Direct Homogeneous Synthesis of Compounds with Two O Atoms and Long-Chain Hydrocarbons from CO and H2: Co-Ru/N-methylpyrrolidone Catalyst.

The homogeneous acetic acid synthesis-type Ru-Co-Li/N-methylpyrrolidone catalyst for CO and H2 transformations has been studied at moderately high pressures. For 1CO:2H2, low acetic acid selectivity has been observed, along with remarkable methyl acetate selectivity, the absence of aldehydes and ethyl acetate and sharp deviations from the Anderson-Schultz-Flory distribution for both alcaohols and long-chain hydrocarbons. For 1CO:1H2 and slightly elevated pressure, acetic acid selectivity slightly increased, notable ethyl acetate formation was detected, and both long-chain hydrocarbons and alcohols disappeared. Hypotheses are discussed about the direct parallel formation of all observed product groups (hydrocarbons, alcohols, esters, and acetic acid) and hydrocarbon chain growth limitations according to the formed Ru-Co cluster size in the presence of the aforementioned catalytic system.

Catalytic Activity of Thermolyzed [Co(NH3)6][Fe(CN)6] in CO Hydrogenation Reaction.

Currently, the processes of obtaining synthetic liquid hydrocarbons and oxygenates are very relevant. Fischer-Tropsch synthesis (FTS) is the most important step in these processes. The products of thermal destruction in argon of the mixture [Co(NH3)6][Fe(CN)6] and Al(OH)3 were used as catalysts for CO hydrogenation. The resulting compositions were studied using powder X-ray diffraction, IR spectroscopy, elemental analysis, SEM micrographs. The specific surface area, pore and particle size distributions were determined. It was determined that the DCS-based catalysts were active in the high-temperature Fischer-Tropsch synthesis. The effect of aluminum in the catalyst composition on the distribution of reaction products was revealed.

Catalytic Design of Matrix-Isolated Ni-Polymer Composites for Methane Catalytic Decomposition.

Targeted synthesis of C/composite Ni-based material was carried out by the method of matrix isolation. The composite was formed with regard to the features of the reaction of catalytic decomposition of methane. The morphology and physicochemical properties of these materials have been characterized using a number of methods: elemental analysis, scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy, temperature programmed reduction (TPR-H2), specific surface areas (SSA), thermogravimetric analysis, and differential scanning calorimetry (TGA/DSC). It was shown by FTIR spectroscopy that nickel ions are immobilized on the polymer molecule of polyvinyl alcohol, and during heat treatment, polycondensation sites are formed on the surface of the polymer molecule. By the method of Raman spectroscopy, it was shown that already at a temperature of 250 °C, a developed conjugation system with sp2-hybridized carbon atoms begins to form. The SSA method shows that the formation of the composite material resulted in a matrix with a developed specific surface area of 20 to 214 m2/g. The XRD method shows that nanoparticles are essentially characterized by Ni, NiO reflexes. The composite material was established by microscopy methods to be a layered structure with uniformly distributed nickel-containing particles 5-10 nm in size. The XPS method determined that metallic nickel was present on the surface of the material. A high specific activity was found in the process of catalytic decomposition of methane-from 0.9 to 1.4 gH2/gcat/h, XCH4, from 33 to 45% at a reaction temperature of 750 °C without the stage of catalyst preliminary activation. During the reaction, the formation of multi-walled carbon nanotubes occurs.