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Recent Developments in Sialon Research in New Zealand

机译:新西兰锡亚隆研究的最新发展

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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°C (100°C 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°C via an O-sialon intermediate by a mechanism which probably involves Si migration assisted by the formation of SiF_4.The effect of mechanochemical activation (high energy grinding) on the SRN formation and sintering of Na and Li a-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:新西兰先后赛隆研究的一个重要方面一直是新的合成方法的开发,包括碳热还原和氮化(CRN)方法的细化,以及使用Sialon前体的机械化学活化(Al和Si氮化物和氧化物或CRN混合物) 。在N_2在N_2中加热的CRN混合物的机械化学活化在1300℃(比在未在下基混合物中低于18℃),但也形成了21R多滴水和刚玉的β-唾液(Z = 2)。最近,我们的注意力侧重于偶尔热还原和氮化(SRN)来合成其他Sialons,包括AlN Polyrytypoids和Na和Liα-Sialons。从它们的预期物理性质(导热率和类似于ALN的良好电绝缘的热导电性和良好的电绝缘)的兴趣,它们的共价粘合和来自其高Al和N内容的相对重量的重量及其细长的晶体形态,这可能改善抗裂性具有α-Sialon的多晶硅复合材料。本文介绍了从粘土,Si和AlN的高纯度致密15R唾液子的SRN单步合成的发展,以及添加剂对产物合成和烧结的影响。还使用氟化物添加剂从粘土,Si和AlN的Na和Liα-Sialons的SRN合成的方法。氟化物具有体积小,电负负电,导致其已知的AlN合成的促进。此外,它们不容易进入唾液结构,但可以通过形成玻璃阶段来强化它。氟化物通过在没有额外氧的情况下引入M〜+,允许在该SRN合成中使用粘土,但具有产生SIF_4作为副产物的缺点。使用LiF的反应通过可能涉及SiF_4的形成辅助的机构,通过O-SiAlon中间体在1200℃的极低温度下进行。通过形成SiF_4,可以涉及Si迁移。机械化学激活(高能磨削)对SRN形成的影响也研究了Na和Li A-Sialons,O和β-Sialon的烧结。凝纹Srn O-Sialon前体促进粉末中的O-Sialon形成,但由于预反应烧结而不是颗粒,这是促进的粒径较小。研磨Na和Liα-Sialon Srn前体形成Sialons的混合物而不是靶单相产品,同时通过研磨其SrN前体来辅助所有Sialons的烧结。

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