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Infrared Study of CO2 Incorporation into Pyrophyllite [Al2Si4O10(OH)2] during Dehydroxylation

Published online by Cambridge University Press:  01 January 2024

Ling Wang
Affiliation:
College of Materials and Bioengineering, Chengdu University of Technology, Chengdu, 610059, Sichuan, PR China
Ming Zhang*
Affiliation:
Department of Earth Sciences, University of Cambridge, Downing Street, Cambridge CB2 3EQ, UK
Simon A. T. Redfern
Affiliation:
Department of Earth Sciences, University of Cambridge, Downing Street, Cambridge CB2 3EQ, UK Research School of Earth Sciences, Australian National University, Mills Road, Canberra, ACT 0200, Australia
*
*E-mail address of corresponding author: mz10001@esc.cam.ac.uk

Abstract

We report infrared spectroscopic observations of the incorporation of CO2 into pyrophyllite that has been heated between 200°C and 1250°C for periods of 15 min, 1 h and 5 days. The presence of CO2 is characterized by the ν3 band of CO2 near 2347 cm−1, detectable in samples in which dehydroxylation has commenced after heating above 450°C. With increasing temperature, the CO2 signal becomes more intense. The signal reaches its maximum intensity near 800°C with an annealing time of 15 min. Further heating leads to a decrease in the CO2 signal and the occurrence of an extra signal near 2156 cm−1 that implies the presence of CO. The process is characterized by significant time-dependence, indicating its kinetic nature. The peak positions of CO2 signals show systematic variations with temperature. Our results suggest that the CO2 molecule is associated with the local structure rather than being present as free gaseous CO2, and that the local structure of pyrophyllite is gradually modified during high-temperature treatments. However, no signals related to carbonate molecules ((CO32−)) were detected. The results suggest that CO2 or other carbon-based molecules may diffuse into some clay minerals during dehydroxylation and may become altered due to structural modifications at high temperatures. This may have significance for possible CO2 sequestration in shales and clay formations.

Type
Research Article
Copyright
Copyright © 2003, The Clay Minerals Society

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References

Bailey, S.W., (1966) The status of clay mineral structures Clays and Clay Minerals 14 123 10.1346/CCMN.1966.0140101.Google Scholar
Bearat, H. McKelvy, M.J. Chizmeshya, A.V.G. Sharma, R. and Carpenter, R.W., (2002) Magnesium hydroxide dehydroxylation/carbonation reaction processes: implications for carbon dioxide mineral sequestration Journal of the American Ceramic Society 85 742748 10.1111/j.1151-2916.2002.tb00166.x.Google Scholar
Brooker, R.A. Kohn, S.C. Holloway, J.R. and McMillian, P.F., (2001) Structural controls on the solubility of CO2 in silicate melts Par II: IR characteristics of carbonate groups in silicate glasses Chemical Geology 174 241254 10.1016/S0009-2541(00)00318-1.Google Scholar
Butt, D.P. Lackner, K.S. Wendt, C.H. Conzone, S.D. Kung, H. Lu, Y.C. and Bremser, J.K., (1996) Kinetics of thermal dehydroxylation and carbonation of magnesium hydroxide Journal of the American Ceramic Society 79 18921898 10.1111/j.1151-2916.1996.tb08010.x.Google Scholar
Drits, V.A. Besson, G. and Muller, F., (1995) An improved model for structural transformations of heat-treated aluminous dioctahedral 2:1 layer silicates Clays and Clay Minerals 43 718731 10.1346/CCMN.1995.0430608.Google Scholar
Fine, G. and Stolper, E., (1985) The speciation of carbon dioxide in sodium aluminosilicate glasses Contributions to Mineralogy and Petrology 91 105121 10.1007/BF00377759.Google Scholar
Fitzgerald, J.J. Dec, S.F. and Hamza, A.I., (1989) Observation of five-coordinated Al in prophyllite dehydroxylate by solid-state 27Al NMR spectroscopy at 14 T American Mineralogist 74 1405 1408.Google Scholar
Fitzgerald, J.J. Hamza, A.I. Dec, S.F. and Bronnimann, C.E., (1996) Solid-state 27Al and 29Si NMR and 1H CRAMPS studies of the 2:1 phyllosilicate pyrophyllite Journal of Physical Chemistry 100 1735117360 10.1021/jp961499f.Google Scholar
Frost, R.L. and Barron, P.F., (1984) Solid-state silicon-29 and aluminium-27 nuclear magnetic resonance investigation of the dehydroxylation of pyrophyllite Journal of Physical Chemistry 88 62066209 10.1021/j150669a030.Google Scholar
Guggenheim, M. Chang, Y.H. and van Koster Groos, A.F., (1987) Muscovite dehydroxylation: High-temperature studies American Mineralogist 72 537 550.Google Scholar
Heller, L., (1962) The thermal transformation of pyrophyllite to mullite American Mineralogist 47 156 157.Google Scholar
Heller, L. Farmer, V.C. Mackenzie, R.C. Mitchell, B.D. and Taylor, H.F.W., (1962) The dehydroxylation and rehydroxylation of triphormic dioctahedral clay minerals Clay Minerals Bulletin 5 5672 10.1180/claymin.1962.005.28.02.Google Scholar
Kloprogge, J.T. and Frost, R.L. (1999) An infrared emission spectroscopic study of synthetic and natural pyrophyllite. Neues Jahrbuch für Mineralogie Monatshefte, 6274.Google Scholar
MacKenzie, K.J.D. Brown, I.W.M. Meinhold, R.H. and Bowden, M.E.J., (1985) Thermal reactions of pyrophyllite studied by high-resolution solid-state 27Al and 29Si nuclear magnetic resonance spectroscopy Journal of the American Ceramic Society 68 266272 10.1111/j.1151-2916.1985.tb15320.x.Google Scholar
Muller, F. Drits, V. Plançon, A. and Robert, J.L., (2000) Structural transformation of 2:1 dioctahedral layer silicates during dehydroxylation-rehydroxylation reactions Clays and Clay Minerals 48 572585 10.1346/CCMN.2000.0480510.Google Scholar
Mysen, B.O., (1976) The role of volatiles in silicate melts: Solubility of carbon dioxide and water in feldspar, pyroxene and feldspathoid melts to 30 Kb and 1625C American Journal of Science 276 969996 10.2475/ajs.276.8.969.Google Scholar
Nakamoto, K., (1978) Infrared and Raman Spectra of Inorganic and Coordination Compounds New York John Wiley and Sons 448 pp.Google Scholar
Rayner, J.H. and Brown, G., (1966) Structure of pyrophyllite Clays and Clay Minerals 25 73 84.Google Scholar
Taylor, W.R., (1990) The dissolved (CO3)2− in alumino-silicate melts — Infrared spectroscopic constraints on the cationic environment of dissolved (CO3)2− European Journal of Mineralogy 2 547563 10.1127/ejm/2/5/0547.Google Scholar
Wang, L. (1994) Metallogeny of pyrophyllite in the coastal region of Southeast China and pyrophyllite’s thermal stability. PhD thesis, Changsha Institute of Geotectonics, Chinese Academy of Sciences (in Chinese).Google Scholar
Wang, L. and Zhang, Z.Y., (1997) High-temperature phases of pyrophyllite and their evolutionary characteristics Chinese Science Bulletin 42 140143 10.1007/BF03182788.Google Scholar
Wang, L. Zhang, M. Redfern, S.A.T. and Zhang, Z.Y., (2002) Dehydroxylation and transformations of the 2:1 phyllosilicate pyrophyllite at elevated temperatures: An infrared spectroscopic study Clays and Clay Minerals 50 272283 10.1346/000986002760832874.Google Scholar
Wang, P. Pan, Z.L. and Weng, L.B., (1984) Systematic Mineralogy Beijing Geological Publishing House 522 pp.Google Scholar
Wardle, R. and Brindley, G.W., (1972) The crystal structures of pyrophyllite, 1Tc, and of its dehydroxylate American Mineralogist 57 732 750.Google Scholar
White, B.W. and Farmer, V.C., (1974) The carbonate minerals The Infrared Spectra of Minerals London Mineralogical Society 227284 10.1180/mono-4.12.Google Scholar