Abstract
Metallic Ti has a strong affinity for O at high temperatures, and methods for removing O directly from Ti are limited. Recently, the authors developed a new sintering process that removes O from Ti using Y metal as a deoxidizing agent in molten salt. However, Y contaminated the sintered Ti body. To address this problem, the authors developed a new Ti deoxidation process using a metal filter. In this process, a Ti green made of Ti powder and Y metal are introduced with molten salt into the respective sides of a room divided by a Ti filter. O removed from the Ti green passes through the Ti filter and reacts with the Y metal. Meanwhile, the small solubility and diffusion coefficient of Y in β-Ti are expected to kinetically prevent Y contamination of the sintered Ti body. It was experimentally demonstrated that a sintered Ti product with a low-O-concentration (< 250 mass ppm O) can be produced while suppressing Y contamination (< 120 mass ppm Y) in the new process. The establishment of this process enables low-cost production of highly functional Ti products and the recycling of Ti scraps in the future.
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Acknowledgments
The authors are grateful to Dr. Gen Kamimura, Mr. Kenta Akaishi, and Mr. Hiromu Hiramatsu at The University of Tokyo for their helpful suggestions and help with the experiments. This work was financially supported by the Japan Society for the Promotion of Science (JSPS) through a Grant-in-Aid for Scientific Research (S) (KAKENHI Grant Nos. 26220910, and 19H05623). This work is also based on results obtained from a project commissioned by the New Energy and Industrial Technology Development Organization (NEDO).
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The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
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Manuscript submitted June 29, 2021; accepted November 20, 2021.
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Iizuka, A., Ouchi, T. & Okabe, T.H. New Deoxidation Method of Titanium Using Metal Filter in Molten Salt. Metall Mater Trans B 53, 1371–1382 (2022). https://doi.org/10.1007/s11663-021-02400-6
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DOI: https://doi.org/10.1007/s11663-021-02400-6