Catalytic Properties of 3D Graphene-Like Microporous Carbons Synthesized in a Zeolite Template

[EN] The inherent properties of a single atomic carbon layer in graphene offer opportunities for the creation of catalytically active centers tailored on a molecular level on a support with high thermal stability and very high specific surface area. We demonstrate that organization of the two-dimensional system of the carbon layer into three-dimensional (3D) graphene-like catalytic materials with the connectivity of a pore network providing good accessibility to the active centers allows the preparation of catalytic materials that exploit the properties of graphene. In this study, 3D graphene-like microporous carbons, denoted as)6 beta-carbon and Y-carbon, were synthesized by nanocasting of beta (*BEA) and faujasite (FAU) zeolite templates. Structural analyses show that the materials are characterized by 3D-assembled and highly stable single-atom graphene an open porous system resembling the regular channel system of the zeolites with a specific surface area comparable to the surface area of graphene. The materials effectively catalyze the hydrogenation of alkenes, alkynes, and cycloalkenes into the corresponding alkanes and cycloalkanes. The materials facilitate catalytic intramolecular rearrangements, including the selective isomerization of double bonds and branching of linear chains, as well as stereoselective isomerization of unsaturated hydrocarbons. layers that formThis work was supported by the Grant Agency of the Czech Republic under project No. 15-12113S. The authors acknowledge the assistance provided by the Research Infrastructures NanoEnviCz (Project No. LM2015073) and Pro-NanoEnviCz (Project No. CZ.02.1.01/0.0/0.0/16_013/0001821), supported by the Ministry of Education, Youth and Sports of the Czech Republic.Sazama, P.; Pastvova, J.; Rizescu, C.; Tirsoaga, A.; Parvulescu, VI.; García Gómez, H.; Kobera, L.... (2018). Catalytic Properties of 3D Graphene-Like Microporous Carbons Synthesized in a Zeolite Template. ACS Catalysis. 8(3):1779-1789. https://doi.org/10.1021/acscatal.7b04086S177917898

Study of the "Fast SCR" -like mechanism of H2-assisted SCR of NOx with ammonia over Ag/Al2O3

It is shown that Ag/Al2O3 is a unique catalytic system for H-2-assisted selective catalytic reduction of NOx by NH3 (NH3-SCR) with both Ag and alumina being necessary components of the catalyst. The ability of Ag/Al2O3 and pure Al2O3 to catalyse SCR of mixtures of NO and NO2 by ammonia is demonstrated, the surface species occurring discussed, and a "Fast SCR"-like mechanism of the process is proposed. The possibility of catalyst surface blocking by adsorbed NOx and the influence of hydrogen on desorption of NOx were evaluated by FTIR and OFT calculations

Mechanistic Study of the NO + NH4NO3 Reaction on H- and Fe/H-BEA Zeolites Using 15N and 18O Labeled Species

Reduction of NO by NH3 over metal-promoted zeolites represents the principal reaction in the selective catalytic reduction (SCR) technology for NOx removal from Diesel engine exhausts. It has been established that addition of ammonium nitrate (AN) to the reaction mixture substantially enhances the rate of this reaction, decreasing the temperature necessary for an efficient deNOx process. Nevertheless, the nature of this effect has not been completely elucidated. To investigate the NO+AN reaction mechanism, we have used individual reactants labeled with either N-15 or O-18 (or both isotopes), thus obtaining an experimental background for proposing the route of the SCR accelerated by AN addition. For this study, we have used as the catalysts H-BEA and Fe/H-BEA zeolites with various Si/Al ratios and various amounts and states of the iron species