showing 12 related works from this author
Adsorption and photocatalytic degradation of acetonitrile: FT-IR investigation
2003
Abstract The photocatalytic degradation of acetonitrile was carried out in liquid–solid regime in a batch reactor by using two types of commercial TiO 2 powders (Merck and Degussa P25) as photocatalysts. The concentration of acetonitrile and non-purgeable organic carbon (NPOC) were monitored. The initial rate of acetonitrile conversion was found higher on TiO 2 Merck than on TiO 2 P25. FT-IR spectroscopy was used to investigate the molecular features of the adsorption and photo-oxidation of acetonitrile on the two TiO 2 powders in a fully surface hydrated form. Acetonitrile was found adsorbed on Ti 4+ surface ions and hydroxyl groups for both types of TiO 2 . This interaction appeared fully…
Photocatalytic oxidation of toluene on irradiated TiO2: comparison of degradation performance in humidified air, in water and in water containing a z…
2003
Photocatalytic degradation of toluene was carried out both in gas–solid and in liquid–solid regime by using polycrystalline samples of TiO2 Merck and TiO2 Degussa P25. For the gas–solid regime two types of continuous photoreactor were used, a fixed bed one of cylindrical shape and a Carberry type photoreactor, both irradiated by near-UV light. The inlet reacting mixture consisted of air containing toluene and water vapours. The influence of the gas flow rate and the presence of water vapour on the photocatalytic process was investigated. CO2 and benzaldehyde were the toluene degradation products detected in the gas phase by using TiO2 Merck. In the presence of water vapour this catalyst exh…
DFT and kinetic evidences of the preferential CO oxidation pattern of manganese dioxide catalysts in hydrogen stream (PROX)
2022
Abstract The oxidation functionality of Mn(IV) sites has been assessed by density functional theory (DFT) analysis of adsorption and activation energies of CO, H2 and O2 on a model Mn4O8 cluster. DFT calculations indicate that Mn(IV) atoms prompt an easy CO conversion to CO2 via a reaction path involving both catalyst and gas-phase oxygen species, while much greater energy barriers hinder H2 oxidation. Accordingly, a MnCeOx catalyst (Mnat/Ceat, 5) with large exposure of Mn(IV) sites shows a remarkable CO oxidation performance at T ≥ 293 K and no H2 oxidation activity below 393 K. Empiric kinetics disclose that the catalyst-oxygen abstraction step determines both CO and H2 oxidation rate, al…
The role of H2O in the photocatalytic oxidation of toluene in vapour phase on anatase TiO2 catalyst
1999
Abstract Photocatalytic oxidation of toluene has been carried out in a gas–solid regime by using polycrystalline anatase TiO2 in a fixed-bed continuous reactor. Air containing toluene and water vapours in various molar ratios was fed to the photoreactor irradiated by a medium pressure Hg lamp. Toluene was mainly photo-oxidised to benzaldehyde, and small amount of benzene, benzyl alcohol and traces of benzoic acid and phenol were also detected. In the presence of water, no decrease of photoreactivity was observed at steady-state conditions. By removing water vapour from the feed, the conversion of toluene to benzaldehyde was almost completely inhibited, and an irreversible deactivation of th…
Photocatalytic oxidation of gaseous toluene on polycrystalline TiO2: FT-IR investigation of surface reactivity of different types of catalysts
2000
Commercial TiO 2 Merck and TiO 2 Degussa P25 powders were employed as the catalysts for the photo-oxidation of toluene. By using TiO 2 Merck benzaldehyde was found in gas phase as the main product of the toluene partial oxidation. After an initial transient period, this catalyst exhibited a high stability in the presence of water vapour in the gaseous mixture, whereas the photoproduction of benzaldehyde sharply decreases after removal of H 2 O from the feed IR spectra of the used catalyst revealed that in the absence of water vapour benzaldehyde is molecularly held on the catalyst surface. This feature was confirmed by co-adsorbing benzaldehyde and water on the fresh catalyst. By contrast, …
VOC's abatement: Photocatalytic oxidation of toluene in vapour phase on anatase TiO2 catalyst
1997
Publisher Summary The photocatalytic oxidation of toluene in the presence of water was performed in the gas–solid regime at room temperature by using TiO2. It has been found that the presence of water was beneficial to achieve the almost complete photo-oxidation of toluene to CO2 and H2O, in fact, only very small amounts of benzaldehyde vapor that is the main product of toluene partial oxidation, were detected. Volatile organic compounds, VOC's, are an important class of air pollutants usually found in the atmosphere of all urban and industrial areas. Toluene is one of these compounds, and because of its noxious nature several strategies have been identified to reduce its presence in indoor…
Photocatalytic oxidation of gaseous toluene on anatase TiO2 catalyst: Mechanistic aspects and FT-IR investigation
1999
Abstract Photo-oxidation of toluene has been carried out in gas–solid regime by using polycrystalline anatase TiO2 as the catalyst. The reacting gaseous mixture was toluene, air and water in various molar ratios. A pyrex fixed-bed continuous photoreactor irradiated by a medium pressure Hg lamp was used for performing the photoreactivity experiments. The main oxidation product was benzaldehyde but benzene, benzyl alcohol and traces of benzoic acid, phenol and unidentified compounds were also detected. The molar conversion to benzaldehyde with respect to the initial amount of toluene was ca. 20% in the best experimental conditions. Benzene was produced only as a transient product during the f…
Photocatalytic degradation of nitrophenols in aqueous titanium dioxide dispersion
1991
Abstract The results are reported of an investigation into the photodegradation of nitrophenol isomers carried out in aqueous titania (anatase) dispersions under various experimental conditions. We investigated the influence of various parameters on the photodegradation rate, such as the concentrations of the catalyst, dissolved oxygen and organic compound, and the presence of various anions in the dispersion. A plausible explanation is proposed for the influence of these parameters, both mechanistic and kinetic factors being accounted for. Gas chromatography and mass spectrometry were used as analytical methods in order to determine intermediate products. Spectroscopic methods (UV-vis and …
Formation of dibutyl carbonate and butylcarbamate via CO2 insertion in titanium(IV) butoxide and reaction with n-butylamine
2016
Abstract The species resulting from insertion of 12CO2 and 13CO2 into titanium(IV) butoxide is for the first time fully characterized by means of infrared and nuclear magnetic resonance spectroscopy. Results show formation of Ti-monobutylcarbonate, that easily undergoes nucleophilic attack by an aliphatic amine. The hydrolysis of the resulting species produces butylcarbamate and dibutylcarbonate as the only main products. Characterization results of the carbonate-like adduct, along with its reactivity with amine molecules open the route to new ways of CO2 utilization as building block for valuable organic compounds.
The role of water in the photocatalytic degradation of acetonitrile and toluene in gas-solid and liquid-solid regimes
2006
Photocatalytic degradation of acetonitrile and toluene was carried out both in gas-solid and in liquid-solid regimes by using commercialTiO2samples (Merck and Degussa P25). The investigation was mainly aimed to study the influence of water present in the reaction environment on the mechanism and degradation rate of two probe molecules. In gas-solid regime, the reacting mixture consisted of toluene or acetonitrile, oxygen, nitrogen, and water vapour. The main degradation product of toluene wasCO2with small amounts of benzaldehyde. In the presence of water vapour, the activity ofTiO2Merck remained stable but greatly decreased if water was absent.TiO2Degussa P25 continuously deactivated, even …
Photocatalytic oxidation of phenol on TiO2 powders. A Fourier transform infrared study
1994
Abstract In the present paper a detailed investigation of a well known photoreaction, i.e. phenol photodegradation in the presence of TiO2, has been carried out. The Fourier transform infrared (FT-IR) technique has been used to characterize the catalyst surface and to follow the photoprocess by “in situ” measurements in a gas—solid regime, simulating the aqueous liquid—solid regime in which this photodegradation reaction has been usually carried out. The influence on the photoprocess of the surface hydroxylation of the catalyst has been investigated and the presence of some reaction intermediates has been revealed by FT-IR. The experimental results have demonstrated that the chosen gas—soli…
Photocatalytic oxidation of acetonitrile in gas–solid and liquid–solid regimes
2005
Il programma NON mi ha consentito di scaricare il PDF di questo articolo. Se lo volete ditemi come inviarlo ABSTRACT Photocatalytic degradation of acetonitrile was carried out in both gas–solid and liquid–solid regimes using two commercial TiO2 catalysts (Merck and Degussa P25). For the gas–solid regime, a continuous annular photoreactor was used. The influence on photodegradation kinetics of the gas flow rate and concentrations of acetonitrile, oxygen, and water was investigated. Acetonitrile degradation products detected in the gas phase included carbon dioxide and hydrogen cyanide. The same photoactivity was exhibited in the presence and in the absence of water vapour. The liquid–solid reg…