Topic 2: Heat and Heat Transfer#

Introduction#

We said earlier that heat flows from a hotter body to a cooler body, but what is heat? Heat is a form of energy. We have said that the temperature of a body is a measure of the average kinetic energy of its component atoms, so to increase the temperature of a body we must add to this kinetic energy. This is what we do when we supply heat, so heat must be another form of energy. The science of thermodynamics, which we will study in this course, is largely the science of how heat, work and the internal energy of a material are converted into each other so as to drive engines, initiate chemical reactions, etc.

Heat transfer mechanisms#

How is heat transferred? There are three possible mechanisms: convection, conduction and radiation.

Convection#

Convection is the transfer of heat by the net bulk motion of fluid (liquid or gas). Examples of heat transfer by convection include boiling water in a kettle, weather systems and cooling fans. We can divide convection systems into two categories: natural convection and forced convection.

Natural convection occurs when a heated fluid expands (thermal expansion). The expanded fluid is less dense than the surrounding, cooler, fluid. The less dense fluid rises and the cooler, denser fluid sinks. This results in a cyclical convection current. An everyday example of this is in central heating systems. The warm air rises above the radiator and the cold air (e.g. near a window) sinks, setting up a convection current cycle.

Fluid viscosity, i.e. the resistance of the fluid to deformation, slows the fluid flow near solid surfaces, resulting in a surface layer of more static fluid (e.g. air) that has an insulating effect. This is one reason why wind gives wind chill - it removes part or all of this static layer. Forced convection occurs when the motion of hot or cold fluid is produced by external means, e.g. a pump or fan. Forced convection can be a very efficient method of transferring heat, and has many practical applications, e.g. fan oven, cooling fans in laptops, car engines, etc.

Conduction#

Conduction is the transfer of energy between atoms in a substance. Unlike convection, there is no bulk motion; instead, collisions at the atomic scale cause the transfer of heat. The atoms of the higher- temperature material have higher average kinetic energy, so collisions between them and the atoms of the lower-temperature material tend to transfer energy from hotter to cooler, increasing the velocity and kinetic energy of the cooler atoms and therefore their temperature. Conductive heat flow is driven by temperature gradient: the greater the difference in average kinetic energy, the more energy will be transferred in each collision. This is described by the heat flow equation,

(6)#\[H = \frac{dQ}{dt} = -k A \frac{dT}{dx},\]

where \(H\) is the heat current, i.e. the derivative of heat \(Q\) with respect to time \(t\), \(A\) is the cross-sectional area through which the heat flows and \(k\) is the thermal conductivity of the material. The negative sign indicates that the direction of heat flow is from hot to cold. Since heat is a form of energy, \(H\) (energy per unit time) is measured in watts; \(k\) is measured in W/m/K.

Thermal conductivity is a property of the material, and depends on the efficiency with which its atoms can transfer kinetic energy to their neighbours. Metals generally have high thermal conductivity, because the free electrons that carry electrical current can also transfer kinetic energy. In non-metallic crystals, kinetic energy is transferred by vibrations in the crystal lattice, and this can also be very efficient (diamond, for example, has an extremely high thermal conductivity). In contrast, gases have low thermal conductivity, because collisions between gas atoms are uncommon - see Table 2.

Table 2 Thermal conductivities#

Substance

\(k\) (W m\(^{-1}\) K\(^{-1}\))

Aluminium

205.0

Copper

385.0

Steel

50.2

Glass

0.96

Ice

1.6

Air

0.026

Radiation#

Any object at a temperature above absolute zero will emit electromagnetic radiation. This can come from many sources: charged particles emit electromagnetic radiation when they are accelerated (and if two atoms collide and change their velocities, they have undergone acceleration), electrons move to lower energy states, molecules move to lower rotational or vibrational states, etc. If the material is dense enough, the photons produced by these various processes will randomise their energies by collisions until they reach a state where the photon energy distribution is independent of the material composition and is determined purely by the temperature of the body. In the ideal case, this is known as blackbody radiation or thermal radiation and the power emitted is

(7)#\[H_{\rm BB} = \frac{dQ}{dt} = A \sigma T^{4}\]

where \(A\) is the surface area of the emitting body and \(\sigma\) is a constant known as Stefan’s constant (or the Stefan-Boltzmann constant); in SI units \(\sigma = 5.670 \times 10^{-8}\) W/m\(^2\)/K\(^4\).

Real bodies are less efficient emitters of electromagnetic radiation than the ideal blackbody (which is defined as an object that is 100% efficient at emitting or absorbing radiation). This is described by the emissivity \(\epsilon\), which is a number between 0 and 1: a body with emissivity \(\epsilon\) will radiate power

(8)#\[H = A \epsilon \sigma T^{4}\]

The emissivity is a property of the material and of the nature of the surface: for example, highly polished stainless steel has an emissivity of 0.075, but rough, weathered stainless steel has an emissivity of 0.85. Generally, shiny, polished surfaces have very low emissivity and rough, dark surfaces have high emissivity.

Since electromagnetic radiation can propagate in a vacuum, radiative heat transfer differs from convective and conductive heat transfer in not requiring the two bodies to be in physical contact - for example, the Sun can heat the Earth by radiative heat transfer. The equilibrium temperature \(T\) of a (rotating) planet of radius \(R\) at a distance \(d\) from its parent star (luminosity \(L\)) can be obtained by balancing the energy received

\[ \frac{L}{4 \pi d^{2}} \pi R^{2} (1-A) \]

where A is the Albedo (or reflectivity), and the energy emitted

\[ 4 \pi R^{2} \epsilon \sigma T^{4}. \]

So the planetary temperature

\[ T^{4} = \frac{L(1-A)}{16 \pi d^2 \epsilon \sigma} \]

is independent of its radius. Inserting suitable quantities for the Earth (\(A\) = 0.3, \(\epsilon\) = 0.6) and the Solar constant (\(L/4 \pi d^{2}\) = 1360 W m\(^{-2}\)) then \(T\) = 289 K for the Earth.

Thermal radiation has a continuous spectrum extending over the whole wavelength range, but the wavelength of peak emission depends on the temperature according to Wien’s law,

(9)#\[\lambda_{\rm max} T = 2.898 \times 10^{-3} {\rm m K}.\]

At temperatures near room temperature, ~300 K, emission peaks around 10 \(\mu\)m, in the infrared part of the spectrum. This is why cameras operating at infrared wavelengths are known as thermal cameras and can be used to measure temperature. It is worth noting that thermal cameras translate to temperature using Equation (7), and therefore will not give accurate readings when pointed at shiny surfaces with low emissivities.

Heat capacity#

Supplying heat to an object will, in general, raise its temperature. But what is the relationship between the amount of heat supplied and the change in temperature? This is quantified by the heat capacity of the object, \(C\):

(10)#\[Q = C \Delta T = mc \Delta T\]

where \(Q\) is the heat supplied, \(\Delta T\) is the resulting temperature change, \(m\) is the mass of the object and \(c\) is the specific heat capacity. The SI units of \(C\) are J/K, and of \(c\), J/kg/K. When dealing with gases, it is often useful to define the molar heat capacity, measured in J/mol/K confusingly, this is also usually denoted \(c\), so if you have a problem involving the heat capacity of a gas, make sure that you know whether you are dealing with specific heat capacity or molar heat capacity. The heat capacity at constant pressure, \(C_P\), differs from the heat capacity at constant volume, \(C_V\). This difference is not generally important for solids and liquids, but is very significant for gases. The specific heat capacity of a given material is also usually dependent on temperature; we will explore this later in the course.

Table 3 Specific heat capacities#

Substance

\(c\) (J kg\(^{-1}\) K\(^{-1}\))

Aluminium

900

Silicon

705

Copper

390

Ice

2100

Water

4190

Latent Heat#

Supplying heat to an object does not always raise its temperature. Sometimes the energy will cause the material to undergo a phase transition, such as melting, vaporisation, or ionisation. For example, supplying heat to a mixture of ice and water at 0\(^{\circ}\) C will not, initially, increase the temperature: instead, it will cause the ice to melt. Only when all the ice has melted will the temperature of the water start to increase (this is why we add ice to drinks to keep them cool). The heat required to cause a phase transition is called the latent heat, is measured in J/kg, and is given by

(11)#\[Q = mL\]

where \(L\) is the (specific) latent heat and \(m\) is the mass of material. The latent heat required to melt a solid is called the latent heat of fusion (\(L_{\rm f}\)); that required to vaporise a liquid is the latent heat of vaporisation (\(L_{\rm v}\). When a vapour condenses into a liquid, or a liquid freezes into a solid, the latent heat is released back into the environment. This feature is commonly used in refrigeration systems, where the refrigerant enters the area to be cooled as a liquid, absorbs heat by evaporating into a vapour, and is subsequently condensed back into a liquid to release the waste heat.

Like specific heat capacity, latent heat is temperature-dependent. In particular, latent heat of vaporisation decreases with increasing temperature and will reach zero at the critical point of the material, at which point the difference between the liquid and gas phases essentially disappears.

Table 4 Latent heats of Fusion (\(L_{f}\)) and Vaporization (\(L_{v}\)) at 1 atmospheric pressure#

Substance

Melting point (K)

\(L_{f}\) (J kg\(^{-1}\))

Boiling point (K)

\(L_{v}\) (J kg\(^{-1}\))

Mercury

234

\(11.8 \times 10^{3}\)

630

\(272 \times 10^{3}\)

Water

273.15

\(334 \times 10^{3}\)

373.15

\(2256 \times 10^{3}\)

Silver

1233.95

\(88.3 \times 10^{3}\)

2466

\(2336 \times 10^{3}\)