The recovery of cathode materials using deep eutectic
solvents
(DESs) still requires a long leaching time and relatively high temperatures.
The poor selectivity of the leaching process leads to the low purity
of the precipitate. Herein, a microwave-assisted choline chlorine–oxalate–water
system was designed to selectively leach Li and recover high-purity
cobalt oxalate simultaneously, which could greatly shorten the extraction
time and decrease the leaching temperature. Fourier transform infrared
spectroscopy, X-ray diffraction, inductively coupled plasma–mass
spectrometry, and X-ray photoelectron spectroscopy methods were used
to explore the mechanism of microwave-assisted DES leaching of valuable
metals from lithium cobalt oxide (LCO). It was found that 99.05% of
Li could be selectively leached and 99.21% of Co could be precipitated
as cobalt oxalate at 100 °C in 10 min simultaneously. The purity
of cobalt oxalate precipitated was 95.36% without any purification
procedures. A new polymer compound Co2+[(Ch+)
x
(Cl–)
y
(HC2O4
–)
z
] was formed during the microwave-assisted
leaching process. The compound could be hydrolyzed, and the cobalt
oxalate precipitate appeared by increasing the water content in the
DES. Finally, the DES for the recovery of LCO could be cycled four
times with favorable selectivity. A low-pollution, efficient, process-simple,
and precipitant-free technology using a microwave-assisted DES for
selective recovery of LCO was proposed, which provided an important
reference method for large-scale recovery of valuable metals from
spent lithium-ion batteries.