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Highly Efficient and Low-Temperature Preparation of Plate-Like ZrB₂-SiC Powders by a Molten-Salt and Microwave-Modified Boro/Carbothermal Reduction Method
To address the various shortcomings of a high material cost, energy-intensive temperature conditions and ultra-low efficiency of the conventional boro/carbothermal reduction method for the industrial preparation of ZrB₂-SiC powders, a novel molten-salt and microwave-modified boro/carbothermal reduct...
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Published in: | Materials 2018-09, Vol.11 (10), p.1811 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | To address the various shortcomings of a high material cost, energy-intensive temperature conditions and ultra-low efficiency of the conventional boro/carbothermal reduction method for the industrial preparation of ZrB₂-SiC powders, a novel molten-salt and microwave-modified boro/carbothermal reduction method (MSM-BCTR) was developed to synthesize ZrB₂-SiC powders. As a result, phase pure ZrB₂-SiC powders can be obtained by firing low-cost zircon (ZrSiO₄), amorphous carbon (C), and boron carbide (B₄C) at a reduced temperature of 1200 °C for only 20 min. Such processing conditions are remarkably milder than not only that required for conventional boro/carbothermal reduction method to prepare phase pure ZrB₂ or ZrB₂-SiC powders (firing temperature of above 1500 °C and dwelling time of at least several hours), but also that even with costly active metals (e.g., Mg and Al). More importantly, the as-obtained ZrB₂ particles had a single crystalline nature and well-defined plate-like morphology, which is believed to be favorable for enhancing the mechanical properties, especially toughness of their bulk counterpart. The achievement of a highly-efficient preparation of such high-quality ZrB₂-SiC powders at a reduced temperature should be mainly attributed to the specific molten-salt and microwave-modified boro/carbothermal reduction method. |
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ISSN: | 1996-1944 1996-1944 |
DOI: | 10.3390/ma11101811 |