: Liquid-phase mutual diffusion coefficients are a key parameter in reservoir simulation models related to both primary production and envisioned secondary recovery processes for heavy oil and bitumen. The measurement of liquid-phase mutual diffusion coefficients in bitumen and heavy oil + light hydrocarbon or gas mixtures present numerous experimental and data analysis challenges due to the viscosity and opacity of the mixtures, the variability of density, viscosity and mutual diffusion coefficient with composition, and the multi-phase nature of these mixtures. Data analysis challenges are particularly acute. For example, recently reported mutual diffusion coefficient values for liquid mixtures of bitumen + carbon dioxide vary over three orders of magnitude when different analysis methods are applied to the same experimental data. In this contribution, we illustrate the importance of measuring composition profiles within liquids as a function of time, as a basis for mutual diffusion coefficient computation, and for allowing explicitly for the variation of diffusion coefficient and liquid density with composition in the analysis of composition profile data. Such inclusions eliminate apparent temporal variations of mutual diffusion coefficients and yield values consistent with relevant theories and exogenous data sets. Liquid-phase mutual diffusion coefficients computed for the mixtures Athabasca Bitumen + pentane and Cold Lake Bitumen + heptane exemplify the experimental and data analysis approaches.
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Zhang et al. (2007) studied this question.
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