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29 - Framework silicates. Zeolites and ion exchange properties of minerals

from Part IV - A systematic look at mineral groups

Hans-Rudolf Wenk
Affiliation:
University of California, Berkeley
Andrei Bulakh
Affiliation:
St Petersburg State University
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Summary

The framework structure

Framework silicates contain a three-dimensional framework of tetrahedra, in which all oxygen atoms are bonded to two tetrahedral cations, resulting in a general formula with a T:O ratio 1:2. Tetrahedral ions can be silicon or aluminum with Al3+ ≤ Si4+. Quartz, SiO2, is an example with no aluminum, while anorthite (CaSi2Al2O8) is an example where aluminum and silicon are equal. The aluminum-containing framework silicates are referred to as alumosilicates with all aluminum atoms tetrahedral, contrary to the alumosilicates discussed in Chapter 26, where at least some aluminum is octahedral. The composition of framework silicates is quite simple compared to pyroxenes and amphiboles: the major cations are silicon and aluminum; in addition, large cavities in the framework may contain cations (e.g., K+, Na+, Ca2 +, Ba2 +, Sr2 +) as well as anions and anion groups (e.g., Cl-, CO2-3, SO2-4, NH+4 and H2O molecules). This is illustrated for scapolite in Figure 29.1. There are no octahedral building units that are an important part of all other silicate structures and therefore framework silicates do not contain octahedral cations (e.g., Mg2+, Fe2+). Among framework silicates, feldspars are most relevant and they have already been discussed in Chapter 19. (We will review some aspects of feldspar structures in this chapter.) Feldspathoids (e.g., nepheline, leucite) are a related group of anhydrous framework silicates, the main difference being that they are deficient in SiO2, and the structure needs to be able to accommodate more large alkali cations than do the alkali feldspars.

Type
Chapter
Information
Minerals
Their Constitution and Origin
, pp. 496 - 508
Publisher: Cambridge University Press
Print publication year: 2004

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References

Baerlocher, C., Meier, W. M. and Olson, D. H. (eds.) (2001). Atlas of Zeolite Framework Types, 5th edn. Elsevier, Amsterdam, 302pp
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Bish, D. L. and Ming, D. W. (eds.) (2001). Natural Zeolites. Occurrence, Properties and Applications. Rev. Mineral. Geochem., vol. 45, Mineralogical Society of America, Washington, DC, 654pp
Breck, D. W. (1974). Zeolite Molecular Sieves: Structure, Chemistry and Use. Wiley, New York, 771pp
Coombs, D. S. et al. (1997). Recommended nomenclature for zeolite minerals: Report of the Subcommittee on Zeolites of the International Mineralogical Association, Committee on New Minerals and Mineral Names. Can. Mineral., 35, 1571–1606
Deer, W. A., Howie, R. A. and Zussman, D. J. (1962). Rock-forming Minerals, vol. IV, Tectosilicates. Longman, London, 435pp
Gottardi, G. and Galli, E. (1985). Natural Zeolites. Springer-Verlag, Berlin, 409pp
Tsitsishvili, G. V., Andronikashvili, T. G., Kirov, G. N. and Filizova, L. D. (1992). Natural Zeolites. Ellis Horwood, New York, 295pp
Van Bekkum, H., Flanigen, E. M., Jansen, J. C. (eds.) (2001). Introduction to Zeolite Science and Practice. Elsevier, Amsterdam, 1062pp
Vaughan, D. J. and Pattrick, R. A. D. (eds.) (1995). Mineral Surfaces. Chapman & Hall, London, 370pp

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