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• W4200473999 endingPage "122864" @default.
• W4200473999 startingPage "122864" @default.
• W4200473999 abstract "• Two methods of fractionation of asphaltenes were employed. • Three subfractions were produced for each method, being characterized by ESI(-). • Subfraction 6–40 V presented a more aromatic profile than of remaining subfractions. • Subfractions with more species of heteroatoms showed higher solubility parameters. • Subfractions in n -hexane have a lower tendency to precipitate in hydrocarbons. Negative ion-mode electrospray (ESI(-)) technique coupled to Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) provides ionization of polar constituents with ultra-high resolution and mass accuracy. This study aimed to characterize asphaltenes and subfractions obtained from precipitation with different n -hexane/asphaltenes ratios (3.5 V, 3.5–6 V, and 6–40 V), and three subfractions obtained from adsorption onto CaCO 3 (non-adsorbed, adsorbed, and irreversibly adsorbed) by FT-ICR MS, and to estimate the solubility parameters (δ) of the molecules with the data generated from ESI(-) analysis. Mean values of solubility parameters between 16 and 24 MPa 0.5 were found for whole asphaltenes and their subfractions. ESI(-) data showed that a higher number of polar species were found for the 6–40 V and irreversibly adsorbed subfraction. Besides, subfraction 6–40 V presented a more aromatic profile than of remaining subfractions. Moreover, 6–40 V and irreversibly adsorbed subfractions presented a shift to higher solubility parameters, indicating that the polarity and aromaticity have influenced the solubility of the subfractions. Species containing multiple heteroatoms showed higher solubility parameters, suggesting that these species appear to be responsible for the lower solubility of subfractions." @default.
• W4200473999 created "2021-12-31" @default.
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• W4200473999 date "2022-03-01" @default.
• W4200473999 modified "2023-10-16" @default.
• W4200473999 title "Asphaltenes subfractions characterization and calculation of their solubility parameter using ESI(-) FT-ICR MS: Part II" @default.
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• W4200473999 doi "https://doi.org/10.1016/j.fuel.2021.122864" @default.
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