The effect of two types of catalysts on the activity of the catalytic hydrogenation of nitrobenzene was studied. Catalysts were prepared by the surface deposition of palladium hydroxide with a simultaneous reduction with formaldehyde in a basic environment and were characterised by X-ray powder diffraction, transmission electron microscopy, adsorption-desorption, and catalytic tests — hydrogenation of nitrobenzene in methanol. The influence of the supports’ (activated carbon and a mixture of activated carbon and multi-walled carbon nanotubes) surface area is discussed. Despite having a size comparable (4–5 nm) to crystallites of metallic palladium, the catalyst prepared on a mixture of activated carbon and nanotubes (Pd/C/CNT) was significantly less active than the catalyst prepared on pure activated carbon (Pd/C); the rate of this reaction was approximately 30 % lower than the initial reaction rate. This feature could be attributed to the lower specific surface area of the Pd/C/CNT (531 m2 g−1) in comparison with the Pd/C (692 m2 g−1).
This paper describes the synthesis of tungsten disulfide (WS2) powder by the sulfurization of tungsten trioxide (WO3) particles in the presence of additive potassium carbonate (K2CO3) in nitrogen (N2) atmosphere, first at lower temperature (200 °C) and followed by reduction at higher temperature (900 °C). In addition, the ultrasonic spray pyrolysis of ammonium meta-tungstate hydrate (AMT) was used for the production of WO3 particles at 650 °C in air. The HSC Chemistry® software package 9.0 was used for the analysis of chemistry and thermodynamic parameters of the processes for WS2 powder synthesis. The crystalline structure and phase composition of all synthesized powders were analyzed by X-ray diffraction (XRD) measurements. The morphology and chemical composition of these samples were examined by scanning electron microscopy (SEM) combined with energy dispersive X-ray analysis (EDX).
Waste generation is a part of every technological process, including galvanizing. The presented paper deals with the characterization of flue dust generated in the process of hot-dip galvanizing, and proposes possible methods for zinc recycling. The flue dust is released into the atmosphere as a white fume above the zinc bath, which is caused by the decomposition of ammonium chloride and zinc chloride present in the flux. This dust is classified as hazardous waste and is a material with a particle size below 90 µm. In addition to zinc and iron compounds, it contains water vapor and oils. The presented elemental, phase, and other characteristic methods of flue dust are important for the subsequent selection of a suitable method for processing the material. At present, this waste is not processed separately due to its low production, which is approximately 0.3 kg per 1 tonne of galvanized steel. The proposed hydrometallurgical recycling method enables the processing of flue dust on a small scale and enables the recovery of high-purity zinc in the form of metallic zinc or zinc oxide.
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