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Ardit, M., Cruciani, G., Dondi, M., Garbarino, G. L., Nestola, F. (2014) Phase transitions during compression of thaumasite, Ca3Si(OH)6(CO3)(SO4)·12H2O: A high-pressure synchrotron powder X-ray diffraction study. Mineralogical Magazine, 78 (5) 1193-1208 doi:10.1180/minmag.2014.078.5.07

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Reference TypeJournal (article/letter/editorial)
TitlePhase transitions during compression of thaumasite, Ca3Si(OH)6(CO3)(SO4)·12H2O: A high-pressure synchrotron powder X-ray diffraction study
JournalMineralogical Magazine
AuthorsArdit, M.Author
Cruciani, G.Author
Dondi, M.Author
Garbarino, G. L.Author
Nestola, F.Author
Year2014 (October)Volume78
Page(s)1193-1208Issue5
PublisherMineralogical Society
DOIdoi:10.1180/minmag.2014.078.5.07Search in ResearchGate
Mindat Ref. ID244559Long-form Identifiermindat:1:5:244559:9
GUIDd17687de-83e5-4da6-a68f-620af3540e0b
Full ReferenceArdit, M., Cruciani, G., Dondi, M., Garbarino, G. L., Nestola, F. (2014) Phase transitions during compression of thaumasite, Ca3Si(OH)6(CO3)(SO4)·12H2O: A high-pressure synchrotron powder X-ray diffraction study. Mineralogical Magazine, 78 (5) 1193-1208 doi:10.1180/minmag.2014.078.5.07
Plain TextArdit, M., Cruciani, G., Dondi, M., Garbarino, G. L., Nestola, F. (2014) Phase transitions during compression of thaumasite, Ca3Si(OH)6(CO3)(SO4)·12H2O: A high-pressure synchrotron powder X-ray diffraction study. Mineralogical Magazine, 78 (5) 1193-1208 doi:10.1180/minmag.2014.078.5.07
Abstract/NotesAbstractThe high-pressure behaviour of the thaumasite structure was investigated using synchrotron powder X-ray diffraction, up to 19.5 GPa. Based on Rietveld refinements, thaumasite retained the roompressure P63space group throughout the whole investigated pressure range while the pressure dependence of the refined unit-cell parameters can be cast into three different compression regimes, each corresponding to a different thaumasite phase (th-I, th-II and th-III) related by isosymmetric phase transitions. In particular, the phase transition in the 7.40–15.02 GPa P-range (i.e. from th-II to th-III) is associated with an inversion of the axial bulk moduli which, by analogy with ettringite, can be rationalized as due to a change in the relative strengths of the iono-covalent bonds along the [Ca3Si(OH)6(H2O)12]4+columns parallel to the c axis vs. the O–H bonds linking the columns within the ab plane. The linear inverse relationship between the low- and high-temperature data from the literature with those collected under high-pressure conditions reveals that the same bonding regime governs the anisotropic expansion and contraction of thaumasite up to ~1.4 GPa and 400 K (HP-HT stability limits of th-I phase).


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