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Physics · Ch 11 — Thermodynamics

Isobaric Process

11.8.5

Isobaric Process

The Isobaric Process: Constant Pressure

An isobaric process is a thermodynamic change that takes place at a constant pressure. The word itself comes from the Greek isos (equal) and baros (weight or pressure). In such a process, the system is free to expand or contract, but the external pressure on it remains fixed. A common example is heating a gas in a cylinder fitted with a movable, frictionless piston that is exposed to the atmosphere — as the gas heats up, it pushes the piston outward, but the pressure inside always matches the constant atmospheric pressure outside.

Because pressure PP is constant, the PP–VV diagram for an isobaric process is a horizontal straight line. If the volume increases (expansion), the process moves from left to right along this line; if the volume decreases (compression), it moves from right to left.


Work Done in an Isobaric Process

The work done by a gas during any thermodynamic process is given by the integral

W=∫ViVfP dV.W = \int_{V_i}^{V_f} P \, dV.

Since PP is constant in an isobaric process, it can be taken out of the integral:

W=P∫ViVfdV=P(Vf−Vi).W = P \int_{V_i}^{V_f} dV = P (V_f - V_i).

Let VfV_f be the final volume and ViV_i the initial volume. Then the work done by the gas is

W=P ΔV,W = P \, \Delta V,

where ΔV=Vf−Vi\Delta V = V_f - V_i.

W=P ΔVW = P \, \Delta V

If the gas expands (ΔV>0\Delta V > 0), WW is positive — the gas does work on its surroundings. If the gas is compressed (ΔV<0\Delta V < 0), WW is negative — work is done on the gas by the surroundings.

Tip

On a PP–VV diagram, the area under the curve (which is just a rectangle of height PP and width ΔV\Delta V) equals the work done. For an isobaric expansion, this area is simply PΔVP \Delta V.


First Law of Thermodynamics for an Isobaric Process

The first law of thermodynamics states

ΔU=Q−W,\Delta U = Q - W,

where ΔU\Delta U is the change in internal energy, QQ is the heat added to the system, and WW is the work done by the system.

For an isobaric process, we substitute W=PΔVW = P \Delta V:

ΔU=Q−PΔV.\Delta U = Q - P \Delta V.

This equation tells us that the heat supplied to the system is partly used to do work (expanding against constant pressure) and partly to change the internal energy (and hence the temperature) of the gas.


Heat Capacity at Constant Pressure (CPC_P)

The molar specific heat capacity at constant pressure, CPC_P, is defined as the amount of heat required to raise the temperature of one mole of a gas by 1 K while keeping the pressure constant. For nn moles, the heat added at constant pressure is

Q=nCPΔT.Q = n C_P \Delta T.

Important

CPC_P is always greater than CVC_V (the molar specific heat at constant volume) because, at constant pressure, the gas expands and does work. Some of the heat supplied goes into this work, so more heat is needed to achieve the same temperature rise.


Relation Between CPC_P and CVC_V (Mayer's Relation)

Consider one mole of an ideal gas undergoing an isobaric process. The first law gives

ΔU=Q−PΔV.\Delta U = Q - P \Delta V.

For one mole, Q=CPΔTQ = C_P \Delta T and ΔU=CVΔT\Delta U = C_V \Delta T (since internal energy of an ideal gas depends only on temperature). Also, from the ideal gas law PV=RTPV = RT, at constant pressure we have PΔV=RΔTP \Delta V = R \Delta T.

Substitute these into the first law: …