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Influence of Aging Temperatures on Precipitation Behaviors of SiC/Al-Zn-Mg-Cu Composites |
ZHANG Ran1,2,3, ZHU Shize1(), LIU Zhenyu1, KE Yubin3,4(), WANG Dong1, XIAO Bolv1, MA Zongyi1 |
1 Shi -changxu Innovation Center for Advanced Materials, Institute of Metal Research, Chinese Academy of Sciences, Shenyang 110016, China 2 School of Materials Science and Engineering, University of Science and Technology of China, Shenyang 110016, China 3 Spallation Neutron Source Science Center, Dongguan 523803, China 4 Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049, China |
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Cite this article:
ZHANG Ran, ZHU Shize, LIU Zhenyu, KE Yubin, WANG Dong, XIAO Bolv, MA Zongyi. Influence of Aging Temperatures on Precipitation Behaviors of SiC/Al-Zn-Mg-Cu Composites. Acta Metall Sin, 2024, 60(8): 1043-1054.
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Abstract A comprehensive understanding of how the addition of SiC particles influences the precipitation-strengthening behaviors of SiC/Al-Zn-Mg-Cu composites is essential for the advancement of high-performance aluminum matrix composites. However, the intrinsic mechanisms have remained unclear for a long time owing to limited characterization methods. Herein, the effect of aging temperatures (100 and 160oC) on the precipitation behaviors and strengthening mechanisms of SiC/Al-7.5Zn-1.8Mg-1.7Cu (mass fraction, %) composites containing 15%SiC (volume fraction) was investigated using in situ small angle neutron scattering, transmission electron microscopy, and tensile testing. A comparison was also made with the Al-7.5Zn-1.8Mg-1.7Cu alloy. As the aging time extended from 0.5 h to 3 h at 100oC, the precipitates in the composites evolved from GPI zones to GPI zones + GPII zones, accompanied by a noticeable increase in size. However, the increase in the volume fraction of precipitates was not substantial owing to slow aging kinetics. This increase in both the size and volume fraction of precipitates can enhance the resistance to dislocation cutting through precipitates, thereby improving the precipitation-strengthening capacity of the composites. Aging kinetics accelerated at 160oC, leading to an increase in both the size and volume fraction of precipitates in the composites with extended aging time. The types of precipitates transitioned from GPII zones + η' phase at 0.5 h to η' phase + η phase at 3 h. Nevertheless, the primary precipitation-strengthening mechanism at this temperature was dislocation bypassing strengthening. Although the expanding volume fraction of precipitates increased the yield strength of the composites, the coarsening of precipitates and the appearance of equilibrium η phase with inferior strengthening capacity imposed limitations on the yield strength increment. Compared with the Al-7.5Zn-1.8Mg-1.7Cu alloy, the composites exhibited low yield strength after aging at 100 and 160oC for 3 h, albeit with differing mechanisms. During aging at 100oC, the type and size of precipitates in both materials were roughly the same, but the composites had a lower volume fraction of precipitates owing to Mg consumption caused by SiC/Al interface reactions, thus weakening the precipitation-strengthening capacity. Conversely, during aging at 160oC, accelerated aging kinetics compensated for the reduction in precipitates volume fraction caused by Mg consumption. However, a low vacancy concentration led to precipitate coarsening and an increased proportion of equilibrium η phase, further weakening the precipitation-strengthening capacity of the composites.
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Received: 29 February 2024
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Fund: National Key Research and Development Program of China(2021YFA1600700);National Natural Science Foundation of China(521932594);National Natural Science Foundation of China(51931009);National Natural Science Foundation of China(U22A20114);CSNS Consortium on High-performance Materials of Chinese Academy of Sciences(JZHKYPT-2021-01);China Postdoctoral Science Foundation(2023M733573);Youth Innovation Promotion Association CAS(2020197) |
Corresponding Authors:
ZHU Shize, Tel: 13998134700, E-mail: szzhu16s@imr.ac.cnKE Yubin, professor, Tel: 15989637569, E-mail: keyb@ihep.ac.cn
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