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41.
A diphasic mullite gel has been synthesized by using Ludox and Al(NO3)3-9H2O in ammoniacal solution. Both DTA and DDTA studies have been performed with a sensitive differential thermal analyzer system. Besides usual exotherm due to mullite formation, a pronounced exotherm between 800–1300°C has been noted. Considering previous XRD data, it is explained as due to formation of Si-Al spinel phase, which is subsequently transformed exothermally at 1320°C to mullite.  相似文献   
42.
The initial oxidation of magnesium at oxygen partial pressures between 1.3 × 10?8 and 1.3 × 10?5 Pa and at temperatures ranging from 273 to 550 K has been investigated in situ with X‐ray photoelectron spectroscopy (XPS), ellipsometry and high resolution elastic recoil detection analysis (HERDA). Quantitative analysis of the XPS spectra showed a clear oxygen deficiency with respect to MgO for the initial oxide. HERDA measurements confirmed this relatively low oxygen content in the thin oxide layers formed. Ellipsometry measurements showed that the electronic structure of the initially formed oxide differs significantly from that of bulk MgO. The band gap values at room temperature for the oxide layers investigated are clearly smaller than the value for bulk MgO. Copyright © 2006 John Wiley & Sons, Ltd.  相似文献   
43.
往复挤压准晶增强快速凝固Mg92.5Zn6.4Y1.1合金   总被引:1,自引:0,他引:1  
采用往复挤压工艺将快速凝固Mg92.5Zn6.4Y1.1合金薄带在330℃挤压2道次和4道次,然后正挤压制成Φ10 mm的棒材。用OM,TEM,XRD及DTA研究了往复挤压过程中准晶相I-Mg3YZn6弥散析出及对力学性能的影响。研究表明,往复挤压有利于快速凝固Mg92.5Zn6.4Y1.1合金薄带的焊合,获得组织致密、均匀、高强韧合金。往复挤压2道次,相组成为-αMg和准晶I-Mg3YZn6,脱溶析出纳米准晶相较少;4道次相组成为-αMg和准晶I-Mg3YZn6及MgZn相,脱溶弥散析出的纳米I-Mg3YZn6准晶相及MgZn相较多。往复挤压提高材料的拉伸性能,其主要原因是细晶强化和析出强化。  相似文献   
44.
IntroductionSupportedPt-Sncatalystsareimpo~inthepdrileumandpthechendcalindustricsbecauseoftheirsuperiorcatalyticperformances.Forexample,Pt-Snsupportedonaneutralsupporthasbeenreportedtoexhibithighdehydrogenationselectivityanddebilitythansupportedplatinumca…  相似文献   
45.
46.
New planar binuclear phthalocyanines sharing the benzene ring were synthesized and their spectral properties were studied. Intense absorption in the near-IR region (∼850 nm) was observed for the first time. Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 7, pp. 1112–1115, July, 2006.  相似文献   
47.
Spinel compound LiNi1−xMnxVO4 (0≤x≤0.4) had been prepared by using the moist chemical method. X-ray diffraction spectra showed that the lattice constant increased with x in the LiNi1−xMnxVO4, XPS spectra indicating that Li1s had a chemical shift towards lesser binding energy, and manganese in LiNi1−xMnxVO4 existing as the mixed valence of Mn2+ and Mn3+. The electrochemical charge and discharge testing at a current density of 0.1 mA/cm2 between the potentials of 4.0 and 3.0 V vs Li/Li+ in 1 mol/dm3 LiPF6/EC+DEC (1:1 by volume) at 25°C showed that LiNi1−xMnxVO4 cell has a better rechargeability, but a lower cell voltage of 4.0 V vs Li/Li+ than that without the doping sample, and the capacity and the cycle efficiency of the Li/LiNi1−xMnxVO4 cells increased with x in the LiNi1−xMnxVO4.  相似文献   
48.
In an investigation of octamethylene bis(malonic acid diamides) and their selectivities for magnesium, it was found that presence of secondary amides within the particular ionophore played a considerable role in the enhancement of magnesium selectivity. Similar effects in other ionophores, i.e. tris(malonic acid diamides), were thus systematically looked at with the help of selectivity measurements with the hope of optimizing the number of secondary and tertiary amides so as to improve the magnesium selectivity. The syntheses of several investigated tris(malonic acid diamide) isologues are equally reported.Deceased in November 1992  相似文献   
49.
Synthesis of the green spinel pigment Co0.46Zn0.55(Ti0.064Cr0.91)2O4 by a novel two-step method of preparation have been investigated. Inorganic pigments are almost always prepared by a solid state reaction. It is classical ceramic method which used oxides, hydroxides or carbonates as precursors. The reaction is performed at temperature higher than 1300°C and an agent of mineralization is usually present. The presented novel method of preparation decreases the calcining temperature necessary for reaching of bright and clear hue of the pigments prepared. Main attention was focused on the influence of two types of titanium raw materials on the temperature region of the spinel structure formation and on the colour properties of the pigments. The mixture of precursors with TiO2 gives a one-phase system when calcining at 1100°C but the colour properties are more interesting at 1150°C. Thermal stability of this pigment is limited by temperature 1300°C. This temperature is connected with partial oxidation of Cr(III) to Cr(VI). Thermal analysis provided the first information about the temperature region of the pigment formation and determined the thermal stability of pigment.  相似文献   
50.
合成了两种新的聚醚取代的水杨醛亚胺Schiff碱锰(III)配合物MnL12Cl和MnL2Cl,研究了它们与表面活性剂2Brij35形成的金属胶束对BNPP的催化水解反应.探讨了催化反应机理,提出了水解反应的动力学数学模型;计算了催化反应的Michanelis常数和表观活化能,并与不含聚醚链的类似物MnL2Cl比较,考查了配合物配体中聚醚支链及其3端基对催化水解反应的影响.结果表明,催化水解反应遵循金属-氢氧离子机理;以羟基作为聚醚链端基的MnL12Cl的催化活性最高,在相同条件下,其表观一级速率常数约为MnL2Cl的3倍,为MnL2Cl的30倍.23  相似文献   
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