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Breaking the Fe3O4-wrapped copper microstructure to enhance copper–slag separation

The precipitation of Fe 3 O 4 particles and the accompanied formation of Fe 3 O 4 -wrapped copper structure are the main obstacles to copper recovery from the molten slag during the pyrometallurgical smelting of copper concentrates. Herein, the commercial powdery pyrite or anthracite is replaced wit...

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Published in:International journal of minerals, metallurgy and materials metallurgy and materials, 2024-10, Vol.31 (10), p.2312-2325
Main Authors: Chi, Xiaopeng, Liu, Haoyu, Xia, Jun, Chen, Hang, Yu, Xiangtao, Weng, Wei, Zhong, Shuiping
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container_title International journal of minerals, metallurgy and materials
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Liu, Haoyu
Xia, Jun
Chen, Hang
Yu, Xiangtao
Weng, Wei
Zhong, Shuiping
description The precipitation of Fe 3 O 4 particles and the accompanied formation of Fe 3 O 4 -wrapped copper structure are the main obstacles to copper recovery from the molten slag during the pyrometallurgical smelting of copper concentrates. Herein, the commercial powdery pyrite or anthracite is replaced with pyrite–anthracite pellets as the reductants to remove a large amount of Fe 3 O 4 particles in the molten slag, resulting in a deep fracture in the Fe 3 O 4 -wrapped copper microstructure and the full exposure of the copper matte cores. When 1wt% composite pellet is used as the reductant, the copper matte droplets are enlarged greatly from 25 µm to a size observable by the naked eye, with the copper content being enriched remarkably from 1.2wt% to 4.5wt%. Density functional theory calculation results imply that the formation of the Fe 3 O 4 -wrapped copper structure is due to the preferential adhesion of Cu 2 S on the Fe 3 O 4 particles. X-ray photoelectron spectroscopy, Fourier transform infrared spectrometer (FTIR), and Raman spectroscopy results all reveal that the high-efficiency conversion of Fe 3 O 4 to FeO can decrease the volume fraction of the solid phase and promote the depolymerization of silicate network structure. As a consequence, the settling of copper matte droplets is enhanced due to the lowered slag viscosity, contributing to the high efficiency of copper–slag separation for copper recovery. The results provide new insights into the enhanced in-situ enrichment of copper from molten slag.
doi_str_mv 10.1007/s12613-024-2861-4
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Herein, the commercial powdery pyrite or anthracite is replaced with pyrite–anthracite pellets as the reductants to remove a large amount of Fe 3 O 4 particles in the molten slag, resulting in a deep fracture in the Fe 3 O 4 -wrapped copper microstructure and the full exposure of the copper matte cores. When 1wt% composite pellet is used as the reductant, the copper matte droplets are enlarged greatly from 25 µm to a size observable by the naked eye, with the copper content being enriched remarkably from 1.2wt% to 4.5wt%. Density functional theory calculation results imply that the formation of the Fe 3 O 4 -wrapped copper structure is due to the preferential adhesion of Cu 2 S on the Fe 3 O 4 particles. X-ray photoelectron spectroscopy, Fourier transform infrared spectrometer (FTIR), and Raman spectroscopy results all reveal that the high-efficiency conversion of Fe 3 O 4 to FeO can decrease the volume fraction of the solid phase and promote the depolymerization of silicate network structure. As a consequence, the settling of copper matte droplets is enhanced due to the lowered slag viscosity, contributing to the high efficiency of copper–slag separation for copper recovery. 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Herein, the commercial powdery pyrite or anthracite is replaced with pyrite–anthracite pellets as the reductants to remove a large amount of Fe 3 O 4 particles in the molten slag, resulting in a deep fracture in the Fe 3 O 4 -wrapped copper microstructure and the full exposure of the copper matte cores. When 1wt% composite pellet is used as the reductant, the copper matte droplets are enlarged greatly from 25 µm to a size observable by the naked eye, with the copper content being enriched remarkably from 1.2wt% to 4.5wt%. Density functional theory calculation results imply that the formation of the Fe 3 O 4 -wrapped copper structure is due to the preferential adhesion of Cu 2 S on the Fe 3 O 4 particles. X-ray photoelectron spectroscopy, Fourier transform infrared spectrometer (FTIR), and Raman spectroscopy results all reveal that the high-efficiency conversion of Fe 3 O 4 to FeO can decrease the volume fraction of the solid phase and promote the depolymerization of silicate network structure. As a consequence, the settling of copper matte droplets is enhanced due to the lowered slag viscosity, contributing to the high efficiency of copper–slag separation for copper recovery. The results provide new insights into the enhanced in-situ enrichment of copper from molten slag.</abstract><cop>Beijing</cop><pub>University of Science and Technology Beijing</pub><doi>10.1007/s12613-024-2861-4</doi><tpages>14</tpages></addata></record>
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subjects Anthracite
Ceramics
Characterization and Evaluation of Materials
Chemistry and Materials Science
Composites
Copper
Copper converters
Copper mattes
Copper sulfides
Corrosion and Coatings
Density functional theory
Depolymerization
Droplets
Fourier transforms
FTIR spectrometers
Glass
Infrared spectrometers
Infrared spectroscopy
Iron oxides
Materials Science
Metallic Materials
Microstructure
Natural Materials
Pellets
Photoelectrons
Pyrite
Raman spectroscopy
Recovery
Reducing agents
Research Article
Separation
Slag
Solid phases
Spectroscopy
Spectrum analysis
Surfaces and Interfaces
Thin Films
Tribology
X ray photoelectron spectroscopy
title Breaking the Fe3O4-wrapped copper microstructure to enhance copper–slag separation
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