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The Sackur–Tetrode equation is an expression for the entropy of a monatomic ideal gas. [ 1 ] It is named for Hugo Martin Tetrode [ 2 ] (1895–1931) and Otto Sackur [ 3 ] (1880–1914), who developed it independently as a solution of Boltzmann's gas statistics and entropy equations, at about the same time in 1912.
The inspiration for adopting the word entropy in information theory came from the close resemblance between Shannon's formula and very similar known formulae from statistical mechanics. In statistical thermodynamics the most general formula for the thermodynamic entropy S of a thermodynamic system is the Gibbs entropy
However, the heat transferred to or from the surroundings is different as well as its entropy change. We can calculate the change of entropy only by integrating the above formula. To obtain the absolute value of the entropy, we consider the third law of thermodynamics: perfect crystals at the absolute zero have an entropy =.
The Van 't Hoff equation has been widely utilized to explore the changes in state functions in a thermodynamic system. The Van 't Hoff plot, which is derived from this equation, is especially effective in estimating the change in enthalpy and entropy of a chemical reaction.
This law of entropy increase quantifies the reduction in the capacity of an isolated compound thermodynamic system to do thermodynamic work on its surroundings, or indicates whether a thermodynamic process may occur. For example, whenever there is a suitable pathway, heat spontaneously flows from a hotter body to a colder one.
As the entropy is a function of state the result is independent of the path. The above relation shows that the determination of the entropy requires knowledge of the heat capacity and the equation of state (which is the relation between P,V, and T of the substance involved). Normally these are complicated functions and numerical integration is ...
The laws of thermodynamics imply the following relations between these two heat capacities (Gaskell 2003:23): = = Here is the thermal expansion coefficient: = is the isothermal compressibility (the inverse of the bulk modulus):
The definition of the Gibbs function is = + where H is the enthalpy defined by: = +. Taking differentials of each definition to find dH and dG, then using the fundamental thermodynamic relation (always true for reversible or irreversible processes): = where S is the entropy, V is volume, (minus sign due to reversibility, in which dU = 0: work other than pressure-volume may be done and is equal ...