Heterogeneous Photocatalysis Using Inorganic Semiconductor Solids 2013
DOI: 10.1007/978-94-007-7775-0_2
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Kinetic Concepts of Heterogeneous Photocatalysis

Abstract: The ABCs of empirical chemical kinetics are highlighted from the scratch. Aspects of dynamics regarding charge carrier trapping and recombination are essential part of this discussion. The effect of imposition of external constrains such as temperature of the reactivity solution, concentration of the subject compound, intensity and wavelength of light on photocatalytic degradation system is emphasised. Because of the crucial position of light intensity in heterogeneous photocatalysis, the principles of operati… Show more

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Cited by 10 publications
(4 citation statements)
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“…It can be noticed that the zero-order kinetics, in this case, comply with most of the experimental results from the anodized Ti–Ta alloy series. According to the literature in heterogeneous photocatalysis, this kinetic model is typical of reactions where the surface available for the catalytic reaction is saturated very quickly and mass diffusion becomes the controlling stage. , This assumption is in good agreement with the results of this study and the potential issue, represented by the reduction of specific surface area available for the catalytic reaction due to the presence of the surface top layer, that has already been addressed. Variation of the zero-order kinetics is shown in Figure B.…”
Section: Resultssupporting
confidence: 90%
“…It can be noticed that the zero-order kinetics, in this case, comply with most of the experimental results from the anodized Ti–Ta alloy series. According to the literature in heterogeneous photocatalysis, this kinetic model is typical of reactions where the surface available for the catalytic reaction is saturated very quickly and mass diffusion becomes the controlling stage. , This assumption is in good agreement with the results of this study and the potential issue, represented by the reduction of specific surface area available for the catalytic reaction due to the presence of the surface top layer, that has already been addressed. Variation of the zero-order kinetics is shown in Figure B.…”
Section: Resultssupporting
confidence: 90%
“…First-order kinetics in contrast, depend on the concentration of at least one reactant and the rate law is given as: where M is the concentration of the reactant, and k is the rate constant in units of per time (s −1 , hr −1 , day −1 ). Therefore, with first-order dissolution processes, the rate of reaction is proportional to the concentration of the reactant, where doubling of the concentration will double the rate [ 62 , 64 ]. However, a reaction can be first-order with respect to one reactant but can have an overall order of greater than 1.…”
Section: Introductionmentioning
confidence: 99%
“…The photocatalytic reaction follows the pseudo‐first‐order rate model as expressed by ln ( C / C 0 )=− kt , where C and C 0 are the concentrations of MO at time t and 0, respectively, and k is the pseudo‐first‐order rate constant . In this respect, Figure shows a good verification of the pseudo‐first‐order kinetic model with R 2 equal to 0.96 and 0.98 for S2 and S1 samples, respectively.…”
Section: Resultsmentioning
confidence: 55%