In thermochemistry, latent heat is the heat released or absorbed by a body during a change of state without change of temperature.[1][2][3][4] The term most often refers to a phase transition such as the melting of ice or the boiling of water.[5][6] The term was introduced around 1750 by Joseph Black. It is derived from the Latin latere (to lie hidden). In its original context of calorimetry set by Black, besides phase changes, the term referred in particular to the heat transferred to a body upon change of volume at constant temperature without phase change.
In meteorology, latent heat flux is the flux of heat from the Earth's surface to the atmosphere that is associated with evaporation or transpiration of water at the surface and subsequent condensation of water vapor in the troposphere. It is an important component of Earth's surface energy budget. Latent heat flux has been commonly measured with the Bowen ratio technique, or more recently since the mid-1900s by the eddy covariance method.
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Two of the more common forms of latent heat (or enthalpies or energies) encountered are latent heat of fusion (melting or freezing) and latent heat of vaporization (boiling or condensing). These names describe the direction of energy flow when changing from one phase to the next: from solid to liquid, and to gas.
In both cases, the change is endothermic, meaning that the system absorbs energy on going from solid to liquid to gas. The change is exothermic (the process releases energy) for the opposite direction. For example, in the atmosphere, when a molecule of water evaporates from the surface of any body of water, energy is transported by the water molecule into a lower temperature air parcel that contains less water vapor than its surroundings. Because energy is needed to overcome the molecular forces of attraction between water particles, the process of transition from a parcel of water to a parcel of vapor requires the input of energy causing a drop in temperature in its surroundings. If the water vapor condenses back to a liquid or solid phase onto a surface, the latent energy absorbed during evaporation is released as sensible heat onto the surface. The large value of the enthalpy of condensation of water vapor is the reason that steam is a far more effective heating medium than boiling water, and is more hazardous.
The terms sensible heat and latent heat are not special forms of energy; instead they characterize the same form of energy, heat, in terms of their effect on a material or a thermodynamic system. Heat is thermal energy in the process of transfer between a system and its surroundings or between two systems with a different temperature.
Both sensible and latent heats are observed in many processes while transporting energy in nature. Latent heat is associated with the phase changes of atmospheric water vapor, mostly vaporization and condensation, whereas sensible heat is energy transferred that affects the temperature of the atmosphere.
The term latent heat was introduced into calorimetry around 1750 by Joseph Black. James Prescott Joule characterized latent energy as the energy of interaction in a given configuration of particles, i.e. a form of potential energy, and the sensible heat as an energy that was indicated by the thermometer,[7] relating the latter to thermal energy.
A specific latent heat (L) expresses the amount of energy in form of heat (Q) required to completely affect a phase change of a unit of mass (m), usually 1kg, of a substance as an intensive property:
Intensive properties are material characteristics and are not dependent on the size or extend of the sample. Commonly quoted and tabulated in the literature are the specific latent heat of fusion and the specific latent heat of vaporization for many substances.
From this definition, the latent heat for a given mass of a substance is calculated by
where:
The following table shows the latent heats and change of phase temperatures of some common fluids and gases.
Substance | Latent Heat Fusion kJ/kg |
Melting Point °C |
Latent Heat Vaporization kJ/kg |
Boiling Point °C |
---|---|---|---|---|
Alcohol, ethyl | 108 | −114 | 855 | 78.3 |
Ammonia | 339 | −75 | 1369 | −33.34 |
Carbon dioxide | 184 | −78 | 574 | −57 |
Helium | 21 | −268.93 | ||
Hydrogen(2) | 58 | −259 | 455 | −253 |
Lead[8] | 24.5 | 327.5 | 871 | 1750 |
Nitrogen | 25.7 | −210 | 200 | −196 |
Oxygen | 13.9 | −219 | 213 | −183 |
R134a | −101 | 215.9 | −26.6 | |
Toluene | −93 | 351 | 110.6 | |
Turpentine | 293 | |||
Water | 334 | 0 | 2260 | 100 |
The latent heat of condensation of water in the temperature range from −40 °C to 40 °C is approximated by the following empirical cubic function:
with a determination coefficient of , where is in °C.
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