Recovery of manganese oxides from spent alkaline and zinc–carbon batteries. An application as catalysts for VOCs elimination
Creators
- 1. Pla.Pi.Mu-Planta Piloto Multipropósito, (CICPBA-UNLP) Cno. Centenario y 505, M.B. Gonnet, Buenos Aires (Argentina)
- 2. Centro de Investigación y Desarrollo en Ciencias Aplicadas, "Dr. J. Ronco" CINDECA (CONICET CCT La Plata), 47 N°257, La Plata, Buenos Aires (Argentina)
Description
Highlights: • Manganese oxides were synthesized using spent batteries as raw materials. • Spent alkaline and zinc–carbon size AA batteries were used. • A biohydrometallurgical process was employed to bio-lixiviate batteries. • Manganese oxides were active in the oxidation of VOCs (ethanol and heptane). - Abstract: Manganese, in the form of oxide, was recovered from spent alkaline and zinc–carbon batteries employing a biohydrometallurgy process, using a pilot plant consisting in: an air-lift bioreactor (containing an acid-reducing medium produced by an Acidithiobacillus thiooxidans bacteria immobilized on elemental sulfur); a leaching reactor (were battery powder is mixed with the acid-reducing medium) and a recovery reactor. Two different manganese oxides were recovered from the leachate liquor: one of them by electrolysis (EMO) and the other by a chemical precipitation with KMnO4 solution (CMO). The non-leached solid residue was also studied (RMO). The solids were compared with a MnOx synthesized in our laboratory. The characterization by XRD, FTIR and XPS reveal the presence of Mn2O3 in the EMO and the CMO samples, together with some Mn4+ cations. In the solid not extracted by acidic leaching (RMO) the main phase detected was Mn3O4. The catalytic performance of the oxides was studied in the complete oxidation of ethanol and heptane. Complete conversion of ethanol occurs at 200 °C, while heptane requires more than 400 °C. The CMO has the highest oxide selectivity to CO2. The results show that manganese oxides obtained using spent alkaline and zinc–carbon batteries as raw materials, have an interesting performance as catalysts for elimination of VOCs
Availability note (English)
Available from http://dx.doi.org/10.1016/j.wasman.2013.03.006Additional details
Identifiers
- DOI
- 10.1016/j.wasman.2013.03.006;
- PII
- S0956-053X(13)00122-0;
Publishing Information
- Journal Title
- Waste Management
- Journal Volume
- 33
- Journal Issue
- 6
- Journal Page Range
- p. 1483-1490
- ISSN
- 0956-053X
- CODEN
- WAMAE2
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 46006537
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- BACTERIA; CARBON DIOXIDE; CATIONS; ELECTRIC BATTERIES; ELECTROLYSIS; ETHANOL; FOURIER TRANSFORM SPECTROMETERS; HEPTANE; INFRARED SPECTRA; LEACHING; MANGANESE; MANGANESE IONS; MANGANESE OXIDES; MATERIALS RECOVERY; OXIDATION; PILOT PLANTS; PRECIPITATION; SODIUM COMPOUNDS; X-RAY DIFFRACTION; X-RAY PHOTOELECTRON SPECTROSCOPY
- Descriptors DEC
- ALCOHOLS; ALKALI METAL COMPOUNDS; ALKANES; CARBON COMPOUNDS; CARBON OXIDES; CHALCOGENIDES; CHARGED PARTICLES; CHEMICAL REACTIONS; COHERENT SCATTERING; DIFFRACTION; DISSOLUTION; ELECTROCHEMICAL CELLS; ELECTRON SPECTROSCOPY; ELEMENTS; ENERGY STORAGE SYSTEMS; ENERGY SYSTEMS; FUNCTIONAL MODELS; HYDROCARBONS; HYDROXY COMPOUNDS; IONS; LYSIS; MANAGEMENT; MANGANESE COMPOUNDS; MEASURING INSTRUMENTS; METALS; MICROORGANISMS; ORGANIC COMPOUNDS; OXIDES; OXYGEN COMPOUNDS; PHOTOELECTRON SPECTROSCOPY; PROCESSING; SCATTERING; SEPARATION PROCESSES; SPECTRA; SPECTROMETERS; SPECTROSCOPY; TRANSITION ELEMENT COMPOUNDS; TRANSITION ELEMENTS; WASTE MANAGEMENT; WASTE PROCESSING
Optional Information
- Copyright
- Copyright (c) 2013 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.