Počet záznamů: 1  

Milling Activation for the Solvent-Free Synthesis of the Zeolite Mordenite

  1. 1.
    0532025 - ÚFCH JH 2021 RIV DE eng J - Článek v odborném periodiku
    Kornas, Agnieszka - Olszówka, Joanna Elżbieta - Urbanová, Martina - Mlekodaj, Kinga - Brabec, Libor - Rathouský, Jiří - Dědeček, Jiří - Pashkova, Veronika
    Milling Activation for the Solvent-Free Synthesis of the Zeolite Mordenite.
    European Journal of Inorganic Chemistry. Roč. 2020, č. 29 (2020), s. 2791-2797. ISSN 1434-1948. E-ISSN 1099-0682
    Grant CEP: GA ČR(CZ) GJ17-09188Y; GA MŠMT(CZ) EF16_013/0001821
    Grant ostatní: GA MŠk(CZ) CZ.02.1.01/0.0/0.0/16_013/0001821
    Institucionální podpora: RVO:61388955
    Klíčová slova: dry-gel conversion * cha zeolite * mechanochemistry * transformation * fau * Solvent elimination * Mechanochemical activation * Planetary mill * Synthesis design * Zeolites
    Obor OECD: Physical chemistry
    Impakt faktor: 2.524, rok: 2020
    Způsob publikování: Omezený přístup

    Milling by a planetary mill was applied as a pretreatment of a reagent mixture for the solvent-free synthesis of the zeolite mordenite. This method was compared with both manual grinding and standard hydrothermal synthesis. The comprehensive characterization of the obtained products was complemented by thorough studies of activated synthesis mixtures before crystallization steps (by Magic Angle Spinning Nuclear Magnetic Resonance and Scanning Electron Microscopy). This experimental approach gave insight into processes behind the synthesis mixture activation by milling. The characteristics of solvent-free zeolite product were comparable with material obtained by the classic hydrothermal route. The automated milling activation made the crystallization possible due to higher energetic impact in comparison to manual grinding. The solvent-free process allowed minimization of the contribution of water to a role of the agent catalyzing silica transformation, as a result, less than 5 % water (compared to the classical synthesis) was necessary to perform the crystallization.
    Trvalý link: http://hdl.handle.net/11104/0310627

     
    Název souboruStaženoVelikostKomentářVerzePřístup
    0532025.pdf32.7 MBVydavatelský postprintvyžádat
     
Počet záznamů: 1  

  Tyto stránky využívají soubory cookies, které usnadňují jejich prohlížení. Další informace o tom jak používáme cookies.