Skip to main content Accessibility help
×
Hostname: page-component-77c89778f8-fv566 Total loading time: 0 Render date: 2024-07-24T23:42:39.015Z Has data issue: false hasContentIssue false
This chapter is part of a book that is no longer available to purchase from Cambridge Core

26 - Orthosilicates and ring silicates. Metamorphic mineral assemblages

from Part IV - A systematic look at mineral groups

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

Summary

General comments on silicates

Silicate minerals constitute over 90 vol.% of the earth's crust and are thus the most common minerals that we encounter. Like other ionic compounds, silicate structures are built up of coordination polyhedra, mainly tetrahedra and octahedra. Among the elements in the crust, oxygen (47 atomic%), silicon (28%), aluminum (8%), iron (5%), and calcium (4%) are the most abundant, and therefore minerals containing silica in combination with these other elements dominate. We have already discussed some silicate minerals in Chapter 19, namely feldspars and silica minerals. In the next four chapters we take a closer look at the large variety of silicates and their significance as rock-forming minerals.

The Si-O bond is only about half ionic, while the remainder is covalent. The covalent Si 3p3- O 2p hybrid bonds (Figure 26.1) have directional properties, contrary to the spherical symmetry of electrostatic attraction in ionic bonding. Because of this, silicates in general have low crystal symmetry, a high anisotropy of physical properties and a complex crystal structure with large unit cells. The bonds define a coordination tetrahedron SiO44-, which is the basic building unit of silicate minerals (see also Figure 19.2).

There are several important cation substitutions in silicates, on tetrahedral, octahedral and larger structural sites (Table 19.2). It is significant that some of these substitutions are between ions of different charge.

Type
Chapter
Information
Minerals
Their Constitution and Origin
, pp. 425 - 447
Publisher: Cambridge University Press
Print publication year: 2004

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Deer, W. A., Howie, R. A. and Zussman, D. J. (1962), Rock-forming Minerals, vol. 1, Ortho- and Ring Silicates. Longman, London, 333pp
Deer, W. A., Howie, R. A. and Zussman, D. J. (1982), Rock-forming Minerals, 2nd edn, vol. 1a, Orthosilicates. Longman, London, 912pp
Kerrick, D. M. (1990). The Al2SiO5Polymorphs. Rev. Mineral., vol. 22, Mineralogical Society of America, Washington, DC, 406pp
Liebau, F. (1985). Structural Chemistry of Silicates. Structure, Bonding, Classification. Springer-Verlag, Berlin, 347ppCrossRef

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×