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Notes · PhysicsUK · A-Levels

Further mechanics and thermal physics

This chapter extends motion to the circular and the oscillatory, then turns to heat and gases. It develops circular motion and the centripetal force, defines simple harmonic motion and derives its solutions and energy, and treats resonance and damping. It then covers thermal energy transfer, the gas laws and, as its culmination, the kinetic-theory derivation that links the pressure of a gas to the motion of its molecules.

6 sections·~17 min reading time·3 competencies·Level Standard 3 · Advanced 3

T·0666 / 13
Exam profile
AO1 · Define angular speed, centripetal acceleration and simple harmonic motion and state the gas laws and kinetic-theory assumptionsAO2 · Calculate centripetal force, SHM periods, speeds and energies, thermal energy transfers and gas-state quantitiesAO3 · Derive pV = (1/3)Nmc-rms-squared, analyse resonance and damping curves and evaluate the thermal required practicals
Operators:definederiveshow thatcalculateexplainsketch

basic level

This is A2 (full A-Level) content, though circular motion and SHM also appear on Paper 1. It requires centripetal force, the SHM equations, thermal energy transfer and the gas laws.

higher level

The full A-Level requires the kinetic-theory derivation of pV = (1/3)Nmc-rms-squared, the link to temperature via (1/2)mc-rms-squared = (3/2)kT, and quantitative treatment of resonance and damping.

Depth

Reading depth: In depth

Text

Text size: Standard

Contents · 6 sections▾
  1. Further mechanics and thermal physics
    • 01Circular motion and centripetal force◐
    • 02Simple harmonic motion: definition and solutions●
    • 03Energy in SHM, resonance and damping●
    • 04Thermal energy, specific heat capacity and latent heat◐
    • 05Ideal gases and the gas laws◐
    • 06Molecular kinetic theory●
§ 01

Circular motion and centripetal force#

●●○StandardLPAQA 7408 3.6.1.1LPDfE GCE Physics - circular motion

Centripetal force in circular motion

Circular motionGeometric figure, centre, object, F (centripetal), v (tangent)centreobjectx1x2F(centripe…v(tangent)
Fig. 1An object moving round a circle has a velocity along the tangent and a centripetal force directed towards the centre; the force is always perpendicular to the velocity.

Key points

An object moving in a circle at constant speed is continually changing direction, and therefore continually accelerating, even though its speed is constant - velocity is a vector. Its angular speed ω\omegaω is the angle swept per unit time, in radians per second, related to the linear speed by v=ωrv = \omega rv=ωr and to the period and frequency by ω=2πT=2πf\omega = \dfrac{2\pi}{T} = 2\pi fω=T2π​=2πf.
The acceleration points towards the centre of the circle and is called the centripetal acceleration, a=v2r=ω2ra = \dfrac{v^2}{r} = \omega^2 ra=rv2​=ω2r. It is caused by a resultant force directed towards the centre - the centripetal force - of magnitude F=mv2r=mω2rF = \dfrac{mv^2}{r} = m\omega^2 rF=rmv2​=mω2r. This is not a new kind of force; it is provided by whatever real force acts towards the centre: gravity for a satellite, tension for a whirled mass, friction for a cornering car.
Because the centripetal force is always perpendicular to the velocity, it does no work on the object and its speed does not change - only its direction. If the force is removed (the string breaks, the road ices over) the object continues in a straight line along the tangent, obeying Newton's first law. This is why cornering demands a sideways force and why that force is felt to be 'missing' when grip is lost.
In a vertical circle the required centripetal force is the same, but gravity now helps or hinders it. At the top of a loop, weight and tension both act downward towards the centre, so the minimum speed to maintain contact is where weight alone provides the centripetal force: mg=mv2rmg = \dfrac{mv^2}{r}mg=rmv2​, giving vmin⁡=grv_{\min} = \sqrt{gr}vmin​=gr​. At the bottom the tension must exceed the weight to provide the centripetal force and support the object.
ω=2πT=2πf,v=ωr\omega = \dfrac{2\pi}{T} = 2\pi f, \qquad v = \omega rω=T2π​=2πf,v=ωr

Angular speed

Relates angular speed to period, frequency and linear speed.

a=v2r=ω2ra = \dfrac{v^2}{r} = \omega^2 ra=rv2​=ω2r

Centripetal acceleration

Directed towards the centre of the circle.

F=mv2r=mω2rF = \dfrac{mv^2}{r} = m\omega^2 rF=rmv2​=mω2r

Centripetal force

The resultant force towards the centre.

Worked example

Tension in a whirled string

A 0.15 kg0.15\,\text{kg}0.15kg mass on a 0.60 m0.60\,\text{m}0.60m string is whirled in a horizontal circle at 2.0 rev s−12.0\,\text{rev s}^{-1}2.0rev s−1. Find the tension, treating the string as horizontal.

  1. 01Angular speed

    ω=2πf=2π×2.0=12.6 rad s−1\omega = 2\pi f = 2\pi \times 2.0 = 12.6\,\text{rad s}^{-1}ω=2πf=2π×2.0=12.6rad s−1.

  2. 02Centripetal force

    The tension provides it: F=mω2r=0.15×(12.6)2×0.60F = m\omega^2 r = 0.15 \times (12.6)^2 \times 0.60F=mω2r=0.15×(12.6)2×0.60.

    F=0.15×158×0.60=14 NF = 0.15 \times 158 \times 0.60 = 14\,\text{N}F=0.15×158×0.60=14N

Result: The string tension is about 14 N14\,\text{N}14N.

Exam focus

  • Use v=ωrv = \omega rv=ωr, a=v2/r=ω2ra = v^2/r = \omega^2 ra=v2/r=ω2r and F=mv2/rF = mv^2/rF=mv2/r for horizontal and vertical circular motion.
  • Identify which real force provides the centripetal force in a given situation and find the minimum speed at the top of a vertical circle.

Typical mistakes

  • Treating 'centrifugal force' as a real outward force - the only real force is the inward (centripetal) one.
  • Forgetting to include the weight when analysing motion in a vertical circle.

Active revision

A 0.20 kg0.20\,\text{kg}0.20kg ball on a string of length 0.80 m0.80\,\text{m}0.80m is whirled in a horizontal circle at 3.0 rev s−13.0\,\text{rev s}^{-1}3.0rev s−1. Find the tension in the string.

Active recall

Recall the key points — then reveal.

Sources: GCE AS and A level subject content for the sciences (Department for Education) · AQA A-level Physics 7408 specification (AQA)

§ 02

Simple harmonic motion: definition and solutions#

●●●AdvancedLPAQA 7408 3.6.1.2LPAQA 7408 3.6.1.3LPDfE GCE Physics - simple harmonic motion

Displacement and velocity in SHM

SHM: displacement and velocityGraph of displacement x, roots at x = 1.571, 4.712, minimum at (3.142, -1), y-intercept at y = 1, on the interval x from 0 to 6.28, Graph of velocity v, roots at x = 0, 3.142, minimum at (1.571, -1), maximum at (4.712, 1), y-intercept at y = 0, on the interval x from 0 to 6.28123456−1−0.50.51displacement xvelocity vx / A and v / (omega A)Time (omega t)
Fig. 2Displacement follows a cosine; velocity is a negative sine a quarter-cycle ahead - zero at the extremes of displacement and greatest as the object passes through the centre.

Key points

Simple harmonic motion (SHM) is defined by a single condition: the acceleration is proportional to the displacement from equilibrium and always directed back towards it, a=−ω2xa = -\omega^2 xa=−ω2x. The constant ω\omegaω is the angular frequency and the minus sign captures the restoring nature of the motion. Any system with a linear restoring force - a mass on a spring obeying F=−kxF = -kxF=−kx, a pendulum for small angles - performs SHM, and the negative-proportional relationship is the acid test in an exam.
Solving the defining equation gives sinusoidal motion. Taking the object released from its maximum displacement (amplitude AAA) at t=0t = 0t=0, the displacement is x=Acos⁡(ωt)x = A\cos(\omega t)x=Acos(ωt). Differentiating gives the velocity v=−Aωsin⁡(ωt)v = -A\omega\sin(\omega t)v=−Aωsin(ωt) and a second differentiation gives a=−Aω2cos⁡(ωt)=−ω2xa = -A\omega^2\cos(\omega t) = -\omega^2 xa=−Aω2cos(ωt)=−ω2x, confirming the definition. Eliminating time between displacement and velocity gives the useful relation v=±ωA2−x2v = \pm\omega\sqrt{A^2 - x^2}v=±ωA2−x2​, so the speed is greatest (vmax⁡=ωAv_{\max} = \omega Avmax​=ωA) at the centre and zero at the extremes.
The period of SHM depends only on the system, not on the amplitude - a property called isochronism, which is why a pendulum keeps good time as its swing decays. For a mass mmm on a spring of stiffness kkk, ω=k/m\omega = \sqrt{k/m}ω=k/m​, so T=2πm/kT = 2\pi\sqrt{m/k}T=2πm/k​; for a simple pendulum of length LLL, T=2πL/gT = 2\pi\sqrt{L/g}T=2πL/g​. The pendulum result gives an accurate laboratory measurement of ggg.
The graphs tell the story. Displacement is a cosine; velocity is a negative sine, a quarter-cycle ahead, zero at the extremes and maximum at the centre; acceleration is a negative cosine, in antiphase with displacement and maximum at the extremes. Recognising these phase relationships - and reading amplitude and period from them - is a routine exam task.
a=−ω2xa = -\omega^2 xa=−ω2x

Defining condition of SHM

Acceleration proportional to, and opposite to, displacement.

x=Acos⁡(ωt),v=± ωA2−x2x = A\cos(\omega t), \qquad v = \pm\,\omega\sqrt{A^2 - x^2}x=Acos(ωt),v=±ωA2−x2​

Displacement and velocity

Solutions of the SHM equation; speed is greatest at the centre.

T=2πmk,T=2πLgT = 2\pi\sqrt{\dfrac{m}{k}}, \qquad T = 2\pi\sqrt{\dfrac{L}{g}}T=2πkm​​,T=2πgL​​

Periods of standard oscillators

Mass-spring and simple pendulum.

Worked example

A mass on a spring

A 0.30 kg0.30\,\text{kg}0.30kg mass on a spring of stiffness 12 N m−112\,\text{N m}^{-1}12N m−1 oscillates with amplitude 0.040 m0.040\,\text{m}0.040m. Find the period and the maximum speed.

  1. 01Angular frequency

    ω=k/m=12/0.30=40=6.32 rad s−1\omega = \sqrt{k/m} = \sqrt{12/0.30} = \sqrt{40} = 6.32\,\text{rad s}^{-1}ω=k/m​=12/0.30​=40​=6.32rad s−1.

  2. 02Period

    T=2π/ω=2π/6.32=0.99 sT = 2\pi/\omega = 2\pi/6.32 = 0.99\,\text{s}T=2π/ω=2π/6.32=0.99s.

  3. 03Maximum speed

    vmax⁡=ωA=6.32×0.040v_{\max} = \omega A = 6.32 \times 0.040vmax​=ωA=6.32×0.040.

    vmax⁡=6.32×0.040=0.25 m s−1v_{\max} = 6.32 \times 0.040 = 0.25\,\text{m}\,\text{s}^{-1}vmax​=6.32×0.040=0.25ms−1

Result: The period is 0.99 s0.99\,\text{s}0.99s and the maximum speed is 0.25 m s−10.25\,\text{m}\,\text{s}^{-1}0.25ms−1.

Exam focus

  • Recognise SHM from the condition a=−ω2xa = -\omega^2 xa=−ω2x and use x=Acos⁡ωtx = A\cos\omega tx=Acosωt, v=±ωA2−x2v = \pm\omega\sqrt{A^2 - x^2}v=±ωA2−x2​ and vmax⁡=ωAv_{\max} = \omega Avmax​=ωA.
  • Apply T=2πm/kT = 2\pi\sqrt{m/k}T=2πm/k​ and T=2πL/gT = 2\pi\sqrt{L/g}T=2πL/g​ and read amplitude, period and phase from displacement, velocity and acceleration graphs.

Typical mistakes

  • Thinking the period of SHM depends on the amplitude - it does not (within the SHM approximation).
  • Losing the minus sign or the phase relationship between displacement, velocity and acceleration.

Active revision

A mass of 0.25 kg0.25\,\text{kg}0.25kg on a spring of stiffness 40 N m−140\,\text{N m}^{-1}40N m−1 oscillates with amplitude 0.050 m0.050\,\text{m}0.050m. Find the period and the maximum speed.

Active recall

Recall the key points — then reveal.

Sources: AQA A-level Physics 7408 specification (AQA)

§ 03

Energy in SHM, resonance and damping#

●●●AdvancedLPAQA 7408 3.6.1.3LPAQA 7408 3.6.1.4LPDfE GCE Physics - SHM energy and resonance

Energy against displacement in SHM

Energy interchange in SHMGraph of potential energy, roots at x = 0, minimum at (0, 0), y-intercept at y = 0, on the interval x from -2 to 2, Graph of kinetic energy, roots at x = -2, 2, maximum at (0, 4), y-intercept at y = 4, on the interval x from -2 to 2−2−1.5−1−0.50.511.521234total energypotential energykinetic energyEnergyDisplacement x
Fig. 3Potential energy (a parabola, minimum at the centre) and kinetic energy (an inverted parabola, maximum at the centre) always add to the constant total energy.

Key points

As an oscillator moves, energy interchanges continuously between kinetic and potential while the total stays constant (in the absence of damping). At the extremes all the energy is potential (the object is momentarily at rest); at the centre all of it is kinetic (maximum speed). The potential energy is 12kx2\tfrac{1}{2}k x^221​kx2, the kinetic energy is 12k(A2−x2)\tfrac{1}{2}k(A^2 - x^2)21​k(A2−x2), and their sum, the total energy 12kA2\tfrac{1}{2}k A^221​kA2, is independent of position. A graph of energy against displacement shows two parabolas that always add to a horizontal line.
Free vibrations occur at the system's own natural frequency f0f_0f0​ once it has been displaced and released. Forced vibrations occur when a periodic driving force is applied; the system then oscillates at the driving frequency. When the driving frequency approaches the natural frequency, the amplitude grows dramatically - this is resonance, and it transfers energy into the oscillator most efficiently.
Damping is any process that removes energy from an oscillator, usually as heat through resistive forces, so the amplitude decays with time. Light damping gives a slowly decaying oscillation; heavy damping slows the return to equilibrium; critical damping returns the system to rest in the shortest time without overshooting - the design goal for car suspension and instrument needles. Increasing the damping lowers and broadens the resonance peak and shifts it slightly to a lower frequency.
Resonance is a double-edged phenomenon. It is exploited in tuned circuits, musical instruments and magnetic resonance imaging, but it must be avoided in structures: bridges, buildings and machinery are engineered so that their natural frequencies differ from the frequencies of likely driving forces (wind, footfall, engine vibration), and damping is added to limit the amplitude if resonance does occur.
Etotal=12kA2E_{\text{total}} = \tfrac{1}{2}kA^2Etotal​=21​kA2

Total energy in SHM

Constant, independent of displacement.

Ep=12kx2,Ek=12k(A2−x2)E_p = \tfrac{1}{2}kx^2, \qquad E_k = \tfrac{1}{2}k(A^2 - x^2)Ep​=21​kx2,Ek​=21​k(A2−x2)

Potential and kinetic energy

Two parabolas that sum to the constant total.

Resonance curves for different damping

Amplitude against driving frequencyGraph of light damping, maximum at (0.987, 4.5), y-intercept at y = 1, on the interval x from 0 to 2.5, Graph of heavier damping, maximum at (0.922, 1.898), y-intercept at y = 1, on the interval x from 0 to 2.50.511.522.512345naturalfrequency f0light dampingheavier dampingAmplitudeDriving frequency / natural f…
Fig. 4As the driving frequency approaches the natural frequency the amplitude peaks; heavier damping lowers and broadens the peak.
Worked example

Total energy of an oscillator

The 12 N m−112\,\text{N m}^{-1}12N m−1 spring oscillator has amplitude 0.040 m0.040\,\text{m}0.040m. Find its total energy and its maximum kinetic energy.

  1. 01Total energy

    E=12kA2=12(12)(0.040)2E = \tfrac{1}{2}kA^2 = \tfrac{1}{2}(12)(0.040)^2E=21​kA2=21​(12)(0.040)2.

    E=0.5×12×1.6×10−3=9.6×10−3 JE = 0.5 \times 12 \times 1.6\times10^{-3} = 9.6\times10^{-3}\,\text{J}E=0.5×12×1.6×10−3=9.6×10−3J
  2. 02Maximum kinetic energy

    At the centre all the energy is kinetic, so Ek,max⁡=E=9.6×10−3 JE_{k,\max} = E = 9.6\times10^{-3}\,\text{J}Ek,max​=E=9.6×10−3J.

Result: The total energy is 9.6 mJ9.6\,\text{mJ}9.6mJ, entirely kinetic as the mass passes through the centre.

Exam focus

  • Describe and use the interchange of kinetic and potential energy in SHM and sketch energy against displacement.
  • Explain resonance and the effect of damping on the amplitude-frequency (resonance) curve, with real examples.

Typical mistakes

  • Thinking the total energy of an undamped oscillator varies through the cycle - it is constant; only the split between kinetic and potential changes.
  • Believing more damping raises the resonance peak - it lowers and broadens it.

Active revision

For the 0.30 kg0.30\,\text{kg}0.30kg, 12 N m−112\,\text{N m}^{-1}12N m−1, 0.040 m0.040\,\text{m}0.040m-amplitude oscillator above, find the total energy and sketch how kinetic and potential energy vary with displacement.

Active recall

Recall the key points — then reveal.

Sources: AQA A-level Physics 7408 specification (AQA)

§ 04

Thermal energy, specific heat capacity and latent heat#

●●○StandardLPAQA 7408 3.6.2.1LPDfE GCE Physics - thermal energy transfer

Key points

The internal energy of a body is the sum of the randomly distributed kinetic and potential energies of its molecules. Raising the temperature increases the average molecular kinetic energy; changing state changes the molecular potential energy (the bonds) at constant temperature. Absolute (kelvin) temperature is proportional to the average kinetic energy per molecule, and 0 K0\,\text{K}0K (absolute zero) is the temperature at which molecular kinetic energy is a minimum.
To raise the temperature of a substance without changing its state, the energy needed is Q=mc ΔθQ = mc\,\Delta\thetaQ=mcΔθ, where ccc is the specific heat capacity - the energy to raise one kilogram by one kelvin. Water's large specific heat capacity of about 4200 J kg−1 K−14200\,\text{J kg}^{-1}\,\text{K}^{-1}4200J kg−1K−1 is why it is used as a coolant and why coastal climates are mild. Specific heat capacity is measured either electrically (an immersion heater) or by the method of mixtures.
To change the state of a substance at constant temperature, the energy needed is Q=mLQ = mLQ=mL, where LLL is the specific latent heat - of fusion for melting/freezing, of vaporisation for boiling/condensing. During a change of state the temperature stays constant because the energy goes into breaking or forming intermolecular bonds (changing potential energy) rather than raising kinetic energy. This is why steam at 100 ∘C100\,^{\circ}\text{C}100∘C scalds far worse than water at 100 ∘C100\,^{\circ}\text{C}100∘C.
A heating curve makes this visible: as energy is supplied at a steady rate, the temperature rises through each phase (slope set by mcmcmc) but plateaus at each melting and boiling point (flat, while mLmLmL is absorbed). Reading such a curve, and allowing for heat losses to the surroundings, is central to the thermal required practical.
Q=mc ΔθQ = mc\,\Delta\thetaQ=mcΔθ

Specific heat capacity

Energy to change the temperature of a mass mmm by Δθ\Delta\thetaΔθ.

Q=mLQ = mLQ=mL

Specific latent heat

Energy to change the state of a mass mmm at constant temperature.

Worked example

Heating and melting ice

Find the energy needed to turn 0.20 kg0.20\,\text{kg}0.20kg of ice at 0 ∘C0\,^{\circ}\text{C}0∘C into water at 20 ∘C20\,^{\circ}\text{C}20∘C. Take Lf=3.3×105 J kg−1L_f = 3.3\times10^{5}\,\text{J kg}^{-1}Lf​=3.3×105J kg−1 and cwater=4200 J kg−1 K−1c_{\text{water}} = 4200\,\text{J kg}^{-1}\,\text{K}^{-1}cwater​=4200J kg−1K−1.

  1. 01Melt the ice

    Q1=mLf=0.20×3.3×105=6.6×104 JQ_1 = mL_f = 0.20 \times 3.3\times10^{5} = 6.6\times10^{4}\,\text{J}Q1​=mLf​=0.20×3.3×105=6.6×104J.

  2. 02Warm the water

    Q2=mc Δθ=0.20×4200×20=1.68×104 JQ_2 = mc\,\Delta\theta = 0.20 \times 4200 \times 20 = 1.68\times10^{4}\,\text{J}Q2​=mcΔθ=0.20×4200×20=1.68×104J.

  3. 03Total

    Add the two stages.

    Q=6.6×104+1.68×104=8.3×104 JQ = 6.6\times10^{4} + 1.68\times10^{4} = 8.3\times10^{4}\,\text{J}Q=6.6×104+1.68×104=8.3×104J

Result: About 8.3×104 J8.3\times10^{4}\,\text{J}8.3×104J (83 kJ) is required, most of it to melt the ice.

Exam focus

  • Use Q=mc ΔθQ = mc\,\Delta\thetaQ=mcΔθ and Q=mLQ = mLQ=mL, including problems combining heating and a change of state.
  • Analyse the electrical determination of specific heat capacity and account for heat losses to the surroundings.

Typical mistakes

  • Expecting the temperature to rise during a change of state - it stays constant while latent heat is absorbed.
  • Using degrees Celsius for a temperature interval where kelvin is required (a temperature difference is the same in K and ∘^{\circ}∘C, but absolute temperatures are not).

Active revision

A 2.0 kW2.0\,\text{kW}2.0kW kettle heats 0.50 kg0.50\,\text{kg}0.50kg of water from 20 ∘C20\,^{\circ}\text{C}20∘C to 100 ∘C100\,^{\circ}\text{C}100∘C. Calculate the minimum time, taking c=4200 J kg−1 K−1c = 4200\,\text{J kg}^{-1}\,\text{K}^{-1}c=4200J kg−1K−1.

Active recall

Recall the key points — then reveal.

Sources: AQA A-level Physics 7408 specification (AQA)

§ 05

Ideal gases and the gas laws#

●●○StandardLPAQA 7408 3.6.2.2LPAQA 7408 3.6.2.3LPDfE GCE Physics - gas laws

Pressure-volume isotherms

Isotherms of an ideal gasGraph of temperature T1, decreasing, on the interval x from 1 to 6, Graph of higher temperature T2, decreasing, on the interval x from 1 to 6123456246810temperature T1highertemperature T2Pressure pVolume V
Fig. 5Each curve is an isotherm (pV=constantpV = \text{constant}pV=constant, Boyle's law); the higher-temperature isotherm lies further from the origin.

Key points

Three experimental gas laws describe how a fixed mass of gas behaves. Boyle's law: at constant temperature, pressure is inversely proportional to volume, pV=constantpV = \text{constant}pV=constant. Charles's law: at constant pressure, volume is proportional to absolute temperature, V/T=constantV/T = \text{constant}V/T=constant. The pressure law: at constant volume, pressure is proportional to absolute temperature, p/T=constantp/T = \text{constant}p/T=constant. All three require temperature in kelvin.
Combining the three gives the ideal gas equation pV=nRTpV = nRTpV=nRT, where nnn is the amount in moles and R=8.31 J mol−1 K−1R = 8.31\,\text{J mol}^{-1}\,\text{K}^{-1}R=8.31J mol−1K−1 is the molar gas constant. Written per molecule it becomes pV=NkTpV = NkTpV=NkT, where NNN is the number of molecules and k=R/NA=1.38×10−23 J K−1k = R/N_A = 1.38\times10^{-23}\,\text{J K}^{-1}k=R/NA​=1.38×10−23J K−1 is the Boltzmann constant. An ideal gas is one that obeys these laws exactly - a good model for real gases at low pressure and well above their boiling point.
On a ppp-VVV diagram, each constant-temperature process (an isotherm) is a hyperbola p∝1/Vp \propto 1/Vp∝1/V; higher temperatures give isotherms further from the origin. Because pV=nRTpV = nRTpV=nRT, doubling the absolute temperature at constant volume doubles the pressure, and cooling a gas at constant pressure shrinks its volume in proportion to TTT - which, extrapolated, points to absolute zero.
Work is done when a gas expands or is compressed: at constant pressure the work done by the gas is W=p ΔVW = p\,\Delta VW=pΔV, the area under the ppp-VVV curve. This links directly to the first law of thermodynamics and, in the engineering-physics option, to engine cycles. For an ideal gas the internal energy depends only on temperature, so an isothermal change involves no change in internal energy.
pV=nRTpV = nRTpV=nRT

Ideal gas equation (moles)

R=8.31 J mol−1 K−1R = 8.31\,\text{J mol}^{-1}\,\text{K}^{-1}R=8.31J mol−1K−1; temperature in kelvin.

pV=NkTpV = NkTpV=NkT

Ideal gas equation (molecules)

k=1.38×10−23 J K−1k = 1.38\times10^{-23}\,\text{J K}^{-1}k=1.38×10−23J K−1 is the Boltzmann constant.

Worked example

Moles and molecules in a flask

A flask of volume 1.5×10−3 m31.5\times10^{-3}\,\text{m}^31.5×10−3m3 holds gas at 2.0×105 Pa2.0\times10^{5}\,\text{Pa}2.0×105Pa and 300 K300\,\text{K}300K. Find the amount in moles and the number of molecules. Take R=8.31 J mol−1 K−1R = 8.31\,\text{J mol}^{-1}\,\text{K}^{-1}R=8.31J mol−1K−1 and NA=6.02×1023 mol−1N_A = 6.02\times10^{23}\,\text{mol}^{-1}NA​=6.02×1023mol−1.

  1. 01Amount in moles

    From pV=nRTpV = nRTpV=nRT, n=pV/RT=(2.0×105)(1.5×10−3)/(8.31×300)n = pV/RT = (2.0\times10^{5})(1.5\times10^{-3})/(8.31 \times 300)n=pV/RT=(2.0×105)(1.5×10−3)/(8.31×300).

    n=3002493=0.120 moln = \dfrac{300}{2493} = 0.120\,\text{mol}n=2493300​=0.120mol
  2. 02Number of molecules

    N=nNA=0.120×6.02×1023=7.2×1022N = n N_A = 0.120 \times 6.02\times10^{23} = 7.2\times10^{22}N=nNA​=0.120×6.02×1023=7.2×1022.

Result: The flask holds 0.12 mol0.12\,\text{mol}0.12mol, about 7.2×10227.2\times10^{22}7.2×1022 molecules.

Exam focus

  • Apply pV=nRTpV = nRTpV=nRT and pV=NkTpV = NkTpV=NkT, converting temperatures to kelvin, to find any state quantity.
  • Use the individual gas laws and interpret ppp-VVV isotherms; calculate work done at constant pressure as p ΔVp\,\Delta VpΔV.

Typical mistakes

  • Using Celsius instead of kelvin in the gas laws - always add 273 to convert.
  • Confusing the amount in moles nnn with the number of molecules NNN (they differ by NAN_ANA​).

Active revision

A sealed flask of volume 2.0×10−3 m32.0\times10^{-3}\,\text{m}^32.0×10−3m3 contains gas at 1.0×105 Pa1.0\times10^{5}\,\text{Pa}1.0×105Pa and 27 ∘C27\,^{\circ}\text{C}27∘C. Calculate the number of moles and the number of molecules.

Active recall

Recall the key points — then reveal.

Sources: AQA A-level Physics 7408 specification (AQA)

§ 06

Molecular kinetic theory#

●●●AdvancedLPAQA 7408 3.6.2.4LPDfE GCE Physics - kinetic theory

Key points

The kinetic theory explains the pressure of a gas as the result of countless molecules colliding with the container walls. It rests on assumptions: the molecules are identical, move randomly and rapidly, are far apart compared with their size (negligible volume), exert no forces except during collisions, and undergo perfectly elastic collisions in a time negligible compared with the time between them. These assumptions define the ideal gas.
The central result derives the pressure from the molecular motion. Consider NNN molecules of mass mmm in a cube of side LLL. A molecule moving with velocity component uuu towards one wall rebounds elastically, reversing its momentum by 2mu2mu2mu; it returns to the same wall every 2L/u2L/u2L/u, so the average force it exerts is 2mu2L/u=mu2L\dfrac{2mu}{2L/u} = \dfrac{mu^2}{L}2L/u2mu​=Lmu2​. Summing over all molecules, dividing by the wall area L2L^2L2 to get pressure, and using the fact that the mean square speed is shared equally among the three directions (u2‾=13c2‾\overline{u^2} = \tfrac{1}{3}\overline{c^2}u2=31​c2), gives pV=13Nmc2‾pV = \tfrac{1}{3}Nm\overline{c^2}pV=31​Nmc2, where c2‾\overline{c^2}c2 is the mean square speed and the root of it, crmsc_{\text{rms}}crms​, is the root-mean-square speed.
Comparing this derived result with the experimental ideal gas equation pV=NkTpV = NkTpV=NkT links the microscopic and the macroscopic: 13Nmc2‾=NkT\tfrac{1}{3}Nm\overline{c^2} = NkT31​Nmc2=NkT, which rearranges to 12mc2‾=32kT\tfrac{1}{2}m\overline{c^2} = \tfrac{3}{2}kT21​mc2=23​kT. This is a profound statement - the average translational kinetic energy of a gas molecule depends only on the absolute temperature. Temperature is, quite literally, a measure of molecular kinetic energy.
Two consequences follow. First, the root-mean-square speed is crms=3kTmc_{\text{rms}} = \sqrt{\dfrac{3kT}{m}}crms​=m3kT​​, so lighter molecules move faster at the same temperature (hydrogen far faster than carbon dioxide), and raising the temperature raises the speed only as T\sqrt{T}T​. Second, the internal energy of NNN molecules of an ideal monatomic gas is entirely kinetic, U=32NkTU = \tfrac{3}{2}NkTU=23​NkT - it depends on temperature alone, confirming that an isothermal change of an ideal gas leaves its internal energy unchanged.
pV=13Nmc2‾pV = \tfrac{1}{3}Nm\overline{c^2}pV=31​Nmc2

Kinetic-theory pressure

Pressure from the mean square speed of the molecules.

12mc2‾=32kT\tfrac{1}{2}m\overline{c^2} = \tfrac{3}{2}kT21​mc2=23​kT

Kinetic energy and temperature

Average molecular translational kinetic energy depends only on temperature.

crms=3kTmc_{\text{rms}} = \sqrt{\dfrac{3kT}{m}}crms​=m3kT​​

Root-mean-square speed

Lighter molecules are faster; speed rises as the square root of temperature.

Worked example

Root-mean-square speed of oxygen

Find the root-mean-square speed of oxygen molecules (mass 5.3×10−26 kg5.3\times10^{-26}\,\text{kg}5.3×10−26kg) at 290 K290\,\text{K}290K. Take k=1.38×10−23 J K−1k = 1.38\times10^{-23}\,\text{J K}^{-1}k=1.38×10−23J K−1.

  1. 01Use the rms-speed formula

    crms=3kT/mc_{\text{rms}} = \sqrt{3kT/m}crms​=3kT/m​.

  2. 02Substitute

    crms=3×1.38×10−23×2905.3×10−26c_{\text{rms}} = \sqrt{\dfrac{3 \times 1.38\times10^{-23} \times 290}{5.3\times10^{-26}}}crms​=5.3×10−263×1.38×10−23×290​​.

    crms=2.27×105=476 m s−1c_{\text{rms}} = \sqrt{2.27\times10^{5}} = 476\,\text{m}\,\text{s}^{-1}crms​=2.27×105​=476ms−1

Result: The oxygen molecules have an rms speed of about 480 m s−1480\,\text{m}\,\text{s}^{-1}480ms−1 - faster than the speed of sound in air.

Exam focus

  • Reproduce the outline derivation of pV=13Nmc2‾pV = \tfrac{1}{3}Nm\overline{c^2}pV=31​Nmc2 from the molecular collisions and state the assumptions.
  • Use 12mc2‾=32kT\tfrac{1}{2}m\overline{c^2} = \tfrac{3}{2}kT21​mc2=23​kT and crms=3kT/mc_{\text{rms}} = \sqrt{3kT/m}crms​=3kT/m​ to find molecular speeds and kinetic energies.

Typical mistakes

  • Confusing the root-mean-square speed with the mean speed - crms=c2‾c_{\text{rms}} = \sqrt{\overline{c^2}}crms​=c2​, not the simple average.
  • Forgetting the factor of 13\tfrac{1}{3}31​ that comes from sharing the mean square speed among the three directions.

Active revision

Calculate the root-mean-square speed of nitrogen molecules (mass 4.7×10−26 kg4.7\times10^{-26}\,\text{kg}4.7×10−26kg) at 300 K300\,\text{K}300K. Take k=1.38×10−23 J K−1k = 1.38\times10^{-23}\,\text{J K}^{-1}k=1.38×10−23J K−1.

Active recall

Recall the key points — then reveal.

Sources: AQA A-level Physics 7408 specification (AQA) · GCE AS and A level subject content for the sciences (Department for Education)

Contents

Section -- / 06

    • 01Circular motion and centripetal force◐
    • 02Simple harmonic motion: definition and solutions●
    • 03Energy in SHM, resonance and damping●
    • 04Thermal energy, specific heat capacity and latent heat◐
    • 05Ideal gases and the gas laws◐
    • 06Molecular kinetic theory●

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References & sources

Sources

Department for Education

  • GCE AS and A level subject content for the sciences

AQA

  • AQA A-level Physics 7408 specification

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