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1.
Sintering kinetics of the system Si3 N4-Y2O3 -Al2 O3 were determined from measurements of the linear shrinkage of pressed disks sintered isothermally at 1500° to 1700°C. Amorphous and crystalline Si3 N4 were studied with additions of 4 to 17 wt% Y2 O3 and 4 wt% A12 O3 . Sintering occurs by a liquid-phase mechanism in which the kinetics exhibit the three stages predicted by Kingery's model. However, the rates during the second stage of the process are higher for all compositions than predicted by the model. X-ray data show the presence of several transient phases which, with sufficient heating, disappear leaving mixtures of β ' -Si3 N4 and glass or β '-Si3 N4 , α '-Si3 N4 , and glass. The compositions and amounts of the residual glassy phases are estimated. 相似文献
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Solid solutions of Fe304-FeV204 and Fe304-FeCr204 were prepared and equilibrated with Pt under controlled streams of CO/CO, gas mixtures at 1673 K. The concentration of Fe in Pt was used to determine the activity of Fe304 in the solid solutions. The activity of the second component was calculated by Gibbshhem integration. From these data, the Gibbs energy of mixing was derived for both systems. The experimental results and theoretical values which are determined from calculated cation distribution compare favorably in the case of vanadite solid solutions but not in the case of chromite solid solutions. The difference is attributed to a heat term arising from lattice distortion due to cation size difference. The positive heat of mixing will give rise to a miscibility gap in the system Fe304-FeCr204 at lower temperatures. 相似文献
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R. K. DATTA 《Journal of the American Ceramic Society》1971,54(5):262-265
High-temperature X-ray diffraction and differential thermal analyses showed that LiGa5 O8 exists in two polymorphs related by the first-order transition at 1138°±3°C of the low-temperature simple-cubic form, space group (probably) O7 , to the high-temperature spinel (fcc) form, space group O h 7 . The transition is rapid, and the high-temperature form in pure LiGa5 O8 could not be quenched to room temperature under the conditions used. However, the high-temperature polymorph can be quenched under equilibrium conditions when 40 mol% or more MgGa2 O4 is present. The subsolidus equilibrium relations in the system MgGa2 O4 -LiGa5 O8 are discussed. 相似文献
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Elena R. Andrievskaya Lidia M. Lopato Vasily P. Smirnov 《Journal of the American Ceramic Society》1996,79(3):714-720
A mathematical model of the liquidus surface based on a reduced polynomial method was proposed for the system HfO2 -Y2 O3 -Er2 O3 . The results of calculations according to this model agree fairly well with the experimental data. Phase equilibria in the system HfO2 -Y2 O3 -Er2 O3 were studied on melted (as-cast) and annealed samples using X-ray diffraction (at room and high temperatures) and micro-structural and petrographic analyses. The crystallization paths in the system HfO2 -Y2 O3 -Er2 O3 were established. The system HfO2 -Y2 O3 -Er2 O3 is characterized by the formation of extended solid solutions based on the fluorite-type (F) form of HfO2 and cubic (C) and hexagonal (H) forms of Y2 O3 and Er2 O3 . The boundary curves of these solid solutions have the minima at 2370°C (15. 5 mol% HfO2 , 49. 5 mol% Y2 O3 ) and 2360°C (10. 5 mol% HfO2 , 45. 5 mol% Y2 O3 ). No compounds were found to exist in the system investigated. 相似文献
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Subsolidus phase relations were established in the system Si3 N4 -SiO2 -Y2 O3 . Four ternary compounds were confirmed, with compositions of Y4 Si2 O7 N2 , Y2 Si3 O3 N4 , YSiO2 N, and Y10 (SiO4 )6 N2 . The eutectic in the triangle Si3 N4 -Y2 Si2 O7 -Y10 (SiO4 )6 N2 melts at 1500°C and that in the triangle Si2 N2 O-SiO2 -Y2 Si2 O7 at 1550°C. The eutectic temperature of the Si3 N4 -Y2 Si2 O7 join was ∼ 1520°C. 相似文献
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The complete phase-equilibrium diagram of the system CaF2 -AlF3 -Na3 AlF6 and the subsolidus portion of the system CaF2 -AlF3 -Na3 AlF6 -Al2 O3 were established from microscopic, powder X-ray diffraction, quench, and DTA data obtained from samples encapsulated in sealed tubes and either reacted in the solid state or melted and recrystallized. The system Na3 AlF6 -CaF2 contains a simple eutectic with no compound formation or solid solution. The system CaF2 -AlF3 -Na3 AlF6 contains two ternary compounds, NaCaAlF6 and NaCaAl2 F9 , which melt incongruently at 735° and 712°C, respectively; NaCaAlF6 exists in three polymorphic forms with transitions at 610° and 722°C and NaCaAl2 F9 is body-centered cubic with a0 = 10.765 Å. The three binary and two ternary compounds divide the system into eight compatibility triangles. Along the NaCaAlF6 -Na3 AlF6 join, 7 mol% NaCaAlF6 is soluble in α-cryolite at 525° and 42% in β-cryolite at 731°C. The quaternary system Na3 AlF6 -AlF3 -CaF2 -Al2 O3 contains eight compatibility tetrahedra. 相似文献
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The quenching technique was used to study subliquidus and subsolidus phase relations in the pseudobinary system Na2 Ti2 Si2 O11 -Na2 Ti2 Si2 O9 . Both narsarukite (Na2 TiSi4 O11 ) and lorenzenite (Na2 Ti2 Si2 O9 ) melt incongruently. Narsarsukite melts at 911°±°C to SiO2 +liquid, with the liquidus at 1016°C. Lorenzenite melts at 910°±5°C to Na2 Ti6 O13 +liquid; Na2 Ti6 O13 reacts with liquid to form TiO2 and is thus consumed by 985°±5°C. The liquidus occurs at 1252°C. 相似文献
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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
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Quadrupole interactions of 11 B and 27 Al in SiO2 -B2 O3 -Al2 O3 -R2 O glass systems were investigated to determine the structure of these glasses, which should be amenable to chemical strengthening. The ratio of BO4 units to BO3 units approached unity as the R2 O/Al2 O3 ratio for compounds having fixed B2 O3 contents approached unity. Nuclear quadrupole coupling constants ( e2 Qq/h =2.73 to 2.93 MHz) were measured for the NMR spectra of 11 B triangles. The line shapes of 27 Al spectra varied with chemical composition, but a few glasses exhibited 27 Al line shapes similar to those of the AlO4 triclusters in SiO2 -Al2 O3 -Na2 O glasses. Compositional trends in the formation of BO4 and AlO4 were deduced from the NMR spectra. 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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The reciprocal salt pair Sr2 SiO4 -Sr2 GeO4 -Ba2 GeO4 -Ba2 SiO4 was investigated using X-ray powder diffraction and DTA. Unlimited solubility in the low-K2 SO4 structure type (α') occurs throughout the system above 85°C. The nonlinear changes of some lattice constants of the solid solutions are discussed. A stable monoclinic low-temperature (β) form of Sr2 SiO4 was found which converts reversibly to the high-temperature α'-modification at 85°C. The enthalpy of the β-α' transition is 51 cal/mol. In the reciprocal salt pair the β-form solid solutions occur in a very narrow region below 85°C. 相似文献
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W. SCHöNWELSKI F. HABEREY R. LECKEBUSCH M. ROSENBERG K. SAHL 《Journal of the American Ceramic Society》1986,69(1):7-9
Solid Solutions with the magnetoplumbite structure in the System LaMgAl11 O19 -LaMgGa11 O19 -LaMgFe11 O19 were studied by X-ray diffractometry of sintered samples. Complete miscibility exists in the subsystem LaMgAl11 O19 -LaMgGa11 O19 and in a narrow adjacent ternary area with low iron content. In the other subsystems and in the major part of the ternary field, a magnetoplumbite phase occurs together with other compounds. 相似文献
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Santanu Basu Amitava Chakraborty Parukuttyamma Sujatha Devi Himadri Sekhar Maiti 《Journal of the American Ceramic Society》2005,88(8):2110-2113
Nanocrystalline La0.9 Sr0.1 Al0.85 Co0.05 Mg0.1 O3 oxide powder was synthesized by a citrate–nitrate auto-ignition process and characterized by thermal analysis, X-ray diffraction, and impedance spectroscopy measurements. Nanocrystalline (50–100 nm) powder with perovskite structure could be produced at 900°C by this process. The powder could be sintered to a density more than 96% of the theoretical density at 1550°C. Impedance measurements on the sintered samples unequivocally established the potential of this process in developing nanostructured lanthanum aluminate-based oxides. The sintered La0.9 Sr0.1 Al0.85 Co0.05 Mg0.1 O3 sample exhibited a conductivity of 2.40 × 10−2 S/cm in air at 1000°C compared with 4.9 × 10−3 S/cm exhibited by La0.9 Sr0.1 Al0.85 Mg0.15 O3 . 相似文献
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Steven A. Markgraf Shiv K. Sharma Amar S. Bhalla 《Journal of the American Ceramic Society》1992,75(9):2630-2632
Raman spectra are reported for fresnoite (Ba2 Ti(Si,Ge)2 O8 glasses, and comparison is made between the Raman spectra of the corresponding crystalline powders and glasses of Ba2 TiSi2 O8 and Ba2 TiGe2 O8 . The Ba2 TiGe2 O8 glass spectra show correspondence with the Ba2 TiGe2 O8 crystalline Raman spectra; the v s (Ge–O–Ge) mode occurs at 518 cm−1 in the glass and at 521 cm−1 in the crystalline material. Five-fold coordinated titanium is the majority species present in the Ba2 TiGe2 O8 glass as revealed by a strong band at 824 cm−1 in the I glass spectrum. The Ba2 TiSi2 O8 glass spectra are similar to the Ba2 TiSi2 O8 crystalline spectrum; the strongest band is found at 836 cm−1 in the I glass spectrum. Through comparison with the previous Raman data of other titania silicate glasses, we conclude that the Ba2 TiSi2 O8 glass has a structure similar to the crystalline phase. 相似文献
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Differential scanning calorimetry studies of As40 Sex Te60-x glasses with 0≤x≤60 show a 2-stage crystallization when 5≤x≤35, followed by a double-peaked melting endotherm. The enthalpy of crystallization for the low-temperature species is independent of composition and equals 11.6±0.9 cal/g for x≤25, whereas that for the high-temperature species decreases from 2.2±0.2 cal/g for x = 5 to 1.1±0.3 cal/g for x =15. The total enthalpy of melting also is independent of composition and equals 18.8±1.2 cal/g for x ≤25. No crystallization was observed for xe40. The high-temperature phase has the mono-clinic As2 Te3 structure; that of the low-temperature phase was not identified. Annealing experiments for compositions with x = 15 or 20 gave time-temperature transformation maps. A kinetic analysis of the data was inconclusive. 相似文献
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Sintering studies of Si3 N4-Y2 O3/Al2 O3 compositions indicated that increased densification could be produced using a dual N2 pressure process. RT modulus of rupture values and microstructures were found to be similar to hot-pressed material. The technique should be adaptable to complex shaped Si3 N4 bodies where high density and strength are required . 相似文献