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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Chemistry of materials 7 (1995), S. 179-184 
    ISSN: 1520-5002
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Catalysis letters 47 (1997), S. 143-154 
    ISSN: 1572-879X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The propane aromatization was studied over H-ZSM5 zeolite modified by Ge, Pt and Pt-Ge. The aromatization was performed in a micro-reactor at 773K and at atmospheric pressure. The addition of germanium on H-ZSM5 increases the activity for propane transformation but decreases the selectivity toward aromatic compounds. The transformation of propane on Pt/H-ZSM5 indicates a significant increase in the activity and a decrease in the selectivity toward aromatics, while on the bimetallic Pt-Ge/H-ZSM5 catalyst both the activity and the selectivity toward aromatics increase. The dehydrogenation of propane over GeO2/SiO2 at 773 K and the n-heptane transformation overH-ZSM5 and Ge/H-ZSM5 at 673 K were performed. Results confirm the dehydrogenation capacity of GeO2 and show similar activity and selectivity for n-heptane conversion on H-ZSM5 and Ge/H-ZSM5. The acidic properties of the catalysts were determined by TPD/NH3 and IR/Pyanalyses. Results show that both the total and strong acidity decrease with the addition of germanium. Therefore, it seems that germanium affects the activity of propane conversion due to the dehydrogenation capacity of GeO2,while the selectivity toward aromatics decreases due to the lower capacity of cyclization, by decreasing the acidity and the number of strong acid sites. In contrast, the Pt-Ge/H-ZSM5 catalyst presents the highest selectivity toward aromatics (53.4%) which is attributed to the decrease in hydrogenolysis capacity of platinum. The TPR results of the Pt-Ge/H-ZSM5 catalyst indicate interaction of Pt-Ge, and from the hydrogen consumption it was seen that Ge4+ is partially reduced to Ge2+, which is attributed to the presence of metallic platinum.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1572-879X
    Keywords: oxidation ; reduction of palladium catalysts ; chlorine effects
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Pd–chloride precursor salt was used to prepare Pd/Al2O3 catalysts. TPSR measurements showed three distinct reactions for the oxidation of propane on palladium surface under excess of hydrocarbon: complete oxidation, steam reforming and propane hydrogenolysis. Propane oxidation on palladium catalysts was related to the Pd2+ sites observed on Pd/Al2O3 through infrared of adsorbed carbon monoxide. In fresh catalysts reduced by H2, the IR spectra showed the linear and bridge adsorbed CO species on the Pd0 surface. After propane reaction, a new band at 2130 cm-1 related to CO adsorption on Pd2+ species was noted. Carbon monoxide species adsorbed on Pd0 were also observed in all samples after reaction. Our results suggest surface ratios of Pd0/PdO during the propane oxidation. On the other hand, time on stream conversions of the complete oxidation of propane were affected by either the water generated during the reaction or added as a reactant at 10 vol%. The water generated by the reaction helped to eliminate chlorine residues in the form of oxychloride species leading to an increasing of the activity. However, the presence of water into the reaction mixture caused a strong decreasing of the activity. The inhibition mechanism of propane oxidation in the presence of water consisted in the dissociative adsorption of water on palladium sites with the possible formation of palladium hydroxide (Pd–OH) at the surface, diminishing the number of active surface sites. Dynamic fluctuations into the reaction conditions supported the idea that a pseudo‐equilibrium adsorption–desorption of water was reached. After water removal or increasing in the reaction temperature the equilibrium was shifted to the direction of OH–Pd decomposition. This behavior suggests that the inhibitory effect of water is a reversible phenomenon, being a function of the amount of water and the reaction temperature.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1572-9540
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The effect of indium addition on alumina-supported platinum catalysts was investigated by measurements of hyperfine interactions. Via lime differential perturbed angular correlation spectroscopy (TDPAC) on111Cd, Pt/Al2O3 catalysts were studied in the flow of a heptane/H2 gas stream. The results indicate that some amount of indium sticks to platinum which is then dispersed on the support surface. The amount of In that is free from platinum is mobile under reaction conditions, being capable of diluting platinum particles and draining off coke precursors from the platinum surface.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0935-6304
    Keywords: Capillary GC ; Alkyl phenols ; Cardanol ; Hydrogenation kinetics ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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