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Physics · Ch 10 — Thermal Properties of Matter

Latent Heat

10.8.1

Latent Heat

The Idea of Change of State

Matter exists in three common states — solid, liquid, and gas. A change from one state to another is not a gradual, continuous process at the microscopic level. Instead, it happens at a fixed temperature for a given substance at a given pressure. For example, ice melts at 0∘C0^\circ\text{C} and water boils at 100∘C100^\circ\text{C} (at standard atmospheric pressure). During the entire phase change, the temperature of the substance remains constant even though heat is being continuously added or removed.

Why does the temperature stay constant? The heat supplied during a phase change does not go into raising the kinetic energy (temperature) of the particles. Instead, it is used to overcome the intermolecular forces that hold the particles together in the original state. This hidden heat is called latent heat (from the Latin latere, meaning "to lie hidden").

Note

The term "latent" means hidden. The heat is "hidden" because it does not show up as a temperature rise — it is stored as potential energy in the new arrangement of molecules.

Latent Heat — Definition

The latent heat of a substance is the quantity of heat required to change the state of unit mass of the substance from one state to another without any change in temperature.

If a mass mm of a substance undergoes a complete change of state, and the heat absorbed or released is QQ, then the latent heat LL is given by:

L=QmL = \frac{Q}{m}

The SI unit of latent heat is J kg−1\text{J kg}^{-1} (joule per kilogram). In the CGS system, it is often expressed in cal g−1\text{cal g}^{-1}.

Q=mLQ = mL

This is the fundamental equation linking heat exchanged, mass, and latent heat. The sign of QQ is positive when heat is absorbed (melting, vaporisation, sublimation) and negative when heat is released (freezing, condensation, deposition).

Two Specific Latent Heats

The section focuses on two important phase changes:

  1. Fusion — change from solid to liquid (melting) or liquid to solid (freezing).
  2. Vaporisation — change from liquid to vapour (boiling/evaporation) or vapour to liquid (condensation).

Correspondingly, we define two specific latent heats:

  • Latent heat of fusion (LfL_f): The heat required to convert 1 kg of a solid into liquid at its melting point, without any temperature change.
  • Latent heat of vaporisation (LvL_v): The heat required to convert 1 kg of a liquid into vapour at its boiling point, without any temperature change.
Important

The latent heat of fusion is always less than the latent heat of vaporisation for the same substance. For example, for water: Lf=3.35×105 J kg−1L_f = 3.35 \times 10^5 \text{ J kg}^{-1} (or 80 cal g−1^{-1}), while Lv=2.256×106 J kg−1L_v = 2.256 \times 10^6 \text{ J kg}^{-1} (or 540 cal g−1^{-1}). This is because the change in intermolecular separation (and hence the work done against intermolecular forces) is much larger when going from liquid to gas than from solid to liquid.

Standard Values for Water (at 1 atm)

The textbook provides these standard values, which are essential for numerical problems:

Phase ChangeLatent HeatValue in SIValue in CGS
Fusion (ice ↔\leftrightarrow water)LfL_f3.35×105 J kg−13.35 \times 10^5 \text{ J kg}^{-1}80 cal g−1^{-1}
Vaporisation (water ↔\leftrightarrow steam)LvL_v2.256×106 J kg−12.256 \times 10^6 \text{ J kg}^{-1}540 cal g−1^{-1}
Tip

In calorimetry problems, you will often use these values. Remember that 1 cal = 4.186 J. So, 80 cal g−1×4.186 J/cal×1000 g/kg≈3.35×105 J kg−180 \text{ cal g}^{-1} \times 4.186 \text{ J/cal} \times 1000 \text{ g/kg} \approx 3.35 \times 10^5 \text{ J kg}^{-1}.

Melting Points, Boiling Points, and Latent Heats of Other Substances

Table 10.5 gives the melting point, latent heat of fusion, boiling point, and latent heat of vaporisation for a few common substances besides water, at 1 atmosphere pressure.

Table 10.5 Temperatures of change of state and latent heats

SubstanceMelting pointLfL_f (105 J kg−110^5\ \text{J kg}^{-1})Boiling pointLvL_v (105 J kg−110^5\ \text{J kg}^{-1})
Ethanol−114∘C-114^\circ\text{C}1.078∘C78^\circ\text{C}8.5
Gold1063∘C1063^\circ\text{C}0.6452660∘C2660^\circ\text{C}15.8
Lead328∘C328^\circ\text{C}0.251744∘C1744^\circ\text{C}8.7
Mercury−39∘C-39^\circ\text{C}0.12357∘C357^\circ\text{C}2.7
Nitrogen−210∘C-210^\circ\text{C}0.26−196∘C-196^\circ\text{C}2.0
Oxygen−219∘C-219^\circ\text{C}0.14−183∘C-183^\circ\text{C}2.1
Water0∘C0^\circ\text{C}3.33100∘C100^\circ\text{C}22.6

Properties of Latent Heat (with Derivations)

The textbook lists and proves several important properties. Each is derived from the definition Q=mLQ = mL and the principle of calorimetry (heat lost = heat gained).

›Proof

Property 1: Heat required to melt a solid at its melting point.

If a mass mm of a solid at its melting point is completely converted into liquid at the same temperature, the heat QQ required is:

Q=mLfQ = m L_f

Derivation: This follows directly from the definition of latent heat of fusion. The heat absorbed per unit mass is LfL_f, so for mass mm, the total heat is m×Lfm \times L_f.

›Proof

Property 2: Heat required to vaporise a liquid at its boiling point.

If a mass mm of a liquid at its boiling point is completely converted into vapour at the same temperature, the heat QQ required is:

Q=mLvQ = m L_v

Derivation: This follows directly from the definition of latent heat of vaporisation. The heat absorbed per unit mass is LvL_v, so for mass mm, the total heat is m×Lvm \times L_v.

›Proof

Property 3: Heat released during freezing (solidification).

If a mass mm of a liquid at its freezing point solidifies completely at the same temperature, the heat QQ released is:

Q=mLfQ = m L_f …

Figure 10.12Temperature versus heat for water at 1 atm pressure (not to scale).
Fig. 10.12 — Temperature versus heat for water at 1 atm pressure (not to scale).

Drawn by us to help you understand the concept clearly, and verified to make sure it's accurate. For exams, practice from your textbook's own diagram.

The figure plots temperature (in °C) on the vertical axis against heat added (in joules, per unit mass) on the horizontal axis. The temperature scale shows two key horizontal lines: one at 0 °C and one at 100 °C. The heat axis is not drawn to scale — the lengths of the plateaus are chosen for clarity, not for exact proportion.

The curve itself is a series of five distinct segments, read from left to right:

  1. Rising ice line — a sloping upward segment where solid ice absorbs heat and its temperature rises from below 0 °C up to 0 °C. The specific heat capacity of ice governs the slope: Q=mciceΔTQ = m c_{\text{ice}} \Delta T.

  2. Melting plateau — a flat horizontal segment at 0 °C. Here, all added heat goes into breaking the crystal lattice of ice, not into raising temperature. The heat absorbed per unit mass is the latent heat of fusion, Lf=3.33×105 J/kgL_f = 3.33 \times 10^5\ \text{J/kg}. The formula is Q=mLfQ = m L_f.

  3. Rising water line — a sloping upward segment where liquid water heats from 0 °C to 100 °C. The specific heat capacity of water is cwater=4186 J/(kg⋅K)c_{\text{water}} = 4186\ \text{J/(kg·K)}, so Q=mcwaterΔTQ = m c_{\text{water}} \Delta T.

  4. Boiling plateau — a flat horizontal segment at 100 °C. Heat now supplies the energy needed to overcome intermolecular forces and turn liquid into vapour, without any temperature change. The latent heat of vaporisation is Lv=22.6×105 J/kgL_v = 22.6 \times 10^5\ \text{J/kg}, and Q=mLvQ = m L_v.

  5. Rising steam line — a final sloping segment where steam (water vapour) heats above 100 °C, with its own specific heat capacity csteam≈2000 J/(kg⋅K)c_{\text{steam}} \approx 2000\ \text{J/(kg·K)}.

Important

The flat plateaus are the central physical lesson: during a phase change, temperature stays constant even though heat continues to flow. The heat is “hidden” (latent) — it changes the internal potential energy of the substance, not its kinetic energy (which is what temperature measures).

The textbook uses this figure to introduce the two key formulas for phase changes:

Q=mLQ = m L

where QQ is the heat absorbed or released during a phase change, mm is the mass of the substance, and LL is the specific latent heat (in J/kg). For melting/freezing, L=LfL = L_f; for boiling/condensation, L=LvL = L_v. …