As we noted in the previous part, the (isothermal) force on a rubber band follows Hooke's Law for small displacements . Interestingly, the force constant is proportional to the temperature with the proportionality factor .
Now consider the case where the rubber band is stretched very quickly so that it can not exchange heat with the environment. In this case, we have an adiabatic process in which the entropy remains constant. We already know that in this case the temperature of the rubber band increases.
Determine the temperature increase in case the rubber band is stretched to three times its original length very quickly. Give the value in units of Kelvin and round the result to the nearest integer.
Details and assumptions: The initial temperature is and the rubber band has an original length of . The elastic behavior is described by the parameter . The rubber has a constant heat capacity for constant length.
Hints: Determine the thermodynamic potential of the free energy of the rubber, which depends on the temperature and the length . Take advantage of the fact that the partial derivatives of the free energy correspond to the force and the entropy: In addition, the entropy is directly linked to the heat capacity: Find an equation for the entropy and solve for the temperature in the case .
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We can determine a part of the free energy when we integrate the force f over l : F ( T , l ) = − ∫ l 0 l f d l + F 0 ( T ) = 2 b T ( l − l 0 ) 2 + F 0 ( T ) Note, that we have a constant of integration, F 0 ( T ) , that still depends on T . Nevertheless, we can get an expression for the entropy S ( T , l ) = − ( ∂ T ∂ F ) l = − 2 b ( l − l 0 ) 2 + F 0 ′ ( T ) We still don't know anything about F 0 ′ ( T ) . But we know, that the entropy is related to the heat capacity via ⇒ ⇒ T ( ∂ T ∂ S ) l d S S ( T , l ) = C l = const = T C l d T for l = const = ∫ T 0 T T C l d T + S 0 ( l ) = C l ln T 0 T + S 0 ( l ) Here, we have constant of integration, S 0 ( l ) , that only depends on l . But if we compare both expressions for the entropy we can derive the full two-dimensional function S ( T , l ) = − 2 b ( l − l 0 ) 2 + C l ln T 0 T + S 0 0 with a constant S 0 0 = S 0 ( l 0 ) . In case of the adiabatic process, we have S ( T , l ) = S 0 0 = const . Therefore, we can solve this equation for T : ⇒ ⇒ Δ S ln T 0 T T = − 2 b ( l − l 0 ) 2 + C l ln T 0 T = 0 = 2 C l b ( l − l 0 ) 2 = T 0 exp ( 2 C l b ( l − l 0 ) 2 ) For l = 3 l 0 = 0 . 3 9 cm we get an temperature increase of Δ T = T − T 0 = ( exp ( 2 ( 0 . 2 6 ) 2 ) − 1 ) ⋅ 2 9 3 K ≈ 1 0 K