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Isobaric process

Thermodynamic process in which pressure remains constant

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Through Thermodynamics, Thermodynamic process and Pressure

Q=ΔU+W

where W is work, U is internal energy, and Q is heat. Pressure-volume work by the closed system is defined as:

W=∫pdV

where Δ means change over the whole process, whereas d denotes a differential. Since pressure is constant, this means that

W=pΔV.

Applying the ideal gas law, this becomes

W=nRΔT

with R representing the gas constant, and n representing the amount of substance, which is assumed to remain constant (e.g., there is no phase transition during a chemical reaction). According to the equipartition theorem, the change in internal energy is related to the temperature of the system by

ΔU=ncV,mΔT,

where cV, m is molar heat capacity at a constant volume.

Substituting the last two equations into the first equation produces:

Q=ncV,mΔT+nRΔTQ=nΔT(cV,m+R)Q=nΔTcP,m

where cP is molar heat capacity at a constant pressure.

Specific heat capacity

To find the molar specific heat capacity of the gas involved, the following equations apply for any general gas that is calorically perfect. The property γ is either called the adiabatic index or the heat capacity ratio. Some published sources might use k instead of γ.

Molar isochoric specific heat:

cV=Rγ−1.

Molar isobaric specific heat:

cp=γRγ−1.

The values for γ are γ = ⁠7/5⁠ for diatomic gases like air and its major components, and γ = ⁠5/3⁠ for monatomic gases like the noble gases. The formulas for specific heats would reduce in these special cases:

Monatomic:

cV=32R and cP=52R

Diatomic:

cV=52R and cP=72R

An isobaric process is shown on a P–V diagram as a straight horizontal line, connecting the initial and final thermostatic states. If the process moves towards the right, then it is an expansion. If the process moves towards the left, then it is a compression.

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