共查询到20条相似文献,搜索用时 31 毫秒
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Yoshiyuki Yokogawa Nobuo Ishizawa Shigeyuki Smiya Masahiro Yoshimura 《Journal of the American Ceramic Society》1991,74(9):2073-2076
The Phase relations of the system Gd2 O3 -Ta2 O5 in the composition range 50 to100 mol% Gd2O3 was studied by solidstate reactions at 1350°, 1500°, or 1700°C and by thermal analyses up to the melting temperatures. Weberite-type orthorhombic phase (W2 phase, space group C2221) with the composition of Gd3 TaO7 seems to melt incongruently; at about 2040°C, although this Gd3 TaO7 Phase was previously reported to melt congruently. A new fluorite-type cubic phase (F phase, space group Fm3m ) was found for the first time above 1500°C in the system. It melts congruently with the composition of about 80mol% Gd2O3at 2318° 3°C. A phase diagram was proposed for the system Gd2 O3–Ta2O5 in the Gd2 O3 –rich portion 相似文献
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The elastic properties of polycrystalline monoclinic Gd2 O3 were determined by the sonic-resonance method. Volume-fraction porosity varied from 0.025 to 0.367 and temperature from room temperature to 1400°C. The Young's and shear moduli are linear functions of volume-fraction porosity, but the rate of their decrease with increasing porosity is less than that expected. The moduli decreased more rapidly than expected with increasing temperature. The Debye temperature is 362°K. With increasing temperature, the first Grueneisen constant, γ, decreases, whereas the second Grueneisen constant, δ, increases. 相似文献
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The phase equilibrium relations in the systems Y2 O3 -Al2 O3 and Gd2 O3 -Fe2 O3 were examined. Each system has two stable binary compounds. A 3:s molar ratio garnet-type compound exists in both systems. The 1:1 distorted perovskite structure is stable in the system Gd2 O3 -Fe2 O3 but only metastable in the system Y2 O3 -AI2 O3 . This interesting example of metastable formation and persistence of a compound with ions of high Z/r values explains the discrepancies in the literature on the structure of the composition YA1O3 . A new 2:1 molar ratio cubic phase has been found in the system Y2 O3 -A12 O3 . Since silicon can be completely substituted for aluminum in this compound, the aluminum ions are presumably in fourfold coordination. 相似文献
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W. R. Xue Walter A. Schulze † Robert E. Newnham 《Journal of the American Ceramic Society》1990,73(6):1783-1784
The electromechanical properties of PbTiO3 ceramics, modified by substitution of Sm or Gd + Nd (same average atomic radius as Sm) for Pb, were studied in the range of 6% to 14% substitution. The modified PbTiO3 ceramics were stable, and the Curie temperature decreased linearly over this composition range. The 10% Sm composition had a large anisotropy in the coupling factor ratio, k t / k p , and a similar, but weaker, effect developed for 12% (1/2 Gd + 1/2 Nd). This indicates that other than average ion size may influence the electromechanical coupling factor ratio. 相似文献
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MADELEINE H. WARZEE MARCEL MAURICE FRANZ HALLA WALTER R. RUSTON 《Journal of the American Ceramic Society》1965,48(1):15-17
In the binary system PbO–Laz O3 only one compound, 4PbO.La2 O3 , exists; it is flanked by two eutectics. The structure of the compound, although of lower symmetry, is intimately related to the C modification of the rare earths. Below 800° to 1000°C, metastable solid solutions are formed from oxide mixtures coprecipitated from mixed solutions of the nitrates, the cubic parameter a = 5.66 A, if extrapolated to pure La2 O3 , corresponding to half the a parameter of the C form of La2 O3 . The solid solutions existing between the compositions La2 O3 –2Pb0 and pure La2 O3 have a cubic face–centered lattice and obey Vegard's rule. The systems of PbO with Sm2 O3 and Gd2 O8 are quite similar to that with La2 O3 . The compound Sm2 O3 .4Pb0 decomposes at 1000°C with evaporation of PbO; Sm2 O3 remains in the B modification. 相似文献
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Pomin Su Anil V. Virkar Camden R. Hubbard O. Burl Cavin Wallace D. Porter 《Journal of the American Ceramic Society》1993,76(10):2513-2520
Gd2 O3 -doped Bi2 O3 polycrystalline ceramics containing between 2 and 7 mol% Gd2 O3 were fabricated by pressureless sintering powder compacts. The as-sintered samples were tetragonal at room temperature. Hightemperature X-ray diffraction (XRD) traces showed that the samples were cubic at elevated temperatures and transformed into the tetragonal polymorph during cooling. On the basis of conductivity measurements as a function of temperature and differential scanning calorimetry (DSC), the cubic → tetragonal as well as tetragonal → cubic → teansition temperatures were determined as a function of Gd2 O3 concentration. The cubic → tetragonal transformation appears to be a displacive transformation. It was observed that additions of ZrO2 as a dopant, which is known to suppress cation interdiffusion in rare-earth oxide–Bi2 O3 systems, did not suppress the transition, consistent with it being a displacive transition. Annealing of samples at temperatures 660°C for several hundred hours led to decomposition into a mixture of monoclinic and rhombohedral phases. This shows that the tetragonal polymorph is a metastable phase. 相似文献
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Jenn-Ming Yang S. M. Jeng Sekyung Chang 《Journal of the American Ceramic Society》1996,79(5):1218-1222
The strength and fracture of a directionally solidified Y3 Al5 O12 /Al2 O3 eutectic fiber were investigated. The fiber was grown continuously by an edge-defined film-fed growth technique. The microstructure was characterized using X-ray diffraction, scanning electron microscopy, and energy-dispersive spectroscopy. The tensile strength and Weibull's modulus of the eutectic fibers were determined in the as-fabricated state and after extended thermal exposure at 1460°C in air. Fractographic analysis was used to identify and classify the strength-limiting mechanisms. The fracture toughness and crack growth behavior were characterized by an indentation technique. A fracture mechanics analysis was also used to establish the relationships between surface flaw size, tensile strength, and fracture toughness of the fiber. 相似文献
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The mechanism of parahydrogen conversion was studied on Gd2 O3 and Y2 O3 powders and on Gd and Y evaporated metal films at low and high temperatures (77° to 90°K and 298° to 418°K). Absolute rates of conversion are compared to theoretical values for 3 possible reaction mechanisms, and it is concluded that a paramagnetic vibrational mechanism is operative on Gd2 O3 , Gd, and Y. On Y2 O3 the reaction rate is enhanced by additional surface paramagnetic sites. The portion of the surface which is active is ∼1 for the metals and ∼0.01 for the oxides. 相似文献
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Ivar E. Reimanis M. E. Hawley T. E. Mitchell D. S. Zhou 《Journal of the American Ceramic Society》1995,78(8):2282-2286
The fracture surfaces of single-crystal Y3 A15 O12 (YAG) have been examined in detail using differential interference microscopy and atomic force microscopy. In YAG crystals grown in 1977 by the Czochralski method strikingly regular undulations of microscopic and submicroscopic dimensions (4–20 nm in amplitude, 1–20 μm in wavelength) are observed on every fracture surface. The undulations do not exhibit typical characteristics of Wallner lines; furthermore, they are not observed in identical fracture tests for YAG crystals grown in 1990 by the Czochralski method. Transmission electron microscopy reveals that the crystals grown in 1977 exhibit a periodic fluctuation of the ratio of the concentrations of aluminum to yttrium, suggesting that the fracture surface features are caused by periodic astoichiometry. 相似文献
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Equilibrium data at liquidus temperatures are presented for compositions in the quaternary system Y-Gd-Fe-O in ambient atmospheres of oxygen gas (pO2 , = 760 mm Hg), air (PO2 , = 159 mm Hg), and CO2 (pO2 variable). Incongruent melting occurred in yttrium-iron and gadolinium-iron garnet phases and in all intermediate garnet solid solutions in the three oxygen pressure sections studied. Fractionation in the yttrium/gadolinium ratio between oxide liquid and crystalline garnet phases in the quaternary system was not observed experimentally, indicating that unzoned (Y,Gd)3 Fe5 O12 crystals may be grown from a melt without special precautions to maintain a fixed Y/Gd ratio. 相似文献
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Oleg Vasylkiv Yoshio Sakka Valeriy V. Skorokhod 《Journal of the American Ceramic Society》2006,89(6):1822-1826
CeCl3 ·7H2 O and GdCl3 ·6H2 O that were dissolved in water were precipitated with urea (NH2 CONH2 ) to produce matrix agglomerates for three-component nano-reactors. Mixing hexamethylenetetramine with dilute nitric acid resulted in the formation of well-dispersed nano-particles of cyclotrimetilene trinitramine (C3 H6 N6 O6 ) (RDX) in the solvent. Nano-reactors were produced by impregnating the nano-C3 H6 N6 O6 into the matrix agglomerates of an intermediate complex of cerium and gadolinium compounds. Blast initiation of the C3 H6 N6 O6 resulted in extremely rapid detonation and gaseous products formation at temperatures of 2000°–5000°C, which were compressed into a volume nearly equal to the initial volume of each RDX nano-particle. Multiple "nano-blasts" occurred in the volume of each nano-reactor. The impact of the blast waves led to fragmentation of the surrounding matter. The evolution of a large volume of gaseous products dissipated the heat of the process and limited temperature increase, thus reducing the possibility of local sintering among the primary particles. The short-term high temperature generated during the blasts enhanced the solid solubility of the metal oxides. Uniform aggregates of 22∼74 nm consisting of 6∼14 nm crystallites of gadolinia in ceria solid solution were synthesized. 相似文献
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The eutectic composition between Y4 Al2 O9 and Y2 O3 was determined using electron probe microanalysis (EPMA) on directionally solidified specimens with hypo- and hypereutectic compositions. The microstructures of the specimens as a function of composition differ considerably with small deviation from the eutectic composition (70.5 mol% Y2 O3 and 29.5 mol% Al2 O3 ). Based on the current results and other published data, the pseudobinary system between Al2 O3 and Y2 O3 is revised. 相似文献
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Studies of the oxidation of Gd and Dy at P O2 's from 10−0.3 to 10−14.5 atm and temperatures from 727° to 1327°C indicate both semiconducting and ionic-conducting domains in the sesquioxides formed. At higher temperatures, where dense coarsegrained oxide layers developed, the rate of oxidation in the high- P 02 semiconducting domain yielded oxygen diffusion coefficients in Dy2 O3 in excellent agreement with literature values derived from oxidation of partially reduced oxide single crystals. Under the same conditions, the oxidation of Gd yielded oxygen diffusion coefficients in cubic Gd2 O3 which are considerably below literature values for monoclinic single-crystal Gd2 O3 . At lower temperatures, porous scales were formed, and apparent diffusion coefficients derived from oxidation rates show a smaller temperature dependence than the high-temperature data. At low P O2 , the oxides behave as ionic conductors, and metal oxidation rates result in estimates of the electronic contribution to the electrical conductivity of the order of 10−6 to 10−7 Ω−1 cm−1 . 相似文献
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Srinivasan Raghavan Hsin Wang Ralph B. Dinwiddie Wallace D. Porter Robert Vaen Detlev Stöver Merrilea J. Mayo 《Journal of the American Ceramic Society》2004,87(3):431-437
Zirconia doped with 3.2–4.2 mol% (6–8 wt%) yttria (3–4YSZ) is currently the material of choice for thermal barrier coating topcoats. The present study examines the ZrO2 -Y2 O3 -Ta2 O5 /Nb2 O5 systems for potential alternative chemistries that would overcome the limitations of the 3–4YSZ. A rationale for choosing specific compositions based on the effect of defect chemistry on the thermal conductivity and phase stability in zirconia-based systems is presented. The results show that it is possible to produce stable (for up to 200 h at 1000°–1500°C), single (tetragonal) or dual (tetragonal + cubic) phase chemistries that have thermal conductivity that is as low (1.8–2.8W/m K) as the 3–4YSZ, a wide range of elastic moduli (150–232 GPa), and a similar mean coefficient of thermal expansion at 1000°C. The chemistries can be plasma sprayed without change in composition or deleterious effects to phase stability. Preliminary burner rig testing results on one of the compositions are also presented. 相似文献
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Hisanori Yamane Mamoru Omori Akira Okubo Toshio Hirai 《Journal of the American Ceramic Society》1993,76(9):2382-2384
Reversible thermal phase transition was observed for Y4 Al2 O9 at 1377°C with a hysteresis width of 78°C using differential scanning calorimetry. The enthalpy of the transition (Δ H ) was about 300 cal/mol. Powder X-ray diffraction peaks of the high-temperature phase, as well as the peaks of the low-temperature phase, were characterized with a monoclinic unit cell. Thermal hysteresis was also confirmed by the temperature dependence of the lattice parameter. The unit cell volume of the high-temperature phase was 0.5% smaller than that of the low-temperature phase at 1400°C. 相似文献
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Yoshihito Mizoguchi Masahiro Kagawa Yasuhiko Syono Toshio Hirai 《Journal of the American Ceramic Society》2001,84(3):651-653
Thin films of yttrium aluminum garnet (YAG, Y3 Al5 O12 ) and yttrium iron garnet (YIG, Y3 Fe5 O12 ) were synthesized on single-crystal Al2 O3 substrates by a modification of spray pyrolysis using a high-temperature inductively coupled plasma at atmospheric pressure (spray–ICP technique). Using this technique, films could be grown at faster rates (0.12 μm/min for YAG and 0.10 μm/min for YIG) than using chemical vapor deposition (0.005–0.008 μm/min for YAG) or sputtering (0.003–0.005 μm/min for YIG). The films were dense and revealed a preferred orientation of (211). The growth of YIG was accompanied by coprecipitation of α-Fe2 O3 . The coprecipitation, however, could be largely suppressed by preliminary formation of a Y2 O3 layer on the substrate. 相似文献
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