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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
1

Pyrite porphyroblast paragenesis at the Cherokee Mine, Ducktown, Tennessee

Brooker, Donald Duane January 1984 (has links)
Pyrite porphyroblasts up to 300 mm in size are common in the polymetamorphosed, iron-rich, stratabound, massive sulfide ore at the Cherokee Mine, Ducktown, Tennessee. These porphyroblasts contain abundant inclusions of sphalerite, calcite, and micas that are used to determine the paragenesis of the porphyroblasts and the metamorphic history of the ore deposit. The ore mineralogy at the mine is: hexagonal pyrrhotite (60%), pyrite (30%), chalcopyrite (4%), sphalerite (3 %), and magnetite (3 %) with minor galena, molybdenum, tetrahedrite, bismuth, ilmenite, and rutile. The ore body is interpreted to have been syngenetic and to have contained both primary pyrrhotite and primary pyrite: additional pyrite may have formed as crusty accretions resulting from oxidation of primary pyrrhotite shortly after deposition. The early pyrites were later deformed and acted as seeds for the formation of the larger porphyroblasts by Ostwald ripening, and by the annealing of small pyrite grains into larger porphyroblasts, during isochemical metamorphism. Sphalerite geobarometry indicates initial growth of the pyrite porphyroblasts began at 6.8± 0.8 kilobars and that many sphalerite grains underwent some degree of re-equilibration at a later stage. Fluid inclusions formed during retrograde metamorphism have salinities near 12 % NaCl with a vapor phase rich in CO₂. Pyrrhotite-pyrite compositional profiles indicate at least partial re-equilibration of hexagonal pyrrhotite down to about 270°C. At lower temperatures further compositional re-equilibration was probably prevented, because the coexisting pyrite was too refractory to release the sulfur needed for the hexagonal pyrrhotite to react to monoclinic pyrrhotite. / Master of Science

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