Thesis (Ph. D.)--University of Wisconsin--Madison, 1961. / Typescript. Vita. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references.

Thesis (Ph. D.)--University of Oregon, 2005. / Typescript. Includes vita and abstract. Includes bibliographical references (leaves 55-58). Also available for download via the World Wide Web; free to University of Oregon users.

No description available.

Thesis (Ph. D.)--University of Washington, 2004. / Vita. Includes bibliographical references (leaves 222-246).

Thesis (Ph. D.)--Rutgers University, 2009. / "Graduate Program in Biomedical Engineering." Includes bibliographical references.

The purpose of this thesis is to design a physical microchannel model for micro-Couette blood flow that provides constant and controlled conditions to study and analyze Red Blood Cell (RBC) aggregation. The innovation of this work is that the Couette blood flow is created by the motion of a second fluid with different properties, thereby entraining the blood. The experimental work is coupled with three-dimensional numerical simulations performed using a research Computational Fluid Dynamic (CFD) Solver, Nek5000, based on the spectral element method, while the experiments are conducted using a micro Particle Image Velocimetry (μPIV) system with a double frame CCD camera and an inverted laser imaging microscope. The design of the channel (150 × 33 μm and 170 × 64 μm microchannels) is based on several parameters determined numerically, such as the velocity and viscosity ratios and the degree of miscibility between the fluids, and the resulting configurations are fabricated in the laboratory using standard photolithography methods. The microchannel designed numerically is then tested experimentally, first, with a Newtonian fluid (glycerol), then with RBC suspensions to be compared to the simulations results. It was found that, numerically, using a velocity ratio of 4 between the two fluids, a third of the channel thickness corresponds to the blood layer. Within that range, it can be concluded, that the velocity profile of the blood layer is approximately linear as confirmed by experimental tests, resulting in the desired profile to study RBC aggregation in controlled conditions. The effect of several parameters, such as the hematocrit and the shear rate, on the RBC aggregates and the velocity profile is investigated, through experiments on the RBC suspensions. The final goal of this research is to ensure the compatibility of the results between the experiments and the Newtonian numerical model for several ranges of shear rate with the future intention of finding an accurate method to be able to quantitatively analyze aggregates and determine the number of RBC in each aggregate depending on the flow conditions (the shear rate).

The purpose of this thesis is to design a physical microchannel model for micro-Couette blood flow that provides constant and controlled conditions to study and analyze Red Blood Cell (RBC) aggregation. The innovation of this work is that the Couette blood flow is created by the motion of a second fluid with different properties, thereby entraining the blood. The experimental work is coupled with three-dimensional numerical simulations performed using a research Computational Fluid Dynamic (CFD) Solver, Nek5000, based on the spectral element method, while the experiments are conducted using a micro Particle Image Velocimetry (μPIV) system with a double frame CCD camera and an inverted laser imaging microscope. The design of the channel (150 × 33 μm and 170 × 64 μm microchannels) is based on several parameters determined numerically, such as the velocity and viscosity ratios and the degree of miscibility between the fluids, and the resulting configurations are fabricated in the laboratory using standard photolithography methods. The microchannel designed numerically is then tested experimentally, first, with a Newtonian fluid (glycerol), then with RBC suspensions to be compared to the simulations results. It was found that, numerically, using a velocity ratio of 4 between the two fluids, a third of the channel thickness corresponds to the blood layer. Within that range, it can be concluded, that the velocity profile of the blood layer is approximately linear as confirmed by experimental tests, resulting in the desired profile to study RBC aggregation in controlled conditions. The effect of several parameters, such as the hematocrit and the shear rate, on the RBC aggregates and the velocity profile is investigated, through experiments on the RBC suspensions. The final goal of this research is to ensure the compatibility of the results between the experiments and the Newtonian numerical model for several ranges of shear rate with the future intention of finding an accurate method to be able to quantitatively analyze aggregates and determine the number of RBC in each aggregate depending on the flow conditions (the shear rate).

Graduation date: 1992

Thesis (Ph. D.)--Rutgers University, 2008. / "Graduate Program in Chemistry and Chemical Biology." Includes bibliographical references.

The purpose of this thesis is to design a physical microchannel model for micro-Couette blood flow that provides constant and controlled conditions to study and analyze Red Blood Cell (RBC) aggregation. The innovation of this work is that the Couette blood flow is created by the motion of a second fluid with different properties, thereby entraining the blood. The experimental work is coupled with three-dimensional numerical simulations performed using a research Computational Fluid Dynamic (CFD) Solver, Nek5000, based on the spectral element method, while the experiments are conducted using a micro Particle Image Velocimetry (μPIV) system with a double frame CCD camera and an inverted laser imaging microscope. The design of the channel (150 × 33 μm and 170 × 64 μm microchannels) is based on several parameters determined numerically, such as the velocity and viscosity ratios and the degree of miscibility between the fluids, and the resulting configurations are fabricated in the laboratory using standard photolithography methods. The microchannel designed numerically is then tested experimentally, first, with a Newtonian fluid (glycerol), then with RBC suspensions to be compared to the simulations results. It was found that, numerically, using a velocity ratio of 4 between the two fluids, a third of the channel thickness corresponds to the blood layer. Within that range, it can be concluded, that the velocity profile of the blood layer is approximately linear as confirmed by experimental tests, resulting in the desired profile to study RBC aggregation in controlled conditions. The effect of several parameters, such as the hematocrit and the shear rate, on the RBC aggregates and the velocity profile is investigated, through experiments on the RBC suspensions. The final goal of this research is to ensure the compatibility of the results between the experiments and the Newtonian numerical model for several ranges of shear rate with the future intention of finding an accurate method to be able to quantitatively analyze aggregates and determine the number of RBC in each aggregate depending on the flow conditions (the shear rate).