Journal of Environmental Science and Health Part A · 2002 · 22 citations · 23 references
Natural SciencesChemical EngineeringEnvironmental EngineeringCatalysisEnvironmental ChemistryWater TreatmentCatalytic Reaction EngineeringCatalytic Reaction KineticsKinetic ModelingPhotocatalysisPhotochemical KineticsPhotochemistryDegradationLangmuir-hinshelwood MechanismLangmuir-hinshelwood ReactionsOrganic Pollutant DegradationPhotocatalytic DegradationPhotocatalytic KineticsPseudo-first-order KineticsRate Constants
A number of chlorophenols, namely 2-chlorophenol, 2,4,-dichlorophenol and 2,4,6-trichlorophenol, were decomposed in aqueous solution by using TiO2 as photoactivated catalyst under UV radiation emitted by a 125W medium pressure Hg lamp in an immersion well-type quartz photoreactor. The organic-bound chlorine was converted into the environmentally harmless inorganic chloride. For catalyst doses between 0.1 and 0.5gl(-1) the reaction mechanisms are elucidated. The corresponding rate constants were obtained by periodically measuring the remaining chlorophenol, and converted chloride in solution. A theoretical model for the degradation pathway is proposed expressing the rate as a linear function of the concentrations of chlorophenol and catalyst. Aside from the model-calculated values, the pseudo-first order rate constants for a rough approximation of chlorophenols degradation as well as the kinetic parameters of Langmuir-Hinshelwood type decomposition are compared. The photodegradation rate of chlorophenols followed the order: C13 x Ph > Cl2 x Ph > Cl x Ph.
23
Limit of detection. A closer look at the IUPAC definition
Gary L. Long, J. D. Winefordner · Analytical Chemistry · 1983 · 1.9K citations
Principles of Instrumental Analysis
A. Townshen · Analytica Chimica Acta · 1983 · 1.1K citations
Natural Sciences, Pharmaceutical Analysis, Analytical Chemistry +9
Introduction to marine chemistry
James I. Drever · Marine Geology · 1972 · 580 citations