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The true interatomic interactions are quantum mechanical in nature, and there is no known way in which the true interactions described by the Schrödinger equation or Dirac equation for all electrons and nuclei could be cast into an analytical functional form. Hence all analytical interatomic potentials are by necessity approximations.
In a simulation, the potential energy of an atom, , is given by [3] = (()) + (), where is the distance between atoms and , is a pair-wise potential function, is the contribution to the electron charge density from atom of type at the location of atom , and is an embedding function that represents the energy required to place atom of type into the electron cloud.
To extend the two atoms approach into solid, consider a simple model, say, a 1-D array of one element with interatomic distance of r, and the equilibrium distance is r 0. Its potential energy-interatomic distance relationship has similar form as the two atoms case, which reaches minimal at r 0, The Taylor expansion for this is:
The following table gives formula for the spring that is equivalent to a system of two springs, in series or in parallel, whose spring constants are and . [1] The compliance c {\displaystyle c} of a spring is the reciprocal 1 / k {\displaystyle 1/k} of its spring constant.)
Flexibility is the inverse of stiffness. For example, consider a spring that has Q and q as, respectively, its force and deformation: The spring stiffness relation is Q = k q where k is the spring stiffness. Its flexibility relation is q = f Q, where f is the spring flexibility. Hence, f = 1/k.
In physics, Hooke's law is an empirical law which states that the force (F) needed to extend or compress a spring by some distance (x) scales linearly with respect to that distance—that is, F s = kx, where k is a constant factor characteristic of the spring (i.e., its stiffness), and x is small compared to the total possible deformation of the spring.
It also features expanded tables and cases, improved notations and figures within the tables, consistent table and equation numbering, and verification of correction factors. The formulas are organized into tables in a hierarchical format: chapter, table, case, subcase, and each case and subcase is accompanied by diagrams.
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