Search results
Results From The WOW.Com Content Network
Hume-Rothery rules, named after William Hume-Rothery, are a set of basic rules that describe the conditions under which an element could dissolve in a metal, forming a solid solution. There are two sets of rules; one refers to substitutional solid solutions, and the other refers to interstitial solid solutions.
Substitutional solid solution strengthening occurs when the solute atom is large enough that it can replace solvent atoms in their lattice positions. Some alloying elements are only soluble in small amounts, whereas some solvent and solute pairs form a solution over the whole range of binary compositions.
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. Substitutional solid solutions, in accordance with the Hume-Rothery rules, may form if the solute and solvent have: Similar atomic radii (15% or less difference)
Notice the strain in the lattice that the solute atoms cause. The interstitial solute could be carbon in iron for example. The carbon atoms in the interstitial sites of the lattice creates a stress field that impedes dislocation movement. This is a schematic illustrating how the lattice is strained by the addition of substitutional solute.
Different atomic mechanisms of alloy formation, showing pure metal, substitutional, interstitial, and a combination of the two. When a molten metal is mixed with another substance, there are two mechanisms that can cause an alloy to form, called atom exchange and the interstitial mechanism. The relative size of each element in the mix plays a ...
Interstitial atoms (blue) occupy some of the spaces within a lattice of larger atoms (red) In materials science, an interstitial defect is a type of point crystallographic defect where an atom of the same or of a different type, occupies an interstitial site in the crystal structure.
This strengthening mechanism is related to solid-solution strengthening and has been observed in a variety of fcc and bcc substitutional and interstitial alloys, metalloids like silicon, and ordered intermetallics within specific ranges of temperature and strain rate. [1]
If the dominant crystallographic defect (mostly interstitial or substitutional point defects) involved in the solid-solution can be chemically intuited beforehand, then using some simple thermodynamic guidelines can considerably reduce the number of samples required to establish maximum solubility. [26]