Papers by Keyword: Platinum

Abstract: Ni and Ni-containing nanoparticles exhibit promising magnetic properties. In a preliminary experiment, these nanoparticles aggregated after synthesis. Because nanoparticle aggregation may degrade their unique properties, a method to prevent their aggregation is required. In this study, Ni-Pt nanoparticles were synthesized and coated with silica to suppress aggregation. A colloidal solution of Ni-Pt nanoparticles was synthesized in water exposed to air using nickel(II) acetate tetrahydrate (Ni source), hexachloroplatinate(IV) hexahydrate (Pt source), sodium borohydride (reducing agent), and citric acid (stabilizer). Silica-coated Ni-Pt nanoparticles (Ni-Pt/SiO₂) were synthesized by adding a tetraethylorthosilicate (TEOS)/ethanol solution to the colloidal Ni-Pt nanoparticle solution. The morphology of the Ni-Pt nanoparticles varied with reaction time. The Ni-Pt/SiO₂ nanoparticles consisted of Ni-Pt cores and SiO₂ shells, with their morphology dependent on the TEOS concentration. Furthermore, the Ni-Pt/SiO₂ nanoparticles were more dispersed than the uncoated Ni-Pt nanoparticles, suggesting that the silica coating suppressed aggregation.

Abstract: The most promising direction in alternative energy is hydrogen energy, using hydrogen as a secondary energy carrier. A key component in hydrogen energy is a fuel cell, especially on solid polymer membranes. Increasing the efficiency, reducing the cost and increasing the service life of such elements is the primary task of this direction. These tasks need to be solved from two sides: by improving the parameters of platinum catalysts in electrochemical reactions of energy sources, as well as by improving the qualities of the membrane. The aim of the work is to synthesize and study composites with palladium and platinum nanoparticles in hydrogen-oxygen fuel cells.

Abstract: Platinum (Pt), a noble metal, is known for its ability to regenerate and be recycled even without any reactivation procedure, and still demonstrated good stability. The cost of the noble metal can be reduced by incorporating the metal into the pores of catalyst support rather than using it individually. Hence, in this research study, 4 wt.% Pt supported on silica-alumina (SiO₂-Al₂O₃) and gamma-alumina (γ-Al₂O₃) was synthesized using wet impregnation method, then followed by catalyst calcination at 500 °C. The catalyst was then characterized using Thermogravimetric Analysis (TGA), Fourier-Transform Infrared Spectroscopy (FTIR), Brunauer–Emmett–Teller (BET), and particle size analyzer where catalyst with high surface area and pore volume demonstrated an excellent performance for the catalytic reaction of cellulose. Experimental results showed that catalyst Pt/SiO₂-Al₂O₃ with the highest surface area and pore volume (466.4 m²/g and 0.1157 cm³/g, respectively) exhibited the highest catalytic performance with the conversion of cellulose up to 65.8% and 30.9% levulinic acid (LA) yield produced at the reaction temperature of 200 °C in a semi-batch reactor for 8 hrs.

Abstract: Increasing durability of catalysts used in fuel cells is a necessary condition for their widespread commercialization. Fulfilling this condition requires understanding the catalyst degradation mechanism to propose how to reduce it. Transmission electron microscopy can help solve this problem thanks to the fact that it enables direct observation and thus unambiguous interpretation of the processes taking place. For this purpose, Identical Location Transmission Electron Microscopy (IL-TEM) was applied for observations of a commercial catalyst (platinum nanoparticles with a diameter of about 2 nm deposited on Vulcan carbon black) before and after durability tests. Obtained results may contribute to the development of better models of phenomena occurring during cell operation.

Abstract: This work is devoted to the study of the activity of 1% platinum catalysts containing rare earth element oxides (OREE) - Gd₂O₃, Ce₂O₃ and aluminum oxide as a carrier in the hydrogenation reactions of nitro compounds on the example of n-nitrotoluene. These catalytic systems in the conditions of liquid-phase hydrogenation provide high selectivity of the process and practically quantitative yield. The process was controlled by the potentiometric method, the reaction rate was judged by the amount of hydrogen absorbed per unit time. It is found that 20% and higher aqueous alcohol solutions can be used as a solvent during hydrogenation. It was found that the initial hydrogenation rate for 1% Pt/Gd₂O₃ is 3.2 times higher, and for 1% Pt/Ce₂O₃ Cerium it is 1.6 times higher relative to the 1% Pt/Al₂O₃ comparison catalyst.

Abstract: The multilayer composite films consisting of poly (diallyldimethylammonium chloride) functionalized graphene (PDDA-rGO) and phosphomolybdic acid functionalized graphene (PMo₁₂-rGO) were prepared by layer-by-layer self-assembly method. The {PDDA-rGO/PMo₁₂-rGO}_n multilayer composite films were used as a support for electro-deposition of Pt particles in situ. Cyclic voltammetry (CV), X-ray photoelectron spectroscopy and scanning electron microscopy were employed for examining the composition, structure, and morphology of the catalyst. Results revealed that the Pt/{PDDA-rGO/PMo₁₂-rGO}_n catalyst is successfully prepared and that the multilayer composite films support improves the dispersion of the Pt particles. CV and chronoamperometry were employed to evaluate the electrocatalytic performance for methanol oxidation. Results revealed that the electrocatalytic activity and stability of the Pt/{PDDA-rGO/PMo₁₂-rGO}₃ catalyst for methanol oxidation are considerably improved in comparison with that of the Pt/GCE catalyst. The current density for the oxidation of methanol increased from 0.66 mA/cm² to 1.21 mA/cm². In addition, the ratio of the forward current density to the backward current density (I_f/I_b) was 1.92 for Pt/{PDDA-rGO/PMo₁₂-rGO}₃ catalyst, corresponding to 1.3 times that of the Pt/GCE catalyst. This result indicated that the multilayer composite films remarkably enhanced the electrocatalytic activity regarding methanol oxidation.

Abstract: 1.25 – 5wt%Pt/Al₂O₃, 1.25 – 5wt%Pd/Al₂O₃, 1wt%Pd/TiO₂, 1 – 5wt%Pd/TiO₂-NF, 1.25wt%Pt+1.25wt%Pd/Al₂O₃, 5wt%Pt/SiO₂, 5wt%Pt/C catalysts were synthesised and tested in the selective oxidation of 1,2-propanediol by molecular oxygen. It was found that all catalysts were active in alkaline water solutions; lactic acid was obtained as the main product of the reaction. The conversion of 1,2-propandiol and the yield of lactic acid depended on the content of active metal in the catalysts. The most active for the oxidation of 1,2-propandiol were palladium-containing catalysts supported on TiO₂ nanofibers (Pd/TiO₂-NF). The highest 1,2-propanediol conversion (100 %) and lactic acid yield (96 %) were obtained using the 5wt%Pd/TiO₂-NF catalyst at the following oxidation parameters: c₀(1,2-propanediol) = 0.3 mol/L, P(O₂) = 1 atm, n (1,2-propanediol)/n (Pd) = 500 mol/mol, t = 60 °C, c₀(NaOH) = 1.5 mol/L.

Abstract: The processing conditions of the of electronic wastes are largely dependent on environmental standards and requirements. Modern technologies for processing electronic waste should meet the increased demand for metals as well as the requirements. Electronic wastes can be classified as hazardous materials, as household and industrial electrical devices, which contain components such as batteries, capacitors, cathode ray tubes, etc. Electronic waste can consist of a large number of components of various sizes, shapes and chemical composition. Some of them contain hazardous metals, including mercury, lead, cadmium. The presence of precious metals in electronic waste such as gold, silver, platinum, palladium, as well as non-ferrous metals (copper, nickel, zinc, tin, etc.) make it attractive for processing. In industry, both hydrometallurgical and pyrometallurgical methods are used to extract valuable metals from electronic waste. Applied technologies may have both advantages and disadvantages.

Abstract: This article presents the technological aspects of experiments on the stable topological patterns formation from thin films of platinum on ceramic membranes. Platinum thin films were deposited by magnetron sputtering on a clean or pre-activated laser ceramics surface. After the deposition of platinum films, the method of various short-term laser irradiation was attempted to form a topological pattern. The results are discussed.

Abstract: It was found that the surfaces of rhodium and platinum electrodes with polarization by direct current in 12 M hydrochloric acid solution are completely covered with oxygen atoms at a potential of +0.68 V (relative to the reference hydrogen electrode), and its increase rate is 10–90 mV/s.