In this study, a Pt/anodized aluminum oxide (AAO) catalyst was prepared by the anodization of an Al alloy (Al6082, 97.5% Al), followed by the incorporation of Pt via an incipient wet impregnation method. Then, the Pt/AAO catalyst was evaluated for autocatalytic hydrogen recombination. The Pt/AAO catalyst’s morphological characteristics were determined by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The average Pt particle size was determined to be 3.0 ± 0.6 nm. This Pt/AAO catalyst was tested for the combustion of lean hydrogen (0.5–4 vol% H2 in the air) in a recombiner section testing station. The thermal distribution throughout the catalytic surface was investigated at 3 vol% hydrogen (H2) using an infrared camera. The Al/AAO system had a high thermal conductivity, which prevents the formation of hotspots (areas where localized surface temperature is higher than an average temperature across the entire catalyst surface). In turn, the Pt stability was enhanced during catalytic hydrogen combustion (CHC). A temperature gradient over 70 mm of the Pt/AAO catalyst was 23 °C and 42 °C for catalysts with uniform and nonuniform (worst-case scenario) Pt distributions. The commercial computational fluid dynamics (CFD) code STAR-CCM+ was used to compare the experimentally observed and numerically simulated thermal distribution of the Pt/AAO catalyst. The effect of the initial H2 volume fraction on the combustion temperature and conversion of H2 was investigated. The activation energy for CHC on the Pt/AAO catalyst was 19.2 kJ/mol. Prolonged CHC was performed to assess the durability (reactive metal stability and catalytic activity) of the Pt/AAO catalyst. A stable combustion temperature of 162.8 ± 8.0 °C was maintained over 530 h of CHC. To confirm that Pt aggregation was avoided, the Pt particle size and distribution were determined by TEM before and after prolonged CHC.

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The aim of this paper is the comparison of structural, morphological and electrical properties of thermally extended graphite synthesized by chemical oxidation of graphite with sulfur of nitric acids at all other same conditions. Thermal treatments of graphite intercalation compounds were performed at a temperature of 600°C on the air for 10 min but additional annealing in temperature range of 100-600oC for 1 hour was done. The obtained materials were characterized by XRD, Raman spectroscopy and impedance spectroscopy. The evolution of structural ordering of thermally extended graphite samples at increasing of annealing temperature was traced. It was determined that the additional annealing allows to control the electrical conductivity and structural disordering degree of extended graphite samples that is useful for preparation of efficient current collectors for electrochemical capacitors.

Passive autocatalytic recombiners (PARs) are used for the removal of accidentally released hydrogen inside confined spaces. The high catalyst surface temperature is an important safety issue to be considered in the use of a PAR. The ability to predict the catalyst surface temperature could be very useful in preventing the self-ignition and explosion of hydrogen inside the PAR. This study seeks to investigate the changes in temperature profiles of the PAR catalytic section upon variation of the inlet hydrogen concentration. Experiments were conducted on a small-scale test setup. The catalytic section comprised cylindrical ceramic elements arranged in parallel and held upright by a stainless-steel frame. The temperature profiles were measured with a high-resolution infrared camera. The commercial computational fluid dynamics (CFD) code STAR-CCM+ was used as a numerical tool for modeling the gas mixture flow inside the experimental setup and the chemical reaction kinetics. The results of numerical studies are presented and compared with experimental results. The presented CFD-based approach and software offer an appropriate numerical tool for the investigation of hydrogen safety issues. Finally, the catalyst was subjected to a prolonged high-temperature combustion fatigue procedure to determine its stability. The surface of the fatigued catalyst was evaluated by scanning electron microscopy and energy-dispersive X-ray spectroscopy. It was found that decomposition of the protective surface layer occurred at elevated temperatures; the catalytic activity was unaffected by this. In addition, a relatively uniform reactive metal particle size was maintained over the entire temperature range, suggesting that no aggregation occurred.

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