RELAXATION OF ASPHALTENES AT THE TOLUENE/WATER INTERFACE: DIFFUSION EXCHANGE AND SURFACE REARRANGEMENT

Upon adsorption at the oil/water interface, asphaltenes slowly form a glassy interphase. This robust, asphaltene-rich interphase is likely the reason for prolonged stability of crude oil/water emulsions and for the propensity of asphaltenic crude oils to alter the wettability of reservoirs. Here we adopt interfacial dilatation rheology using the oscillating pendant drop with axisymmetric drop shape analysis (ADSA) to investigate the relaxation mechanisms of asphaltenes adsorbed at the toluene/water interface. We compare classical viscoelastic models with the measured rheologic data and find that the frequency response of the dilatational moduli fits a combination of diffusion-exchange and surface-rearrangement mechanisms. The combined relaxation model is verified by solvent washing the asphaltenes from the interface and measuring the dilatational response of the resulting irreversibly adsorbed species. After washout, the oil-phase diffusion component of the frequency response disappears, and the relaxation time of the adsorbed film increases by an order of magnitude. Since the studied asphaltenes prove insoluble in the synthetic aqueous brine (pH = 8.0), this result suggests that reversibly exchanging species in the oil phase weakens an interconnected asphaltene-gel/glass phase at the interface. Our experiments show, for the first time, that most of the surface-active asphaltenic molecules are irreversibly adsorbed from the oil phase.