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Hierarchies of nonclassical reaction kinetics due to anisotropic confinements

dc.contributor.authorAhn, Jaewooken_US
dc.contributor.authorKopelman, Raoulen_US
dc.contributor.authorArgyrakis, Panosen_US
dc.date.accessioned2010-05-06T21:44:53Z
dc.date.available2010-05-06T21:44:53Z
dc.date.issued1999-01-22en_US
dc.identifier.citationAhn, Jaewook; Kopelman, Raoul; Argyrakis, Panos (1999). "Hierarchies of nonclassical reaction kinetics due to anisotropic confinements." The Journal of Chemical Physics 110(4): 2116-2121. <http://hdl.handle.net/2027.42/70174>en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/70174
dc.description.abstractIn contrast to classical chemical reaction kinetics, for diffusion limited chemical reactions the anisotropy of the geometry has far reaching effects. We use tubular two and three-dimensional spaces to illustrate and discuss the dimensional crossover in A+B→0A+B→0 reactions due to dimensional compactification. We find that the crossover time tc = Wαtc=Wα scales as α = β/(a−b),α=β/(a−b), where a, b, and β are given by the earlier and the late time inverse density scaling of ρ−1 ∼ taρ−1∼ta and ρ−1 ∼ tbWβ,ρ−1∼tbWβ, respectively. We also obtain a critical width WcWc below (above) which the chemical reaction progresses without (with) traversing a two or three-dimensional Ovchinnikov–Zeldovich (OZ) reaction regime. As a result we find that there exist different hierarchies of dimensionally forced crossovers, depending on the initial conditions and geometric restrictions. Kinetic phase diagrams are employed, and exponents are given for various Euclidean and fractal compactified geometries, for the A+BA+B and A+AA+A elementary reactions. Monte Carlo simulations illustrate some of the kinetic hierarchies. © 1999 American Institute of Physics.en_US
dc.format.extent3102 bytes
dc.format.extent122918 bytes
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dc.format.mimetypeapplication/pdf
dc.publisherThe American Institute of Physicsen_US
dc.rights© The American Institute of Physicsen_US
dc.titleHierarchies of nonclassical reaction kinetics due to anisotropic confinementsen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelPhysicsen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartments of Chemistry and Physics, University of Michigan, Ann Arbor, Michigan 48109-1055en_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, Michigan 48109-1055en_US
dc.contributor.affiliationotherDepartment of Physics, University of Thessaloniki, 54006 Thessaloniki, Greeceen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/70174/2/JCPSA6-110-4-2116-1.pdf
dc.identifier.doi10.1063/1.477820en_US
dc.identifier.sourceThe Journal of Chemical Physicsen_US
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dc.owningcollnamePhysics, Department of


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