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1.
Large, hard ZrO2 agglomerates remained in an Al2 O3 /ZrO2 composite suspension after inefficient ball-milling. The ZrO2 agglomerates shrank away from the consolidated Al2 O3 /ZrO2 powder matrix during sintering, producing crack-like voids which were responsible for strength degradation. 相似文献
2.
Heromichi Okamura Eric A. Barringer H. Kent Bowen 《Journal of the American Ceramic Society》1986,69(2):22-C-
An unagglomerated, monosized Al2 O3 TiO2 composite powder was prepared by the stepwise hydrolysis of titanium alkoxide in an Al2 O3 dispersion. Particle size was controlled by selecting the particle size of the starting Al2 O3 powder; TiO2 content was determined by the amount of alkoxide hydrolyzed. A composite-powder compact containing 50 mol% TiO2 , when fired at 1350°C for 30 min, showed nearly theoretical density with aluminum titanate phase formation. 相似文献
3.
A method is proposed to prepare Al2 O3 -AlN-Ni composites. The composites are prepared by sintering Al2 O3 /NiAl powder mixtures at 1600°C in a mixture of nitrogen and carbon monoxide. The presence of NiAl particles raises the green density of Al2 O3 /NiAl powder compacts. During sintering, NiAl reacts with nitrogen to form AlN and Ni inclusions. A volume expansion accompanies the reaction. Because of the high green density and the reaction, the volume shrinkage of the Al2 O3 -AlN-Ni composite decreases with the increase of added NiAl content. 相似文献
4.
P. L. ROEDER F. P. GLASSER† E. F. OSBORN 《Journal of the American Ceramic Society》1968,51(10):585-593
Liquidus phase equilibrium data are presented for the system Al2 O3 -Cr2 O3 -SiO2 . The liquidus diagram is dominated by a large, high-temperature, two-liquid region overlying the primary phase field of corundum solid solution. Other important features are a narrow field for mullite solid solution, a very small cristobalite field, and a ternary eutectic at 1580°C. The eutectic liquid (6Al2 O3 -ICr2 O3 -93SiO2 ) coexists with a mullite solid solution (61Al2 O3 -10Cr2 O3 -29SiO2 ), a corundum solid solution (19Al2 O3 -81Cr2 O3 ), and cristobalite (SO2 ). Diagrams are presented to show courses of fractional crystallization, courses of equilibrium crystallization, and phase relations on isothermal planes at 1800°, 1700°, and 1575°C. Tie lines were sketched to indicate the composition of coexisting mullite and corundum solid solution phases. 相似文献
5.
Masahide Okamoto Hironori Kodama Kazuo Shinozaki 《Journal of the American Ceramic Society》2008,91(4):1110-1114
The sintering of a composite of MgO–B2 O3 –Al2 O3 glass and Al2 O3 filler is terminated due to the crystallization of Al4 B2 O9 in the glass. The densification of a composite of MgO–B2 O3 –Al2 O3 glass and Al2 O3 filler using pressureless sintering was accomplished by lowering the sintering temperature of the composite. The sintering temperature was lowered by the addition of small amounts of alkali metal oxides to the MgO–B2 O3 –Al2 O3 glass system. The resultant composite has a four-point bending strength of 280 MPa, a coefficient of thermal expansion (RT—200°C) of 4.4 × 10−6 K−1 , a dielectric constant of 6.0 at 1 MHz, porosity of approximately 1%, and moisture resistance. 相似文献
6.
Koji Tsukuma 《Journal of the American Ceramic Society》2000,83(12):3219-3221
Composites of β-Ce2 O3 ·11Al2 O3 and tetragonal ZrO2 were fabricated by a reductive atmosphere sintering of mixed powders of CeO2 , ZrO2 (2 mol% Y2 O3 ), and Al2 O3 . The composites had microstructures composed of elongated grains of β-Ce2 O3 ·11Al2 O3 in a Y-TZP matrix. The β-Ce2 O3 ·11Al2 O3 decomposed to α-Al2 O3 and CeO2 by annealing at 1500°C for 1 h in oxygen. The elongated single grain of β-Ce2 O3 ·11Al2 O3 divided into several grains of α-Al2 O3 and ZrO2 doped with Y2 O3 and CeO2 . High-temperature bending strength of the oxygen-annealed α-Al2 O3 composite was comparable to the β-Ce2 O3 ·11Al2 O3 composite before annealing. 相似文献
7.
Transparent Nano-Composites Ceramics by Annealing of Amorphous Phase in the HfO2 -Al2 O3 -GdAlO3 System
Shunji Araki Masahiro Yoshimura 《International Journal of Applied Ceramic Technology》2004,1(2):155-160
We have succeeded in fabricating transparent nano-structured ceramics by annealing of the amorphous phase obtained by the solidification of the eutectic melt in the ternary system HfO2 − Al2 O3 − GdAlO3 . The ceramics annealed at 1273 K for 6 hr contained 5-10-nm cubic hafnia grains, and those annealed at 1273 K for 72 hr contained both cubic hafnia and gadolinium aluminum garnet grains 5-10 nm in size. They showed high transparency. Annealing at 1473 K, however, resulted in grain growths that brought about non-transparency. 相似文献
8.
The system Na3 AlF6 -AlF3 -Al2 O3 was investigated by a combination of quenching, optical microscopy, and X-ray powder diffraction techniques in order to define liquidus temperatures, univariant lines, and invariant points. Phase fields for the primary crystallization of cryolite, chiolite, aluminum fluoride, α-alumina, and η-alumina were located. A ternary peritectic point contained 28.3% AlF3 -4.4% Al2 O3 -67.3% Na3 AlF6 at 723°C. A eutectic point of composition 37.3% AlF3 -3.2% Al2 O3 -59.5% Na3 AlF6 occurs at 684°C. 相似文献
9.
Ken-ichi Tajima † Hae Jin Hwang Mutsuo Sando Koichi Niihara 《Journal of the American Ceramic Society》2000,83(3):651-653
Hard lead zirconate titanate (PZT) and PZT/Al2 O3 composites were prepared and the alternating-electric-field-induced crack growth behavior of a precrack above the coercive field was evaluated via optical and scanning electron microscopy. The crack extension in the 1.0 vol% Al2 O3 composite was significantly smaller than that in monolithic PZT and the 0.5 vol% Al2 O3 composite. Secondary-phase Al2 O3 dispersoids were found both at grain boundaries and within grains in the composites. A large number of dispersoids were observed at the grain boundaries in the 1.0 vol% Al2 O3 composite. It appears that the Al2 O3 dispersoids reinforce the grain boundaries of the PZT matrix as well as act as effective pins against microcrack propagation. 相似文献
10.
The UO2 –Al2 O3 phase equilibrium system was found to contain no new compounds or solid solutions. Uranium dioxide melted at 2878°± 22°C. and Al2 O3 melted at 2034°± 16°C. The eutectic temperature was approximately 1930°C. There is an indication that two immiscible liquids formed above the eutectic temperature between 53 and 74 mole % Al2 O3 . 相似文献
11.
Silvia Schicker Daniel E. García Igor Gorlov Rolf Janssen Nils Claussen 《Journal of the American Ceramic Society》1999,82(10):2607-2612
Wet milling of Al2 O3 -aluminide alloy (3A) precursor powders in acetone has been investigated by milling Fe/Al/Al2 O3 and Fe2 O3 /Al/Al2 O3 powder mixtures. The influence of the milling process on the physical and chemical properties of the milled powders has been studied. Particle refinement and homogenization were found not to play a dominant role, whereas plastic deformation of the metal particles leads to the formation of dislocations and a highly disarranged polycrystalline structure. Although no chemical reactions among the powder components in Fe2 O3 /Al/Al2 O3 powder mixtures were observed, the formation of a nanocrystalline, ordered intermetallic FeAl phase in Fe/Al/Al2 O3 powder mixtures caused by mechanical alloying was detected. Chemical reactions of Fe and Al particle surfaces with the atmosphere and the milling media lead to the formation of highly porous hydroxides on the particle surfaces. Hence the specific surface area of the powders increases, while the powder density decreases during milling. The fraction of Fe oxidized during milling was determined to be 0.13. The fraction of Al oxidized during milling strongly depends on the metal content of the powder mixture. It ranges between 0.4 and 0.8. 相似文献
12.
A. T. PRINCE 《Journal of the American Ceramic Society》1951,34(2):44-51
The system MgO–Al2 O3 –2CaO·SiO2 comprises a plane through the tetrahedron CaO–MgO–Al2 O3 –SiO2 . A total of 108 compositions were prepared having an alumina content below the line joining 2CaO·Al2 O3 SiO2 (gehlenite) and MgO·Al2 O3 (spinel). Quenching experiments were carried out on 96 of these compositions at temperatures up to 1590°C. Three binary eutectic systems and two ternary eutectic systems are described. Compositions on this plane are of significance in an investigation of the constitution of basic refractory clinkers made from Canadian dolomitic magnesites. They also concern the compositions of certain blast furnace slags. 相似文献
13.
Koji Tsukuma Kuniyoshi Ueda Masahiko Shimada 《Journal of the American Ceramic Society》1985,68(1):4-C-5
Composites of Al2 O3 and Y2 O3 partially-stabilized ZrO2 were isostatically hot-pressed using submicrometer powders as the starting material. The addition of Al2 O3 resulted in a large increase in bending strength. The average bending strength for a composite containing 20 wt% Al2 O3 was 2400 MPa, and its fracture toughness was 17 MN·w−3/2 相似文献
14.
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
15.
J. LLorca José Y. Pastor Pedro Poza José I. Peña Isabel de Francisco Angel Larrea Victor M. Orera 《Journal of the American Ceramic Society》2004,87(4):633-639
The effect of Y2 O3 content on the flexure strength of melt-grown Al2 O3 –ZrO2 eutectics was studied in a temperature range of 25°–1427°C. The processing conditions were carefully controlled to obtain a constant microstructure independent of Y2 O3 content. The rod microstructure was made up of alternating bands of fine and coarse dispersions of irregular ZrO2 platelets oriented along the growth axis and embedded in the continuous Al2 O3 matrix. The highest flexure strength at ambient temperature was found in the material with 3 mol% Y2 O3 in relation to ZrO2 (Y2 O3 ). Higher Y2 O3 content did not substantially modify the mechanical response; however, materials with 0.5 mol% presented a significant degradation in the flexure strength because of the presence of large defects. They were nucleated at the Al2 O3 –ZrO2 interface during the martensitic transformation of ZrO2 on cooling and propagated into the Al2 O3 matrix driven by the tensile residual stresses generated by the transformation. The material with 3 mol% Y2 O3 retained 80% of the flexure strength at 1427°C, whereas the mechanical properties of the eutectic with 0.5 mol% Y2 O3 dropped rapidly with temperature as a result of extensive microcracking. 相似文献
16.
Pierre E. Debély Eric A. Barringer H. Kent Bowen 《Journal of the American Ceramic Society》1985,68(3):76-C-
A fine, uniform A12 O3 -SiO2 powder was prepared by heterocoagulation of narrow Al2 O3 and SiO2 powders. This composite powder was dispersed, compacted, and fired in air at 900° to 1580°C for 1 to 13 h. Full density was achieved at 1550°C with the formation of a mullite phase. Relative densities of 83% and 98% (0.3 μm grain size) were measured for samples sintered at 1200°C for 13 h and at 1400°C for 1 h, respectively. 相似文献
17.
High-purity polycrystalline MgO and Al2 O3 were thermally grooved at 1500° and 1600°C. Accurate techniques were developed for following the growth of a single groove. For high-purity samples growth kinetics were essentially similar to those reported in the literature but were determined to be controlled by volume diffusion. Specimens for thermal grooving were prepared from Al2 O3 to which transition metal oxides (Fe2 O39 , MnO, and TiO2 ), which are known to accelerate shrinkage and sintering of Al2 O3 powder compacts, had been added; the rate of groove growth was increased remarkably by minor amounts of these additives. Control of partial pressure indicated that Fe2+ and Ti4+ are the species active in promoting groove growth. Substantial evidence was found for volume diffusion as the mechanism controlling groove formation. 相似文献
18.
Electroconductive Al2 O3 –NbN ceramic composites were prepared by hot pressing. Dense sintered bodies of ball-milled Al2 O3 –NbN composite powders were obtained at 1550°C and 30 MPa for 1 h under a nitrogen atmosphere. The bending strength and fracture toughness of the composites were enhanced by incorporating niobium nitride (NbN) particles into the Al2 O3 matrix. The electrical resistivity of the composites decreased with increasing amount of NbN phase. For a 25 vol% NbN–Al2 O3 composite, the values of bending strength, fracture toughness, Vickers hardness, and electrical resistivity were 444.2 MPa, 4.59 MPa·m1/2 , 16.62 GPa, and 1.72 × 10−2 Ω·cm, respectively, making the composite suitable for electrical discharge machining. 相似文献
19.
Tai-Il Mah Kristin A. Keller Sankar Sambasivan Ronald J. Kerans 《Journal of the American Ceramic Society》1997,80(4):874-878
Heat treatments in several environments were performed on a series of compounds in the Al2 O3 and Y2 O3 system: Al2 O3 Y3 Al5 O12 eutectic, Y3 Al5 O12 , YAlO3 , Y4 Al2 O9 , and Y2 O3 . The yttrium aluminates were found to be stable at high temperatures under vacuum and in air. However, when they were heat-treated under vacuum in proximity to SiC, degradation was observed. This was found to be primarily a result of carbothermal reduction. In a similarly reducing environment without Si, the yttrium aluminates, and Al2 O3 and Y2 O3 , all exhibited degradation by carbothermal reduction. Based upon the experimental results, a degradation mechanism for yttrium aluminates was proposed. 相似文献
20.
Porous Cr3 C2 grains (∼300 to 500 μm) with ∼10 wt% of Cr2 O3 were prepared by heating a mixture of MgCr2 O4 grains and graphite powder at 1450° to 1650°C for 2 h in an Al2 O3 crucible covered by an Al2 O3 lid with a hole in the center. The porous Cr3 C2 grains exhibited a three-dimensional network skeleton structure. The mean open pore diameter and the specific surface area of the porous grains formed at 1600°C for 2 h were ∼3.5 (μm and ∼6.7 m2 /g, respectively. The present work investigated the morphology and the formation conditions of the porous Cr3 C2 grains, and this paper will discuss the formation mechanism of those grains in terms of chemical thermodynamics. 相似文献