Search results for " catalysts"

showing 10 items of 99 documents

Influence of SMSI effect on the catalytic activity of a Pt(1%)/ Ce0.6Zr0.4O2 catalyst: SAXS, XRD, XPS and TPR investigations

2004

Abstract The steady-state activity of NO reduction by C3H6, in lean conditions, was studied on a Pt(1%)/Ce0.6Zr0.4O2 catalyst, in a plug-flow reactor, in the temperature range 100–500 °C. The influence of reductive pre-treatments on the catalytic performance at low temperature (250 °C) was investigated. Enhancement of the activity was found for the catalyst pre-treated in hydrogen at 350 °C as compared to the sample pre-treated in H2 at 800 and 1050 °C. Moreover, transient reactivity tests of NO reduction by hydrogen were also carried out. As previously observed, the sample reduced at 350 °C was the most active catalyst. In both types of reactions the temperature and the nature of pre-treat…

HydrogenProcess Chemistry and TechnologyReducing atmosphereInorganic chemistryAnalytical chemistrychemistry.chemical_elementAtmospheric temperature rangeCatalysisCatalysischemistryTransition metalX-ray photoelectron spectroscopyTemperature-programmed reductionPlatinumCerium compounds Catalysts capacity OSCGeneral Environmental Science
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DESIGN OF NOVEL IMIDAZOLIUM BASED NANOSTRUCTURES FOR SUSTAINABLE CATALYTIC APPLICATIONS

Imidazolium SaltHeterogeneous CatalystsCarbon Dioxide ConversionSettore CHIM/06 - Chimica OrganicaPolyhedral Oligomeric SilsesquioxaneCarbon NanostructureC-C CouplingPalladium
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Ziegler–Natta catalysts based on vanadium halides: a DFT study

2003

Abstract Ziegler–Natta ethylene insertion into the carbon–metal bond for a number of fragments containing vanadium on different oxidation states as well as the halogen ligands has been studied by means of DFT. It is shown that the complexation and insertion energies are strongly influenced by the charge on the transition metal atom and, to some extent, by the electronegativity of the halogen atom. Complexation energy varies in the range −129 to −159 kJ/mol for charged species and −64 to −77 kJ/mol for neutral ones. Insertion energy follows a similar pattern and ranges from −28 to −62 and −82 to −100 kJ/mol, respectively. The calculated values are compared with the experimental results and d…

Inorganic chemistryHalideVanadiumchemistry.chemical_elementVanadiumGeneral ChemistryDFTCatalysisTransition stateCatalysisElectronegativityTransition metalchemistryolefin polymerisationHalogenPhysical chemistryZiegler–Natta catalystsZiegler–Natta catalystCatalysis Today
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Highly Loaded Multi-Walled Carbon Nanotubes Non-Covalently Modified with a Bis-Imidazolium Salt and their Use as Catalyst Supports

2016

The surfaces of multi-walled carbon nanotubes (MWCNTs) were non-covalently modified using two bis-imidazolium dibromide derivatives having phenyl or pyrene groups. Due to the presence of the two pyrene groups the bis(pyren-1-ylmethylimidazolium) dibromide derivative was immobilised at a loading of about 15-16 wt %, whereas only <3 wt % of the phenyl derivative was immobilised. The presence of the two imidazolium cations helped the immobilisation of tetrachloropalladate ions after exchange with bromide ions. Tetrachloropalladate was used as pre-catalyst in several Suzuki-Miyaura carbon-carbon cross-coupling reactions in water or water/ethanol at 50 °C in only 0.1 mol % and compared with the …

Inorganic chemistrySalt (chemistry)supported catalyst02 engineering and technologyCarbon nanotube010402 general chemistryHeterogeneous catalysis01 natural sciencessupramolecular chemistryCatalysislaw.inventionnanotubeschemistry.chemical_compoundlawPhenylboronic acidsupported catalystschemistry.chemical_classificationChemistryChemistry (all)General ChemistrySettore CHIM/06 - Chimica Organica021001 nanoscience & nanotechnology0104 chemical sciencesheterogeneous catalysisCovalent bondnanotubePyreneheterogeneous catalysiCarbon nanotube supported catalystC-C coupling0210 nano-technologyNuclear chemistry
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Synergetic effect of gold in Au/Pd catalysts during hydrodesulfurization reactions of model compounds

2003

Abstract The simultaneous formation of colloidal dispersions of Pd and Au metal particles protected by the organic polymer polyvinylpyrrolidone (PVP) in reducing alcohol solution was used for the synthesis of new silica-supported monometallic and bimetallic Au x Pd y catalysts with different x / y ratios. The samples, with a 2 wt% total metal loading, after air calcinations at 673 K to remove the PVP, were characterized by X-ray diffraction, X-ray photoelectron spectroscopy, and FTIR spectra of chemisorbed CO. Formation of alloyed Au x Pd y particles of different metal composition with consequent modification of their electronic and geometric properties was ascertained. The catalytic activi…

Inorganic chemistrychemistry.chemical_elementCatalysisCatalysisMetalchemistry.chemical_compoundAu-Pd catalysts; Polyvinylpyrrolidone; Hydrodesulfurization; HDS; Thiophene; DibenzothiophenechemistryTransition metalDibenzothiophenevisual_artThiophenevisual_art.visual_art_mediumPhysical and Theoretical ChemistryBimetallic stripHydrodesulfurizationPalladiumJournal of Catalysis
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The importance of supramolecular reaction media in catalysis

Ionic liquids supramolecular gels ionogels chiral catalysts
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Energy and environmental assessment of powder and structured Ni/GDC catalysts

2019

Power -to-Gas technologies have been recently introduced as a relevant strategy allowing higher shares of renewable generation in the energy sector

LCA Energy and environmental assessment Ni/GDC catalysts decarbonization power to gas
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Gas-phase hydrogenation of propionitrile on copper-lanthanide oxides

2009

Abstract The hydrogenation of propionitrile on copper-lanthanide oxide catalysts (2Cu·CeO 2 and 4Cu·Ln 2 O 3 (Ln = La, Pr, Nd)) was studied in the gas phase. The activity of the catalysts varies with the lanthanide in the order 2Cu·CeO 2  > 4Cu·Pr 2 O 3  > 4Cu·La 2 O 3  ≥ 4Cu·Nd 2 O 3 , while the activation energies varies in the opposite order, except for 2Cu·CeO 2 . The main product was the primary amine, n -propylamine. The formation of the unstable imine CH 3 CH 2 N CHCH 3 as a major product over 2Cu·CeO 2 seems to be consistent with the acidity of the catalyst. The catalysts were more selective than conventional copper impregnation catalysts, Cu (10 wt.%) on SiO 2 , La 2 O 3 or CeO 2 ,…

LanthanideCopper oxideInorganic chemistryImineprimary aminechemistry.chemical_element010402 general chemistryHeterogeneous catalysis01 natural sciencesCatalysisCatalysischemistry.chemical_compound[ CHIM.CATA ] Chemical Sciences/Catalysisgas-phase hydrogenationPhysical and Theoretical Chemistrysupported catalystsComputingMilieux_MISCELLANEOUS010405 organic chemistryProcess Chemistry and Technologypropionitrile[CHIM.CATA]Chemical Sciences/CatalysisCopper0104 chemical scienceschemistrycopperAmine gas treatingPropionitrile
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Di- and Tetrairon(III) μ-Oxido Complexes of an N3S-Donor Ligand: Catalyst Precursors for Alkene Oxidations

2019

The new di- and tetranuclear Fe(III) μ-oxido complexes [Fe 4 (μ-O) 4 (PTEBIA) 4 ](CF 3 SO 3 ) 4 (CH 3 CN) 2 ] (1a), [Fe 2 (μ-O)Cl 2 (PTEBIA) 2 ](CF 3 SO 3 ) 2 (1b), and [Fe 2 (μ-O)(HCOO) 2 (PTEBIA) 2 ](ClO 4 ) 2 (MeOH) (2) were prepared from the sulfur-containing ligand (2-((2,4-dimethylphenyl)thio)-N,N-bis ((1-methyl-benzimidazol-2-yl)methyl)ethanamine (PTEBIA). The tetrairon complex 1a features four μ-oxido bridges, while in dinuclear 1b, the sulfur moiety of the ligand occupies one of the six coordination sites of each Fe(III) ion with a long Fe-S distance of 2.814(6) A. In 2, two Fe(III) centers are bridged by one oxido and two formate units, the latter likely formed by methanol oxidati…

MECHANISMFe-S interactionoxidation116 Chemical sciencesThio-rautaSULFURHomogeneous catalysis02 engineering and technology010402 general chemistry01 natural sciencesMedicinal chemistrythioetherCatalysislcsh:Chemistrychemistry.chemical_compoundThioetheriron-oxo complexAcetonitrileta116Fe-S interaction; homogeneous catalysis; iron-oxo complex; oxidation; thioetherOriginal Researchchemistry.chemical_classificationeetteritFUNCTIONAL-MODELCOORDINATIONPEROXIDEAlkeneLigandACTIVE-SITEhapettuminenGeneral Chemistrykompleksiyhdisteet021001 nanoscience & nanotechnology540COPPER-COMPLEXEShomogeneous catalysis0104 chemical sciencesChemistrychemistrylcsh:QD1-999katalyysiACIDOXO0210 nano-technologySelectivityNONHEME IRON CATALYSTSFrontiers in Chemistry
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Robust Mesoporous CoMo/γ-Al2O3 Catalysts from Cyclodextrin-Based Supramolecular Assemblies for Hydrothermal Processing of Microalgae: Effect of the P…

2018

Hydrothermal liquefaction (HTL) is a promising technology for the production of biocrude oil from microalgae. Although this catalyst-free technology is efficient under high-temperature and high-pressure conditions, the biocrude yield and quality can be further improved by using heterogeneous catalysts. The design of robust catalysts that preserve their performance under hydrothermal conditions will be therefore very important in the development of biorefinery technologies. In this work, we describe two different synthetic routes (i.e., impregnation and cyclodextrin-assisted one-pot colloidal approach), for the preparation in aqueous phase of six high surface area CoMo/γ-Al2O3 catalysts. Cat…

Materials science02 engineering and technology010402 general chemistrybiocrude01 natural sciencesHydrothermal circulationCatalysisCopolymer[CHIM]Chemical SciencesGeneral Materials ScienceComputingMilieux_MISCELLANEOUSbiocrude; cyclodextrin; heterogeneous catalysts; hydrothermal liquefaction; microalgaeheterogeneous catalystsmicroalgaeheterogeneous catalystAqueous two-phase systemhydrothermal liquefaction[CHIM.CATA]Chemical Sciences/CatalysisSettore ING-IND/27 - Chimica Industriale E Tecnologica021001 nanoscience & nanotechnologyBiorefinery0104 chemical sciencesHydrothermal liquefactioncyclodextrinChemical engineeringYield (chemistry)Materials Science (all)0210 nano-technologyMesoporous materialACS Applied Materials &amp; Interfaces
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