3D-RISM-KH molecular theory of solvation and density functional theory investigation of the role of water in the aggregation of model asphaltenes

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DOIResolve DOI: http://doi.org/10.1039/c2cp23131j
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TypeArticle
Journal titlePhysical Chemistry Chemical Physics
ISSN1463-9076
1463-9084
Volume14
Issue11
Pages39223934
AbstractWe applied a multiscale modeling approach that involves the statistical–mechanical three-dimensional reference interaction site model with the Kovalenko–Hirata closure approximation (3D-RISM-KH molecular theory of solvation) as well as density functional theory (DFT) of electronic structure to study the role of water in aggregation of the asphaltene model compound 4,4′-bis(2-pyren-1-yl-ethyl)-2,2′-bipyridine (PBP) [X. Tan, H. Fenniri and M. R. Gray, Energy Fuels, 2008, 22, 715]. The solvation free energy and potential of mean force predicted by 3D-RISM-KH reveal favorable pathways for disaggregation of PBP dimers in pure versus water-saturated chloroform solvent. The water density distribution functions elucidate hydrogen bonding preferences and water bridge formation between PBP monomers. The ΔG298 values of −5 to −7 kcal mol−¹ for transfer of water molecules in chloroform to a state interacting with PBP molecules are in agreement with experimental results. Geometry optimization and thermochemistry analysis of PBP dimers with and without water bridges using WB97Xd/6-31G(d,p) predict that both PBP dimerization and dimer stabilization by water bridges are spontaneous (ΔG298 < 0). The ¹H NMR chemical shifts of PBP monomers and dimers predicted using the gauge-independent atomic orbital method and polarizable continuum model for solvation in chloroform are in an excellent agreement with the experimental results for dilute and concentrated PBP solutions in chloroform, respectively [X. Tan, H. Fenniri and M. R. Gray, Energy Fuels, 2009, 23, 3687]. The DFT calculations of PBP dimers with explicit water show that bridges containing 1–3 water molecules lead to stabilization of PBP dimers. Additional water molecules form hydrogen bonds with these bridges and de-shield the PBP protons, negating the effect of water on the ¹HC3 NMR chemical shift of PBP, in agreement with experiment. The ΔG298 results show that hydrogen bonding to water and water-promoted polynuclear assembly bridging is as important as π–π interactions for asphaltene aggregation.
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LanguageEnglish
AffiliationNational Institute for Nanotechnology; National Research Council Canada
Peer reviewedYes
NPARC number21268934
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Record identifierd5e1277c-5544-43c2-9f35-37c570888d12
Record created2013-11-27
Record modified2016-05-09
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