Abstract

The transformation of schwertmannite to goethite and/or hematite in high pH solutions was studied between 60 and 240 °C using synchrotron-based, in-situ energy-dispersive X-ray diffraction (EDXRD). Powder diffraction and electron microscopy indicate that the crystallization of hematite and goethite occurred via intermediate ferrihydrite. At temperatures ≤80 °C goethite was the only crystallization product, while at temperatures >80 °C goethite and hematite crystallized almost simultaneously. At temperatures ≥150 °C a secondary crystallization stage was observed in which goethite transformed to hematite. The activation energies of nucleation for goethite and hematite are 27 ± 1 and 25 ± 1 kJ/mol, respectively, while the activation energies of crystallization are 33 ± 1 and 28 ± 1 kJ/mol. Most of the sulfate was released from the schwertmannite during the early stages of crystallization with <5% of the sulfate remaining associated with the solid phase after crystallization was complete. Sulfate from the initial schwertmannite retarded the dissolution of ferrihydrite, which inhibited the nucleation and the early stages of goethite formation, but did not significantly affect the later stages of goethite crystallization. At high temperatures the presence of sulfate favored the crystallization of hematite over goethite. The activation energy of crystallization for the secondary transformation of goethite to hematite is 103 ± 3 kJ/mol.

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.