Search results for "dehydrogenation"

Oxidative dehydrogenation of n-butane on MgO-supported vanadium oxide catalysts

1998

Abstract Vanadium–magnesium oxide (VMgO) catalysts have been prepared, characterized and tested in the ODH of n-butane. The catalysts were prepared by two variations of the wet-impregnation method using aqueous ammonium metavanadate or organically-based methanolic vanadyl acetylacetonate solutions. The catalyst surface area depends on the vanadium content and the preparation method. Catalyst characterization (i.e. XRD, 51V NMR, FTIR, LRS) results indicate the presence of poor crystalline Mg-orthovanadate (Mg3V2O8), while the presence of other Mg-vanadates is not clear. Oxygen isotopic-exchange experiments on VMgO catalysts indicate an R2 process: [ 18 O 2 +2 16 O 2− (s) → ( 18 O 18 O 16 O 1…

Selective Oxidation of n-Butane and Butenes over Vanadium-Containing Catalysts

2000

Abstract The oxidative dehydrogenation (OXDH) of n-butane, 1-butene, and trans-2-butene on different vanadia catalysts has been compared. MgO, alumina, and Mg–Al mixed oxides with Mg/(Al+Mg) ratios of 0.25 and 0.75 were used as supports. The catalytic data indicate that the higher the acid character of catalysts the lower is both the selectivity to C4-olefins from n-butane and the selectivity to butadiene from both 1-butene or trans-2-butene. Thus, OXDH reactions are mainly observed from n-butane and butenes on basic catalysts. The different catalytic performance of both types of catalysts is a consequence of the isomerization of olefins on acid sites, which appears to be a competitive reac…

Enzymatic and pharmacokinetic studies on the metabolism of branched chain alpha-keto acids in the rat.

1983

Michaelis-constants and enzyme activities for dehydrogenation and transamination of the three branched chain alpha-keto acids in liver, kidney, skeletal muscle, and brain of rats are reported. After oral load only 11-22% of the keto acids pass the liver unchanged. Blood levels in pharmacokinetic and absorption studies are related to the Michaelis-constants. At the low keto-acid concentrations after oral application, dehydrogenation in the non-hepatic tissues is supposed to prevail over transamination. Data on feed efficiency of branched chain alpha-keto acids reported in the literature support this view. The chance for transamination is better after intravenous administration. The transfera…

Metal‐ and Reagent‐Free Anodic Dehydrogenative Cross‐Coupling of Naphthylamines with Phenols

2018

Oxidative dehydrogenation of ethane on Te-containing MoVNbO catalysts

2004

Abstract Ethylene has selectively been obtained during the oxidative dehydrogenation of ethane on a Mo–V–Te–Nb–O mixed oxide catalyst. The catalyst was prepared hydrothermally and heat-treated at 600 °C for 2 h in a N2-stream. For comparison, undoped and Te-doped Mo–V–Nb–O catalysts and Mo–V–Te–O and Mo–Te–Nb–O mixed oxides have also been prepared. The catalytic performance of the Mo–V–Nb–Te–O mixed oxide catalyst cannot be explained by the incorporation of Te on the surface of a Mo–V–Nb–O mixed oxide but by the presence of an orthorhombic Te2M20O57 (M=Mo, V, Nb) crystalline phase. The role of tellurium in these catalysts is also discussed.

Polycyclic aromatic chains on metals and insulating layers by repetitive [3+2] cycloadditions

2020

The vast potential of organic materials for electronic, optoelectronic and spintronic devices entails substantial interest in the fabrication of π-conjugated systems with tailored functionality directly at insulating interfaces. On-surface fabrication of such materials on non-metal surfaces remains to be demonstrated with high yield and selectivity. Here we present the synthesis of polyaromatic chains on metallic substrates, insulating layers, and in the solid state. Scanning probe microscopy shows the formation of azaullazine repeating units on Au(111), Ag(111), and h-BN/Cu(111), stemming from intermolecular homo-coupling via cycloaddition reactions of CN-substituted polycyclic aromatic az…

The Hydrogen‐Storage Challenge: Nanoparticles for Metal‐Catalyzed Ammonia Borane Dehydrogenation

2021

International audience; Dihydrogen is one of the sustainable energy vectors envisioned for the future. However, the rapidly reversible and secure storage of large quantities of hydrogen is still a technological and scientific challenge. In this context, this review proposes a recent state-of-the-art on H 2 production capacities from the dehydrogenation reaction of ammonia borane (and selected related amine-boranes) as a safer solid-source of H 2 by hydrolysis (or solvolysis), according to the different developed nanoparticle-based catalysts. The review groups the results according to the transition metals constituting the catalyst according a special view to current cost/availability consid…

Mixed oxide Ti Si O prepared by non-hydrolytic Xerogel method as a diluter of nickel oxide for the oxidative dehydrogenation of ethane

2018

Abstract Mixed Ti Si O materials prepared by non-hydrolytic xerogel method have been employed as diluters for nickel oxide and used in the catalytic oxidative dehydrogenation of ethane. These catalysts have been characterized by several physicochemical techniques such as N2 adsorption, XRD, TPR, TEM, HR-TEM, and XPS. Supported nickel oxide catalysts have been reported to be efficient but only if the nature and the amount of support are controlled. In the present article it is shown that highly loaded (80 wt% NiO) nickel catalysts are more efficient when diluted on mixed Ti Si O materials with appropriate Ti/Si ratios than on pure TiO2 and SiO2 diluters. The catalytic results have been expla…

Front Cover: Metal‐ and Reagent‐Free Anodic Dehydrogenative Cross‐Coupling of Naphthylamines with Phenols (ChemElectroChem 9/2018)

2018

Nanoconfined mixed Li and Mg borohydrides as materials for solid state hydrogen storage

2012

Abstract Several mixtures of LiBH4 and Mg(BH4)2 borohydrides in different stoichiometric ratios (1:0, 2:1, 1:1, 1:2, 0:1), prepared by high energy ball milling, have been investigated with X-ray powder diffraction and thermal programmed desorption (TPD) volumetric analysis to test the dehydrogenation kinetics in correlation with the physical mixture composition. Afterwards mixed and unmixed borohydrides were dispersed on high specific surface area ball milled graphite by means of the solvent infiltration technique. BET and statistical thickness methods were used to characterize the support surface properties, and SEM micrographs gave a better understanding of the preparation techniques. It …