High-temperature Water–Gas Shift catalysts for hydrogen enrichment of a gas produced by biomass steam gasification

To improve the hydrogen content of a biomass steam gasification syngas, Water–Gas Shift Fe/CeO₂ catalysts supported on ceramic foams were developed. The impregnation of ceria as washcoat led to an increase in the support surface area (BET) and to the formation of well-dispersed iron particles (XRD and TPR) by iron oxide impregnation. Catalytic tests were performed at atmospheric pressure with minor pressure drops, under a gas mixture similar to that produced at the gasifier outlet. A satisfactory CO conversion and a large increase in H₂ content were reached by adjusting the operating parameters of the WGS and the catalysts’ composition. After-test characterizations indicated in situ catalysts activation with no over-reduction and a positive action of ceria on iron dispersion and sintering prevention.     

Synthesis and characterization of BaGa2O4 and Ba3Co2O6(CO3)0.6 compounds in the search of alternative materials for Proton Ceramic Fuel Cell (PCFC)

BaGa₂O₄ and Ba₃Co₂O₆(CO₃)_0.6 compounds were studied as electrolyte and cathode materials for Proton Ceramic Fuel Cells (PCFC), respectively. Not only BaGa₂O₄ rapidly reacts with atmospheric H₂O and CO₂ and leads to a progressive material decomposition, but it does not present real hydration properties in normal conditions of pressure. On the other hand, the basic cobalt oxocarbonate Ba₃Co₂O₆(CO₃)_0.6 exhibits an interesting tendency for weight uptake and formation of hydrogencarbonate groups in moist heating/cooling conditions. This material was therefore considered for complementary studies in order to confirm its potential use as mixed proton-electron conductor, taking into account the ordered intergrowth of carbonates and face sharing Co-octahedra columns forming a pseudo-one-dimensional structure. Some preliminary results concerning electrochemical properties of the barium cobalt oxocarbonate as a PCFC cathode are also described and show at the moment modest performance, possibly related to a hydrated/carbonated surface layer contribution and/or the lack of electron percolation within the electrode layer.     

阴极微弧电沉积制备Al2O3陶瓷层技术及研究进展

阴极微弧电沉积技术是一种在材料表面通过微弧放电沉积陶瓷层的表面处理技术,利用该技术可以在金属及非金属表面生成耐磨、耐蚀性能优异的陶瓷膜层.本文介绍了阴极微弧电沉积技术的研究现状以及应用阴极微弧电沉积技术制备Al2O3陶瓷层的方法和基本原理,并且对阴极微弧电沉积技术的影响因素进行了总结,阐述了阴极微弧电沉积技术的应用前景和存在的问题.     

反相高效液相色谱法测定陶瓷饰品中六价铬的溶出量

提出了柱前衍生反相高效液相色谱法测定陶瓷饰品中六价铬溶出量的方法。采用人工汗液萃取陶瓷饰品,用1,5-二苯卡巴肼与萃取液中的六价铬在酸性条件下进行衍生反应,衍生物在Waters SunFire ODS C18色谱柱上分离,以pH 2.5的10mmol·L-1磷酸二氢钾缓冲溶液和丙酮为流动相进行梯度洗脱,于波长540nm处进行测定。六价铬的质量浓度在5.0~200.0μg·L-1范围内与峰面积呈线性关系,相关系数为0.999 1,检出限(3S/N)为0.037μg·L-1。空白(实际样品)的加标回收率在97%~101%之间,测定值的相对标准偏差在1.9%~3.2%之间。     

Resistance switching memory in perovskite oxides

The resistance switching behavior has recently attracted great attentions for its application as resistive random access memories (RRAMs) due to a variety of advantages such as simple structure, high-density, high-speed and low-power. As a leading storage media, the transition metal perovskite oxide owns the strong correlation of electrons and the stable crystal structure, which brings out multifunctionality such as ferroelectric, multiferroic, superconductor, and colossal magnetoresistance/electroresistance effect, etc. The existence of rich electronic phases, metal–insulator transition and the nonstoichiometric oxygen in perovskite oxide provides good platforms to insight into the resistive switching mechanisms.     

Micromechanics of residual stress and texture development due to poling in polycrystalline ferroelectric ceramics

This paper presents micromechanics based analysis of elastic strain and changes in the texture of poled polycrystalline ferroelectric PZT ceramics for direct comparison with synchrotron X-ray measurements. The grains are modelled as spherical inclusions, to which transformation strains are assigned depending on the fractions of different ferroelectric domains. Eshelby's inclusion problem with the classical self-consistent method is applied to evaluate the elastic state of the grains. In particular, the elongation due to lattice elastic strain is calculated as a function of inclination Ψ relative to the polar axis. The ratio of diffraction peak intensities, corresponding to the domain fractions, is also expressed as a function of Ψ. This analysis identifies the special character of the reflection, for which the lattice strain along in the stress free state is independent of ferroelectric domain population and hence unaffected by poling. The elongation due to the lattice strain parallel to and peak intensity ratio are expressed in terms of the overall macroscopic strain of a poled specimen, each having a dependence.     

Dynamic compressive responses of intact and damaged ceramics from a single split Hopkinson pressure bar experiment

A novel dynamic compressive experimental technique has been developed based on a split Hopkinson pressure bar. This new method dynamically loads the ceramic specimen by two consecutive stress pulses. The first pulse determines the dynamic response of the intact ceramic materiaal and then crushes the specimen, and the second pulse determines the dynamic compressive constitutive behavior of the ceramic rubble. Precise pulse shaping ensures that the specimen deforms at nearly constant strain rates under dynamic stress equilibrium during the loading by both stress pulses. Pulse shaping also controls the amplitudes of loading pulses, the values of strain rates, the maximum strains in the rubble specimens, and the proper separation time between the two loading pulses. The feasibility of the new technique is demonstrated by the experimental results obtained on an AD995 alumina.     

Effects of interface dislocations on properties of ferroelectric thin films

Effects of interfacial dislocations on properties of thin-film ferroelectric materials, such as the self-polarization distribution, Curie temperature, dielectric constant and the switching behaviors, are investigated via the system dynamics based on the Landau-Devonshire functional. Dislocation generation in the film is found to reduce the overall self-polarization and the Curie temperature. The spatial variations are both very strong, particularly in the immediate neighborhood of the dislocation cores. In agreement with previous results based on a stationary model, a dead layer exists near the film/substrate interface, in which the average self-polarization is much reduced. Moreover, it is evident from our results that interface dislocations play an important role in suppressing the remnant polarization and the coercive field of the polarization.