从炼钢过程中产生的炉渣中分离出磁性部分

K. Foniok, V. Matějka, P. Maierová, P. Matějková, J. Vlček
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引用次数: 0

摘要

生铁和钢铁生产过程中产生的冶金渣是无机材料的宝贵来源。它们回收的限制通常与分离成分的昂贵方法有关。钢炉渣(FS)和钢包渣(LS)含有一定量的不同形式的铁,主要以氧化铁形式存在。本文报道了用干法和湿法分离分离FS和LS中磁性组分的结果。结果表明,干式磁选法不适合此目的,而湿式磁选法是有前途的。在本研究中,FS包含约。30 wt%的fe2o3和LS含有大约。将17wt %的fe2o3磨成小于0.1 mm的分数,然后对磁选分数进行干湿分离。结果表明,干燥分选是不合适的,因为100%的物料被回收,表明在磨矿过程中磁性部分均匀化强烈。另一方面,湿法分离对FS和LS的磁性组分的分离率分别为26%和30%。分离的磁性组分在FS和LS的情况下分别含有41%和40%的fe2o3。分离得到的馏分进行了化学和物相分析,并用扫描电镜研究了颗粒的形貌。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Separation of the magnetic fraction from the slags originated during steel production
Metallurgical slags originating during pig iron and steel manufacturing, are valuable sources of the inorganic materials. The limitation of their recycling is usually connected to the expensive methods of the separation of the components. The steel furnace slags (FS) as well as ladle slags (LS) contains reasonable amount of iron bonded in different forms, predominantly in iron oxides. In this paper we are reporting the results of the dry and wet separation techniques used for the isolation of the magnetic fraction presented in FS and LS. The results obtained indicate the dry magnetic separation as not suitable for this purpose, while wet method was found to be promising. In this research the FS containing approx. 30 wt% of Fe 2 O 3 and LS containing approx. 17 wt% of Fe 2 O 3 were milled to the fraction less than 0.1 mm and then subjected to the process of dry and wet separation of the magnetic fraction. It was observed that the dry separation is not suitable, since 100 % of the materials were recovered showing the intensive homogenization of the magnetic fraction during the milling process. On the other hand, the wet separation led to the isolation of 26 and 30 wt% of magnetic fractions for FS and LS, respectively. The isolated magnetic fractions contained 41 and 40 wt% of Fe 2 O 3 in the case of the FS and LS, respectively. The fractions obtained during the separation were subjected to the chemical and phase analysis, the morphology of the particles was studied using scanning electron microscopy.
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