The above expression gives value of internal energy for .
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We can assume that internal energy of a homogeneous and pure phase is a function of temperature and volume, so u = u ( T , v ) d u = ( ∂ T ∂ u ) v d T + ( ∂ v ∂ u ) T d v We know that heat capacity at constant volume is defined as c v = ( ∂ T ∂ u ) v , thus d u = c v d T + ( ∂ v ∂ u ) T d v ( 1 ) Now remember from Thermodynamic square that d u = T d s − P d v , where s is entropy, and divide both sides of this differential relation by d v in constant temperature to get ( ∂ v ∂ u ) T = T ( ∂ v ∂ s ) T − P ( 2 ) From Maxwell relations we know that ( ∂ v ∂ s ) T = ( ∂ T ∂ P ) v ; Put this back in ( 2 ) : ( ∂ v ∂ u ) T = T ( ∂ T ∂ P ) v − P And finally put the last relation in ( 1 ) : d u = c v d T + [ T ( ∂ T ∂ P ) v − P ] d v Therefore, this relation is true for both ideal and real gases.