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评估 GC-MS 分析烃类时固相萃取技术的可靠性。

Evaluating the reliability of solid phase extraction techniques for hydrocarbon analysis by GC-MS.

机构信息

Aramco Americas- Houston Research Center, 16300 Park Row Drive, Houston, TX 77084, USA.

Aramco Americas- Houston Research Center, 16300 Park Row Drive, Houston, TX 77084, USA.

出版信息

J Chromatogr A. 2024 Nov 22;1737:465435. doi: 10.1016/j.chroma.2024.465435. Epub 2024 Oct 12.

DOI:10.1016/j.chroma.2024.465435
PMID:39427508
Abstract

Saturate and aromatic compounds are essential in the petroleum industry for assessing the thermal maturity of source rocks and oils, which is critical for basin modeling and sweet-spot mapping. These compounds also play a role in environmental applications, such as oil spill fingerprinting and biogeochemistry. However, the analysis of these compounds by gas chromatography-mass spectrometry (GC-MS) requires meticulous and time-consuming separation processes. Traditional methods like normal-phase liquid column chromatography (LCC) involve large volumes of harmful solvents. This study evaluates the effectiveness of five different sorbents using solid-phase extraction (SPE) techniques-neutral Si, SiOH, Ag-ion, neutral Al, and Ag-ion mixed with activated silica-compared to LCC. The goal was to discern differences in peak resolution, concentration, and isomer ratios of saturate and aromatic compounds for thermal maturity and source rock assessments. The results show that SiOH, neutral Si, and neutral Al do not fully separate aromatic compounds from the saturate fraction, sometimes leaving 40-100% of aromatics within the saturate fraction. Ag-ion mixed with activated silica provided the best separation, resulting in up to 23 times higher aromatic concentration than SiOH. This method is more reliable for quantifying both saturate and aromatic compounds, increases the efficiency of hydrocarbon evaluations, and reduces solvent consumption by 63%, offering a more sustainable approach to hydrocarbon analysis.

摘要

饱和烃和芳烃化合物在石油工业中对于评估源岩和油的热成熟度至关重要,这对于盆地模拟和甜点区预测至关重要。这些化合物在环境应用中也有作用,例如溢油指纹分析和生物地球化学。然而,通过气相色谱-质谱联用(GC-MS)分析这些化合物需要细致和耗时的分离过程。传统方法如正相液相色谱(LCC)涉及大量有害溶剂。本研究评估了五种不同吸附剂(中性 Si、SiOH、Ag 离子、中性 Al 和 Ag 离子混合活性硅)的固相萃取(SPE)技术相对于 LCC 的有效性。目标是辨别在用于热成熟度和源岩评估的饱和烃和芳烃化合物的峰分辨率、浓度和异构体比例方面的差异。结果表明,SiOH、中性 Si 和中性 Al 并不能将芳烃化合物与饱和烃完全分离,有时会使 40-100%的芳烃留在饱和烃中。Ag 离子混合活性硅提供了最佳的分离效果,导致芳烃浓度比 SiOH 高 23 倍。这种方法更可靠地定量分析饱和烃和芳烃化合物,提高了烃类评价的效率,并减少了 63%的溶剂消耗,为烃类分析提供了更可持续的方法。

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