Search results for "Catalyst support"

showing 10 items of 23 documents

2020

Worldwide, tons of lignin is produced annually in pulping plants and it is mainly considered as a waste material. Usually lignin is burned to produce energy for the pulping reactors. The production of value-added materials from renewable materials like lignin, has proved to be challenging. In this study, the effects of addition of three different types of lignin in the production of tannin/furanic foams is investigated. The foams were matured, first at 373 K and finally carbonized at 1073 K and the properties of them including mechanical strength, specific surface area and pore development are investigated before and after thermal treatment. According to the results, higher mechanical stren…

0301 basic medicineSolid-state chemistryMultidisciplinaryMaterials scienceCarbonizationCatalyst supportThermal treatmentCatalysis03 medical and health scienceschemistry.chemical_compound030104 developmental biology0302 clinical medicineAdsorptionChemical engineeringchemistrySpecific surface areaLignin030217 neurology & neurosurgeryHeliyon
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CoOx catalysts supported on alumina and alumina-baria: influence of the support on the cobalt species and their activity in NO reduction by C3H6 in l…

2003

Abstract CoO x catalysts (Co 1 and 3 wt.%) were prepared by incipient-wetness impregnation of the supports, Al 2 O 3 and Al 2 O 3 (80 wt.%)-BaO (20 wt.%), and calcined at 500 and 800 °C. The samples were characterized by X-ray diffraction (XRD) and BET techniques. H 2 -temperature programmed reduction (TPR) and UV-Vis diffuse reflectance spectroscopy (DRS) spectra were recorded with the aim to identify the different Co species formed. The presence of Co 2+ species tetrahedrally and octahedrally coordinated appears strongly influenced by the nature of the support and the cobalt content. Co 3 O 4 particles were detected after calcination at 500 °C, a successive treatment at 800 °C promotes th…

Barium oxideChemistryProcess Chemistry and TechnologyCatalyst supportInorganic chemistrychemistry.chemical_elementSelective catalytic reductionCatalysisCatalysislaw.inventionchemistry.chemical_compoundlawCalcinationTemperature-programmed reductionCobalt oxideCobaltApplied Catalysis A: General
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Thermal stability, structural properties and catalytic activity of Pd catalysts supported on Al2O3–CeO2–BaO mixed oxides prepared by sol–gel method

2003

Abstract Al2O3–CeO2–BaO oxides with constant Al/Ba mass ratio and increasing cerium content were prepared, using the sol–gel procedure, and calcined at 1000 °C for 5 h. The influence of barium oxide on the thermal stability and on the morphological and structural properties of the corresponding supports, in terms of increasing surface area of alumina and ceria dispersion, was studied. The corresponding Pd (1 wt.%) catalysts were prepared by a stepwise impregnation method with a solution of palladium acetylacetonate in benzene. Palladium was introduced in two sequential steps by impregnation 0.5 wt.% of Pd each time. The structural and textural properties of the materials were studied by X-r…

Barium oxideProcess Chemistry and TechnologyCatalyst supportInorganic chemistrychemistry.chemical_elementCatalysisCatalysislaw.inventionCeriumchemistry.chemical_compoundchemistrylawThermal stabilityCalcinationPhysical and Theoretical ChemistryBET theoryPalladiumJournal of Molecular Catalysis A: Chemical
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Catalytic transesterification of Pistacia chinensis seed oil using HPW immobilized on magnetic composite graphene oxide/cellulose microspheres

2018

Abstract In the present study, magnetic composite graphene oxide/cellulose (GO/CM@Fe3O4) microspheres were prepared as support material, which are cost-efficient, non-toxic and environmental friendly. The microspheres with higher adsorption capacity were further modified using triethylene tetramine (TETA), and H3PW12O40 (HPW) was immobilized to form GO/CM-NH2@Fe3O4-HPW microspheres as heterogeneous catalyst for biodiesel production. The novel heterogeneous catalyst was characterized by scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), Brunauer-Emmett-Teller (BET) and X-ray diffractometry (XRD). For the first time, GO/CM-NH2@Fe3O4--HPW was applied in the tr…

BiodieselMaterials scienceRenewable Energy Sustainability and the EnvironmentCatalyst support02 engineering and technologyTransesterification010402 general chemistry021001 nanoscience & nanotechnologyHeterogeneous catalysis01 natural sciences0104 chemical sciencesCatalysischemistry.chemical_compoundAdsorptionChemical engineeringchemistryBiodiesel productionMethanol0210 nano-technologyRenewable Energy
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Pt–CeO thin film catalysts for PEMFC

2015

Abstract Platinum is the mostly used element in catalysts for fuel cell technology, but its high price limits large-scale applications. Platinum doped cerium oxide represents an alternative solution due to very low loading, typically few micrograms per 1 cm2, at the proton exchange membrane fuel cell (PEMFC) anode. High efficiency is achieved by using magnetron sputtering deposition of cerium oxide and Pt of 30 nm thick nanoporous films on large surface carbon nanoparticle substrates. Thin film techniques permits to grow the catalyst film characterized by highly dispersed platinum, mostly in ionic Pt2+ state. Such dispersed Pt species show high activity and stability. These new materials ma…

Cerium oxideMaterials scienceNanoporousCatalyst supportInorganic chemistryProton exchange membrane fuel cellchemistry.chemical_elementGeneral ChemistrySputter depositionCatalysisCatalysischemistryThin filmPlatinumCatalysis Today
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Enhanced Activity and Stereoselectivity of Polystyrene-Supported Proline-Based Organic Catalysts for Direct Asymmetric Aldol Reaction in Water

2009

Several polystyrene-supported proline dipeptides and a prolinamide derivative were prepared by thiol–ene coupling. These materials were used as catalysts for the direct asymmetric aldol reaction in water, and results compared with unsupported catalysts in water. Such an approach gave more active or stereoselective catalysts compared to the unsupported compounds, showing that our immobilization procedure may be useful to develop catalytic materials with enhanced performance. Moreover, these catalysts can be recovered and reused for at least nine times without loss of activity or can be easily regenerated when their activity has decreased. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, …

ChemistryCatalyst supportOrganic ChemistryEnantioselective synthesisSettore CHIM/06 - Chimica OrganicaChemical synthesisCatalysisAldol reactionOrganocatalysisOrganic chemistryDipeptide Organocatalysis Prolinamide Proline Supported catalystAldol condensationStereoselectivityPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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HC-SCR of NOx over Ag/alumina: a combination of heterogeneous and homogeneous radical reactions?

2005

Matrix isolation combined with EPR and FT-IR technique at low temperature has been used to study the gas phase species involved in HC-SCR over a highly active Ag/alumina catalyst. A combination of heterogeneous and homogeneous (radical) reactions is proposed to take place over a Ag/alumina catalyst during HC-SCR. Radicals of low molecular weight were trapped in a growing argon matrix behind the Ag/alumina catalyst. In the same matrix, cyanogen isocyanate was detected and is suggested to be a key intermediate for the formation of amines and ammonia via the hydrolysis of isocyanate species.

ChemistryCyanogenRadicalCatalyst supportInorganic chemistryMatrix isolationGeneral ChemistryHeterogeneous catalysisIsocyanateCatalysisCatalysischemistry.chemical_compoundOrganic chemistryNOxCatalysis Today
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Gold catalysts supported on CeO2 and CeO2–Al2O3 for NO reduction by CO

2006

Abstract The reduction of NO x by CO was studied over gold catalyst supported on ceria and ceria–alumina. The mixed supports with different CeO 2 /Al 2 O 3 ratios were prepared by co-precipitation. The catalysts were characterized by means of XRD, TPR, XPS and Raman spectroscopy. The addition of alumina led to a slight enlargement of the gold particles, while the ceria particle size was decreased. Deeper oxygen vacancies formation in the presence of alumina was detected by TPR, XPS and Raman spectroscopy, compared to the pure ceria support. The samples exhibited a high and stable activity and 100% selectivity towards N 2 was reached at 200 °C.

ChemistryProcess Chemistry and TechnologyCatalyst supportInorganic chemistryHeterogeneous catalysisCatalysisCatalysischemistry.chemical_compoundsymbols.namesakeX-ray photoelectron spectroscopyTransition metalAluminium oxidesymbolsParticle sizeRaman spectroscopyGeneral Environmental ScienceApplied Catalysis B: Environmental
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Effect of silica-type sol–gel carrier’s structure and morphology on a supported Ziegler–Natta catalyst for ethylene polymerization

2006

Abstract Silica xerogels with different structures and morphology, synthesized using a sol–gel procedure, were used as a carrier of vanadium catalysts (VOCl 3 /AlEt 2 Cl) for ethylene polymerization. Two techniques of catalyst synthesis were applied: slurry impregnation and gas-phase adsorption and the relevant polymerization methods were then employed. The effect of the carrier structure and morphology on the vanadium loading in the catalysts, the catalyst’s activity and kinetic stability were investigated.

Ethylene polymerizationPolymers and PlasticsSilica gelCatalyst supportUHMWPEOrganic ChemistrySupported catalystsGeneral Physics and AstronomyVanadiumchemistry.chemical_elementSilicaPolyethyleneSol–gelCatalysischemistry.chemical_compoundchemistryPolymerizationPolymer chemistryMaterials ChemistryZiegler–Natta catalystSol-gelEuropean Polymer Journal
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Polymerization of ethylene by oxide-supported titanium halide catalyst: kinetic model with a deactivation of active species

2000

Abstract The effect of the calcination temperature of alumina, which was then used as a support for a titanium halide catalyst [TiCl4/Et2AlCl], on the catalyst activity in ethylene polymerization was investigated. α-Al2O3 was found to make a more advantageous catalyst support as compared to γ-Al2O3 despite the fact that the former offered a clearly lower specific surface area and its content of surface OH groups was inferior. The ethylene polymerization in the presence of the catalytic system on different alumina supports was investigated on the basis of a proposed kinetic model, taking into consideration the deactivation of active sites in the process. The improved activity was found to re…

EthylenePolymers and PlasticsCatalyst supportOrganic Chemistrytechnology industry and agriculturechemistry.chemical_elementPolymerization of ethyleneCatalysisTitanium chloridechemistry.chemical_compoundchemistryPolymerizationSpecific surface areaPolymer chemistryMaterials ChemistryTitanium Ziegler–Natta type catalystZiegler–Natta catalystOxide-type supportTitaniumPolymer
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