Factors affecting aluminum depletion during cyclic oxidation of Fe-base alumina-forming alloys

Abstract

In order to develop an improved oxidation-limited lifetime model, experiments are being conducted to assess the critical factors that affect the rate of Al loss from Fe-base alumina-forming alloys during cyclic oxidation. Both wrought and dispersion strengthened ferritic and intermetallic Fe–Al±Cr alloys are being investigated at exposure temperatures from 1100–1300°C. Higher temperatures, thinner specimens and cycle frequency are used to accelerate degradation during oxidation. However, the effects of these experimental choices often have not been critically assessed in prior work. Electron probe microanalysis has been used to measure the residual Al content under various conditions and at various stages of life. For 0.5–2mm thick specimens, lifetime repeatedly showed a linear relationship to thickness. Increasing the oxidation temperature appears to be the most viable strategy to accelerate the evaluation of oxidation resistance for comparing and developing alloys.     

Size dependent ferromagnetism in dodecyl amine capped ZnO nanoparticles

We investigated the size dependent ferromagnetism in dodecyl amine capped zinc oxide nanoparticle. X-ray diffraction and X-ray photoelectron spectroscopy analysis demonstrated that density of oxygen vacancies was enhanced due to an increase in compressive strain concomitant with the decrease in particle size. Magnetic measurements showed increased ferromagnetic ordering in ZnO nanoparticles with reduced particle size. It was also found that the increase in coercive field, saturation magnetization and magnetic hysteresis loop area were invariably associated with increased oxygen defect population. The observed ferromagnetism in organic capped zinc oxide nanocrystals has therefore been assigned to defect induced phenomena. Results of sample characterization using optical absorption spectroscopy, photo luminescence spectroscopy and high resolution transmission electron microscope have also been presented.     

Electrochemical Study on the Reduction Mechanism of Uranium Oxide in a LiCl-Li2O Molten Salt

By means of a linear sweep voltammetry, a cyclic voltammetry and a chronopotentiometry, the electrolytic reduction of uranium oxide has been studied to establish the reduction mechanisms, which are based on a simultaneous uranium oxide reduction and a Li₂O electrowinning, and the formation and electrolysis of lithium uranate. From the voltammograms, the reduction potentials of the uranium oxide and Li₂O were obtained. From the chronopotentiometries based on the results of the voltammograms, the uranium oxide was reduced to uranium metal through the reduction mechanisms showing a more than 99% conversion. For a verification of the reduction mechanisms feasibility, basic data on the electrolytic reduction of the uranium oxide was obtained from the experiments and the characteristics of the closed recycle of Li₂O were discussed.     

Harnessing power from sea water using nano material as photocatalyst and solar energy as light source: the role of hydrocarbon as dual agent

The splitting of water in the presence of ordinary and nano TiO₂ was carried out using hydrocarbon as a dual agent and solar energy as a light source for these experiments. The hydrogen gas evolved was tested and measured using downward displacement of water. The observed results show that more hydrogen was evolved when nano TiO₂ was used as catalyst due to the larger surface area of the nano material. The splitting of sea water yields more hydrogen compared with ordinary water due to the presence of electron donating sodium ions in water. The added hydrocarbon plays a dual role as electron donor and as a trapping agent, which enhances the production of hydrogen to a greater extent compared with the regular donors such as olefin. Copyright © 2013 John Wiley & Sons, Ltd.     

WO3/BiVO4 composite photoelectrode prepared by improved auto-combustion method for highly efficient water splitting

We report on the improvement in the water splitting efficiency of a WO₃/BiVO₄ composite photoelectrode by the application of an improved auto-combustion method to the preparation of porous BiVO₄ thin films. The unique feature of this preparation method is the addition of both NH₄NO₃, as a strong oxidizing agent, and an organic additive into BiVO₄ precursor solution. The local decomposition heat of the organic additive and oxidizing agent created a porous film with small, highly crystalline BiVO₄ particles. The photoelectrode has many advantages over existing ones, such as the high light-harvesting efficiency (LHE), a single BiVO₄ phase, the facile access of the holes to the photoelectrode/electrolyte interface, and the ease of water and oxygen diffusion. The maximum incident photon-to-current efficiency (IPCE) was estimated to be 64% (at 440 nm, 1.23 V vs. RHE) and the applied bias photon-tocurrent efficiency (ABPE) reached as high as 1.28%. This ABPE value is highest among all oxide semiconductor photoelectrodes reported previously, except for the case of a stacking photoelectrode system.     

Recent progress in integration of reforming catalyst on metal-supported SOFC for hydrocarbon and logistic fuels

The metal-supported solid oxide fuel cell (MS-SOFC) is of current research interest in the clean energy field due to its high performance, quick start-up, thermal cycle stability, and lower raw material cost compared to the conventional cermet-based SOFC. To efficiently operate a MS-SOFC using complex hydrocarbon and logistic fuels, it is required to introduce an internal reforming catalyst within the anode metal scaffold. This review article discusses some examples of the performance of MS-SOFCs under hydrocarbon and logistic fuels with and without an additional reforming catalyst. We also discuss the performance improvement of conventional cermet-based SOFCs by adding reforming catalysts via the infiltration method. This information can be directly applied to future MS-SOFC applications. Furthermore, this review article proposes possible novel methods such as direct precursor infiltration, catalyst-anode premixing, and atomic layer deposition methods to introduce the reforming catalyst into a MS-SOFC for improving its initial electrochemical performance and long-term stability under hydrocarbon and logistics fuel.     

Production of biodiesel from castor oil using iron (II) doped zinc oxide nanocatalyst

The depletion of fossil fuels has caused the price of petroleum to rise remarkably and created need for alternative energy such as biodiesel. In the present study, the biodiesel was produced from castor oil using ferromagnetic zinc oxide nanocomposite as heterogeneous catalyst for transesterification reaction. Single phase of nanocatalyst were confirmed by X-Ray Diffraction analysis. The spherical shape of the aggregated nanocatalyst was observed in Scanning Electron Microscopy. Magnetic properties were analysed using vibrating sample magnetometer. Atomic Force Microscopic analysis revealed the larger surface area and roughness of nanocatalyst. The biodiesel yield of 91% (w/w) was obtained in 50 min at 55 °C with 14 wt % catalyst loading and 12:1 methanol/oil ratio and was confirmed by Gas chromatograph with Mass Spectrometer. The result showed that the iron (II) doped ZnO nanocatalyst is a promising catalyst for the production of biodiesel via heterogeneous catalytic transesterification under milder reaction conditions.     

One-step production of biodiesel through simultaneous esterification and transesterification from highly acidic unrefined feedstock over efficient and recyclable ZnO nanostar catalyst

Zinc oxide (ZnO) nanostar synthesized by simple and up-scalable microwave-assisted surfactant free hydrolysis method was applied as catalyst for biodiesel synthesis through one-step simultaneous esterification and transesterification from high free fatty acid (FFA) contaminated unrefined feedstock. It was found that ZnO nanostar catalyst was reacted with FFA to yield zinc oleate (ZnOl) as intermediate and finally became zinc glycerolate (ZnGly). With the re-deposition of ZnGly back to the ZnO nanostar catalyst at the end of the reaction, the catalyst can be easily recovered and stay active for five cycles. Furthermore, the rate of transesterification is highly promoted by the presence of FFA (6 wt.%) which makes it an efficient catalyst for low grade feedstock like waste cooking oil and crude plant oils.     

Synthesis of composite of graphene and UO3 composite via one-step solution chemical reaction and its application to UO2-based accident tolerant fuel

In this paper, two kinds of composites constructed by UO₃ nanoflakes (which is UO₃·yNH₃·xH₂O, precisely) and different graphene oxide (GO) nanosheets (homemade GO, GO-h, and commercial GO, GO-c) were prepared via solution chemical reaction. The two kinds of GO share similar morphology and possess the same species of functional groups. Nevertheless, GO-h possesses higher oxidization degree and thus could adsorb more uranyl ions, and the corresponding composite shows a much more regular shape: UO₃ nanoflakes and GO nanosheets cross each other, which would help overcome the disadvantage of graphene aggregation. As a result, homemade reduced graphene oxide (RGO-h) sheets inside the final UO₂ pellets (named as UO₂/GO-h) could construct a well-bulit thermally conductive network to enhance its thermal conductivity. However, similar RGO-c network cannot be observed in the UO₂/GO-c pellest originated from GO-c. Therefore, only the thermal conductivity of UO₂/GO-h pellet acquires a dramatic increase, 37.30% relative to UO₂ pellet at 1200 °C, showing that UO₂/GO-h possesses great potential for the development of novel UO₂-based ATF fuels.