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An analytical investigation of 24 oxygenated-PAHs (OPAHs) using liquid and gas chromatography–mass spectrometry

机译:液相和气相色谱-质谱法分析24种含氧多环芳烃(OPAH)

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摘要

We developed two independent approaches for separation and quantitation of 24 oxygenated polycyclic aromatic hydrocarbons (OPAHs) using both liquid chromatography-atmospheric pressure chemical ionization/mass spectrometry (LC-APCI/MS) and gas chromatography-electron impact/mass spectrometry (GC-EI/MS). Building on previous OPAH research, we examined laboratory stability of OPAHs, improved existing method parameters, and compared quantification strategies using standard addition and an internal standard on an environmental sample. Of 24 OPAHs targeted in this research, 19 compounds are shared between methods, with 3 uniquely quantitated by GC-EI/MS and 2 by LC-APCI/MS. Using calibration standards, all GC-EI/MS OPAHs were within 15 % of the true value and had less than 15 % relative standard deviations (RSDs) for interday variability. Similarly, all LC-APCI/MS OPAHs were within 20 % of the true value and had less than 15 % RSDs for interday variability. Instrument limits of detection ranged from 0.18 to 36 ng mL−1 on the GC-EI/MS and 2.6 to 26 ng mL−1 on the LC-APCI/MS. Four standard reference materials were analyzed with each method, and we report some compounds not previously published in these materials, such as perinaphthenone and xanthone. Finally, an environmental passive sampling extract from Portland Harbor Superfund, OR was analyzed by each method using both internal standard and standard addition to compensate for potential matrix effects. Internal standard quantitation resulted in increased precision with similar accuracy to standard addition for most OPAHs using 2-fluoro-fluorenone-13C as an internal standard. Overall, this work improves upon OPAH analytical methods and provides some considerations and strategies for OPAHs as focus continues to expand on this emerging chemical class.>FigureOPAH chromatograms from GC-EI/MS and LC-APCI/MS methods for NIST SRM 1650b (diesel particulate matter)
机译:我们开发了两种独立的方法,分别使用液相色谱-常压化学电离/质谱(LC-APCI / MS)和气相色谱-电子碰撞/质谱(GC-EI)分离和定量分析24种氧化多环芳烃(OPAH)。 /多发性硬化症)。在先前的OPAH研究的基础上,我们检查了OPAH的实验室稳定性,改进了现有方法的参数,并在环境样品上使用标准添加和内标比较了定量策略。本研究针对的24种OPAH中,方法之间共有19种化合物,其中3种通过GC-EI / MS进行了唯一定量,另外2种通过LC-APCI / MS进行了定量。使用校准标样,所有GC-EI / MS OPAH均在真实值的15%以内,并且日间变异性的相对标准偏差(RSD)小于15%。同样,所有LC-APCI / MS OPAH均在真实值的20%以内,并且日间变化的RSD小于15%。仪器的检测限在GC-EI / MS上为0.18至36 ng mL -1 ,在LC-APCI / MS上为2.6至26 ng mL -1 。每种方法都分析了四种标准参考物质,我们报告了一些以前未在这些物质中发表的化合物,例如哌那萘醌和x吨酮。最后,使用内标和标准添加物通过每种方法对俄勒冈州波特兰港超级基金的环境被动采样提取物进行了分析,以补偿潜在的基质效应。内标定量法以2-氟芴酮- 13 C作为内标物,导致大多数OPAH的精密度提高,准确性与标准添加品相似。总体而言,这项工作改进了OPAH的分析方法,并为OPAH提供了一些考虑因素和策略,因为人们将重点继续扩展到这一新兴的化学类别上。<!-fig ft0-> <!-fig @ position =“ anchor” mode =文章f4-> <!-fig mode =“ anchored” f5-> > Figure <!-fig / graphic | fig / alternatives / graphic mode =“ anchored” m1-> <!-标题NIST SRM 1650b(柴油颗粒物)的GC-EI / MS和LC-APCI / MS方法的a7-> OPAH色谱图

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