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采用XRD、XPS和MLA等检测研究海相火山岩型黄铜矿及斑岩型黄铜矿化学浸出的差异性。结果表明:在化学浸出过程中,海相火山岩型黄铜矿与斑岩型黄铜矿浸出特性有很大的差异,这是由于两种黄铜矿表面形成中间产物的性质不同。两种黄铜矿化学浸出的产物除单质硫S 8之外,还有非化学计量的中间产物Cu 3.5 Fe 4 S 2.5、Cu 5 Fe 4 S及Cu 3.5 Fe 1.5 S 5生成。海相火山岩型黄铜矿的中间产物以Cu 3.5 Fe 4 S 2.5为主,斑岩型黄铜矿的中间产物以Cu 3.5 Fe 1.5 S 5为主。海相火山岩型黄铜矿与斑岩型黄铜矿具有不同的溶解途径:海相火山岩型黄铜矿受到H+的腐蚀后矿物中的Cu—S断裂,Cu2+与Fe2+同时溶解,而斑岩型黄铜矿受到H+腐蚀后Fe2+优先溶解。

The chemical leaching different characteristics of chalcopyrite with different genetic types (marine volcanic and porphyry) were investigated by XRD, XPS and MLA analysis. The results show that the difference between marine volcanic chalcopyrite and porphyry chalcopyrite during chemical leaching is generated by intermediate formed on the surface of chalcopyrite with different chemical and structural properties. Nonstoichiometric intermediate products, such as Cu3.5Fe4S2.5, Cu5Fe4S and Cu3.5Fe1.5S5, also form during two kinds of chalcopyrite leaching, besides sulphur S8. The main intermediate product of marine volcanic chalcopyrite is Cu 3.5 Fe 4 S 2.5 , while Cu 3.5 Fe 1.5 S 5 is mainly in porphyry chalcopyrite. The leaching mechanism of marine volcanic chalcopyrite and porphyry chalcopyrite is different. During the leaching process of marine volcanic chalcopyrite, Cu2+and Fe2+are dissolved simultaneously after the broken of Cu—S bond attacked by proton. However, Fe2+dissolves preferentially after the porphyry chalcopyrite is corroded by H+.

参考文献

[1] Pathak, A;Dastidar, MG;Sreekrishnan, TR .Bioleaching of heavy metals from sewage sludge: A review[J].Journal of Environmental Management,2009(8):2343-2353.
[2] HIROYOSHI N;HIROTA M;HIRAJIMA T;TSUNEKAWA M .A case of ferrous sulfate addition enhancing chalcopyrite leaching[J].HYDROMETALLURGY,1997,47(01):37-45.
[3] Yasuhiro Konishi;Masahiko Tokushige;Satoru Asai .Copper recovery from chalcopyrite concentrate by acidophilic thermophile Acidianus brierleyi in batch and continuous-flow stirred tank reactors[J].Hydrometallurgy,2001(2/3):271-282.
[4] J. Vilcaez;K. Suto;C. Inoue .Bioleaching of chalcopyrite with thermophiles: Temperature-pH-ORP dependence[J].International Journal of Mineral Processing,2008(1/2):37-44.
[5] 白静,温建康,黄松涛,武彪,姚国成.不同成矿条件下黄铜矿微生物浸出研究概况[J].稀有金属,2012(04):644-650.
[6] 傅开彬,林海,莫晓兰,董颖博,汪涵.不同成因类型黄铜矿细菌浸出钝化[J].中南大学学报(自然科学版),2011(11):3245-3250.
[7] FATHI H.Chalcopyrite:its chemistry and metallurgy[M].New York:McGraw-Hill Book Company,1978:26-28.
[8] HILLER J E;PROBSTHAIN K .Thermische und r?ntgenographische Untersuchungen am Kupferkies[J].Z Krist,1956,108:108-129.
[9] NAMBU M;KANO S .Phase relation between chalcopyrite and the so-called cubic chalcopyrite[J].Ganeski Kobutsu Kosho Gakkaishi,1968,60(05):127-145.
[10] BJ?RLING G;LESIDRENSKI P.Aktivierung von mineralsulfiden für hydrometallurgische behandlung[M].Leningrad:Proc VIII Intern Congr,1968:16-20.
[11] Wolfgang Sand;Tilman Gehrke;Peter-Georg Jozsa .(Bio) chemistry of bacterial leaching-direct vs. indirect bioleaching[J].Hydrometallurgy,2001(2/3):159-175.
[12] CóRDOBA E M;MU?OZ J A;BLáZQUEZ M L;GONZáLEZ F BALLESTER A .Passivation of chalcopyrite during its chemical leaching with ferric ion at 68 ℃[J].Minerals Engineering,2009,22(03):229-235.
[13] E.M. Cordoba;J.A. Munoz;M.L. Blazquez .Leaching of chalcopyrite with ferric ion--Part I: General aspects[J].Hydrometallurgy,2008(3/4):81-87.
[14] E.M. Cordoba;J.A. Munoz;M.L. Blazquez .Leaching of chalcopyrite with ferric ion--Part II: Effect of redox potential[J].Hydrometallurgy,2008(3/4):88-96.
[15] AMMOU-CHOKROUM M;SEN P K;FOUQUES F.Electrooxidation of chalcopyrite in acid chloride medium;kinetics, stoichiometry and reaction mechanism[A].Warsaw:Elsevier Scientific Publishing Company,1981:759-807.
[16] 方明山,肖仪武,童捷矢.MLA在铅锌氧化矿物解离度及粒度测定中的应用[J].有色金属(选矿部分),2012(03):1-3,9.
[17] HACKL R P;DREISINGER D B;PETERS E;KING J A .Passivation of chalcopyrite during oxidative leaching in sulfate media[J].HYDROMETALLURGY,1995,39(1/3):25-48.
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