Zobrazeno 1 - 10
of 17
pro vyhledávání: '"O. V. Buyevskaya"'
Autor:
P. Rybarczyk, M.-M. Pohl, Angelika Brückner, Jörg Radnik, O. V. Buyevskaya, M. Baerns, H. Berndt
Publikováno v:
Journal of Catalysis. 202:45-58
Me –V–O catalysts ( Me = Mg, Zn, Pb) of different Me : V ratios were characterized with respect to phase composition, structure and valence state of vanadium sites as well as composition and acid–base properties of the surface using XRD, TEM, T
Publikováno v:
Catalysis Today. 67:369-378
An evolutionary approach was applied to create five generations of α-Al 2 O 3 -supported multi-metal-oxides to be used as catalytic materials for the oxidative dehydrogenation of propane at 773 K. Each generation consisted of 56 differently composed
Publikováno v:
Catalysis Today. 62:91-99
Selected aspects related to the mode of reactor operation and to the development of catalysts for the oxidative dehydrogenation of ethane and propane to their respective olefins are dealt with. The differences in the catalytic conversion when applyin
Publikováno v:
Applied Catalysis A: General. 200:63-77
A methodical basis of the evolutionary method for selection and optimization of heterogeneous catalytic materials was developed. For validation, the oxidative dehydrogenation of propane was used as a model reaction. Various oxides (V 2 O 5 , MoO 3 ,
Publikováno v:
Catalysis Letters. 63:153-159
For elucidating the mechanism of oxygen adsorption and its effect on selectivity in the oxidative coupling of methane (OCM) transient experiments were carried out in the TAP-2 reactor by pulsing oxygen over Na2O/CaO catalysts at temperatures between
Publikováno v:
Catalysis Today. 33:85-96
Results are discussed on the direct oxidation of propane to acrolein on MexOγ-supported Ag0.01Bi0.85V0.54Mo0.45Ox (MexOγ = γ-Al2O3, TiO2, SiO2) and on Me7Bi5Mo12Ox (Me = Mg, Ca, Zn) catalysts. Almost no formation of acrolein was observed over MexO
Publikováno v:
Zeitschrift für Physikalische Chemie. 197:49-65
Publikováno v:
Catalysis Letters. 38:81-88
The nature of surface sites responsible for methane activation and COx formation on Rh catalysts for the partial oxidation of methane to syngas was investigated. The interaction of H4 with Rh-black after oxidative and reductive pretreatments was stud
Publikováno v:
Catalysis Letters. 29:261-270
Reaction steps in the oxidation of CH4 to CO and H2 over a Rh(1 wt%)/γ-Al2O3 catalyst were studied using in situ DRIFTS at 973 K and 0.1 MPa. Product distribution and the resulting absorption band intensities of the respective adsorbates were strong
Publikováno v:
Catalysis Letters. 29:249-260
The reaction of methane with surface oxygen as well as the interaction of methane/oxygen mixtures with a Rh(1 wt%)/γ-Al2O3 catalyst was studied by applying the temporal-analysisof-product (TAP) reactor. The product distribution was strongly affected