首页|钼精矿焙烧过程中杂质化合物对烧结行为的影响

钼精矿焙烧过程中杂质化合物对烧结行为的影响

Effect of impurity compounds on sintering behavior of molybdenum concentrate during roasting process

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在钼精矿焙烧过程中,伴生元素转化及其与二硫化钼的相互作用会引起粉体部分熔化、结块、团聚等烧结现象,严重影响钼焙砂质量和炉子寿命.本文研究了钼精矿焙烧时赋存的杂质(种类和含量)以及焙烧温度对其烧结行为的影响,对其烧结程度进行定量化计算,并观察烧结物中各成分黏结形态的微观形貌.结果表明:钼精矿中SiO2和Al2O3对钼精矿焙烧烧结行为影响很小,而CaO、MgO、Fe2O3、CuO和K2CO3会强化烧结行为;增大反应温度达到MoO3与钼酸盐共晶的临界温度后会加剧团聚现象;增大CaO、CuO和K2CO3含量,对钼精矿烧结行为影响最大.烧结物中各组分之间的黏结形态分为三类,即加SiO2或Al2O3后呈孤立型,加CaO或MgO后呈交叉型,以及加Fe2O3、CuO或K2CO3后呈包裹型.
During the roasting process of molybdenum concentrate,the sintering phenomena such as partial melting,lumping and agglomeration of powder caused by the transformation of accessory elements and their interaction with molybdenum disulfide greatly affect the quality of molybdenum calcine and furnace life.This article studied the effects of impurities(types and contents)and roasting temperature during the roasting of molybdenum concentrate on the sintering behavior.The sintering degree was quantitatively calculated,and the microscopic morphology of the bonding forms of each component in the sintered material was observed.The results show that SiO2 and Al2O3 in molybdenum concentrate have little effect on the roasting and sintering behavior of molybdenum concentrate,while CaO,MgO,Fe2O3,CuO,and K2CO3 in molybdenum concentrate strengthen the sintering behavior;the agglomeration phenomenon will be intensified when the reaction temperature reaches the critical temperature of MoO3 and molybdate eutectic;increasing the content of CaO,CuO and K2CO3 has the greatest influence on the sintering behavior of molybdenum concentrate.The bonding forms between each component in the sintered material can be divided into three types,that is,isolated after adding SiO2 or Al2O3,crossover after adding CaO or MgO,and coated after adding Fe2O3,CuO or K2CO3.

molybdenum concentratethermodynamicsroastingimpuritysintering

李小明、翟钰华、邹冲、王伟安、李彬

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西安建筑科技大学 冶金工程学院,西安 710055

钼精矿 热力学 焙烧 杂质 烧结

国家自然科学基金

U22A20175

2024

中国有色金属学报
中国有色金属学会

中国有色金属学报

CSTPCD北大核心
影响因子:1.108
ISSN:1004-0609
年,卷(期):2024.34(2)
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