Search results for "Selective catalytic reduction"

showing 10 items of 17 documents

Catalytic reduction of nitrates and nitrites in water solution on pumice-supported Pd–Cu catalysts

2000

Abstract Two series of pumice-supported palladium and palladium–copper catalysts, prepared by impregnation with different palladium and copper precursors, were tested for the hydrogenation of aqueous nitrate and nitrite solutions. Measurements were performed in a stirred tank reactor, operating in batch conditions, in buffered water solution at atmospheric pressure and at 293 K. The activities of the catalysts were calculated in terms of nitrate and/or nitrite removal. With the monometallic Pd/pumice, the reduction of nitrite is highly selective; only 0.2% of the initial nitrite content is converted to ammonium ions. The activity in terms of turn over frequency (TOF) is higher as compared t…

Aqueous solutionProcess Chemistry and TechnologyInorganic chemistrychemistry.chemical_elementSelective catalytic reductionCopperCatalysisCatalysischemistry.chemical_compoundchemistryNitrateAmmoniumNitriteGeneral Environmental SciencePalladiumApplied Catalysis B: Environmental
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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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Efficient and rapid transformation of high silica CHA zeolite from FAU zeolite in the absence of water

2017

High silica CHA zeolite plays an important role in selective catalytic reduction of NOx with NH3 (NH3-SCR), but its synthesis is not highly efficient due to the use of a relatively high-cost structural directing agent (SDA) N,N,N-trimethyl-adamantammonium hydroxide (TMAdaOH) and relatively long crystallization time under hydrothermal conditions. Herein, we report an efficient and rapid synthesis of a high silica CHA zeolite possessing good crystallinity and uniform crystals (CHA-ST). The method includes interzeolite transformation of high silica FAU zeolite in the absence of water but the presence of zeolite seeds and a bromide form of the SDA. The absence of water in the synthesis signific…

ChabaziteMaterials scienceRenewable Energy Sustainability and the EnvironmentInorganic chemistrySelective catalytic reduction02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesCatalysislaw.inventionSSZ-13chemistry.chemical_compoundchemistryChemical engineeringBromidelawHydroxideGeneral Materials ScienceCrystallization0210 nano-technologyZeoliteJournal of Materials Chemistry A
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Reduction of ferricytochrome c catalyzed by optically active chromium(III) complexes

2009

The reduction rates of horse heart ferricytochrome c by amalgamated zinc or by electrolysis at fixed potential on a mercury pool as the cathode have been measured in a buffered solution at pH 7.5 by absorption spectrophotometry. In both cases, the reaction was strongly accelerated by the presence of the optically active complexes Lambda-[Cr(III)((S,S)-promp)H(2)O](+) (H(2)promp = N,N'-[(pyridine-2,6-diyl)bis(methylene)]-bis[(S)-proline]), Delta-[Cr(III)((R,R)-alamp)H(2)O](+) (H(2)alamp = N,N'-[(pyridine-2,6-diyl)bis(methylene)]-bis[(R)-alanine]) and Lambda-[Cr(III)((S,S)-alamp)(H(2)O)(2)](+). These were shown to undergo reversible one-electron reduction to the corresponding labile chromium(…

ChromiumModels MolecularAbsorption spectroscopyInorganic chemistrychemistry.chemical_elementZinc010402 general chemistryCrystallography X-Ray01 natural sciencesMedicinal chemistryCatalysislaw.inventionCatalysisInorganic ChemistryChromiumchemistry.chemical_compoundlawElectrochemistryOrganometallic CompoundsAnimals[CHIM.COOR]Chemical Sciences/Coordination chemistryHorsesPhysical and Theoretical ChemistryMethyleneComputingMilieux_MISCELLANEOUSElectrolysisMolecular Structure010405 organic chemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistryCytochromes cSelective catalytic reductionHeart0104 chemical sciences3. Good healthKineticschemistryCyclic voltammetryOxidation-Reduction
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Recent advances in the preparation of zeolites for the selective catalytic reduction of NOx in diesel engines

2019

Metal-exchanged zeolites with small pore sizes have attracted much attention in recent years due to their application in the selective catalytic reduction (SCR) of NOx in diesel engines. Typically, copper-chabazite (e.g. Cu-SSZ-13) has been gradually used as an SCR catalyst in heavy-duty diesel vehicles over the last decade due to its relatively excellent catalytic performance and stability. However, most SSZ-13 zeolites are still prepared via the traditional hydrothermal process in the presence of organic templates, requiring consecutive solid separation and thermal treatment steps to achieve the final zeolite products. In recent years, several strategies for the environmentally friendly p…

Fluid Flow and Transfer ProcessesDiesel fuelMaterials scienceChemical engineeringChemistry (miscellaneous)Process Chemistry and TechnologyChemical Engineering (miscellaneous)Selective catalytic reductionZeoliteEnvironmentally friendlyCatalysisNOxCatalysisReaction Chemistry & Engineering
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One‐Pot Synthesis of a New High‐Aluminium‐Content Super‐Microporous Aluminosilicate

2006

A new super-microporous aluminosilicate having a high aluminium content (Si/Al ca. 1) has been prepared through a surfactant-assisted procedure with the use of a commercially available binary precursor (di-sec-butoxyaluminooxytriethoxysilane) as a single source of both Al and Si. The formation of super-micropores is a result of a significant network shrinkage associated with the thermal elimination of the surfactant. This solid has been studied by X-ray powder diffraction, electron microscopy, nuclear magnetic resonance spectroscopy and porosimetry. A preliminary analysis of the acidity and the catalytic activity of the super-microporous solid for the selective catalytic reduction of NOx is…

Inorganic ChemistrychemistryChemical engineeringAluminosilicateAluminiumOne-pot synthesischemistry.chemical_elementOrganic chemistrySelective catalytic reductionMicroporous materialPorosimetryPowder diffractionCatalysisEuropean Journal of Inorganic Chemistry
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Rare-earth ion exchanged Cu-SSZ-13 zeolite from organotemplate-free synthesis with enhanced hydrothermal stability in NH3-SCR of NOx

2019

The relatively low hydrothermal stability of Al-rich Cu-SSZ-13 catalysts hinders their practical application in ammonia selective catalytic reduction (NH3-SCR) reaction. Rare-earth ions were introduced into the Al-rich SSZ-13 zeolite using an organotemplate-free synthesis prior to the exchange of Cu2+ ions. Among the rare-earth ions tested (Ce, La, Sm, Y, Yb), Y shows significant enhancement of the hydrothermal stability and NH3-SCR activities after severe hydrothermal aging at 800 °C for 16 h when compared with Cu-SSZ-13 without Y. Cu–Y-SSZ-13 catalysts with various amounts of Y were prepared, and it is found that with increasing Y content, the low temperature NO conversions can be improve…

Materials science010405 organic chemistryInorganic chemistryInfrared spectroscopySelective catalytic reduction010402 general chemistry01 natural sciencesCatalysisHydrothermal circulation0104 chemical sciencesCatalysisSSZ-13AdsorptionTemperature-programmed reductionZeoliteCatalysis Science & Technology
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Highly Active Hydrogenation Catalysts Based on Pd Nanoparticles Dispersed along Hierarchical Porous Silica Covered with Polydopamine as Interfacial G…

2020

New catalysts based on Pd(0) nanoparticles (Pd NPs) on a bimodal porous silica of the UVM-7/polydopamine (PDA) support have been synthesized following two preparative strategies based on the sequential or joint incorporation of two components of the composite (Pd and PDA). We analyzed the role played by the PDA as &lsquo

Materials scienceCatalitzadorsComposite numberbimodal porositychemistry.chemical_elementNanoparticle02 engineering and technologylcsh:Chemical technology010402 general chemistry01 natural sciencesCatalysis4-nitrophenolCatalysislcsh:Chemistrychemistry.chemical_compoundlcsh:TP1-1185mesoporous silicaPhysical and Theoretical ChemistrypolydopamineSubstrate (chemistry)Selective catalytic reduction4-NitrophenolMesoporous silicapalladium021001 nanoscience & nanotechnology0104 chemical scienceslcsh:QD1-999chemistryChemical engineeringcatalytic reductionnanoparticlesMaterials nanoestructurats0210 nano-technologyPalladiumCatalysts
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A new approach for crystallization of copper(II) oxide hollow nanostructures with superior catalytic and magnetic response.

2015

We report the synthesis of copper(II) oxide hollow nanostructures at ambient pressure and close to room temperature by applying the soft templating effect provided by the confinement of droplets in miniemulsion systems. Particle growth can be explained by considering a mechanism that involves both diffusion and reaction control. The catalytic reduction of p-nitrophenol in aqueous media is used as a model reaction to prove the catalytic activity of the materials: the synthesized hollow structures show nearly 100 times higher rate constants than solid CuO microspheres. The kinetic behavior and the order of the reduction reaction change due to the increase of the surface area of the hollow str…

Materials scienceOxidechemistry.chemical_elementNanotechnologySelective catalytic reductionCopperlaw.inventionCopper(II) oxideCatalysisMiniemulsionchemistry.chemical_compoundReaction rate constantchemistryChemical engineeringlawGeneral Materials ScienceCrystallizationNanoscale
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Biomimetic oxygen reduction by cofacial porphyrins at a liquid-liquid interface.

2012

Oxygen reduction catalyzed by cofacial metalloporphyrins at the 1,2-dichlorobenzene−water interface was studied with two lipophilic electron donors of similar driving force, 1,1'-dimethylferrocene (DMFc) and tetrathiafulvalene (TTF). The reaction produces mainly water and some hydrogen peroxide, but the mediator has a significant effect on the selectivity, as DMFc and the porphyrins themselves catalyze the decomposition and the further reduction of hydrogen peroxide. Density functional theory calculations indicate that the biscobaltporphyr- in, 4,5-bis(5-(2,8,13,17-tetraethyl-3,7,12,18-tetramethylporphyrinyl))-9,9-dimethylxanthene, Co2(DPX), actually catalyzes oxygen reduction to hydrogen p…

Models MolecularPorphyrinsMolecular Conformationchemistry.chemical_element02 engineering and technology010402 general chemistryPhotochemistry01 natural sciencesBiochemistryOxygenCatalysisCatalysisElectron Transportchemistry.chemical_compoundColloid and Surface ChemistryBiomimeticsHeterocyclic CompoundsMoleculePerchloric acidFerrous CompoundsHydrogen peroxideta116ElectrodesSelective catalytic reductionGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesOxygenchemistryQuantum Theory0210 nano-technologySelectivityHydrophobic and Hydrophilic InteractionsTetrathiafulvaleneJournal of the American Chemical Society
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