163 research outputs found

    Sharp estimates on minimum travelling wave speed of reaction diffusion systems modelling autocatalysis

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    This article studies propagating wave fronts in an isothermal chemical reaction A + 2B - \u3e 3B involving two chemical species, a reactant A and an autocatalyst B, whose diffusion coefficients, D-A and D-B, are unequal due to different molecular weights and/or sizes. Explicit bounds v(*) and v* that depend on D-B/D-A are derived such that there is a unique travelling wave of every speed v \u3e = v* and there does not exist any travelling wave of speed v \u3c v*. New to the literature, it is shown that v(*) proportional to v* proportional to D-B/D-A when D-B = v(min). Estimates on v(min) significantly improve those of early works. The framework is built upon general isothermal autocatalytic chemical reactions A + nB - \u3e (n + 1)B of arbitrary order n \u3e = 1

    Mass conserved Allen-Cahn equation and volume preserving mean curvature flow

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    We consider a mass conserved Allen-Cahn equation u_t=\Delta u+ \e^{-2} (f(u)-\e\lambda(t)) in a bounded domain with no flux boundary condition, where \e\lambda(t) is the average of f(u(⋅,t))f(u(\cdot,t)) and −f-f is the derivative of a double equal well potential. Given a smooth hypersurface γ0\gamma_0 contained in the domain, we show that the solution u^\e with appropriate initial data approaches, as \e\searrow0, to a limit which takes only two values, with the jump occurring at the hypersurface obtained from the volume preserving mean curvature flow starting from γ0\gamma_0

    Propagation of Local Disturbances in Reaction Diffusion Systems Modeling Quadratic Autocatalysis

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    This article studies the propagation of initial disturbance in a quadratic autocatalytic chemical reaction in one-dimensional slab geometry, where two chemical species A, called the reactant, and B, called the autocatalyst, are involved in the simple scheme A + B - \u3e 2B. Experiments demonstrate that chemical systems for which quadratic or cubic catalysis forms a key step can support propagating chemical wavefronts. When the autocatalyst is introduced locally into an expanse of the reactant, which is initially at uniform concentration, the developing reaction is often observed to generate two wavefronts, which propagate outward from the initial reaction zone. We show rigorously that with such an initial setting the spatial region is divided into three regions by the two wavefronts. In the middle expanding region, the reactant is almost consumed so that A approximate to 0, whereas in the other two regions there is basically no reaction so that B approximate to 0. Most of the chemical reaction takes place near the wavefronts. The detailed characterization of the concentrations is given for each of the three zones

    Analysis of an Optimal Stopping Problem Arising from Hedge Fund Investing

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    The final publication is available at Elsevier via https://doi.org/10.1016/j.jmaa.2019.123559. © 2020. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/We analyze the optimal withdrawal time for an investor in a hedge fund with a first-loss or shared-loss fee structure, given as the solution of an optimal stopping problem on the fund's assets with a piecewise linear payoff function. Assuming that the underlying follows a geometric Brownian motion, we present a complete solution of the problem in the infinite horizon case, showing that the continuation region is a finite interval, and that the smooth-fit condition may fail to hold at one of the endpoints. In the finite horizon case, we show the existence of a pair of optimal exercise boundaries and analyze their properties, including smoothness and convexity.NSERC, RGPIN-2017-04220
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