Nesquehonite sequesters transition metals and CO2 during accelerated carbon mineralisation

Jessica Hamilton, Siobhan A. Wilson, Bree Morgan, Connor Charles Turvey, David Paterson, Colin MacRae, Jenine McCutcheon, Gordon Southam

Research output: Contribution to journalArticleResearchpeer-review

13 Citations (Scopus)


Acid leaching of ultramafic rocks to produce Mg2+- and Ca2+-rich solutions for mineral carbonation may inadvertently leach toxic trace metals. This study investigates the capacity of nesquehonite (MgCO3·3H2O), a common product of mineral carbonation at Earth's surface conditions, to sorb Cr, Ni, Mn, Co and Cu from solution. Our results demonstrate that upon precipitation, nesquehonite rapidly sequesters transition metals present in solution at concentrations from 10 to 100 mg/L. Trace metal uptake appears to occur by substitution for Mg2+ in the nesquehonite crystal structure, and also by incorporation into minor, metal-rich phases, such as Fe-oxyhydroxides. This indicates that first row transition metals will likely be trapped and stored within Mg-carbonate minerals produced in industrial mineral carbonation reactors and in landscapes modified to capture atmospheric CO2 via enhanced weathering. Thus, it is unlikely that trace metals will pose an environmental risk in the event of accidental release of wastewater.

Original languageEnglish
Pages (from-to)73-81
Number of pages9
JournalInternational Journal of Greenhouse Gas Control
Publication statusPublished - 1 Dec 2016


  • Carbon sequestration
  • Enhanced weathering
  • Mg-carbonate minerals
  • Mineral carbonation
  • Nesquehonite
  • Trace metals
  • X-ray fluorescence microscopy

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