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Crichton, W. A., Ross, N. L. (2000) Equation of state of phase E. Mineralogical Magazine, 64 (3) 561-567 doi:10.1180/002646100549427

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Reference TypeJournal (article/letter/editorial)
TitleEquation of state of phase E
JournalMineralogical Magazine
AuthorsCrichton, W. A.Author
Ross, N. L.Author
Year2000 (June)Volume64
Issue3
PublisherMineralogical Society
DOIdoi:10.1180/002646100549427Search in ResearchGate
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Mindat Ref. ID243175Long-form Identifiermindat:1:5:243175:2
GUID0
Full ReferenceCrichton, W. A., Ross, N. L. (2000) Equation of state of phase E. Mineralogical Magazine, 64 (3) 561-567 doi:10.1180/002646100549427
Plain TextCrichton, W. A., Ross, N. L. (2000) Equation of state of phase E. Mineralogical Magazine, 64 (3) 561-567 doi:10.1180/002646100549427
Abstract/NotesAbstractThe isothermal equation of state (EoS) of phase E, Mg1.96(7)Fe0.072(5)Si1.04(5)H3.7(8)O6, has been determined using high-pressure single-crystal X-ray diffraction. A third-order Birch Murnaghan EoS fit to pressue-volume data collected from room pressure and temperature to 6.7 GPa reveals that phase E has the lowest bulk modulus, KT = 92.9(7) GPa, and highest pressure derivative of the bulk modulus, K' = 7.3(2), for any dense hydrous magnesium silicate (DHMS) yet measured. A parameterized third-order Birch-Murnaghan EoS was also fit to the unit-cell parameters which display significant curvature with increasing pressure. This analysis shows that the c-axis (Kc = 89.1(10) GPa) is 6% more compressible than the a-axis (Ka = 94.8(6) GPa), with little of the anisotropy commonly observed in other layered structures. The high K' is indicative of the similarity to layers of the brucite structure. The introduction of interlayer cation polyhedra to the structure serves to reduce both the anisotropy, by reducing the compressibility perpendicular to the sheets, and the ability to shear, by increasing the coherence between layers.


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