A discussion on the expansion and compression of ideal gases, also considering the particular cases of isothermal and adiabatic processes

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The expansion and compression of ideal gases are regularly considered to be polytropic processes. Therefore, they satisfy the equation:

PV^n = const.
(13)

where n is called the polytropic index.

However, we also know that ideal gases follow the so-called combined gas law (for a more detailed discussion also see Thermodynamics of Ideal Gases ), which states that:

\frac{PV}{T} = const.
(14)

Therefore, when dividing equation (#1) by \displaystyle \frac{PV}{T} we will also get a constant:

PV^n \div \frac{PV}{T} = const.
(15)

or, written in a different form:

PV^n \cdot \frac{T}{PV} = const.
(16)

from which we obtain that, during an expansion or compression, ideal gases satisfy:

TV^{n-1} = const.
(17)

Also, we can rewrite equation (#2) as:

V = const. \cdot \frac{T}{P}
(18)

By using the expression form of the volume from (#6) in equation (#1), we get that:

\frac{PT^n}{P^n} = const.
(19)

which leads to another equation which is satisfied during the expansion or compression of ideal gases:

\frac{T}{P^\frac{n-1}{n}} = const.
(20)

Let us now consider the work done during a polytropic expansion or compression. We know that the work done by a gas which is expanding from state 1 to state 2 is given by:

W = \int_1^2 PdV
(21)

As this is a polytropic expansion, we also have that:

PV^n = C
(22)

or, furthermore, that:

P = \frac{C}{V^n}
(23)

where C is a constant, and n the polytropic index. By using the expression of pressure from (#11) in equation (#9), we get the work done by the gas as:

W = C \int_1^2 V^{-n} dV
(24)

which, integrated, leads to:

W = C \left( \frac{V^{-n+1}}{-n+1} \right) \bigg|_1^2
(25)

By using identity (#10) again, we can rewrite (#13) as:

W = \left( PV^n \frac{V^{1-n}}{1-n} \right) \bigg|_1^2
(26)

or, furthermore, as:

W = \left( \frac{PV}{1-n} \right) \bigg|_1^2
(27)

Thus, we obtain the work done by the gas during a polytropic expansion as:

W = \frac{P_2 V_2 - P_1 V_1}{1-n}
(28)

However, from the ideal gas law we also have that:

PV = m \tilde{R} T
(29)

where m is the mass, and \tilde{R} the universal gas constant (for additional information also see Thermodynamics of Ideal Gases ). Therefore, we have that:

P_1 V_1 = m \tilde{R} T_1
(30)

and:

P_2 V_1 = m \tilde{R} T_2
(31)

By using (#18) and (#19), the work done from equation (#16) becomes:

W = \frac{m \tilde{R} T_2 - m \tilde{R} T_1}{1-n}
(32)

from which we obtain the work done by the gas during a polytropic expansion also as:

W = \frac{m \tilde{R} (T_2 - T_1)}{1-n}
(33)

In order to calculate the work done on a gas undergoing a polytropic compression from state 1 to state 2, we follow a similar reasoning, but this time starting from:

W = - \int_1^2 PdV
(34)

Therefore, equations (#16) and (#21) can be rewritten in order to express the work done during a polytropic compression as:

W = - \frac{(P_2 V_2 - P_1 V_1)}{1-n}
(35)

and:

W = - \frac{m \tilde{R} (T_2 - T_1)}{1-n}
(36)

respectively. Hence, we obtain that the work done during a polytropic compression can be expressed as:

W = \frac{P_1 V_1 - P_2 V_2}{1-n}
(37)

or as:

W = \frac{m \tilde{R} (T_1 - T_2)}{1-n}
(38)

Let us now consider the heat supplied during a polytropic expansion. From the first law of thermodynamics we know that the heat added to the system Q equals the change in internal energy \Delta U plus the work done by the system W:

Q = \Delta U + W
(39)

As the change in internal energy is given by:

\Delta U = m C_V (T_2 - T_1)
(40)

where m is the mass, and C_V the heat capacity at constant volume (for a more detailed discussion also see Thermodynamics of Ideal Gases ), and also taking into account the expression of the work done during a polytropic expansion from (#20), the heat supplied during a polytropic expansion becomes:

Q = m C_V (T_2 - T_1) + \frac{m \tilde{R} (T_2 - T_1)}{1-n}
(41)

which can also be written as:

Q = (T_2 - T_1) \left( m C_V + \frac{m \tilde{R}}{1-n} \right)
(42)

We know that the universal gas constant \tilde{R} relates the heat capacity at constant volume C_V to the heat capacity at constant pressure C_P by:

C_P - C_V = \tilde{R}
(43)

(for a more detailed discussion also see Thermodynamics of Ideal Gases ). However, from the definition of the heat capacity ratio \gamma:

\gamma = \frac{C_P}{C_V}
(44)

we also have that:

C_P = \gamma C_V
(45)

By using the expression of C_P from (#33) in equation (#31), we get that:

\gamma C_V - C_V = \tilde{R}
(46)

or, furthermore, that:

C_V (\gamma - 1) = \tilde{R}
(47)

from which we obtain C_V as:

C_V = \frac{\tilde{R}}{\gamma - 1}
(48)

By using the expression of C_V from (#36) in equation (#30), we get the heat supplied during a polytropic expansion as:

Q = (T_2 - T_1) \left( \frac{m \tilde{R}}{\gamma - 1} + \frac{m \tilde{R}}{1-n} \right)
(49)

or, furthermore, as:

Q = m \tilde{R} (T_2 - T_1) \left( \frac{1}{\gamma - 1} + \frac{1}{1-n} \right)
(50)

Equation (#38) leads to:

Q = m \tilde{R} (T_2 - T_1) \left[ \frac{1-n+\gamma - 1}{(\gamma -1)(1-n)} \right]
(51)

or, furthermore, to:

Q = m \tilde{R} (T_2 - T_1) \frac{(\gamma - n)}{(\gamma - 1)(1-n)}
(52)

Taking into account that \displaystyle \frac{m \tilde{R} (T_2 - T_1)}{1-n} = W (see equation #21), we obtain the heat supplied during a polytropic expansion as:

Q = W \frac{(\gamma - n)}{\gamma - 1}
(53)

where \gamma is the heat capacity ratio, n the polytropic index, and W the work done during the expansion.

Isothermal Expansion or Compression

For different values of the polytropic index n, the polytropic process defined by (#1) will be equivalent to other particular processes. For instance, if n=1, equation (#1) will be rewritten as:

PV = const.
(54)

However, taking into account the ideal gas law (see #17), this also means that:

m \tilde{R} T = const.
(55)

As m and \tilde{R} are constants, this leads to:

T = const.
(56)

which means that for n=1, we are dealing with isothermal processes.

As the work done during a process which changes the system from state 1 to state 2 is given by W=\int_1^2 PdV, and also taking into account that \displaystyle P=\frac{m \tilde{R} T}{V} (see the ideal gas law, equation #17), we get the work done during an isothermal expansion or compression as:

W = \int_1^2 \frac{m \tilde{R} T}{V} dV
(57)

from which we obtain:

W = m \tilde{R} T ln \frac{V_2}{V_1}
(58)

Let us now consider the heat changed during an isothermal expansion or compression. The change in internal energy in this case is \Delta U = 0, as T_1=T_2 (see equation #28). Therefore, from the first law of thermodynamics (see #27), we obtain that, for an isothermal process, the heat changed equals the work done:

Q = W
(59)

Adiabatic Expansion or Compression

Another particular case of the polytropic processes is when the polytropic index equals the heat capacity ratio, i.e. when n=\gamma. In this case, the heat changed during the process (see equation #41) will be:

Q = 0
(60)

Therefore, when n=\gamma, we are dealing with adiabatic processes. This can also be demonstrated the other way around. Consider, for example, that we are dealing with an adiabatic process. As \delta Q = 0 and \delta W = PdV, we obtain from the first law of thermodynamics (see #27) written for infinitesimal changes, that:

PdV = -dU
(61)

We can write the infinitesimal change in internal energy as (see equation #28):

dU = m C_V dT
(62)

where m is the mass, C_V the heat capacity at constant volume, and dT the infinitesimal change in temperature. Therefore, equation (#49) becomes:

PdV = - m C_V dT
(63)

However, \displaystyle P=\frac{m \tilde{R} T}{V} (see the ideal gas law, equation #17). Hence, we can also write equation (#51) as:

\frac{m \tilde{R} T}{V} dV = -m C_V dT
(64)

or, furthermore, as:

\tilde{R} \frac{dV}{V} = - C_V \frac{dT}{T}
(65)

By integrating equation (#53) we get that:

R ln V + C_V ln T = const.
(66)

which can also be written as:

ln V^R + ln T^{C_V} = const.
(67)

or, furthermore, as:

ln (V^R \cdot T^{C_V}) = const.
(68)

By raising e to equation (#56), we get that:

V^R \cdot T^{C_V} = const.
(69)

Then, by raising equation (#57) to the \displaystyle \frac{1}{C_V} power, we get that:

V^\frac{\tilde{R}}{C_V} \cdot T = const.
(70)

From equation (#35) we can also write that:

\frac{\tilde{R}}{C_V} = \gamma - 1
(71)

Therefore, equation (#58) becomes:

V^{\gamma - 1} \cdot T = const.
(72)

However, we know that all polytropic processes satisfy V^{n-1} \cdot T = const. (see equation #5). By coupling this with equation (#60) we obtain that, indeed, for adiabatic processes, n=\gamma.

Let us now consider the work done during an adiabatic expansion or compression. As n=\gamma, the work done during an adiabatic expansion is given by (see equation #21):

W = \frac{m \tilde{R} (T_2 - T_1)}{1-\gamma}
(73)

However, as \displaystyle \frac{\tilde{R}}{1-\gamma} = - C_V (see #36), equation (#61) becomes:

W = -m C_V (T_2 - T_1)
(74)

Taking into account equation (#50), we obtain the work done during an adiabatic expansion as:

W = -\Delta U
(75)

where \Delta U is the change in internal energy.

By following a similar reasoning, we obtain the work done during an adiabatic compression (given by equation #26 when n=\gamma) as:

W = \Delta U
(76)

where \Delta U is the change in internal energy.