Natural and synthetic ferroglaucophane |
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| Authors: | Christoph Hoffmann |
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| Institution: | 1. Department of Geology, University of California, 90024, Los Angeles, California
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| Abstract: | Amphiboles approximating the composition of the ferroglaucophane end member, Na2Fe3Al2Si8O22(OH)2, have not been found in nature prior to 1969. Chemical, physical and petrologic data of four specimens of that mineral are given, two from Southern Italy and two from New Caledonia (Black, 1970). The ferroglaucophane end member was synthesized in seeded runs at 500° C, 5000 bars fluid pressure with oxygen fugacity defined by the wüstite-magnetite (WM) buffer. X-ray data and cell dimensions (a=9.686 Å, b=17.89, c=5.317, β=103° 45.2′ V=894.9 Å3) are presented along with microprobe data that confirm the end member composition. Under these conditions of synthesis the ferroglaucophane grew metastably, however. Stability relations of the synthetic end member and of one natural specimen were investigated in a temperature range from 250° C to 500° C and at 3 and 5 kb with different oxygen buffers. At relatively low oxygen fugacities (WM buffer, QFM buffer) ferroglaucophane breaks down above 350–360° C. Under more oxidizing conditions (HM buffer) ferroglaucophane may not be stable even at very low temperatures. Mineral facies and chemical bulk composition of rocks that would favor the natural occurrence of ferroglaucophane are discussed. As assemblages with ferroglaucophane can have crystallized only below a very specific upper temperature limit, it is proposed to direct some attention towards that mineral. |
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