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柴油燃料酸蚀的化学表征:基于瓦片式费舍尔比率和组合阈值测定的二维气相色谱-飞行时间质谱非靶向分析

Chemical characterization of the acid alteration of diesel fuel: Non-targeted analysis by two-dimensional gas chromatography coupled with time-of-flight mass spectrometry with tile-based Fisher ratio and combinatorial threshold determination.

作者信息

Parsons Brendon A, Pinkerton David K, Wright Bob W, Synovec Robert E

机构信息

Department of Chemistry, University of Washington, Box 351700, Seattle, WA 98198, USA.

Pacific Northwest National Laboratory, Battelle Boulevard, P.O. Box 999, Richland, WA 99352, USA.

出版信息

J Chromatogr A. 2016 Apr 1;1440:179-190. doi: 10.1016/j.chroma.2016.02.067. Epub 2016 Feb 27.

Abstract

The illicit chemical alteration of petroleum fuels is of keen interest, particularly to regulatory agencies that set fuel specifications, or taxes/credits based on those specifications. One type of alteration is the reaction of diesel fuel with concentrated sulfuric acid. Such reactions are known to subtly alter the chemical composition of the fuel, particularly the aromatic species native to the fuel. Comprehensive two-dimensional gas chromatography coupled with time-of-flight mass spectrometry (GC×GC-TOFMS) is well suited for the analysis of diesel fuel, but may provide the analyst with an overwhelming amount of data, particularly in sample-class comparison experiments comprised of many samples. Tile-based Fisher-ratio (F-ratio) analysis reduces the abundance of data in a GC×GC-TOFMS experiment to only the peaks which significantly distinguish the unaltered and acid altered sample classes. Three samples of diesel fuel from differently branded filling stations were each altered to discover chemical features, i.e., analyte peaks, which were consistently changed by the acid reaction. Using different fuels prioritizes the discovery of features likely to be robust to the variation present between fuel samples and may consequently be useful in determining whether an unknown sample has been acid altered. The subsequent analysis confirmed that aromatic species are removed by the acid alteration, with the degree of removal consistent with predicted reactivity toward electrophilic aromatic sulfonation. Additionally, we observed that alkenes and alkynes were also removed from the fuel, and that sulfur dioxide or compounds that degrade to sulfur dioxide are generated by the acid alteration. In addition to applying the previously reported tile-based F-ratio method, this report also expands null distribution analysis to algorithmically determine an F-ratio threshold to confidently select only the features which are sufficiently class-distinguishing. When applied to the acid alteration of diesel fuel, the suggested per-hit F-ratio threshold was 12.4, which is predicted to maintain the false discovery rate (FDR) below 0.1%. Using this F-ratio threshold, 107 of the 3362 preliminary hits were deemed significantly changing due to the acid alteration, with the number of false positives estimated to be about 3. Validation of the F-ratio analysis was performed using an additional three fuels.

摘要

石油燃料的非法化学改性备受关注,尤其是对于那些制定燃料规格或基于这些规格征收税费/给予信贷的监管机构而言。其中一种改性类型是柴油与浓硫酸的反应。已知此类反应会微妙地改变燃料的化学成分,特别是燃料中天然存在的芳烃种类。全二维气相色谱与飞行时间质谱联用(GC×GC - TOFMS)非常适合分析柴油,但可能会给分析人员提供大量数据,尤其是在由许多样品组成的样品类别比较实验中。基于图块的费舍尔比率(F比率)分析将GC×GC - TOFMS实验中的数据丰度仅减少到能显著区分未改性和酸改性样品类别的峰。对来自不同品牌加油站的三个柴油样品分别进行改性,以发现化学特征,即分析物峰,这些峰因酸反应而持续变化。使用不同的燃料优先发现可能对燃料样品之间存在的变化具有稳健性的特征,因此可能有助于确定未知样品是否已被酸改性。后续分析证实,芳烃种类通过酸改性被去除,去除程度与对亲电芳香磺化的预测反应性一致。此外,我们观察到烯烃和炔烃也从燃料中被去除,并且酸改性会生成二氧化硫或降解为二氧化硫的化合物。除了应用先前报道的基于图块的F比率方法外,本报告还扩展了空分布分析,以通过算法确定F比率阈值,从而有信心地仅选择具有足够类别区分能力的特征。当应用于柴油的酸改性时,建议的每次命中F比率阈值为12.4,预计可将错误发现率(FDR)保持在0.1%以下。使用此F比率阈值,3362个初步命中结果中有107个被认为由于酸改性而有显著变化,估计假阳性数量约为3个。使用另外三种燃料对F比率分析进行了验证。

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