4.6 Article

Imperfect mixing as a dominant factor leading to stochastic behavior: a new system exhibiting crazy clock behavior

Journal

PHYSICAL CHEMISTRY CHEMICAL PHYSICS
Volume 20, Issue 20, Pages 14145-14154

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c8cp01156g

Keywords

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Funding

  1. Hungarian Research Fund NKFIH-OTKA Grant [K116591]
  2. European Union
  3. European Social Fund Grant [EFOP-3.6.1.-16-2016-00004]
  4. Ministry of Human Capacities [UNKP-17-3-I]
  5. [GINOP-2.3.2-15-2016-00022]

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It is clearly demonstrated that the arsenous acid-periodate reaction displays crazy-clock behavior when a statistically meaningful number of kinetic runs are performed under exactly the same conditions. Both extensive experimental and numerical simulation results gave convincing evidence that the stochastic feature of the title reaction originates from the imperfection of the mixing process, and neither local random fluctuation nor initial inhomogeneity alone is capable of explaining adequately the observed phenomena. Imperfect mixing is manifestedin practicein the unintentional and inherent formation of dead volumes where the concentration of the reactants may even significantly differ from the ones measured in the case of a completely uniform concentration distribution, and the system may spend enough time there under imperfectly mixed conditions to complete the nonlinear chemical process. Furthermore, it is also shown that a more efficient mixing, i.e. a smaller dead volume size and shorter residence time being spent in the dead volume, does not necessarily mean Landolt times are smaller than the one measured under completely homogeneous conditions. Evidently, the initial concentration of the reagents in the dead volumeand of course in the rest of the solutiongreatly influences the Landolt time to be measured in the case of an individual kinetic run and may therefore show either positive or negative deviation from the Landolt time for the completely homogeneous state. As a result, less efficient mixing may either accelerate or decelerate the rate of a nonlinear autocatalytic reaction at a macroscopic volume level.

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