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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 96 (1992), S. 7714-7718 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 98 (1994), S. 1933-1938 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Catalysis letters 11 (1991), S. 365-374 
    ISSN: 1572-879X
    Keywords: TiO2-Al2O3 ; Mo/Al2O3 ; Mo/TiO2-Al2O3 ; temperature programmed reduction (TPR) ; X-ray photoelectron spectroscopy (XPS)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The effect of TiO2 modified Al2O3 surface on the reducibility of MoO3 has been studied by TPR and XPS. The results show that Mo6+ in Mo/TiO2-Al2O3 can be reduced to much lower valency, especially at low Mo loading. The influence of the calcination temperature on the reduction of Mo6+ on Al2O3 and TiO2-Al2O3 carriers is different. The data reveals that the reducibility of Mo6+ on Al2O3 slightly decreased, while that on TiO2-Al2O3 increased when the calcination temperature was raised. It is suggested that the stronger tetrahedral site of the Al2O3 surface was first occupied by TiO2 and main octahedral Mo6+ in polymeric species-; and a small crystalline MoO3 formed on TiO2-Al2O3, whereas the formation of tetrahedral Mo6+ species and Al2(MoO4)3 phase was inhibited.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1572-879X
    Keywords: Interaction ; molybdenum oxide ; cobalt oxide ; alumina ; dehydration ; Raman spectroscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A set of Co promoted 10% Mo/Al2O3 samples have been characterized by means of Raman spectroscopy under ambient as well as in situ dehydrated conditions. Under ambient conditions, the degree of the polymerization of surface molybdenum oxide species decreases with increasing Co loading. Under dehydrated conditions, the polymeric molybdenum oxide species is absent with the addition of only 0.2% Co. At low Co loadings (⩽2%), before the formation of CoMoO4 compound, the spectral features are very similar under ambient conditions. Dehydration causes the upward shift of the Mo=O symmetric stretching mode. A broad band around 920–930 cm−1 was thus observed. This band has been suggested to be associated with the Co-Mo interaction species. In contrast to crystalline CoMoO4, this species shows a reversibility on H2 reduction-O2 reoxidation treatments. From the results obtained, it is proposed that cobalt oxide interacts with the most polymerized molybdenum oxide species to form Co-Mo interaction species and/or crystalline CoMoO4; therefore, the amount of the surface molybdenum oxide species decreases with a change in the molecular structure as a function of the Co concentration.
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  • 5
    ISSN: 1572-879X
    Keywords: Citrate method ; magnesium vanadates ; redox property ; selective oxidation of propane to propene
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Three magnesium vanadate phases, i.e., MgV2O6 (metavanadate), α-Mg2V2O7 (pyrovana-date) and Mgs V2O8 (orthovanadate), have been successfully prepared with high purity by the citrate method at a relatively low temperature (550°C). FT-IR, LRS, XRD and SEM techniques have been used to characterize these vanadate phases. The effect of calcination temperature has also been investigated. It was found that the particle size and morphology of the MgV2O6 phase, which is a function of calcination temperature, appear to have a strong effect on the infrared spectra. Furthermore, the catalytic properties of the three phases were examined in the oxidative dehydrogenation of propane. The propene selectivity follows the order: α-Mg2V2O7 〉 Mg3 Vg2O8 〉 MgV2O6, which is consistent with their redox properties. This fact suggests that there is some correlation between the catalytic and redox properties of these magnesium vanadate phases.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Catalysis letters 24 (1994), S. 249-256 
    ISSN: 1572-879X
    Keywords: Methane adsorption ; alumina ; hydroxyls ; FT-IR ; coadsorption ; CO adsorption
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Methane adsorption on alumina was investigated by FT-IR spectroscopy at 173 K. Adsorbed methane gives four distinct IR bands at 3008, 3000, 2900 and 1305 cm−1 which are attributed to v1 (2900 cm−1), v3 (3008, 3000 cm−1), and v4 (1305 cm−1) modes of methane respectively. The appearance of the v1 mode indicates that the Td symmetry of methane is distorted by the adsorption. The intensities of these bands increase significantly with outgassing temperatures of alumina, reach their maxima at an outgassing temperature near 773 K, and then decrease with further higher outgassing temperatures. Two hydroxyls with IR bands at 3750 and 3665 cm−1 are perturbed evidently by the adsorbed CH4 thereby resulting in two redshifted bands at 3707 and 3640 cm−1. Coadsorbed CO slightly affects the adsorbed CH4 indicating the very weak interaction between CH4 and surface cations of alumina. It is proposed that the adsorbed CH4 on alumina is formed mainly via the interaction of CH4 with both surface hydroxyl and c.u.s. oxygen anion.
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  • 7
    ISSN: 1572-879X
    Keywords: methane ; adsorption ; hydroxyl groups ; H-D exchange reaction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Infrared investigations on the interaction of methane with silica, aluminas (η,γ and α) and HZSM-5 zeolite have been carried out. At low temperature (173 K), methane adsorption was observed over these oxides and HZSM-5 zeolite. Our findings featured that the infrared inactiveΝ 1 band (2917 cm−1) of a gaseous methane molecule became active and shifted to lower frequencies (2900 and 2890 cm−1) when it adsorbed on the surfaces of these adsorbents. Our results also demonstrate that hydroxyl groups played a very important role in methane adsorption over the acidic oxides and the HZSM-5 zeolite. When interaction between the hydroxyl groups and methane took place, the band shift of the hydroxyl groups varied with different oxides. The strength of the interaction decreased according to the following sequence, Si-OH-Al〉Al-OH〉Si-OH, which is in accordance with the order of their acidities. At higher temperatures, methane interacted quite differently with various oxides and HZSM-5 zeolite. It has been observed that the hydroxyl groups of silica, γ-alumina and HZSM-5 zeolite could exchange with CD4 at temperatures higher than 773K, while those on η-alumina could exchange at a temperature as low as 573 K. Another interesting observation was the formation of formate species over Al2O3 (both η and γ) at temperatures higher than 473 K. The formate species would decompose to CO2, or produce carbonate at much higher temperatures. Formation of formate species was not observed over silica and HZSM-5 under similar conditions, α-Al2O3 did not adsorb or react with methane in any case.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Catalysis letters 15 (1992), S. 255-267 
    ISSN: 1572-879X
    Keywords: Temperature programmed sulfiding ; laser Raman spectroscopy ; Mo/Al2O3 ; Mo/TiO2-Al2O3
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A series of Mo/Al2O3 and Mo/TiO2-Al2O3 catalysts were investigated by temperature programmed sulfiding (TPS) and laser Raman spectroscopy (LRS). The effect of TiO2 on the sulfidability of molybdena was studied in detail. It is found that Mo/Al2O3 catalysts can be partially sulfided by O-S exchange at low temperature, forming molybdenum oxysulfide. The Mo-S bond subsequently ruptures in the presence of H2 to produce H2S. At 530–550 K deep sulfiding of molybdenum oxysulfide occurs forming crystalline MoS2. When the surface of Al2O3 was covered by a monolayer of TiO2, the sulfiding rate of molybdena at low temperature was not only greatly increased, but H2S produced in the reduction of Mo-S species caused deep sulfiding of the catalyst which resulted in a decrease of the TPS peak temperature by 80–100 K. The results indicate that this promotion of the sulfiding of molybdena is enhanced with TiO2 loading. The function of TiO2 is explained by the weakened interaction between MoO3 and Al2O3 due to the coverage of the Al2O3 surface by TiO2.
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  • 9
    ISSN: 1572-879X
    Keywords: Cerium oxide ; mild oxidation ; oxygen species ; rare earth oxide ; FT-IR ; ethylene oxidation ; isotopic technique
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Surface oxidation of ethylene on cerium oxide was studied at mild temperatures (293–473K) by usingin situ FT-IR spectroscopy, and isotopic technique. Ethylene oxidation took place even at around 330 K on a well outgassed cerium oxide independent of the presence of gaseous O2. At mild temperatures, the surface adsorbed product was mainly formate species. Adsorbed Superoxide (O 2 − ) species was definitely observed at temperatures up to 373 K when gaseous oxygen was present. However isotopic experiment confirmed that the Superoxide was not the active form of oxygen due to the mild oxidation of ethylene. The principal oxygen species participating in the mild oxidation of ethylene was surface lattice oxygen which is supposed to be in O−-like form created by an outgassing at high temperatures. The mild oxidation of ethylene could be also initiated by surface peroxide (O 2 2− ) and O− species which were formed via the adsorption of O2 on a partially reduced cerium oxide.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1572-879X
    Keywords: methane ; oxygen ; aromatization ; Mo/HZSM‐5 ; coke formation ; UV‐Raman spectroscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The aromatization of methane over a Mo/HZSM‐5 catalyst was carried out in the presence of oxygen. It is shown that the addition of a small amount of oxygen is beneficial to improve the durability of the catalyst. UV‐Raman spectra disclose that the carbonaceous deposits formed on the HZSM‐5 are mainly polyolefinic and aromatic, while that on the Mo/HZSM‐5 is mainly polyaromatic. The small amount of O2 added may partly remove the coke deposits on the active sites and keep the catalyst as MoOxCy/HZSM‐5, thus resulting in an improvement of the catalytic performance of the Mo/HZSM‐5 catalyst.
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