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The specific heat capacity of a substance, especially a gas, may be significantly higher when it is allowed to expand as it is heated (specific heat capacity at constant pressure) than when it is heated in a closed vessel that prevents expansion (specific heat capacity at constant volume).
Table of specific heat capacities at 25 °C (298 K) unless otherwise noted. [citation needed] Notable minima and maxima are shown in maroon. Substance Phase Isobaric mass heat capacity c P J⋅g −1 ⋅K −1 Molar heat capacity, C P,m and C V,m J⋅mol −1 ⋅K −1 Isobaric volumetric heat capacity C P,v J⋅cm −3 ⋅K −1 Isochoric ...
In thermal physics and thermodynamics, the heat capacity ratio, also known as the adiabatic index, the ratio of specific heats, or Laplace's coefficient, is the ratio of the heat capacity at constant pressure (C P) to heat capacity at constant volume (C V).
The heat capacity depends on how the external variables of the system are changed when the heat is supplied. If the only external variable of the system is the volume, then we can write: d S = ( ∂ S ∂ T ) V d T + ( ∂ S ∂ V ) T d V {\displaystyle dS=\left({\frac {\partial S}{\partial T}}\right)_{V}dT+\left({\frac {\partial S}{\partial V ...
The SI unit of heat capacity is joule per kelvin (J/K). Heat capacity is an extensive property. The corresponding intensive property is the specific heat capacity, found by dividing the heat capacity of an object by its mass. Dividing the heat capacity by the amount of substance in moles yields its molar heat capacity.
Heat capacity (constant pressure) C p: J/K Specific heat capacity (constant pressure) c p: J/(kg·K) Heat capacity (constant volume) C v: J/K Specific heat capacity (constant volume) c v: J/(kg·K) Helmholtz free energy: A, F: J Helmholtz free entropy: Φ: J/K Internal energy: U: J Specific internal energy: u: J/kg
ĉ V is the dimensionless specific heat capacity at constant volume, approximately 3 / 2 for a monatomic gas, 5 / 2 for diatomic gas, and 3 for non-linear molecules if we treat translations and rotations classically and ignore quantum vibrational contribution and electronic excitation.
This quantity is used almost exclusively for liquids and solids, since for gases it may be confused with the "specific heat capacity at constant volume", which generally has very different values. International standards now recommend that "specific heat capacity" always refer to capacity per unit of mass. [2]