Small-angle X-ray scattering (SAXS) analyses of an asphaltene (a heptane-insoluble fraction in Canadian oil sand bitumen (CaAs)), at various concentrations in bromobenzene (BB) were performed at a synchrotron facility. BB is the first trial medium in which the aggregation behavior of asphaltenes has been elucidated, and is considered to be one of the "best" pure solvents for CaAs when determining the Hansen Solubility Parameters (HSP). Although the aggregation behavior of the CaAs in toluene (TL) and toluene-pentane mixed solvent (TL-PT10, containing 10% pentane on a volume basis) was confirmed to be similar to that reported in previous SAXS studies, the behavior in BB was markedly different. The results indicated that aggregates with a soft boundary of ~30-60 Å in the radius of gyration (R g ), which were observable in TL and TL-PT10, disappeared in BB and larger aggregates with a clear boundary appeared simultaneously. This phenomenon supported a colloidal aggregation model, with HSP analyses suggesting that BB dispersed the colloid surface fraction at the molecular level and isolated the colloid core fraction, which led to the formation of a rigid aggregation of the core fraction. The HSP analyses enabled us to evaluate the aggregation behavior quantitatively, and the results obtained by SAXS were consistent with those obtained by Rayleigh scattering that we reported previously.

Hydrocarbons including a methylene group are generally considered a hydrophobic building block, in the sense that the density of their hydration water is lower than that of bulk water. However, is the methylene group always hydrophobic? In this study, we experimentally determined the partial molar volume of a methylene group in water as 14.01 ± 0.46 cm mol for 1-alkyne, 9.83 ± 0.35 cm mol for 2-alkyne, and 11.39 ± 0.55 cm mol for 3-alkyne. These values are all unusually small compared to the ∼16 cm mol for model compounds from the literature. The subsequent volumetric analysis on the basis of the Kirkwood-Buff parameter indicates that the hydration water is enriched by the addition of a methylene group for 2-alkyne, while it is depleted for the reported model compounds that contain hydrophilic functional groups, 1-alkyne, and 3-alkyne. Our findings suggest that the triple bonded carbons in 2-alkyne that reduce hydration water act as a hydrophobic group in 2-alkyne. Thus, the methylene group should be called "hydrophilic" in this case because it actually recovers the hydration water when placed next to more hydrophobic groups. Therefore, we conclude that the hydrophobicity of a methylene group varies depending on its hydration environment due to other functional groups in the solute.

No abstract

No abstract

No abstract