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Mechanical properties and microstructure of in situ synthesized ZrB2-ZrN1-x composites

机译:原位合成ZrB2-ZrN1-x复合材料的力学性能和微观结构

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摘要

ZrB2-ZrN1-x composites were in situ synthesized from Zr and BN powders by hot-pressing at high temperatures. Thermodynamic calculation indicates that ZrN will be formed preferentially than ZrB2 in Zr-BN system. Three samples with Zr/BN molar ratios of 3:2, 3.5:2 and 2:1 were investigated at temperatures above 1650 degrees C. All mixtures of Zr and BN transformed to ZrB2-ZrN1-x composites completely without any other detectable phases. Nonstoichiometric zirconium nitride, ZrN1-x, is supposed to be formed in 3.5:2- and 2:1-samples. The microstructural morphology of well-sintered ZrB2-ZrN1-x composites is characterized by quadrate column-shaped ZrB2 distributed evenly in the interwoven acicular ZrN1-x matrix. A certain amount of hollow rectangular-shaped ZrB2 with open ends is found in 3.5:2-sample hot-pressed at 1700 degrees C, while some large spherical particles with lots of acicular ZrN1-x, sticked on its surface are observed in 2:1-sample hot-pressed at 1800 degrees C. Excessive Zr compared to the stoichiometric Zr/BN molar ratio of 3:2 will facilitate the densification process. Acicular ZrN1-x, is apparently beneficial to the improvement of bending strength and fracture toughness of ZrB2-ZrN1-x composites. (c) 2006 Springer Science + Business Media, Inc.
机译:ZrB2-ZrN1-x复合材料是由Zr和BN粉末通过高温热压原位合成的。热力学计算表明,在Zr-BN体系中,ZrN优先于ZrB2形成。在高于1650摄氏度的温度下研究了Zr / BN摩尔比为3:2、3.5:2和2:1的三个样品。Zr和BN的所有混合物完全转化为ZrB2-ZrN1-x复合材料,没有任何其他可检测相。非化学计量的氮化锆ZrN1-x可能以3.5:2-和2:1的样品形成。烧结良好的ZrB2-ZrN1-x复合材料的微观结构形态为方形柱状ZrB2均匀分布在交织的针状ZrN1-x基质中。在1:700摄氏度下热压的3.5:2样品中发现了一定数量的中空矩形ZrB2,在2:2中观察到一些表面上粘附有许多针状ZrN1-x的大球形颗粒: 1-样品在1800摄氏度下热压。与化学计量的Zr / BN摩尔比为3:2相比,过量的Zr会促进致密化过程。针状ZrN1-x显然有利于提高ZrB2-ZrN1-x复合材料的弯曲强度和断裂韧性。 (c)2006年Springer Science + Business Media,Inc.

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