Enthalpy of Fusion and Enthalpy of Vaporization

Submitted by ChemPRIME Staff on Thu, 12/16/2010 - 13:37

When heatEnergy transferred as a result of a temperature difference; a form of energy stored in the movement of atomic-sized particles. energyA system's capacity to do work. is supplied to a solidA state of matter having a specific shape and volume and in which the particles do not readily change their relative positions. at a steady rate by means of an electrical heating coil, we find that the temperatureA physical property that indicates whether one object can transfer thermal energy to another object. climbs steadily until the melting pointThe temperature at which a solid becomes a liquid. Also called freezing point. is reached and the first signs of liquidA state of matter in which the atomic-scale particles remain close together but are able to change their positions so that the matter takes the shape of its container formation become evident. Thereafter, even though we are still supplying heat energy to the system, the temperature remains constant as long as both liquid and solid are present. Only when the last vestiges of the solid have disappeared does the temperature start to climb again.

This macroscopic behavior demonstrates quite clearly that energy must be supplied to a solid in order to melt it. On a microscopic level meltingThe process of a liquid forming from a solid. involves separating molecules which attract each other. This requires an increase in the potential energy of the molecules, and the necessary energy is supplied by the heating coil. The kinetic energy of the molecules (rotation, vibration, and limited translation) remains constant during phase changes, because the temperature does not change.

The heat energy which a solid absorbs when it melts is called the enthalpyA thermodynamic state function, symbol H, that equals internal energy plus pressure x volume; the change in enthalpy corresponds to the energy transferred as a result of a temperature difference (heat transfer) when a reaction occurs at constant pressure. of fusionA nuclear reaction in which small nuclei are united to form larger ones. or heat of fusionThe heat energy transfer into a system as a substance melts. and is usually quoted on a molar basis. (The word fusion means the same thing as “melting.”) When 1 mol of ice, for example, is melted, we find from experiment that 6.01 kJ are needed. The molar enthalpy of fusion of ice is thus +6.01 kJ mol–1, and we can write


H2O(s) → H2O(l)      (0°C)      ΔHm = 6.01 kJ mol–1


Selected molar enthalpies of fusion are tabulated below. Solids like ice which have strong intermolecular forces have much higher values than those like CH4 with weak ones. Note that the enthalpies of fusion and vaporizationThe formation of a vapor from a liquid; evaporation or boiling. change with temperature.

When a liquid is boiled, the variation of temperature with the heat energy supplied is similar to that found for melting. When heat is supplied at a steady rate to a liquid at atmospheric pressureForce per unit area; in gases arising from the force exerted by collisions of gas molecules with the wall of the container., the temperature rises until the boiling pointThe temperature at which the vapor pressure of a liquid equals the pressure of the gas in contact with the liquid; usually this is atmospheric pressure. is attained. After this the temperature remains constant until the enthalpy of vaporization has been supplied. Once all the liquid has been converted to vapor, the temperature again rises. In the case of water the molar enthalpy of vaporization is 40.67 kJ mol–1. In other words


H2O(l) → H2O(g)      (100°C)      ΔHm = 40.67 kJ mol–1


Molar Enthalpies of Fusion and Vaporization of Selected Substances.

Substance Formula ΔH(fusion)
/ kJ mol1
Melting Point / K ΔH(vaporization) / kJ mol-1 Boiling Point / K (ΔHv/Tb)
/ JK-1 mol-1
Neon Ne 0.33 24 1.80 27 67
Oxygen O2 0.44 54 6.82 90.2 76
Methane CH4 0.94 90.7 8.18 112 73
Ethane C2H6 2.85 90.0 14.72 184 80
Chlorine Cl2 6.40 172.2 20.41 239 85
Carbon tetrachloride CCl4 2.67 250.0 30.00 350 86
Water* H2O 6.00678 at 0°C, 101kPa
6.354 at 81.6 °C, 2.50 MPa
273.1 40.657 at 100 °C,
45.051 at 0 °C,
46.567 at -33 °C
373.1 109
n-Nonane C9H20 19.3 353 40.5 491 82
Mercury Hg 2.30 234 58.6 630 91
Sodium Na 2.60 371 98 1158 85
Aluminum Al 10.9 933 284 2600 109
Lead Pb 4.77 601 178 2022 88

*http://www1.lsbu.ac.uk/water/data.html



Heat energy is absorbed when a liquid boils because molecules which are held together by mutual attraction in the liquid are jostled free of each other as the gasA state of matter in which a substance occupies the full volume of its container and changes shape to match the shape of the container. In a gas the distance between particles is much greater than the diameters of the particles themselves; hence the distances between particles can change as necessary so that the matter uniformly occupies its container. is formed. Such a separation requires energy. In general the energy needed differs from one liquid to another depending on the magnitude of the intermolecular forces. We can thus expect liquids with strong intermolecular forces to have larger enthalpies of vaporization. The list of enthalpies of vaporization given in the table bears this out.

Example

Compare the heat energy required to vaporize 100 g of lead to the energy required (1)to melt 100 g of lead; (2) to melt 100 g water; and (3) to vaporize 100 g of water.

Solution

To vaporize 100 g of lead:

Pb(l) → Pb(g)      (1749°C)      ΔHm = 178 kJ mol–1

100 g ~ \times ~\frac {1 mol Pb}{207.2 ~g~ Pb}~ \times ~\frac{178~ kJ}{mol} = 85.9~ kJ

(1) To melt 100 g of lead:


Pb(s) → Pb(l)      (328 °C)      ΔHm = 4.77 kJ mol–1


100 g ~\times~ \frac {1 mol Pb}{207.2 ~g~ Pb} ~\times ~\frac{4.77~ kJ}{mol} = 2.30~ kJ


(2) To melt 100 g of water:


100 g ~\times~ \frac {1 mol}{18.0 ~g}~ \times~ \frac{6.01~ kJ}{mol} = 33.4~ kJ


(3) To vaporize 100 g of water:

100 g ~\times ~\frac {1 mol}{18.0~ g} ~\times ~\frac{40.657~ kJ}{mol} = 226~ kJ


It might be surprising that the heat required to melt or vaporize 100 g of lead is so much less than that require to melt or vaporized water. First, the temperature at which the substance melts has nothing to do with the enthalpy of fusion, although in practice we would have to add more heat to get lead to the melting point. The molar enthalpy of fusion is actually smaller for lead, because of smaller bonding energies between particles. The molar enthalpy of vaporization of lead is larger than that of water, but this problem reminds us that in some cases a massA measure of the force required to impart unit acceleration to an object; mass is proportional to chemical amount, which represents the quantity of matter in an object.-based result can be of practical value, showing that less heat is required to vaporize an equal mass of lead.


Two other features of the table deserve mention. One is the fact that the enthalpy of vaporization of a substance is always higher than its enthalpy of fusion. When a solid melts, the molecules are not separated from each other to nearly the same extent as when a liquid boils. Second, there is a close correlation between the enthalpy of vaporization and the boiling point measured on the thermodynamic scale of temperature. Periodic trends in boiling point closely follow periodic trends in heat of vaporiation. If we divide the one by the other, we find that the result is often in the range of 75 to 90 J K–1 mol–1. To a first approximation therefore the enthalpy of vaporization of a liquid is proportional to the thermodynamic temperature at which the liquid boils. This interesting result is called Trouton’s rule. An equivalent rule does not hold for fusion. The energy required to melt a solid and the temperature at which this occurs depend on the structure of the crystalA solid with a regular polyhedral shape; for example, in sodium chloride (table salt) the crystal faces are all at 90° angles. A solid in which the atoms, molecules, or ions are arranged in a regular, repeating lattice structure. as well as on the magnitude of the intermolecular forces.