MadSci Network: Earth Sciences |
Water, which is present in rocks in small quantities, is usually treated in its dissociated form as OH-. It is a "network modifier" which means that it disrupts the silicon-oxygen bonds and therefore disrupts the polymerization of silica tetrahedra that form the backbones of silicate minerals. Once disrupted, the minerals are much easier to melt, which simply involves further disruption. Since the structures take less energy to melt, they can melt at lower temperatures. Silicate melts do not consist of isolated ions or ionic groups, rather they contain long and short fragments of chains, sheets, and framework structures. These structures interfere with each other as the melt flows and so contribute to viscosity. As water is added, it not only lowers density, it also lowers viscosity. Water percentages in melts are usually given as weight percent. This can be misleading, since water has such low molecular weight compared to minerals. The mole percent water may be much higher. The equations needed to predict the thermodynamic relationships of minerals and melts are derived from simple thermodynamic relationships such as those for ideal gases. Unfortunately, the relationships for minerals are not simple, in part because the materials are not ideal and in part because the materials have such complex chemistries. The treatment of those equations is well beyond what I am capable of here. Whole books have been written on this subject. Go to GeoRef and search on mineral thermodynamics or melt thermodynamics. Go to a science bookstore or your professors and look for 'Thermodynamics of Minerals and Melts' or 'Physics and Chemisrty of Earth Materials', both by Alexandra Navrotsky, or Krauskoff's 'Thermodynamics for Geologists' (not sure if that is exactly the right name) or others. David Smith, Ph.D. Discovery Center of Science and Technology, Bethlehem, PA
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