期刊
CERAMICS INTERNATIONAL
卷 42, 期 8, 页码 9565-9570出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.ceramint.2016.03.037
关键词
Sintering; UHTCs; Zirconium diboride; Additive; SPS
资金
- Office of Naval Research Global (ONRG), USA [N62909-13-1-N055]
Zirconium diboride (ZrB2) was synthesized by a solution-based technique using zirconyl chloride (ZrOCl2 center dot 8H(2)O, ZOO), boric acid (H3BO3, BA) and gum karaya (GM) as the sources of zirconium, boron and carbon, respectively. The initial formation temperature of ZrB2 was 1200 degrees C and complete conversion was achieved by 1400 degrees C. Preceramic precursors and as-synthesized ZrB2 powders were characterized by XRD, TG-DTA, SEM, TEM, EDX and compared with commercial ZrB2 powder made by carbothermic reduction. FT-IR of as-synthesized dried preceramic precursor revealed the formation of Zr-O-C and Zr-O-B whereas SEM showed agglomerated spherical particles with mean diameter of < 1 mu m. Commercial ZrB2 and as-synthesized fine ZrB2 powder were spark plasma sintered (SPS) at 1900 degrees C for 10 min. Addition of 10 wt% of synthesized fine powder improved the fired density from 87% to 93% of theoretical. A significant cost benefit arises for the utilization of cheap synthesized fine powder as an additive for the densification of the more expensive commercial powder. (C) 2016 Elsevier Ltd and Techna Group S.r.l. All rights reserved.
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