Heat capacity: Difference between revisions
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The difference between the heat capacity at constant pressure and the heat capacity at constant volume is given by | The difference between the heat capacity at constant pressure and the heat capacity at constant volume is given by | ||
:<math>C_p -C_V = \left( p + \left. \frac{\partial U}{\partial V} \right\vert_T \right) \left. \frac{\partial V}{\partial T} \right\vert_p</math> | :<math>C_p -C_V = \left( p + \left. \frac{\partial U}{\partial V} \right\vert_T \right) \left. \frac{\partial V}{\partial T} \right\vert_p</math> | ||
==Excess heat capacity== | |||
In a classical system the excess heat capacity for a monatomic fluid is given by subtracting the [[Ideal gas: Energy |ideal internal energy]] (which is kinetic in nature) | |||
:<math>C_v^{ex} = C_v - \frac{3}{2}Nk_BT</math> | |||
in other words the excess heat capacity is associated with the component of the internal energy due to the intermolecular potential, and for that reason it is also known as the ''configurational'' heat capacity. Given that the excess internal energy for a pair potential is given by (Eq. 2.5.20 in <ref>J-P. Hansen and I. R. McDonald "Theory of Simple Liquids", Academic Press (2006) (Third Edition) ISBN 0-12-370535-5 </ref>): | |||
:<math>U^{ex} = 2\pi N \rho \int_0^{\infty} \Phi_{12}(r) g(r) r^2 ~{\rm d}{\mathbf r}</math> | |||
where <math>\Phi_{12}(r)</math> is the [[intermolecular pair potential]] and <math>g(r)</math> is the [[radial distribution function]], | |||
one has | |||
:<math>C_v^{ex} = 2\pi N \rho \int_0^{\infty} \Phi_{12}(r) \left. \frac{\partial g(r)}{\partial T} \right\vert_V r^2 ~{\rm d}{\mathbf r} </math> | |||
For many-body distribution functions things become more complicated <ref>[http://dx.doi.org/10.1063/1.468220 Ben C. Freasier, Adam Czezowski, and Richard J. Bearman "Multibody distribution function contributions to the heat capacity for the truncated Lennard‐Jones fluid", Journal of Chemical Physics '''101''' pp. 7934-7938 (1994)]</ref>. | |||
==Liquids== | ==Liquids== | ||
<ref>[http://dx.doi.org/10.1063/1.1667469 Claudio A. Cerdeiriña, Diego González-Salgado, Luis Romani, María del Carmen Delgado, Luis A. Torres and Miguel Costas "Towards an understanding of the heat capacity of liquids. A simple two-state model for molecular association", Journal of Chemical Physics '''120''' pp. 6648-6659 (2004)]</ref> | |||
==Solids== | ==Solids== | ||
====Petit and Dulong==== | ====Petit and Dulong==== |
Revision as of 15:28, 11 May 2012
The heat capacity is defined as the differential of heat with respect to the temperature ,
where is heat and is the entropy.
At constant volume
From the first law of thermodynamics one has
thus at constant volume, denoted by the subscript , then ,
At constant pressure
At constant pressure (denoted by the subscript ),
where is the enthalpy. The difference between the heat capacity at constant pressure and the heat capacity at constant volume is given by
Excess heat capacity
In a classical system the excess heat capacity for a monatomic fluid is given by subtracting the ideal internal energy (which is kinetic in nature)
in other words the excess heat capacity is associated with the component of the internal energy due to the intermolecular potential, and for that reason it is also known as the configurational heat capacity. Given that the excess internal energy for a pair potential is given by (Eq. 2.5.20 in [1]):
where is the intermolecular pair potential and is the radial distribution function, one has
For many-body distribution functions things become more complicated [2].
Liquids
Solids
Petit and Dulong
Einstein
Debye
A low temperatures on has
where is the Boltzmann constant, is the temperature and is an empirical parameter known as the Debye temperature.
See also
References
- ↑ J-P. Hansen and I. R. McDonald "Theory of Simple Liquids", Academic Press (2006) (Third Edition) ISBN 0-12-370535-5
- ↑ Ben C. Freasier, Adam Czezowski, and Richard J. Bearman "Multibody distribution function contributions to the heat capacity for the truncated Lennard‐Jones fluid", Journal of Chemical Physics 101 pp. 7934-7938 (1994)
- ↑ Claudio A. Cerdeiriña, Diego González-Salgado, Luis Romani, María del Carmen Delgado, Luis A. Torres and Miguel Costas "Towards an understanding of the heat capacity of liquids. A simple two-state model for molecular association", Journal of Chemical Physics 120 pp. 6648-6659 (2004)
- ↑ Alexis-Thérèse Petit and Pierre-Louis Dulong "Recherches sur quelques points importants de la Théorie de la Chaleur", Annales de Chimie et de Physique 10 pp. 395-413 (1819)