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Mills, S. J., Wilson, S. A., Dipple, G. M., Raudsepp, M. (2010) The decomposition of konyaite: importance in CO2 fixation in mine tailings. Mineralogical Magazine, 74 (5) 903-917 doi:10.1180/minmag.2010.074.5.903

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Reference TypeJournal (article/letter/editorial)
TitleThe decomposition of konyaite: importance in CO2 fixation in mine tailings
JournalMineralogical Magazine
AuthorsMills, S. J.Author
Wilson, S. A.Author
Dipple, G. M.Author
Raudsepp, M.Author
Year2010 (October)Volume74
Page(s)903-917Issue5
PublisherMineralogical Society
Download URLhttps://rruff.info/rruff_1.0/uploads/MM74_903.pdf+
DOIdoi:10.1180/minmag.2010.074.5.903Search in ResearchGate
Classification
Not set
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Not set
Mindat Ref. ID244111Long-form Identifiermindat:1:5:244111:9
GUIDf1e32185-3ec9-455c-85f1-f8cc30774cf7
Full ReferenceMills, S. J., Wilson, S. A., Dipple, G. M., Raudsepp, M. (2010) The decomposition of konyaite: importance in CO2 fixation in mine tailings. Mineralogical Magazine, 74 (5) 903-917 doi:10.1180/minmag.2010.074.5.903
Plain TextMills, S. J., Wilson, S. A., Dipple, G. M., Raudsepp, M. (2010) The decomposition of konyaite: importance in CO2 fixation in mine tailings. Mineralogical Magazine, 74 (5) 903-917 doi:10.1180/minmag.2010.074.5.903
Abstract/NotesThe sodium-magnesium hydrated double salt konyaite, Na2Mg(SO4)2·5H2O, has been studied by single-crystal X-ray diffraction and thermogravimetry on synthetic samples and by quantitative X-ray diffraction utilizing the Rietveld method on natural samples from the Mount Keith mine, Western Australia. Konyaite crystallizes in space group P21/c, with the cell parameters: a = 5.7594(10), b = 23.914(4), c = 8.0250(13) Å, β = 95.288(9)°, V = 1100.6(3) Å3 and Z = 4. The crystal structure has been refined to R1 = 3.41% for 2155 reflections [Fo>4σ(Fo)] and 6.44% for all 3061 reflections, with all atoms located.Quantitative phase analysis utilizing the Rietveld method was undertaken on five samples of konyaite-bearing mine tailings from the Mount Keith Nickel Mine, Western Australia. Konyaite was found to decompose over time and after 22 months had transformed to other sulphate and amorphous phases. Blödite did not increase in any ofthe samples indicating that konyaite may not always transform to blödite. Over the same time frame, synthetic konyaite completely decomposed to a mixture of thenardite (Na2SO4), hexahydrite (MgSO4·6H2O), blödite (Na2Mg(SO4)2·4H2O) and löweite (Na12Mg7(SO4)13). Detection of konyaite and other Mg-rich sulphates is important in terms of CO2 fixation. Magnesium bound to sulphate mineral phases reduces the overall potential of tailings piles to lock up atmospheric carbon in Mg carbonates, such as hydromagnesite. Amorphous sulphates are also highly reactive and may contribute to acid mine drainage ifpresent in large quantities, and may dissolve carbonate phases which have already sequestered carbon.

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LocalityCitation Details
Mount Keith Open Pit, Mount Keith, Wiluna Shire, Western Australia, Australia

Mineral Pages

MineralCitation Details
Konyaite

Mineral Occurrences

LocalityMineral(s)
Mount Keith Open Pit, Mount Keith, Wiluna Shire, Western Australia, Australia Antigorite, Blödite, Hexahydrite, Hydromagnesite, Konyaite, Lizardite, Magnesite, Thénardite, Woodallite


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