Catalytic Pd-Ag nanoparticles immobilized on fiber glass by surface self-propagating thermal synthesis

Pd–Ag nanoparticles with different Pd/Ag ratio were deposited onto fiber glass by using the technique of surface self-propagating thermal synthesis (SSTS) and characterized by X-ray photoelectron spectroscopy (XPS), atomic absorption spectroscopy (ААS), and EXAFS spectroscopy. The samples reduced in hydrogen exhibited the formation of Pd–Ag alloy whose tentative structure and composition were suggested. Thermally scheduled reduction of Pd–Ag catalysts in hydrogen made the Ag atoms partially oxidized. Reported are the catalytic properties of synthesized Pd–Ag samples in selective hydrogenation of acetylene

Catalytic Pd-Ag nanoparticles immobilized on fiber glass by surface self-propagating thermal synthesis

Pd–Ag nanoparticles with different Pd/Ag ratio were deposited onto fiber glass by using the technique of surface self-propagating thermal synthesis (SSTS) and characterized by X-ray photoelectron spectroscopy (XPS), atomic absorption spectroscopy (ААS), and EXAFS spectroscopy. The samples reduced in hydrogen exhibited the formation of Pd–Ag alloy whose tentative structure and composition were suggested. Thermally scheduled reduction of Pd–Ag catalysts in hydrogen made the Ag atoms partially oxidized. Reported are the catalytic properties of synthesized Pd–Ag samples in selective hydrogenation of acetylene

Modified Ag/TiO2 systems: Promising catalysts for liquid-phase oxidation of alcohols

The current work is the first study concerning the liquid-phase oxidation of n-octanol and betulin over modified and unmodified Ag/TiO2 catalysts. Catalytic activity of nanosilver catalysts supported on titania for alcohols selective oxidation can be enhanced by modification of the support with Ce, Fe or Mg oxides. In most cases reductive or oxidative pretreatments of these catalysts were detrimental for their activity. The main reason for performance of Ag/MxOy/TiO2 catalysts is changes of the electronic state of the supported Ag, and especially changes in the surface concentration of Ag+ ions. Monovalent Ag+ ions are active sites in silver-containing catalysts for n-octanol, as well as for betulin oxidation. The obtained results show a potential of silver-containing catalysts for liquid phase oxidation of alcohols, and by selecting the optimum modifier and the support as well as, pretreatment conditions the catalytic properties and stabilization of the active sites can be optimized

Modified Ag/TiO2 systems: Promising catalysts for liquid-phase oxidation of alcohols

The current work is the first study concerning the liquid-phase oxidation of n-octanol and betulin over modified and unmodified Ag/TiO2 catalysts. Catalytic activity of nanosilver catalysts supported on titania for alcohols selective oxidation can be enhanced by modification of the support with Ce, Fe or Mg oxides. In most cases reductive or oxidative pretreatments of these catalysts were detrimental for their activity. The main reason for performance of Ag/MxOy/TiO2 catalysts is changes of the electronic state of the supported Ag, and especially changes in the surface concentration of Ag+ ions. Monovalent Ag+ ions are active sites in silver-containing catalysts for n-octanol, as well as for betulin oxidation. The obtained results show a potential of silver-containing catalysts for liquid phase oxidation of alcohols, and by selecting the optimum modifier and the support as well as, pretreatment conditions the catalytic properties and stabilization of the active sites can be optimized