Densification of ZrB2–SiC nanocomposites prepared using ZrSi2, B4C, and C additives
Source abstract
Abstract
Dense ZrB2–SiC nanocomposites were fabricated at 1450 °C by the high-energy ball milling (HEBM) of ZrB2powder with ZrSi2–B4C–C additives and reactive spark plasma sintering (R-SPS). The sizes of ZrB2and SiC grains were 80–350 nm, and the phases were homogeneously distributed because of the molecular-level homogeneity of the constituents in ZrSi2and the homogeneous mixing of the raw powders by HEBM. The deformation of ZrSi2or the reactions between the additives during R-SPS did not strongly promote the densification. Fine and homogeneously distributed ZrB2and SiC particles formed by HEBM and R-SPS were the major reasons for the low temperature densification. The fine particles which had high surface energy provided the driving force for densification at low temperatures. Also, the fine SiC grains suppressed the growth of ZrB2grains during densification. The 4-point bending strength of the composites sintered at 1500 °C was 354 MPa.
Source: expertdata · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Advanced ceramic materials synthesis · Aluminum Alloys Composites Properties · MXene and MAX Phase Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (28)
Show source-provided references
1. 10.1016/j.jeurceramsoc.2010.01.02810.1016/j.jeurceramsoc.2010.01.028 ↗
2. 2008 · 4-15
3. 10.1016/j.jeurceramsoc.2010.03.02210.1016/j.jeurceramsoc.2010.03.022 ↗
4. 10.1111/j.1744-7402.2010.02594.x10.1111/j.1744-7402.2010.02594.x ↗
5. 10.1016/j.jeurceramsoc.2015.09.02410.1016/j.jeurceramsoc.2015.09.024 ↗
6. 10.2109/jcersj2.121.48010.2109/jcersj2.121.480 ↗
7. 10.1016/j.jeurceramsoc.2014.05.02010.1016/j.jeurceramsoc.2014.05.020 ↗
8. 10.1111/j.1551-2916.2011.04873.x10.1111/j.1551-2916.2011.04873.x ↗
9. 10.1016/j.jeurceramsoc.2006.11.07410.1016/j.jeurceramsoc.2006.11.074 ↗
10. 10.1111/j.1551-2916.2010.04051.x10.1111/j.1551-2916.2010.04051.x ↗
11. J. Am. Ceram. Soc. · 2000 · 83 · 233010.1111/j.1151-2916.2000.tb01558.x ↗
12. 10.1016/j.ceramint.2013.02.02810.1016/j.ceramint.2013.02.028 ↗
13. 10.1002/adem.20100001210.1002/adem.201000012 ↗
14. 10.1016/j.scriptamat.2007.04.02510.1016/j.scriptamat.2007.04.025 ↗
15. 10.1016/j.scriptamat.2011.12.03610.1016/j.scriptamat.2011.12.036 ↗
16. 10.1111/j.1551-2916.2010.04317.x10.1111/j.1551-2916.2010.04317.x ↗
17. 10.1016/j.jeurceramsoc.2013.05.00310.1016/j.jeurceramsoc.2013.05.003 ↗
18. 10.1016/j.ceramint.2013.09.03110.1016/j.ceramint.2013.09.031 ↗
19. 10.1016/j.scriptamat.2010.06.00510.1016/j.scriptamat.2010.06.005 ↗
20. 2005 · 45
21. 1996 · 73
22. 2001 · 956
23. Phys. Rev. · 1969 · 179 · 609
24. 2014 · 309
25. 10.1016/S1359-6462(03)00022-810.1016/S1359-6462(03)00022-8 ↗
26. Am. Ceram. Soc. Bull. · 1973 · 52 · 170
27. 10.1016/j.ceramint.2012.11.00110.1016/j.ceramint.2012.11.001 ↗
28. 10.1111/jace.1226710.1111/jace.12267 ↗