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Moon, Deok Hyun; Wazne, Mahmoud; Jagupilla, Santhi Chandra; Christodoulatos, Christos; Kim, Min Gyu; Koutsospyros, Agamemnon, E-mail: mwazne@stevens.edu2008
AbstractAbstract
[en] A long-term bench scale treatability study was performed to assess the ability to remediate chromite ore processing residue (COPR) using calcium polysulfide (CaS5). COPR materials were characterized with respect to particle size, pH, curing period and mineralogy. A stoichiometric ratio of sulfide species to hexavalent chromium (Cr6+) of 2 was used for the long-term treatment of COPR. The effectiveness of CaS5 treatment was assessed using the toxicity characteristic leaching procedure (TCLP), alkaline digestion, and X-ray absorption near edge structure (XANES) analyses. The formation of ettringite, known as a heaving agent, was investigated following the treatment of CaS5, using X-ray powder diffraction (XRPD) and scanning electron microscopy (SEM) along with an energy dispersive X-ray spectroscopy (EDX). Overall, after a curing period of 18 months, the TCLP total chromium (Cr) and alkaline digestion (Cr6+) results obtained from the treatability study showed that the concentrations were lower than 5 mg L-1 and 9 mg kg-1, respectively. However, XANES results obtained from samples cured for 18 months showed that all of the treated samples had higher Cr6+ concentrations than shown using alkaline digestion. The lowest XANES Cr6+ concentration of 610.2 mg kg-1 was obtained from the sample with a particle size less than 0.075 mm and a pH value of 9. Particle size reduction prior to the addition of the reductant, along with pH reduction was found to be strongly associated with the treatment performance. Ettringite formation, due to pH increase over time in the samples, where the initial pH was adjusted to 9, was verified by XRPD and SEM-EDX analyses, indicating that a pH less than 9 should be maintained to avoid ettringite formation
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S0048-9697(08)00338-0; Available from http://dx.doi.org/10.1016/j.scitotenv.2008.03.040; Copyright (c) 2008 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; Country of input: International Atomic Energy Agency (IAEA)
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Journal Article
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ALKALINE EARTH METALS, CHALCOGENIDES, CHARGED PARTICLES, CHROMIUM COMPOUNDS, COHERENT SCATTERING, DIFFRACTION, DISSOLUTION, ELECTRON MICROSCOPY, ELEMENTS, IONS, METALS, MICROSCOPY, OXYGEN COMPOUNDS, PROCESSING, SCATTERING, SEPARATION PROCESSES, SIZE, SORPTION, SPECTROSCOPY, SULFUR COMPOUNDS, TRANSITION ELEMENT COMPOUNDS, TRANSITION ELEMENTS
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