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Sample Preparation for Solid Petroleum-Based Matrices Based on Direct Matrix Introduction Oriented to Hydrocarbon Profiling

Multicomponent mixtures may be considered complex because of the overwhelming number of sample constituents and their broad range of physical–chemical properties. Such features translate into challenges in resolving all components using separation techniques but also impact sample preparation, which...

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Published in:Energy & fuels 2020-09, Vol.34 (9), p.10705-10712
Main Authors: de Oliveira, Amilton Moreira, Castiblanco, Julián Eduardo Ballen, Fleming, Felipe Pereira, de Souza, Emanoel Nazareno Ramalho, Hantao, Leandro Wang
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cited_by cdi_FETCH-LOGICAL-a350t-6c34e923b169f3ff16f5de1a62af95fee68d8c0dacd319cbfe52aafaa70188d63
cites cdi_FETCH-LOGICAL-a350t-6c34e923b169f3ff16f5de1a62af95fee68d8c0dacd319cbfe52aafaa70188d63
container_end_page 10712
container_issue 9
container_start_page 10705
container_title Energy & fuels
container_volume 34
creator de Oliveira, Amilton Moreira
Castiblanco, Julián Eduardo Ballen
Fleming, Felipe Pereira
de Souza, Emanoel Nazareno Ramalho
Hantao, Leandro Wang
description Multicomponent mixtures may be considered complex because of the overwhelming number of sample constituents and their broad range of physical–chemical properties. Such features translate into challenges in resolving all components using separation techniques but also impact sample preparation, which is often underestimated in modern practices of oil industry. While the former may be effectively tackled using comprehensive two-dimensional gas chromatography (GC×GC), analyte mass discrimination remains overlooked. In the analysis of whole crude oils or heavy distillates, it is well known that pentatriacontane (C35) precipitates at room temperature in many solvents, such as carbon disulfide, n-hexane, and toluene. Therefore, solvent-based sample preparation methods are biased for analytes heavier than C35, which are found in unusual crude oils. Although, current methods using conventional thermal desorption are limited for C40 hydrocarbons, direct matrix introduction (DMI) may be used for sample introduction. In this work, we expanded the effective operating range of DMI for hydrocarbon analysis by GC. Two case studies were evaluated. First, an uncommonly heavy paraffinic oil fraction was characterized by DMI-GC to illustrate the effect of solubility-based discrimination during sample preparation. Second, we extended the benefits of DMI for the sample preparation of soil contaminated by oil spill, bypassing the need for solvent extraction. Relative standard deviations of 6.7–9.4% were observed for the measurement of n-alkanes, allowing for reliable qualitative analysis of weathered soils. Furthermore, calibration curves of n-alkanes from 6.25 μg g–1 to 100 μg mL–1 (Pearson coefficient, r 2 = 0.99) demonstrated the potential of the DMI-based method for quantitative analysis.
doi_str_mv 10.1021/acs.energyfuels.0c01613
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title Sample Preparation for Solid Petroleum-Based Matrices Based on Direct Matrix Introduction Oriented to Hydrocarbon Profiling
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