So far we have discussed temperature change due to heat transfer. No temperature change occurs from heat transfer if ice melts and becomes liquid water (i.e., during a phase change). For example, consider water dripping from icicles melting on a roof warmed by the Sun. Conversely, water freezes in an ice tray cooled by lower-temperature surroundings.

Energy is required to melt a solid because the cohesive bonds between the molecules in the solid must be broken apart such that, in the liquid, the molecules can move around at comparable kinetic energies; thus, there is no rise in temperature. Similarly, energy is needed to vaporize a liquid, because molecules in a liquid interact with each other via attractive forces. There is no temperature change until a phase change is complete. The temperature of a cup of soda initially at [latex]0º\text{C}[/latex] stays at [latex]0º\text{C}[/latex] until all the ice has melted. Conversely, energy is released during freezing and condensation, usually in the form of thermal energy. Work is done by cohesive forces when molecules are brought together. The corresponding energy must be given off (dissipated) to allow them to stay together (Figure).

The energy involved in a phase change depends on two major factors: the number and strength of bonds or force pairs. The number of bonds is proportional to the number of molecules and thus to the mass of the sample. The strength of forces depends on the type of molecules. The heat [latex]Q[/latex] required to change the phase of a sample of mass [latex]m[/latex] is given by

where the latent heat of fusion, [latex]{L}_{\text{f}}[/latex], and latent heat of vaporization, [latex]{L}_{\text{v}}[/latex], are material constants that are determined experimentally. See ((Figure)).

Latent heat is measured in units of J/kg. Both [latex]{L}_{\text{f}}[/latex] and [latex]{L}_{\text{v}}[/latex] depend on the substance, particularly on the strength of its molecular forces as noted earlier. [latex]{L}_{\text{f}}[/latex] and [latex]{L}_{\text{v}}[/latex] are collectively called latent heat coefficients. They are latent, or hidden, because in phase changes, energy enters or leaves a system without causing a temperature change in the system; so, in effect, the energy is hidden. (Figure) lists representative values of [latex]{L}_{\text{f}}[/latex] and [latex]{L}_{\text{v}}[/latex], together with melting and boiling points.

The table shows that significant amounts of energy are involved in phase changes. Let us look, for example, at how much energy is needed to melt a kilogram of ice at [latex]0º\text{C}[/latex] to produce a kilogram of water at [latex]0°\text{C}[/latex]. Using the equation for a change in temperature and the value for water from (Figure), we find that [latex]Q={\text{mL}}_{\text{f}}=\left(1\text{.}0\phantom{\rule{0.25em}{0ex}}\text{kg}\right)\left(\text{334}\phantom{\rule{0.25em}{0ex}}\text{kJ/kg}\right)=\text{334}\phantom{\rule{0.25em}{0ex}}\text{kJ}[/latex] is the energy to melt a kilogram of ice. This is a lot of energy as it represents the same amount of energy needed to raise the temperature of 1 kg of liquid water from [latex]0º\text{C}[/latex] to [latex]\text{79}\text{.}8º\text{C}[/latex]. Even more energy is required to vaporize water; it would take 2256 kJ to change 1 kg of liquid water at the normal boiling point ([latex]\text{100º}\text{C}[/latex] at atmospheric pressure) to steam (water vapor). This example shows that the energy for a phase change is enormous compared to energy associated with temperature changes without a phase change.

Phase changes can have a tremendous stabilizing effect even on temperatures that are not near the melting and boiling points, because evaporation and condensation (conversion of a gas into a liquid state) occur even at temperatures below the boiling point. Take, for example, the fact that air temperatures in humid climates rarely go above [latex]\text{35}\text{.}0º\text{C}[/latex], which is because most heat transfer goes into evaporating water into the air. Similarly, temperatures in humid weather rarely fall below the dew point because enormous heat is released when water vapor condenses.

We examine the effects of phase change more precisely by considering adding heat into a sample of ice at [latex]-\text{20º}\text{C}[/latex] ((Figure)). The temperature of the ice rises linearly, absorbing heat at a constant rate of [latex]0\text{.}\text{50 cal/g}\cdot º\text{C}[/latex] until it reaches [latex]0º\text{C}[/latex]. Once at this temperature, the ice begins to melt until all the ice has melted, absorbing 79.8 cal/g of heat. The temperature remains constant at [latex]0º\text{C}[/latex] during this phase change. Once all the ice has melted, the temperature of the liquid water rises, absorbing heat at a new constant rate of [latex]1\text{.}\text{00 cal/g}\cdot º\text{C}[/latex]. At [latex]\text{100º}\text{C}[/latex], the water begins to boil and the temperature again remains constant while the water absorbs 539 cal/g of heat during this phase change. When all the liquid has become steam vapor, the temperature rises again, absorbing heat at a rate of [latex]0\text{.}\text{482 cal/g}\cdot º\text{C}[/latex].

Water can evaporate at temperatures below the boiling point. More energy is required than at the boiling point, because the kinetic energy of water molecules at temperatures below [latex]\text{100º}\text{C}[/latex] is less than that at [latex]\text{100º}\text{C}[/latex], hence less energy is available from random thermal motions. Take, for example, the fact that, at body temperature, perspiration from the skin requires a heat input of 2428 kJ/kg, which is about 10 percent higher than the latent heat of vaporization at [latex]\text{100º}\text{C}[/latex]. This heat comes from the skin, and thus provides an effective cooling mechanism in hot weather. High humidity inhibits evaporation, so that body temperature might rise, leaving unevaporated sweat on your brow.

We have seen that vaporization requires heat transfer to a liquid from the surroundings, so that energy is released by the surroundings. Condensation is the reverse process, increasing the temperature of the surroundings. This increase may seem surprising, since we associate condensation with cold objects—the glass in the figure, for example. However, energy must be removed from the condensing molecules to make a vapor condense. The energy is exactly the same as that required to make the phase change in the other direction, from liquid to vapor, and so it can be calculated from [latex]Q={\text{mL}}_{\text{v}}[/latex].

Sublimation is the transition from solid to vapor phase. You may have noticed that snow can disappear into thin air without a trace of liquid water, or the disappearance of ice cubes in a freezer. The reverse is also true: Frost can form on very cold windows without going through the liquid stage. A popular effect is the making of “smoke” from dry ice, which is solid carbon dioxide. Sublimation occurs because the equilibrium vapor pressure of solids is not zero. Certain air fresheners use the sublimation of a solid to inject a perfume into the room. Moth balls are a slightly toxic example of a phenol (an organic compound) that sublimates, while some solids, such as osmium tetroxide, are so toxic that they must be kept in sealed containers to prevent human exposure to their sublimation-produced vapors.

All phase transitions involve heat. In the case of direct solid-vapor transitions, the energy required is given by the equation [latex]Q={\mathrm{mL}}_{\text{s}}[/latex], where [latex]{L}_{\text{s}}[/latex] is the heat of sublimation, which is the energy required to change 1.00 kg of a substance from the solid phase to the vapor phase. [latex]{L}_{\text{s}}[/latex] is analogous to [latex]{L}_{\text{f}}[/latex] and [latex]{L}_{\text{v}}[/latex], and its value depends on the substance. Sublimation requires energy input, so that dry ice is an effective coolant, whereas the reverse process (i.e., frosting) releases energy. The amount of energy required for sublimation is of the same order of magnitude as that for other phase transitions.

The material presented in this section and the preceding section allows us to calculate any number of effects related to temperature and phase change. In each case, it is necessary to identify which temperature and phase changes are taking place and then to apply the appropriate equation. Keep in mind that heat transfer and work can cause both temperature and phase changes.