摘要
Functionally gradient samples are prepared by getting metal Ni or Cu bonded with Ni-matrix composites reinforced by TiB2 particles by field activated diffusion bonding process. The intermetallic compound of Ni3Al has been applied as a mediate layer in order to reduce residual stress. The microstracture, phase composition of the interfaces between the metal and Ni3Al are determined and the mechanical properties of the gradient materials are characterized. Elemental concentration profiles across the interfaces between layers showed significant diffusion dissolution and formation of firm bonds. Measured micro-hardness values of the sample increased monotonically from the metal substrate to the surface layer of composites. The values for the surface composite layer ranged from about 2 000 HK to 3 300 HK. The results of this investigation demonstrate the feasibility of field activated diffusion bonding process for rapid preparation of FGMs.
Functionally gradient samples are prepared by getting metal Ni or Cu bonded with Ni-matrix composites reinforced by TiB2 particles by field activated diffusion bonding process. The intermetallic compound of Ni3Al has been applied as a mediate layer in order to reduce residual stress. The microstracture, phase composition of the interfaces between the metal and Ni3Al are determined and the mechanical properties of the gradient materials are characterized. Elemental concentration profiles across the interfaces between layers showed significant diffusion dissolution and formation of firm bonds. Measured micro-hardness values of the sample increased monotonically from the metal substrate to the surface layer of composites. The values for the surface composite layer ranged from about 2 000 HK to 3 300 HK. The results of this investigation demonstrate the feasibility of field activated diffusion bonding process for rapid preparation of FGMs.
基金
Acknowledgment The authors wish to thank the financial support for this research from the National Natural Science Foundation of China (Grant No. 50975190) and the Army Office of Research (ZAM).