首页 | 本学科首页   官方微博 | 高级检索  
     

高硫精矿配比对烧结矿性能的影响
引用本文:王桂林,张建良,刘征建,王耀祖,刘福成,佟振.高硫精矿配比对烧结矿性能的影响[J].钢铁,2022,57(2):19-27.
作者姓名:王桂林  张建良  刘征建  王耀祖  刘福成  佟振
作者单位:1.北京科技大学冶金与生态工程学院, 北京 100083;
2.北京科技大学人工智能研究院, 北京 100083;
3.凌源钢铁股份有限公司科技质量部, 辽宁 凌源 122500
基金项目:中央高校基本科研业务费资助项目(06500170);广东省基础与应用基础研究联合区域基金-青年基金资助项目(2020A1515111008)。
摘    要: 相比进口富矿粉,精矿品位较高,可广泛应用于铁矿石烧结工序。为了探究高硫精矿对烧结矿产质量的影响以及精矿中硫元素对烧结过程的影响,利用烧结杯试验装置进行了高硫精矿配比在25%~45%范围内的烧结杯试验。并通过微观结构、技术指标及冶金性能等方面表征了高硫精矿配比对烧结矿性能的影响。试验结果表明,精矿配比为25%时,烧结矿还原的界面反应条件较差,硅酸盐相阻碍了还原气体的扩散,致使烧结矿还原度为77.80%,软化开始温度为1 200 ℃,软熔带透气性能恶化。精矿配比为30%时,烧结利用系数提升至1.19 t/(m2·h)、垂直烧结速度达到22.22 mm/min。精矿配比为40%时,有效改善了烧结矿还原性能,恶化了低温还原粉化性能。精矿配比为45%时,烧结利用系数最高,为1.20 t/(m2·h),还原性能和低温还原粉化性能适宜。整体而言,在试验范围内,适当增加高硫精矿配比有利于提升烧结矿的还原性能和荷重软化熔滴性能,但精矿配比为45%时烧结矿的熔滴S特性值为281.02 kPa·℃,透气性能恶化。烧结烟气方面,精矿配比为40%时,烧结烟气的CO2和NOx含量较高,烧结过程氧化性气氛较强,降低了烧结矿中铁橄榄石等低还原性矿物含量,恶化了低温还原性能。烟气分析结果表明,高硫精矿烧结时硫元素基本都进入烧结烟气中,并未恶化烧结矿性能。

关 键 词:高硫精矿  烧结指标  微观结构  冶金性能  烧结烟气  
收稿时间:2021-07-19

Effect of high-sulfur concentrate on properties of sinter
WANG Gui-lin,ZHANG Jian-liang,LIU Zheng-jian,WANG Yao-zu,LIU Fu-cheng,TONG Zhen.Effect of high-sulfur concentrate on properties of sinter[J].Iron & Steel,2022,57(2):19-27.
Authors:WANG Gui-lin  ZHANG Jian-liang  LIU Zheng-jian  WANG Yao-zu  LIU Fu-cheng  TONG Zhen
Affiliation:1. School of Metallurgical and Ecological Engineering, University of Science and Technology Beijing, Beijing 100083, China;2. Institute of Artificial Intelligence, University of Science and Technology Beijing, Beijing 100083, China;3. Technical Quality Control Department, Lingyuan Iron and Steel Co., Ltd., Lingyuan 122500, Liaoning, China
Abstract:Concentrate is widely used in iron ore sintering process because its higher grade than that of imported ore-rich powder. However, there are few studies about the effect of high-sulfur concentrate on properties of sinter. Therefore, in order to study the effects of high-sulfur concentrate on the properties of sinter and influence of S element in concentrate on sintering process, a series of sinter cup experiments with high-sulfur concentrate concentration of 25%-45% were carried out, and the influences were characterized through microstructure, sintering indices, and metallurgical properties. The experimental results showed that when the concentration of concentrates was 25%, the interface reaction conditions of reduction were poor, and the diffusion of reduction gas were hindered by silicate phase. This resulted in a lower reduction index with 77.80%, the initial softening temperature was 1 200 ℃, and the permeability of cohesive zone deteriorated. The concentrates with 30% increased the sintering utilization index to 1.19 t/(m2·h), and improved vertical sintering speed to 22.22 mm/min. The sinter with high-sulfur concentrate concentration of 40% had improved reduction property and deteriorated the low temperature reduction degradation property. When the concentration was 45%, the sintering utilization index was the highest with 1.20 t/(m2·h), the reduction performance and reduction degradation property were suitable. On the whole, an appropriate increase in high-sulfur concentrate content was beneficial to improve the reduction performance and softening-melting performance of the sinter, but when the concentrate ratio was 45%, the S-value was 281.02 kPa·℃, meaning poor permeability performance of sinter. In the terms of sintering flue gas, when concentration of concentrates was 40%, the CO2 and NOx content of sintering flue gas were high, showing a high oxidizing atmosphere in the sintering process, which decreased the content of low-reducibility minerals such as iron olivine in the sinter and deteriorated the reduction degradation index. The results of flue gas analysis showed that the S element of high-sulfur concentrate basically entered sintering flue gas during sintering process, and the performance of sinter was not deteriorated.
Keywords:high-sulfur concentrate  sinter index  microstructure  metallurgical properties  sintering flue gas
本文献已被 维普 万方数据 等数据库收录!
点击此处可从《钢铁》浏览原始摘要信息
点击此处可从《钢铁》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号