Kazan (Volga region) Federal University, KFU
KAZAN
FEDERAL UNIVERSITY
 
TRANSFORMATION OF THE ACTIVE COMPONENT DURING OXIDATIVE AND REDUCTIVE ACTIVATION OF THE PALLADIUM HYDROGENATION CATALYST
Form of presentationArticles in international journals and collections
Year of publication2020
Языканглийский
  • Ilyasov Ildar Ravilevich, author
  • Lamberov Aleksandr Adolfovich, author
  • Laskin Artem Igorevich, author
  • Bibliographic description in the original language Laskin A. Transformation of the active component during oxidative and reductive activation of the palladium hydrogenation catalyst / Laskin A., Il'Yasov I., Lamberov A. // New Journal of Chemistry. - 2020. - 44. p. 1719-1732.
    Annotation Palladium catalysts supported on aluminium oxide with acetate and acetylacetonate as precursors were synthesized. The properties of palladium in Pd(Ac)2/(δ+ϰ)-Al2O3 and Pd(Acac)2/(δ+ϰ)-Al2O3 systems treated in oxidizing and reducing atmospheres in a wide temperature range of 300 - 700 ? C were investigated. According to the results of UV-vis/DR and TPR the Pd(Ac)2/(δ+ϰ)-Al2O3 systems oxidized at 300 - 700 ? C are characterized by the presence of large particles of PdO и Pd2+ in the structure of aluminate phases. The subsequent reduction at 500 ? С of pre-oxidized Pd(Ac)2/(δ+ϰ)-Al2O3 systems according to the TEM results is accompanied by the formation of large palladium particles with D = 4.0–4.5 nm and small particles with D = 1.1 nm. At the same time, palladium particles with a diameter of more than 4.0 nm are characterized by the presence of a hydride form of hydrogen. The oxidation of Pd(Acac)2/(δ+ϰ)-Al2O3 in the temperature range of 300-700 ? C leads to the formation of small clusters of PdO and palladium-aluminate phases of non-stoichiometric composition. When reducing, only cluster forms of palladium with D = 1.3 - 1.5 nm are formed from them. At the same time, according to the IRS data, Pd(Ac)2/(δ+ϰ)-Al2O3 catalysts oxidized and reduced at 500 ? C are characterized by a larger number of active centers with a bridge coordination of CO, compared to the Pd(Acac)2/(δ+ϰ)-Al2O3 system. This fact combined with the presence of catalysts of the hydride form of hydrogen for Pd(Ac)2/(δ+ϰ)-Al2O3 leads to a high conversion of methylacetylene and propadiene, but to a low selectivity of their conversion to propylene. An increase in the temperature of the sequential oxidative reduction treatments of Pd(Ac)2/(δ+ϰ)-Al2O3 and Pd(Acac)2/(δ+ϰ)-Al2O3 systems to 600 ? C is accompanied by an increase in the particle size of palladium and the number of atoms with the terminal coordinates of CO molecules. This leads to a significant increase in the conversion of methylacetylene and propadiene.
    Keywords palladium catalyst, selective hydrogenation
    The name of the journal NEW JOURNAL OF CHEMISTRY
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