Bao Quoc Tang

Dr. Bao Quoc Tang


Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2017 in SIAM Journal on Mathematical Analysis
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Journal Article
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LDLaurent Desvillettes
Laurent Desvillettes
KFKlemens Fellner
Klemens Fellner
BTBao Quoc Tang
Bao Quoc Tang
The quantitative convergence to equilibrium for reaction-diffusion systems arising from complex balanced chemical reaction networks with mass action kinetics is studied using the so-called entropy ...

1 April 2020 in Annales de l'Institut Henri Poincaré C, Analyse non linéaire
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KFKlemens Fellner
Klemens Fellner
JMJeff Morgan
Jeff Morgan
BTBao Quoc Tang
Bao Quoc Tang
The global existence of classical solutions to reaction-diffusion systems in arbitrary space dimensions is studied. The nonlinearities are assumed to be quasi-positive, to have (slightly super-) quadratic growth, and to possess a mass control, which includes the important cases of mass conservation and mass dissipation. Under these assumptions, the local classical solution is shown to be global, and in the case of mass conservation or mass dissipation, to have the L^{\infty } -norm growing at most polynomially in time. Applications include skew-symmetric Lotka-Volterra systems and quadratic reversible chemical reactions.

13 April 2018 in Zeitschrift für angewandte Mathematik und Physik
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KFKlemens Fellner
Klemens Fellner
BTBao Quoc Tang
Bao Quoc Tang
The convergence to equilibrium for renormalised solutions to nonlinear reaction–diffusion systems is studied. The considered reaction–diffusion systems arise from chemical reaction networks with mass action kinetics and satisfy the complex balanced condition. By applying the so-called entropy method, we show that if the system does not have boundary equilibria, i.e. equilibrium states lying on the boundary of \({\mathbb {R}}_+^N\), then any renormalised solution converges exponentially to the complex balanced equilibrium with a rate, which can be computed explicitly up to a finite-dimensional inequality. This inequality is proven via a contradiction argument and thus not explicitly. An explicit method of proof, however, is provided for a specific application modelling a reversible enzyme reaction by exploiting the specific structure of the conservation laws. Our approach is also useful to study the trend to equilibrium for systems possessing boundary equilibria. More precisely, to show the convergence to equilibrium for systems with boundary equilibria, we establish a sufficient condition in terms of a modified finite-dimensional inequality along trajectories of the system. By assuming this condition, which roughly means that the system produces too much entropy to stay close to a boundary equilibrium for infinite time, the entropy method shows exponential convergence to equilibrium for renormalised solutions to complex balanced systems with boundary equilibria.

1 July 2010 in Nonlinear Analysis
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CACung The Anh
Cung The Anh
BTBao Quoc Tang
Bao Quoc Tang


1 January 2017 in Kinetic and Related Models
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Journal Article
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KFKlemens Fellner
Klemens Fellner
WPWolfang Prager
Wolfang Prager
BTBao Quoc Tang
Bao Quoc Tang
In this paper, the applicability of the entropy method for the trend towards equilibrium for reaction-diffusion systems arising from first order chemical reaction networks is studied. In particular, we present a suitable entropy structure for weakly reversible reaction networks without detail balance condition. We show by deriving an entropy-entropy dissipation estimate that for any weakly reversible network each solution trajectory converges exponentially fast to the unique positive equilibrium with computable rates. This convergence is shown to be true even in cases when the diffusion coefficients of all but one species are zero. For non-weakly reversible networks consisting of source, transmission and target components, it is shown that species belonging to a source or transmission component decay to zero exponentially fast while species belonging to a target component converge to the corresponding positive equilibria, which are determined by the dynamics of the target component and the mass injected from other components. The results of this work, in some sense, complete the picture of trend to equilibrium for first order chemical reaction networks.