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Recent Developments in Sialon Research in New Zealand

机译:新西兰Sialon研究的最新进展

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An important aspect of previous sialon research in NZ has been the development of new synthesis methods, including refinements in carbothermal reduction and nitridation (CRN) methods and the use of mechanochemical activation of sialon precursors (either Al and Si nitrides and oxides or CRN mixtures). Mechanochemical activation of CRN mixtures of clay and carbon heated in N_2 formed β-sialon (z = 2) at 1300℃ (100℃ lower than in unground mixtures) but 21R polytypoid and corundum were also formed. More recently, our attention has focussed on the technique of silicothermal reduction and nitridation (SRN) to synthesise other sialons, including the AlN polytypoids and Na and Li α-sialons. The interest in the polytypoids springs from their expected physical properties (thermal conductivity and good electrical insulation similar to AlN), their covalent bonding and relatively light weight arising from their high Al and N contents and their elongated crystal morphology which may improve the crack resistance of polytypoid composites with α-sialon. This paper describes the development of SRN single-step synthesis of high-purity dense 15R sialon from clay, Si and AlN, and the effect of additives on the synthesis and sintering of the product. A method is also described for SRN synthesis of Na and Li α-sialons from clay, Si and AlN using fluoride additives. Fluorides have the advantage of small size, high electronegativity, leading to their known facilitation of AlN synthesis. Furthermore, they do not readily enter the sialon structure but may toughen it by formation of glassy phases. Fluorides allow use of clay in this SRN synthesis by introducing M~+ without additional oxygen, but have the disadvantage of generating SiF_4 as a byproduct. The reaction using LiF proceeds readily at the very low temperature of 1200℃ via an O-sialon intermediate by a mechanism which probably involves Si migration assisted by the formation of SiF4.The effect of mechanochemical activation (high energy grinding) on the SRN formation and sintering of Na and Li α-sialons, O and β-sialon has also been studied.Grinding the SRN O-sialon precursor promotes O-sialon formation in powders but not in pellets due to pre-reaction sintering, which is facilitated by the smaller particle size. Grinding Na and Li α-sialon SRN precursors forms a mixture of sialons rather than the target monophase product, while sintering of all the sialons is assisted by grinding their SRN precursors.
机译:新西兰以前的赛隆研究的一个重要方面是开发新的合成方法,包括改进碳热还原和氮化(CRN)方法以及对赛隆前体(Al和Si氮化物和氧化物或CRN混合物)进行机械化学活化。在N_2中加热的CRN粘土和碳的CRN混合物的机械化学活化在1300℃(比未研磨的混合物低100℃)下形成了β-sialon(z = 2),但同时也形成了21R多型和刚玉。最近,我们的注意力集中在硅热还原和氮化(SRN)技术上,以合成其他Sialons,包括AlN多型和Na和Liα-Sialons。人们对聚类肽的兴趣来自其预期的物理性能(导热性和与AlN相似的良好电绝缘性),它们的共价键和较高的Al和N含量以及延长的晶体形态(可改善其抗裂性)而产生的相对较轻的重量。 α-赛隆的多型复合材料。本文描述了由粘土,Si和AlN一步合成SRN一步合成高纯度致密15R赛隆的方法,以及添加剂对产物的合成和烧结的影响。还描述了一种使用氟化物添加剂由粘土,Si和AlN SRN合成Na和Liα-赛隆的方法。氟化物具有体积小,电负性高的优点,从而导致已知的促进AlN合成。此外,它们不容易进入赛隆结构,而是可能通过形成玻璃相而使其增韧。氟化物通过在不添加氧的情况下引入M +从而允许在SRN合成中使用粘土,但具有产生副产物SiF_4的缺点。使用LiF的反应可通过O-赛隆中间体在1200℃的极低温度下轻松进行,其机理可能涉及Si迁移并伴随形成SiF4。机械化学活化(高能研磨)对SRN形成和还研究了Na和Liα-赛隆,O和β-赛隆的烧结。由于预反应烧结,对SRN O-赛隆的前体进行研磨会促进粉末中的O-赛隆的形成,但不会促进颗粒中的O-赛隆的形成。粒度。研磨Na和Liα-sialonSRN前驱体形成的是赛隆的混合物,而不是目标单相产物,而所有赛隆的烧结都通过研磨SRN前驱体来辅助。

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