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The synergy between catalysis and plasma chemistry often enhances the yield of chemical reactions in plasma-driven reactors. In the case of CO2 splitting into CO and O2, no positive synergistic effect was observed in earlier studies with plasma reactors, except for dielectric barrier discharges, that do not have a high yield and a high efficiency. Here, we demonstrate that introducing metal meshes into radio frequency-driven plasma reactors increases the relative reaction yield by 20%–50%, while supported metal oxide catalysts in the same setups have no effect. We attribute this to the double role of the metal mesh, which acts both as a catalyst for direct CO2 dissociation as well as for oxygen recombination. [ABSTRACT FROM AUTHOR]

MXenes are a new family of 2D carbides or nitrides that have attracted attention due to their layered structure, tunable surface groups and high electrical conductivity. Here, we report for the first time that the Ti2CTx MXene catalyses the selective oxidative dehydrogenation of n‐butane to butenes and 1,3‐butadiene. This catalyst showed higher intrinsic activity compared to a commercial TiC and TiO2 samples in terms of C4 olefin formation rate. We propose that the stabilisation of structural vacancies and the change in composition (from a carbide to a mixed phase oxide) in the MXene causes its higher catalytic activity. These vacancies can lead to a higher concentration of unpaired electrons in the MXene‐derived material, enhancing its nucleophilic properties and favouring the production of olefins. [ABSTRACT FROM AUTHOR]

In Podzols, organic matter ( OM) is stabilized mainly by interaction with minerals, as a direct consequence of pedogenic processes. Metal-organic associations strongly affect OM surface features, particularly microporosity. Cemented ortstein horizons ( CM) may form during podzolization, accompanied by a spatial arrangement of OM on mineral surfaces, which differs from that in non-cemented horizons ( N-CM). To investigate the metal-organic associations and their changes during pedogenesis, we selected both N-CM and CM podzolic horizons, isolated NaClO-resistant OM and compared the specific surface area ( SSA) before and after OM oxidation. The SSA was assessed by using N2, to detect the pores in the range of micropores (< 2 nm) and mesopores (2-50 nm), and CO2, to measure a smaller microporosity (< 0.5 nm), which is not accessible to N2. Only the N-CM samples showed the typical increase in N2-SSA after the removal of labile OM, while a decrease was found in all CM horizons. The CO2-SSA revealed a large number of small micropores characterizing OM, both before and after oxidation. The smallest micropore classes (< 0.5 nm) were, however, more abundant in NaClO-resistant OM, which had therefore a larger number of N2-inaccessible surfaces than the labile pool. The N2-SSA data thus indicated a more homogeneous coverage of mineral surfaces by stabilized OM in CM samples. Because of the abundance of small micropores, OM in these podzolic B horizons had extremely large CO2-SSA values (about 800 m2 g−1), with sharp differences between the NaClO-labile OM (290-380 m2 g−1) and the NaClO-stabilized pool (1380-1860 m2 g−1), thus indicating very reactive illuvial organic materials. [ABSTRACT FROM AUTHOR]

In the search for new materials and concepts in materials science, metallo-organic hybrids are attractive candidates; they can combine the rich diversity of organic molecules with the advantages of metals. Transition metals such as palladium are widely applied in catalysis, and small organic molecules such as those in the cinchona alkaloid family can control the stereochemistry of a number of organic reactions. Here, we show that reducing a metal salt in the presence of a cinchona alkaloid dopant gives a chirally imprinted metallo-organic hybrid material that is catalytically active and shows moderate enantioselectivity in hydrogenation. Furthermore, using photoelectron emission spectroscopy, we show that the metal retains some chiral character even after extraction of the dopant. This simple and effective methodology opens exciting opportunities for developing a variety of chiral composite materials. [ABSTRACT FROM AUTHOR]

Abstract: The advantages of two-step oxidative dehydrogenation as an alternative method for manufacturing small alkenes are outlined. In a nutshell, the process is based on separating the gaseous oxygen and hydrocarbon feeds in time. In the first step, alkanes are dehydrogenated in the presence of a solid oxygen carrier (without gaseous oxygen). Subsequently, the carrier is reoxidised using a gaseous feed. This process requires a dehydrogenation catalyst that is selective and stable under severe redox cycling. In search for such a catalyst, we prepare and study various platinum/tin catalysts supported on alumina. The catalysts are doped with either magnesia or potassium oxide. The activity, selectivity, and stability of these catalysts in the dehydrogenation of ethane to ethylene are then investigated under severe redox cycling conditions (600°C and 10% (v/v) oxygen in the regeneration step). Pt0.02Sn0.003Mg0.06 is found to be the most stable combination. The catalysts’ dispersion and the metal–support interactions are studied using transmission electron microscopy (TEM) and temperature-programmed hydrogen desorption (TPD). The effects of the (earth)alkali promoter and the interaction between the metal catalyst and support are discussed. [Copyright &y& Elsevier]