journal article·2022-03

Diffusion bonding of Ti‐coated C f ‐SiC f /SiBCN composites to Nb using Ag–Pd interlayer

Jincheng Lin, Xunye Zhang, Wei Wang, Di Yu, Dechang Jia, Tiesong Lin, Panpan Lin, Peng He

Publisher page

Abstract

Abstract The Ti‐coated C f ‐SiC f /SiBCN ceramic was diffusion‐bonded to Nb using an Ag–Pd interlayer. At a ceramic/Ag–Pd interface, it is found that Ti first reacted with C and Pd to form a TiC x /Ti(Pd) double‐layer structure, and then Ti(Pd) completely converted into TiC x with the increase of holding time or temperature. Meanwhile, the infiltration of Pd along TiC x grain boundary reacted with Si to form brittle Pd 2 Si compound. By contrary, only a simple NbPd 3 layer was formed at the Nb/Ag–Pd interface during the whole process. A maximum shear strength of 16 ± 3 MPa is obtained for the joint prepared at 900°C for 30 min. The plastic deformation of the Ag–Pd interlayer and pullout of fibers inside ceramic contributed to the superior performance. Nevertheless, as the holding time and temperature reached 90 min and 950°C, the high chemical affinity of the Pd–Si system and enhanced atomic diffusion led to the massive formation of Pd 2 Si, which increased the joint brittleness and degraded the ceramic performance.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Advanced ceramic materials synthesis · Advanced materials and composites · Aluminum Alloys Composites Properties

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

Affiliations

State Key Laboratory of Advanced Welding and Joining Harbin Institute of Technology Harbin China

Institute for Advanced Ceramics School of Materials Science and Engineering Harbin Institute of Technology Harbin China

Funding

National Natural Science Foundation of China

References (23)

Show source-provided references
1. 10.1111/jace.1620210.1111/jace.16202 ↗
2. 10.1007/s40145-015-0128-210.1007/s40145-015-0128-2 ↗
3. 10.1016/j.corsci.2014.01.00610.1016/j.corsci.2014.01.006 ↗
4. 10.1016/j.ceramint.2015.03.14410.1016/j.ceramint.2015.03.144 ↗
5. 10.1179/174328009X46107810.1179/174328009X461078 ↗
6. 10.1016/j.ceramint.2019.10.00310.1016/j.ceramint.2019.10.003 ↗
7. 10.1016/j.scriptamat.2011.04.01510.1016/j.scriptamat.2011.04.015 ↗
8. 10.1016/j.matdes.2016.03.07210.1016/j.matdes.2016.03.072 ↗
9. 10.1007/s10853-018-3025-610.1007/s10853-018-3025-6 ↗
10. 10.1007/s11665-019-04420-510.1007/s11665-019-04420-5 ↗
11. 10.1016/j.jmst.2018.01.00110.1016/j.jmst.2018.01.001 ↗
12. 10.1016/j.jmst.2017.01.03210.1016/j.jmst.2017.01.032 ↗
13. 10.1016/j.vacuum.2018.07.01610.1016/j.vacuum.2018.07.016 ↗
14. 10.1016/j.jeurceramsoc.2012.07.00510.1016/j.jeurceramsoc.2012.07.005 ↗
15. 10.1179/1362171812Y.000000008310.1179/1362171812Y.0000000083 ↗
16. 10.1134/S003602442013017810.1134/S0036024420130178 ↗
17. 10.1016/j.ceramint.2013.11.00810.1016/j.ceramint.2013.11.008 ↗
18. 10.1016/j.jallcom.2013.04.03710.1016/j.jallcom.2013.04.037 ↗
19. 10.1007/s11663-999-0090-x10.1007/s11663-999-0090-x ↗
20. 10.1016/0022-5088(89)90178-110.1016/0022-5088(89)90178-1 ↗
21. 10.1016/0925-8388(93)90406-D10.1016/0925-8388(93)90406-D ↗
22. 10.1016/j.ssi.2008.07.02110.1016/j.ssi.2008.07.021 ↗
23. 10.1111/jace.1601810.1111/jace.16018 ↗