Thermodynamics (HL)
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Define internal energy U of a gas.
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2.4.115 cards
Define internal energy U of a gas.
The **total energy of all the particles**: their random **kinetic energy** + the **potential energy** of the forces between them.
What does the internal energy of an **ideal gas** depend on?
**Temperature only** — an ideal gas has no inter-particle PE, so U is fixed by the random KE of the particles.
State the first law of thermodynamics.
$Q = \Delta U + W$ — the heat **added** equals the rise in **internal energy** plus the **work done by** the gas.
Rearrange the first law for ΔU.
$\Delta U = Q - W$ (heat in **minus** work done by the gas).
In Q = ΔU + W, what is the sign of Q when heat is **removed**?
**Negative** — Q is the heat **added** to the gas, so heat leaving makes Q < 0.
In Q = ΔU + W, what is the sign of W when the gas is **compressed**?
**Negative** — W is the work done **by** the gas; on compression the surroundings do work on it, so W < 0.
Work done by a gas at constant pressure?
$W = P\,\Delta V$ — pressure times the change in volume.
Units for W = PΔV?
P in **pascals (Pa)**, ΔV in **cubic metres (m³)**, giving W in **joules (J)**.
Internal energy vs heat — what's the difference?
**Internal energy** is energy a gas **already has** inside; **heat** is energy **flowing** in or out due to a temperature difference.
For an ideal gas at **constant temperature**, what is ΔU?
**ΔU = 0** — U depends on temperature alone, so no temperature change means no change in internal energy.
500 J heat added, gas does 200 J work — find ΔU.
$\Delta U = Q - W = 500 - 200 = 300$ J (the gas warms).
Quick way to handle the signs in the first law?
Write each sign in **words** first ('heat removed → Q negative', 'gas compressed → W negative'), then plug into $\Delta U = Q - W$.
Change in internal energy of a monatomic ideal gas?
**ΔU = 3/2 Nk_BΔT = 3/2 nRΔT**: set by the temperature change alone.
How do you find the work done by a gas whose pressure changes?
The **area under the p–V graph**; positive when the gas expands, negative when compressed.
Closed system v isolated system?
**Closed**: no mass crosses, energy can (heat or work). **Isolated**: neither mass nor energy crosses.
2.4.215 cards
What does entropy S measure?
The **disorder** of a system — the **number of microstates** (microscopic arrangements) available. Unit: **J K⁻¹**.
What is a microstate?
One specific microscopic arrangement of the particles that gives the same overall (macroscopic) state. **More microstates ⇒ higher entropy**.
Formula for entropy change?
$\Delta S = \dfrac{\Delta Q}{T}$, with **T in kelvin**.
In ΔS = ΔQ/T, what are the units?
$\Delta S$ in **J K⁻¹**, $\Delta Q$ in **J**, $T$ in **K**.
Sign of ΔQ for heat flowing in vs out?
Heat **in** ⇒ ΔQ is **positive** (entropy rises); heat **out** ⇒ ΔQ is **negative** (entropy falls).
State the second law of thermodynamics.
The **entropy of an isolated system never decreases** — it increases for any irreversible (real) process.
Can one part of a system lose entropy?
Yes — but only if another part gains **more**, so the **total** entropy of the isolated system still does not decrease.
Why does heat flow hot → cold by itself?
Because it **increases the total entropy** of the universe ($\Delta S_{total} > 0$); the reverse would decrease it, so it never happens unaided.
What is 'time's arrow'?
The **direction** of time set by the second law: real processes always run the way that **increases total entropy**.
How do you test if a process is allowed?
Calculate $\Delta S_{total}$ for the isolated system. If it is **positive**, the process can occur (and is irreversible).
Why is the cold body's entropy gain larger?
$\Delta S = \Delta Q/T$, and the **cold** body has the **smaller T**, so for the same ΔQ it gains **more** entropy than the hot body loses.
Entropy unit vs energy unit?
Entropy is the **joule per kelvin (J K⁻¹)**; energy is the **joule (J)** — do not confuse them.
Entropy in terms of microstates?
**S = k_B ln Ω**, where Ω is the number of (equally likely) microstates.
Clausius form of the second law?
Heat cannot flow from a colder body to a hotter body **on its own**.
Kelvin form of the second law?
No engine working in a cycle can convert heat from a hot reservoir **completely** into work.
2.4.314 cards
Isothermal process — what is constant, and the consequence?
**T** is constant, so $\Delta U = 0$ and therefore $Q = W$.
Isobaric process — what is constant, and the work?
**P** is constant; the work done by the gas is $W = P\,\Delta V$.
Isovolumetric process — what is constant, and the consequence?
**V** is constant, so $W = 0$ and therefore $Q = \Delta U$.
Adiabatic process — what is zero, and the consequence?
**Q = 0** (no heat flows), so $\Delta U = -W$.
On a p–V diagram, what is the work done by the gas?
The **area under the curve** between the start and end volumes.
What does a heat engine do each cycle?
Takes in **Q_in** from the hot reservoir, does useful **work W**, and rejects **Q_out** to the cold reservoir. $W = Q_{in} - Q_{out}$.
Give the efficiency formula for a heat engine.
$\eta = \dfrac{\text{useful work}}{\text{energy input}} = 1 - \dfrac{Q_{out}}{Q_{in}}$.
Give the Carnot (maximum) efficiency formula.
$\eta_{Carnot} = 1 - \dfrac{T_{cold}}{T_{hot}}$, with both temperatures in **kelvin**.
Why is a real engine's efficiency below the Carnot value?
Friction, turbulence and unwanted heat loss waste energy, so the real efficiency is always **lower** than the Carnot ceiling.
Worked example — efficiency from Q_in = 800 J, Q_out = 600 J?
$\eta = 1 - \dfrac{600}{800} = 0.25$, i.e. **25%**.
Worked example — Carnot efficiency between 500 K and 300 K?
$\eta_{Carnot} = 1 - \dfrac{300}{500} = 0.40$, i.e. **40%**.
Adiabatic law for a monatomic ideal gas?
**pV^5/3 = constant** (so also TV^2/3 = constant).
Net work done by a gas in one cycle?
The **area inside the loop** on the p–V diagram; ΔU = 0 over the cycle.
Which processes make up a Carnot cycle?
**Two isothermal** (hot expansion, cold compression) and **two adiabatic** processes.
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