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Processing of Reaction-Bonded and Post-Sintered Silicon Nitride Micro Parts

机译:处理反应键合和烧结后氮化硅微零件

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Components for a micromechanical system comprising micro turbine and micro planetary gear were manufactured of silicon nitride. Owing to the near-net-shape capability and in view of mass production injection molding was applied as forming technology. In the field of Microsystems Technology very narrow tolerances of few μm are required; therefore it was the aim to reduce sintering shrinkage significantly as it is considered to be one of the main sources for size deviation. Reaction-bonded silicon nitride (RBSN) can be produced nearly without shrinkage, but it offers only poor mechanical strength because of high residual porosity. Post-densification by liquid phase sintering of RBSN is an appropriate way to improve the mechanical properties. Even though this is at the expense of increasing shrinkage - and thereby potential size deviation - the total amount of sintering shrinkage is clearly reduced when compared to conventional processing of silicon nitride powder. In the present work a paraffin based feedstock for low-pressure injection molding containing silicon powder and Y_2O_3/Al_2O_3 as sintering aid was applied. Nitridation of the debindered components was performed in N_2/5%H_2 atmosphere (0.15MPa) at a temperature of 1390°C. The reaction-bonding process is driven by a solid/gas phase reaction where nitrogen diffusion into the Si-powder compact limits the Si_3N_4 formation. It was found that for the micro samples already after 2-4 h dwell time 90% conversion of silicon to silicon nitride was obtained. Therefore this process is especially suited for the fabrication of micro components with inherently high surface-to-volume ratio and small wall thickness. After subsequent sintering in pure nitrogen samples could be densified to 97% of theoretical density. XRD measurements confirmed a complete conversion from - to β-Si_3N_4. The overall linear shrinkage from green body to sintered reaction bonded silicon nitride accumulates to 11%.
机译:对于包括微涡轮机和微行星齿轮的微机械系统组件制造的氮化硅构成。由于近净形状的能力,并鉴于大量生产注射成型的涂布作为形成技术。在微系统技术领域几μm的非常窄的公差是必需的;因此它是降低,因为它被认为是对尺寸偏差的主要来源之一显著烧结收缩的目的。反应烧结氮化硅(RBSN)可以制造几乎不收缩,但它提供了由于高的残余孔隙的唯一差的机械强度。后致密化通过RBSN的液相烧结是改善机械性能的适当方式。虽然这是在增加的收缩为代价 - 并由此潜在尺寸偏差 - 烧结收缩的总量相比,氮化硅粉末的常规处理时明显减少。在目前的工作石蜡基于用于低压注射成型含有硅粉末和Y_2O_3 / Al_2O_3的作为施加烧结助剂的原料。在1390℃的温度下在N_2 / 5%H_2气氛(为0.15MPa)进行脱粘结剂的成分的氮化。将反应粘结过程是通过一个固/气相反应从动其中氮扩散到Si粉末压块限制Si_3N_4形成。结果发现,对于微样品已经经过硅氮化硅的2〜4小时的停留时间的90%的转化率获得。因此,该方法特别适用于微组件具有固有的高表面积 - 体积比和壁厚小的制造。后纯氮样品中随后的烧结可致密化到理论密度的97%。 XRD测量证实完全转化为 - 至β-Si_3N_4。从坯体到烧结反应烧结氮化硅的整体的线性收缩率累积到11%。

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