Atmospheric Carbon Mineralization in an Industrial-Scale Chrysotile Mining Waste Pile

Magnesium-rich minerals that are abundant in ultramafic mining waste have the potential to be used as a safe and permanent sequestration solution for carbon dioxide (CO2). Our understanding of thermo-hydro-chemical regimes that govern this reaction at an industrial scale, however, has remained an im...

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Veröffentlicht in:Environmental science & technology 2018-07, Vol.52 (14), p.8050-8057
Hauptverfasser: Nowamooz, Ali, Dupuis, J. Christian, Beaudoin, Georges, Molson, John, Lemieux, Jean-Michel, Horswill, Micha, Fortier, Richard, Larachi, Faïçal, Maldague, Xavier, Constantin, Marc, Duchesne, Josée, Therrien, René
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Sprache:eng
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Zusammenfassung:Magnesium-rich minerals that are abundant in ultramafic mining waste have the potential to be used as a safe and permanent sequestration solution for carbon dioxide (CO2). Our understanding of thermo-hydro-chemical regimes that govern this reaction at an industrial scale, however, has remained an important challenge to its widespread implementation. Through a year-long monitoring experiment performed at a 110 Mt chrysotile waste pile, we have documented the existence of two distinct thermo-hydro-chemical regimes that control the ingress of CO2 and the subsequent mineral carbonation of the waste. The experimental results are supported by a coupled free-air/porous media numerical flow and transport model that provides insights into optimization strategies to increase the efficiency of mineral sequestration at an industrial scale. Although functioning passively under less-than-optimal conditions compared to laboratory-scale experiments, the 110 Mt Thetford Mines pile is nevertheless estimated to be sequestering up to 100 tonnes of CO2 per year, with a potential total carbon capture capacity under optimal conditions of 3 Mt. Annually, more than 100 Mt of ultramafic mine waste suitable for mineral carbonation is generated by the global mining industry. Our results show that this waste material could become a safe and permanent carbon sink for diffuse sources of CO2.
ISSN:0013-936X
1520-5851
DOI:10.1021/acs.est.8b01128