K-, CeO2-, and Mn-promoted Ni/Al2O3 catalysts for stable CO2 reforming of methane

Reforming of methane with carbon dioxide into syngas over Ni/γ-Al₂O₃ catalysts modified by potassium, MnO and CeO₂ was studied. The catalysts were prepared by impregnation technique and were characterized by N₂ adsorption/desorption isotherm, BET surface area, pore volume, and BJH pore size distribution measurements, and by X-ray diffraction and scanning electron microscopy. The performance of these catalysts was evaluated by conducting the reforming reaction in a fixed bed reactor. The coke content of the catalysts was determined by oxidation conducted in a thermo-gravimetric analyzer. Incorporation of potassium and CeO₂ (or MnO) onto the catalyst significantly reduced the coke formation without significantly affecting the methane conversion and hydrogen yield. The stability and the lower amount of coking on promoted catalysts were attributed to partial coverage of the surface of nickel by patches of promoters and to their increased CO₂ adsorption, forming a surface reactive carbonate species. Addition of CeO₂ or MnO reduced the particle size of nickel, thus increasing Ni dispersion. For Ni–K/CeO₂–Al₂O₃ catalysts, the improved stability was further attributed to the oxidative properties of CeO₂. Results of the investigation suggest that stable Ni/Al₂O₃ catalysts for the carbon dioxide reforming of methane can be prepared by addition of both potassium and CeO₂ (or MnO) as promoters.     

A Synergic Blend of Newly Isolated <Emphasis Type=Italic>Pseudomonas mandelii</Emphasis> KJLPB5 and [hmim]Br for Chemoselective 2° Aryl Alcohol Oxidation in H<Subscript>2</Subscript>O<Subscript>2</Subscript>: Synthesis of Aryl Ketone or Aldehydes via Sequential Dehydration-Oxidative C=C Cleavage

Abstract  

Pseudomonas mandelii KJLPB5 is reported for the oxidation of aryl alcohols in ionic liquid [hmim]Br (1-hexyl-3-methyl imidazolium bromide) with H₂O₂. With a slight alteration of reaction conditions, the developed protocol leads either to (i) chemoselective oxidation of 2° aryl alcohols over 1° and aliphatic counterparts or (ii) direct one pot-two step sequential conversion of 2° aryl alcohols into corresponding one or two carbons shorter aryl aldehydes through oxidative cleavage pathway, thus providing a new facet to metal-free oxidations. The key operational parameters such as substrate concentration, incubation temperature, incubation time, ionic liquid type and ionic liquid concentration are also optimized.     

On the hazard function of Birnbaum-Saunders distribution and associated inference

In this paper, we discuss the shape of the hazard function of Birnbaum-Saunders distribution. Specifically, we establish that the hazard function of Birnbaum-Saunders distribution is an upside down function for all values of the shape parameter. In reliability and survival analysis, as it is often of interest to determine the point at which the hazard function reaches its maximum, we propose different estimators of that point and evaluate their performance using Monte Carlo simulations. Next, we analyze a data set and illustrate all the inferential methods developed here and finally make some concluding remarks.     

Just-in-time dynamic voltage scaling: Exploiting inter-node slack to save energy in MPI programs

Although users of high-performance computing are most interested in raw performance, both energy and power consumption have become critical concerns. As a result, improving energy efficiency of nodes on HPC machines has become important, and the prevalence of power-scalable clusters, where the frequency and voltage can be dynamically modified, has increased.