Synthesis of Al2O3-SiC powder from electroceramics waste and its application in low-carbon MgO-C refractories

被引:40
作者
Ma, Beiyue [1 ]
Ren, Xinming [1 ]
Gao, Zhi [1 ]
Tian, Jialong [1 ]
Jiang, Zhouhua [1 ]
Zan, Wenyu [1 ]
Yu, Jingkun [1 ,2 ]
Qian, Fan [3 ]
Cao, Yingnan [3 ]
Fu, Gaofeng [1 ]
机构
[1] Northeastern Univ, Sch Met, Shenyang 110819, Peoples R China
[2] Northeastern Univ, State Key Lab Rolling & Automat, Shenyang, Peoples R China
[3] Sinosteel Luoyang Inst Refractories Res Co Ltd, State Key Lab Adv Refractories, Luoyang 471039, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
Al2O3-SiC powder; electroceramics waste; low-carbon MgO-C refractories; oxidation resistance; slag resistance; CORROSION-RESISTANCE; COMPOSITE; PERFORMANCE; GRAPHITE;
D O I
10.1111/ijac.13934
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Composite additives are an efficient means to improve the high-temperature stability and slag resistance of low-carbon MgO-C refractories. In this work, Al2O3-SiC powder was firstly synthesized from electroceramics waste by carbon embedded method at 1500 degrees C, 1550 degrees C, and 1600 degrees C for 4 h, and then the as-synthesized Al2O3-SiC powder was used as an additive to low-carbon MgO-C refractories. The effects of its addition amounts of 0, 2.5 wt.%, 5.0 wt.%, and 7.5 wt.% on the properties of the refractories were investigated in detail. It was found that increasing the heat treatment temperature is beneficial to the phase conversion of mullite and quartz to alumina and silicon carbide in the electroceramics waste. Furthermore, the addition of Al2O3-SiC powder effectively improves the performance of low-carbon MgO-C samples, and the formation of spinel dense layer and high-viscosity isolation layer is the internal reason for the improvement of the oxidation resistance and slag resistance of low-carbon MgO-C samples. This work provides ideas for the reuse of electroceramics waste and presents an alternative strategy for the performance optimization of low-carbon MgO-C refractories.
引用
收藏
页码:1265 / 1273
页数:9
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