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Specific heat capacity and latent heat (VCE Physics Unit 1)

Syllabus dot point

“Investigate and apply theoretically and practically the relationships Q=mcΔTQ = mc\Delta T (specific heat capacity) and Q=mLQ = mL (latent heat of fusion and vaporisation), including multi-stage heating problems”

7 min read

Quick answer

Use Q=mcΔTQ = mc\Delta T for heating within one phase and Q=mLQ = mL for a phase change at constant temperature (for water Lf=3.34×105L_f = 3.34 \times 10^5, Lv=2.26×106L_v = 2.26 \times 10^6 J kg−1^{-1}); multi-stage problems split at each phase boundary.

Jump to a section
  1. What this dot point is asking
  2. Specific heat capacity
  3. Latent heat
  4. Conservation of energy in heat exchanges
  5. VCAA exam style
  6. Common traps
  7. In one sentence
  8. Examples in context
  9. Try this
  10. Exam-style questions

What this dot point is asking

VCAA wants you to apply two formulas: Q=mcΔTQ = mc\Delta T for temperature change within a phase, and Q=mLQ = mL for energy absorbed or released during a phase change at constant temperature. Both combine in the standard multi-stage heating problem.

Specific heat capacity

Q=mcΔTQ = m c \Delta T

  • QQ = heat energy (J)
  • mm = mass (kg)
  • cc = specific heat capacity (J kg−1^{-1} K−1^{-1})
  • ΔT\Delta T = temperature change (K or °C; same size unit)

Typical values to know: cwater=4186c_{\rm water} = 4186, cice=2100c_{\rm ice} = 2100, csteam=2010c_{\rm steam} = 2010, caluminium=900c_{\rm aluminium} = 900, ccopper=385c_{\rm copper} = 385.

Water has an unusually high specific heat, which is why coastal climates are mild and why water is used as a coolant.

Latent heat

During a phase change, energy is absorbed or released at constant temperature. The energy goes into breaking or forming intermolecular bonds.

Q=mLQ = m L

  • LfL_f = specific latent heat of fusion (solid ↔\leftrightarrow liquid). For water, Lf=3.34×105L_f = 3.34 \times 10^5 J kg−1^{-1}.
  • LvL_v = specific latent heat of vaporisation (liquid ↔\leftrightarrow gas). For water, Lv=2.26×106L_v = 2.26 \times 10^6 J kg−1^{-1}.

Vaporisation is several times more energy-intensive than fusion because all intermolecular bonds must be broken to form a gas.

Conservation of energy in heat exchanges

In an insulated container, heat lost by hot bodies equals heat gained by cold bodies:

Qlost=QgainedQ_{\rm lost} = Q_{\rm gained}

Calorimetry questions set up this equation, substitute mcΔTmc\Delta T on each side, and solve for the final temperature or unknown specific heat.

VCAA exam style

Multi-stage heating problems are the standard. Watch for the phase boundary (the moment ΔT\Delta T stops applying and LL takes over). Convert grams to kilograms before substituting. Report energy in scientific notation.

Common traps

Forgetting the phase change
A problem like "ice at −5-5°C to water at 2020°C" has three stages. Missing Q2=mLfQ_2 = mL_f gives an answer about 4.54.5 times too small (it leaves out 78%78\% of the energy).
Using ΔT\Delta T across a phase change
Inside a phase change, temperature is constant. Q=mcΔTQ = m c \Delta T does not apply.
Mixing units
Specific heats are written for SI units. A 200200 g sample is 0.2000.200 kg.
Treating LfL_f and LvL_v as interchangeable
They differ by an order of magnitude. Use LfL_f for melting/freezing, LvL_v for boiling/condensing.

In one sentence

Within a single phase, heat is related to temperature change by Q=mcΔTQ = mc\Delta T (specific heat capacity), and at a phase change heat is absorbed or released at constant temperature according to Q=mLQ = mL (latent heat of fusion or vaporisation), with energy conserved in insulated heat exchanges.

Examples in context

Example 1. Snowy 2.0 reservoir thermal mass. Tantangara Reservoir, the upper storage for Snowy 2.0, holds 254254 GL (2.54×10112.54 \times 10^{11} kg) of water. To cool this reservoir from 15∘15^\circC to 5∘5^\circC overnight in autumn would require removing Q=mcΔT=2.54×1011×4186×10=1.06×1016Q = mc\Delta T = 2.54 \times 10^{11} \times 4186 \times 10 = 1.06 \times 10^{16} J. By comparison, Australia's entire daily electricity demand is approximately 5.6×10145.6 \times 10^{14} J, so the reservoir's thermal mass is enormous. This thermal inertia stabilises water temperature for turbine bearings and reduces ice-formation risk on the spillway gates during cold snaps.

Example 2. Latrobe Valley brown coal moisture and energy penalty. Latrobe Valley brown coal contains about 60%60\% water by mass. Drying 11 kg of raw coal requires removing 0.60.6 kg of water. Energy to heat that water from 20∘20^\circC to 100∘100^\circC is Q1=0.6×4186×80=2.01×105Q_1 = 0.6 \times 4186 \times 80 = 2.01 \times 10^5 J; energy to vaporise it at 100∘100^\circC is Q2=mLv=0.6×2.26×106=1.36×106Q_2 = mL_v = 0.6 \times 2.26 \times 10^6 = 1.36 \times 10^6 J. Total moisture penalty per kg of coal is 1.561.56 MJ, against a dry-coal heat value of around 2626 MJ. Around 6%6\% of Loy Yang A's energy output is therefore spent evaporating water, which is part of why brown coal generation has lower thermal efficiency than black coal.

Try this

Q1. Define specific heat capacity and state SI units. [2 marks]

  • Cue. Energy required to raise the temperature of 11 kg of a substance by 1∘1^\circC (or 11 K); J kg−1^{-1} K−1^{-1}.

Q2. A 500500 g aluminium block (c=900c = 900 J kg−1^{-1} K−1^{-1}) absorbs 13.513.5 kJ. Calculate the temperature rise. [3 marks]

  • Cue. ΔT=Q/(mc)=13500/(0.5×900)=30∘\Delta T = Q/(mc) = 13500/(0.5 \times 900) = 30^\circC.

Q3. A 200200 g ice cube at −10∘-10^\circC is added to 400400 g of water at 25∘25^\circC in an insulated cup. Take cice=2100c_{\rm ice} = 2100, cwater=4186c_{\rm water} = 4186 J kg−1^{-1} K−1^{-1}, Lf=3.34×105L_f = 3.34 \times 10^5 J kg−1^{-1}. (a) Calculate the energy required to warm the ice to 0∘0^\circC. (b) Calculate the energy required to melt the ice at 0∘0^\circC. (c) Determine the final equilibrium temperature. [2+2+3 marks]

  • Cue. (a) 0.2×2100×10=42000.2 \times 2100 \times 10 = 4200 J. (b) 0.2×3.34×105=668000.2 \times 3.34 \times 10^5 = 66800 J. (c) The water can release only 0.4×4186×25=41 8600.4 \times 4186 \times 25 = 41\,860 J cooling to 0∘0^\circC, which is less than the 71 00071\,000 J needed to warm and melt all the ice. So the final temperature is 0∘0^\circC. After warming the ice (4 2004\,200 J), the remaining 37 66037\,660 J melts 37 660/(3.34×105)=0.11337\,660 / (3.34 \times 10^5) = 0.113 kg, leaving about 0.0870.087 kg of ice.

Exam-style questions

Questions in the style of VCAA exam questions on this dot point, each with a worked answer. They are written by ExamExplained unless tagged "Past paper"; the year shows the paper a question is modelled on.

Year 11 SAC-style5 marks
Calculate the total energy required to heat 300300 g of ice from −5-5°C to water at 2020°C, using cice=2100c_{\rm ice}=2100 J kg−1^{-1} K−1^{-1}, cwater=4186c_{\rm water}=4186 J kg−1^{-1} K−1^{-1} and Lf=3.34×105L_f = 3.34 \times 10^5 J kg−1^{-1}.
Show worked answer →

Three stages.

Stage 1 (ice −5-5°C →\to ice 00°C). Q1=(0.300)(2100)(5)=3150Q_1 = (0.300)(2100)(5) = 3150 J.

Stage 2 (melt at 00°C). Q2=mLf=(0.300)(3.34×105)=100 200Q_2 = m L_f = (0.300)(3.34 \times 10^5) = 100\,200 J.

Stage 3 (water 00°C →\to water 2020°C). Q3=(0.300)(4186)(20)=25 116Q_3 = (0.300)(4186)(20) = 25\,116 J.

Total: Q=3150+100 200+25 116=1.28×105Q = 3150 + 100\,200 + 25\,116 = 1.28 \times 10^5 J.

Markers reward splitting at the phase boundary, mass in kg, and a final answer in scientific notation.

Practise this

Sources & how we know this

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