Procedure to use phosphogypsum industrial waste for mineral CO2 sequestration
Creators
- 1. Instituto de Ciencia de Materiales de Sevilla (CSIC-US), Av. Américo Vespucio, 49, 41092 Seville (Spain)
- 2. Departamento de Física de la Materia Condensada, Facultad de Física, Universidad de Sevilla, Av. Reina Mercedes s/n, 41012 Seville (Spain)
- 3. Instituto de Diagnóstico Ambiental y Estudios del Agua (IDÆA-CSIC), Jordi Girona 18, 08034 Barcelona (Spain)
- 4. Departamento de Geología, Facultad de Ciencias Experimentales, Universidad de Huelva, Campus Universitario Campus del Carmen, Avenida de las Fuerzas Armadas, 21071 Huelva (Spain)
- 5. Departamento de Ciencias de la Tierra, Universidad de Cádiz, Campus del Río San Pedro, Av. República Saharaui s/n, 11510 Puerto Real (Spain)
Description
Highlights: ► Phosphogypsum wastes are proposed to reduce CO2 greenhouse gas emissions. ► Phosphogypsum dissolution with NaOH results in Ca(OH)2 precipitation and Na2SO4. ► Aqueous carbonation of Ca(OH)2 with CO2 results in the CaCO3 precipitation. ► Metals contained in the phosphogypsum are transferred to the final calcite. ► Applications of CaCO3 and Na2SiO4 by-products are proposed to improve viability. - Abstract: Industrial wet phosphoric acid production in Huelva (SW Spain) has led to the controversial stockpiling of waste phosphogypsum by-products, resulting in the release of significant quantities of toxic impurities in salt marshes in the Tinto river estuary. In the framework of the fight against global climate change and the effort to reduce carbon dioxide emissions, a simple and efficient procedure for CO2 mineral sequestration is presented in this work, using phosphogypsum waste as a calcium source. Our results demonstrate the high efficiency of portlandite precipitation by phosphogypsum dissolution using an alkaline soda solution. Carbonation experiments performed at ambient pressure and temperature resulted in total conversion of the portlandite into carbonate. The fate of trace elements present in the phosphogypsum waste was also investigated, and trace impurities were found to be completely transferred to the final calcite. We believe that the procedure proposed here should be considered not only as a solution for reducing old stockpiles of phosphogypsum wastes, but also for future phosphoric acid and other gypsum-producing industrial processes, resulting in more sustainable production.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.jhazmat.2011.09.039Additional details
Identifiers
- DOI
- 10.1016/j.jhazmat.2011.09.039;
- PII
- S0304-3894(11)01139-3;
Publishing Information
- Journal Title
- Journal of Hazardous Materials
- Journal Volume
- 196
- Journal Page Range
- p. 431-435
- ISSN
- 0304-3894
- CODEN
- JHMAD9
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 44108031
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; S36: MATERIALS SCIENCE;
- Descriptors DEI
- CALCITE; CALCIUM; CALCIUM CARBONATES; CALCIUM HYDROXIDES; CARBON DIOXIDE; DISSOLUTION; EFFICIENCY; EMISSION; ESTUARIES; GYPSUM; IMPURITIES; INDUSTRIAL WASTES; PHOSPHORIC ACID; PRECIPITATION; SODIUM CARBONATES; SODIUM HYDROXIDES; SODIUM SULFATES; SOLUTIONS; TRACE AMOUNTS
- Descriptors DEC
- ALKALI METAL COMPOUNDS; ALKALINE EARTH METAL COMPOUNDS; ALKALINE EARTH METALS; CALCIUM COMPOUNDS; CARBON COMPOUNDS; CARBON OXIDES; CARBONATE MINERALS; CARBONATES; CHALCOGENIDES; COASTAL WATERS; DISPERSIONS; ELEMENTS; HOMOGENEOUS MIXTURES; HYDROGEN COMPOUNDS; HYDROXIDES; INORGANIC ACIDS; INORGANIC COMPOUNDS; METALS; MINERALS; MIXTURES; OXIDES; OXYGEN COMPOUNDS; PHOSPHORUS COMPOUNDS; SEPARATION PROCESSES; SODIUM COMPOUNDS; SULFATE MINERALS; SULFATES; SULFUR COMPOUNDS; SURFACE WATERS; WASTES
Optional Information
- Copyright
- Copyright (c) 2011 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.