Abstract
The quartz-coesite transition was determined by reversed experiments in a piston-cylinder apparatus in the range 500-1200°C. The equilibrium transition boundary can be expressed as P (kbar) = 21.945 (±0.1855) + 0.006901 (± 0.0003)T (K). It is subparallel to, but ~1.5 kbar higher than, the transition boundary determined by Bohlen and Boettcher (1982). The entropy [39.56 ± 0.2 J/(mol.K)] and enthalpy of formation (-907.25 ± 0.007 kJ/mol) were also retrieved from elements of coesite at 1 bar, 298 K, from phase-equilibrium data and selected thermochemical data from the literature. From the characteristics of the hysteresis loop it is concluded that the practice of maintaining a constant nominal pressure by repeated pressure adjustment during an experiment leads to variation of pressure on the sample. -from Authors
| Original language | English (US) |
|---|---|
| Pages (from-to) | 231-238 |
| Number of pages | 8 |
| Journal | American Mineralogist |
| Volume | 80 |
| Issue number | 3-4 |
| DOIs | |
| State | Published - 1995 |
ASJC Scopus subject areas
- Geophysics
- Geochemistry and Petrology
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