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Magnetically enhanced centrifugation for continuous biopharmaceutical processing

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dc.contributor.advisor T. Alan Hatton and Kenneth A. Smith. en_US
dc.contributor.author Chen, Fei, Ph. D. Massachusetts Institute of Technology en_US
dc.contributor.other Massachusetts Institute of Technology. Dept. of Chemical Engineering. en_US
dc.date.accessioned 2010-02-09T16:45:32Z
dc.date.available 2010-02-09T16:45:32Z
dc.date.copyright 2009 en_US
dc.date.issued 2009 en_US
dc.identifier.uri http://hdl.handle.net/1721.1/51565
dc.description Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Chemical Engineering, 2009. en_US
dc.description Includes bibliographical references. en_US
dc.description.abstract Effective separation and purification of biopharmaceutical products from the media in which they are produced continues to be a challenging task. Such processes usually involve multiple steps and the overall product loss can be significant. As an integrative technique, high gradient magnetic separation (HGMS), together with the application of functional magnetic particles, provides many advantages over traditional techniques. However, HGMS has a number of drawbacks; and its application is limited because it is inherently a batch process and it is difficult to recycle the magnetic nanoparticles. This thesis explores the development of a new type of continuous magnetic separation process, called magnetically enhanced centrifugation (MEC), which exploits the interactions of magnetic particles with magnetic field gradients, forced convective flows and large centrifugal forces. Magnetically susceptible wires in a uniform magnetic field facilitate the capture and aggregation of magnetic particles on wires, and a centrifugal force perpendicular to the magnetic force conveys the particle sludge parallel to the wires in a continuous mode. The primary focus of this thesis is multi-scale modeling and simulation to understand the underlying physics of MEC processes. The potential of MEC as an effective unit operation for biopharmaceutical downstream processing has been demonstrated. Unlike traditional batch-mode HGMS, MEC has a great advantage in that it can be operated continuously as magnetic particles captured on wire surface are constantly removed. en_US
dc.description.abstract (cont.) A dimensionless model for simulating the trajectories of magnetic particles in combined magnetic and flow fields has been developed. The model was first applied to single wire configurations and then extended to multi-wire arrays. It was shown that modified rhombic arrays can provide high capture efficiency while maintaining low pressure drop. It is also shown that capture efficiencies based on results for clean, particle-free wires, may be seriously in error because the particle buildup that accumulates on the wire significantly distorts the flow and the magnetic fields and thus influences the particle trajectories. The dynamic buildup growth process was treated as a moving-boundary problem. Simulation results have shown that the capture efficiency decreases dramatically as particle buildup volume increases. In addition, the influence of particle chaining under magnetic dipole-dipole forces on separation efficiency has been investigated. Magnetic particles form chains as soon as they enter a background magnetic field, and are captured in the form of particle chains. The hydrodynamic force on particle chains was calculated using a 3-D CFD simulation. The capture radius calculated with considering the chaining effect is few times as great as the capture radius calculated assuming individual particles. Bench-top MEC experiments have shown that magnetic particle buildup generally comprises two layers with distinct structures: a spiky layer with all chains parallel to the magnetic field, and a densely-packed layer near the wire. en_US
dc.description.abstract (cont.) This unique structure reflects the dominance of magnetic forces near the wire and of magnetic dipole-dipole interactions at locations further from the wire. As more and more particles accumulate on the wire surface, the centrifugal force can overcome the cohesion of the layer or the adhesion of the layer to the wire, leading to movement of the buildup material. The onset of such movement can be achieved either by increasing the centrifugal force or by increasing the buildup height. Energy and force analyses have been carried out to study various scenarios of buildup movement. For monodisperse magnetic particles, four scenarios can be expected: chain-like layer collapsing down (I), rigid body movement (II), buildup breakage (III), and mixed behavior of rigid body movement and buildup breakage (IV). A set of design formulas were derived to predict buildup structure and different scenarios. Useful scenario and operating regime diagrams were obtained. A discrete element modeling (DEM) package was developed to study the dynamics and rheological behavior of highly concentrated magnetic particle systems. For monodisperse magnetic particles, simulation results confirmed the four regions of the scenario diagram as predicted by force arguments. For polydisperse magnetic particles, DEM simulations showed that the buildup exhibits solid-like behavior when centrifugal effects are small, and liquid-like behavior with a continuous velocity profile when centrifugal effects are large. en_US
dc.description.abstract (cont.) DEM simulations were able to predict the three dimensional effects, including the buildup profiles at the wire tip. Taken together, the results of this work provide a general strategy that can be used as a starting point for the design, evaluation, and optimization of magnetically enhanced processes that are suitable for biopharmaceutical downstream processing. en_US
dc.description.statementofresponsibility by Fei Chen. en_US
dc.format.extent xxiv, 257 p. en_US
dc.language.iso eng en_US
dc.publisher Massachusetts Institute of Technology en_US
dc.rights M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission. en_US
dc.rights.uri http://dspace.mit.edu/handle/1721.1/7582 en_US
dc.subject Chemical Engineering. en_US
dc.title Magnetically enhanced centrifugation for continuous biopharmaceutical processing en_US
dc.type Thesis en_US
dc.description.degree Ph.D. en_US
dc.contributor.department Massachusetts Institute of Technology. Dept. of Chemical Engineering. en_US
dc.identifier.oclc 466155242 en_US


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