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Reactive Sintering of NiAl-Al2O3 and NiAl-SiC Composites

机译:Nial-Al2O3和Nial-SiC复合材料的反应性烧结

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In this work we have recognized the possibilities to obtain "in-situ" near net-shape composites of NiAl-SiC and NiAl-Al_2O_3, by combustion synthesis technique, starting from mixtures of Nickel-Aluminum metallic powders and ceramic reinforcement of Al_2O_3 and SiC. These composites cannot be shaped due to their limited ductility and are difficult to cast due to their high melting point and reactivity. The reactive sintering is performed at temperatures of 890-910 K in tubular furnace under argon pressure. The compacts of the Ni-Al intermetallic compound and ceramic reinforcement (Al_2O_3 and SiC) have been obtained, below aluminum melting point, due to the large amount of exothermic heat liberated during the formation of NiAl compound. The most significant disadvantage of the intermetallic NiAl phase is the brittleness at room temperature; in this work we show that it is possible to obtain a reduction of the hardness values by grain refinement with the utilization of the reactive sintering in the powder-metallurgy technique as well as with the addition of a third alloying element, such as iron, to Aluminum and Nickel powders before the reactive process. The results of the composites NiAl-SiC are very interesting as well; these present a significant raising of the Vickers microhardness values of the intermetallic matrix (from 300 HV_(0,2) to 750 HV_(0,2)) compared to those measured in NiAl-Al_2O_3 composites, caused by the presence of Si and C in the NiAl phase.
机译:在这项工作中,我们已经认识到通过燃烧合成技术从镍 - 铝金属粉末和Al_2O_3和SiC的陶瓷增强的混合物开始获得Nial-SiC和Nial-Al_2O_3的“原位”近净形状复合材料。 。由于其有限的延展性,这些复合材料不能形,并且由于其高熔点和反应性而难以浇铸。在氩气下管状炉中的890-910k的温度下进行反应烧结。由于在形成Nial化合物期间释放的大量放热热,已经获得了Ni-Al金属间化合物和陶瓷增强(Al_2O_3和SiC)的块。金属间Nial阶段的最显着缺点是室温下的脆性;在这项工作中,我们表明,通过利用粉末冶金技术的反应性烧结以及添加第三合金元件(例如铁),可以通过晶粒细化获得硬度值的降低。反应过程前铝和镍粉。复合材料的结果也非常有趣;与在Nial-Al_2O_3复合材料中测量的那些相比,这些对金属间基质的维持量显微硬度值(从300 HV_(0.2)至750HV_(0,2))一起提出了显着提高,由Si和C的存在引起的在Nial阶段。

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