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SCIENCE · INVESTIGATE AND EXPLAIN

Cool an expanding gas without removing heat

Distinguish reversible adiabatic expansion, isothermal expansion and free expansion.

Learning outcome: Use an adiabatic energy balance, compare pressure and temperature endpoints and state when the constant-gamma path relation applies.

Starting recap

Adiabatic means no heat crosses the system boundary. Work can still change internal energy.

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Try

An insulated gas expands against a load and cools. Has energy disappeared even though no heat escaped?

Open the experiment

Predict

For expansion from 20 to 40 L at initial 300 K, predict which process ends colder and which supplies more work.

Experiment

Compare final temperatures, pressures and work at 40 L. Reverse the volume change by selecting 10 L; check which process now requires more work input. At 20 L verify the unchanged-state limit. Explain why neither drawn path describes a rapid free expansion.

Compare isothermal and reversible adiabatic gas processes

Worked teaching model · synthetic values · One mole of a classical monatomic ideal gas initially occupies 20 L. R = 8.314 L kPa/(mol K), Cv = 3R/2 and gamma = 5/3 are constant. Both processes are reversible ideal limits with quasistatic load matching, only pressure-volume work, and no bulk kinetic/potential-energy change. Isothermal heat exchange maintains the initial temperature; adiabatic insulation prevents heat exchange. They share a final volume, generally not a final pressure or temperature. No elapsed time, friction, free-expansion trajectory or real-species validity range is modeled.

Reset keeps your prediction, captures and practice history.

P (kPa absolute) · same start; final volume 40 L010020030040050060001020304045Volume (L) · start at filled point; finish at open pointsSolid: isothermal · dashed: reversible adiabatic

Expansion: travel right from the common start. The adiabatic pressure falls more steeply. The signed area under each pressure curve gives work by the gas for these reversible processes. Curves use 65 sampled states; work uses the analytic formulas, not the drawn segments.

Final states and signed energy transfers
ProcessFinal V (L)Final T (K)Final P (kPa absolute)W by gas (kJ)Q into gas (kJ)ΔU (kJ)
Isothermal40300.00062.3551.7291.7290.000
Reversible adiabatic40188.98839.2811.3840.000-1.384

Check each row: Q − W = ΔU. A zero Q means no heat transfer, not necessarily no temperature change. The adiabatic curve describes work against a changing load, not free expansion into vacuum.

Same initial state and final volume; different final temperatures and pressures.

Isothermal: final T = 300.000 K; W = 1.729 kJ; Q = 1.729 kJ; ΔU = 0.000 kJ. Reversible adiabatic: final T = 188.988 K; W = 1.384 kJ; Q = 0.000 kJ; ΔU = -1.384 kJ. Positive W is work by the gas; positive Q enters it.

Captures preserve recipes and replay their calculated results. They are synthetic model evidence, not physical measurements.

Understand

Insulation prevents heat exchange, not energy transfer

Predict what will happen when the same starting gas expands against a load with its walls thermally insulated. With Q = 0, the first law becomes ΔU = −W. If the gas does positive work, its internal energy falls. For this ideal gas, the temperature falls too. Energy leaves through work even though no heat leaves.

Select initial 300 K and final 40 L. The solid isothermal path ends at 300 K. The dashed reversible adiabatic path ends at approximately 188.988 K. The paths share a starting state and final volume, not a final state. Their different internal-energy changes are therefore consistent with internal energy being a state property.

Specify the gas and the process

The lab models one mole of a classical monatomic ideal gas with molar heat capacity Cv = 3R/2, measured in J/(mol K). It assumes constant heat capacities and only pressure-volume work. For this model Cp = 5R/2, so their ratio gamma = Cp/Cv = 5/3. These constants do not describe every gas or every temperature range.

For the reversible adiabatic path, Tf = Ti(Vi/Vf)^(gamma − 1). Subscripts i and f mean initial and final states. Volumes use the same units, temperatures use kelvin, and the exponent here is 2/3. For doubling volume, Tf = 300 × (20/40)^(2/3) ≈ 188.988 K. The final pressure from nRTf/Vf is approximately 39.281 kPa.

Then ΔU = nCv(Tf − Ti) ≈ −1384.429 J. With Q = 0, W ≈ 1384.429 J. Compare the ledger with the isothermal work, about 1728.848 J: the isothermal pressure stays higher during expansion because the bath replenishes energy. The extra work is not evidence of a more efficient cyclic engine; neither displayed path is a complete cycle.

Reverse the volume change

Select final 10 L. The adiabatic temperature rises to about 476.220 K, and the gas requires approximately 2197.644 J of work input. Work by the gas is negative; ΔU is positive. The isothermal compression instead stays at 300 K and rejects approximately 1728.848 J as heat.

Capture the comparison. Explain why the dashed pressure curve is above the solid one during compression but below it during expansion. Set the final volume to 20 L and check that both processes collapse to the unchanged initial state.

Do not apply the curve to every insulated process

Adiabatic only specifies zero heat transfer. The plotted relation additionally requires a reversible ideal path with quasistatic mechanical balance and constant heat capacity. An equivalent relation is Pf Vf^gamma = Pi Vi^gamma. Insulation alone does not justify that equation.

Consider gas released into an evacuated compartment of a rigid, insulated container. There is no opposing external pressure for the expansion work and no heat crossing the outer boundary. Between equilibrium states, Q = W = ΔU = 0. For an ideal gas the final temperature is unchanged. The rapid intermediate states are not the equilibrium points on our dashed curve. This is a counterexample to “every adiabatic expansion cools a gas.” The OpenStax adiabatic-process reference distinguishes free expansion from quasistatic adiabatic work.

Transfer using the energy account

An insulated gas does 600 J of work against a load. Its amount is 2 mol and its constant Cv is 12 J/(mol K). Find its temperature change. Then replace that process with free expansion into vacuum under the stated ideal-gas assumptions.

Check the adiabatic transfer

ΔU = −600 J. The total heat capacity is nCv = 24 J/K, so ΔT = −600/24 = −25 K. Free expansion instead has W = 0 and hence ΔT = 0. The first calculation uses the energy balance and specified heat capacity; it does not need the reversible pressure-volume relation.

Apply

An insulated ideal gas freely expands into a vacuum inside a rigid container. Compare its final equilibrium temperature with its initial temperature:

Public practice checks a specific claim. It does not establish independent mastery.

Explain the cooling through work transfer, distinguish insulation from fixed temperature, and give a counterexample to the claim that every adiabatic expansion cools an ideal gas.

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