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Room Temperature Electrorefining of Rare Earth Metals from End-of-use Nd-Fe-B Magnets

Recovering rare earth elements (REE) from used permanent magnets, which contains about 30 wt.% of rare earth elements, has been persistent technological challenge. Current recycling methods relies on pyrometallurgical or hydrometallurgical processes which are energy- and chemical- intensive and not economically and environmentally viable for rare earth containing magnets. Enabling efficient and simplistic recovery and refining of REEs contained in End-of-Use (EoU) products, such as Neodymium-Iron-Boron (Nd-Fe-B) based magnets will play an important and complementary role in the total supply of REEs in the future. We designed a new electrochemical method and demonstrated a room temperature one-pot process that concurrently separates and electroplates REE from commercial Nd-Fe-B magnets. By establishing selective oxidation and reductive potential as electrochemical control parameter along with electrochemically compatible non-aqueous electrolyte system, we demonstrated selective electroleaching of lanthanides (Nd and Preseodymium (Pr)) from anode and concurrent plating as alloy at Pt cathode. The morphological and chemical evolution of the Nd-Fe-B magnets during electroleaching reveals the electrochemical stimuli and rate of dissolution depends on microstructural complexities of the Nd-Fe-B magnet. The concomitant electroplating process leads to Nd-Pr based alloy which can be used as raw metallic alloy for manufacturing new permanent magnet and other devices. Our study demonstrates a scalable separation and refining methodology, based on widely available organic electrolyte system and without any consumptive chemical use, for selective lanthanide recovery from waste magnets.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Materials Data on PrNd3 by Materials Project

Nd3Pr is Copper-derived structured and crystallizes in the tetragonal I4/mmm space group. The structure is three-dimensional. there are two inequivalent Nd sites. In the first Nd site, Nd is bonded to eight Nd and four equivalent Pr atoms to form NdPr4Nd8 cuboctahedra that share corners with twelve equivalent NdPr4Nd8 cuboctahedra, edges with eight equivalent PrNd12 cuboctahedra, edges with sixteen NdPr4Nd8 cuboctahedra, faces with four equivalent PrNd12 cuboctahedra, and faces with fourteen NdPr4Nd8 cuboctahedra. There are four shorter (3.68 Å) and four longer (3.69 Å) Nd–Nd bond lengths. All Nd–Pr bond lengths are 3.69 Å. In the second Nd site, Nd is bonded to eight equivalent Nd and four equivalent Pr atoms to form NdPr4Nd8 cuboctahedra that share corners with four equivalent NdPr4Nd8 cuboctahedra, corners with eight equivalent PrNd12 cuboctahedra, edges with twenty-four NdPr4Nd8 cuboctahedra, faces with six equivalent PrNd12 cuboctahedra, and faces with twelve NdPr4Nd8 cuboctahedra. All Nd–Pr bond lengths are 3.68 Å. Pr is bonded to twelve Nd atoms to form PrNd12 cuboctahedra that share corners with four equivalent PrNd12 cuboctahedra, corners with eight equivalent NdPr4Nd8 cuboctahedra, edges with eight equivalent PrNd12 cuboctahedra, edges with sixteen equivalent NdPr4Nd8 cuboctahedra, faces with four equivalent PrNd12 cuboctahedra, and faces with fourteen NdPr4Nd8 cuboctahedra.

36 MATERIALS SCIENCE↗