A clean process for the recovery of rare earth and transition metals from NiMH battery based on primary amine and lauric acid.

J Environ Manage

CAS Key Laboratory of Design and Assembly of Functional Nanostructures, Fujian Key Laboratory of Nanomaterials, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian, 350002, PR China; Jiangxi Province Key Laboratory of Cleaner Production of Rare Earths, Ganjiang Innovation Academy, Chinese Academy of Sciences, Ganzhou, 341000, PR China; Fujian Research Center for Rare Earth Engineering Technology, Xiamen Institute of Rare Earth Materials, Haixi Institute, Chinese Academy of Sciences, Xiamen, 361021, PR China; School of Rare Earths, University of Science and Technology of China, Hefei, 230026, PR China. Electronic address:

Published: February 2024

A novel rare earth separation system composed of lauric acid (LA) and primary ammonium (RNH) was studied. Compared with individual LA and RNH, the mixed extraction system can significantly improve the extraction and separation ability of rare earth (RE). When LA and RNH are mixed in an equal molar ratio, the synergistic coefficient for extracting Nd(III) in the system reaches 136.85. Effective separation of Nd from Co and Ni can be achieved, with the separation coefficients of 1503 and 2762 for Nd/Co and Nd/Ni, respectively. The ion association mechanism of developed extraction system can avoid the generation of saponification wastewater. Thus, the negative impact of saponification wastewater on the economy and environment can be reduced. The extraction system is simple to be prepared and easy to be stripped, which helps to reduce acid and alkali consumption. Application of this extraction system can effectively realize the separation of RE elements La, Ce, Pr, Nd and transition metals Co, Ni, Mn in nickel-metal hydride (NiMH) battery. This paper provides a new strategy for the development of ionic liquid saponification technology without saponified wastewater.

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Source
http://dx.doi.org/10.1016/j.jenvman.2023.119788DOI Listing

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