6 Basic Thermodynamic Processes

Compare the defining conditions, energy transfers, boundary work, and ideal-gas relations for five basic thermodynamic processes.

Processes and the energy balance

A changes a system from one equilibrium state to another. It can be represented on a pressure–volume diagram; for a , the area under the path gives the work done by the system.

Use the sign convention that heat entering the system is positive and work done by the system is positive. For a closed system with negligible changes in kinetic and potential energy, the is

ΔU=Q−W.\Delta U=Q-W.

The relations in this guide focus on a fixed amount of ideal gas. Let mm be its mass, RR its specific gas constant, and cvc_v and cpc_p its specific heats. When specific heats are constant, the internal-energy change is ΔU=mcvΔT\Delta U=mc_v\Delta T; for an ideal gas, cp−cv=Rc_p-c_v=R.

Constant-pressure process

In an , pressure remains fixed:

P=constant.P=\text{constant}.

The boundary work is

W=P(V2−V1).W=P(V_2-V_1).

For an ideal gas, PΔV=mRΔTP\Delta V=mR\Delta T. With constant specific heats, ΔU=mcvΔT\Delta U=mc_v\Delta T, so the gives Q=mcpΔTQ=mc_p\Delta T. During heating and expansion, some energy raises the gas’s internal energy and some is transferred as work. A weighted piston can approximate constant pressure as the gas expands.

Constant-volume process

In an , volume remains fixed:

V=constant.V=\text{constant}.

Because the boundary does not move, there is no boundary work, and the heat transfer equals the internal-energy change:

W=0,Q=ΔU.W=0,\qquad Q=\Delta U.

For an ideal gas with constant specific heat, Q=mcvΔTQ=mc_v\Delta T. For example, heating gas in a rigid, sealed tank raises its internal energy and temperature without boundary work.

In an , temperature remains fixed:

T=constant.T=\text{constant}.

For an ideal gas, PV=mRTPV=mRT, so PV=constantPV=\text{constant}. Because ideal-gas internal energy depends only on temperature, ΔU=0\Delta U=0, and the gives Q=WQ=W.

For a quasi-equilibrium expansion or compression, the work is

W=mRTln⁡ ⁣(V2V1).W=mRT\ln\!\left(\frac{V_2}{V_1}\right).

During expansion, the gas does positive work and must receive an equal amount of heat to remain at the same temperature. This idealization requires enough time and heat transfer to maintain a uniform temperature.

An has no heat transfer, so Q=0Q=0. The then becomes

ΔU=−W.\Delta U=-W.

Consequently, an expanding gas that does work cools, while a gas compressed by work done on it warms. Adiabatic does not by itself mean reversible or constant entropy.

For a reversible (or quasi-static) of an ideal gas with constant specific heats, the process is isentropic and obeys

PVγ=constant,TVγ−1=constant,γ=cpcv.PV^{\gamma}=\text{constant},\qquad TV^{\gamma-1}=\text{constant},\qquad \gamma=\frac{c_p}{c_v}.

These pressure–volume and temperature–volume relations do not generally apply to an irreversible .

A follows the model relation

PVn=constant,PV^n=\text{constant},

where nn is the polytropic exponent. For a fixed mass of ideal gas, boundary work in a is

W={P2V2−P1V11−n,n≠1,mRTln⁡ ⁣(V2V1),n=1.W= \begin{cases} \dfrac{P_2V_2-P_1V_1}{1-n}, & n\ne 1,\\[6pt] mRT\ln\!\left(\dfrac{V_2}{V_1}\right), & n=1. \end{cases}

The special case n=1n=1 is isothermal for an ideal gas. Constant pressure corresponds to n=0n=0, while a reversible adiabatic ideal-gas process with constant specific heats corresponds to n=γn=\gamma. For any polytropic path, heat transfer can be found from Q=ΔU+WQ=\Delta U+W. The relation is a useful model for processes such as gas compression and expansion; the exponent describes the path, not a universal property of the gas.

Choosing and applying a process model

Identify the process from the quantity held fixed or its defining relation: pressure for an , volume for an , temperature for an , no heat transfer for an , and PVn=constantPV^n=\text{constant} for a .

Then calculate boundary work and apply ΔU=Q−W\Delta U=Q-W. Use special ideal-gas relations only when their stated assumptions apply.