Related Experiment Video
Updated: May 30, 2025

Biomass Conversion to Produce Hydrocarbon Liquid Fuel Via Hot-vapor Filtered Fast Pyrolysis and Catalytic Hydrotreating
Published on: December 25, 2016
Highly efficient recovery of total components from spent hydroprocessing catalysts (HPCs) with minimal CO2 & SO2
Guodong Xu1, Junlian Wang1, Fei Xu1
1School of Civil and Resource Engineering, University of Science and Technology Beijing, Beijing, 100083, China.
Abstract:
It is imperative to recover the valuable components of spent HPCs. We have proposed a hydrometallurgical process and recovered 99.9% of V, 99.9% of Mo, and 95% of Al in our previous work. In this study, we focused on the Co and Ni recovery from the alkaline leaching residue of spent HPCs. We characterized the leaching residue by SEM-EDS, XPS, TGA, Laser Particle Size Analyzer, and ICP-OES. The Ni and Co leaching rates both reached around 95% with 2.0 mol/L H2SO4 at 120 °C for 75 min. The impurity of Al in the leachate was removed via solvent extraction with 30% P204 at A/O of 1 and pHequilibrium of 2.0. The Co and Ni in the raffinate was separated via two stages of counter-current extraction with 20% Cyanex 272 at A/O of 1 and pHequilibrium of 5.7. The CoSO4 and NiO products were characterized by XRD, and there are no impurity peaks. We also did DFT calculations, which show the binding energies of Al3+ with extractants are in the order of Al3+-P204 > Al3+-P507 > Al3+-Cyanex 272, and Cyanex 272 exhibits the highest difference in binding energies of Ni2+ and Co2+. The process of Ni and Co recovery from the alkaline leaching residue of spent HPCs was proposed. Only 8 t CO2 and 120 kg SO2 emissions were generated during all the component recovery per ton of the spent HPCs using our proposed process. They are much less than pyro-hydrometallurgical processes.
More Related Videos
Related Concept Videos
Bioremediation
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Washing, Drying, and Ignition of Precipitates

