1992
DOI: 10.1111/j.1151-2916.1992.tb05538.x
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Densification and Sintering Kinetics in Sintered Silicon Nitride

Abstract: The sintering sequence of Y2O3-AI2O3-doped Si3N4 was investigated with respect to the relationship between densification, (Y -+ p transformation, and microstructural development. Quenching studies were performed to reveal these interactions during a complete sintering cycle. Isothermal studies were conducted to examine the sintering kinetics and compared to Kingery's liquid-phase sintering model. The bulk density increased to >90% of theoretical density with only minor transformation taking place. Major transf… Show more

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Cited by 56 publications
(31 citation statements)
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“…For example, the lowest eutectic temperature of yttria-alumina-silica was reported as 1618 K [12] while that of yttria-silica is 1933 K [13]. Therefore, only a small amount of alumina needs to be added to significantly improve the density of silicon nitride sintered with yttria, as reported by Smith and Quackenbush [14].…”
Section: Introductionmentioning
confidence: 85%
“…For example, the lowest eutectic temperature of yttria-alumina-silica was reported as 1618 K [12] while that of yttria-silica is 1933 K [13]. Therefore, only a small amount of alumina needs to be added to significantly improve the density of silicon nitride sintered with yttria, as reported by Smith and Quackenbush [14].…”
Section: Introductionmentioning
confidence: 85%
“…The grain structure and constitution of an insulating composite are greatly determined by dynamic parameters of temperature treatment-billet heating modes and sinter cooling modes. The former governs the chemistry and kinetics of interaction between the phase components and compaction environment [2], while the latter influences the dynamics of crystallization in a material. It is believed that a substance is easily decrystallized if the critical cooling rate is no more than 60 deg/min [3].…”
Section: Introductionmentioning
confidence: 99%
“…11) Distribution of activation energies of low-temperature E 1 (1) and high-temperature E 2(2) conductivity areas of the composites with TiO 2 additive…”
mentioning
confidence: 99%
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“…Time can be precisely determined and controlled, whereas temperature irreversible α →ß phase transformation simultaneously occurred during this heat-treatment cycle [44]. The microstructure of the material evolved from equiaxed primary α-phase particles and ~50% open porosity to interlocking needle-like ß-phase grains and <5% closed porosity [45,46]. Components were fired in nitrogen in a batch furnace with a slight N 2 overpressure (+ 13.7 kPa), or in a continuous furnace at ambient pressure under flowing N 2 (Centorr Vacuum Industries, Nashua, NH, USA), or in a hot-isostatic press (HIP) (QIH-21 Avure Technologies Columbus, OH) at pressures ranging from about 0.7 MPa, to 10 MPa.…”
Section: Process Validation Studiesmentioning
confidence: 99%