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Unprecedented propane?SCR-NOx activity over template-free synthesized Al-rich Co-BEA* zeolite

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F15%3A00450878" target="_blank" >RIV/61388955:_____/15:00450878 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1016/j.jcat.2015.10.007" target="_blank" >http://dx.doi.org/10.1016/j.jcat.2015.10.007</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.jcat.2015.10.007" target="_blank" >10.1016/j.jcat.2015.10.007</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Unprecedented propane?SCR-NOx activity over template-free synthesized Al-rich Co-BEA* zeolite

  • Original language description

    An Al-rich Co-BEA* zeolite (Si/Al 4.2, Co/Al 0.5) was prepared by organotemplate-free hydrothermal synthesis and [Co(II)(H2O)6]2+ ion exchange. The structure of the Co species and their activity in C3H8?SCR-NOx were compared to that of Si-rich Co-BEA* (Si/Al 11.3). The high population of AlSiAl sequences in Al-rich BEA* with AlO4 facing different channels, contrary to their absence in Si-rich BEA*, results in dehydrated Co-BEA* in easily reducible counter-ion [Co(III)O]+ species attached to one AlO4. The high concentration and density of these Co-oxo species in Al-rich Co-BEA* facilitates extra-ordinarily high SCR-NOx rate even under water vapor up to 10 vol.%, twelve-times outperforming Si-rich Co-BEA*. The five-to-six times increased TOF and easier reducibility suggest a synergetic redox effect of water-resistant Co-oxo species. The Al-rich Co-BEA* provides the highest reaction rate at conditions of wet NOx streams, exceeding that previously reported for metal ion/oxo zeolite catalys

  • 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

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2015

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Journal of Catalysis

  • ISSN

    0021-9517

  • e-ISSN

  • Volume of the periodical

    332

  • Issue of the periodical within the volume

    DEC 2015

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    11

  • Pages from-to

    201-211

  • UT code for WoS article

    000366073500022

  • EID of the result in the Scopus database

    2-s2.0-84946820322