Efficient Electrochemical Recovery of Fine Tellurium Powder from Hydrochloric Acid Media Via Mass Transfer Enhancement
Abstract
Recovery of tellurium from industrial waste streams is of significant importance for the supply of this scattered element. In order to overcome the bottlenecks of high reagents consumption and low recovery efficiency in conventional processes, a novel electrochemical recovery of Te from hydrochloric acid solution was first developed using low-cost stainless steel plate. Due to the high mobility of Te in HCl systems, there is a good electrodeposition behavior of Te(IV) from both the thermodynamic and kinetic considerations. It has been identified that Te electrodeposition is diffusion controlled quasi-reversible reaction, in which the mass transfer can significantly determine the recovery performance and deposit quality. Therefore, a cylinder turbulent reactor with larger surface area cathode was employed for the extraction of tellurium from dilute solution. Microscale Te powder was successfully obtained with a recovery ratio of 96.1% and a current efficiency of 84.3%, while the side reactions of chlorine evolution and TeO2 formation were efficiently inhibited. This mass transfer-enhanced electrodeposition may serve as a promising alternative to overcome the drawbacks of existing valuable element recovery and water purification.
Recommended Citation
W. Jin et al., "Efficient Electrochemical Recovery of Fine Tellurium Powder from Hydrochloric Acid Media Via Mass Transfer Enhancement," Separation and Purification Technology, vol. 203, pp. 117 - 123, Elsevier B.V., Sep 2018.
The definitive version is available at https://doi.org/10.1016/j.seppur.2018.04.026
Department(s)
Materials Science and Engineering
Keywords and Phrases
Electrodeposition; Mass transfer; Recovery; Scattered metals; Tellurium
International Standard Serial Number (ISSN)
1383-5866
Document Type
Article - Journal
Document Version
Citation
File Type
text
Language(s)
English
Rights
© 2018 Elsevier B.V., All rights reserved.
Publication Date
01 Sep 2018
Comments
The authors acknowledge the funding support from National Natural Science Foundation of China (Grant No. 51604253 and U1460108); MOE & SAFEA for the 111 Project (B13025).