Abstract
B-modified MoSi2 coatings were prepared on pure Mo through pack Si–B co-deposition process. The effects of pack mixture, co-deposition temperature and time on the formation of the Si–B co-deposition coating were studied by preparing the coatings in the pack mixtures 16Si–xB–4NaF–Bal.Al2O3 (wt.%, x=0.5–4) at 1100–1400°C for 2.5–10h. XRD, EDS, and WDS techniques were used to examine the microstructures of the coatings. Thermodynamics calculation about the equilibrium partial pressures of the volatile fluoride vapors in the pack aided experimental observation was introduced to reveal the coating formation mechanism. The results showed that the Si–B co-deposition coating had four layers: the MoSi2 outer layer with MoB precipitates distributed within its lower part, the Mo5Si3 second layer, the MoB third layer and the Mo2B inner layer. Pack mixture, co-deposition temperature and time made negligible effect on coating structure. The growth of the coating was dominated by the inward diffusion of Si and B. The deposited Si atoms mainly formed MoSi2 phase; the deposited B atoms either diffused into the substrate to form the MoB and Mo2B layers or generated MoB precipitates within the MoSi2 outer layer. The effects of B atoms within the Si–B co-deposition coating on coating oxidation manifested in two aspects: firstly, B atoms diffused to coating surface and oxidized to B2O3, which promoted the formation of a dense scale and reduced the coating weight loss; and secondly, the MoB layer acted as a barrier to the inward diffusion of Si, which slowed the degradation of MoSi2 to poor oxidation-resistant Mo5Si3 and would increase the coating lifetime.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
More From: International Journal of Refractory Metals and Hard Materials
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.