In this work, the reactions of ethane and ethene in an oxidizing and non-oxidizing atmosphere over γ-alumina were investigated under temperature-programmed conditions, in an attempt to estimate the possible contribution and functionality of the support in the reaction pathway of ethane ODH over MoO3/Al2O3 catalysts. The results indicate that alumina contributes to the primary deep oxidation and dehydrogenation routes of ethane to COx and coke respectively, which proceed effectively over the acidic OH groups and the Al3+–O2− acidic centers. On the contrary, the formation of ethylene seems to be coupled to the presence of redox sites on the catalytic surface and requires the presence of the molybdena phase. Moreover, the redox sites of the MoOx species were found to unselectively activate the further overoxidation of the olefin to carbon oxides. Therefore, Al2O3 catalyzes the unselective primary oxidation of ethane to carbon oxides, whereas the molybdena phase is involved in the selective oxidative dehydrogenation (ODH) of ethane to ethene and the secondary overoxidation of ethene to COx. 相似文献
Summary: The effect of impurities on the coordination polymerization has generally been classified and discussed in different ways and has been investigated in detail in the syndiospecific homo‐ and copolymerization of styrene. With regard to impurities of styrene, phenylacetylene as an unpolar impurity containing separate multiple bonds, 1‐phenyl‐1,2‐ethanediol and ω‐hydroxyacetophenone as examples of polar impurities, and ethylbenzene as an other unpolar impurity have been investigated regarding the effect on the polymerization rate and the influence on the molecular properties of the syndiotactic polystyrenes. In the syndiospecific copolymerization with p‐methylstyrene, indene shows a different behavior regarding the decrease of the polymerization conversion depending on the comonomer concentrations present in the monomer mixture. Additionally, the effect of impurities of the catalyst system on the syndiospecific styrene polymerization has been demonstrated, particularly of octahydrofluorene as a component of the transition metal compound and of trimethylaluminium as a component of the cocatalyst methylaluminoxane. All results have been discussed with respect to the mechanisms of the effects on polymerization behavior and on polymer properties.
Dependence of the relative polymerization conversion on the amount of indene added to the monomer mixture in styrene (ST)/p‐methylstyrene (PMS) copolymerization (catalyst n‐ratio: 0.5; molar ratio MAO:Ti = 110:1; polymerization temperature: 60 °C; polymerization time: 45 min). 相似文献
The reaction pathway of the ammoxidation of toluene on (VO)2P2O7 used as catalyst and the interaction of potential intermediates with the pyrophosphate were studied by spectroscopic techniques (FTIR, EPR), temperature-programmed chemisorptions/ reactions (TPD, TPRS) and transient studies such as the temporal analysis of products (TAP) technique. NH3 is chemisorbed on the catalyst surface, forming three different species, i.e., NH
4+
ions located on BrØnsted sites, coordinatively bound NH3 on Lewis sites and NH
2–
groups, presumably P-NH2. Toluene that is probably adsorbed on Lewis sites reacts in a first step to a benzyl radical. A subsequent partial oxidation by interaction of VIV=O groups generates a V...O=CH-C6H5 surface structure. This benzaldehyde-like surface species reacts with adsorbed NH3 according to a Langmuir-Hinshelwood mechanism. TAP experiments on ammonium-containing vanadium phosphates revealed that NH
4+
ions could act as potential N-insertion species. No formation of benzylamine as well as the generation of V=NH surface groups as possible intermediates or N-insertion sites were observed. 相似文献
Methane was pulsed over pure CuO and NiO as well as Cu/La2O3 and Ni/La2O3 catalysts at 600° C. Results indicate that the mechanisms for methane activation over copper and nickel are quite different. Over CuO, methane is converted to CO2 and H2O, most likely via the combustion mechanism; whereas metallic copper does not activate methane. Over NiO in the presence of metallic nickel sites, methane activation follows the pyrolysis mechanism to give CO, CO2, H2 and H2O. Similar results were obtained over the Cu/La2O3 and Ni/La2O3 catalysts. XRD investigations indicate that copper and nickel existed as CuLa2O4 and LaNiO3 respectively in the La2O3-supported catalysts. The effect of La2O3 on the activation of methane is discussed. 相似文献
The hexane-soluble fractions of hydroliquefied products from three Yallourn brown coal lithotypes have been separated into five fractions by combined silica-alumina packed column chromatography. Analyses of various fractions by g.c.-m.s. permitted the identification of ≈50 components in the saturate fraction and 40 components in the diaromatic fraction, together with 30 components in the monoaromatics. The components identified were quite similar among hexane-soluble portions of all three lithotypes. A marked predominance of even carbon number alkane (C23-C29) was observed in the hydrocarbon fractions from pale lithotype over , and medium light lithotype over both pure ZnCl2 and . However, medium dark lithotype over both melt catalysts produced a saturate fraction with an odd carbon number(C22-C28) preference. Based on spectral methods, Soxhlet extracts obtained from untreated lithotypes (hexane and benzene solubles) were characterized as complex mixtures of higher molecular weight(300–1000) aliphatic hydrocarbons, which were supposed to be a precursor of the saturates produced from the corresponding lithotype in the catalytic hydroliquefaction. 相似文献
Monolayer vanadium species are mainly in the V(V) valence state, but with XPS a small fraction of V4+ species are identified. Prolonged analysis treatment increases the V4+ concentration. With increasing vanadium concentration, a monolayer coverage corresponding to 1 mg V2O5 per m2 develops, and it contains additional layers with a thickness of about 250 Å at 4 mg V2O5 per m2, covering 3% of its surface area. 相似文献
MCM-41- and silica gel-supported MoS2 catalysts were prepared. MCM-41 was synthesized and impregnated with precursor, then activated to obtain the active phase. The sol–gel method was used for providing the SiO2 support as well as for including the catalyst precursors in one single step of preparation. Such catalysts have applications particularly in hydrodesulfurization (HDS) and hydrodenitrogenation (HDN) processes. A comparison of the activities of the catalysts was made. The catalytic activity results showed the method of preparation used in this study was successful in producing very efficient catalysts for the HDS of dibenzothiophene (DBT).A higher selectivity for direct C–S bond cleavage was observed for the MoS2 catalyst supported on SiO2 by the sol–gel method. X-ray diffraction studies showed that the catalysts were poorly crystallized with a very weak intensity of the (002) line of 2H-MoS2. 相似文献