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Recycling of rare earth elements from SmCo_5-Magnets via solid-state chlorination

机译:通过固态氯化法回收SmCo_5-磁铁中的稀土元素

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The recycling of rare earths from End-of-Life permanent magnets is a widely studied field of research. However, with rare earth prices falling, recycling processes have become increasingly uneconomical. In this context, solid-state chlorination has been intensively studied as this method has the potential to serve as an alternative to acid leaching. Instead of a mineral acid dissolving the magnets, a chlorination takes place by decomposing NH4Cl at temperatures between 225 and 325 degrees C. The resulting dry HCl forms water-soluble chlorides from the magnet material. For rare earth recycling from Fe14Nd2B magnets, the method was found to provide significant advantages in terms of consumption of chemicals as well as and chemical costs. The present work sheds light on another obstacle of magnet recycling, which is the inhomogeneous composition of the starting material. Only 2% of the total end-of-life magnet waste material contains SmCo magnets. Fe14Nd2B magnets account for most of the waste material. SmCo magnets are nevertheless the second most important group of rare-earth-based permanent magnets. However, they are not collected separately, and recycling processes have to focus on recovering both magnet alloys within one process. Therefore, the solid-state chlorination of SmCo5 magnets was examined in detail. The present work focusses consequently on three major issues: (i) Adjustment of solid state chlorination so that SmCo alloys can be chlorinated under the same conditions as Fe14Nd2B magnets. This is the most important requirement for a recycling process that utilizes both types of rare earth magnets. (ii) Examination of the reaction of SmCo with NH4Cl. It was found that the chlorination behaviour differs significantly from that of the Fe14Nd2B magnets. The particles arising from SmCo5 disintegrate more rapidly than expected during chlorination, which eventually enables an almost selective chlorination of samarium. (iii) Furthermore, Sm yields were optimised to reach 99.7% by applying a design of experiments. (C) 2019 Elsevier Ltd. All rights reserved.
机译:从报废永久磁铁中回收稀土是一个广泛研究的研究领域。但是,随着稀土价格的下跌,回收过程变得越来越不经济。在这种情况下,已经对固态氯化法进行了深入研究,因为这种方法具有替代酸浸的潜力。代替无机酸溶解磁体,而是通过在225至325摄氏度之间的温度下分解NH4Cl进行氯化。生成的干燥HCl从磁体材料中形成水溶性氯化物。对于从Fe14Nd2B磁体中回收稀土,发现该方法在化学药品的消耗以及化学药品成本方面具有明显的优势。本工作揭示了磁铁回收的另一个障碍,即原料的不均匀组成。报废的磁铁废料总量中只有2%包含SmCo磁铁。 Fe14Nd2B磁体占了大部分废料。 SmCo磁体仍然是稀土基永磁体的第二重要组成部分。但是,它们不是单独收集的,回收过程必须集中于在一个过程中回收两种磁铁合金。因此,详细研究了SmCo5磁体的固态氯化。因此,目前的工作集中在三个主要问题上:(i)调整固态氯化,以便SmCo合金可以在与Fe14Nd2B磁体相同的条件下进行氯化。这是利用两种稀土磁体的回收过程中最重要的要求。 (ii)检验SmCo与NH4Cl的反应。发现氯化行为与Fe14Nd2B磁体的氯化行为显着不同。由SmCo5产生的颗粒崩解的速度比氯化过程中预期的要快,最终使enables几乎可以选择性地氯化。 (iii)此外,通过设计实验,将Sm的收率优化至99.7%。 (C)2019 Elsevier Ltd.保留所有权利。

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