Chamosite
| Chamosite | |
|---|---|
 A 3.6 by 2.2 cm of Axinite-Fe covered on both sides by greenish microcrystals of Chamosite | |
| General | |
| Category | Phyllosilicate |
| Formula (repeating unit) | (Fe2+,Mg)5Al(AlSi3O10)(OH)8 |
| IMA symbol | Chm[1] |
| Strunz classification | 9.EC.55 |
| Crystal system | Monoclinic |
| Crystal class | Prismatic (2/m) (same H-M symbol) |
| Space group | C2/m |
| Unit cell | a = 5.37 Å, b = 9.3 Å, c = 14.22 Å; β = 97.88°; Z = 2 |
| Identification | |
| Color | Green, grey-green, black |
| Mohs scale hardness | 3 |
| References | [2][3][4] |
Chamosite is the Fe2+end member of the chlorite group. A hydrous aluminium silicate of iron, which is produced in an environment of low-to-moderate-grade metamorphosed iron deposits, as gray or black crystals in oolitic iron ore. Like other chlorites, it is a product of the hydrothermal alteration of pyroxenes, amphiboles and biotite in igneous rock. The composition of chlorite is often related to that of the original igneous mineral, so that more Fe-rich chlorites are commonly found as replacements of the Fe-rich ferromagnesian minerals (Deer et al., 1992).
History
[edit]In 1820, Pierre Bertier, a mineralogist and mining engineer from Nemours, France, discovered chamosite. The new mineral was found in an area of low-to-moderate-grade metamorphosed iron deposits. Early samples of chamosite (which is a chlorite) stirred some controversy after they were found to possess the structure of kaolin rather than chlorite; however, further research proved that chamosite was found in nature largely alongside another phyllosilicate called berthierine, which has a kaolin-type structure and is rather difficult to distinguish from chamosite. Chamosite is named after the municipality of Chamoson, between Sion and Martigny, in the canton of Valais, Switzerland.
Structure
[edit]X-ray diffraction (XRD) indicates that the proportion of 7 Å B layers in bertherine-chamosite ranges from 5 to 28%, and chemical analysis by scanning electron microscope-energy-dispersive X-ray spectroscopy (SEM-EDS) indicates positive correlation between %B and Fe/(Fe + Mg) (Ryan and Hillier, 2002). The chamosite structure is very similar to typical chlorite in which they are alternated regular layers with tetrahedral and tri-octahedral components (Rivas Sanchez et al., 2006). Its 2:1 layer structure is similar to that of mica, with a basal spacing of 14 Å. (Rivas Sanchez et al., 2006). In most common chlorites, there are 12.0 octahedral cations per O20(OH)16 and approximately equivalent amounts of aluminium in tetrahedral and octahedral sites [e.g. the magnesia chlorite, clinochlore, (Mg10Al2)(Si6Al2O20)(OH)16] (Deer et al., 1992).
Physical properties
[edit]Chamosite has a laminar shape; sheets measure from 20 to 200 μm (Rivas Sanchez et al., 2006). Chamosite may be greenish-gray or brown in color. The cleavage is length-slow; the orientation may be α ∧ c=small, β=b, γ ∧ α=small, optic plane= [0 10] (Heinrich, 1965) and has good cleavage on the {001} axis. It has a dull luster and grayish-green streak. Birefringence is much lower than that of the micas, illite, montmorillonite and vermiculite, and refractive indices are higher than those of kaolinite (Deer et al. 1992). The chamosite spectra shows the reflection d=7.18 Å (main value of the chlorite) and the reflection d=14.4 Å (that confirms the presence of chlorite) (Rivas Sanchez et al., 2006).
Geologic occurrence
[edit]Chamosite is a relatively uncommon mineral in nature. Since its discovery in Chamoson, only about 15 localities around the world are known to be associated with iron deposits. Chamosite may be found in occurrence with other chlorite minerals. In recent years, berthierine, a more abundant chlorite, was discovered in occurrence with chamosite in the iron deposit of Peña Colorada, Mexico. Chamosite is related to the beginning of a hydrothermal phase and occurs mainly in a mineralized breccia type stock-work in which it fills open spaces and replaces the hot rock through fissures (Rivas Sanchez et al., 2006). The Mamu-Nkporo formation in the locality of Okigwe, Nigeria, was studied by Akande and Mucke (1993), and they concluded that the carbonate discovered with associated chamosite was formed in a shallow marine subtidal to intertidal environment developed during periods of rise and fall in sea level. Formations of chamosite-bearing oolites record periods of increasing wave energy corresponding to storm conditions between quiet shallow marine sedimentation (Akande and Mucke, 1993). Chamosite is a mineral from which elements may be extracted for commercial purpose. Xuanwei City in Yunnan Province has one of the highest lung cancer mortality rates in China (Dai et al., 2008). This epidemic had long been blamed on hydrocarbons released from the burning of coal. Dai et al. (2008) conducted a mineralogical and geochemical study of coal from two coal mines in this region, and identified chamosite as one of the main minerals in the coal. The chamosite was suspected as the main carcinogen for local high lung cancer incidence in Xuanwei.
References
[edit]- ^ Warr, L.N. (2021). "IMA–CNMNC approved mineral symbols". Mineralogical Magazine. 85 (3): 291–320. Bibcode:2021MinM...85..291W. doi:10.1180/mgm.2021.43. S2CID 235729616.
- ^ Webmineral.com
- ^ Mindat.org
- ^ Handbook of Mineralogy
Further reading
[edit]- Akande, S.O.; Mucke, A. (1993). "Depositional environment and diagnosis of carbonates at the Mamu-Nkporo formation, Anambra basin, Southern Nigeria". Journal of African Earth Sciences. 17 (4): 445–456. Bibcode:1993JAfES..17..445A. doi:10.1016/0899-5362(93)90003-9.
- Brindley, G.W.; Youell, R.F. (1953). "Ferrous chamosite and ferric chamosite". Mineralogical Magazine and Journal of the Mineralogical Society. 30 (220): 57–70. Bibcode:1953MinM...30...57B. doi:10.1180/minmag.1953.030.220.07.
- Dai, S.; Chou, C.L. (2007). "Occurrence and origin of minerals in a chamosite-bearing coal of Late Permian age, Zhaotong, Yunnan, China". American Mineralogist. 92 (8–9): 1253–1261. Bibcode:2007AmMin..92.1253D. doi:10.2138/am.2007.2496. S2CID 55597302.
- Dai, S.; Tian, L.; Chou, C.L.; Zhou, Y.; Zhang, M.; Zhao, L.; Wang, J.; Yang, Z.; Cao, H.; Ren, D. (2008). "Mineralogical and compositional characteristics of Late Permian coals from an area of high lung cancer rate in Xuan Wei, Yunnan, China: Occurrence and origin of quartz and chamosite". International Journal of Coal Geology. 76 (4): 318–327. doi:10.1016/j.coal.2008.09.001.
- Deer, W.A.; Howie, R.A.; Zussman, J. (1992). An introduction to the rock-forming minerals. Prentice Hall.
- Delaloye, M.F.; Odin, G.S. (1988). Chamosite, the green marine clay from Chamoson; A study of Swiss oolitic ironstones. ISBN 978-0-444-87120-6.
- Heinrich, E.W. (1965). Microscopic Identification of Minerals. McGraw-Hill.
- Iijima, A.; Matsumoto, R. (1982). "Berthierine and Chamosite in coal measures of Japan". Clays and Clay Minerals. 30 (4): 264–274. Bibcode:1982CCM....30..264I. doi:10.1346/ccmn.1982.0300403.
- Rivas Sanchez, M.L.; et al. (2006). "Berthierine and chamosite hydrothermal: Genatic guides in the Peña Colorada magnetite-ore bearing deposit". Earth Planets Space. 58: 1389–1400. doi:10.1186/BF03352635.
- Ryan, P.C.; Hillier, S. (2002). "Berthierine / Chamosite and discrete chlorite from evolved Verdine and evaporate-associated facies in the Jurassic sundance formation, Wyoming". American Mineralogist. 87: 1607–1615. doi:10.2138/am-2002-11-1210. S2CID 16947162.
- Saccocia, P.J.; Seyfried, W.E. (1993). "A resolution of discrepant thermodynamic properties For chamosite retrieved from experimental and empirical techniques". American Mineralogist. 78: 607–611.
- Youell, R.F. (1955). "Mineralogy and Crystal structure of chamosite". Nature. 176 (4481): 560–561. Bibcode:1955Natur.176..560Y. doi:10.1038/176560b0. S2CID 4160997.
