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基于全二维气相色谱-飞行时间质谱获得的指纹图谱追踪原油的来源

[Tracing the origin of crude oil based on fingerprint profiles obtained by comprehensive two-dimensional gas chromatography-time-of-flight mass spectrometry].

作者信息

Zhang Wei-Ya, Chen Pin, Xie Wei-Xin, Gao Xuan-Bo, Zhang Wan-Feng, Dai Wei, Lin Si-Yuan, Zhu Shu-Kui

机构信息

Testing and Technology Center for Industrial Products of Shenzhen Customs,Shenzhen 518067,China.

State Key Laboratory of Geomicrobiology and Environmental Changes,China University of Geosciences,Wuhan 430074,China.

出版信息

Se Pu. 2025 Jun;43(6):688-695. doi: 10.3724/SP.J.1123.2025.02005.

DOI:10.3724/SP.J.1123.2025.02005
PMID:40394748
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12093212/
Abstract

Crude oils are complex mixtures of thousands of organic compounds that differ significantly in relative molecular mass, volatility, content, and polarity. Traditional methods for analyzing crude oil often involve complicated steps, consume large amounts of organic solvents, and require long sample-preparation times. These limitations lead to inefficient and time-consuming analysis processes. Crude oil is commonly analyzed by gas chromatography-mass spectrometry (GC-MS). However, this technique is incapable of effectively separating complex crude-oil components owing to its low resolution and peak capacity, resulting in overlapping peaks that can lead to inaccurate compound identification and quantification. These challenges highlight the need for advanced analytical techniques. Comprehensive two-dimensional gas chromatography (GC×GC) is a novel separation technique that has been widely used to analyze complex samples, such as food, environmental samples, natural products, and crude oil. GC×GC has several advantages over traditional GC. Firstly, it offers higher resolution and peak capacity, thereby improving separation efficiency. Secondly, its high separation power reduces the need for complex sample pretreatment. Thirdly, the ordered separation and "tile effect" in a GC×GC chromatogram facilitate easier compound identification and quantification in complex mixtures.In this study, we developed a gas purge microsyringe extraction (GPMSE) method for the rapid pretreatment of crude-oil samples. This method reduces sample processing time to only 10 min while minimizing organic solvent consumption. The chemical compositions of 45 crude oil samples were analyzed using GC×GC-time-of-flight mass spectrometry (GC×GC-TOFMS), which helped to establish detailed chemical fingerprints for each sample. The GC×GC-TOFMS data were processed using multivariate statistical methods, including redundancy analysis (RDA) and Monte Carlo permutation testing, which identified 36 biomarkers that are strongly associated with the origin of the crude oil (p<0.05). A classification model was constructed using a training set of 28 samples. Four single-source and 13 mixed-source samples were used to validate the model. The GPMSE-GC×GC-TOFMS method was demonstrated to be highly efficient and accurate. A discrimination accuracy of 97.8% was achieved during the identification of crude-oil sources. The developed method not only provides a powerful tool for tracing crude oil but also has broad applications potential, including for the detection of adulterated crude oil, tracking oil-spill sources, and monitoring oilfield development. This study offers several significant benefits. For example, it helps to address crude-oil trade fraud and supports national energy security. Additionally, it provides scientific support in relation to crude-oil quality control and risk assessment. The developed method is fast, reliable, and environmentally friendly; hence, it is expected to be a valuable tool for use in the oil industry. The GPMSE-GC×GC-TOFMS method is cost-effective and requires minimal solvent; consequently, it is an attractive option for reducing environmental impacts in laboratory and industrial settings. Furthermore, the high throughput and accuracy of the developed method make it suitable for large-scale analyses. In conclusion, this study demonstrated the effectiveness of combining GPMSE with GC×GC-TOFMS for analyzing crude oil; the ability of the method to identify biomarkers and classify crude-oil sources in a highly accurate manner represents a significant advancement in the field. Future studies are expected to further explore its applications in related areas, such as oil refining and environmental monitoring.

摘要

原油是由数千种有机化合物组成的复杂混合物,这些化合物在相对分子质量、挥发性、含量和极性方面存在显著差异。传统的原油分析方法通常涉及复杂的步骤,消耗大量有机溶剂,且需要较长的样品制备时间。这些局限性导致分析过程效率低下且耗时。原油通常通过气相色谱 - 质谱联用(GC-MS)进行分析。然而,由于其低分辨率和峰容量,该技术无法有效分离复杂的原油成分,导致峰重叠,从而可能导致化合物鉴定和定量不准确。这些挑战凸显了对先进分析技术的需求。全二维气相色谱(GC×GC)是一种新型分离技术,已广泛用于分析复杂样品,如食品、环境样品、天然产物和原油。GC×GC相对于传统GC具有多个优点。首先,它具有更高的分辨率和峰容量,从而提高了分离效率。其次,其高分离能力减少了对复杂样品预处理的需求。第三,GC×GC色谱图中的有序分离和“瓦片效应”便于在复杂混合物中更轻松地进行化合物鉴定和定量。在本研究中,我们开发了一种气体吹扫微注射器萃取(GPMSE)方法用于原油样品的快速预处理。该方法将样品处理时间缩短至仅10分钟,同时最大限度地减少了有机溶剂的消耗。使用GC×GC - 飞行时间质谱(GC×GC - TOFMS)分析了45个原油样品的化学成分,这有助于为每个样品建立详细的化学指纹图谱。使用包括冗余分析(RDA)和蒙特卡罗置换检验在内的多元统计方法对GC×GC - TOFMS数据进行处理,确定了36种与原油来源密切相关的生物标志物(p<0.05)。使用28个样品的训练集构建了一个分类模型。使用4个单源和13个混合源样品对该模型进行验证。结果表明,GPMSE - GC×GC - TOFMS方法高效且准确。在原油来源鉴定过程中实现了97.8%的判别准确率。所开发的方法不仅为追踪原油提供了有力工具,而且具有广泛的应用潜力,包括用于检测掺假原油、追踪溢油源和监测油田开发。本研究带来了几个显著益处。例如,它有助于解决原油贸易欺诈问题并支持国家能源安全。此外,它为原油质量控制和风险评估提供了科学支持。所开发的方法快速、可靠且环保;因此,它有望成为石油行业中一种有价值的工具。GPMSE - GC×GC - TOFMS方法具有成本效益且所需溶剂最少;因此,它是减少实验室和工业环境中环境影响的一个有吸引力的选择。此外,所开发方法的高通量和准确性使其适用于大规模分析。总之,本研究证明了将GPMSE与GC×GC - TOFMS相结合用于分析原油的有效性;该方法以高度准确的方式识别生物标志物和分类原油来源的能力代表了该领域的一项重大进展。未来的研究有望进一步探索其在炼油和环境监测等相关领域的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3979/12093212/09cb2ee38318/4ACFEFCF-25F9-4439-AECA-5034EFF20F90-F004.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3979/12093212/09cb2ee38318/4ACFEFCF-25F9-4439-AECA-5034EFF20F90-F004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3979/12093212/9933389d610c/4ACFEFCF-25F9-4439-AECA-5034EFF20F90-F001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3979/12093212/ff563cd3d033/4ACFEFCF-25F9-4439-AECA-5034EFF20F90-F002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3979/12093212/d558bff2ca30/4ACFEFCF-25F9-4439-AECA-5034EFF20F90-F003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3979/12093212/09cb2ee38318/4ACFEFCF-25F9-4439-AECA-5034EFF20F90-F004.jpg

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