Search results for "LYST"

showing 10 items of 904 documents

Heterogeneous Photocatalysis for Selective Formation of High-Value-Added Molecules: Some Chemical and Engineering Aspects

2018

This review deals with the parameters that influence heterogeneous photocatalysis (PC) for selective synthesis of high-value chemicals by itself or in combination with other technologies. In particular, the parameters related to the photocatalysts, such as crystallinity degree, type of polymorph, surface acid-base properties, exposure of particular crystalline facets, coupling of different semiconductors, position of the valence and conduction band edge, addition of doping agents, and those related to the reaction system, such as setup configuration and reactor geometry, type of solvent, type and amount of photocatalyst, affecting the selectivity toward specific products are described and d…

high value-added chemicals; photocatalyst features; reactor configuration optimization; selective photocatalysis; selectivity enhancement; Catalysis; Chemistry (all)selectivity enhancement02 engineering and technology010402 general chemistry01 natural sciencesCatalysisCatalysisCatalysiMoleculeselective photocatalysihigh value-added chemicalsphotocatalyst featuresSettore ING-IND/24 - Principi Di Ingegneria Chimicareactor configuration optimizationselective photocatalysisChemistryChemistry (all)General Chemistry021001 nanoscience & nanotechnologyphotocatalyst feature0104 chemical sciencesChemical engineeringPhotocatalysisSettore CHIM/07 - Fondamenti Chimici Delle Tecnologie0210 nano-technologyhigh value-added chemical
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Influence of a Cu–zirconia interface structure on CO2 adsorption and activation

2021

CO2 adsorption and activation on a catalyst are key elementary steps for CO2 conversion to various valuable products. In the present computational study, we screened different Cu–ZrO2 interface structures and analyzed the influence of the interface structure on CO2 binding strength using density functional theory calculations. Our results demonstrate that a Cu nanorod favors one position on both tetragonal and monoclinic ZrO2 surfaces, where the bottom Cu atoms are placed close to the lattice oxygens. In agreement with previous calculations, we find that CO2 prefers a bent bidentate configuration at the Cu–ZrO2 interface and the molecule is clearly activated being negatively charged. Strain…

hiilidioksidiinterface propertiestiheysfunktionaaliteoriazirkoniumoksidikuparikatalyytittermodynamiikkathermodynamic cyclesnanoparticlesnanohiukkasetnanorodsadsorptiohiilidioksidin talteenotto ja varastointidensity functional theorycatalysts and catalysis
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Highly Active and Stable NiCuMo Electrocatalyst Supported on 304 Stainless Steel Porous Transport Layer for Hydrogen Evolution in Alkaline Water Elec…

2023

Several functionalized porous transport layers with Pt-free electrocatalysts for hydrogen evolution reaction in alkaline conditions, based on Ni, Cu, and Mo, are prepared through electrodeposition onto a 304 stainless steel mesh. Morphological characterization confirms the fabrication of electrodes with high electrochemical surface active area due to the formation of hierarchical nanostructures. Mo presence into the electrocatalysts increases the activity toward the hydrogen evolution reaction. The optimization of electrodeposition process leads to the preparation of highly active NiCuMo electrocatalyst that exhibits near zero onset overpotential and overpotentials of 15 and 113 mV at 10 an…

hydrogen evolutionSettore ING-IND/23 - Chimica Fisica ApplicataPt-free electrocatalystsRenewable Energy Sustainability and the Environmentelectrocatalysisalkaline electrolyzersporous transport layersGeneral Environmental Science
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Characterization of Cobalt Catalysts on Biomass-Derived Carbon Supports

2017

Cobalt catalysts are known to have a high activity and selectivity in the Fischer–Tropsch reaction converting synthesis gas to higher hydrocarbons (C5+). These catalysts have been supported by different porous materials. Porous carbon materials like activated carbon (AC) have physical and chemical surface properties that affect the preparation of supported metal catalysts and can easily be tailored. In this study, AC was produced by carbonization and steam activation of lignin, a waste fraction from the Kraft pulping process. A series of Co/AC-catalysts was produced and characterized by several techniques. According to the results, tailored properties (high surface area, mesoporosity) were …

inorganic chemicalsActivated carbonaktiivihiilicharacterizationCobaltSupportkobolttikannatuscatalyst
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Cross-Linked Imidazolium Salts as Scavengers for Palladium.

2014

Five imidazolium-based materials have been synthesised and used for the first time as palladium scavengers. Radical reactions of suitable bis-vinylimidazolium salts led to a series of insoluble materials through homo-polymerisation, immobilisation with a 3-mercaptopropyl-modified silica gel or co-polymerisation with ethylene glycol dimethylacrylate. These materials were screened as palladium scavengers with a set of palladium(0) and palladium(II) compounds in different solvents and at different starting amounts of palladium. In many cases, residual amounts of palladium were lower than 5 ppm, as requested for the manufacture of active pharmaceutical ingredients and fine chemicals. The applic…

inorganic chemicalsActive ingredientSilica gelchemistry.chemical_elementGeneral ChemistrySettore CHIM/06 - Chimica OrganicaScavenger (chemistry)chemistry.chemical_compoundchemistrySuzuki reactionIonic liquidOrganic chemistryEthylene glycolcross-coupling imidazolium salts ionic liquids palladium supported catalystsPalladiumChemPlusChem
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Dual stereocontrolled alkylation of aldehydes with polystyrene-supported nickel complexes derived from α-amino amides

2015

Nickel(II) complexes derived from α-amino amide ligands anchored to gel-type and monolithic polymers act as efficient catalysts for the enantioselective addition of dialkylzinc reagents to aldehydes. Similar to the analogous homogeneous systems, dual stereocontrol in addition products can be achieved by controlling the stoichiometry of the immobilized nickel complex. Aromatic and aliphatic aldehydes were alkylated in good yields with enantioselectivities comparable to those obtained with the homogeneous analogues. These polymer-supported catalysts offer significant advantages as no metal leaching is observed and they can be easily recovered from the reaction mixture by simple filtration and…

inorganic chemicalsAldehydesCatalystsGeneral Chemical EngineeringPolymer supported catalystsEnantioselective synthesischemistry.chemical_elementEnantioselectivityGeneral ChemistryAlkylationAmidesCatalysischemistry.chemical_compoundNickelchemistryCatàlisiNickelAmideReagentOrganic chemistryPolystyreneQuímica orgànicaStoichiometry
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A new application for nickel foam in alkaline fuel cells

2009

The use of nickel foam as an electrode substrate in alkaline fuel cells (AFCs) has been investigated for bi-polar cells incorporating an electrically conducting gas diffusion layer. This contribution focuses on the cathode, and draws comparisons between nickel foam and nickel mesh substrates. One of the principal electrocatalysts for the cathodic reduction of oxygen is silver, so an improvement in electrochemical performance was obtained by electroplating the nickel foam with silver. The electrodeposition process was optimised to maximise electrochemical performance with a minimum of silver deposited. Nickel foam, which is less expensive than the usual nickel mesh, appears to be a good subs…

inorganic chemicalsAlkaline fuel cellGas diffusion electrodeRenewable Energy Sustainability and the EnvironmentGraphene foamMetallurgyEnergy Engineering and Power Technologychemistry.chemical_elementCondensed Matter PhysicsElectrochemistryElectrocatalystNickelFuel TechnologychemistryChemical engineeringElectrodeotorhinolaryngologic diseasesElectroplatingInternational Journal of Hydrogen Energy
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TAP reactor study of the deep oxidation of propane using cobalt oxide and gold-containing cobalt oxide catalysts

2009

Abstract A transient reactor study of the oxidation of propane to CO 2 on gold-free and gold-doped CoO x catalysts has been carried out. It has been demonstrated that the presence of gold markedly promotes the catalytic reactivity of cobalt oxide in the total oxidation of propane. Both catalysts oxidised propane directly to CO 2 via a Mars–Van Krevelen mechanism, and this was confirmed using isotopically labelled oxygen experiments. The increased activity of the gold catalyst is related to the faster reoxidation of the cobalt oxide when gold is present in the catalyst, since the reaction step in which the catalyst is reduced, due to propane oxidation, is similar for both catalysts. The fast…

inorganic chemicalsChemistryorganic chemicalsProcess Chemistry and TechnologyCatalyst supportInorganic chemistrychemistry.chemical_elementHeterogeneous catalysisOxygenCatalysisCatalysischemistry.chemical_compoundCatalytic oxidationTransition metalPropaneheterocyclic compoundsCobalt oxideApplied Catalysis A: General
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Enhanced Heterogeneous Catalytic Conversion of Furfuryl Alcohol into Butyl Levulinate

2014

We study the catalytic condensation of furfuryl alcohol with 1-butanol to butyl levulinate. A screening of several commercial and as-synthesized solid acid catalysts shows that propylsulfonic acid-functionalized mesoporous silica outperforms the state-of-the-art phosphotungstate acid catalysts. The catalyst is prepared via template-assisted sol-gel polycondensation of TEOS and MPTMS. It gives 96 % yield (and 100 % selectivity) of butyl levulinate in 4h at 110 °C. Reaction profiles before and after a hot filtration test confirm that the active catalytic species do not leach into the solution. The catalyst synthesis, characterization, and mode of operation are presented and discussed. Sour ca…

inorganic chemicalsCondensation polymerGeneral Chemical EngineeringesterificationNiobiumHeterogeneous catalysisCatalysisCatalysisFurfuryl alcoholalcoholschemistry.chemical_compoundEnvironmental ChemistryOrganic chemistryGeneral Materials ScienceFuransbiomassorganic chemicalsCondensationMesoporous silicasolid acidsSilicon DioxideLevulinic AcidsGeneral Energyheterogeneous catalysischemistryYield (chemistry)ZeolitesPolystyrenesSulfonic AcidsSelectivityChemSusChem
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The reduction of molecular oxygen by iron porphyrins

2002

Abstract Molecular assemblies have been synthesised to reproduce the structure of the cytochrome c oxidase (C c O) active site and to explore the roles played by its different features. It was discovered that a single iron porphyrin, adsorbed at the surface of a graphite electrode, is a selective catalyst for the four-electron reduction of dioxygen to water, at pH 7. To cite this article: D. Ricard et al., C. R. Chimie 5 (2002) 33–36

inorganic chemicalsCytochromebiology010405 organic chemistryGeneral Chemical EngineeringInorganic chemistryActive sitechemistry.chemical_elementGeneral Chemistry010402 general chemistryElectrochemistryElectrocatalyst01 natural sciencesPorphyrinOxygen[ CHIM ] Chemical Sciences0104 chemical scienceschemistry.chemical_compoundchemistryPolymer chemistry[CHIM] Chemical Sciencesbiology.proteinCytochrome c oxidase[CHIM]Chemical SciencesGraphite
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