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