A transient isotopic study for investigating important design parameters of NiCo/Ce0.75Zr0.25O2-δ catalyst for the dry reforming of methane

The effects of metal loading and particle size of NiCo alloy deposited on Ce0.75Zr0.25O2-δ carrier on the carbon reaction paths of dry reforming of methane at 750 °C with respect to the observed long-term activity profiles was elucidated. Small NiCo nanoparticles (7.8 nm) showed progressive deactivation as opposed to the larger ones (43 nm) which exhibited self-regeneration. Towards this goal, appropriate transient kinetic isotopic experiments (use of 18O2 and 13CO2) and other catalyst characterization studies (transient isothermal reduction, XPS, HAADF-STEM-EDX) were conducted. This work paves the way for the design of highly active and coke-resistant reducible metal oxides-supported NiCo

Alkali and earth alkali modified CuO_x/SiO₂ catalysts for propylene partial oxidation: What determines the selectivity?

In this work, CuOx/SiO2 catalysts were investigated in the propylene partial oxidation reaction. Ordered mesoporous silica (KIT-6) was used to deposit 1–10 wt. copper and subsequently modified with Na, K and Ca. The synthesized materials were characterized by N2 physisorption, XRD, TEM-EDS, CO2-TPD, operando UV/Vis DRS, operando XANES and pyridine DRIFT spectroscopy. Regardless of the CuOx loading, catalyst deactivation was observed during propylene oxidation reaction in non-modified catalysts, which was related to sintering of oligomeric [Cu-O-Cu]n species. Sintering of CuOx is strongly promoted under a reducing propylene atmosphere and related to the presence of Cu+1. The resulting bulk CuOx promotes acrolein selectivity. We produced modified catalysts with finely dispersed alkali metal cations, associated with the subnanometer CuOx phase, resulting in a greatly stabilized morphology and catalytic activity. Operando XANES analysis revealed that a substantial fraction of Cu2+ is transformed to Cu+ during the propylene oxidation reaction (52–68, depending on the modifying atom). Also, the dynamics of reaching the quasi steady oxidation state differ strongly. The kinetics of oxygen abstraction and replenishment are substantially different, indicative of modified chemistry of the nucleophilic oxygen species, present in 5CuNa catalyst in contrast to others (5Cu and 5CuCa). We propose that Cu+ is not crucial for PO formation. Instead the electropositive Na+ and K+ decrease the nucleophilic strength of oxygen in CuOx, by attracting its electrons. Consequently, the catalytic action of oxygen changes from oxidative attack on the allylic hydrogen to oxygen insertion into the C[dbnd]C bond of propylene. This results in a noticeable selectivity shift from acrolein to propylene oxide. The effect of calcium on decreasing the nucleophilic character of O species in CuOx is negated by charge compensation by strongly adsorbed hydroxyl groups and Ca modification for PO selectivity is inefficient. Additionally we found, that further oxidation of propylene oxide is, most likely, the main factor determining high selectivity for COx products. The alkali modification which increases the PO selectivity does not function via elimination of LAS, but exclusively through attenuation of nucleophilic character of oxygen species. © 2018 Elsevier B.V