Publications by authors named "Orlando M Alfano"

Article Synopsis
  • - Researchers synthesized pure TiO and palladium-modified TiO (Pd-TiO) films using a sol-gel method to compare their properties and effectiveness in degrading the contaminant 17-α-ethinylestradiol (EE2) under simulated sunlight using a planar microreactor.
  • - Characterization of the films included several advanced techniques, revealing that the addition of palladium improved the crystallite size, increased surface area, and enhanced radiation absorption capabilities of the TiO.
  • - The Pd-TiO film demonstrated an 80% higher reaction rate for degrading EE2 compared to pure TiO, showing improved radiation absorption efficiency and better utilization of photons in the degradation process.
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The degradation of paracetamol (PCT) in an aqueous medium using the Fenton and photo-Fenton reactions was investigated. The aim of this research was the development of a kinetic model based on a reaction mechanism, which includes two main intermediates of PCT degradation and the local volumetric rate of photon absorption (LVRPA). Ferrioxalate was used as a catalyst and the working pH was adjusted to 5.

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Since COVID-19 pandemic, indoor air quality control has become a priority, and the development of air purification devices effective for disinfecting airborne viruses and bacteria is of outmost relevance. In this work, a photocatalytic device for the removal of airborne microorganisms is presented. It is an annular reactor filled with TiO-coated glass rings and irradiated internally and externally by UV-A lamps.

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The removal of indoor and outdoor air pollutants is crucial to prevent environmental and health issues. Photocatalytic building materials are an energy-sustainable technology that can completely oxidize pollutants, improving the air quality of contaminated sites. In this work, different photoactive TiO catalysts (anatase or modified anatase) and amounts were used to formulate photocatalytic paints in replacement of the normally used TiO (rutile) pigment.

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A theoretical and experimental study of bisphenol A (BPA) degradation by the UV/HO process in water is presented. The effects of the HO concentration and the specific rate of photon emission (E) on BPA degradation were investigated. A kinetic model derived from a reaction sequence was employed to predict BPA and hydrogen peroxide concentrations over time using an annular photochemical reactor in batch recirculation mode.

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A methodology for photocatalytic reactor modeling applied to advanced oxidation processes for chemical pollution abatement is presented herein. Three distinct reactor configurations typically employed in the field of air and water purification-wall reactors, slurry reactors, and fixed-bed reactors-are considered to illustrate the suggested approach. Initially, different mechanistically derived kinetic expressions to represent the photocatalytic rate of pollutant degradation are reviewed, indicating the main assumptions made by the authors in the published contributions.

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A regional raw clay was used as the starting material to prepare iron-pillared clays with different iron contents. The catalytic activity of these materials was tested in the heterogeneous photo-Fenton process, applied to the degradation of 2-chlorophenol chosen as the model pollutant. Different catalyst loads between 0.

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The combination of kinetic and spectroscopic tools has become a key scientific methodology for the understanding of catalytic behavior but its application in photocatalysis has inherent difficulties due to the nature of the energy source of the reaction. This review article provides an overview of its use by, first, presenting mechanistically derived kinetic formulations and spectroscopic data handling methods including intrinsic expressions for light and, second, highlighting representative examples of application. To do it we consider universal catalytic systems, particularly (although not exclusively) titania-based materials, and the most frequent hole and/or electron triggered reaction schemes.

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The photocatalytic inactivation of Bacillus subtilis spores in air was evaluated employing a fixed-bed reactor with TiO2-coated glass rings, under artificial UV-A radiation. Calculations of the radiation effectively absorbed inside the reactor were carried out by Monte Carlo simulations. The photocatalytic inactivation was assessed by analyzing the viability of the microorganisms retained by the coated glass rings inside the reactor at different irradiation periods.

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A kinetic model describing Fenton and photo-Fenton degradation of paracetamol (PCT) and consumption of hydrogen peroxide (HO) was proposed. A set of Fenton and photo-Fenton experiments (18 runs in total) was performed by fixing the initial concentration of PCT to 40 mg L and varying the initial concentrations of HO and ferrous ion, Fe. The experimental set-up was a well-stirred annular photoreactor equipped with an actinic BL TL-DK 36 W/10 1SL lamp.

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SBA-15 and KIT-6 materials have been synthesized and modified with iron salts by the wet impregnation method with different metal loadings. The different mesostructures obtained were characterized by N adsorption-desorption at 77 K, X-ray diffraction, temperature-programmed reduction, and ultraviolet-visible spectroscopy. These iron-containing mesostructured materials have been successfully tested for the heterogeneous photo-Fenton degradation of aqueous solutions of dangerous herbicides, such as atrazine, using UV-visible light irradiation, at room temperature and close to neutral pH.

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The effects of four inorganic anions (Cl, SO-, HCO, NO) usually present in groundwater were investigated on the photo-Fenton degradation of 2,4-dichlorophenoxyacetic acid (2,4-D). A kinetic model derived from a reaction sequence is proposed using the ferrioxalate complex as iron source at pH close to natural conditions (pH = 5). It was demonstrated that oxalate not only maintained iron in solution for the natural groundwater system, but also increased the photochemical activation of the process.

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An integral reactor design methodology was developed to address the optimal design of photocatalytic wall reactors to be used in air pollution control. For a target pollutant to be eliminated from an air stream, the proposed methodology is initiated with a mechanistic derived reaction rate. The determination of intrinsic kinetic parameters is associated with the use of a simple geometry laboratory scale reactor, operation under kinetic control and a uniform incident radiation flux, which allows computing the local superficial rate of photon absorption.

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The aims of this work were to design and build a photocatalytic reactor (UV-A/TiO) to study the inactivation of phages contained in bioaerosols, which constitute the main dissemination via phages in industrial environments. The reactor is a close system with recirculation that consists of a stainless steel camera (cubic form, side of 60 cm) in which air containing the phage particles circulates and an acrylic compartment with six borosilicate plates covered with TiO. The reactor is externally illuminated by 20 UV-A lamps.

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This work presents the photocatalytic degradation of the pharmaceutical drug clofibric acid in a fixed-bed reactor filled with TiO-coated glass rings. Experiments were carried out under UV radiation. A kinetic model that takes into account radiation absorption by means of the local surface rate of photon absorption (LSRPA) has been developed.

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The solar photo-Fenton degradation of the herbicide 2,4-dichlorophenoxyacetic acid (2,4-D) in aqueous solution at a natural pH (pH = 5) using ferrioxalate as iron source was investigated. The kinetic model proposed and validated in a previous contribution was used to predict the reactants concentrations during the oxidation process in a non-concentrating pilot-plant solar reactor. The effects of hydrogen peroxide to 2,4-D initial concentration ratios (R), temperature, and radiation levels were studied.

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A theoretical and experimental study of the photo-Fenton degradation of the herbicide 2,4-dichlorophenoxyacetic acid (2,4-D) in water is presented. A kinetic model derived from a reaction sequence is proposed using the ferrioxalate complex as iron source for conditions of pH = 5. The kinetic model was employed to predict the concentrations of 2,4-D, 2,4-dichlorophenol (2,4-DCP), hydrogen peroxide (HP) and oxalate (Ox) in a flat plate laboratory reactor irradiated with a solar simulator.

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This study reports the application of the photo-Fenton process for the degradation of the herbicide 2,4-dichlorophenoxyacetic (2,4-D). The objective of this research was the evaluation of the procedure at natural pH (pH = 5) using the ferrioxalate complex as iron source at two incident irradiation levels. For this purpose, different combinations of attenuation filters from a solar simulator were tested.

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A kinetic study of the photocatalytic degradation of the pharmaceutical clofibric acid is presented. Experiments were carried out under UV radiation employing titanium dioxide in water suspension. The main reaction intermediates were identified and quantified.

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Iron pillared clay (Fe-PILC) was prepared from a montmorillonite and was characterized by scanning electron microscopy and X-ray fluorescence. Fe-PILC catalytic activity was evaluated in photo-Fenton processes applied to the degradation of 2-clorophenol. Different catalyst loads were assayed.

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A methodology for modeling photocatalytic reactors for their application in indoor air pollution control is carried out. The methodology implies, firstly, the determination of intrinsic reaction kinetics for the removal of formaldehyde. This is achieved by means of a simple geometry, continuous reactor operating under kinetic control regime and steady state.

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In the present work the degradation of 2-chlorophenol (2-CP) used as model compound, applying the Heterogeneous photo-Fenton reaction, was studied. Small particles of goethite or iron oxyhydroxide were used as a source of iron. The influence of catalyst loading, radiation intensity and the molar ratio between hydrogen peroxide and contaminant were examined.

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This work analyzes the kinetic modelling of the photocatalytic inactivation of E. coli in water using different types of kinetic models; from an empirical equation to an intrinsic kinetic model including explicit radiation absorption effects. Simple empirical equations lead to lower fitting errors, but require a total of 12 parameters to reproduce the results of four inactivation curves when the catalyst concentration was increased.

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In a broad sense, photochemical reactions proceed through pathways involving several reaction steps. The initiation step is the absorption of energy both by the reactant or sensitizer molecules and in some cases, by the catalyst, leading to intermediate products that ultimately give rise to stable end products. Preferably, the reaction rate expression is derived from a proposed mechanism together with sound simplifying assumptions; otherwise, it may be adopted on an empirical basis.

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