Microfluidic Solvent Extraction of Rare Earth Elements

Canadian Institute of Mining, Metallurgy and Petroleum
Frederik H. Kriel Elisabeth Kolar Rossen Sedev Rik Catthoor Scott Middlemas Army Research Laboratory Gareth Hatch Craig Priest
Organization:
Canadian Institute of Mining, Metallurgy and Petroleum
Pages:
8
File Size:
856 KB
Publication Date:
Jan 1, 2016

Abstract

"This paper reports solvent extraction of rare earth elements (REEs) carried out using a microfluidic device and considers the REE loading limit of the organic phase under laminar flow. The microfluidic device contacts aqueous and organic phase streams for a precisely defined contact time (subsecond resolution) and then separates them for offline analysis. Experiments are reported examining the effect of contact time on extraction. We focus on three REEs: one ‘light’ (Nd), one ‘mid’ (Dy), and one ‘heavy’ (Yb) REE, which are extracted using Cyanex® 572. It appears that loading limits may be locally exceeded in the organic phase near to the liquid-liquid interface, where third phase deposits are observed. Third phase formation was also observed close to the liquid-liquid interface in two-dimensional confinement, showing similar third phase adsorption on glass plates. It is also shown that, under microfluidic flow, a typical first ‘split’ between heavy REEs and light REEs can be carried out without exceeding loading limits.INTRODUCTIONMicrofluidic solvent extraction has emerged as a useful tool for studying extraction of metals in a mineral processing context (Ciceri, Mason, Harvie, Perera, & Stevens, 2013; Ciceri, Perera, & Stevens, 2011; Kriel et al., 2015; Mason, Ciceri, Harvie, Perera, & Stevens, 2013; Priest, Zhou, Klink, Sedev, & Ralston, 2012; Priest et al., 2011). The main advantages are the extremely well-defined and tunable flow behaviour, large surface-to-volume ratios, short contact times, and minimisation of sample and reagent amounts. Two main flow configurations have been studied to date: droplet-based and co-flowing streambased extraction. In the former, droplets are formed at a microchannel junction (usually a T-junction or flow-focusing junction) and flow downstream as plugs or ‘free’ droplets. In our case, stream-based extraction, the chip is a plate (often glass) with embedded microchannels (i.e. with cross-sections of tens of micrometres) that carry the aqueous and organic phases in contact without forming droplets. Thus, these chips play the role of a mixer in a conventional mixer-settler and phase separation takes place by branching the streams or collection in a vessel at the chip outlet. Stream-based extraction requires stable streams that are usually supported by a particular channel geometry (e.g. guide structure or small ‘pillars’) or surface chemistry, and flow parallel bounded by the liquid-liquid interface(Aota, Nonaka, Hibara, & Kitamori, 2006; Hibara et al., 2005; Hibara et al., 2002). Phases are disengaged downstream at a Y-junction, which is a qualitative difference between microfluidic and bulk extractions."
Citation

APA: Frederik H. Kriel Elisabeth Kolar Rossen Sedev Rik Catthoor Scott Middlemas Army Research Laboratory Gareth Hatch Craig Priest  (2016)  Microfluidic Solvent Extraction of Rare Earth Elements

MLA: Frederik H. Kriel Elisabeth Kolar Rossen Sedev Rik Catthoor Scott Middlemas Army Research Laboratory Gareth Hatch Craig Priest Microfluidic Solvent Extraction of Rare Earth Elements. Canadian Institute of Mining, Metallurgy and Petroleum, 2016.

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