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Precursors of active Ni species in Ni/Al2O3 catalysts for oxidative dehydrogenation of ethane

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F13%3A39896225" target="_blank" >RIV/00216275:25310/13:39896225 - isvavai.cz</a>

  • Alternative codes found

    RIV/61989100:27640/13:86087557

  • Result on the web

    <a href="http://www.sciencedirect.com/science/article/pii/S187220671260672X" target="_blank" >http://www.sciencedirect.com/science/article/pii/S187220671260672X</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/S1872-2067(12)60672-X" target="_blank" >10.1016/S1872-2067(12)60672-X</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Precursors of active Ni species in Ni/Al2O3 catalysts for oxidative dehydrogenation of ethane

  • Original language description

    Ni/Al2O3 catalysts for oxidative dehydrogenation (ODH) of ethane were prepared by impregnation of Al2O3 with nickel acetate or nickel nitrate, and by mechanical mixing of NiO and Al2O3. The Ni-based catalysts were characterized by N-2 adsorption-desorption, X-ray diffraction, diffuse reflectance UV-visible diffuse reflectance spectroscopy, and temperature-programmed reduction of hydrogen. The results showed that formation of crystalline NiO particles with a size of { 8 nm and/or non-stoichiometric NiO species in the Ni/Al2O3 catalysts led to more active species in ODH of ethane under the investigated reaction conditions. In contrast, tetrahedral Ni species present in the catalysts led to higher selectivity for ethene. Formation of large crystalline NiOparticles (22-32 nm) over Ni/Al2O3 catalysts decreased the selectivity for ethene.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    CF - Physical chemistry and theoretical chemistry

  • OECD FORD branch

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2013

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Chinese Journal of Catalysis

  • ISSN

    0253-9837

  • e-ISSN

  • Volume of the periodical

    34

  • Issue of the periodical within the volume

    10

  • Country of publishing house

    CN - CHINA

  • Number of pages

    9

  • Pages from-to

    1905-1913

  • UT code for WoS article

    000325601000016

  • EID of the result in the Scopus database