In this paper, an example of the effect of sample matrix on the quantitative determination of total petroleum hydrocarbons (TPH) by GC-FID in soil is presented. Two types of soil were selected for the evaluation. Extraction and analysis of the soil samples was in accordance with CEN prEN 14039. The relative systematic error resulting from the matrix effect was obtained for three different TPH concentrations by statistical comparison of the slopes of the matrix-matched calibration lines and a pure solvent calibration line. Too high TPH concentrations were obtained when conventional solvent calibration was used for quantitation. This demonstrates that matrix-matched calibration should be exploited in the determination of petroleum hydrocarbons in soil samples. However, there was also significant enhancement of the response due to an interfering matrix with decreasing analyte concentration. Enhancement seems to be especially evident in the quantification of TPH over the concentration range encountered in polluted environments. As a result, even when matrix-matched calibration is used for quantitation, it is still necessary to establish the range over which a linear response can be expected. Otherwise too high results for sample TPH concentrations will be obtained. (C) 2007 Elsevier B.V. All rights reserved.
机译:分析的不同领域的研究论文表明,基质诱导的色谱响应增强效应(矩阵效应)是气相色谱应用中经常遇到的问题。本文以样品基质对GC-FID定量测定土壤中总石油烃(TPH)的影响为例。选择两种土壤进行评估。土壤样品的提取和分析符合CEN prEN14039。通过对基质匹配的校准线和纯溶剂校准线的斜率进行统计比较,获得了三种不同TPH浓度的基质效应引起的相对系统误差。 。当使用常规溶剂校准进行定量时,TPH浓度太高。这表明在土壤样品中石油烃的测定中应采用基质匹配的校准方法。但是,由于基质干扰而降低了分析物浓度,因此响应也显着增强。在受污染环境中遇到的浓度范围内对TPH进行定量时,增强作用尤其明显。结果,即使将矩阵匹配的校准用于定量分析,仍然有必要建立可预期线性响应的范围。否则,将无法获得样品TPH浓度过高的结果。 (C)2007 Elsevier B.V.保留所有权利。

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