Slurry Erosive Wear Evaluation of HVOF-Spray Cr2O3 Coating on Some Turbine Steels

In this study, Cr₂O₃ coatings were deposited on CF8M and CA6NM turbine steels by high-velocity oxy-fuel (HVOF)-spray process and analyzed with regard to their performance under slurry erosion conditions. High Speed Erosion Test Rig was used for slurry erosion tests, and the effects of three parameters, namely, average particle size, speed (rpm), and slurry concentration on slurry erosion of these materials were investigated. SEM micrographs on the surface of samples, before and after slurry erosion tests, were taken to study the erosion mechanism. For the uncoated steels, CA6NM steel showed better erosion resistance in comparison with CF8M steel. The HVOF-sprayed Cr₂O₃-coated CF8M and CA6NM steels showed better slurry erosion resistance in comparison with their uncoated counterparts. It may be due to the higher hardness as a result of HVOF-sprayed Cr₂O₃ coating in comparison with the uncoated CF8M and CA6NM steels.     

Three-dimensional phase-field modeling of martensitic microstructure evolution in steels

In the present work a 3-D elastoplastic phase-field (PF) model is developed, based on the PF microelasticity theory proposed by A.G. Khachaturyan and by including plastic deformation as well as anisotropic elastic properties, for modeling the martensitic transformation (MT) by using the finite-element method. PF simulations in 3D are performed by considering different cases of MT occurring in an elastic material, with and without dilatation, and in an elastic perfectly plastic material with dilatation having isotropic as well as anisotropic elastic properties. As input data for the simulations the thermodynamic parameters corresponding to an Fe-0.3%C alloy as well as the physical parameters corresponding to steels acquired from experimental results are considered. The simulation results clearly show autocatalysis and morphological mirror image formation, which are some of the typical characteristics of a martensitic microstructure. The results indicate that elastic strain energy, anisotropic elastic properties, plasticity and the external clamping conditions affect MT as well as the microstructure.     

在表面活性剂存在下铬铁矿表土中镍的微生物萃取(英文)

加入表面活性剂吐温20,用Aspergillus niger对预处理过的印度Sukinda铬铁矿表土在摇瓶中生物浸取镍。考察添加表面活性剂吐温20对黑曲霉菌Aspergillus niger生长及浸镍效果的影响。结果表明,添加低浓度的表面活性剂吐温20对黑曲霉菌从预处理过的铬铁矿表土中提取镍是有利的。通常,Aspergillus niger利用培养基中的碳源来进行细胞代谢,产生有机代谢物,从而生物浸出矿。添加表面活性剂吐温20加速了黑曲霉菌对碳源的消耗,从而改善了镍浸出效果。在预处理矿浆浓度为2%和温度为30°C的条件下,添加表面活性剂吐温20的镍浸取率能达到39%,没有表面活性剂的镍浸取率只有24%。     

High Temperature Thermodynamics of RE(La,Ce,Pr,Y,Tb)-S-F Systems

ＨｉｇｈＴｅｍｐｅｒａｔｕｒｅＴｈｅｒｍｏｄｙｎａｍｉｃｓｏｆＲＥ（Ｌａ，Ｃｅ，Ｐｒ，Ｙ，Ｔｂ）－Ｓ－ＦＳｙｓｔｅｍｓＨｏｎｇＹａｎｒｕｏ；Ｒ．ＶａｓａｎｔＫｕｍａｒ＊ａｎｄＬｉＬｉａｎｓｈｅｎｇ（洪彦若）（李联生）（ＵｎｉｖｅｒｓｉｔｙｏｆＳｃｉｅ...     

Effects of Silver Addition on Properties and Performance of Plasma Sprayed La0.6Sr0.4Co0.2Fe0.8O3−δ Interconnect Layer

Interconnect layers on stainless steel substrates (STS430) for solid oxide fuel cells (SOFC) were built up by atmospheric plasma spraying (APS) using spray dried La_0.6Sr_0.4Co_0.2Fe_0.8O_3?δ (LSCF) and blended LSCF/Ag composites. The microstructure and phase of each coating were analyzed using scanning electron microscopy (SEM) and x-ray diffraction (XRD) studies, respectively. Furthermore, bond strength, microhardness, performance in a thermal cycle test and in an oxidation test, and electrical conductivity were measured and compared. The coatings prepared from spray dried LSCF have higher porosity and more cracks within the splats and at intersplat boundaries. In contrast, the coatings prepared from LSCF/Ag had fewer cracks and less porosity due to the relatively high ductility of silver. After oxidation testing at 800 °C for 200 h, the weight change of the STS430 substrate and the LSCF and LSCF/Ag-coated alloys were found to be 0.06833, 0.01950, and 0.01656 mg/cm², respectively. Also the electrical conductivity of LSCF and LSCF/Ag coatings were higher than that of STS430 by two orders.     

Electrochemical membrane reactor: Synthesis of quaternary ammonium hydroxide from its halide by in situ ion substitution

Electrochemical membrane reactors (EMRs) with two compartments (EMR-2: anion-exchange membrane (AEM) separated catholyte and anolyte) and three compartments (EMR-3: three compartments separated by two AEMs to avoid contact between the product and the electrodes) were developed for the synthesis of tetrabutylammonium hydroxide (TBAOH) from tetrabutylammonium bromide (TBABr) by in situ ion substitution. In house prepared AEM with good physicochemical, electrochemical properties and excellent stabilities was used. Schematic diagrams are presented for the possible synthesis of TBAOH from TBABr by in situ ion substitution in EMR-2 and EMR-3. Synthesis of TBAOH using EMR-2 and EMR-3 was achieved under different experimental conditions and process parameters (rate of synthesis, current efficiency (CE) and energy consumption) were estimated. In EMR-2, relatively slow synthesis of TBAOH with low recovery was explained due to Hofmann elimination of TBAOH in contact with the electrode. While in EMR-3, relatively faster rate of TBAOH synthesis with its high recovery and current efficiency indicated practical application of the developed process for the efficient synthesis of TBAOH without the use of any additives or reagents.     

A Novel Oxidation of Valine by N-Bromophthalimide in the Presence of Ruthenium(III) Chloride as a Homogeneous Catalyst

Kinetics of Ruthenium(III) [Ru(III)] chloride catalyzed oxidation of valine (Val) has been studied by N-bromophthalimide (NBP) in the acidic medium at 35 °C. The reaction rate follows first-order and zero-order dependence with respect to [NBP] and [Val]. First-order kinetics was observed for Ru(III) chloride at low range of concentrations and tending towards zero-order at higher concentrations. A negative effect was observed for [H⁺] and [phthalimide], while a positive effect was observed for [Cl^?] on the reaction rate. Hg(OAc)₂, ionic strength (I), and dielectric constant (D) of the medium did not change significantly the reaction rate. The rate constants as a function of temperature (298–318 K) were used to calculate activation parameters of the oxidation of Val by NBP. A plausible mechanism was proposed to explain the results of kinetic studies, reaction stoichiometry and product analysis.     

Influence of Mg Addition on the Catalytic Activity of Alumina Supported Ag for C3H6-SCR of NO

The influence of different magnesium (Mg) weight percentages (1, 2.5, 5, 7.5 and 10) over silver (3 wt%) impregnated alumina (SA) catalyst was investigated for the reduction of NO by C₃H₆. Mg doped SA catalysts were prepared by conventional impregnation method and characterized by XRD, BET-SA, ICP-MS, XPS, SEM, UV-DRS, H₂-TPR and O₂-TPD. The existence of MgO and MgAl₂O₄ phases on Mg doped SA catalysts were observed from XRD and XPS analyses. Existence of high percentage MgAl₂O₄ phase on 5% Mg doped SA catalyst (Mg (5) SA) enhances the dispersion and stabilization of silver phases (Ag₂O). Mg (5) SA catalyst shows a 51% of high selectivity (NO to N₂) in presence of SO₂ (80 ppm) at low temperatures (350 °C) and maintained high selectivity’s with a wide temperature window (350–500 °C). An optimal high surface availability of Ag⁰ and Ag⁺ species were observed from XPS analysis over Mg (5) SA catalyst. H₂-TPR analysis shows high temperature reduction peak over Mg (5) SA compared to SA catalyst. XPS analysis confirms the high percent availability of MgAl₂O₄ species over Mg (5) SA catalyst. DRIFTS study reveals the molecular evidences for the evolution of enolic species during NO reduction over the highly active Mg (5) SA catalyst at low temperatures. It also confirms further transformation of enolic species into –NCO species with NO + O₂ and finally into N₂ and CO₂.     

Synthesis and emission analysis of RE (Eu or Dy):Li2TiO3 ceramics

The development and photoluminescence analysis of Eu³⁺or Dy³⁺ ions in the matrix of lithium titanate (Li₂TiO₃) ceramics by using a solid state reaction method are reported. Emission spectra of Eu³⁺:Li₂TiO₃ ceramics have shown strong red emission at 611 nm (⁵D₀ → ⁷F₂) with λ_exci = 392 nm (⁷F₀ → ⁵L₆) and from the Dy³⁺:Li₂TiO₃, a blue emission at 493 nm (⁴F_9/2 → ⁶H_15/2) and also an yellow emission at 582 nm (⁴F_9/2 → ⁶H_13/2) have been observed with λ_exci = 366 nm (⁶H_15/2 → ⁶P_5/2). Both the rare-earth ions containing ceramics have displayed their brighter emission performance from their measured spectral results. In addition, X-ray diffraction (XRD), Fourier transform infra red (FTIR) spectroscopy, scanning electron microscopy (SEM) and energy dispersive X-ray analysis (EDAX) have been used to characterize the structural properties of (Eu³⁺ or Dy³⁺):Li₂TiO₃ ceramics.