采用电化学方法研究LIX84I萃取Cu^(2+)的界面转移过程  

Interfacial transfer process of Cu^(2+) assisted by LIX84I using electrochemical methods

作　　者：周文辉[1] 胡久刚[1] 唐晖[1] 李娅[1] 付明波 孙乐行 陈启元[1] 

机构地区：[1]中南大学化学化工学院,长沙410083

出　　处：《中国有色金属学报》2015年第5期1387-1393,共7页The Chinese Journal of Nonferrous Metals

基　　金：国家重点基础研究发展计划资助项目(2014CB643401);国家自然科学基金资助项目(51134007;51304244);中国博士后科学基金资助项目(2014M552152);中南大学博士后基金资助项目

摘　　要：为了研究铜的萃取过程,通过构建互不相溶微孔界面电化学方法,研究Cu2+在水/1,2-二氯乙烷界面上与LIX84I的配位转移过程,获得Cu2+与LIX84的扩散动力学参数和界面转移机理。结果表明:当LIX84配体浓度过量时,萃取过程中Cu2+从水相线性扩散至界面的过程为控制步骤,并与LIX84I在界面发生配位反应后,铜配合物以球形扩散迁移至有机相中;当Cu2+离子过量时,LIX84I从有机相球形扩散至两相界面与Cu2+配位后,铜配合物也以球形扩散迁移至有机相中。Cu2+与LIX84I的萃取过程在两相界面进行,符合界面络合转移和界面离解转移的扩散机理。In order to study the copper extraction process, based on the electrochemical methods for ion transfer at micro-oil/water interface, the transfer process of Cu2＋ assisted by LIX84I at the water/1, 2-dichloroethane interface was investigated. The dynamics parameters of the extraction process and the transfer mechanism of copper（II） were obtained. The results indicate that, when the LIX84I is excess, Cu2＋ transfers from aqueous phase to oil/water interface and complexes with LIX84I controlled by a linear diffusion, whereas, the transfer process of LIX84I from the organic phase to oil/water interface and complex with Cu2＋ controlled by spherical diffusion when Cu2＋ is greatly excess. In both cases, the Cu2＋ complexes transfer to the organic phase with a spherical diffusion. The Cu2＋ complexes form at interface with an interface complexation transfer and interface dissociative transfer mechanism.

关 键 词：液/液界面 铜萃取 离子转移 电化学 

分 类 号：TF811[冶金工程—有色金属冶金]