2015
DOI: 10.1016/j.ceramint.2015.06.068
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Novel synthesis of ZrB2 powder by low temperature direct molten salt reaction

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Cited by 14 publications
(3 citation statements)
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“…Moreover, according to Table , the temperature for MSM‐BCTR synthesis of ZrB 2 was only 1200°C, which was almost the lowest among that reported for preparation of ZrB 2 or ZrB 2 –SiC powders by the methodologies based on thermal‐reduction . It was worth noting that, the demanding soaking time of 20 minutes was evidently shorter than not only that (several hours or more) required for conventional BCTR, but also that required even with costly active metals (eg, Mg and Al) or boron as the additional reducing agents. More importantly, the as‐obtained ZrB 2 –SiC powders had well‐defined single‐crystalline anisotropic morphologies as well as the resulting great potential in enhancing the mechanical properties of their bulk counterparts, which was rarely reported for the powder product of thermal‐reduction‐based methodologies.…”
Section: Resultsmentioning
confidence: 95%
“…Moreover, according to Table , the temperature for MSM‐BCTR synthesis of ZrB 2 was only 1200°C, which was almost the lowest among that reported for preparation of ZrB 2 or ZrB 2 –SiC powders by the methodologies based on thermal‐reduction . It was worth noting that, the demanding soaking time of 20 minutes was evidently shorter than not only that (several hours or more) required for conventional BCTR, but also that required even with costly active metals (eg, Mg and Al) or boron as the additional reducing agents. More importantly, the as‐obtained ZrB 2 –SiC powders had well‐defined single‐crystalline anisotropic morphologies as well as the resulting great potential in enhancing the mechanical properties of their bulk counterparts, which was rarely reported for the powder product of thermal‐reduction‐based methodologies.…”
Section: Resultsmentioning
confidence: 95%
“…It should be emphasized that the preparation conditions (1200 °C/20 min) for phase pure ZrB 2 -SiC powders was almost the lowest according to Table 2, among that reported for synthesizing ZrB 2 or ZrB 2 -SiC by the methodologies based on thermal-reduction process [5,14,15,27,28,29,30,31,32,33,34,35,36,37,38], not only remarkably milder than that (several hours or more) required for conventional BCTR to prepare phase pure ZrB 2 or ZrB 2 -SiC powders, but also that even with costly active metals (e.g., Mg and Al) [30,39] or boron [29,31,35] as the additional reducing agent. Such great enhancement to the synthetic result of ZrB 2 -SiC powders should be attributed to the combined effects of microwave heating and molten-salt medium.…”
Section: Resultsmentioning
confidence: 99%
“…Several techniques have been established for ZrB 2 powder preparation . Solid‐state synthesis such as the self‐propagating high temperature (SHS) technique always produces ZrB 2 in the form of aggregates, which requires being ground by ball milling and attrition milling into the required size.…”
Section: Introductionmentioning
confidence: 99%