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Journal ArticleDOI

Factors affecting the efficiency of a photocatalyzed process in aqueous metal-oxide dispersions: Prospect of distinguishing between two kinetic models

TLDR
In this article, the photooxidative degradation of phenol in aqueous TiO2 dispersions has been revisited to determine the dependencies of the rate on the concentration of the phenol and on the photon flow (ρ) of the actinic light at 365nm.
Abstract
The photooxidative degradation of phenol in aqueous TiO2 dispersions has been revisited to determine the dependencies of the rate on the concentration of phenol and on the photon flow (ρ) of the actinic light at 365 nm. The principal objective was to assess the factors that influence the efficiency of the photocatalytic process, the rate of which is described by the function d C d t (ρ,C)=( const )C n ρ m where n and m are orders of the reaction with respect to concentration and photon flow (light intensity), respectively. The reaction order m varies with reagent concentration C, whereas the order n depends on photon flow ρ. The description indicates that m→1 if n→0, whereas n→1 if m→0. Therefore, the reaction orders m and n of phenol photodegradation are interdependent. A detailed kinetic description of the process is given based on two well-known mechanistic/kinetic models, namely (i) the Langmuir–Hinshelwood (LH) model whereby the organic reagent is pre-adsorbed on the photocatalyst surface prior to UV illumination, and (ii) the Eley–Rideal (ER) model for which the organic reagent diffuses from the solution bulk onto the photocatalyst surface to interact with the activated state of the photocatalyst. The kinetic treatment infers that it is possible (under certain conditions) to delineate between the LH and ER mechanistic models on the basis of the magnitude of the Langmuir constant KL at very high photon flow, i.e. when ρ→∞ {for the LH pathway, KL→K; for the ER model KL→0}, and on the dependence of kobs of the process on ρ. For the ER model, kobs scales linearly with ρ at high photon flow, whereas for the LH pathway kobs displays a sub-linear dependence on ρ and tends toward saturation at high photon flow.

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Citations
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Journal ArticleDOI

Inorganic and organic UV filters: Their role and efficacy in sunscreens and suncare products

TL;DR: In this article, the photostabilities of sunscreen organic active agents in neat polar and apolar solvents and in actual commercial formulations have been examined, confirming the recent findings by Sayre et al. that the titanium dioxide particle surface was modified to produce TiO2 specimens of considerably reduced photoactivity.
Journal ArticleDOI

Enhanced photocatalytic degradation of methylene blue and methyl orange by ZnO:Eu nanoparticles

TL;DR: In this paper, the influence of europium doping and solvents on size, particles agglomeration, light absorption and photocatalytic activity was analyzed in ZnO nanoparticles.
ReportDOI

Bibliography of Work on the Heterogeneous Photocatalytic Removal of Hazardous Compounds from Water and Air

TL;DR: The state of the art in catalysts are forms of titanium dioxide or modifications thereof, but work on other heterogeneous catalysts is included in this article, where the subject of the report is chemistry and engineering for the application of heterogeneous photocatalysts.
Journal ArticleDOI

Thermodynamic and kinetic analysis of heterogeneous photocatalysis for semiconductor systems.

TL;DR: The thermodynamic driving force of photocatalysis was explained, and the functions of light and heat in photoc atalysis were distinguished, and some applications of the D-I model to study photocatalytic kinetics were discussed.
Journal ArticleDOI

Dogmas and Misconceptions in Heterogeneous Photocatalysis. Some Enlightened Reflections

TL;DR: This short article reexamines the a priori assumed validity of the LH kinetic model in heterogeneous photocatalysis, the recombination of photogenerated free charge carriers on the solid (metal oxide) photocatalyst by the band-to-band recombination pathway, and the mistaken assertion that the kinetics of a heterogeneous photoreaction are either only first-order dependent or half- order dependent on photon flow.
References
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Journal ArticleDOI

Photocatalytic degradation of organic water contaminants: Mechanisms involving hydroxyl radical attack

TL;DR: In this article, it is proposed that the hydroxyl radical, OH·, is the primary oxidant in the photocatalytic system and four possible mechanisms are suggested, all based on OH· attack of the organic reactant.
Journal ArticleDOI

Photolysis of chloroform and other organic molecules in aqueous titanium dioxide suspensions

TL;DR: In this article, the photocatalytic degradation of chloroform has been investigated in aqueous suspensions of TiO_2 over the wavelength range of 310-380 nm, and a detailed reaction mechanism has been proposed in which the rate-determining mechanism is the reaction of surface-bound *OH with======adsorbed CHCl_3.
Journal ArticleDOI

Photodegradation kinetics of 4-nitrophenol in TiO2 suspension

TL;DR: In this paper, a two-phase swirl-flow monolithic type reactor was designed to study the kinetics of heterogeneous photocatalytic processes on semiconductor catalysts, and the photomineralization of 4-nitrophenol (4-NP) sensitized by Degussa P25 TiO2 in aqueous solution has been investigated as a function of the following different experimental parameters: initial concentration of pollutant (CS0), light intensity (Ia), partial pressure of oxygen (pO2), catalyst concentration, pH, chloride ion and temperature
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