110 Coal Geology (Posters)
VAPOUR DEPOSITION OF ARSENIC-BEARING MINERALS ORIGINATING FROM A BURNING CULM BANK: ST. ETIENNE, THE LOIRE REGION, FRANCE
Paper number: 110-10
Program: Technical Sessions
Time: 1:30 PM – 5:30 PM
Authors
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M. Naze-Nancy Masalehdani Presenting AuthorUniversité des Sciences et Technologie de Lille 1, Lille, N/A
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Yves PaquetteINERIS, Verneuil-en-Halatte, N/A
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Jean-Luc BouchardonEcole Nationale Supérieure Des Mines, Saint Etienne, N/A
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Bernard GuyEcole Nationale Supérieure Des Mines, Saint Etienne, N/A
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Glenn B. StracherEast Georgia College, Swainsboro, GA
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Jean ChalierSaint Etienne, N/A
Abstract
Ion-coupled plasma mass spectrometry and energy dispersive spectrometry-scanning electron microscopy analyses of unbaked shales, the main component of the culm bank, revealed that they are naturally rich in arsenic and sulphur (pyrite and/or arsenopyrite), the primary source of arsenic and sulphur in the coal-fire minerals, whereas porcellainites (baked shales) contain higher concentrations of iron-oxides (mainly hematite). The oxidation of sulphide minerals in the shales during baking possibly mobilized arsenic and sulphur into a gas phase, concentrating iron oxides in the porcellanites. Fluorine originated from muscovite and/or fluorapatite in the shales and antimony is thought to have originally been in solid solution with the Fe-sulphides. The source of bismuth is unknown.
The minerals described herein were formed from harmful coal-fire gas components (NOx, SOx, AsOx, HCl, etc.), harmful to human health. The minerals are soluble in water and a potential environmental hazard because of the slow but prolonged release of their toxins into the hydrologic system. Consequently, the study of minerals that form from burning culm banks is worthy of intense research.