P
P. De Kepper
Researcher at University of Bordeaux
Publications - 52
Citations - 2971
P. De Kepper is an academic researcher from University of Bordeaux. The author has contributed to research in topics: Bistability & Reaction–diffusion system. The author has an hindex of 28, co-authored 52 publications receiving 2867 citations. Previous affiliations of P. De Kepper include Centre national de la recherche scientifique & Université libre de Bruxelles.
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Journal ArticleDOI
Experimental evidence of a sustained standing Turing-type nonequilibrium chemical pattern.
TL;DR: The experimental observation of a sustained standing nonequilibrium chemical pattern in a single-phase open reactor is interpreted as the first unambiguous experimental evidence of a Turing structure.
Journal ArticleDOI
Transitions from bistability to limit cycle oscillations. Theoretical analysis and experimental evidence in an open chemical system
Jacques Boissonade,P. De Kepper +1 more
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Turing-type chemical patterns in the chlorite-iodide-malonic acid reaction
TL;DR: In this paper, experimental observations of symmetry breaking stationary patterns are interpreted as the first unambiguous evidence of Turing-type structures in a single-phase isothermal chemical reaction system, and a phase diagram gathering the domain of existence of symmetry-breaking and no-symmetry-breaking standing patterns is discussed.
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Experimental Studies and Quantitative Modeling of Turing Patterns in the (Chlorine Dioxide, Iodine, Malonic Acid) Reaction
TL;DR: In this paper, the formation of Turing patterns in the (chlorine dioxide, iodine, malonic acid) reaction is performed in a spatial open gel disk reactor where all the input species are fed onto one side by a continuous stirred tank reactor.
Journal ArticleDOI
One-dimensional "spirals": Novel asynchronous chemical wave sources.
J.-J. Perraud,J.-J. Perraud,A. De Wit,A. De Wit,E. Dulos,E. Dulos,P. De Kepper,P. De Kepper,Guy Dewel,Guy Dewel,Pierre Borckmans,Pierre Borckmans +11 more
TL;DR: The experimental observation of an endogeneous antisymmetric wave source in a quasi-one-dimensional chemical system is reported and a theoretical interpretation relying on the interaction between Turing and Hopf modes is proposed.