TY - JOUR
T1 - Dissolution of natural serpentinite in mineral and organic acids
AU - Teir, Sebastian
AU - Revitzer, Hannu
AU - Eloneva, Sanni
AU - Fogelholm, Carl Johan
AU - Zevenhoven, Ron
N1 - Funding Information:
We thank Esko Pöyliö and Rita Kallio at Ruukki for generously providing us with XRF and XRD services, and the Laboratory of Energy Engineering and Environmental Protection for facilitating this work. We thank Mika Järvinen for helpful comments and proof-reading, and Jaakko Savolahti for assisting us with the experiments. We acknowledge the Nordic Energy Research, the Finnish Funding Agency for Technology and Innovation (TEKES) and the Finnish Recovery Boiler Committee for financial support. Ron Zevenhoven acknowledges the Academy of Finland for an Academy Researcher position (2004–2005).
Copyright:
Copyright 2008 Elsevier B.V., All rights reserved.
PY - 2007/7/4
Y1 - 2007/7/4
N2 - Abundant resources of magnesium silicates make an interesting prospect for long-term storage of CO2 by mineral carbonation. Several carbonation processes proposed in literature for CO2 storage employ extraction of silicate minerals using a liquid solvent. In this study, the dissolution of natural serpentinite in respective solutions of acids, bases and ammonium salts has been investigated. Experiments performed at room temperature showed that H2SO4 was most efficient at extracting magnesium from serpentinite, followed by HCl, HNO3, HCOOH and CH3COOH. Experiments for determining the dissolution kinetics was performed at temperatures of 30, 50 and 70 °C in 2 M solutions of H2SO4, HCl, and HNO3. At 70 °C temperatures all magnesium was extracted from serpentinite in each of the three acid solutions tested during 1-2 h. Also a large part of iron in serpentinite was extracted, while very little silicon dissolved (< 4%). The dissolution rate seemed to be limited by product layer diffusion for serpentinite particles with a size distribution of 74-125 μm. The apparent activation energies were 68 kJ mol- 1 for dissolution in H2SO4, 70 kJ mol- 1 for dissolution in HCl, and 74 kJ mol- 1 for dissolution in HNO3.
AB - Abundant resources of magnesium silicates make an interesting prospect for long-term storage of CO2 by mineral carbonation. Several carbonation processes proposed in literature for CO2 storage employ extraction of silicate minerals using a liquid solvent. In this study, the dissolution of natural serpentinite in respective solutions of acids, bases and ammonium salts has been investigated. Experiments performed at room temperature showed that H2SO4 was most efficient at extracting magnesium from serpentinite, followed by HCl, HNO3, HCOOH and CH3COOH. Experiments for determining the dissolution kinetics was performed at temperatures of 30, 50 and 70 °C in 2 M solutions of H2SO4, HCl, and HNO3. At 70 °C temperatures all magnesium was extracted from serpentinite in each of the three acid solutions tested during 1-2 h. Also a large part of iron in serpentinite was extracted, while very little silicon dissolved (< 4%). The dissolution rate seemed to be limited by product layer diffusion for serpentinite particles with a size distribution of 74-125 μm. The apparent activation energies were 68 kJ mol- 1 for dissolution in H2SO4, 70 kJ mol- 1 for dissolution in HCl, and 74 kJ mol- 1 for dissolution in HNO3.
KW - Extraction
KW - Kinetics
KW - Leaching
KW - Mineral carbonation
KW - Serpentine
KW - Serpentinite
UR - http://www.scopus.com/inward/record.url?scp=34249857647&partnerID=8YFLogxK
U2 - 10.1016/j.minpro.2007.04.001
DO - 10.1016/j.minpro.2007.04.001
M3 - Article
AN - SCOPUS:34249857647
SN - 0301-7516
VL - 83
SP - 36
EP - 46
JO - International Journal of Mineral Processing
JF - International Journal of Mineral Processing
IS - 1-2
ER -