Search results for "Catalyst"

showing 10 items of 516 documents

Catalytic conversion of glucose to 5-hydroxymethylfurfural over biomass-based activated carbon catalyst

2020

Selective and efficient dehydration of glucose to 5-hydroxymethylfurfural (HMF) has been widely explored research problem recently, especially from the perspective of more sustainable heterogeneous catalysts. In this study, activated carbon was first produced from a lignocellulosic waste material, birch sawdust. Novel heterogeneous catalysts were then prepared from activated carbon by adding Lewis or Brønsted acid sites on the carbon surface. Prepared catalysts were used to convert glucose to HMF in biphasic water:THF system at 160 °C. The highest HMF yield and selectivity, 51% and 78%, respectively, were obtained in 8 h with a catalytic mixture containing both Lewis and Brønsted acid sites…

5-hydroxymethylfurfuralaktiivihiiliActivated carbonCatalystGlucose conversion
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Hydrogenolysis of hydroxymatairesinol on Y derived catalysts: a computational study

2010

Hydrogenolysis of 7-hydroxymatairesinol (HMR) to matairesinol (MAT) occurs on palladium supported acidic catalysts. HMR has three stereochemical centres and naturally exists as a mixture of two diastereoisomers, namely RRR-HMR and SRR-HMR. The latter is significantly more reactive than the former, in the reaction above. In order to elucidate the hydrogenolysis mechanism, simple surface events involving HMR derivatives on aluminated faujasite (H-Y) fragments were simulated by quantum chemical calculations. The metallic function of a Pd/H-Y acidic catalyst was also mimicked by a minimal palladium cluster. Stereochemical evidences pointed already out that water β-elimination on the epimeric ce…

7-HydroxymatairesinolProcess Chemistry and TechnologySupported catalystschemistry.chemical_elementDFT calculationFaujasiteengineering.materialHeterogeneous catalysisMedicinal chemistryHydrogenation/dehydration processeCatalysisCatalysisReaction rateHydroxymatairesinolchemistryHydrogenolysisengineeringOrganic chemistryReactivity (chemistry)Physical and Theoretical ChemistryPalladiumH-Y zeolite
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Nano-magnetic potassium impregnated ceria as catalyst for the biodiesel production

2019

Abstract The main objective of this work comprises the investigation of biodiesel production from rapeseed oil using potassium impregnated Fe3O4-CeO2 nanocatalyst. The various concentration of potassium impregnated Fe3O4-CeO2 was screened for catalytic conversion of rapeseed oil to triglyceride methyl ester. The 25 wt % potassium impregnated Fe3O4-CeO2 nanocatalyst showed best biodiesel production. Nanocatalyst was characterized by FTIR, XRD, SEM, TEM, BET and Hammett indicator for basicity test. The characterization of biodiesel was performed with GC-MS, 1H and 13C NMR. Moreover, the optimum reaction parameters such as catalyst amount (wt %), oil to methanol ratio, reaction time and reacti…

Acid valuekasviöljyt020209 energyPotassiumchemistry.chemical_elementbiodiesel02 engineering and technologyrapeseed oilCatalysischemistry.chemical_compoundkatalyytit0202 electrical engineering electronic engineering information engineering0601 history and archaeologyta116ta215ta218Biodiesel060102 archaeologyRenewable Energy Sustainability and the Environment06 humanities and the artsTransesterificationtransesterificationchemistryYield (chemistry)Biodiesel productionoksiditnanohiukkasetMethanolFe3O4-CeO2 nanocatalystrapsiöljyNuclear chemistryRenewable Energy
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Carbons from second generation biomass as sustainable supports for catalytic systems

2018

In this study activated carbons were produced from the wood of three different wood species (pine, birch, spruce). The resulting activated carbons were characterized in bulk for ash content, carbon content (elemental analyses), specific surface area, and pore size distribution, and at the surface by measuring the autogenerated pH and studying their structure by XPS. All the samples presented high surface areas and appeared to be mesoporous materials (mesopores >80%). The carbons were then used as support for AuPt nanoparticles and tested in the liquid phase oxidation of glycerol (GLY) and in the hydrogenation of levulinic acid (LA), two important chemicals from cellulose-based biomass. The …

Activated mesoporous carbonskatalyytitaktiivihiiliLevulinic acid hydrogenationbiomassa (teollisuus)Carbon supported catalystsGlycerol oxidationGVL production
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Alkaline fuel cell technology - A review

2021

Abstract The realm of alkaline-based fuel cells has with the arrival of anionic exchange membrane fuel cells (AEMFCs) taken a great step to replace traditional liquid electrolyte alkaline fuel cells (AFCs). The following review summarises progress, bottleneck issues and highlights the most recent research trends within the field. The activity of alkaline catalyst materials has greatly advanced, however achieving long-term stability remains a challenge. Great AEMFC performances are reported, though these are generally obtained through the employment of platinum group metals (PGMs), thus emphasising the importance of R&D related to non-PGM materials. Thorough design strategies must be utilise…

Alkaline fuel cellMaterials scienceRenewable Energy Sustainability and the Environmentbusiness.industryEnergy Engineering and Power Technology02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical sciencesVDP::Teknologi: 500Fuel TechnologyFuel cells0210 nano-technologyProcess engineeringbusinessAlkaline catalystInternational Journal of Hydrogen Energy
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Nucleophilic benzoylation using a mandelic acid dioxolanone as a synthetic equivalent of the benzoyl carbanion. Oxidative decarboxylation of α-hydrox…

2004

The synthesis of alkyl aryl ketones using a mandelic acid dioxolanone as a synthetic equivalent (Umpolung) of the benzoyl carbanion is reported. The methodology involves alkylation of the mandelic acid dioxolanone, hydrolysis of the dioxolanone moiety in the alkylated products and oxidative decarboxylation of the resulting alpha-hydroxyacids. The last step is carried out in a catalytic aerobic way using a Co (III) complex in the presence of pivalaldehyde under very mild conditions.

AlkylationDecarboxylationCarbonatesPharmaceutical ScienceAlkylationdioxolanoneArticlecatalystsAnalytical ChemistryUmpolunglcsh:QD241-441chemistry.chemical_compoundNucleophilelcsh:Organic chemistryDrug DiscoveryMoietyOrganic chemistryPhysical and Theoretical ChemistrydecarboxylationOxidative decarboxylationCarbanionMolecular StructureChemistryOrganic ChemistryDioxolanesBenzoic AcidKetonesMandelic acidcobaltChemistry (miscellaneous)Umpolung.Molecular MedicineMandelic AcidsHydroxy AcidsOxidation-Reduction
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ENANTIOSELECTIVE REDUCTION OF PROCHIRAL KETONES PROMOTED BY AMINO AMIDE RUTHENIUM COMPLEXES: A DFT STUDY

2021

International audience; The origin of enantioselectivity in the reaction of chiral Ru amino amide complexes in the asymmetric transfer hydrogenation of acetophenone was investigated using DFT calculations. For the most stable active catalysts, the full free energy profiles for the reaction were calculated according to the concerted hydrogen transfer mechanism. We succeeded in reproducing the experimentally observed enantioselectivity for the studied Ru amino amide complexes. Our results indicate that the high enantioselectivity can be explained by a stabilizing CH-π interaction existing between the phenyl group of acetophenone and the aromatic substituent of the catalyst, which plays a sign…

Amidoamide Ruthenium CatalystEnantioselective ReductionSubstituentchemistry.chemical_elementConformers010402 general chemistryTransfer hydrogenation01 natural sciencesBiochemistryDFTCatalysisInorganic Chemistrychemistry.chemical_compoundComputational chemistryMaterials ChemistryPhenyl groupPhysical and Theoretical ChemistryEnantiomeric excess010405 organic chemistryOrganic ChemistryEnantioselective synthesis3. Good health0104 chemical sciencesRuthenium[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistryMechanismAcetophenone
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Hybrid TiO2 @ phthalocyanine catalysts in photooxidation of 4-nitrophenol: Effect of the matrix and sensitizer type

2020

Abstract Microcrystalline and nanocrystalline anatase (TiO2) based hybrid photocatalysts including selected phthalocyanine sensitizers were explored in photooxidation of 4-nitrophenol (4-NP) in water. Composites obtained with the homemade pure nano-anatase displayed a very poor catalytic performance compared to the other ones prepared from the commercial Tioxide-Huntsman (micro) and Evonik P25 (nano) products. In particular, the microcrystalline anatase impregnated with sandwich phthalocyanines of Gd or Yb showed excellent results both in photooxidation of 4-NP and hydroquinone, and proved the only ones which completely removed these two compounds from the system during the same reaction cy…

AnataseGeneral Chemical EngineeringHydroquinoneGeneral Physics and Astronomy02 engineering and technology010402 general chemistry01 natural sciences4-nitrophenolCatalysisChemical kineticsReaction ratechemistry.chemical_compoundMetallophthalocyaninesLanthanideLanthanidesHybrid photocatalystHydroquinoneChemistry4-NitrophenolGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesMicrocrystallineChemical engineeringPhthalocyanineTitanium dioxideMetallophthalocyanine0210 nano-technologyHybrid photocatalystsJournal of Photochemistry and Photobiology A: Chemistry
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NiO diluted in high surface area TiO2 as efficient catalysts for the oxidative dehydrogenation of ethane

2017

[EN] Catalysts consisting of NiO diluted in high surface area TiO2 can be as efficient in the oxidative dehydrogenation of ethane as the most selective NiO-promoted catalysts reported previously in the literature. By selecting the titania matrix and the NiO loading, yields to ethylene over 40% have been obtained. In the present article, three different titanium oxides (TiO2) have been employed as supports or diluters of nickel oxide and have been tested in the oxidative dehydrogenation of ethane to ethylene. All TiO2 used present anatase as the main crystalline phase and different surface areas of 11,55 and 85 m(2) g(-1). It has been observed that by selecting an appropriate nickel loading …

AnataseInorganic chemistrychemistry.chemical_element02 engineering and technology010402 general chemistry01 natural sciencesCatalysisCatalysisEthyleneSurface coverageNiO diluted in TiO2DehydrogenationOxidative dehydrogenation of ethaneTitanium oxideChemistryProcess Chemistry and TechnologyNickel oxideNon-blocking I/O021001 nanoscience & nanotechnologyNickel oxide catalysts0104 chemical sciencesTitanium oxideNickel(ODH)0210 nano-technologyTitanium
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Activity of phthalocyanine-sensitized TiO2-anatase in photooxidation of sulfite ions

2015

Abstract Hybrid catalysts based on the TiO2 matrix impregnated with Nd, Eu and Yb diphthalocyanines proved effective in oxidation of sulfite ions under irradiation with light from the UV-visible range. Micro- and nano-crystalline anatase powders were used in preparation of the photocatalysts, which were applied in the form of a suspension in the water phase. The reaction yield was found to depend on the phthalocyanine sensitizer used and the conditions of TiO2 impregnation. The best results were obtained when micro-anatase impregnated with Yb-diphthalocyanine was used.

AnataseMaterials scienceGeneral Chemical EngineeringphotooxidationIndustrial chemistryGeneral ChemistryPhotochemistryIonChemistrychemistry.chemical_compoundchemistrySulfitePhthalocyanineTiO2hybrid photocatalystsanataseQD1-999Biotechnologyphthalocyanine sensitizerPolish Journal of Chemical Technology
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