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Francisco J. Real

Researcher at University of Extremadura

Publications -  73
Citations -  3004

Francisco J. Real is an academic researcher from University of Extremadura. The author has contributed to research in topics: Reaction rate constant & Radical. The author has an hindex of 31, co-authored 72 publications receiving 2637 citations.

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Degradation of carbofuran by using ozone, UV radiation and advanced oxidation processes.

TL;DR: The improvement in the decomposition levels of carbofuran reached by the combined processes in relation to the single oxidants, due to the generation of the very reactive hydroxyl radicals, is also established in every process.
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The role of hydroxyl radicals for the decomposition of p-hydroxy phenylacetic acid in aqueous solutions.

TL;DR: An improvement in the decomposition of the phenolic acid in the combined UV/H2O2 oxidation is observed, due to the generation of OH radicals, and the contribution of the radical reaction to the global process is determined.
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Comparison of different chemical oxidation treatments for the removal of selected pharmaceuticals in water matrices

TL;DR: In this article, the degradation of selected pharmaceuticals in some water matrices was studied by using several chemical treatments, including UV radiation alone, ozone, Fenton's reagent, photo-Fenton system, and combinations of UV radiation and ozone with H 2 O 2, TiO 2, Fe(II), and Fe(III).
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Kinetics of aqueous chlorination of some pharmaceuticals and their elimination from water matrices.

TL;DR: Apparent rate constants for the reactions of four selected pharmaceutical compounds with chlorine in ultra-pure (UP) water were determined as a function of the pH, and the efficiency of the chlorination process with respect to the pharmaceuticals elimination and the formation THMs was established.
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Kinetics of the Chemical Oxidation of the Pharmaceuticals Primidone, Ketoprofen, and Diatrizoate in Ultrapure and Natural Waters

TL;DR: In this article, the rate constants for the reactions with ozone, UV radiation, and Fenton's reagent were determined by means of a competition kinetic model, and the results showed that reaction with OH radicals was the major pathway for the oxidative transformation of these compounds.