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Kinetics of diffusion-limited bimolecular reactions in low-dimensional media.

dc.contributor.authorClement, Eric Andre Alexandre
dc.contributor.advisorKopelman, Raoul
dc.contributor.advisorSander, Leonard M.
dc.date.accessioned2016-08-30T16:48:41Z
dc.date.available2016-08-30T16:48:41Z
dc.date.issued1989
dc.identifier.urihttp://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqm&rft_dat=xri:pqdiss:9013878
dc.identifier.urihttps://hdl.handle.net/2027.42/128413
dc.description.abstractWe investigate three cases of bimolecular reaction kinetics in the diffusion limited regime when the medium is not necessarily a three dimensional euclidean space. This work is a theoretical approach that connects the fluctuations of reactant distribution at steady state, to the fundamental properties of a random walk. We use the fractal model as a topological extension of euclidean spaces. We show that for spectral dimensions below the critical dimension d$\sb{\rm s}$ = 2, a self-organization of reactants takes place in the system. The three examples of biomolecular reaction are the homomolecular annihilation A+A$\to$0, the heteromolecular annihilation A+B$\to$0 and the trapping problem A+T$\to$T where T is a fixed trap. In the A+A$\to$0 case we observe a mesoscopic self-organization characterized by an averaged depletion zone around each particle and an anomalous order of reaction X = 1 + 2/d$\sb{\rm s}$, in the low density limit. In the A+B$\to$0 case we observe a segregation that may be microscopic, mesoscopic or macroscopic according to the nature of the source term. We separate two types of sources, the ones with a strict conservation and the ones with a statistical conservation in the number of As and Bs in the system. In the strict conservation case we have a classical order of reaction X = 2 and segregation to a size determined by the nature of the source. In this case we study sources with random and correlated A-B separations. In the statistical conservation case, we have a non-reactive steady state with a saturation of the system in one of the reactants. If a vertical annihilation mechanism is present, we find segregation to a scale fixed by the external rate of particles and an effective order of reaction X = 4/d$\sb{\rm s}$. If a first order symmetric decay mechanism A$\to$0 and B$\to$0 is present, we find a mesoscopic segregation defined by the decay rate constant and a classical order of reaction X = 2. For the trapping problem, we find for d$\sb{\rm s} <$ 2, an anomalous partial order of reaction relative to the trap concentration X = 2/d$\sb{\rm s}$. The theoretical predictions are tested via Monte-Carlo simulations on lattices.
dc.format.extent175 p.
dc.languageEnglish
dc.language.isoEN
dc.subjectBimolecular
dc.subjectDiffusion
dc.subjectDimensional
dc.subjectKinetics
dc.subjectLimited
dc.subjectLow
dc.subjectMedia
dc.subjectReactions
dc.titleKinetics of diffusion-limited bimolecular reactions in low-dimensional media.
dc.typeThesis
dc.description.thesisdegreenamePhDen_US
dc.description.thesisdegreedisciplineCondensed matter physics
dc.description.thesisdegreedisciplinePhysics
dc.description.thesisdegreedisciplinePure Sciences
dc.description.thesisdegreegrantorUniversity of Michigan, Horace H. Rackham School of Graduate Studies
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/128413/2/9013878.pdf
dc.owningcollnameDissertations and Theses (Ph.D. and Master's)


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