Current oil production technologies recover only about one‐third to one‐half of the oil originally present in an oil reservoir. Given current oil prices, even a modest increase in oil recovery efficiency is fiscally attractive. One novel approach to increase oil recovery efficiency is a process called microbial enhanced oil recovery (MEOR), where microorganisms are either used as a clogging agent to redirect flow or to produce biosurfactant that reduces interfacial tension. This dissertation aims to understand the MEOR pore‐scale mechanisms relevant to oil recovery by taking a two‐fold approach where transparent 2‐dimensional micromodel experiments imaged with stereo microscopy and 3‐dimensional column experiments imaged with x‐ray computed microtomography (CMT) are utilized. Micromodel experiments allow for direct visualization of the biological phase (i.e. biofilm), however, only 2‐dimensional information is provided. Conversely, CMT experiments provide 3‐dimensional pore‐scale information, but lack the ability to image the biological phase. With this two‐fold approach, it is possible to distinguish multiple fluid interfaces, quantify fluid phase saturations, measure oil blob size distributions, and visualize the biological phase. Furthermore, a method to measure interfacial curvature from 3‐dimensional images is developed, providing researchers a new perspective from which to study multiphase flow experiments. Overall, the presented research utilizes pore‐scale imaging techniques to study the interfacial interactions occurring during MEOR in an effort to better explain the physics, and thus, increase the efficacy of MEOR. / Graduation date: 2012

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Certain strains of hydrophobic bacteria are known to play critical roles in petroleum-related applications. The aim of this study was to investigate how hydrophobic bacteria in their stationary phase could adsorb onto the hexadecane-water interface and alter its mechanical properties. The two strains of bacteria used in forming the interfacial films were Acinetobacter venetianus RAG-1 (a Gram-negative bacterium) and Rhodococcus erythropolis 20S-E1-c (Gram-positive). Experiments at two different length scales (millimetre and micrometre) were conducted and the results were compared. In addition, a simple flow experiment was designed in a constricted channel and the results were related to the intrinsic mechanical properties of bacteria-adsorbed films. On the millimetre scale, using the pendant drop technique, the film interfacial tension was monitored as the surface area was made to undergo changes. Under static conditions, both types of bacteria showed no significant effect on the interfacial tension. When subjected to transient excitations, the two bacterial films exhibited qualitatively similar, yet quantitative distinct rheological properties (including film elasticities and relaxation times). Under continuous reduction of surface area, the RAG-1 system showed a “paper-like” interface, while the interface of the 20S-E1-c system was “soap film-like.” These macroscopic observations could be explained by the surface ultrastructures of the two cell strains. On the micrometre scale, using the micropipette technique, colloidal stability of the bacteria-coated oil droplets was examined through direct-contact experiments. Both types of bacteria were seen to function as effective stabilizers. In addition, the adsorbed bacteria also interacted with one another at the interface, giving rise to higher order 2-D rheological properties. A technique of directly probing the mechanical properties of the emulsion drop surfaces revealed that (a) the films behaved as purely elastic sheets, and (b) with a reduction in cell concentration in the aqueous phase, less oil was emulsified, but the elastic moduli of the adsorbed films remained unchanged. These results are in contrast to the above millimetre-scale study. Therefore the rheological properties of these bacteria-adsorbed films appear to be length scale-dependent. An oil displacement experiment was designed to investigate the flow behaviour of micron-scale emulsion drops in a constricted channel. The qualitative results can be correlated with the interfacial rheological properties and may have valuable relevance to the study of multiphase flow through constricted channels in porous rocks (e.g. in MEOR operations). / Chemical Engineering

Thesis (M.S.)--Mississippi State University. Department of Geosciences. / Title from title screen. Includes bibliographical references.

The Lowry Method of Protein Assay is an effective alternative to point count or culture methods to determine the relative abundance of microorganisms in geologic samples. Results of this project show that the outcome of the Lowry assay is not affected by the constituents of a sandstone reservoir and that a relationship exists between microbes and clay minerals. Core samples were taken from the Carter sandstone at the North Blowhorn Creek Unit in Lamar County, Alabama. Samples were chosen based on mineralogic heterogeneity. The samples were placed in an anaerobic glove bag and given nutrients to induce the growth of in situ microorganisms. Samples were then assayed. Results of the protein assays show that the Lowry Method of Protein Assay is effective in determining protein concentrations in geologic samples with varying mineralogies. The assays also indicated that samples with abundant clay minerals show the greatest amount of microbial growth.