快速凝固Al—Li—Cu—Mg—Zr合金中H相的Z相的TEM研究

用ＨＲＴＥＭ、ＴＥＭ及ＥＤＡＸ分析研究了Ａｌ－Ｌｉ－Ｃｕ－Ｚｒ合金中的一种新相（暂名Ｈ相）和六角Ｚ相的结构，确定Ｈ相具有四方点阵，点阵参数为ａ＝２．８ｎｍ，ｃ＝２．４ｎｍ，ＥＤＡＸ分析表明Ｈ明和Ｚ相均含有Ａｌ，Ｍｇ，Ｃｕ。发现Ｈ相与Ｚ相的共存取向关系为［１００］ｈ｜｜［１１２０］ｚ，［０１０］｜｜［０００１］Ｚ。还观察到Ｚ相中一种特有有的旋转畴结构。     

Controllable synthesis of pure monodispersed zirconia nanopowders with tetragonal phase

Nanopowders of pure zirconia have been synthesized using citric acid (CA)-assisted lamellar liquid crystal template method. The microstructure of the zirconia powder prepared at the different mole ratios of CA to zirconium oxynitrate (ZN) was characterized by FT-IR, X-ray diffraction (XRD), laser particle size analyzer, Raman spectroscopy, and scanning electron microscope (SEM) methods. The phase structure of the sodium dodecyl sulfate (SDS)/C₁₀H₂₁OH/H₂O system before and after adding mixing solution CA and ZN was determined by POM (Polarizing Optical Microscope). The results show that lamellar structure of the SDS/C₁₀H₂₁OH/H₂O system after adding mixing solution CA and ZN is stable. The presence of CA inhibits agglomeration and growth of zirconia particle. The crystallite size of zirconia powders decreases and agglomerates lowly with addition of CA. Fourier transform infrared spectrometry (FI-IR) analyses reveal that the structure of chelating organic complex is maintained in zirconia structure at high-temperature calcination to cause oxygen vacancies which stabilizes the tetragonal phase of zirconia. The zirconia powders remained the single metastable tetragonal phase at the molar ratios of CA to ZN ranging from 1:3 to 5:1. The crystallite size of zirconia with spherical morphology varied from 32.2 to 20.1 nm with the increase of the molar ratio of CA to ZN in the range of 1:3 to 5:1.     

Catalytic activities and properties of mesoporous sulfated Al2O3–ZrO2

Mesoporous sulfated Al₂O₃–ZrO₂ (MSAZ) catalysts with large surface areas and pore volumes after calcination at high temperature (650 °C) and with higher Al₂O₃ content than 20wt% were successfully prepared from a template of block copolymer (P84). The MSAZ catalysts were characterized by X-ray diffraction (XRD), N₂ adsorption, transmission electron microscopy (TEM), ²⁷Al magic-angle spinning nuclear magnetic resonance (MAS NMR), thermogravimetric analysis (TG–DTG), temperature-programmed desorption of ammonia (NH₃-TPD) and infrared spectra (IR) of adsorbed pyridine. It is shown that the resulting mesostructured sulfated Al₂O₃–ZrO₂ samples have a well-developed textural mesoporosity. The number of acid sites present on MSAZ catalysts is higher than that on conventional sulfated zirconia, and the former catalysts are more active than the latter one for various acid-catalyzed reactions.     

n-Butane Isomerization Over SO4 =/NiO/Al2O3/ZrO2 Catalysts. Effect of the Reaction Pressure and Metal Loading

The effect of alumina and nickel in sulfated ZrO₂ as a catalyst for n-butane isomerization was investigated. Samples were synthesized by supporting nickel sulfated zirconia on boehmite and then calcining the material. The crystalline structure of ZrO₂ was studied by X-ray powder diffraction and refined by the Rietveld method. Surface areas were determined by N₂ adsorption and BET analysis, while the acid properties were studied by NH₃ adsorption. The chemical reaction was carried out in a fixed-bed microreactor at 338 K under atmospheric (78 kPa) or 245 kPa total pressure. Results showed that either nickel or alumina improved the catalytic activity, but a synergic effect was observed when both components assisted. The catalytic activity was related to the relative content of tetragonal zirconia and acid site density. Alumina stabilized tetragonal zirconia increased the acid site density and presumably led to a better dispersion of nickel oxide. The catalytic activity could be related to both oxidation and acid sites produced by nickel. A bimolecular reaction mechanism helps explain the observed trends. The increase in the reaction rate would be explained by the increase in the rate of the initial step of dehydrogenation either caused by a better dispersion of nickel or higher operating pressure.     

四角螺母级进模设计

针对零件需多次拉伸、冲孔、翻边、倒角、切边弯曲等工序 ,成功地设计和制造了1副级进模 ,合理地选用了模具材料,满足了四角螺母大批量生产的要求 ,可为类似零件的成形提供参考。     

Structural instabilities and superconductivity in La-214 compounds

In La_2–x Ba _x CuO₄ (LBCO) the transition to a low-temperature tetragonal phase and the suppression of superconductivity occur at the carrier concentration p 1/8 per copper. We will discuss the roles of various material parameters that control this instability. An unusual lattice softening has been found by ultrasonic measurement on La_2–x Sr _x CuO₄ (LSCO). This softening is present only in an in-plane shearing mode and is ascribed to the growth of structural fluctuations in the normal state.These phenomena are closely related because both the structural change in LBCO and the applied strain in LSCO lift the degeneracy of in-plane oxygen sites. They clarify the importance of strong coupling between the normal-state electronic system and the lattice by a Peierls-type mechanism.     

Strength Analysis of Yttria-Stabilized Tetragonal Zirconia Polycrystals

Tensile strength of Y₂O₃-stabilized ZrO₂ polycrystals (Y-TZP) was measured by a newly developed tensile testing method with a rectangular bar. The tensile strength of Y-TZP was lower than that of the three-point bend strength, and the shape of the tensile strength distribution was quite different from that of the three-point bend strength distribution. It was difficult to predict the distribution curve of the tensile strength using the data of the three-point bend strength by one-modal Weibull distribution. The distribution of the tensile strength was analyzed by two- or three-model Weibull distribution coupled with an analysis of fracture origins. The distribution curve of the three-point bend strength which was estimated by multimodal Weibull distribution agreed favorably with that of the measured three-point bend strength values. A two-modal Weibull distribution function was formulated approximately from the distributions of the tensile and three-point bend strengths, and the estimated two-modal Weibull distribution function for the four-point bend strength agreed well with the measured four-point bend strength.     

Y_2O_3-MgO共稳定ZrO_2的相研究

通过化学组成和相含量设计,采用湿混法制备了MgO和Y2O3共同稳定ZrO2粉末,在不同的温度下烧结,获得了室温下单斜相和四方相含量不同的烧结样品,用X射线峰宽化法测定并计算了粒子尺寸。结果表明:随着Y2O3含量的增加,单斜相含量降低,四方相含量增加。温度对相含量的影响较小,而晶粒尺寸受Y2O3和温度的影响并不明显。     

Insight into t->m transition of MW treated 3Y-PSZ ceramics by grazing incidence X-ray diffraction

The influence of a microwave hybrid heat treatment (MHH) on the surface and in-depth mineralogical transformation of pre-sintered 3Y-PSZ was investigated. 3Y-PSZ samples were prepared by slip casting and sintered by conventional firing (1270 °C). Then, different MHH treatments from 5 to 15 min. at 1200 °C were applied to obtain a fully stabilized 3Y-TZP. The monoclinic fraction depth profiles in the first micrometres (up to 5) of thickness were investigated by means of the grazing incident X-ray diffraction technique (GIXRD). A good sintering degree with practically nil closed porosity and grain growth was achieved after MHH of 15 min. MHH increases the tetragonal phase content both in the surface and in-depth, reducing completely the monoclinic phase shell typically found after conventional sintering. A new parabolic model is proposed for the convoluted monoclinic fraction depth profile, which through the value of its horizontal asymptote allows the determination of the monoclinic shell thickness.