Optimized Synthesis Approaches of Metal Nanoparticles with Antimicrobial Applications

According to the literature data, metal nanoparticles can be synthesized by various methods but the chemical reduction methods are mostly applied getting more advantageous comparing with the other methods. This work emphasizes also that the combination of synthetized methods could lead to the spectacular results depending on the application. Among the chemical methods, this work analyzed the polyol method, radiolytic process, microemulsion method, solvo-thermal method, microwave-assisted synthesis, and electrochemical synthesis. It also presents the main application of metal nanoparticles in biomedical fields, empathizing on their antimicrobial potential.

Enhanced CO Oxidation Catalysis of Pt0.1Cu0.9/Fe2O3 Synthesized by Radiolytic Process

ABSTRACTCatalysts in which Pt and Cu are immobilized on support particles of γ-Fe2O3 were synthesized by the radiolytic process and were evaluated for CO oxidation in a gas flow mixture (1% CO, 0.5% O2, 67.2% H2 and N2 balance) by measuring the CO concentration in the outlet gas. The Pt/Cu atomic ratios of the as-synthesized catalysts were determined to be 100:0, 90:10, 78:22, 50:50, 21:79, and 11:89, and the total metal loadings determined by chemical analyses were 10 wt%. Material characterization was performed using X-ray diffraction, X-ray absorption near edge structure, and transmission electron microscopy, and it was indicated that the composite catalysts consist of Pt-Cu bimetallic grains immobilized on the support at higher Pt-loading, while CuO with poor crystallinity is also observed at lower Pt-loading. The catalytic activity decreased as the Pt-loading was decreased to 50 at%, and also with increasing temperature. However, as the Pt-loading was further decreased, the activity contrariwise increased, and increased with increasing temperature up to 100 °C. The sample containing only 11 at% Pt exhibited the highest activity at 100 °C, which is higher than that of the commercial catalyst measured for comparison, and given at a lower temperature than that for the commercial catalyst. This enhanced activity, despite the low Pt-loading, could be attributed to oxygen supply via CuO from the O2-poor atmosphere to PtCu bimetallic grains trapping CO molecules. This new material is promising for use as a catalyst to purify hydrogen gas fed to a polymer electrolyte fuel cell.

Improved Electrochemical Durability of PtRuAu/C Catalyst Synthesized by Radiolytic Process

ABSTRACTNanoparticle catalyst of PtRuAu/C for direct methanol fuel cell anodes was synthesized by a radiolytic process. Its methanol oxidation activity and the electrochemical durability were evaluated by using the linear sweep voltammetry and the cyclic voltammety. The Au addition significantly improved the durability in comparison with PtRu/C catalyst without losing its high activity. The atomic structure was characterized with techniques of the transmission electron microscopy, the X-ray diffraction, the X-ray fluorescence spectroscopy and the X-ray absorption fine structure. These results implied that the arrangement of Pt and Ru atoms in the PtRuAu/C has no significant difference from that without Au, possessing a structure of Pt rich core and PtRu alloy shell. We concluded that the improvement in durability could originate from these PtRu nanoparticles decorated with Au, but not from particles with high Au contents.

Studies on Spent Fuel Alterations During Storage and Radiolysis Effects on Corrosion Behaviour Using Alpha-Doped UO2

UO2 containing different fractions of short-lived alpha-emitters, the so-called alpha-doped UO2 simulates the level of activity of spent fuel after different storage times, and can be used to study the effects of radiolysis on the corrosion behaviour of aged spent fuel exposed to groundwater in a geologic repository. Furthermore, the integral over time of the alpha-decay in alpha-doped UO2 can simulate the decay damage accumulated in spent fuel during storage. This allows investigating property modifications occurring to the fuel during storage periods of interest (e.g. in view of spent fuel retrieval or in view of final disposal) within a laboratory-acceptable timescale. Periodical measurements of lattice parameter are performed on high activity alpha-doped UO2 to investigate the build-up of radiation damage and evaluate possible dose rate effects. Additionally, annealing tests combined with He-release measurements using a Knudsen cell and with microstructure examination using TEM are performed to establish a correlation among the annealing of damage in the microstructure (mainly characterized by dislocation loops) and the release behaviour of He. The effects on the microstructure due to the accumulation of He and α-decay damage are of interest as they may considerably affect the mechanical integrity of the fuel rods, by causing e.g. swelling or cracking in the fuel and/or overpressurization of the cladding. Alpha-doped UO2 with specific activities spanning over three orders of magnitude and undoped UO2 were used in static leaching experiments at room temperature in deionized water under nominally anoxic conditions. Under these experimental conditions (single effect studies) a clear dissolution enhancing effect of alpha-radiolysis was observed coupled with the establishment of higher redox potential due to the radiolytic process. An alpha-activity dependence of the dissolution behaviour was observed.

Silicon Hydride Formation in Co-60 Irradiated Optical Fibers

ABSTRACTDoping with hydrogen is shown to reduce the sensitivity of optical fibers to form optical attenuation bands as a result of ionizing radiation and to increase the recovery rate in the near infrared after the exposure. In this case silicon hydride is shown to form in low-OH, pure silica fibers upon Co-60 irradiation. The ratio of radiolytically induced changes in silicon hydride to silicon hydroxide is estimated to be greater than ten. The more numerous radiolytic formation of SiH species implies the participation of oxygen vacancy type defects in the radiolytic process.