共查询到18条相似文献,搜索用时 78 毫秒
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以TiSi2作为烧结助剂,采用热压烧结制备了TiB2陶瓷.对烧结试样进行了XRD、SEM与EDS分析,对TiB2-x% TiSi2系统进行了热力学计算分析,探讨了TiSi2促进TiB2陶瓷低温烧结致密的机理.结果表明:添加6.0wt%TiSi2作为烧结助剂,可以使TiB2陶瓷在1650℃热压烧结致密.TiSi2促进TiB2陶瓷烧结致密机理为:一是TiSi2熔点低于烧结温度,通过液相传质提高了烧结速率;二是通过高温烧结反应,形成了高熔点的Ti5Si3相以及SiO2玻璃相,SiO2以玻璃相的形式填充气孔并促进液相传质,使坯体致密. 相似文献
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以固体废弃物粉煤灰为主要原料,通过对原料进行预烧处理工艺得到活化粉煤灰粉体,分别在850 ℃、875℃、900 ℃、925 ℃、950 ℃度进行真空热压烧结,制备粉煤灰建筑陶瓷复合材料.利用XRD对复合材料的物相组成进行分析、采用SEM分析样品的微观结构,结合烧成样品的吸水率、体积密度、硬度等,分析不同的烧结温度对陶瓷性能的影响.结果表明:真空热压烧结过程中,随着温度升高,样品低共熔相增多,致密化程度增加.当烧结温度达到925℃时,所得复合陶瓷材料晶粒分布均匀、细小,晶粒尺寸为0.4~0.5 μm;陶瓷样品的体积密度、吸水率、硬度分别为2.62 g/cm3、0.05%、6.5 GPa. 相似文献
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按照不同的实验方案对碳化硼原料进行烧结,结果发现在2 108~2 226℃下进行无压烧结能得到高纯碳化硼制品,使用Al气和由SiC制得的Si气做为助烧结气,在2 226℃可得到高致密性的B4C制品,体积密度为2.455g.cm-3,约为理论密度的97.4%。 相似文献
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BN基复合陶瓷致密化的主要障碍 总被引:4,自引:0,他引:4
本文对BN基复合陶瓷进行了热压和无压烧结试验,对烧结体的密度变化和显微结构进行了研究,分析了影响BN基复合致密化的主要因素,认为卡片房式结构是妨BN基复合陶瓷致密化的主要原因。热压过程中施加的压力足够大时,可以破坏这种卡片房式结构,使片状BN定向排列,因而能获得同致密度的BN基复合陶瓷,热压过程中若有液相出现,有利于片状BN定向排列,因而能促进BN基复合陶瓷的致密化。无压烧结因不能消除坯体中的卡片 相似文献
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Jun Wang Kaijie Ning Jian Zhang Dewei Luo Jie Ma Danlei Yin Dingyuan Tang Ling Bing Kong 《Journal of the American Ceramic Society》2016,99(6):1935-1942
This paper reports on the influence of rapid rate sintering (RRS) on densification and microstructure evolution of yttria transparent ceramics by using vacuum sintering. The presence of temperature gradient has been confirmed during the RRS process. The higher the heating rate (HR), the larger the temperature gradient in the samples would be. By using RRS, e.g., HR = 40°C/min, the samples could be densified very fast to a relative density of 99.6%. However, these samples could not be further densified, due to the presence of difference in densification caused by a heating rate‐induced temperature gradient. By using a two‐step RRS with an intermediate‐temperature thermal treatment, this problem has been successfully addressed. The intermediate‐temperature treatment allowed for the particle neck growth, so that effective thermal conductivity of the compacts was increased greatly. Therefore, the temperature gradient and differentiate densification were effectively prevented. Samples sintered using the two‐step RRS process could be fully densified and excellent in‐line optical transmittance was achieved. It is believed this strategy is applicable to other transparent ceramics, as well as other engineering ceramics. 相似文献
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Mohamed N. Rahaman Lutgard C. De Jonghe May-Ying Chu 《Journal of the American Ceramic Society》1991,74(3):514-519
The effect of green density on both the densification rate and the creep rate was measured simultaneously during sintering by loading dilatometry. The experiments were performed on zinc oxide powder compacts with five different green densities covering a range of 0.39 to 0.73 of theoretical. The samples were heated at a constant rate of 4°C/min up to 1100°C in air. The densification rate at any temperature increases significantly with decreasing green density. The data for the densification rate and creep rate as a function of density show two quite distinct regimes of behavior; the rates were strongly dependent on density below 0.80, while above this value they were weakly dependent on density. The ratio of the densification rate to the creep rate was almost independent of temperature but increased almost linearly with increasing green density. The representation of the data in terms of models for sintering and creep is discussed. 相似文献
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High-Pressure Self-Combustion Sintering of Alumina-Titanium Carbide Ceramic Composite 总被引:4,自引:0,他引:4
Seiji Adachi Takahiro Wada Toshihiro Mihara Yoshinari Miyamoto Mitsue Koizumi 《Journal of the American Ceramic Society》1990,73(5):1451-1452
Al2 O3 -TiC ceramic composites were fabricated by highpressure self-combustion sintering (HPCS). The samples had a unique microstructure which was quite different from that of commercial Al2 O3 -TiC materials made by conventional processing. A possible mechanism for combustion reaction is suggested on the basis of the microstructure of the samples and the thermodynamical data. The HPCS sample had a higher K IC value than commercial Al2 O3 -TiC materials. 相似文献