从废钕铁硼磁体中回收稀土元素的无酸电气化工艺

Prakash Venkatesan*, Jilt Sietsma and Yongxiang Yang, 
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摘要

从钕铁硼磁体中回收稀土元素(REE)是减轻稀土供应链相关风险的重要策略。在本文中,我们提出了一种回收稀土的电化学工艺,其中稀土浸出和沉淀所需的所有试剂都是原位电化学生成的。采用三室电化学反应器,将含稀土盐和添加盐氨基甲酸铵送入中间的室。电解后,盐被分解成酸和稀土氢氧化物。利用阳极液室产生的酸对废钕铁硼磁铁进行浸出。将稀土氢氧化物收集在阴极室中,煅烧得到稀土氧化物。在同一步骤中,95%以上的稀土元素和钴被萃取到溶液中,85%以上的铁以Fe(OH)3沉淀的形式被去除。随后,渗滤液被氧化和中和,以去除99%以上的铁。通过使用电子作为绿色试剂,该工艺在单个反应器中结合了浸出和沉淀,使工艺强化。末端产生的渗滤液富含稀土元素,可再次进入中间隔间,形成一个完整的闭环过程。总的来说,这个过程不消耗酸,只消耗电,用于中和的氢氧化铵和一种添加剂盐,磺胺酸铵。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

An Acid Free Electrified Process for Recycling Rare-Earth Elements from NdFeB Magnet Waste

An Acid Free Electrified Process for Recycling Rare-Earth Elements from NdFeB Magnet Waste

Recycling of rare-earth elements (REEs) from NdFeB magnets is an important strategy to mitigate the risks associated with the REE supply chain. In this article, we propose an electrochemical process to recover REEs wherein all the reagents required for both leaching of REEs as well as the precipitation are generated in situ electrochemically. A three compartment electrochemical reactor was used in which a rare-earth containing salt along with an additive salt, ammonium sulfamate, was fed into the middle compartment. Upon electrolysis, the salts were split into acid and rare-earth hydroxides. The acid generated in the anolyte compartment was used to leach the NdFeB magnet waste. The rare-earth hydroxides were collected in the catholyte compartment and calcined to obtain rare-earth oxides. More than 95% of REEs and cobalt were extracted into the solution, and more than 85% of iron was removed as Fe(OH)3 precipitate in the same step. Subsequently, the leachate was oxidized and neutralized to remove more than 99% of iron. By using electrons as green reagents, this process combines leaching and precipitation in a single reactor enabling process intensification. The leachate produced at the end is rich in REEs and can be fed again into the middle compartment, forming a completely closed-loop process. Overall, the process consumes no acid, only electricity, ammonium hydroxide for neutralization, and an additive salt, ammonium sulfamate.

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