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spelling paper:paper_03043894_v155_n1-2_p45_Nieto2023-06-08T15:29:25Z Photocatalyzed degradation of flumequine by doped TiO2 and simulated solar light Candal, Roberto Jorge Sileo, Elsa Ester Antibiotic Doped titanium dioxide Flumequine Photocatalysis Sol-gel Antibiotics Photocatalysis Rietveld refinement Sol-gel process Doped titanium dioxide Flumequine Toxic materials flumequine thiourea titanium dioxide Antibiotics Photocatalysis Rietveld refinement Sol-gel process Toxic materials antibiotics catalysis experimental design infrared spectroscopy multivariate analysis optimization oxide pH photodegradation solar radiation titanium urea X-ray diffraction article crystallography degradation diffuse reflectance spectroscopy infrared spectroscopy pH photocatalysis solar energy solar radiation X ray diffraction Anti-Bacterial Agents Catalysis Fluoroquinolones Photochemistry Sunlight Titanium Water Pollutants, Chemical Water Purification Titanium dioxide was obtained in its pure form (TiO2) and in the presence of urea (u-TiO2) and thiourea (t-TiO2) using the sol-gel technique. The obtained powders were characterized by BET surface area analysis, Infrared Spectroscopy, Diffuse Reflectance Spectroscopy and the Rietveld refinement of XRD measurements. All the prepared catalysts show high anatase content (>99%). The a and b-cell parameters of anatase increase in the order TiO2 < u-TiO2 < t-TiO2, while the c-parameter presents the opposite trend. Because of the interplay in cell dimensions, the cell grows thicker and shorter when prepared in the presence of urea and thiourea, respectively. The cell volume decreases in the order t-TiO2 > u-TiO2 > TiO2. The photocatalytic activities of the samples were determined on flumequine under solar-simulated irradiation. The most active catalysts were u-TiO2 and t-TiO2, reaching values over 90% of flumequine degradation after 15 min irradiation, compared with values of 55% for the pure TiO2 catalyst. Changing simultaneously the catalyst amount (t-TiO2) and pH, multivariate analysis using the response surface methodology was used to determine the roughly optimal conditions for flumequine degradation. The optimized conditions found were pH below 7 and a catalyst amount of 1.6 g L-1. © 2007 Elsevier B.V. All rights reserved. Fil:Candal, R.J. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Sileo, E.E. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2008 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03043894_v155_n1-2_p45_Nieto http://hdl.handle.net/20.500.12110/paper_03043894_v155_n1-2_p45_Nieto
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Antibiotic
Doped titanium dioxide
Flumequine
Photocatalysis
Sol-gel
Antibiotics
Photocatalysis
Rietveld refinement
Sol-gel process
Doped titanium dioxide
Flumequine
Toxic materials
flumequine
thiourea
titanium dioxide
Antibiotics
Photocatalysis
Rietveld refinement
Sol-gel process
Toxic materials
antibiotics
catalysis
experimental design
infrared spectroscopy
multivariate analysis
optimization
oxide
pH
photodegradation
solar radiation
titanium
urea
X-ray diffraction
article
crystallography
degradation
diffuse reflectance spectroscopy
infrared spectroscopy
pH
photocatalysis
solar energy
solar radiation
X ray diffraction
Anti-Bacterial Agents
Catalysis
Fluoroquinolones
Photochemistry
Sunlight
Titanium
Water Pollutants, Chemical
Water Purification
spellingShingle Antibiotic
Doped titanium dioxide
Flumequine
Photocatalysis
Sol-gel
Antibiotics
Photocatalysis
Rietveld refinement
Sol-gel process
Doped titanium dioxide
Flumequine
Toxic materials
flumequine
thiourea
titanium dioxide
Antibiotics
Photocatalysis
Rietveld refinement
Sol-gel process
Toxic materials
antibiotics
catalysis
experimental design
infrared spectroscopy
multivariate analysis
optimization
oxide
pH
photodegradation
solar radiation
titanium
urea
X-ray diffraction
article
crystallography
degradation
diffuse reflectance spectroscopy
infrared spectroscopy
pH
photocatalysis
solar energy
solar radiation
X ray diffraction
Anti-Bacterial Agents
Catalysis
Fluoroquinolones
Photochemistry
Sunlight
Titanium
Water Pollutants, Chemical
Water Purification
Candal, Roberto Jorge
Sileo, Elsa Ester
Photocatalyzed degradation of flumequine by doped TiO2 and simulated solar light
topic_facet Antibiotic
Doped titanium dioxide
Flumequine
Photocatalysis
Sol-gel
Antibiotics
Photocatalysis
Rietveld refinement
Sol-gel process
Doped titanium dioxide
Flumequine
Toxic materials
flumequine
thiourea
titanium dioxide
Antibiotics
Photocatalysis
Rietveld refinement
Sol-gel process
Toxic materials
antibiotics
catalysis
experimental design
infrared spectroscopy
multivariate analysis
optimization
oxide
pH
photodegradation
solar radiation
titanium
urea
X-ray diffraction
article
crystallography
degradation
diffuse reflectance spectroscopy
infrared spectroscopy
pH
photocatalysis
solar energy
solar radiation
X ray diffraction
Anti-Bacterial Agents
Catalysis
Fluoroquinolones
Photochemistry
Sunlight
Titanium
Water Pollutants, Chemical
Water Purification
description Titanium dioxide was obtained in its pure form (TiO2) and in the presence of urea (u-TiO2) and thiourea (t-TiO2) using the sol-gel technique. The obtained powders were characterized by BET surface area analysis, Infrared Spectroscopy, Diffuse Reflectance Spectroscopy and the Rietveld refinement of XRD measurements. All the prepared catalysts show high anatase content (>99%). The a and b-cell parameters of anatase increase in the order TiO2 < u-TiO2 < t-TiO2, while the c-parameter presents the opposite trend. Because of the interplay in cell dimensions, the cell grows thicker and shorter when prepared in the presence of urea and thiourea, respectively. The cell volume decreases in the order t-TiO2 > u-TiO2 > TiO2. The photocatalytic activities of the samples were determined on flumequine under solar-simulated irradiation. The most active catalysts were u-TiO2 and t-TiO2, reaching values over 90% of flumequine degradation after 15 min irradiation, compared with values of 55% for the pure TiO2 catalyst. Changing simultaneously the catalyst amount (t-TiO2) and pH, multivariate analysis using the response surface methodology was used to determine the roughly optimal conditions for flumequine degradation. The optimized conditions found were pH below 7 and a catalyst amount of 1.6 g L-1. © 2007 Elsevier B.V. All rights reserved.
author Candal, Roberto Jorge
Sileo, Elsa Ester
author_facet Candal, Roberto Jorge
Sileo, Elsa Ester
author_sort Candal, Roberto Jorge
title Photocatalyzed degradation of flumequine by doped TiO2 and simulated solar light
title_short Photocatalyzed degradation of flumequine by doped TiO2 and simulated solar light
title_full Photocatalyzed degradation of flumequine by doped TiO2 and simulated solar light
title_fullStr Photocatalyzed degradation of flumequine by doped TiO2 and simulated solar light
title_full_unstemmed Photocatalyzed degradation of flumequine by doped TiO2 and simulated solar light
title_sort photocatalyzed degradation of flumequine by doped tio2 and simulated solar light
publishDate 2008
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03043894_v155_n1-2_p45_Nieto
http://hdl.handle.net/20.500.12110/paper_03043894_v155_n1-2_p45_Nieto
work_keys_str_mv AT candalrobertojorge photocatalyzeddegradationofflumequinebydopedtio2andsimulatedsolarlight
AT sileoelsaester photocatalyzeddegradationofflumequinebydopedtio2andsimulatedsolarlight
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