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作 者:陶明昱 戴普林 陈航 陈禄政[1] TAO Mingyu;DAI Pulin;CHEN Hang;CHEN Luzheng(School of Land and Resources Engineering,Kunming University of Science and Technology,Kunming Yunnan 650093,China)
机构地区:[1]昆明理工大学国土资源工程学院,云南昆明650093
出 处:《矿物学报》2024年第3期428-435,共8页Acta Mineralogica Sinica
基 金:云南省高层次人才引进计划项目(编号:140520210124);昆明理工大学长江学者引进人才平台建设项目(编号:109720190145)。
摘 要:黄铜矿与毒砂浮选分离中,Cu^(2+)总是不可避免地活化毒砂,使其混入铜精矿产品中,从而降低产品的质量。石灰作为毒砂的有效抑制剂,其有效成分为CaOH^(+)。本研究采用密度泛函理论(DFT),分析CaOH^(+)对毒砂的抑制机理。DFT计算结果表明,CaOH^(+)能够使Cu^(2+)离开毒砂表面,削弱其活化作用;毒砂表面的Fe^(2+)和Cu^(2+)失去的电子对与CaOH^(+)的LUMO+1轨道形成反馈π键,导致Fe、Cu的活性被CaOH^(+)降低,从而对毒砂形成强抑制作用。这表明无论毒砂是否被Cu^(2+)活化,CaOH^(+)均能吸附在其表面,达到抑制效果。In the flotation separation process of chalcopyrite and arsenopyrite,arsenopyrite was inevitably activated by Cu^(2+),and then was mixed into the copper concentrate product whose product quality was thus reduced.Lime is an effective inhibitor of arsenopyrite,with its acitve component of CaoH^(+).In this investigation,the inhibition mechanism of CaOH^(+)on arsenopyrite has been analysed using the Density Dunctional Theory(DFT).The DFT calculation results show that the CaOH^(+)can cause Cu^(2+)leave the surface of arsenopyrite,and weaken the activation capacity of Cu^(2+).The lost electron pairs of Fe^(2+)and Cu^(2+)on the surface of arsenopyrite formed a feedbackπbond with the LUMO+1 orbital of CaOH^(+),resulting in the reduction of the activity of Fe and Cu by CaOH^(+).Thus,CaOH^(+)has strong inhibiton effect on arsenopyrite.This phenomenon suggests that CaOH^(+)could be adsorbed on the surface of arsenopyrite to achieve its inhibition effect on arsenopyrite,whether arsenopyrite was activated by Cu^(2+)or not.
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