{"title":"Enhancement of copper mobilization using acidic AlCl3 − rich lixiviant","authors":"","doi":"10.1016/j.mineng.2024.108953","DOIUrl":null,"url":null,"abstract":"<div><p>Copper (Cu) extraction from low-grade ores is limited by the formation of secondary minerals that can passivate the surfaces of Cu-sulphide minerals in these ores. Hence, a novel approach utilizing AlCl<sub>3</sub> as a lixiviant was developed to modify coupled dissolution-reprecipitation processes at the mineral interface. The formation of Al-rich phases instead of Fe-hydroxysulphates enhanced Cu extraction through combined ferric-iron and proton-promoted dissolution. AlCl<sub>3</sub> accelerated chalcopyrite and bornite dissolution by forming soluble intermediate Cu-phases (e.g., covellite) at consistently high Eh (550–650 mV) and acidity due to the Lewis acid property of AlCl<sub>3</sub>. X-ray diffraction analysis revealed that Na-bearing jarosite [(K<sub>0.61</sub>Na<sub>0.41</sub>)<!--> <!-->Fe<sub>3</sub>(SO<sub>4</sub>)<sub>2</sub>(OH)] and sideronatrite [Na<sub>2</sub>Fe(SO<sub>4</sub>)<sub>2</sub>(OH)(H<sub>2</sub>O)] formation in lixiviants without AlCl<sub>3</sub> decreased Fe<sup>3+</sup><sub>(aq)</sub> availability for Cu-sulphide minerals dissolution. In contrast, significant amounts of AlSO<sub>4</sub><sup>+</sup><sub>(aq)</sub> formed in the AlCl<sub>3</sub>-rich lixiviant at pH 1–3, which reduced the sulphate activity and decreased the saturation state of the Fe-hydroxysulphates. Further, AlCl<sub>3</sub> promoted the formation of amorphous, porous Al-rich phases, facilitating quick Fe diffusion through the passivating layer and improving Cu recovery compared to lixiviants containing CaCl<sub>2</sub>, NaCl, or acid-only.</p></div>","PeriodicalId":18594,"journal":{"name":"Minerals Engineering","volume":null,"pages":null},"PeriodicalIF":4.9000,"publicationDate":"2024-08-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S0892687524003820/pdfft?md5=cc4c082f7c87acc261a4b6a88fe5472a&pid=1-s2.0-S0892687524003820-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Minerals Engineering","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0892687524003820","RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Copper (Cu) extraction from low-grade ores is limited by the formation of secondary minerals that can passivate the surfaces of Cu-sulphide minerals in these ores. Hence, a novel approach utilizing AlCl3 as a lixiviant was developed to modify coupled dissolution-reprecipitation processes at the mineral interface. The formation of Al-rich phases instead of Fe-hydroxysulphates enhanced Cu extraction through combined ferric-iron and proton-promoted dissolution. AlCl3 accelerated chalcopyrite and bornite dissolution by forming soluble intermediate Cu-phases (e.g., covellite) at consistently high Eh (550–650 mV) and acidity due to the Lewis acid property of AlCl3. X-ray diffraction analysis revealed that Na-bearing jarosite [(K0.61Na0.41) Fe3(SO4)2(OH)] and sideronatrite [Na2Fe(SO4)2(OH)(H2O)] formation in lixiviants without AlCl3 decreased Fe3+(aq) availability for Cu-sulphide minerals dissolution. In contrast, significant amounts of AlSO4+(aq) formed in the AlCl3-rich lixiviant at pH 1–3, which reduced the sulphate activity and decreased the saturation state of the Fe-hydroxysulphates. Further, AlCl3 promoted the formation of amorphous, porous Al-rich phases, facilitating quick Fe diffusion through the passivating layer and improving Cu recovery compared to lixiviants containing CaCl2, NaCl, or acid-only.
期刊介绍:
The purpose of the journal is to provide for the rapid publication of topical papers featuring the latest developments in the allied fields of mineral processing and extractive metallurgy. Its wide ranging coverage of research and practical (operating) topics includes physical separation methods, such as comminution, flotation concentration and dewatering, chemical methods such as bio-, hydro-, and electro-metallurgy, analytical techniques, process control, simulation and instrumentation, and mineralogical aspects of processing. Environmental issues, particularly those pertaining to sustainable development, will also be strongly covered.