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American Mineralogist; April 1998; v. 83; no. 3-4; p. 205-212
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Phase relation in the system MgO-NaCl-H 2 O; the dehydroxylation of brucite in the presence of NaCl-H 2 O fluids

T. B. Bai, and A. F. Koster van Groos

University of Illinois at Chicago, Department of Earth and Environmental Sciences, Chicago, IL, United States

The dehydroxylation of brucite was determined in the presence of NaCl-H 2 O fluids containing 0, 2, 6, 11, 14, 18, 30, and 38 mol% NaCl (0.0, 5.5, 17.0, 28.8, 34.5, 41.7, 58.2, and 66.6 wt% NaCl) to approximately 2500 bars and approximately 700 degrees C by high-pressure differential thermal analysis (HP-DTA). At pressures below 150 bars, brucite dehydrates in two separate reactions involving at least one intermediate phase. The dehydroxylation reaction of brucite at pressure to approximately 2 kbars follows InP(bars) = 22.23-13620/T(K). In the presence of NaCl-H 2 O fluids, the dehydroxylation temperature is lowered because of the reduction of the activity of H 2 O in these fluids. At 1 kbar pressure, mixing in the NaCl-H 2 O fluids is virtually ideal, assuming a nearly complete association of NaCl, but at 2 kbars, the dissociation of NaCl is substantial. The phase relations in the system MgO-NaCl-H 2 O show five univariant reactions emanating from an invariant assemblage, periclase + brucite + halite + liquid + vapor, located at 565+ or -5 degrees C and 440+ or -30 bars.

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J. Horita, T. Driesner, and D. R. Cole
Pressure Effect on Hydrogen Isotope Fractionation Between Brucite and Water at Elevated Temperatures
Science, November 19, 1999; 286(5444): 1545 - 1547.
[Abstract] [Full Text]




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