Abstract

Automobile catalysts sector is the largest consumption field of platinum group metals (PGMs) worldwide, and they are the most important secondary resources of Pt, Pd, and Rh once they reach the end of life. However, recycling PGMs from spent automotive catalysts is of great difficulty due to their complex physicochemical characteristics and low concentrations. A highly efficient technology for recovery of Pt, Pd, and Rh by iron melting collection was proposed. Owing to the same face-centred cubic structure and close atomic radius, iron powder is used as collector since Fe and PGMs can form continuous solid solution. PGMs are concentrated and formed Fe-PGMs alloy phase at a relatively low temperature of 1300–1400 °C through adjustment of slag compositions. The principles of slag design were put forward, and the effects of basicity, slag compositions and collector dosage on the recovery efficiency of PGMs were studied. Factsage 7.0 software (CRCT-Thermfact and GTT-Technologies) was used to calculate slag viscosity and simulate slag reaction equilibrium during the melting process. The recovery efficiency of PGMs was 99.25 % under the optimized conditions: mass ratio of CaO/Na2O=35:20, CaF2 5 wt.%, Na2B4O7 8.5 wt.%, collector Fe 15 wt.%, and 5 wt.% C, where the concentration of Pt, Pd and Rh in slag phase were 2.398, 3.879, and 0.976 g/t, respectively. Meanwhile, the formation of ferrosilicon (FeSi2, FeSi) was avoided. 50 kg pilot-scale experiments also achieved over 99 % recovery efficiency of PGMs.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.