A novel reductive alkali roasting of chromite ores for carcinogen-free Cr6+-ion extraction of chromium oxide (Cr2O3) – A clean route to chromium product manufacturing!
- 1. School of Chemical and Process Engineering, Faculty of Engineering, University of Leeds, Woodhouse Lane, Leeds, LS2 9JT (United Kingdom)
Description
Highlights: • The reduction of chromite ores with alkali eliminates the risk of carcinogenic Cr6+- ion production during the extraction of chroimum oxide and Fe-Cr-alloy. The alumina is also extracted as a by-product of the process. • The CO generated in the process is partly utilized for energy generation by combustion via CO+0.5O2 = CO2 reaction. Less than 10 % of CO2 may be sequestrated for alumina recovery. • There is no solid and water waste in the process which contains carcinogenic Cr6+- ions. A novel reduction reaction for extracting Cr2O3 from chromite ores is demonstrated by excluding the formation of carcinogenic chromate (Cr6+) intermediates. We have investigated in detail the underpinning high-temperature reduction reaction: FeCr2O4+Na2CO3+2[C]=[Fe]+Na2Cr2O4+3CO(g), which defines the process chemistry for the formation of sodium chromite (Na2CrO2) as an intermediate product for Cr2O3 extraction. After high-temperature reduction, the magnetic separation, aqueous and acid leaching of reaction products yielded 81 wt% and 70 wt% pure Cr2O3 from low (∼4 wt%) and high (>8 wt%) silica-containing chromite ores, respectively. The process diagram explains the extraction of Cr2O3, Fe-Cr alloy, Al2O3, and MgO-Al2O3-silicate, reuse of CO2 for Na2CO3 recovery, and energy generation from CO combustion for demonstrating Cr6+-free extraction of metallic and mineral values from chromite ores. The process chemistry demonstrates the extraction of 75–80 % pure Cr2O3 from NaCrO2 by leaching with 0.05−0.5 M dilute H2SO4 in controlled pH conditions. The detailed chemical analysis of leachates after Cr2O3 extraction shows that the acid leachates with residual concentrations of ∼150 ppm Cr3+-ions can be recycled in situ for reusing water, for eliminating the risk of Cr6+-ion formation from atmospheric oxidation. The novel extraction route may be able to displace the current oxidative process for chromite ore processing by retrofitting.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.jhazmat.2020.123589Additional details
Identifiers
- DOI
- 10.1016/j.jhazmat.2020.123589;
- PII
- S0304389420315752;
Publishing Information
- Journal Title
- Journal of Hazardous Materials
- Journal Volume
- 403
- Journal Page Range
- vp.
- ISSN
- 0304-3894
- CODEN
- JHMAD9
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 54051587
- Subject category
- S36: MATERIALS SCIENCE;
- Descriptors DEI
- CARBON DIOXIDE; CARBON MONOXIDE; CHROMATES; CHROMIUM; CHROMIUM IONS; LEACHING; OXIDATION; SILICA; SILICATES; SODIUM CARBONATES; SOLIDS; SULFURIC ACID
- Descriptors DEC
- ALKALI METAL COMPOUNDS; CARBON COMPOUNDS; CARBON OXIDES; CARBONATES; CHALCOGENIDES; CHARGED PARTICLES; CHEMICAL REACTIONS; CHROMIUM COMPOUNDS; DISSOLUTION; ELEMENTS; HYDROGEN COMPOUNDS; INORGANIC ACIDS; INORGANIC COMPOUNDS; IONS; METALS; MINERALS; OXIDE MINERALS; OXIDES; OXYGEN COMPOUNDS; SEPARATION PROCESSES; SILICON COMPOUNDS; SODIUM COMPOUNDS; SULFUR COMPOUNDS; TRANSITION ELEMENT COMPOUNDS; TRANSITION ELEMENTS
Optional Information
- Copyright
- Copyright (c) 2020 The Authors. Published by Elsevier B.V.