Lesson 4 of 4
Phase change and latent heat
I can define and apply specific heat capacity and specific latent heat under the stated thermal and process conditions.Syllabus
Syllabus 9478, 13(g). Define and apply specific heat capacity and specific latent heat under the stated thermal and process conditions.
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Ice at 0 degrees C is heated until it has all become water at 0 degrees C. What happens to its internal energy?
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It increases, as the potential energy of the molecules rises.
Energy is supplied to break the rigid structure. The mean kinetic energy stays the same, but the molecular potential energy rises, so the internal energy increases.
Decide whether the energy changes temperature or changes phase. At a phase change, energy can enter while temperature stays constant under the stated pressure and conditions.
Define specific latent heat
Specific latent heat l is the energy required by heating per unit mass for a stated change of phase at constant temperature under stated conditions. Its unit is J/kg.
Specific latent heat of fusion concerns melting; specific latent heat of vaporisation concerns liquid becoming vapour. Their values need not be equal. Freezing and condensation transfer energy out under the corresponding reversed conditions.
Here lowercase l denotes the specific quantity. Some references use L for it; check the definition and unit. A value in J/kg is not the total energy for an arbitrary sample.
During a phase change, energy can change microscopic potential energy and supply expansion work without raising temperature. Q = mcΔT describes warming within a phase, so setting ΔT = 0 in that equation does not prove that no energy entered during a phase change.
Split a multi-stage change
Before calculating precisely, roughly 0.1 kg multiplied by a supplied fusion latent heat of order 3 × 105 J/kg needs energy of order 3 × 104 J. Melting should therefore dominate the following account compared with its short warming stages.
Worked warming and melting
Ice at -5.0°C to water at 25.0°C
A 0.0800 kg ice sample ends as liquid water. Use cice = 2100 J/(kg K), lf = 3.34 × 105 J/kg and cwater = 4200 J/(kg K). The stated melting temperature is 0°C. Assume constant properties over each interval, negligible losses and container heat capacity, and negligible volume work for these condensed phases.
| Stage | Calculation | Energy / J |
|---|---|---|
| Warm ice from -5 to 0°C | 0.0800 × 2100 × 5.0 | 840 |
| Melt all ice at 0°C | 0.0800 × 3.34 × 105 | 26720 |
| Warm water from 0 to 25°C | 0.0800 × 4200 × 25.0 | 8400 |
= 35960 J ≈ 36.0 kJ
Use cumulative energy to separate warming from melting
For the stated 0.0800 kg ice/water sample, assume the supplied heat capacities and fusion latent heat, negligible loss and vessel capacity, and negligible volume work. The horizontal coordinate is energy supplied to the sample, not time.
A: 0 kJ, -5 °C. B: 0.840 kJ, 0 °C. C: 27.560 kJ, 0 °C. D: 35.960 kJ, 25 °C.
A-B warms ice; B-C melts it; C-D warms water. The initial stage is genuinely narrow on this energy scale. A flat temperature segment does not mean that energy input has stopped.
The first 840 J warms the ice. The next 26720 J melts it, so complete melting occurs at cumulative input 27560 J. Only after this can further input warm an entirely liquid sample in this model. The graph's energy widths do not by themselves specify stage durations.
Check whether all the material changes phase
Suppose a separate 0.0200 kg ice sample is already at its melting point and receives 5000 J, with negligible other transfers. Complete melting would require:
Mass melted = 5000/(3.34 × 105)
= 0.01497 kg ≈ 15.0 g
About 5.03 g of ice remains. Ice and water coexist at the melting temperature under the stated conditions; there is insufficient energy to melt everything and then warm the liquid.
Try it step by step
Work it out in steps: Energy for the change of state, Q = mL, in J, then Time at the heater power, t = Q / P, in s.
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Problem 1.
Energy for the change of state, Q = mL, in J: Q = 0.20 x 3.34 x 105 = 6.68 x 104 J
Time at the heater power, t = Q / P, in s: t = 6.68 x 104 / 100 = 668 s
Problem 2.
Energy for the change of state, Q = mL, in J: Q = 0.050 x 3.34 x 105 = 1.67 x 104 J
Time at the heater power, t = Q / P, in s: t = 1.67 x 104 / 50 = 334 s
Problem 3.
Energy for the change of state, Q = mL, in J: Q = 0.30 x 2.26 x 106 = 6.78 x 105 J
Time at the heater power, t = Q / P, in s: t = 6.78 x 105 / 2000 = 339 s
Check your understanding
A 20.0 g ice sample is already at its melting point. It receives 5000 J with negligible other transfers. Use l_f = 3.34 x 105 J/kg. What happens?
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About 15.0 g melts and the temperature stays at the melting point.
Melted mass = 5000/(3.34 x 105) = 0.01497 kg. The energy is insufficient to melt all 20.0 g, so ice and water remain together at the melting temperature.
Account for work during vaporisation
Latent heating need not all become an internal-energy increase when the sample expands significantly. Choose a fixed sample as the system and use ΔU = Q + Won.
Worked phase-change energy account
Separate heating from expansion work
In a separate supplied model, 0.0100 kg vaporises at constant temperature against external pressure 2.0 × 105 Pa. Use lv = 1.80 × 106 J/kg and a volume increase of 0.0060 m3. These are supplied model properties, not stated values for water.
Wby = pextΔV = 1200 J
Won = -1200 J
ΔU = 18000 - 1200 = 16800 J
The heating supplies both the internal-energy increase and the work output. Constant temperature does not mean zero ΔU, and Q = ml does not automatically make ΔU equal to Q.
Measure fusion latent heat with a matched control
A melting investigation can compare water collected with a measured heater input against a comparable no-heater control. Begin with ice and apparatus at the melting temperature, drain pre-existing water before timed collection, and use the same collection geometry and duration. Measure collected mass with a tared collector and record the input and timing resolutions.
Compare collected melt with a matched no-input control
Begin with ice and apparatus at the melting temperature, and drain pre-existing water before each timed collection. The two runs use the same arrangement and 300 s interval. The supplied model assumes equal background heating and complete collection of the relevant melt.
Heater-on collection
Matched control: no heater input
The extra collected mass is 20.00 - 5.00 = 15.00 g. The measured heater input is 16.7 × 300 = 5010 J, giving lf = 5010/0.01500 = 3.34 × 105 J/kg under the stated assumptions.
This is an input-versus-extra-melt comparison. Initial warming, trapped water or a changed background transfer would undermine the simple subtraction. Because meltwater leaves the holder, a closed fixed-mass account for the holder would omit the outflow.
In the supplied comparison, measured heater power is 16.7 W = 16.7 J/s for 300 s. The heated run collects 20.00 g of water; the comparable control collects 5.00 g.
Extra melted mass = (20.00 - 5.00) g = 0.01500 kg
lf = 5010/0.01500
= 3.34 × 105 J/kg
This calculation assumes complete collection, equal background transfer in the two runs, and that the measured heater input accounts for the additional melting rather than appreciable apparatus warming or an unmatched loss. The control is a conditional correction, not a guarantee that every error has disappeared.
- Ice initially below its melting point: part of the input first warms it. Treating all that input as melting energy can make the inferred l too high.
- Water retained in the apparatus: the collected extra mass can be smaller than the mass actually melted. Dividing input by that underestimated mass can also give too large an l.
- Different background conditions: a heater can change temperature gradients or losses. A control that no longer matches these conditions cannot simply be subtracted as an equal background.
Water leaving the vessel crosses its boundary. Do not apply a closed, fixed-mass first-law account to that vessel while ignoring the outflow. The matched input-and-mass calculation above states the required assumptions without treating the draining vessel as such a system.
Practise an exam question
Write your answer first, then tick the mark points it makes.
Exam-style question
The specific latent heat of vaporisation of water is much larger than its specific latent heat of fusion. Explain why. [3]
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