journal article·2024-07Open access

Rapid synthesis of high‐yield Ti 3 AlC 2 MAX phase powders from TiC 0.67 and Al with induction heating assistance

Anna Gubarevich, Kenshin Miura, Katsumi Yoshida

Abstract

Abstract The development of new low‐carbon emission methods for the synthesis and processing of materials is an urgent task today. Here, we present a rapid, efficient, and low‐energy‐consuming synthesis method for high‐yield Ti 3 AlC 2 MAX phase powders. Our method is based on induction heating‐assisted combustion synthesis (IH‐CS), where the heat of the reaction is used as a driving force of the process, and the conditions of the process are finely controlled using IH at the same time. Ti 3 AlC 2 MAX phase was synthesized using TiC 0.67 and Al powders as starting materials. The introduction of TiC 0.67 reduced the total exothermic effect of the reaction, facilitating better control of the reaction process. IH was used to ignite the reaction and to hold the temperature after ignition at an optimal value to complete the synthesis process. The effects of holding temperature, Al, and Si addition on Ti 3 AlC 2 yield were investigated. As a result, Ti 3 AlC 2 MAX phase powders containing only .7 wt% of the secondary phase were synthesized in a very short time. Our findings suggest that IH‐CS is a highly effective and promising alternative for the facile fabrication of high‐purity MAX phase powders.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: MXene and MAX Phase Materials · Aluminum Alloys Composites Properties · Advanced ceramic materials synthesis

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Laboratory for Zero‐Carbon Energy Institute of Innovative Research Tokyo Institute of Technology Meguro‐ku Tokyo Japan

Graduate Major in Nuclear Engineering Department of Materials Science and Engineering School of Materials and Chemical Technology Tokyo Institute of Technology Meguro‐ku Tokyo Japan

References (23)

Show source-provided references
1. 10.1111/j.1151-2916.2000.tb01281.x10.1111/j.1151-2916.2000.tb01281.x ↗
2. 10.1016/S1005-0302(10)60064-310.1016/S1005-0302(10)60064-3 ↗
3. 10.1016/j.trechm.2019.02.01610.1016/j.trechm.2019.02.016 ↗
4. 10.1016/j.actamat.2020.03.00810.1016/j.actamat.2020.03.008 ↗
5. 10.1016/j.jeurceramsoc.2014.11.03410.1016/j.jeurceramsoc.2014.11.034 ↗
6. 10.1021/acs.jpcc.6b1024110.1021/acs.jpcc.6b10241 ↗
7. 10.1016/j.jeurceramsoc.2021.10.03010.1016/j.jeurceramsoc.2021.10.030 ↗
8. 10.1111/jace.1754410.1111/jace.17544 ↗
9. 10.1016/j.jallcom.2014.02.14910.1016/j.jallcom.2014.02.149 ↗
10. 10.1111/jace.1684610.1111/jace.16846 ↗
11. 10.1016/j.ceramint.2023.04.23610.1016/j.ceramint.2023.04.236 ↗
12. 10.1111/j.1551-2916.2007.01728.x10.1111/j.1551-2916.2007.01728.x ↗
13. 10.1016/j.ceramint.2017.09.20210.1016/j.ceramint.2017.09.202 ↗
14. 10.1007/BF0114472910.1007/BF01144729 ↗
15. 10.1007/BF0265391910.1007/BF02653919 ↗
16. 10.1016/j.scriptamat.2023.11573110.1016/j.scriptamat.2023.115731 ↗
17. 10.1016/j.matpr.2019.05.24410.1016/j.matpr.2019.05.244 ↗
18. 10.1007/BF0286872910.1007/BF02868729 ↗
19. 10.1007/s11661-004-0267-510.1007/s11661-004-0267-5 ↗
20. 10.1016/j.jallcom.2007.02.03810.1016/j.jallcom.2007.02.038 ↗
21. 10.1016/j.matdes.2019.10814310.1016/j.matdes.2019.108143 ↗
22. 10.1016/j.ceramint.2020.09.21810.1016/j.ceramint.2020.09.218 ↗
23. 10.1021/acsnano.0c0835710.1021/acsnano.0c08357 ↗