University Physics Volume 2

# 1.5Phase Changes

## Learning Objectives

By the end of this section, you will be able to:

• Describe phase transitions and equilibrium between phases
• Solve problems involving latent heat
• Solve calorimetry problems involving phase changes

Phase transitions play an important theoretical and practical role in the study of heat flow. In melting (or “fusion”), a solid turns into a liquid; the opposite process is freezing. In evaporation, a liquid turns into a gas; the opposite process is condensation.

A substance melts or freezes at a temperature called its melting point, and boils (evaporates rapidly) or condenses at its boiling point. These temperatures depend on pressure. High pressure favors the denser form, so typically, high pressure raises the melting point and boiling point, and low pressure lowers them. For example, the boiling point of water is $100°C100°C$ at 1.00 atm. At higher pressure, the boiling point is higher, and at lower pressure, it is lower. The main exception is the melting and freezing of water, discussed in the next section.

## Phase Diagrams

The phase of a given substance depends on the pressure and temperature. Thus, plots of pressure versus temperature showing the phase in each region provide considerable insight into thermal properties of substances. Such a pT graph is called a phase diagram.

Figure 1.12 shows the phase diagram for water. Using the graph, if you know the pressure and temperature, you can determine the phase of water. The solid curves—boundaries between phases—indicate phase transitions, that is, temperatures and pressures at which the phases coexist. For example, the boiling point of water is $100°C100°C$ at 1.00 atm. As the pressure increases, the boiling temperature rises gradually to $374°C374°C$ at a pressure of 218 atm. A pressure cooker (or even a covered pot) cooks food faster than an open pot, because the water can exist as a liquid at temperatures greater than $100°C100°C$ without all boiling away. (As we’ll see in the next section, liquid water conducts heat better than steam or hot air.) The boiling point curve ends at a certain point called the critical point—that is, a critical temperature, above which the liquid and gas phases cannot be distinguished; the substance is called a supercritical fluid. At sufficiently high pressure above the critical point, the gas has the density of a liquid but does not condense. Carbon dioxide, for example, is supercritical at all temperatures above $31.0°C31.0°C$. Critical pressure is the pressure of the critical point.

Figure 1.12 The phase diagram (pT graph) for water shows solid (s), liquid (l), and vapor (v) phases. At temperatures and pressure above those of the critical point, there is no distinction between liquid and vapor. Note that the axes are nonlinear and the graph is not to scale. This graph is simplified—it omits several exotic phases of ice at higher pressures. The phase diagram of water is unusual because the melting-point curve has a negative slope, showing that you can melt ice by increasing the pressure.

Similarly, the curve between the solid and liquid regions in Figure 1.12 gives the melting temperature at various pressures. For example, the melting point is $0°C0°C$ at 1.00 atm, as expected. Water has the unusual property that ice is less dense than liquid water at the melting point, so at a fixed temperature, you can change the phase from solid (ice) to liquid (water) by increasing the pressure. That is, the melting temperature of ice falls with increased pressure, as the phase diagram shows. For example, when a car is driven over snow, the increased pressure from the tires melts the snowflakes; afterwards, the water refreezes and forms an ice layer.

As you learned in the earlier section on thermometers and temperature scales, the triple point is the combination of temperature and pressure at which ice, liquid water, and water vapor can coexist stably—that is, all three phases exist in equilibrium. For water, the triple point occurs at $273.16K(0.01°C)273.16K(0.01°C)$ and 611.2 Pa; that is a more accurate calibration temperature than the melting point of water at 1.00 atm, or $273.15K(0.0°C)273.15K(0.0°C)$.

## Interactive

View this video to see a substance at its triple point.

At pressures below that of the triple point, there is no liquid phase; the substance can exist as either gas or solid. For water, there is no liquid phase at pressures below 0.00600 atm. The phase change from solid to gas is called sublimation. You may have noticed that snow can disappear into thin air without a trace of liquid water, or that ice cubes can disappear in a freezer. Both are examples of sublimation. The reverse also happens: Frost can form on very cold windows without going through the liquid stage. Figure 1.13 shows the result, as well as showing a familiar example of sublimation. Carbon dioxide has no liquid phase at atmospheric pressure. Solid $CO2CO2$ is known as dry ice because instead of melting, it sublimes. Its sublimation temperature at atmospheric pressure is $−78°C−78°C$. Certain air fresheners use the sublimation of a solid to spread a perfume around a room. 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.

Figure 1.13 Direct transitions between solid and vapor are common, sometimes useful, and even beautiful. (a) Dry ice sublimes directly to carbon dioxide gas. The visible “smoke” consists of water droplets that condensed in the air cooled by the dry ice. (b) Frost forms patterns on a very cold window, an example of a solid formed directly from a vapor. (credit a: modification of work by Windell Oskay; credit b: modification of work by Liz West)

## Equilibrium

At the melting temperature, the solid and liquid phases are in equilibrium. If heat is added, some of the solid will melt, and if heat is removed, some of the liquid will freeze. The situation is somewhat more complex for liquid-gas equilibrium. Generally, liquid and gas are in equilibrium at any temperature. We call the gas phase a vapor when it exists at a temperature below the critical temperature, as it does for water at $20.0°C20.0°C$. Liquid in a closed container at a fixed temperature evaporates until the pressure of the gas reaches a certain value, called the vapor pressure, which depends on the gas and the temperature. At this equilibrium, if heat is added, some of the liquid will evaporate, and if heat is removed, some of the gas will condense; molecules either join the liquid or form suspended droplets. If there is not enough liquid for the gas to reach the vapor pressure in the container, all the liquid eventually evaporates.

If the vapor pressure of the liquid is greater than the total ambient pressure, including that of any air (or other gas), the liquid evaporates rapidly; in other words, it boils. Thus, the boiling point of a liquid at a given pressure is the temperature at which its vapor pressure equals the ambient pressure. Liquid and gas phases are in equilibrium at the boiling temperature (Figure 1.14). If a substance is in a closed container at the boiling point, then the liquid is boiling and the gas is condensing at the same rate without net change in their amounts.

Figure 1.14 Equilibrium between liquid and gas at two different boiling points inside a closed container. (a) The rates of boiling and condensation are equal at this combination of temperature and pressure, so the liquid and gas phases are in equilibrium. (b) At a higher temperature, the boiling rate is faster, that is, the rate at which molecules leave the liquid and enter the gas is faster. This increases the number of molecules in the gas, which increases the gas pressure, which in turn increases the rate at which gas molecules condense and enter the liquid. The pressure stops increasing when it reaches the point where the boiling rate and the condensation rate are equal. The gas and liquid are in equilibrium again at this higher temperature and pressure.

For water, $100°C100°C$ is the boiling point at 1.00 atm, so water and steam should exist in equilibrium under these conditions. Why does an open pot of water at $100°C100°C$ boil completely away? The gas surrounding an open pot is not pure water: it is mixed with air. If pure water and steam are in a closed container at $100°C100°C$ and 1.00 atm, they will coexist—but with air over the pot, there are fewer water molecules to condense, and water boils away. At any given temperature, including when boiling, vapor is generated at the corresponding saturation vapor pressure. This may be less than the ambient pressure, but part of the ambient pressure is due to air, so the pressure of the vapor above the pot can be less than the pressure of the vapor being generated at that temperature, and evaporation continues. Incidentally, the equilibrium vapor pressure of solids is not zero, a fact that accounts for sublimation.

Explain why a cup of water (or soda) with ice cubes stays at $0°C,0°C,$ even on a hot summer day.

## Phase Change and Latent Heat

So far, we have discussed heat transfers that cause temperature change. However, in a phase transition, heat transfer does not cause any temperature change.

For an example of phase changes, consider the addition of heat to a sample of ice at $−20°C−20°C$ (Figure 1.15) and atmospheric pressure. The temperature of the ice rises linearly, absorbing heat at a constant rate of $2090J/kg·ºC2090J/kg·ºC$ until it reaches $0°C.0°C.$ Once at this temperature, the ice begins to melt and continues until it has all melted, absorbing 333 kJ/kg of heat. The temperature remains constant at $0°C0°C$ 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 At $100°C,100°C,$ the water begins to boil. The temperature again remains constant during this phase change while the water absorbs 2256 kJ/kg of heat and turns into steam. When all the liquid has become steam, the temperature rises again, absorbing heat at a rate of $2020J/kg·ºC2020J/kg·ºC$. If we started with steam and cooled it to make it condense into liquid water and freeze into ice, the process would exactly reverse, with the temperature again constant during each phase transition.

Figure 1.15 Temperature versus heat. The system is constructed so that no vapor evaporates while ice warms to become liquid water, and so that, when vaporization occurs, the vapor remains in the system. The long stretches of constant temperatures at $0°C0°C$ and $100°C100°C$ reflect the large amounts of heat needed to cause melting and vaporization, respectively.

Where does the heat added during melting or boiling go, considering that the temperature does not change until the transition is complete? Energy is required to melt a solid, because the attractive forces between the molecules in the solid must be broken apart, so that in the liquid, the molecules can move around at comparable kinetic energies; thus, there is no rise in temperature. Energy is needed to vaporize a liquid for similar reasons. Conversely, work is done by attractive forces when molecules are brought together during freezing and condensation. That energy must be transferred out of the system, usually in the form of heat, to allow the molecules to stay together (Figure 1.18). Thus, condensation occurs in association with cold objects—the glass in Figure 1.16, for example.

Figure 1.16 Condensation forms on this glass of iced tea because the temperature of the nearby air is reduced. The air cannot hold as much water as it did at room temperature, so water condenses. Energy is released when the water condenses, speeding the melting of the ice in the glass. (credit: Jenny Downing)

The energy released when a liquid freezes is used by orange growers when the temperature approaches $0°C0°C$. Growers spray water on the trees so that the water freezes and heat is released to the growing oranges. This prevents the temperature inside the orange from dropping below freezing, which would damage the fruit (Figure 1.17).

Figure 1.17 The ice on these trees released large amounts of energy when it froze, helping to prevent the temperature of the trees from dropping below $0°C0°C$. Water is intentionally sprayed on orchards to help prevent hard frosts. (credit: Hermann Hammer)

The energy involved in a phase change depends on the number of bonds or force pairs and their strength. The number of bonds is proportional to the number of molecules and thus to the mass of the sample. The energy per unit mass required to change a substance from the solid phase to the liquid phase, or released when the substance changes from liquid to solid, is known as the heat of fusion. The energy per unit mass required to change a substance from the liquid phase to the vapor phase is known as the heat of vaporization. The strength of the forces depends on the type of molecules. The heat Q absorbed or released in a phase change in a sample of mass m is given by

$Q=mLf(melting/freezing)Q=mLf(melting/freezing)$
1.7
$Q=mLv(vaporization/condensation)Q=mLv(vaporization/condensation)$
1.8

where the latent heat of fusion $LfLf$ and latent heat of vaporization $LvLv$ are material constants that are determined experimentally. (Latent heats are also called latent heat coefficients and heats of transformation.) These constants 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 1.18 (a) Energy is required to partially overcome the attractive forces (modeled as springs) between molecules in a solid to form a liquid. That same energy must be removed from the liquid for freezing to take place. (b) Molecules become separated by large distances when going from liquid to vapor, requiring significant energy to completely overcome molecular attraction. The same energy must be removed from the vapor for condensation to take place.

Table 1.4 lists representative values of $LfLf$ and $LvLv$ in kJ/kg, together with melting and boiling points. Note that in general, $Lv>LfLv>Lf$. The table shows that the amounts of energy involved in phase changes can easily be comparable to or greater than those involved in temperature changes, as Figure 1.15 and the accompanying discussion also showed.

$LfLf$ $LvLv$
Substance Melting Point $(°C)(°C)$ kJ/kg kcal/kg Boiling Point $(°C)(°C)$ kJ/kg kcal/kg
Helium[2] 5.23 1.25 $−268.9(4.2K)−268.9(4.2K)$ 20.9 4.99
Hydrogen $−259.3(13.9K)−259.3(13.9K)$ 58.6 14.0 $−252.9(20.2K)−252.9(20.2K)$ 452 108
Nitrogen $−210.0(63.2K)−210.0(63.2K)$ 25.5 6.09 $−195.8(77.4K)−195.8(77.4K)$ 201 48.0
Oxygen $−218.8(54.4K)−218.8(54.4K)$ 13.8 3.30 $−183.0(90.2K)−183.0(90.2K)$ 213 50.9
Ethanol –114 104 24.9 78.3 854 204
Ammonia –75 332 79.3 –33.4 1370 327
Mercury –38.9 11.8 2.82 357 272 65.0
Water 0.00 334 79.8 100.0 2256[3] 539[4]
Sulfur 119 38.1 9.10 444.6 326 77.9
Lead 327 24.5 5.85 1750 871 208
Antimony 631 165 39.4 1440 561 134
Aluminum 660 380 90 2450 11400 2720
Silver 961 88.3 21.1 2193 2336 558
Gold 1063 64.5 15.4 2660 1578 377
Copper 1083 134 32.0 2595 5069 1211
Uranium 1133 84 20 3900 1900 454
Tungsten 3410 184 44 5900 4810 1150
Table 1.4 Heats of Fusion and Vaporization[1] [1]Values quoted at the normal melting and boiling temperatures at standard atmospheric pressure ($1 atm 1 atm$). [2]Helium has no solid phase at atmospheric pressure. The melting point given is at a pressure of 2.5 MPa. [3]At $37.0 ° C 37.0 ° C$ (body temperature), the heat of vaporization $L v L v$ for water is 2430 kJ/kg or 580 kcal/kg. [4]At $37.0 ° C 37.0 ° C$ (body temperature), the heat of vaporization, $L v L v$ for water is 2430 kJ/kg or 580 kcal/kg.

Phase changes can have a strong stabilizing effect on temperatures that are not near the melting and boiling points, since evaporation and condensation occur even at temperatures below the boiling point. For example, temperatures in humid weather rarely fall below the dew point—the temperature where condensation occurs given the concentration of water vapor in the air—because so much heat is released when water vapor condenses.

More energy is required to evaporate water below the boiling point than at the boiling point, because the kinetic energy of water molecules at temperatures below $100°C100°C$ is less than that at $100°C100°C$, so less energy is available from random thermal motions. For example, at body temperature, evaporation of sweat from the skin requires a heat input of 2428 kJ/kg, which is about 10% higher than the latent heat of vaporization at $100°C100°C$. This heat comes from the skin, and this evaporative cooling effect of sweating helps reduce the body temperature in hot weather. However, high humidity inhibits evaporation, so that body temperature might rise, while unevaporated sweat might be left on your brow.

## Example 1.9

### Calculating Final Temperature from Phase Change

Three ice cubes are used to chill a soda at $20°C20°C$ with mass $msoda=0.25kgmsoda=0.25kg$. The ice is at $0°C0°C$ and each ice cube has a mass of 6.0 g. Assume that the soda is kept in a foam container so that heat loss can be ignored and that the soda has the same specific heat as water. Find the final temperature when all ice has melted.

### Strategy

The ice cubes are at the melting temperature of $0°C.0°C.$ Heat is transferred from the soda to the ice for melting. Melting yields water at $0°C,0°C,$ so more heat is transferred from the soda to this water until the water plus soda system reaches thermal equilibrium.

The heat transferred to the ice is

$Qice=miceLf+micecW(Tf−0°C).Qice=miceLf+micecW(Tf−0°C).$

The heat transferred by the soda is

$Qsoda=msodacW(Tf−20°C).Qsoda=msodacW(Tf−20°C).$

Since no heat is lost, $Qice=−Qsoda,Qice=−Qsoda,$ as in Example 1.7, so that

$miceLf+micecW(Tf−0°C)=−msodacW(Tf−20°C).miceLf+micecW(Tf−0°C)=−msodacW(Tf−20°C).$

Solve for the unknown quantity $TfTf$:

$Tf=msodacw(20°C)−miceLf(msoda+mice)cw.Tf=msodacw(20°C)−miceLf(msoda+mice)cw.$

### Solution

First we identify the known quantities. The mass of ice is $mice=3×6.0g=0.018kgmice=3×6.0g=0.018kg$ and the mass of soda is $msoda=0.25kg.msoda=0.25kg.$ Then we calculate the final temperature:
$Tf=20,930J−6012J1122J/°C=13°C.Tf=20,930J−6012J1122J/°C=13°C.$

### Significance

This example illustrates the large energies involved during a phase change. The mass of ice is about 7% of the mass of the soda but leads to a noticeable change in the temperature of the soda. Although we assumed that the ice was at the freezing temperature, this is unrealistic for ice straight out of a freezer: The typical temperature is $−6°C−6°C$. However, this correction makes no significant change from the result we found. Can you explain why?

Like solid-liquid and liquid-vapor transitions, direct solid-vapor transitions or sublimations involve heat. The energy transferred is given by the equation $Q=mLsQ=mLs$, where $LsLs$ is the heat of sublimation, analogous to $LfLf$ and $LvLv$. The heat of sublimation at a given temperature is equal to the heat of fusion plus the heat of vaporization at that temperature.

We can now 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. Keep in mind that heat transfer and work can cause both temperature and phase changes.

## Problem-Solving Strategy

### The Effects of Heat Transfer

1. Examine the situation to determine that there is a change in the temperature or phase. Is there heat transfer into or out of the system? When it is not obvious whether a phase change occurs or not, you may wish to first solve the problem as if there were no phase changes, and examine the temperature change obtained. If it is sufficient to take you past a boiling or melting point, you should then go back and do the problem in steps—temperature change, phase change, subsequent temperature change, and so on.
2. Identify and list all objects that change temperature or phase.
3. Identify exactly what needs to be determined in the problem (identify the unknowns). A written list is useful.
4. Make a list of what is given or what can be inferred from the problem as stated (identify the knowns). If there is a temperature change, the transferred heat depends on the specific heat of the substance (Heat Transfer, Specific Heat, and Calorimetry), and if there is a phase change, the transferred heat depends on the latent heat of the substance (Table 1.4).
5. Solve the appropriate equation for the quantity to be determined (the unknown).
6. Substitute the knowns along with their units into the appropriate equation and obtain numerical solutions complete with units. You may need to do this in steps if there is more than one state to the process, such as a temperature change followed by a phase change. However, in a calorimetry problem, each step corresponds to a term in the single equation $Qhot+Qcold=0Qhot+Qcold=0$.
7. Check the answer to see if it is reasonable. Does it make sense? As an example, be certain that any temperature change does not also cause a phase change that you have not taken into account.

Why does snow often remain even when daytime temperatures are higher than the freezing temperature?

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