Comparative study on the passivation layers of copper sulphide minerals during bioleaching
The bioleaching of copper sulphide minerals was investigated by using A. ferrooxidans ATF6. The result shows the preferential order of the minerals bioleaching as djurleite〉bomite〉pyritic chalcopyrite〉covellite〉porphyry chalcopyfite. The residues were characterized by X-ray diffraction (XRD) and sca...
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Published in | International journal of minerals, metallurgy and materials Vol. 19; no. 10; pp. 886 - 892 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Springer Berlin Heidelberg
University of Science and Technology Beijing
01.10.2012
Springer Nature B.V School of Civil and Environmental Engineering, University of Science and Technology Beijing, Beijing 100083, China Key Laboratory of Solid Waste Treatment and Resource Recycle(Ministry of Education), Southwest University of Science and Technology, Mianyang 621010, China%School of Civil and Environmental Engineering, University of Science and Technology Beijing, Beijing 100083, China |
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Online Access | Get full text |
ISSN | 1674-4799 1869-103X |
DOI | 10.1007/s12613-012-0643-x |
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Abstract | The bioleaching of copper sulphide minerals was investigated by using A. ferrooxidans ATF6. The result shows the preferential order of the minerals bioleaching as djurleite〉bomite〉pyritic chalcopyrite〉covellite〉porphyry chalcopyfite. The residues were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). It is indicated that jarosite may not be responsible for hindered disso- lution. The elemental sulfur layer on the surface of pyritic chalcopyrite residues is cracked. The compact surface layer of porphyry chalcopy- rite may strongly hinder copper extraction. X-ray photoelectron spectroscopy (XPS) further confirms that the passivation layers of covellite, pyritic chalcopyrite, and porphyry chalcopyrite are copper-depleted sulphide Cu4S11, S8, and copper-rich iron-deficient polysulphide CtuFe2S9, resoectivelv. The ability of these oassivation layers was found as Cu4Fe2S9〉Cu4S11〉S8〉iarosite. |
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AbstractList | The bioleaching of copper sulphide minerals was investigated by using A. ferrooxidans ATF6. The result shows the preferential order of the minerals bioleaching as djurleite〉bomite〉pyritic chalcopyrite〉covellite〉porphyry chalcopyfite. The residues were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). It is indicated that jarosite may not be responsible for hindered disso- lution. The elemental sulfur layer on the surface of pyritic chalcopyrite residues is cracked. The compact surface layer of porphyry chalcopy- rite may strongly hinder copper extraction. X-ray photoelectron spectroscopy (XPS) further confirms that the passivation layers of covellite, pyritic chalcopyrite, and porphyry chalcopyrite are copper-depleted sulphide Cu4S11, S8, and copper-rich iron-deficient polysulphide CtuFe2S9, resoectivelv. The ability of these oassivation layers was found as Cu4Fe2S9〉Cu4S11〉S8〉iarosite. The bioleaching of copper sulphide minerals was investigated by using A. ferrooxidans ATF6. The result shows the preferential order of the minerals bioleaching as djurleite>bornite>pyritic chalcopyrite>covellite>porphyry chalcopyrite. The residues were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). It is indicated that jarosite may not be responsible for hindered dissolution. The elemental sulfur layer on the surface of pyritic chalcopyrite residues is cracked. The compact surface layer of porphyry chalcopyrite may strongly hinder copper extraction. X-ray photoelectron spectroscopy (XPS) further confirms that the passivation layers of covellite, pyritic chalcopyrite, and porphyry chalcopyrite are copper-depleted sulphide Cu4S11, S8, and copper-rich iron-deficient polysulphide Cu4Fe2S9, respectively. The ability of these passivation layers was found as Cu4Fe2S9>Cu4S11>S8>jarosite. The bioleaching of copper sulphide minerals was investigated by using A. ferrooxidans ATF6. The result shows the preferential order of the minerals bioleaching as djurleite>bornite>pyritic chalcopyrite>covellite>porphyry chalcopyrite. The residues were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). It is indicated that jarosite may not be responsible for hindered dissolution. The elemental sulfur layer on the surface of pyritic chalcopyrite residues is cracked. The compact surface layer of porphyry chalcopyrite may strongly hinder copper extraction. X-ray photoelectron spectroscopy (XPS) further confirms that the passivation layers of covellite, pyritic chalcopyrite, and porphyry chalcopyrite are copper-depleted sulphide Cu(4)Sn(11), S8, and copper-rich iron-deficient polysulphide Cu(4)Fe(2)S(9), respectively. The ability of these passivation layers was found as Cu(4)Fe(2)S(9)>Cu(4)S(11)>Sg>jarosite. The bioleaching of copper sulphide minerals was investigated by using A. ferrooxidans ATF6. The result shows the preferential order of the minerals bioleaching as djurleite>bornite>pyritic chalcopyrite>covellite>porphyry chalcopyrite. The residues were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). It is indicated that jarosite may not be responsible for hindered dissolution. The elemental sulfur layer on the surface of pyritic chalcopyrite residues is cracked. The compact surface layer of porphyry chalcopyrite may strongly hinder copper extraction. X-ray photoelectron spectroscopy (XPS) further confirms that the passivation layers of covellite, pyritic chalcopyrite, and porphyry chalcopyrite are copper-depleted sulphide Cu 4 S 11 , S8, and copper-rich iron-deficient polysulphide Cu 4 Fe 2 S 9 , respectively. The ability of these passivation layers was found as Cu 4 Fe 2 S 9 >Cu 4 S 11 >S 8 >jarosite. |
Author | Kai-bin Fu Hai Lin Xiao-lan Mo Han Wang Hong-wei Wen Zi-long Wen |
AuthorAffiliation | School of Civil and Environmental Engineering, University of Science and Technology Beijing, Beijing 100083, China Key Laboratory of Solid Waste Treatment and Resource Recycle (Ministry of Education), Southwest University of Science and Technology, Mianyang 621010, China |
AuthorAffiliation_xml | – name: School of Civil and Environmental Engineering, University of Science and Technology Beijing, Beijing 100083, China;Key Laboratory of Solid Waste Treatment and Resource Recycle(Ministry of Education), Southwest University of Science and Technology, Mianyang 621010, China%School of Civil and Environmental Engineering, University of Science and Technology Beijing, Beijing 100083, China |
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Cites_doi | 10.1016/j.minpro.2007.09.003 10.1016/j.hydromet.2006.03.032 10.1016/S0304-386X(03)00165-8 10.1016/j.gca.2006.02.007 10.1016/S0016-7037(02)01371-6 10.1016/j.mineng.2008.07.004 10.1016/j.bioelechem.2004.01.006 10.1016/0304-386X(95)00111-S 10.1016/0304-386X(95)00023-A 10.1016/S0022-0728(81)80549-9 10.1179/000844389795576230 10.1016/j.hydromet.2006.05.001 10.1016/j.mineng.2004.08.004 10.1016/0304-386X(87)90002-8 10.1149/1.2114117 10.1016/S0304-386X(00)00165-1 10.1016/S0304-386X(00)00115-8 10.1127/0935-1221/2007/0019-1714 10.1016/j.proeps.2009.09.111 10.1016/S0301-7516(00)00045-4 10.1016/S0301-7516(02)00003-0 10.1021/cr60301a003 10.1016/S1572-4409(99)80022-4 |
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Keywords | copper ore treatment passivation bioleaching copper sulphide |
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Notes | The bioleaching of copper sulphide minerals was investigated by using A. ferrooxidans ATF6. The result shows the preferential order of the minerals bioleaching as djurleite〉bomite〉pyritic chalcopyrite〉covellite〉porphyry chalcopyfite. The residues were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). It is indicated that jarosite may not be responsible for hindered disso- lution. The elemental sulfur layer on the surface of pyritic chalcopyrite residues is cracked. The compact surface layer of porphyry chalcopy- rite may strongly hinder copper extraction. X-ray photoelectron spectroscopy (XPS) further confirms that the passivation layers of covellite, pyritic chalcopyrite, and porphyry chalcopyrite are copper-depleted sulphide Cu4S11, S8, and copper-rich iron-deficient polysulphide CtuFe2S9, resoectivelv. The ability of these oassivation layers was found as Cu4Fe2S9〉Cu4S11〉S8〉iarosite. 11-5787/T copper ore treatment; copper sulphide; bioleaching; passivation ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Article-2 ObjectType-Feature-1 content type line 23 |
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PublicationTitle | International journal of minerals, metallurgy and materials |
PublicationTitleAbbrev | Int J Miner Metall Mater |
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Publisher | University of Science and Technology Beijing Springer Nature B.V School of Civil and Environmental Engineering, University of Science and Technology Beijing, Beijing 100083, China Key Laboratory of Solid Waste Treatment and Resource Recycle(Ministry of Education), Southwest University of Science and Technology, Mianyang 621010, China%School of Civil and Environmental Engineering, University of Science and Technology Beijing, Beijing 100083, China |
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Snippet | The bioleaching of copper sulphide minerals was investigated by using A. ferrooxidans ATF6. The result shows the preferential order of the minerals bioleaching... The bioleaching of copper sulphide minerals was investigated by using A. ferrooxidans ATF6. The result shows the preferential order of the minerals bioleaching... |
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SubjectTerms | Bacterial leaching Bornite Ceramics Chalcopyrite Characterization and Evaluation of Materials Chemistry and Materials Science Comparative studies Composites Copper Copper sulfides Corrosion and Coatings Covellite Glass Jarosite Leaching Materials Science Metallic Materials Minerals Natural Materials Passivation Passivity Photoelectrons Residues Scanning electron microscopy Sulfides Sulfur Surface layers Surfaces and Interfaces Thin Films Tribology X ray photoelectron spectroscopy X-ray diffraction X-rays X-射线光电子能谱 X-射线衍射 多硫化物 扫描电子显微镜 氧化亚铁硫杆菌 生物浸出 硫化铜矿物 钝化层 |
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Title | Comparative study on the passivation layers of copper sulphide minerals during bioleaching |
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