共查询到20条相似文献,搜索用时 15 毫秒
1.
Mamoru Mitomo Yoh-ichiro Sato Nobuo Ayuzawa Isamu Yashima 《Journal of the American Ceramic Society》1991,74(4):856-858
Plasma etching of β-Si3 N4 , α-sialon/β-Si3 N4 and α-sialon ceramics were performed with hydrogen glow plasma at 600°C for 10 h. The preferential etching of β-Si3 N4 grains was observed. The etching rate of α-sialon grains and of the grain-boundary glassy phase was distinctly lower than that of β-Si3 N4 grains. The size, shape, and distribution of β-Si3 N4 grains in the α-sialon/β-Si3 N4 composite ceramics were revealed by the present method. 相似文献
2.
Dong-Duk Lee Suk-Joong L. Kang Gunter Petzow Duk N. Yoon 《Journal of the American Ceramic Society》1990,73(3):767-769
By using α-Si3 N4 and β-Si3 N4 starting powders with similar particle size and distribution, the effect of α-β (β') phase transition on densification and microstructure is investigated during the liquid-phase sintering of 82Si3 N4 ·9Al2 O3 ·9Y2 O3 (wt%) and 80Si3 N4 ·13Al2 O3 ·5AIN·5AIN·2Y2 O3 . When α-Si3 N4 powder is used, the grains become elongated, apparently hindering the densification process. Hence, the phase transition does not enhance the densification. 相似文献
3.
Fengxia Li Li Fu Xiaojian Ma Changhui Sun LianCheng Wang Chunli Guo Yitai Qian Yitai Qian 《Journal of the American Ceramic Society》2009,92(2):517-519
Starting from Si powder, NaN3 and different additives such as N -aminothiourea, iodine, or both, Si3 N4 nanomaterials were synthesized through the nitridation of silicon powder in autoclaves at 60°–190°C. As the additive was only N -aminothiourea, β-Si3 N4 nanorods and α-Si3 N4 nanoparticles were prepared at 170°C. If the additive was only iodine, α-Si3 N4 dendrites with β-Si3 N4 nanorods were obtained at 190°C. However, when both N -aminothiourea and iodine were added to the system of Si and NaN3 , the products composed of β-Si3 N4 nanorods and α, β-Si3 N4 nanoparticles could be prepared at 60°C. 相似文献
4.
Gui-hua Peng Min Liang Zhen-hua Liang Qing-yu Li Wen-lan Li Qian Liu 《Journal of the American Ceramic Society》2009,92(9):2122-2124
Silicon nitride ceramics were prepared by spark plasma sintering (SPS) at temperatures of 1450°–1600°C for 3–12 min, using α-Si3 N4 powders as raw materials and MgSiN2 as sintering additives. Almost full density of the sample was achieved after sintering at 1450°C for 6 min, while there was about 80 wt%α-Si3 N4 phase left in the sintered material. α-Si3 N4 was completely transformed to β-Si3 N4 after sintering at 1500°C for 12 min. The thermal conductivity of sintered materials increased with increasing sintering temperature or holding time. Thermal conductivity of 100 W·(m·K)−1 was achieved after sintering at 1600°C for 12 min. The results imply that SPS is an effective and fast method to fabricate β-Si3 N4 ceramics with high thermal conductivity when appropriate additives are used. 相似文献
5.
Gas-pressure sintering of α-Si3 N4 was carried out at 1850 ° to 2000°C in 980-kPa N2 . The diameters and aspect ratios of hexagonal grains in the sintered materials were measured on polished and etched surfaces. The materials have a bimodal distribution of grain diameters. The average aspect ratio in the materials from α-Si3 N4 powder was similar to that in the materials from β-Si3 N4 powder. The aspect ratio of large and elongated grains was larger than that of the average for all grains. The development of elongated grains was related to the formation of large nuclei during the α-to-β phase transformation. The fracture toughness of gaspressure-sintered materials was not related to the α content in the starting powder or the aspect ratio of the grains, but to the diameter of the large grains. Crack bridging was the main toughening mechanism in gas-pressure-sintered Si3 N4 ceramics. 相似文献
6.
Effect of Sintering Additives on Microstructure and Mechanical Properties of Porous Silicon Nitride Ceramics 总被引:2,自引:0,他引:2
Jun Yang Jian-Feng Yang Shao-Yun Shan Ji-Qiang Gao Tatsuki Ohji 《Journal of the American Ceramic Society》2006,89(12):3843-3845
Porous silicon nitride (Si3 N4 ) ceramics with about 50% porosity were fabricated by pressureless sintering of α-Si3 N4 powder with 5 wt% sintering additive. Four types of sintering aids were chosen to study their effect on the microstructure and mechanical properties of porous Si3 N4 ceramics. XRD analysis proved the complete formation of a single β-Si3 N4 phase. Microstructural evolution and mechanical properties were dependent mostly on the type of sintering additive. SEM analysis revealed the resultant porous Si3 N4 ceramics as having high aspect ratio, a rod-like microstructure, and a uniform pore structure. The sintered sample with Lu2 O3 sintering additive, having a porosity of about 50%, showed a high flexural strength of 188 MPa, a high fracture toughness of 3.1 MPa·m1/2 , due to fine β-Si3 N4 grains, and some large elongated grains. 相似文献
7.
Tzer-Shin Sheu 《Journal of the American Ceramic Society》1994,77(9):2345-2353
The in situ β-Si3 N4 /α'-SiAlON composite was studied along the Si3 N4 –Y2 O3 : 9 AlN composition line. This two phase composite was fully densified at 1780°C by hot pressing Densification curves and phase developments of the β-Si3 N4 /α'-SiAlON composite were found to vary with composition. Because of the cooperative formation of α'-Si AlON and β-Si3 N4 during its phase development, this composite had equiaxed α'-SiAlON (∼0.2 μm) and elongated β-Si3 N4 fine grains. The optimum mechanical properties of this two-phase composite were in the sample with 30–40%α', which had a flexural strength of 1100 MPa at 25°C 800 MPa at 1400°C in air, and a fracture toughness 6 Mpa·m1/2 . α'-SiAlON grains were equiaxed under a sintering condition at 1780°C or lower temperatures. Morphologies of the α°-SiAlON grains were affected by the sintering conditions. 相似文献
8.
Jun-Qi Li Fa Luo Dong-Mei Zhu Wan-Cheng Zhou 《Journal of the American Ceramic Society》2007,90(6):1950-1952
The influence of phase formation on the dielectric properties of silicon nitride (Si3 N4 ) ceramics, which were produced by pressureless sintering with additives in MgO–Al2 O3 –SiO2 system, was investigated. It seems that the difference in the dielectric properties of Si3 N4 ceramics sintered at different temperatures was mainly due to the difference of the relative content of α-Si3 N4 , β-Si3 N4 , and the intermediate product (Si2 N2 O) in the samples. Compared with α-Si3 N4 and Si2 N2 O, β-Si3 N4 is believed to be a major factor influencing the dielectric constant. The high-dielectric constant of β-Si3 N4 could be attributed to the ionic relaxation polarization. 相似文献
9.
Electrical conductivity was measured from 850° to 1400°C for β-sialon and pure X phase as well as for the sintered system Si3 N4 -Al2 O3 , containing β-sialon, X phase, β-Si3 N4 , and glassy phase. Ionic conductivity was measured at >1000°C. The charge carriers were identified by electrolysis. The results showed that pure β-sialon is ionically conducting because of Si4+ migration for the temperature range studied. Pure X phase shows ionic conduction by Si4+ above 1000°; below 1000°C, it shows electronic conduction because of impurities. The conductivity of the sintered system Si3 N4 -Al2 O3 containing β-sialon, β-Si3 N4 X phase, and glassy phase changes as the relative quantities of β -sialon and X phase change. The apparent activation energies for the ionic and electronic conductivities are 45 and 20 kcal/mol, respectively. 相似文献
10.
Wei-Wu Chen Xin-Lu Su Pei-Ling Wang Dong-Sheng Yan Yi-Bing Cheng Koji Watari 《Journal of the American Ceramic Society》2005,88(10):2955-2956
Dy-α-sialon and β-Si3 N4 materials containing Dy-oxynitride glass were hot pressed at 1800°C for 1 h. The luminescence spectra of Dy3+ in these samples were compared when excited at 350 nm. The results showed that two strong emission bands in the region 470–500 nm and 570-600 nm, associated with the 4 F9/2 →6 H15/2 and 4 F9/2 →6 H13/2 transitions of Dy3+ ions, were observed in Dy-α-sialon. However, no emission peak was detected from the β-Si3 N4 sample, despite it containing the same amount of Dy3+ cations. This proved that only the Dy3+ cations in the α-sialon structure, not those in the oxynitride glass, produce the luminescence spectrum. 相似文献
11.
Branko Matovic Georg Rixecker Fritz Aldinger 《Journal of the American Ceramic Society》2004,87(4):546-549
This paper deals with the densification and phase transformation during pressureless sintering of Si3 N4 with LiYO2 as the sintering additive. The dilatometric shrinkage data show that the first Li2 O- rich liquid forms as low as 1250°C, resulting in a significant reduction of sintering temperature. On sintering at 1500°C the bulk density increases to more than 90% of the theoretical density with only minor phase transformation from α-Si3 N4 to β-Si3 N4 taking place. At 1600°C the secondary phase has been completely converted into a glassy phase and total conversion of α-Si3 N4 to β-Si3 N4 takes place. The grain growth is anisotropic, leading to a microstructure which has potential for enhanced fracture toughness. Li2 O evaporates during sintering. Thus, the liquid phase is transient and the final material might have promising mechanical properties as well as promising high-temperature properties despite the low sintering temperature. The results show that the Li2 O−Y2 O3 system can provide very effective low-temperature sintering additives for silicon nitride. 相似文献
12.
The microstructure, crystal structure, and chemical composition of reaction-sintered Si3 N4 containing iron were studied using conventional and scanning transmission electron microscopy. It was found that the grains of β -Si3 N4 were large and blocklike with well-developed facets, a series of voids along some grain boundaries, a subgrain of iron silicide near the periphery, and penetration of iron silicide into the three-grain junctions and grain boundaries. At some distance from each β -Si3 N4 grain was a region of small α-Si3 N4 grains, with no evidence of iron silicide. Between this region and the β -Si3 N4 grain was a zone containing both α- and β -Si3 N4 and iron silicide. These observations suggest that the large β -Si3 N4 grains grow in liquid iron silicide, that the smaller α-Si3 N4 grains grow from the vapor, and that the latter are converted to the β form by solution in, and reprecipitation from, liquid iron silicide. 相似文献
13.
C. Greskovich 《Journal of the American Ceramic Society》1981,64(2):31-C-
The development of microstructure in hot-pressed Sia N4 was studiehd for a typical Si3 N4 powder with and without BeSiN2 as a densification aid. The effect of hot-pressing temperature on density, α- to β-Si3 N4 conversion and specific surface area showed that BeSiN2 appears to increase the mobility of the system by enhancing densification, α- to β-Si3 N4 transformation, and grain growth at temperatures between 1450° and 1800°. These processes appear to occur in the presence of a liquid phase. 相似文献
14.
Shock Synthesis of Cubic Silicon Nitride 总被引:2,自引:0,他引:2
Toshimori Sekine 《Journal of the American Ceramic Society》2002,85(1):113-116
The phase transitions of α-Si3 N4 and β-Si3 N4 have been investigated by shock compression through the recovery technique and Hugoniot measurements. α- and β-Si3 N4 are transformed into a cubic spinel structure ( c -Si3 N4 ). The yield of c -Si3 N4 increases with increasing shock pressure and reaches 100% at 63 GPa. The shock-synthesized c -Si3 N4 powders are nanocrystals and display a high-temperature metastability up to about 1620 K. c -Si3 N4 is one of the hard materials based on the measured equation of state. c -Si3 N4 powders have been characterized by electron microscopy and 29 Si magic angle spinning NMR spectroscopy. The purification and separation method has been developed to obtain pure c -Si3 N4 powders. 相似文献
15.
New Strategies for Preparing NanoSized Silicon Nitride Ceramics 总被引:2,自引:0,他引:2
Xin Xu Toshiyuki Nishimura Naoto Hirosaki Rong-Jun Xie Yinchun Zhu Yoshinobu Yamamoto Hidehiko Tanaka 《Journal of the American Ceramic Society》2005,88(4):934-937
We report the preparation of nanosized silicon nitride (Si3 N4 ) ceramics via high-energy mechanical milling and subsequent spark plasma sintering. A starting powder mixture consisting of ultrafine β-Si3 N4 and sintering additives of 5-mol% Y2 O3 and 2-mol% Al2 O3 was prepared by high-energy mechanical milling. After milling, the powder mixture was mostly transformed into a non-equilibrium amorphous phase containing a large quantity of well-dispersed nanocrystalline β-Si3 N4 particles. This powder precursor was then consolidated by spark plasma sintering at a temperature as low as 1600°C for 5 min at a heating rate of 300°C/min. The fully densified sample consisted of homogeneous nano-Si3 N4 grains with an average diameter of about 70 nm, which led to noticeable high-temperature ductility and elevated hardness. 相似文献
16.
Mikito Kitayama Kiyoshi Hirao Motohiro Toriyama Shuzo Kanzaki 《Journal of the American Ceramic Society》1999,82(10):2931-2933
A powder mixture of α-Si3 N4 , Y2 O3 , and SiO2 was heat-treated in a loose powder state in the temperature range of 1750°–1900°C for 2 h; then, the mixture was acid-rinsed to remove the glassy phase. The widths and lengths of the resulting β-Si3 N4 crystals were analyzed quantitatively. The width–aspect-ratio distribution of the β-Si3 N4 crystals initially showed a strong negative correlation, and then the aspect ratio of crystals with small widths quickly decreased. After a stage in which aspect ratio was almost constant, regardless of the width, the width-aspect-ratio distribution evolved to show a positive correlation in the final stage. This pattern of morphology evolution of the β-Si3 N4 crystals was in good agreement with that predicted by the anisotropic Ostwald ripening model. 相似文献
17.
Ibram Ganesh 《International Journal of Applied Ceramic Technology》2009,6(1):89-101
In this paper, a new net-shaping process, an hydrolysis-induced aqueous gelcasting (GC) (GCHAS) has been reported for consolidation of β-Si4 Al2 O2 N6 ceramics from aqueous slurries containing 48–50 vol%α-Si3 N4 , α-Al2 O3 , AlN, and Y2 O3 powders mixture. Dense ceramics of same composition were also consolidated by aqueous GC and hydrolysis assisted solidification routes. Among three techniques used, the GCHAS process was found to be superior for fabricating defect-free thin wall β-Si4 Al2 O2 N6 crucibles and tubes. Before use, the as purchased AlN powder was passivated against hydrolysis. The sintered β-Si4 Al2 O2 N6 ceramics exhibited comparable properties with those reported for similar materials in the literature. 相似文献
18.
β-Si3 N4 ceramics sintered with Yb2 O3 and ZrO2 were fabricated by gas-pressure sintering at 1950°C for 16 h changing the ratio of "fine" and "coarse" high-purity β-Si3 N4 raw powders, and their microstructures were quantitatively evaluated. It was found that the amount of large grains (greater than a few tens of micrometers) could be drastically reduced by mixing a small amount of "coarse" powder with a "fine" one, while maintaining high thermal conductivity (>140 W·(m·K)−1 ). Thus, this work demonstrates that it is possible for β-Si3 N4 ceramics to achieve high thermal conductivity and high strength simultaneously by optimizing the particle size distribution of raw powder. 相似文献
19.
Gui-hua Peng Guo-jian Jiang Wen-lan Li Bao-lin Zhang Li-dong Chen 《Journal of the American Ceramic Society》2006,89(12):3824-3826
α/β-Si3 N4 composites with various α/β phase ratios were prepared by hot pressing at 1600°–1650°C with MgSiN2 as sintering additives. An excellent combination of mechanical properties (Vickers indentation hardness of 23.1 GPa, fracture strength of about 1000MPa, and toughness of 6.3 MPa·m1/2 ) could be obtained. Compared with conventional Si3 N4 -based ceramics, this new material has obvious advantages. It is as hard as typical in-situ-reinforced α-Sialon, but much stronger than the latter (700 MPa). It has comparable fracture strength and toughness, but is much harder than β-Si3 N4 ceramics (16 GPa). The microstructures and mechanical properties can be tailored by choosing the additive and controlling the heating schedule. 相似文献
20.
Chunli Guo Zheng Xing Xiaojian Ma Liqiang Xu Yitai Qian 《Journal of the American Ceramic Society》2008,91(5):1725-1728
Silicon nitride nanowires or nanorods have been synthesized from SiCl4 , NaN3 , and metallic Mg at temperatures ranging from 200° to 300°C. X-ray powder diffraction patterns indicated that the as-obtained products were mainly β-Si3 N4 . Scanning electron microscope and high-resolution transmission electronic microscopy showed that the samples mostly consisted of Si3 N4 nanowires or nanorods. As metallic iron powder was used, α-Si3 N4 was mainly formed at 250°C. 相似文献