Search results for "heterogeneous"

showing 10 items of 460 documents

The effect of potassium on the selective oxidation ofn-butane and ethane over Al2O3-supported vanadia catalysts

1995

The catalytic properties of undoped and K-doped (K/V atomic ratio of 0.5) Al2O3-supported vanadia catalysts (∼4.5 wt% of V2O5) for the oxidation ofn-butane and ethane were studied. Isolated tetrahedral V5+ species are mainly observed in both undoped and K-doped samples. The incorporation of potassium decreases both the reducibility of surface vanadium species and the number of surface acid sites. Potassium-free vanadium catalysts show a high selectivity during the oxidative dehydrogenation (ODH) of ethane but a low selectivity during the ODH ofn-butane. However, the presence of potassium on the vanadium catalysts strongly influences their catalytic properties, increasing the selectivity to …

chemistry.chemical_classificationPotassiumInorganic chemistrychemistry.chemical_elementVanadiumButaneGeneral ChemistryHeterogeneous catalysisCatalysisCatalysischemistry.chemical_compoundHydrocarbonchemistryDehydrogenationSelectivityCatalysis Letters
researchProduct

Influence of preparation conditions of nano-crystalline ceria catalysts on the total oxidation of naphthalene, a model polycyclic aromatic hydrocarbon

2007

Abstract Nano-crystalline ceria catalysts prepared by homogeneous precipitation with urea were tested for the total oxidation of naphthalene, a model polycyclic aromatic hydrocarbon (PAH). Systematic variation of preparation conditions, including calcination temperature, calcination time and aging time, resulted in differences in surface area, reducibility, morphology and crystallite size of the CeO 2 catalyst and hence differences in catalytic performance. A combination of high surface area, small crystallite size and high oxygen defect concentration was found to favor the efficiency of the ceria catalysts for the total oxidation of naphthalene. Optimum preparation conditions for this stud…

chemistry.chemical_classificationProcess Chemistry and TechnologyInorganic chemistryPolycyclic aromatic hydrocarbonHeterogeneous catalysisCatalysisCatalysislaw.inventionchemistry.chemical_compoundHydrocarbonCatalytic oxidationchemistrylawCalcinationCrystalliteGeneral Environmental ScienceNaphthaleneApplied Catalysis B: Environmental
researchProduct

Spin-State-Dependent Redox-Catalytic Activity of a Switchable Iron(II) Complex

2017

The spin state of catalytically active 3d metal centers plays a significant role for their activity in enzymatic processes and organometallic catalysis. Here we report on the catalytic activity of a Fe(II) coordination compound that can undergo a cooperative switch between low-spin (LS) and high-spin (HS) states. Catalytic measurements within 291 - 318 K temperature region reveal a drastic drop of the catalytic activity upon conversion of metallic centers from the LS to the HS form. For a thermoswitchable [Fe(NH2trz)3]Br2 complex (Tup = 305 K), an activation energy is found to be considerably lower for the LS state (158 kJ mol-1) comparing to the HS state (305 kJ mol-1). Mossbauer analysis …

chemistry.chemical_classificationSpin statesInorganic chemistry02 engineering and technologyActivation energy010402 general chemistry021001 nanoscience & nanotechnologyHeterogeneous catalysis01 natural sciencesRedox0104 chemical sciencesCoordination complexCatalysisInorganic ChemistryMetalCrystallographychemistrySpin crossovervisual_artvisual_art.visual_art_medium0210 nano-technologyEuropean Journal of Inorganic Chemistry
researchProduct

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)
researchProduct

Exploiting the CNC Side Chain in Heterocyclic Rearrangements: Synthesis of 4(5)-Acylamino-imidazoles

2010

A new variation on the Boulton-Katritzky reaction is reported, namely, involving use of a CNC side chain. A novel Montmorillonite-K10 catalyzed nonreductive transamination of a 3-benzoyl-1,2,4-oxadiazole afforded a 3-(alpha-aminobenzyl)-1,2,4-oxadiazole, which was condensed with benzaldehydes to afford the corresponding imines. In the presence of strong base, these imines underwent Boulton-Katritzky-type rearrangement to afford novel 4(5)-acylaminoimidazoles.

chemistry.chemical_classificationchemistryTransaminationStereochemistryOrganic ChemistrySide chainSettore CHIM/06 - Chimica OrganicaPhysical and Theoretical Chemistryoxadiazole imidazole heterocyclic rearrangement transamination heterogeneous catalysisBiochemistryCatalysisOrganic Letters
researchProduct

ChemInform Abstract: Novel Prolinamide-Supported Polystyrene as Highly Stereoselective and Recyclable Organocatalyst for the Aldol Reaction.

2008

A new prolinamide derivative anchored to a polystyrene support has been straightforwardly prepared and employed as heterogeneous catalyst in the direct asymmetric aldol reaction with good results in terms of yield and stereoselectivity. The optimal reaction conditions were found when a 1:2 (v/v) water/chloroform mixture was used. This mixture was the best compromise between the good swelling properties of chloroform and the formation of a concentrated organic phase due to the presence of water. Noticeably, the enantioselectivities obtained employing acetone as ketone were, to the best of our knowledge, the highest achieved with a supported proline derivative. This catalyst can be easily rec…

chemistry.chemical_classificationchemistry.chemical_compoundAddition reactionKetoneChloroformchemistryAldol reactionAcetoneOrganic chemistryGeneral MedicinePolystyreneHeterogeneous catalysisCatalysisChemInform
researchProduct

Effective Removal and Mineralization of 8-Hydroxyquinoline-5-sulfonic Acid through a Pressurized Electro-Fenton-like Process with Ni−Cu−Al Layered Do…

2020

Ni−Cu−Al layered double hydroxide (Ni−Cu−Al LDH) was proposed as an electro‐Fenton‐like catalyst for 8‐hydroxyquinoline‐5‐sulfonic acid (8‐HQS) removal in water. The properties of the prepared catalysts were characterized by using X‐ray, SEM and EDAX analyses. The effect of numerous operative parameters on the removal of 8‐HQS and total organic carbon (TOC) was studied. Very high level removal of both 8‐HQS and TOC (87 and 79 %, respectively) were obtained by using a pressurized electro‐Fenton‐like process (PrEFL‐LDH) at P=10 bars, using a Ti/IrO2‐Ta2O5 anode for 6 h. The process presented good performances in a large range of pH (3–10) and gave better removals of 8‐HQS and TOC with respect…

chemistry.chemical_classificationchemistry.chemical_compoundChemistry8-hydroxyquinoline-5-sulfonic acid heterogeneous catalysis Ni−Cu−Al layered double hydroxide nitrogen heterocycles pressurized-electro-FentonElectrochemistryHydroxide8-HydroxyquinolineMineralization (soil science)Sulfonic acidSettore ING-IND/27 - Chimica Industriale E TecnologicaHeterogeneous catalysisCatalysisNuclear chemistry
researchProduct

Heterogeneous salt distribution in hot snacks enhances saltiness without loss of acceptability

2013

clef UT: 000318667000026; International audience; Abstract Health issues have led worldwide organisations to encourage the food industry to reduce salt in processed foods. Therefore, different strategies for salt reduction have been investigated. Here, the effect of heterogeneous salt distribution on saltiness perception intensity was assessed to compensate for salt reduction in snack foods. Two models of hot-served baked foods were developed. One model is made of two layers that vary in composition (cream-based and cereal-based layers) and salt (NaCl) concentration; the other one is made of four cream-based layers that vary in salt concentrations. Consumer panels rated the saltiness intens…

chemistry.chemical_classificationlikingTasteFood industrybusiness.industryChemistry[ SDV.AEN ] Life Sciences [q-bio]/Food and Nutritiondigestive oral and skin physiologySalt reductionfood and beveragesSalt (chemistry)layered food productsSnack foodConsumer panelstaste enhancementFood processingheterogeneous tastant distributionFood sciencesalt reductionbusiness[SDV.AEN]Life Sciences [q-bio]/Food and NutritionFood ScienceFood Research International
researchProduct

Selective oxidation of propane and ethane on diluted Mo–V–Nb–Te mixed-oxide catalysts

2007

Abstract Te-free and Te-containing Mo–V–Nb mixed oxide catalysts were diluted with several metal oxides (SiO 2 , γ -Al 2 O 3 , α -Al 2 O 3 , Nb 2 O 5 , or ZrO 2 ), characterized, and tested in the oxidation of ethane and propane. Bulk and diluted Mo–V–Nb–Te catalysts exhibited high selectivity to ethylene (up to 96%) at ethane conversions 10 % , whereas the corresponding Te-free catalysts exhibited lower selectivity to ethylene. The selectivity to ethylene decreased with the ethane conversion, with this effect depending strongly on the diluter and the catalyst composition. For propane oxidation, the presence of diluter exerted a negative effect on catalytic performance (decreasing the forma…

chemistry.chemical_compoundEthylenechemistryPropaneInorganic chemistryAluminium oxideMixed oxidePhysical and Theoretical ChemistryHeterogeneous catalysisSelectivityCatalysisVanadium oxideCatalysisJournal of Catalysis
researchProduct

Steam-activated FeMFI zeolites. Evolution of iron species and activity in direct N2O decomposition

2003

Abstract In this paper the effect of the composition and steaming conditions of FeMFI catalysts on activity in direct N2O decomposition is investigated. MFI zeolites with different framework compositions (FeAlSi, FeGaSi, and FeSi) and without iron ( 100 mbar H2O in N2) favor the extraction of framework iron, enabling the application of lower activation temperatures. The optimum temperature during steam activation is that at which extraction of framework iron is complete without extensive clustering of extra-framework iron species into oxide particles, as was demonstrated by transmission electron microscopy and electrochemical characterization of the samples. Additional experiments show…

chemistry.chemical_compoundTransition metalChemistryInorganic chemistryExtraction (chemistry)OxidePhysical and Theoretical ChemistryMolecular sieveHeterogeneous catalysisZeoliteDecompositionCatalysisCatalysisJournal of Catalysis
researchProduct