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Compositional variation of a crystalline substance due to substitution or omission of various atomic constituents within a crystal structure. Solid solutions can be classified as substitutional, interstitial, or omissional. They may also be categorized by the nature of their thermodynamic properties, such as enthalpy, entropy, and free energy (for example ideal, nonideal, and regular solid solutions).
The concept of solid solution can be understood by considering a specific mineral group such as olivine. Although olivine-group minerals may exhibit a range of compositions they all have a similar crystal structure. Thus all of the minerals in the olivine group are isostructural (having a similar crystal structure). Yet within this structural framework, compositions vary considerably. Such chemical variation can be described by defining the nature and extent of the atomic substitutions involved or by describing intermediate compositions in terms of limiting end-member compositions. In addition to substitution within the crystal structure, compositional variation may take place by interstitial substitution or omission solid solution. Interstitial solid solution occurs when ions or atoms occupy a position in a crystal structure that is usually vacant. Omission solid solution occurs when an atom or ion is missing from a specific crystallographic position. See also Olivine.
Solid solution is widespread among minerals. In fact, very few naturally occurring minerals exist as pure end-member substances but exhibit trace to extensive solid solution. The extent of solid solution depends upon the relative sizes of the atoms or ions involved, the charges of the ions, the coexistence and composition of other minerals or liquid (for example, magma), and the temperature and pressure conditions of formation (with temperature having a more pronounced effect).
| Dental Dictionary: solid solution |
An alloy all of whose constituents are mutually soluble in the solid state.
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A solid solution is a solid-state solution of one or more solutes in a solvent. Such a mixture is considered a solution rather than a compound when the crystal structure of the solvent remains unchanged by addition of the solutes, and when the mixture remains in a single homogeneous phase.This often happens when the two elements (generally metals) involved are close together on the periodic table; conversely, a chemical compound is generally a result of the non proximity of the two metals involved on the periodic table.[1]
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The solute may incorporate into the solvent crystal lattice substitutionally, by replacing a solvent particle in the lattice, or interstitial, by fitting into the space between solvent particles. Both of these types of solid solution affect the properties of the material by distorting the crystal lattice and disrupting the physical and electrical homogeneity of the solvent material.[2]
Some mixtures will readily form solid solutions over a range of concentrations, while other mixtures will not form solid solutions at all. The propensity for any two substances to form a solid solution is a complicated matter involving the chemical, crystallographic, and quantum properties of the substances in question. Solid solutions, in accordance with the Hume-Rothery rules, may form if the solute and solvent have:
The phase diagram in Fig. 1 displays an alloy of two metals which forms a solid solution at all relative concentrations of the two species. In this case, the pure phase of each element is of the same crystal structure, and the similar properties of the two elements allow for unbiased substitution through the full range of relative concentrations.
Solid solutions have important commercial and industrial applications, as such mixtures often have superior properties to pure materials. Many metal alloys are solid solutions. Even small amounts of solute can affect the electrical and physical properties of the solvent.
The binary phase diagram in Fig. 2 at right shows the phases of a mixture of two substances in varying concentrations, α and β. The region labeled "α" is a solid solution, with β acting as the solute in a matrix of α. On the other end of the concentration scale, the region labeled "β" is also a solid solution, with α acting as the solute in a matrix of β. The large solid region in between the α and β solid solutions, labeled "solid α and β", is not a solid solution. Instead, an examination of the microstructure of a mixture in this range would reveal two phases — solid solution α-in-β and solid solution β-in-α would form separate phases, perhaps lamella or grains.
In the phase diagram, the unalloyed extreme left and right concentrations, and the dip in the center, the material will be solid and become liquid as heat is added, where at other proportions the material will enter a mushy or pasty phase. The mixture at dip point of the diagram is called a eutectic alloy. Lead-tin mixtures formulated at that point (37/63 mixture) are useful when soldering electronic components, particularly if done manually, since the solid phase is quickly entered as the solder cools. In contrast, when lead-tin mixtures were used to solder seams in automobile bodies a pasty state enableed a shape to be formed with a wooden paddle or tool, so a 70-30 lead to tin ratio was used. (Lead is being removed from such applications owing to its toxicity and consequent difficulty in recycling devices and components that include lead.)
When a solid solution becomes unstable — due to a lower temperature, for example — exsolution occurs and the two phases separate into distinct microscopic to megascopic lamellae. An example of this is the alkali feldspar mineral variety perthite in which thin white albite layers alternate between typically pink microcline.
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