IB Physics HL Thermodynamics Paper 1 & 2 The Four Processes ~12 min read

Thermodynamic Processes

A gas can change in endless ways, but four clean changes cover almost everything you’ll meet in the exam. Each one holds a single quantity fixed — and their names all start with “iso“, Greek for “same”. The trick is lovely and simple: once you know what stays constant, the first law (Q = ΔU + W) hands you everything else. (Throughout, the gas is assumed ideal.)

📚 What you need to know

Four processes, one rule each

Every one of these keeps a single quantity constant. Spot which one, set the matching term in the first law to zero, and read off the rest:

ProcessHeld constantFirst law gives
Isovolumetricvolume (ΔV = 0)Q = ΔU
Isobaricpressure (Δp = 0)Q = ΔU + pΔV
Isothermaltemperature (ΔT = 0)Q = W
Adiabaticno heat (ΔQ = 0)W = −ΔU

Here’s the story behind each one:

WE 1

Heat is supplied to three ideal gases. Gas P is kept at constant volume, gas Q at constant temperature, and gas R at constant pressure. For each, state whether the work done W, the change in internal energy ΔU, and the temperature change ΔT are positive, zero, or negative.

P (constant volume): no work → W = 0. Then Q = ΔU so ΔU > 0, and ΔT > 0 Q (constant temperature): ΔT = 0, so ΔU = 0. Then Q = W so W > 0 R (constant pressure): gas expands so W > 0; heat also raises ΔU > 0, so ΔT > 0 Same starting move every time: pick what’s constant, zero that term, then use Q = ΔU + W.

Seeing them on a p–V graph

Each process has its own signature shape on a pressure–volume graph — and since the work done is the area under the line, the shape tells you the work at a glance.

THE FOUR PROCESSES ON A p–V GRAPH ISOBARIC (Δp = 0)pVconstant pressure · W = pΔV ISOVOLUMETRIC (ΔV = 0)pVno work · Q = ΔU ISOTHERMAL (ΔT = 0)pVΔU = 0 · Q = W ADIABATIC (ΔQ = 0)pVno heat · W = −ΔU
Isobaric runs horizontal (constant pressure); isovolumetric runs vertical (constant volume, no area, so no work); isothermal and adiabatic are curves that fall as the gas expands.

Isothermal vs adiabatic: the confusing pair

These two look alike — both are downward curves — and students mix them up constantly. The key difference is steepness: the adiabatic curve always drops faster.

ISOTHERMAL vs ADIABATIC A isothermal adiabatic (steeper) PRESSURE, p VOLUME, V adiabatic drops faster: no heat in, so the gas also cools
Starting from the same point A, the adiabatic curve falls below the isothermal one. In an isothermal expansion the temperature is held up by incoming heat; in an adiabatic expansion no heat comes in, so the gas also cools, and its pressure drops faster.
Think of it this way: in an isothermal expansion, heat keeps flowing in to keep the temperature up, propping the pressure. In an adiabatic expansion there’s no such help — the gas pays for its own work out of its internal energy, cools down, and so its pressure sinks more steeply. Steeper curve = the adiabatic one.

The adiabatic equation (monatomic gas)

Adiabatic changes are special enough to get their own equation. For a monatomic ideal gas (helium, neon, argon), pressure and volume are tied together by:

Adiabatic change, monatomic gas pV5/3 = constant p1V15/3 = p2V25/3

Combine this with the ideal gas law pV = nRT and the pressures drop out, leaving a handy version in terms of temperature and volume:

Temperature form T1V12/3 = T2V22/3
WE 2

A monatomic ideal gas is compressed adiabatically from a pressure of 1.0 × 105 Pa and volume 6.0 × 10−3 m3 to a volume of 2.0 × 10−3 m3. Find the new pressure.

Step 1 — rearrange p₁V₁5/3 = p₂V₂5/3 for p₂ p₂ = p₁ × (V₁/V₂)5/3 p₂ = (1.0×10⁵) × (6.0/2.0)5/3 = (1.0×10⁵) × 35/3 p₂ ≈ 6.2 × 10⁵ Pa Compression squeezes the gas, so the pressure jumps up — sensible.
WE 3

A monatomic ideal gas at 600 K expands adiabatically from 2.0 × 10−3 m3 to 5.0 × 10−3 m3. Find the new temperature.

Step 1 — use T₁V₁2/3 = T₂V₂2/3, so T₂ = T₁(V₁/V₂)2/3 T₂ = 600 × (2.0/5.0)2/3 = 600 × (0.4)2/3 T₂ ≈ 326 K Expanding with no heat in, the gas cools from 600 K to about 326 K — exactly why adiabatic curves are steeper.
One caution: the exponent 53 is for monatomic gases, whose atoms only move in straight lines. Gases made of bigger molecules can also spin, so their exponent is different — but for IB, the monatomic case is the one you need.

Entropy in each process

Because ΔS = ΔQ/T, entropy simply follows the heat. Any process that takes heat in raises the gas’s entropy; any that lets heat out lowers it. The special case is adiabatic: no heat flows, so ΔQ = 0 and the entropy doesn’t change at all.

ProcessHeat ΔQEntropy ΔS
Isothermal / isobaric / isovolumetric — heat in> 0increases
… the same, heat out< 0decreases
Adiabatic (either direction)= 0no change
Tuck this away for later: a reversible adiabatic change keeps entropy exactly constant. That “no entropy change” step is one of the ingredients of the perfect engine cycle — the Carnot cycle — you’ll meet at the end of the topic.
Name the
process
what’s
constant?
Zero that term
in Q = ΔU + W
read off
The rest
(W, ΔU, Q)

💡 Top tips

⚠ Common mistakes

Quick recap: Four “iso” processes, each fixing one quantity: isovolumetric (W = 0, Q = ΔU), isobaric (W = pΔV), isothermal (ΔU = 0, Q = W), adiabatic (Q = 0, W = −ΔU). On a p–V graph they’re horizontal, vertical, and two curves — the adiabatic steeper. A monatomic adiabatic obeys pV5/3 = constant, and adiabatic changes keep entropy constant.
That’s the whole toolkit of gas changes. Real machines don’t use them one at a time — they string several into a repeating loop to turn heat into work over and over. Next, in Heat Engines, we join these processes into a cycle and work out exactly how much useful work you can get.

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