共查询到20条相似文献,搜索用时 15 毫秒
1.
Osamu Yamaguchi Akira Narai Kiyoshi Shimizu 《Journal of the American Ceramic Society》1986,69(2):36-C-
A new compound, 12SrO·7Al2 O3 , is formed from an amorphous material prepared by the simultaneous hydrolysis of strontium and aluminum alkoxides. It has a cubic unit cell with a =1.2325 nm. The structure contains tetrahedral AlO4 groups and octahedral AlO6 groups. This compound decomposes into 3SrO·Al2 O3 and SrO·Al2 O3 at higher temperatures. 相似文献
2.
Osamu Yamaguchi Koji Sugiura Akihiro Mitsui Kiyoshi Shimizu 《Journal of the American Ceramic Society》1985,68(2):44-C-
A new compound, 5La2 O3 -2Al2 O3 , is formed from an amorphous material prepared by the simultaneous hydrolysis of lanthanum and aluminurn alkoxides. It has an orthorhombic unit cell with a=0.9704 nm, b=0.5967 nm, and c=1.5473 nm. The structure contains tetrahedral AlO4 groups and octahedral AlO6 groups. 相似文献
3.
Tomohiro Yamakawa Junichi Tatami Toru Wakihara Katsutoshi Komeya Takeshi Meguro Kenneth J. D. MacKenzie Shinichi Takagi Masahiro Yokouchi 《Journal of the American Ceramic Society》2006,89(1):171-175
Aluminum nitride (AlN) powders were synthesized by gas reduction–nitridation of γ-Al2 O3 using NH3 and C3 H8 as the reactant gases. AlN was identified in the products synthesized at 1100°–1400°C for 120 min in the NH3 –C3 H8 gas flow confirming that AlN can be formed by the gas reduction–nitridation of γ-Al2 O3 . The products synthesized at 1100°C for 120 min contained unreacted γ-Al2 O3 . The 27 A1 MAS NMR spectra show that Al–N bonding in the product increases with increasing reaction temperature, the tetrahedral AlO4 resonance decreasing prior to the disappearance of the octahedral AlO6 resonance. This suggests that the tetrahedral AlO4 sites of the γ-Al2 O3 are preferentially nitrided than the AlO6 sites. AlN nanoparticles were directly formed from γ-Al2 O3 at low temperature because of this preferred nitridation of AlO4 sites in the reactant. AlN nanoparticles are formed by gas reduction–nitridation of γ-Al2 O3 not only because the reaction temperature is sufficiently low to restrict grain growth, but also because γ-Al2 O3 contains both AlO4 and AlO6 sites, by contrast with α-Al2 O3 which contains only AlO6 . 相似文献
4.
Osamu Yamaguchi Masakazu Shirai Masaru Yoshinaka 《Journal of the American Ceramic Society》1988,71(12):510-C
In the system ZrO2 -Al2 O3 , cubic ZrO2 solid solutions containing up to 40 mol% Al2 O3 crystallize at low temperatures from amorphous materials prepared by the simultaneous hydrolysis of zirconium and aluminum alkoxides. The values of the lattice parameter, a, increase linearly from 0.5095 to 0.5129 nm with increasing Al2 O3 content. At higher temperatures, the solid solutions transform into tetragonal ZrO2 and α-Al2 O3 . Pure ZrO2 crystallizes in the tetragonal form at 415° to 440°C. 相似文献
5.
Osamu Yamaguchi Daijo Tomihisa Tatsuji Uegaki Kiyoshi Shimizu 《Journal of the American Ceramic Society》1987,70(11):335-C
In the system Ta2 O3 -Al2 O5 solid solutions of metastable δ-Ta2 O5 (hexagonal) are formed up to 50 mol% Al2 O3 from amorphous materials prepared by the simultaneous hydrolysis of tantalum and aluminum alkoxides. The values of the lattice parameters decrease linearly with increasing Al2 O3 , content. The to β-Ta2 O5 (orthorhombic, low-temperature form) transformation occurs at ∼950°C. The solid solution containing 50 mol% Al2 O3 transforms at 1040° to 1100°C to orthorhombic TaAlO4 . Orthorhombic TaAlO4 contains octahedral TaO6 groups in the structure. 相似文献
6.
ROBERT S. ROTH JOSEPH J. RITTER HARRY S. PARKER DENNIS B. MINOR 《Journal of the American Ceramic Society》1986,69(12):858-862
Only ZrO2 was found to stabilize the phase previously reported as "Ba2 Ti5 O12 ." A metastable phase corresponding to this compound was found to form between 650° and 675°C from hydrolyzed ethoxide precursors. The stability was increased to ∼850°C by the addition of 1 to 2 mol% Nb2 O5 to the precursor solutions. Addition of 5 mol% SnO2 failed to yield appreciable amounts of this phase in solid-state preparations, contrary to the previous report. Addition of 8 mol% ZrO2 , however, did produce the desired phase as reported, both with and without additional Nb2 O5 , apparently stable to >1300°C. Small single crystals, picked from a ZrO2 -stabilized specimen with 1 mol% Nb2 O5 , showed the compound Ba2 Ti5- x Zrx O12 to be a 10-layer structure, triclinic, pseudo-orthorhombic with A-centered symmetry and a =9.941(5), b = 11.482(4), c = 23.528 (10) × 10–1 nm. The corresponding reduced triclinic unit cell has a = 9.941, b = 11.482, c = 13.090 × 10–1 nm, α= 116.01°, β= 90.0°, γ= 90.0°. 相似文献
7.
In the system TiO2 —Al2 O3 , TiO2 (anatase, tetragonal) solid solutions crystallize at low temperatures (with up to ∼ 22 mol% Al2 O3 ) from amorphous materials prepared by the simultaneous hydrolysis of titanium and aluminum alkoxides. The lattice parameter a is relatively constant regardless of composition, whereas parameter c decreases linearly with increasing Al2 O3 . At higher temperatures, anatase solid solutions transform into TiO2 (rutile) with the formation of α-Al2 O3 . Powder characterization is studied. Pure anatase crystallizes at 220° to 360°C, and the anatase-to-rutile phase transformation occurs at 770° to 850°C. 相似文献
8.
J. P. COUTURES 《Journal of the American Ceramic Society》1985,68(3):105-107
A tentative phase diagram for the system Al2 03 -Nd2 O3 is presented. Three compounds were obtained: a β -A12 O3 -type compound, the perovskite NdAlO3 , and Nd4 Al2 O9 . The perovskite melts congruently (mp 2090°C), and the two other compounds exhibit incongruent melting behavior: β -Nd/Al2 O3 , mp 1900°C; Nd4 Al2 O9 , mp 1905°C. Two eutectics exist with the following compositions and melting points: 80 mol% Al2 O3 , 1750°C; 23 mol% Al2 O3 ,1800°C. Nd4 Al2 O9 decomposes in the solid state at 1780°C. 相似文献
9.
Phase relations in the system Na2 O· Al2 O3 -CaO· Al2 O3 -Al2 O3 at 1200°C in air were determined using the quenching method and high-temperature X-ray diffraction. The compound 2Na2 O · 3CaO · 5Al2 O3 , known from the literature, was reformulated as Na2 O · CaO · 2Al2 O3 . A new compound with the probable composition Na2 O · 3CaO · 8Al2 O3 was found. Cell parameters of both compounds were determined. The compound Na2 O · CaO-2Al2 O3 is tetragonal with a = 1.04348(24) and c = 0.72539(31) nm; it forms solid solutions with Na2 O · Al2 O3 up to 38 mol% Na2 O at 1200°C. The compound Na2 O · 3CaO · 8Al2 O3 is hexagonal with) a = 0.98436(4) and c = 0.69415(4) nm. The compound CaO · 6Al2 O3 is not initially formed from oxide components at 1200°C but behaves as an equilibrium phase when it is formed separately at higher temperatures. The very slow transformation kinetics between β and β "-Al2 O3 make it very difficult to determine equilibrium phase relations in the high-Al2 O3 part of the diagram. Conclusions as to lifetime processes in high-pressure sodium discharge lamps can be drawn from the phase diagram. 相似文献
10.
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
11.
Akira Kato Hisao Yamashita Hiroshi Kawagoshi Shimpei Matsuda 《Journal of the American Ceramic Society》1987,70(7):157-C
Mixtures of La2 O3 and Al2 O3 with various La contents were prepared by co-precipitation from La(NO3 )3 and Al(NO3 )3 solutions and calcined at 800° to 1400°C. The addition of small amounts of La2 O3 (2 to 10 mol%) to Al2 O3 gives rise to the formation of lanthanum β-alumina (La 2 O3 ·11–14Al2 O3 ) upon heating to above 1000°C and retards the transformation of γ-Al2 O3 to α-Al2 O3 and associated sintering. 相似文献
12.
The syntheses and the results of unit-cell determinations ofBa3 V4 O13 and the two forms (low- and high-temperature) of Ba3 P4 O13 are presented. Ba3 V4 O13 crystallizes in the monoclinic system, space group Cc or C2/c with unit-cell dimensions a=16.087, b=8.948, c=10.159 (x10nm), β=114.52° Low-Ba3 P4 O13 crystallizes in the triclinic system, space group P1 or P1 with unit-cell dimensions a=5.757, b=7.243, c=8.104 (x10 nm) α=82.75°, β=73.94°, γ=70.71°. Low-Ba3 P4 O13 transforms at 870°C into high-Ba3 P4 O13 which crystallizes in the orthorhombic system, space group Pbcm (No. 57) (or Pbc2, No. 29) with unit-cell dimensions a =7.107, b=13.883, c=19.219 (x10 nm). No relations have been found between the structures of the tribarium tetravanadate and the tribarium tetraphosphate. 相似文献
13.
Heidi L. Rutz Delbert E. Day Charles F. Spencer Jr. 《Journal of the American Ceramic Society》1990,73(6):1788-1790
In the Y2 O3 –Al2 O3 –B2 O3 system, homogeneous glasses were obtained from compositions containing from 50 to 65 mol% B2 O3 . The density, refractive index, and thermal expansion increase as Y2 O3 replaces either B2 O3 or Al2 O3 . These glasses have a dilatometric softening temperature above 665°, and below 300°C their dc electrical resistivity exceeds that of fused silica. The infrared absorption spectra indicate that BO3 , BO4 , and AlO4 , groups are present in these glasses. 相似文献
14.
Koji Ishida Ken Hirota Osamu Yamaguchi Hideki Kume Suguru Inamura Hiroki Miyamoto 《Journal of the American Ceramic Society》1994,77(5):1391-1395
In the system ZrO2 –Al2 O3 , a new method for preparing ZrO2 solid solutions from ZrCl4 and AlCl3 using hydrazine monohydrate is investigated. c -ZrO2 solid solutions containing up to ∼40 mol% Al2 O3 crystallize at low temperatures from amorphous materials. The formation mechanism is discussed from IR spectral data. The values of the lattice parameter α increase linearly from 0.5072 to 0.5105 nm with increasing Al2 O3 content. At higher temperatures, transformation of the solid solutions proceeds as follows: c ( SS ) → t ( ss ) → t ( ss ) +α-Al2 O3 → m +α-Al2 O3 . m -ZrO2 –α-Al2 O3 composite ceramics are fabricated by hot isostatic pressing for 2 h at 1250°C and 196 MPa. Microstructures and mechanical properties are examined, in connection with increasing Al2 O3 content. 相似文献
15.
Mari Lou Balmer Fred F. Lange Carlos G. Levi 《Journal of the American Ceramic Society》1994,77(8):2069-2075
Aqueous solutions of zirconium acetate and aluminum nitrate were spray pyrolyzed at 250°C and upquenched to different temperatures to yield metastable solid solutions of composition Zr(1− x ) Alx O(2− x /2) . An amorphous oxide forms first during pyrolysis which subsequently crystallizes as a single phase for x ≤ 0.57 (≤40 mol% Al2 O3 ). The crystallization temperature increased with Al2 O3 content. Electron diffraction, supported by Raman spectroscopy, indicates that the initial phase is tetragonal. At higher temperatures, the initial solid solation partitions to other metastable phases, viz., t -ZrO2 +γ-Al2 O3 , prior to achieving their equilibrium phase assemblage, m -ZrO2 +α-Al2 O3 . Partitioning yields a nanocomposite microstructure with grain sizes of 20–100 nm, compared to the 3 to 5 nm in the initial, single phase. Compositions containing 45 to 50 mol% Al2 O3 concurrently crystallize and partition. The structure selected during crystallization and the partitioning phenomena are discussed in terms of diffusional constraints during crystallization, which are conceptually similar to those operating during rapid solidification. 相似文献
16.
Yttria-ceria-doped tetragonal zirconia (Y,Ce)-TZP)/alumina (Al2 O3 ) composites were fabricated by hot isostatic pressing at 1400° to 1450°C and 196 MPa in an Ar–O2 atmosphere using the fine powders prepared by hydrolysis of ZrOCl2 solution. The composites consisting of 25 wt% Al2 O3 and tetragonal zirconia with compositions 4 mol% YO1.5 –4 mol% CeO2 –ZrO2 and 2.5 mol% YO1.5 –5.5 mol% CeO2 –ZrO2 exhibited mean fracture strength as high as 2000 MPa and were resistant to phase transformation under saturated water vapor pressure at 180°C (1 MPa). Postsintering hot isostatic pressing of (4Y, 4Ce)-TZP/Al2 O3 and (2.5Y, 5.5Ce)-TZP/Al2 O3 composites was useful to enhance the phase stability under hydrothermal conditions and strength. 相似文献
17.
Yosuke Matsumoto Ken Hirota Osamu Yamaguchi Suguru Inamura Hiroki Miyamoto Nobuaki Shiokawa Kazuhiro Tsuji 《Journal of the American Ceramic Society》1993,76(10):2677-2680
Amorphous Al2 O3 –ZrO2 composite powders with 5–30 mol% ZrO2 have been prepared by adding aqueous ammonia to the mixed solution of aqueous aluminum sulfate and zirconium alkoxide containing 2-propanol. Simultaneous crystallization of γ-Al2 O3 and t -ZrO2 occurs at 870°–980°C. The γ-Al2 O3 transforms to α-Al2 O3 at 1160°–1220°C. Hot isostatic pressing has been performed for 1 h at 1400°C under 196 MPa using α-Al2 O3 – t -ZrO2 composite powders. Dense ZrO2 -toughened Al2 O3 (ZTA) ceramics with homogeneous-dispersed ZrO2 particles show excellent mechanical properties. The toughening mechanism is discussed. The microstructures and t / m ratios of ZTA are examined, with emphasis on the relation between strength and fracture toughness. 相似文献
18.
Thermal reactions in 93% Al2 O3 -7% MgO and 95.8% Al2 O3 -4.2% MgO gels seeded with α-Al2 O3 , MgAl2 O4 , α-Fe2 O3 , and SiO2 , sols were investigated by differential thermal analysis to determine the extent of nucleation catalysis of solid-state reactions. Seeding with α-Al2 O3 lowered the α-Al2 O3 crystallization temperature in these xerogels by 100° to 150°C. Spinel seeds have much less effect on the γ-α transition, and α-Fe2 O3 and SiO2 seeds do not affect it significantly. Isostructural seeding of gels may therefore permit lower ceramic processing temperatures. 相似文献
19.
Formation and Sintering of Yttria-Doped Tetragonal Zirconia with 50 mol% Alumina Prepared by the Hydrazine Method 总被引:1,自引:0,他引:1
Shinya Kimoto Ken Hirota Osamu Yamaguchi Hideki Kume Suguru Inamura Hiroki Miyamoto 《Journal of the American Ceramic Society》1994,77(6):1694-1696
Al2 O3 /Y2 O3 -doped ZrO2 composite powders with 50 mol% Al2 O3 are prepared by the hydrazine method. As-prepared powders are mixtures of AlO(OH) gel and amorphous ZrO2 solid solutions containing Y2 O3 and Al2 O3 . The formation process leading to α-Al2 O3 - t -ZrO2 composite powders is examined. Hot isostatic pressing is performed for 2 h at 1400°C under 196 MPa using θ-Al2 O3 - t -ZrO2 composite powders. The resulting dense, sintered α-Al2 O3 - t -ZrO2 composites show excellent mechanical strength. 相似文献
20.
Gradient, porous alumina ceramics were prepared with the characteristics of microsized tabular α-Al2 O3 grains grown on a surface with a fine interlocking feature. The samples were formed by spin-coating diphasic aluminosilicate sol on porous alumina substrates. The sol consisted of nano-sized pseudo-boehmite (AlOOH) and hydrolyzed tetraethyl orthosilicate [Si(OC2 H5 )4 ]. After drying and sintering at 1150°–1450°C, the crystallographic and chemical properties of the porous structures were investigated by analytical electron microscopy. The results show that the formation of tabular α-Al2 O3 grains is controlled by the dissolution of fine Al2 O3 in the diphasic material at the interface. The nucleation and growth of tabular α-Al2 O3 grains proceeds heterogeneously at the Al2 O3 /glass interface by ripening nano-sized Al2 O3 particles. 相似文献