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采用 X 射线衍射(XRD),扫描电镜(SEM)及能谱(EDAX)等方法,研究了 Cr5.0 Co8.0 Mo0.9 W5.5 Ta7.4 Al6.0 Re4.2合金在900和1000℃的氧化行为.结果表明,氧化动力学曲线遵循氧化初期氧化增重速率较快,氧化期间氧化动力学曲线呈波浪式变化,且呈现氧化温度越高波浪式越明显的特征.在900℃氧化300 h 后合金表面氧化物膜分为3层,外层为 NiO、Ni2 Cr2 O 4、Ni2 CoO 4和 CrTaO 4;中间层为平直的Al2 O 3层,内氧化层为Al2 O 3,氧化期间,分布在外层的 CrTaO 4抑制基体中 Al 向外扩散,并抑制氧化膜的生长,使氧化速度降低.1000℃时合金表面的氧化物膜分为2层,外层为 NiO、Ni2 Cr2 O 4、Ni2 CoO 4和CrTaO 4;内氧化层为 Al2 O 3.在900和1000℃氧化期间,合金均发生元素 Al 的内氧化和内氮化,与外氧化膜相邻的区域为元素 Al 的内氧化区,远离外氧化膜的基体内部形成元素 Al 的内氮化区,随氧化温度升高,内氧化区和内氮化区的深度增加,内氧化物和内氮化物的尺寸增大.

The oxidation behaviour of Cr5.0 Co8.0 Mo0.9 W5.5 Ta7.4 Al6.0 Re4.2 superalloy at 900 and 1 000 ℃in air has been investigated by means of measuring the kinetics curves of the oxidation and analysis method of TGA,XRD and SEM/EDAX.Results show that the oxidation initial oxidation rate is rapid,with the oxidation time,the increasing of oxidation weight overall tends to be smooth,but the oxidation kinetics curve for superal-loy later has a wavy change and obviously for the higher oxidation temperature.The oxidation film are consist of three layers at 900 ℃.The outer layer is mainly composed of NiO,Ni2 Cr2 O 4 ,Ni2 CoO 4 ,CrTaO 4 and continuous middle layer and disconnected inner layer of Al2 O 3 .The phase CrTaO 4 decreases the diffusion rate of Al.As a result,a continuous oxide layer of Al2 O 3 is formed in the middle layer to restrain the growth of oxide film and decrease the oxidation rate.The oxidation film are consist of two layers at 1 000 ℃.The outer layer is mainly composed of NiO,Ni2 Cr2 O 4 ,Ni2 CoO 4 ,CrTaO 4 ,and disconnected inner layer of Al2 O 3 .The internal oxide (Al2 O 3 )and internal nitride(AlN)precipitates formed inside the superalloy after exposure for 300h during oxi-dation at 900 ℃ and 1 000 ℃;the internal oxidation zone forms on the near-surface area of the superalloy,in-ternal nitridation zone forms below the internal oxidation zone inside the superalloy;with the increasing of tem-perature the internal oxidation zone and internal nitridation zone are wider,simultaneity the size of internal ni-tride and internal oxide increase.

参考文献

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