Abstract

The relatedness of copper and iron speciation to chalcopyrite bioleaching by acidophilic Acidithiobacillus ferrooxidans was analyzed by synchrotron radiation-based X-ray diffraction (SR-XRD) and Cu, Fe K-edge X-ray absorption near edge structure (XANES) spectroscopy, accompanying with the determination of leaching parameters and the observation of chalcopyrite surface modification by scanning electron microscopy. The results showed that chalcopyrite was leached gradually by A. ferrooxidans, with ~70.58% of Cu2+ dissolution after 30days of bioleaching when the mineral surface was evidently attacked. During the bioleaching, bornite and chalcocite were detected at day 3 and day 9 when the redox potential was less than 500mV, but they disappeared at day 18 and day 30 when covellite was detected and the redox potential was about 550mV. The linear fitting of Cu and Fe XANES spectra quantitatively demonstrated the composition of leaching residue: the copper species comprised ~84.8% of chalcopyrite, ~10.2% of bornite and ~5.0% of chalcocite at day 3, then changed to ~90.1% of chalcopyrite, ~6.5% of bornite and ~3.4% of chalcocite at day 9; the composition became ~89.8% of chalcopyrite and ~10.2% of covellite at day 18, and ~80.3% of chalcopyrite and ~19.7% of covellite at day 30. The iron species comprised ~26% of chalcopyrite and ~74% of jarosite at day 30. Elemental sulfur and jarosite were detected from day 3 but without evident negative effect on the copper extraction.

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.