201 resultados para CUO-CEO2


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随着大规模集成电路的发展,需要一种高介质材料来代替传统的SiO2,介绍了可能替代SiO2的几种二元材料的研究现状,主要包括Si3N4,Ta2O5,TiO2,ZrO2,Y2O3,Gd2O3和CeO2几种材料的结构和电学性能,以及制备薄膜的几种方法;蒸发法,化学气相沉积和离子束沉积。

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Ce1-XNiXO2 oxides with X varying from 0.05 to 0.5 were prepared by different methods and characterized by XRD and TPR techniques. Ce(0.7)Mi(0.3)O(2) sample prepared by sol-gel method shows the highest reducibility and the highest catalytic activity for methane combustion. Three kinds of Ni phases co-exist in the Ce1-XNiXO2 catalysts prepared by sol-gel method: (i) aggregated NiO on the support CeO2, (ii) highly dispersed NiO with strong interaction with CeO2 and (iii) Ni atoms incorporated into CeO2 lattice. The distribution of different Ni species strongly depends on the preparation methods. The highly dispersed NiO shows the highest activity for methane combustion. The NiO aggregated on the support CeO2 shows lower catalytic activity for methane combustion, while the least catalytic activity is found for the Ni species incorporated into CeO2. Any oxygen vacancy formed in CeO2 lattice due to the incorporating of Ni atoms adsorbs and activates the molecular oxygen to form active oxygen species. So the highest catalytic activity for methane combustion on Ce0.7Ni0.3O2 catalyst is attributed not only to the highly dispersed Ni species but also to the more active oxygen species formed. (C) 2002 Elsevier Science B.V. All rights reserved.

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Ag-CuCl catalysts were found to be active and selective for the epoxidation of propylene using air as the oxidant. Ag catalyst gives a propylene conversion of 31.6%, with a propylene oxide (PO) selectivity of 0.42% at a reaction temperature of 350 degreesC after 220 min of reaction. Addition of CuCl significantly improves the selectivity to PO, and suppresses the conversion of propylene. The Ag-CuCl (1/0.6) catalyst gives propylene conversion of about 3% and a PO selectivity of about 30% at a reaction temperature of 350 degreesC after 500 min of reaction. The activity of the Ag-CuCl catalyst increases with the reaction time and the selectivity to PO is very stable for this catalyst. It is found that AgCl and CuO phases formed during the catalyst preparation are beneficial to the epoxidation of propylene.

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zero point of charge of freshly precipitated cu(oh)2 has been determined to lie at pH 7.7 by means of microclectrophoresis technique. Day aged hydroxide shows an acid zpc shift to pH 7.3. these experimental values approximate the equivalence points of cu+ and oh_ ,which can be estimated from the solubility diagram constructed fo gu(oh)2 and cuo.

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掺杂的CeO2基固体电解质因其在中低温条件下(500 ̄700℃)具有高氧离子电导率而成为有希望的IT-SOFCs(intermediate temperature-solid oxide fuel

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Pd-Au/C and Pd-Ag/C were found to have a unique characteristic of evolving high-quality hydrogen dramatically and steadily from the catalyzed decomposition of liquid formic acid at convenient temperature, and further this was improved by the addition of CeO2(H2O)(x).

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采用高温固相法合成了Nd2CexO3+2x(x=2.0,2.25,2.5,2.75,3.0)复合氧化物,在高温合金基体上采用等离子喷涂制备了该材料热障涂层。XRD分析结果表明Nd2CexO3+2x粉末和涂层均为立方萤石晶体结构。考察了CeO2含量对Nd2CexO3+2x的力学性能(弹性模量、维氏硬度和断裂韧性)和等离子喷涂涂层在1250℃抗热震性能的影响。随着CeO2含量增加,材料的弹性模量降低,维氏硬度和断裂韧性提高。通过提高初始粉末中CeO2的含量,获得了组成接近化学计量比Nd2Ce2O7的涂层,涂层的抗热震性能增强,热循环次数达到1000次以上。Nd2CexO3+2x涂层的失效原因主要是:与金属基体之间...

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Lanthanum-zirconium-cerium composite oxide (La-2(Zr0.7Ce0.3)(2)O-7, LZ7C3) as a candidate material for thermal barrier coatings (TBCs) was prepared by electron beam-physical vapor deposition (EB-PVD). The composition, crystal structure, thermophysical properties, surface and cross-sectional morphologies and cyclic oxidation behavior of the LZ7C3 coating were studied. The results indicated that LZ7C3 has a high phase stability between 298 K and 1573 K, and its linear thermal expansion coefficient (TEC) is similar to that of zirconia containing 8 wt% yttria (8YSZ). The thermal conductivity of LZ7C3 is 0.87 W m(-1) K-1 at 1273 K, which is almost 60% lower than that of 8YSZ. The deviation of coating composition from the ingot can be overcome by the addition of excess CeO2 and ZrO2 during ingot preparation or by adjusting the process parameters.

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Rare earths are a series of minerals with special properties that make them essential for applications including miniaturized electronics, computer hard disks, display panels, missile guidance, pollution controlling catalysts, H-2-storage and other advanced materials. The use of thermal barrier coatings (TBCs) has the potential to extend the working temperature and the life of a gas turbine by providing a layer of thermal insulation between the metallic substrate and the hot gas. Yttria (Y2O3), as one of the most important rare earth oxides, has already been used in the typical TBC material YSZ (yttria stabilized zirconia). In the development of the TBC materials, especially in the latest ten years, rare earths have been found to be more and more important. All the new candidates of TBC materials contain a large quantity of rare earths, such as R2Zr2O7 (R=La, Ce, Nd, Gd), CeO2-YSZ, RMeAl11O19 (R=La, Nd; Me=Mg, Ca, Sr) and LaPO4. The concept of double-ceramic-layer coatings based on the rare earth materials and YSZ is effective for the improvement of the thermal shock life of TBCs at high temperature.

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Nanocrystalline 8YSZ (8 mol% yttria stabilized zirconia) bulk samples with grain sizes of 20-30 nm were synthesized by Sol-Gel method and then densified under a high pressure of 4.5 GPa at 1273 K for 10 min. The method led to the densification of 8YSZ to a relative density higher than 92% without grain growth. Fourier transmission Raman spectroscopy suggested that 8YSZ underwent a phase transition from the cubic phase to a phase mixture (tetragonal plus a trace of monoclinic) after the densification, which decreased the electrical conductivity to a certain degree as concluded from the impedance spectroscopy.

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采用沉淀法制备了CuO 水溶胶, 用油酸萃取并包覆CuO纳米水溶胶,制备了CuO纳米有机溶胶,对有机溶胶的制备条件进行了系统地研究。由TEM 分析表明,有机溶胶中CuO纳米 粒子呈球形,粒径约为20nm,粒子分布均匀, 无明显团聚现象。