Search results for "HETEROGENEOUS CATALYSIS"
showing 10 items of 233 documents
Steam-activated FeMFI zeolites. Evolution of iron species and activity in direct N2O decomposition
2003
Abstract In this paper the effect of the composition and steaming conditions of FeMFI catalysts on activity in direct N2O decomposition is investigated. MFI zeolites with different framework compositions (FeAlSi, FeGaSi, and FeSi) and without iron ( 100 mbar H2O in N2) favor the extraction of framework iron, enabling the application of lower activation temperatures. The optimum temperature during steam activation is that at which extraction of framework iron is complete without extensive clustering of extra-framework iron species into oxide particles, as was demonstrated by transmission electron microscopy and electrochemical characterization of the samples. Additional experiments show…
Influence of the preparation method on the thiophene HDS activity of silica supported CoMo catalysts
2002
Abstract The effect of the preparation method of CoMo/SiO2 catalysts with and without sodium ions, on the hydrodesulfurization (HDS) of thiophene was investigated by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and N2 physisorption (BET). The samples were prepared by total sol–gel route, by classic wetness impregnation and by co-impregnation, in the presence of nitrilotriacetic acid (NTA), of commercial and sol–gel prepared silica. The influence of sodium ions added to the sol mixture and to the silica before the impregnation with Co and Mo salt solution, was also considered. The presence of sodium favoured the phase transition of amorphous silica to cristobalite with con…
Selective Gold Recovery and Catalysis in a Highly Flexible Methionine-Decorated Metal–Organic Framework
2016
A novel chiral 3D bioMOF exhibiting functional channels with thio-alkyl chains derived from the natural amino acid l-methionine (1) has been rationally prepared. The well-known strong affinity of gold for sulfur derivatives, together with the extremely high flexibility of the thioether "arms" decorating the channels, account for a selective capture of gold(III) and gold(I) salts in the presence of other metal cations typically found in electronic wastes. The X-ray single-crystal structures of the different gold adsorbates Au(III)@1 and Au(I)@1 suggest that the selective metal capture occurs in a metal ion recognition process somehow mimicking what happens in biological systems and protein r…
Templating effect of carbon nanoforms on highly cross-linked imidazolium network: Catalytic activity of the resulting hybrids with Pd nanoparticles
2019
Two different carbon nanoforms (CNFs), namely multi-walled carbon nanotubes (MWCNTs) and carbon nanohorns (CNHs), have been chosen as support for the direct polymerization of a bis-vinylimidazolium salt. Transmission electron microscopy analyses revealed a templating effect of the CNFs on the growth of the polymeric network, which perfectly covers their whole surfaces creating a cylindrical or spherical coating for MWCNTs and CNHs, respectively. Subsequently, the CNFs-polyimidazolium have been used as stabilizers for Pd nanoparticles (Pd NPs), and the obtained materials have been characterized by means of analytical and spectroscopic techniques and then employed as easily recoverable and re…
Palladium-based catalytic systems for the synthesis of conjugated enynes by Sonogashira reactions and related alkynylations
2007
Conjugated alkynes are recurring building blocks in natural products, a wide range of industrial intermediates, pharmaceuticals and agrochemicals, and molecular materials for optics and electronics. The palladium-catalyzed cross-coupling between sp(2)-hybridized carbon atoms of aryl, heteroaryl, and vinyl halides with sp-hybridized carbon atoms of terminal acetylenes is one of the most important developments in the field of alkyne chemistry over the past 50 years. The seminal work of the 1970s has initiated an intense search for more general and reliable reaction conditions. The interest in the catalytic activation of demanding substrates, the need to minimize the consumption of depletive r…
“Supported Co3O4-CeO2 monoliths: effect of preparation method and Pd-Pt promotion on the CO/CH4 oxidation activity”
2006
Abstract Two structured composite oxides, Co3O4(30wt%)-CeO2(70wt%), have been prepared by washcoating commercial cordierite monoliths with a CeO2-γAl2O3 layer, on which the active phase Co3O4-CeO2 was added through two different methods: dip-coating from a suspension containing the preformed active oxide or impregnation with a solution of the cobalt and cerium precursors. Morphological characterizations of the monoliths have been performed by BET, and SEM-EDAX analyses. Electronic and reduction properties have been evaluated by XPS and H2-TPR, respectively. The effect of the preparation method has been investigated in the catalytic oxidation of CO, whereas the promotion by a low content of …
Escaping scaling relationships for water dissociation at interfacial sites of zirconia-supported Rh and Pt clusters
2019
<p>Water dissociation is an important reaction involved in many industrial processes and a good model reaction for probing the activity of catalytic sites. In this computational study, the dissociation of water at interfacial sites of globally optimized ZrO2 sup- ported Pt and Rh clusters is investigated under the framework of density functional theory. Our findings demonstrate that the perimeter sites of these small clusters can activate water, but the dissociation behavior varies considerably between sites. It is shown that the studied clusters break scaling relationships for water dissociation, suggesting these catalysts may achieve activities beyond the maximum imposed by such rel…
Reduction and catalytic behaviour of heterobimetallic copper–lanthanide oxides
2008
Abstract The reduction of the heterobimetallic copper–lanthanide oxides 2CuO·CeO2 and 3CuO·Ln2CuO4 (Ln = La, Pr, Nd) was studied by H2-TG/DTA and H2-TPR. All systems exhibit two main reduction steps accompanied by mass losses in the temperature range 20–1000 °C. The first step was attributed to CuO reduction, whereas the second step is due either to copper reduction in the Ln2CuO4 phase with the concomitant formation of Ln2O3 or to the surface reduction of CeO2. The products were characterized by XRD, SEM, EDX, and BET techniques and are better described as supported copper type materials. They were active for the mesityl oxide (4-methyl-2-penten-2-one) gas phase hydrogenation.
COMPUTATIONAL APPROACHES EMPLOYED IN THE SusFuelCat PROJECT
2013
Elementary steps in heterogeneous catalysis: The basis for environmental chemistry
2017
Kataliza stała się obecnie alternatywnym sposobem na natychmiastowe tworzenie produktu chemicznego z uwagi na niższą barierę energetyczną (między cząsteczkami a katalizatorami). Kataliza heterogenna obejmuje przyspieszenie reakcji chemicznej poprzez oddziaływanie cząsteczek związanych z powierzchnią ciała stałego. Jest to dyscyplina, która obejmuje różne aspekty chemii: chemię nieorganiczną i analityczną w celu scharakteryzowania katalizatorów i form tych katalizatorów. Chemia przemysłowa następnie łączy te wszystkie zagadnienia razem, aby zrozumieć chemiczną manipulację ciał stałych, reakcję chemiczną i inżynierię energetyczną oraz przenoszenie ciepła i masy w tych procesach katalitycznych…