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Method for the determination of perfluorinated compounds (PFCs) in water by solid-phase extraction and liquid chromatography/tandem mass spectrometry (LC/MS/MS)

机译:固相萃取和液相色谱/串联质谱法(LC / MS / MS)测定水中全氟化合物(PFC)的方法

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A solid phase extraction-liquid chromatography tandem mass spectrometry (SPE-LC/MS/MS) analytical method for the analysis of perfluorinated compounds (PFCs) in water is presented. The method incorporates a stable isotope internal standard (IS) for each target analyte added prior to sample collection. Method validation for perfluorinated carboxylic acids (PFCAs) (C4-C12), perfluorinated sulfonic acids (PFSAs) (C4, C6, and C8), and perfluorooctane sulfonamide (PFOSA) in laboratory Milli Q water evaluated the following: (1) method accuracy and precision over the concentration range 0.025 ng mL~(-1) to 25 ng mL~(-1); (2) internal standard calibration; (3) quantitation of mixed branched and linear isomers of perfluorooctanoate (PFOA) and perfluorooctane sulfonate (PFOS) with linear isomer calibration; (4) method minimum reporting levels (MRLs) (Shoemaker et al, http://www.epa.gov/ nerlcwww/Method%20537_FINAL_revl. 1 .pdf, and Winslowetal, Environ. Sci. Technol., 2006,40,281-288); and (5) 28 day holding time at the MRL, low, and mid range of the calibration range. IS calibration with IS addition to the sample bottle prior to sample collection demonstrated an overall method accuracy of at least 100 ± 10% with a precision of ±15% and a 28-day sample holding time at the MRLs for all target analytes. Method application to groundwater, production facility non-contact cooling water, and production facility wastewater treatment effluent samples demonstrated a method accuracy of at least 100 ± 19% with a precision of ±25% for all target analytes.
机译:提出了一种固相萃取-液相色谱串联质谱(SPE-LC / MS / MS)分析方法,用于分析水中的全氟化合物(PFC)。该方法为样品收集前添加的每种目标分析物均加入了稳定的同位素内标(IS)。在实验室Milli Q水中对全氟羧酸(PFCA)(C4-C12),全氟磺酸(PFSA)(C4,C6和C8)和全氟辛烷磺酰胺(PFOSA)的方法验证评估了以下内容:(1)方法的准确性在0.025 ng mL〜(-1)至25 ng mL〜(-1)的浓度范围内具有较高的精度; (2)内标校准; (3)用线性异构体校准定量全氟辛酸酯(PFOA)和全氟辛烷磺酸(PFOS)的混合支链和线性异构体; (4)方法最低报告水平(MRL)(Shoemaker等,http://www.epa.goverlcwww/Method%20537_FINAL_revl。1 .pdf,以及Winslowetal,Environ。Sci。Technol。,2006,40,281-288 ); (5)在MRL,校准范围的中低范围中保持28天。在样品收集之前向样品瓶中添加IS进行的IS校准表明,所有目标分析物的总体方法准确度至少为100±10%,精度为±15%,并且在MRL处的样品保存时间为28天。在地下水,生产设施非接触式冷却水和生产设施废水处理废水样品中的方法应用证明,方法精度至少为100±19%,所有目标分析物的精度为±25%。

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