- Thermodynamic free energy
In

thermodynamics , the term**thermodynamic free energy**refers to the amount of work that can be extracted from asystem , and is helpful inengineering applications. It is a subtraction of theentropy of a system ("useless energy") from the total energy, yielding a thermodynamicstate function which represents the "useful energy".**Overview**In short, free energy is that portion of any First-Law energy that is available for doing thermodynamic work; "i.e.", work mediated by thermal energy. Since free energy is subject to

irreversible loss in the course of such work and First-Law energy is always conserved, it is evident that free energy is an expendable, Second-Law kind of energy that can make things happen within finite amounts of time.The free energy functions are Legendre transforms of the

internal energy . For processes involving a system atconstant pressure "p" andtemperature "T", theGibbs free energy is the most useful because, in addition to subsuming any entropy change due merely to heatflux , it does the same for the "p"d"V" work needed to "make space for additional molecules" produced by various processes. (Hence its utility tosolution -phase chemists, including biochemists.) TheHelmholtz free energy has a special theoretical importance since it is proportional to thelogarithm of the partition function for thecanonical ensemble instatistical mechanics . (Hence its utility to physicists; and togas -phase chemists and engineers, who do not want to ignore "p"d"V" work.)The (historically earlier)

Helmholtz free energy is defined as "A" = "U" − "TS", where "U" is the internal energy, "T" is the absolute temperature, and "S" is theentropy . Its change is equal to the amount of reversible work done on, or obtainable from, a system at constant "T". Thus its appellation "work content ", and the designation "A" from "arbeit", the German word for work. Since it makes no reference to any quantities involved in work (such as "p" and "V"), the Helmholtz function is completely general: its decrease is the maximum amount of work which can be done "by" a system, and it can increase at most by the amount of work done "on" a system.The

Gibbs free energy "G" = "H" − "TS", where "H" is theenthalpy . ("H" = "U" + "pV", where "p" is the pressure and "V" is the volume.)There has been historical controversy:

* Inphysics , “free energy” most often refers to the "Helmholtz free energy ", denoted by "F".

* Inchemistry , “free energy” most often refers to the "Gibbs free energy ".Since both fields use both functions, a

compromise has been suggested, using "A" to denote the Helmholtz function, with "G" for the Gibbs function. While "A" is preferred byIUPAC , "F" is sometimes still in use, and the correct free energy function is often implicit in manuscripts and presentations.**Application**The

experiment al usefulness of these functions is restricted to conditions where certain variables ("T", and "V" or "external" "p") are held constant, although they also have theoretical importance in derivingMaxwell relations . Work other than "p"d"V" may be added, e.g., for electrochemical cells, or**"f ˑ**"d**"x**" work in elastic materials and inmuscle contraction. Other forms of work which must sometimes be considered are stress-strain, magnetic, as in adiabatic demagnetization used in the approach toabsolute zero , and work due to electric polarization. These are described bytensor s.In most cases of interest there are internal degrees of freedom and processes, such as

chemical reaction s andphase transition s, which create entropy. Even for homogeneous "bulk" materials, the free energy functions depend on the (often suppressed) composition, as do all properthermodynamic potentials (extensive functions), including the internal energy."N"

_{"i"}is the number of molecules (alternatively, moles) of type "i" in the system. If these quantities do not appear, it is impossible to describe compositional changes. The differentials for "reversible processes" are (assuming only "pV" work):$mathrm\{d\}A\; =\; -\; p,mathrm\{d\}V\; -\; Smathrm\{d\}T\; +\; sum\_i\; mu\_i\; ,mathrm\{d\}N\_i,$

:$mathrm\{d\}G\; =\; Vmathrm\{d\}P\; -\; Smathrm\{d\}T\; +\; sum\_i\; mu\_i\; ,mathrm\{d\}N\_i,$

where μ

_{"i"}is thechemical potential for the "i"-th component in the system. The second relation is especially useful at constant "T" and "p", conditions which are easy to achieve experimentally, and which approximately characterize living creatures.:$(mathrm\{d\}G)\_\{T,p\}\; =\; sum\_i\; mu\_i\; ,mathrm\{d\}N\_i,$

Any decrease in the Gibbs function of a system is the upper limit for any isothermal, isobaric work that can be captured in the

surroundings , or it may simply be dissipated, appearing as "T" times a corresponding increase in the entropy of the system and/or its surrounding.**ee also***

Gibbs free energy

*Helmholtz free energy

*Exergy

*Merle Randall

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2010.*