Qiao, P, Harbottle, D orcid.org/0000-0002-0169-517X, Li, Z et al. (2 more authors) (2018) Interactions of Asphaltene Subfractions in Organic Media of Varying Aromaticity. Energy & Fuels, 32 (10). pp. 10478-10485. ISSN 0887-0624
Abstract
Whole asphaltenes were fractionated by extended-saturates, aromatics, resins, and asphaltenes (E-SARA) analysis into four asphaltene subfractions: toluene-extracted interfacially active asphaltenes (T-IAA), toluene-extracted remaining asphaltenes (T-RA), Heptol 50/50-extracted interfacially active asphaltenes (HT-IAA), and Heptol 50/50-extracted remaining asphaltenes (HT-RA). The aggregation kinetics of fractionated asphaltenes measured by dynamic light scattering (DLS) showed that decreasing solvent aromaticity promoted asphaltene aggregation for all subfractions. In a given solvent, T-IAA exhibited the strongest aggregation tendency, followed by HT-IAA, then T-RA, and HT-RA. Such differences were attributed to the higher oxygen and sulfur contents (highlighted in sulfoxide content) in IAA subfractions than RA subfractions, as confirmed by elemental analysis and X-ray photoelectron spectroscopy (XPS). The interaction forces between immobilized fractionated asphaltenes were measured using an atomic force microscope (AFM) to obtain a fundamental understanding of asphaltene interactions in organic media of varying aromaticity. The results showed that decreasing solvent aromaticity reduced steric repulsion and increased adhesion between asphaltenes with asphaltenes adopting a more compressed conformation. IAA subfractions, in particular T-IAA, exhibited higher adhesion forces than RA subfractions during separation of two asphaltene films in contact. The results of AFM colloidal force measurements were in good agreement with the DLS data. In spite of the small sulfoxide content in asphaltenes, the sulfoxide groups are believed to play a critical role in enhancing asphaltene aggregation in the bulk oil phase.
Metadata
Item Type: | Article |
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Authors/Creators: |
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Copyright, Publisher and Additional Information: | © 2018 American Chemical Society. This is an author produced version of a paper published in Energy & Fuels. Uploaded in accordance with the publisher's self-archiving policy. |
Dates: |
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Institution: | The University of Leeds |
Academic Units: | The University of Leeds > Faculty of Engineering & Physical Sciences (Leeds) > School of Chemical & Process Engineering (Leeds) |
Depositing User: | Symplectic Publications |
Date Deposited: | 30 Nov 2018 09:59 |
Last Modified: | 07 Sep 2019 01:01 |
Status: | Published |
Publisher: | American Chemical Society |
Identification Number: | 10.1021/acs.energyfuels.8b02170 |
Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:139427 |