Search results for "Catalysis"

showing 10 items of 5944 documents

Paramagnetic ionic liquids as “liquid fixed-bed” catalysts in flow application

2011

Abstract The structural diversity of Ionic Liquids is well-known and widely used to generate solvents designed for special applications. Magnetic as well as catalytic properties have been described previously. To our best knowledge we report the first time about the combination of both, the magnetic and catalytic behaviour of imidazole based magnetic ionic liquids was used to establish a so-called liquid fixed-bed (LFB) in a micro-/meso-structured reactor. As proof of priciple the esterification of Ac 2 O with cyclohexanol was investigated by bubbling generated regular microdroplets of the reaction mixture through the magnetically fixed ionic liquid catalyst. With residence times of approx.…

General Chemical EngineeringCyclohexanolGeneral ChemistryFlow chemistryIndustrial and Manufacturing EngineeringCatalysischemistry.chemical_compoundParamagnetismchemistryChemical engineeringYield (chemistry)Ionic liquidEnvironmental ChemistryImidazoleOrganic chemistryMoleculeChemical Engineering Journal
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Numerical evidence for a thermal driving force during adsorption of butane in silicalite.

2009

International audience; The transport properties of nano-porous materials determine their applicability, e.g. as separators or catalysts (J. Ka¨rger, D. Ruthven. Diffusion in zeolites, Wiley, New York (1991); L.V.C. Rees, D. Shen. Adsorption of gases in zeolite molecular sieves. In Introduction to Zeolite Science and Practice, Studies in surface science and catalysis, H.V.C. van Bekkum, E.M. Flanigen, P.A. Jacobs, J.C. Jansen (Eds.), vol. 137, pp. 579–631, Elsevier, Amsterdam (2001)). Adsorption in zeolites is explained as a two-step process; adsorption to the external crystal surface and subsequent intra-crystalline diffusion (R. M. Barrer. Porous crystal membranes. J. Chem. Soc. Faraday T…

General Chemical EngineeringDiffusion02 engineering and technology010402 general chemistryMolecular sieve01 natural sciencesIsothermal processCatalysis[PHYS.PHYS.PHYS-CHEM-PH] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Crystalchemistry.chemical_compoundAdsorptionGeneral Materials ScienceZeoliteComputingMilieux_MISCELLANEOUSChemistryButaneGeneral Chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry[CHIM.THEO] Chemical Sciences/Theoretical and/or physical chemistry[ PHYS.PHYS.PHYS-CHEM-PH ] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]13. Climate actionModeling and SimulationPhysical Sciences[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistryPhysical chemistry[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]0210 nano-technologyInformation Systems
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Two Decades of Progress in the Asymmetric Intramolecular aza-Michael Reaction.

2021

The asymmetric intramolecular aza-Michael reaction (IMAMR) is a very convenient strategy for the generation of heterocycles bearing nitrogen-substituted stereocenters. Due to the ubiquitous presence of these skeletons in natural products, the IMAMR has found widespread applications in the total synthesis of alkaloids and biologically relevant compounds. The development of asymmetric versions of the IMAMR are quite recent, most of them reported in this century. The fundamental advances in this field involve the use of organocatalysts. Chiral imidazolidinones, diaryl prolinol derivatives, Cinchone-derived primary amines and quaternary ammonium salts, and BINOL-derived phosphoric acids account…

General Chemical EngineeringEnantioselective synthesisTotal synthesisStereoisomerismGeneral ChemistryBiochemistryCombinatorial chemistryStereocenterProlinolchemistry.chemical_compoundAlkaloidschemistryNucleophileIntramolecular forceOrganocatalysisMaterials ChemistryMichael reactionIminesAminesChemical record (New York, N.Y.)
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Formaldehyde: Catalytic Oxidation as a Promising Soft Way of Elimination

2013

International audience; Compared to other molecules such as benzene, toluene, xylene, and chlorinated compounds, the catalytic oxidation of formaldehyde has been studied rarely. However, standards for the emission level of this pollutant will become more restrictive because of its extreme toxicity even at very low concentrations in air. As a consequence, the development of a highly efficient process for its selective elimination is needed. Complete catalytic oxidation of formaldehyde into CO2 and H2O using noble-metal-based catalysts is a promising method to convert this pollutant at room temperature, making this process energetically attractive from an industrial point of view. However, th…

General Chemical EngineeringFormaldehyde02 engineering and technologyengineering.material010402 general chemistryHeterogeneous catalysis01 natural sciences7. Clean energyCatalysisCatalysis[ CHIM.CATA ] Chemical Sciences/Catalysischemistry.chemical_compound[ CHIM.ORGA ] Chemical Sciences/Organic chemistryFormaldehyde[ CHIM.OTHE ] Chemical Sciences/OtherEnvironmental ChemistryOrganic chemistryGeneral Materials SciencePollutantAir Pollutants[CHIM.ORGA]Chemical Sciences/Organic chemistryXylene[CHIM.CATA]Chemical Sciences/Catalysis021001 nanoscience & nanotechnologyToluene0104 chemical sciencesGeneral EnergychemistryCatalytic oxidation13. Climate actionAir Pollution IndoorengineeringNoble metal[CHIM.OTHE]Chemical Sciences/Other0210 nano-technologyOxidation-ReductionChemSusChem
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Selective photooxidation of ortho-substituted benzyl alcohols and the catalytic role of ortho-methoxybenzaldehyde

2016

It has been recently reported by Palmisano et al. (2015) [1] that the oxidation of 2-methoxybenzyl alcohol (2-MBA) to 2-methoxybenzaldehyde (2-MBAD) proceeds in water under near-UV light with an unexpected catalytic effect of 2-MBAD. In order to investigate the catalytic role of aldehyde in photolytic oxidation of ortho-substituted benzyl alcohols (OSBAs), reactivity runs were carried out with 2-methylbenzyl alcohol (2-MeBA), 2-nitrobenzyl alcohol (2-NBA), 2-hydroxybenzyl alcohol (2-HBA) and 2-chlorobenzyl alcohol (2-CIBA) in the absence and in the presence of their corresponding aldehyde. None of those alcohols showed a measurable oxidation rate even in the presence of their aldehydes but …

General Chemical EngineeringGeneral Physics and AstronomyAlcohol2-MethoxybenzaldehydeHomogeneous photocatalysi010402 general chemistry01 natural sciencesAldehydeCatalysisFerulic acidPhysics and Astronomy (all)chemistry.chemical_compoundBenzyl alcoholOrganic chemistryChemical Engineering (all)Reactivity (chemistry)chemistry.chemical_classificationSettore ING-IND/24 - Principi Di Ingegneria Chimica010405 organic chemistryChemistryChemistry (all)General Chemistry0104 chemical sciencesAutocatalytic photooxidationAlcohol oxidationPhotocatalysis2-Methoxybenzaldehyde; Autocatalytic photooxidation; Benzyl alcohols; Homogeneous photocatalysis; Chemistry (all); Chemical Engineering (all); Physics and Astronomy (all)Selectivity
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Blue light activated photodegradation of biomacromolecules by N-doped titanium dioxide in a chitosan hydrogel matrix

2023

The use of photocatalysis activated by titanium dioxide nanostructured materials is a promising solution for many biomedical applications ranging from drug-free antibacterial to anticancer therapies, as well as for innovative hydrogel-supported phototherapies. This makes the effects of photocatalysis on the structure of biomolecules of a great relevance in order to define the applicability of photocatalytic materials in the biomedical fields. In this work, the effects of nitrogen-doped titanium dioxide (N-TiO2) dispersed in a biocompatible chitosan/PEG hydrogel on myoglobin and bovine serum albumin as target model proteins were investigated. The efficiency of this composite biocompatible ma…

General Chemical EngineeringGeneral Physics and AstronomyPhotocatalysis Proteins Hydrogel Spectroscopy Nitrogen-doped TiO2General ChemistrySettore CHIM/02 - Chimica Fisica
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Effect of silver deposits on the photocatalytic activity of titanium dioxide samples for the dehydrogenation or oxidation of 2-propanol

1991

Abstract Until now, the effect of the deposition of metal particles onto a powdered semiconductor oxide on its photocatalytic activity has been determined for group VIII transition metals only. In this study, AGTiO2 samples were prepared by photodeposition, characterized by transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS) and tested, under band-gap illumination, using the oxidation of 2-propanol (neat liquid phase or mixed with water) in the absence or presence of molecular oxygen. The silver deposits were found to be metallic both before and after use, but the size of the particles and their distribution on the support were markedly influenced by the type …

General Chemical EngineeringInorganic chemistryGeneral Physics and Astronomychemistry.chemical_elementGeneral ChemistrySilver nanoparticleCatalysisMetalchemistry.chemical_compoundchemistryTransition metalvisual_artTitanium dioxidevisual_art.visual_art_mediumPhotocatalysisDehydrogenationPlatinumJournal of Photochemistry and Photobiology A: Chemistry
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Catalytic systems based on transition metals for the carbonylation of methanol to dimethylcarbonate

1997

Abstract The results of an investigation on catalytic systems arising from the electrochemical activation of salts and complexes of several transition metals for the carbonylation of methanol to dimethylcarbonate (DMC) are reported. Metals were tested as inorganic salts or complexes with ligands such as 2,2′-bipyridine (bipy), 1,6-bis (2-oxyphenyl)-2,5-diaza-1,5-hexadiene (salen), 2,4-pentanedionate (acac), triphenylphosphine (TPP) in methanol at room temperature saturated with carbon monoxide at atmospheric pressure. Best faradic yields vs DMC were observed as follows: CuCl(bipy): 84.8%; PdCl 2 (bipy): 64.0%; CoCl 2 : 26.0%; RhCl 3 : 25.0%; AgBF 4 (bipy): 10.2%; AuCl 3 : 9.4%; Cr(acac) 3 :…

General Chemical EngineeringInorganic chemistryPrimary alcoholElectrosynthesisMedicinal chemistryCatalysischemistry.chemical_compoundTransition metalchemistryElectrochemistryMethanolTriphenylphosphineCarbonylationCarbon monoxide
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Vanadium‐Doped Zircon and Zirconia Materials Prepared from Gel Precursors as Site‐Selective Electrochemical Sensors

2003

Abstract Polymer film electrodes incorporating vanadium‐doped zircon (V x ZrSiO4, 0.00 < x < 0.10) and vanadium‐doped monoclinic and tetragonal zirconias (V x ZrO2, 0.00 < x < 0.15), prepared by heat treatment of gel precursors, exhibit a significant site‐selective electrocatalytic activity towards the oxidation of amino acids, polyalcohols, and polyhydroxycarboxylic acids in alkaline media. Catalysis of the oxidation of carboxylate and alcohol groups involves a relatively slow chemical reaction between the substrate and vanadium centers, while the oxidation of thiolate in cysteine can be attributed to the oxidation of an adduct formed by vanadium centers and the substrate.

General Chemical EngineeringInorganic chemistrySubstrate (chemistry)Vanadiumchemistry.chemical_elementElectrocatalystElectrochemistryCatalysischemistry.chemical_compoundchemistryCubic zirconiaCarboxylateInstrumentationGeneral Environmental ScienceSol-gelInstrumentation Science &amp; Technology
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Transesterification of rapeseed oil over acid resins promoted by supercritical carbon dioxide

2011

The methanolysis of rapeseed oil catalyzed by commercial styrene-divinylbenzene macroporous acid resins was performed in a batch reactor at 100-140 °C and 10-46 MPa to study the effect of supercritical carbon dioxide (scCO2) on the performances of the process. Reaction temperatures of 120-140 °C were necessary to obtain high enough yields of fatty acid methyl esters. Upon addition of scCO2 faster transesterification kinetics was obtained also at the lowest investigated operating pressure (10-11 MPa), working in two fluid phase systems. Experiments performed changing the reaction time indicated that most of the esters were formed during the first 3 h. When the pressure was increased at 38-46…

General Chemical EngineeringMethanolysiKineticsBatch reactorOperating pressurePolymeric acidHeterogeneous catalysisCatalysiCatalysisHeterogeneous catalysiIon exchange resinSupercritical carbon dioxideOrganic chemistryFatty acid methyl esterRapeseed oilEsterPhysical and Theoretical ChemistryVegetable oils Supercritical fluid extractionIon-exchange resinStyreneReaction systemReaction timeBiodieselFluid phasiTwo-fluid Batch reactorSupercritical carbon dioxideEsterificationChemistryReaction kineticTransesterificationSettore ING-IND/27 - Chimica Industriale E TecnologicaFatty acidCondensed Matter PhysicsPhase behaviourTransesterificationCarbon dioxideReaction temperatureMacroporouStyrene-divinylbenzeneBiodieselEnhancement effectIon exchangeThe Journal of Supercritical Fluids
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