Influence of 1%Nb Solute Addition on the Thermal Stability of In Situ Consolidated Nanocrystalline Cu
Source abstract
Abstract
Nanocrystalline (nc) Cu and Cu–1% Nb bulk materials are synthesized using a combination of cryogenic and room temperature ball milling. The grain size values of these in situ consolidated Cu and Cu–1% Nb, determined using transmission electron microscopy, are found to be 22 nm and 18 nm, respectively. In this investigation, isochronal heat treatments are performed for 1 h to establish grain size and microstructural changes as a function of temperature. The annealing of nc Cu–1% Nb at a temperature of 1073 K reveals a slight increase in the average grain size from 18 to 45 nm. The grain size of nc Cu, however, increases from 22 nm to about 3 μm after annealing at the same conditions. The present results indicate that solute entrapment plays a major role in thermal stability of the high purity contaminant‐free Cu with the addition of only 1 at% Nb after annealing for 1 h up to a homologous temperature of 0.8. Kinetic stabilization via clustering of Nb atoms on the grain boundaries and the triple junctions is also observed after annealing at high temperature for longer times.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Microstructure and mechanical properties · Metallic Glasses and Amorphous Alloys · Aluminum Alloys Composites Properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials Science and Technology Qatar University Doha 2713 Qatar
Department of Materials Science and Engineering North Carolina State University Raleigh NC 27606‐7907 USA
Funding
Qatar National Research Fund
References (41)
Show source-provided references
1. 10.1557/S088376940005155110.1557/S0883769400051551 ↗
2. 10.1557/S088376940005154X10.1557/S088376940005154X ↗
3. 10.1016/j.msea.2017.11.06010.1016/j.msea.2017.11.060 ↗
4. 10.1063/1.203412210.1063/1.2034122 ↗
5. 10.1126/science.109290510.1126/science.1092905 ↗
6. 10.1016/S1359-6462(03)00397-X10.1016/S1359-6462(03)00397-X ↗
7. 10.1016/0965-9773(93)90088-S10.1016/0965-9773(93)90088-S ↗
8. Sutton A. P. · 1995 · 819
9. 10.1016/j.jcrysgro.2003.12.02110.1016/j.jcrysgro.2003.12.021 ↗
10. 10.1016/j.scriptamat.2008.04.04510.1016/j.scriptamat.2008.04.045 ↗
11. 10.1557/JMR.1998.016910.1557/JMR.1998.0169 ↗
12. 10.1557/JMR.2007.040310.1557/JMR.2007.0403 ↗
13. 10.1016/j.actamat.2006.03.02110.1016/j.actamat.2006.03.021 ↗
14. 10.1016/j.scriptamat.2012.04.01010.1016/j.scriptamat.2012.04.010 ↗
15. 10.1016/j.actamat.2016.12.05710.1016/j.actamat.2016.12.057 ↗
16. 10.1063/1.32457310.1063/1.324573 ↗
17. de Boer F. R. · 1989 · 758
18. 10.1016/S1003-6326(08)60264-210.1016/S1003-6326(08)60264-2 ↗
19. 10.1016/j.jallcom.2014.11.19310.1016/j.jallcom.2014.11.193 ↗
20. 10.1007/s11837-015-1644-910.1007/s11837-015-1644-9 ↗
21. 10.1016/j.msea.2012.01.10410.1016/j.msea.2012.01.104 ↗
22. 10.1016/j.scriptamat.2005.09.02810.1016/j.scriptamat.2005.09.028 ↗
23. 10.1063/1.203412210.1063/1.2034122 ↗
24. 10.1557/JMR.1999.056910.1557/JMR.1999.0569 ↗
25. 10.1016/S1359-6454(01)00338-X10.1016/S1359-6454(01)00338-X ↗
26. Krill C. E. · Z. Metallkd. Res. Adv. Tech · 2005 · 96 · 1134
27. Weissrmiller J. · J. Mater. Res · 1994 · 9 · 21
28. 10.1007/s10853-008-2870-010.1007/s10853-008-2870-0 ↗
29. 10.1103/PhysRevB.79.09411210.1103/PhysRevB.79.094112 ↗
30. 10.1016/j.actamat.2006.11.02810.1016/j.actamat.2006.11.028 ↗
31. 10.1007/BF0258609610.1007/BF02586096 ↗
32. 10.1016/S1359-6454(99)00079-810.1016/S1359-6454(99)00079-8 ↗
33. 10.1016/0956-716X(91)90144-P10.1016/0956-716X(91)90144-P ↗
34. 10.3139/146.01794110.3139/146.017941 ↗
35. 10.1016/0965-9773(94)90100-710.1016/0965-9773(94)90100-7 ↗
36. 10.1016/j.msea.2012.07.04510.1016/j.msea.2012.07.045 ↗
37. Abaza M. A. · 2017
38. Cullity B. D. · 2001 · 388
39. 10.1016/0956-716X(93)90436-V10.1016/0956-716X(93)90436-V ↗
40. 10.1016/j.actamat.2007.07.02610.1016/j.actamat.2007.07.026 ↗
41. 10.1016/j.scriptamat.2016.11.02510.1016/j.scriptamat.2016.11.025 ↗