Phase equilibria in the Al–Si–V system: The vanadium rich part

The V-rich part of the Al–Si–V phase diagram was determined by a combination of optical microscopy, powder X-ray diffraction (XRD), differential thermal analysis (DTA) and electron probe microanalysis (EPMA). Phase equilibria were investigated at two isothermal sections at 850 and 1300 °C. High temperature DTA was performed to identify the ternary invariant reactions yielding a ternary reaction scheme and the vertical section at 50 at.% V. As cast samples were investigated in order to gain additional information about primary crystallization fields. A liquidus surface projection was constructed for the entire ternary system by combining our experimental data with those from literature.     

接地故障中和器全补偿技术及应用

目前世界上普遍应用的配电系统消弧线圈接地方式在一定程度上保证了系统的供电可靠性,但仍然存在接地残流较大和高阻型故障检测难等问题。GFN(接地故障全中和器)具有消除接地电流、准确定位故障点,以及提升供电稳定性和可靠性的作用。介绍了瑞典GFN接地故障全补偿技术的基本原理、功能特点、应用实例和功能扩展等。实用情况表明GFN接地故障全补偿技术可以较为成功地减少特殊瞬时故障。     

德国中小城镇在国土开发中扮演的重要角色

与大多数欧洲城市相比,德国的城镇体系属于均衡发展的典范。地区的高度自治、联邦体制以及强有力的州政府使德国在两千多年的城市发展历程中,逐渐形成了大中小城市遍布全国的空间形态。这些城市都具有相似的生活质量、便捷的交通和便利的服务。基于对中小城镇的概括定义,本文将首先简要介绍城市均衡发展的历史渊源及小城镇在德国的重要作用,并举例分析一些进行中的都市化过程,随后将选取纽伦堡城市区域作为中小城镇的成功案例重点介绍,最后简要说明支持城镇发展的联邦政策规划。     

Quantification of Yttria in Stabilized Zirconia by Raman Spectroscopy

The relationship between Y₂O₃ content in tetragonal and cubic ZrO₂ phases and the shift of the Raman band at ～645/cm was investigated. With increasing Y₂O₃ content, the 645/cm Raman band position decreases to lower Raman shift values. A fit of x = Y₂O₃ content in wt% and y = Raman band position in per cm, was found to be valid for low Y₂O₃‐stabilized t‐ZrO₂, t′′‐ZrO₂ transition, and fully stabilized c‐ZrO₂. Modeling the change in lattice parameters due to the incorporation of Y₂O₃ in ZrO₂ as obtained from Rietveld‐refined XRD data confirms that the peculiar sigmoidal form of the band shift with Y₂O₃ content is mainly due to a variation of the amount of oxygen vacancies. The resultant method is highly attractive in fields of Y₂O₃ determination in ZrO₂ materials where a fast, spatially resolved, and nondestructive analysis is required.     

Structural characterization of octadecyl modified MCM-41 silica by NMR and FTIR

Mesoporous MCM-41 silica spheres were prepared via the pseudomorphic route, using commercial prontosil silica spheres. Surface modification offers a great opportunity to adjust both the pore structure and surface properties of MCM-41 type materials which results in materials of improved hydrothermal and mechanical stability to make them promising candidates for chromatographic applications. In the present context, the obtained MCM-41 silica spheres were surface modified with octadecyl (C₁₈) alkyl chains, by using direct grafting and surface polymerization methods, in order to vary the degree of surface hydrophobicity. The resulting materials were characterized before and after surface modification using various characterization techniques, with special emphasis on NMR and FTIR spectroscopies, for studying the attachment, mobility and the conformational order of the attached alkyl chains.     

Synthesis,characterization, and application of oligomer‐type‐based phosphites

Organic alkyl and aryl phosphites are effective antioxidants and photostabilizers with applications in a wide range of polymers. The primary role of phosphites is to decompose hydroperoxide. However, aryl phosphites are also capable of reacting as antioxidants by affecting the kinetics. In particular, oligomer‐type phosphites have a greater effect on polymer degradation because of their high compatibility, reactivity, and solubility with almost all polymers. Generally, phosphites are sensitive to hydrolysis. In order to overcome this hydrolytic sensitivity in phosphites, a novel hydrolytically stable oligomeric phosphite incorporating a sterically hindered aromatic alcohol (2,4‐di‐tert‐butyl‐6‐methylphenol) that gives hydrolytic stability to the phosphite was synthesized and characterized, and its performance as an antioxidant for polypropylene was investigated. J. VINYL ADDIT. TECHNOL., 22:146–155, 2016. © 2014 Society of Plastics Engineers     

Time‐resolved investigation of Cu(In,Ga)Se2 growth and Ga gradient formation during fast selenisation of metallic precursors

Ga segregation at the backside of Cu(In,Ga)Se₂ solar cell absorbers is a commonly observed phenomenon for a large variety of sequential fabrication processes. Here, we investigate the correlation between Se incorporation, phase formation and Ga segregation during fast selenisation of Cu–In–Ga precursor films in elemental selenium vapour. Se incorporation and phase formation are analysed by real‐time synchrotron‐based X‐ray diffraction and fluorescence analysis. Correlations between phase formation and depth distributions are gained by interrupting the process at several points and by subsequent ex situ cross‐sectional electron microscopy and Raman spectroscopy. The presented results reveal that the main share of Se incorporation takes place within a few seconds during formation of In–Se at the top part of the film, accompanied by outdiffusion of In out of a ternary Cu–In–Ga phase. Surprisingly, CuInSe₂ starts to form at the surface on top of the In–Se layer, leading to an intermediate double graded Cu depth distribution. The remaining Ga‐rich metal phase at the back is finally selenised by indiffusion of Se. On the basis of a proposed growth model, we discuss possible strategies and limitations for the avoidance of Ga segregation during fast selenisation of metallic precursors. Solar cells made from samples selenised with a total annealing time of 6.5 min reached conversion efficiencies of up to 14.2 % (total area, without anti‐reflective coating). The evolution of the Cu(In,Ga)Se₂ diffraction signals reveals that the minimum process time for high‐quality Cu(In,Ga)Se₂ absorbers is limited by cation ordering rather than Se incorporation. Copyright © 2014 John Wiley & Sons, Ltd.