Search results for "Titanium"

showing 10 items of 878 documents

Heterogeneous oxidation of pyrimidine and alkyl thioethers in ionic liquids over mesoporous Ti or Ti/Ge catalysts.

2004

Heterogeneous catalytic oxidation of a series of thioethers (2-thiomethylpyrimidine, 2-thiomethyl-4,6-dimethyl-pyrimidine, 2-thiobenzylpyrimidine, 2-thiobenzyl-4,6-dimethylpyrimidine, thioanisole, and n-heptyl methyl sulfide) was performed in ionic liquids by using MCM-41 and UVM-type mesoporous catalysts containing Ti, or Ti and Ge. A range of triflate, tetrafluoroborate, trifluoroacetate, lactate and bis(trifluoromethanesulfonyl)-imide-based ionic liquids were used. The oxidations were carried out by using anhydrous hydrogen peroxide or the urea-hydrogen peroxide adduct and showed that ionic liquids are very effective solvents, achieving greater reactivity and selectivity than reactions p…

chemistry.chemical_classificationTitaniumMolecular StructureChemistryGermaniumOrganic ChemistryThioanisoleInorganic chemistryGeneral ChemistrySulfidesHeterogeneous catalysisSilicon DioxidePeroxideCatalysisCatalysischemistry.chemical_compoundPyrimidinesCatalytic oxidationIonic liquidSolventsParticle SizeTrifluoromethanesulfonateOxidation-ReductionPorosityAlkylChemistry (Weinheim an der Bergstrasse, Germany)
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Photoreactivity of Iron-Doped Titanium Dioxide Powders for Dinitrogen Reduction to Ammonia

1989

The production of NH3 from N2 and H2O on Fe/TiO2 has been studied in a continuous photoreactor under UV radiation. An ESR study of the catalysts shows that Fe3+ ions are better electron traps than Ti4+ ions. This trapping can be irreversible if the corresponding holes originate stable species adsorbed on the catalyst surface. The charge separation, thus favoured by the Fe3+ ions, helps the N2 adsorption by its reaction with surface species activated by holes. The best activity is found when no excess Fe is segregated at the surface; overall turnover for N2 reduction as high as 6 e−/Fe atom can be reached before catalyst deactivation.

chemistry.chemical_compoundAmmoniaAdsorptionChemistryInorganic chemistryTitanium dioxideAtomTrappingElectronPhotochemistryCatalysisIon
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Influence of hydrogen peroxide on the kinetics of phenol photodegradation in aqueous titanium dioxide dispersion

1990

Abstract The influence of hydrogen peroxide on the phenol photodegradation rate under near UV radiation was investigated in homogeneous and heterogeneous systems: the heterogeneous systems were aqueous dispersions of titanium dioxide (anatase). The hydrogen peroxide photodecomposition reaction was also investigated for all the systems used. The highest rate of phenol photodegradation was observed in the heterogeneous system for the contemporary presence of hydrogen peroxide and oxygen. The rate equations for phenol photodegradation and hydrogen peroxide photodecomposition for both systems were obtained. A mechanistic model able to explain the main experimental results is also proposed.

chemistry.chemical_compoundAnataseReaction rate constantchemistryTitanium dioxideInorganic chemistryGeneral EngineeringPhotocatalysisPhenolPhotochemistryPhotodegradationHydrogen peroxideCatalysisApplied Catalysis
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Influence of operational variables on the photodegradation kinetics of Monuron in aqueous titanium dioxide dispersions

1994

The degradation of Monuron [N′—(4-chlorophenyl)—N, N dimethyl urea] in aqueous TiO 2 dispersions irradiated in the near-UV region has been investigated using a Pyrex batch photoreactor. The influence on the degradation kinetics of pH, initial Monuron concentration and catalyst concentration has been studied. The mineralization of the pollutant was also investigated. Measurements of photon absorbed flows allowed to determine the quantum yield values; they were found to increase by increasing the initial pH of the dispersion.

chemistry.chemical_compoundAqueous solutionChemistryInorganic chemistryKineticsTitanium dioxideQuantum yieldMineralization (soil science)PhotodegradationDispersion (chemistry)Catalysis
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Photocatalytic oxidation of acetonitrile in aqueous suspension of titanium dioxide irradiated by sunlight

2004

The photocatalytic oxidation of acetonitrile (CH3CN) was carried out in aqueous suspensions of polycrystalline TiO2 P25 Degussa irradiated by sunlight. A plug flow photoreactor in a total recycle loop was used for carrying out reactivity experiments in which the concentrations of acetonitrile, of its intermediate oxidation products and of not-purgeable organic carbon (NPOC) were monitored. The influence of the presence of strong oxidant species (H2O2, S2O82−, ClO−) on the process rate was studied. The dependence of acetonitrile photo-oxidation rate on the substrate concentration and on the catalyst amount was also investigated. The photodegradation rate of substrate and NPOC followed first …

chemistry.chemical_compoundAqueous solutionchemistryTitanium dioxideInorganic chemistryPhotocatalysisSubstrate (chemistry)Reactivity (chemistry)PhotodegradationAcetonitrileGeneral Environmental ScienceCatalysisAdvances in Environmental Research
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A Straightforward Route to Homoallyl-Homocrotylamines Promoted by a Titanium Complex

2012

I�-Allyltitanium complexes, generated in situ from 1,3-dienes and Cp2TiH, react with benzotriazole derivatives to give homoallylic amines in good yields. Under similar conditions, triple cascade reactions (allyltitanation followed by cationic 2-aza-Cope rearrangement followed by a second allyltitanation) occur from bis(benzotriazolyl) compounds affording a straightforward route to homoallyl-(E)-homocrotylamines. A theoretical study provides further insight into the factors that govern the selectivity of this sequence of reactions. The titanium-promoted reductive coupling of 1,3-dienes with bis(benzotriazolyl) compounds as substrates led selectively to homoallyl-homocrotylamines through a tr…

chemistry.chemical_compoundBenzotriazoleCascade reactionChemistryOrganic ChemistryCationic polymerizationOrganic chemistryPhysical and Theoretical ChemistrySigmatropic reactionSelectivityCombinatorial chemistryA titaniumEuropean Journal of Organic Chemistry
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Photoinduced Charge Separation of Self-Organized Semiconducting Superstructures Composed of a Functional Polymer-TiO2 Hybrid

2013

chemistry.chemical_compoundMaterials sciencePolymers and PlasticschemistryPhotoinduced charge separationOrganic ChemistryTitanium dioxideMaterials ChemistryCopolymerNanotechnologySelf-assemblyPhysical and Theoretical ChemistryCondensed Matter PhysicsMacromolecular Chemistry and Physics
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Oxidation of Titanium, Zirconium and their Alloys, Texture of their Oxide Scales

1994

chemistry.chemical_compoundMaterials sciencechemistryMechanics of MaterialsMechanical EngineeringMetallurgyOxideZirconium oxideGeneral Materials ScienceCondensed Matter PhysicsTitanium zirconiumTitanium oxideMaterials Science Forum
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The Photocatalytic Activity of Novel, Substituted Porphyrin/TiO2-Based Composites

2010

Four novel porphyrins, 5-[3-(3-phenoxy)-propoxy]phenyl porphyrin, 5,15-di-[3-(3-phenoxy)-propoxy] phenyl porphyrin, 5,10,15-tri-[3-(3-phenoxy)-propoxy]phenyl porphyrin, 5,10,15,20-tetra-[3-(3-phenoxy)- propoxy]phenyl porphyrin, and their corresponding Cu(II) porphyrins, were synthesized and characterized spectroscopically. The photodegradation of 4-nitrophenol in aq. suspension was used to determine the photocatalytic activity of polycrystalline TiO2 samples which had been impregnated with the Cu(II) porphyrins, as sensitizers. The photocatalytic activity of the composite depends mainly on the amount of sensitizer on the TiO2 surface rather than the nature of the substituted porphyrins.

chemistry.chemical_compoundchemistryProcess Chemistry and TechnologyGeneral Chemical EngineeringPolymer chemistryTitanium dioxidePhotocatalysisPhotosensitizerCrystallitePhotodegradationPhotochemistryPorphyrinPorphyrins Cu(II)-porphyrins Substitutions Photosensitizers Photodegradation Titanium Dioxide
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Titanium dioxide in dental enamel as a trace element and its variation with bleaching

2017

Background Titanium is a less studied trace element in dental enamel. Literature relates an increased Titanium concentration with a decreased enamel crystal domain size, which in turn is related to a higher color value. The aim of our study was to analyze the effect of tooth bleaching agents on its concentration in dental enamel by means of confocal Raman spectroscopy. Material and methods Human teeth were randomly distributed in six experimental groups (n=10) and submitted to different bleaching protocols according to the manufacturer´s instructions. Confocal Raman spectroscopy was carried out in order to identify and quantify the presence of titanium dioxide molecules in enamel prior to a…

chemistry.chemical_elementOdontología01 natural sciences010309 optics03 medical and health sciencessymbols.namesakechemistry.chemical_compound0302 clinical medicinestomatognathic systemwhitening0103 physical sciencesHydrogen peroxideGeneral DentistryTooth Bleaching AgentsEnamel painttitanium dioxidecarbamide peroxideChemistryDental enameltechnology industry and agricultureTrace elementbleaching030206 dentistryHydrogen peroxide:CIENCIAS MÉDICAS [UNESCO]stomatognathic diseasesvisual_artRaman spectroscopyUNESCO::CIENCIAS MÉDICASTitanium dioxidevisual_art.visual_art_mediumsymbolsRaman spectroscopyNuclear chemistryTitaniumJournal of Clinical and Experimental Dentistry
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