Internal Energy of An Ideal Gas

Internal Energy of an Ideal Gas
Consider n mole of monatomic ideal gas. The internal energy of the

gas is the sum of the translational kinetic energies of the atoms.
If N is the total number of atoms then the internal energy,
𝑬=𝒏 𝑵 𝑨 𝑲 𝒂𝒗𝒈 𝟑
∴ 𝑬= 𝒏𝑹𝑻
𝟐
𝟑 𝑲𝑻
𝑬 =( 𝒏 𝑵 𝑨 ) ( )
𝟐 and ΔEint =
Thus the internal energy Eint of an

ideal gas is a function of the gas
𝑹 temperature only.
[𝒂𝒔 𝑲 = ]
𝑵𝑨
Molar Specific Heat at Constant Volume
If Q amount of heat is added to n mole of ideal gas to
increase the temperature by keeping the volume constant
then the molar specific heat,
∆ 𝑸=𝒏 𝑪𝑽 ∆ 𝑻
The Work done at constant volume,
The change in internal energy of the system,

From the 1st law of thermodynamics,
𝟑
𝑪𝑽 = 𝑹
𝟐
J/mol.K
Molar Specific Heat at Constant Pressure
If Q amount of heat is added to n mole of ideal gas to
increase the temperature by keeping the pressure
constant then the molar specific heat,
∆ 𝑸 =𝒏 𝑪 𝑷 ∆ 𝑻
The Work done at constant pressure,
The change in internal energy of the system,

From the 1st law of thermodynamics,
𝟑
𝒏 𝑪 𝑷 ∆ 𝑻 = 𝑷 ∆ 𝑽 + 𝒏𝑹 ∆ 𝑻
𝟐
𝟓
𝑪 𝑷= 𝑹
𝟐
𝑪 𝑷 =𝟐𝟎 .𝟖J / mol .K
Relation Between and
We Know,
∴ 𝑪 𝑷 − 𝑪 𝑽 =𝑹
Thus Cp is greater than the molar specific heat at

constant volume CV
Internal Energy in Terms of
Internal energy,
The change in internal energy,

Degrees of freedom and molar specific heats: Eint = ( and CV = (
Let us try to explain that molecules with more than one atom can store internal energy in forms
other than translational kinetic energy.
Figure 19-13 shows common models of helium (a monatomic molecule,

containing a single atom), oxygen (a diatomic molecule, containing two
atoms), and methane (a polyatomic molecule).
James Clerk Maxwell introduced the theorem of the

equipartition of energy:
Every kind of molecule has a certain number f of degrees of

freedom (independent ways). Each degree of freedom can
store energy of per molecule (or per mole).
[f( per molecule]
For the translational motion, superimpose an xyz coordinate system on any gas. The molecules
will, in general, have velocity components along all three axes. Thus, gas molecules of all types
have three degrees of translational freedom (three ways to move in translation) and, on
average, an associated energy of 3( ) per molecule.
For the rotational motion, imagine the origin of our xyz coordinate
system at the center of each molecule. In a gas, each molecule should
be able to rotate with an angular velocity component along each of the
three axes, so each gas should have three degrees of rotational
freedom and, on average, an additional energy of 3( ) per molecule.
However, experiment shows this is true only for the polyatomic

molecules. According to quantum theory, the physics dealing with
the allowed motions and energies of molecules and atoms, a
monatomic gas molecule does not rotate and so has no rotational
[0( ) = 0] (a single atom cannot rotate like a top). A diatomic
molecule can rotate like a top only about axes perpendicular to the
line connecting the atoms and not about that line itself. Therefore, a
diatomic molecule can have only two degrees of rotational freedom
and a rotational energy of only 2( ) per molecule.
To extend our analysis of molar specific heats to ideal diatomic and polyatomic gases, it is
necessary to retrace the derivations of that analysis in detail. First, we replace E int = (3/2) nRT
with Eint = (f/2) nRT, where f is the number of degrees of freedom [Table 19-3]. Doing so leads
to the prediction
CV = (
This agrees for monatomic gases (f = 3). As Table 19-3 shows, this prediction also agrees with
experiment for diatomic gases (f =5), but it is too low for polyatomic gases (f = 6 for molecules
comparable to CH4).
47. The temperature of 2.00 mol of an ideal monatomic gas is raised 15.0 K at
constant volume. What are (a) the work W done by the gas, (b) the energy
transferred as heat Q, (c) the change ΔEint in the internal energy of the gas, and
(d) the change ΔK in the average kinetic energy per atom?
Solution:
Here, ΔT= 15 K
n = 2.00 mol k=
ΔV = V - V = 0
(a) W = pΔV = p(0) = 0
(b) Q = nCVΔT = n ( ΔT = 2.00 (15) = 373.95 J [CV = (

[
(c) ΔEint = Q – W = 373.95 – 0 = 373.95 J
(d) ΔK = (ΔT = (15 = 31.05 J

48. When 20.9 J was added as heat to a particular ideal gas, the volume of the gas
changed from 50.0 cm3 to 100 cm3 while the pressure remained at 1.00 atm. (a) By
how much did the internal energy of the gas change? If the quantity of gas present
was 2.00x10-3 mol, find (b) Cp and (c) CV.
Solution:
Here, Q = 20.9 J
ΔV = (100 – 50) cm3 = 50 cm3 =50(10-2 m)3 = 50x10-6 m3
p = 1.00 atm = 1x105 Pa

n = 2.00x10-3 mol
(a) ΔEint = Q – W = Q – p ΔV = 20.9 – 1x105(50x10-6) = 20.9 – 5.0 = 15.9 J
(b) Q = nCpΔT [p = constant]
Cp =
Ideal gas law, pV = nRT
(pV) = (nRT)
p = nR
p = nR
pΔV = nR ΔT
= n ΔT
Cp =
Cp = = = = 34.74 J/mol-K
(c) Cp – CV = R
CV = Cp – R = 34.74 – 8.31 = 26.43 J/mol-K

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Internal Energy of an Ideal Gas

Consider n mole of monatomic ideal gas. The internal energy of the

Thus the internal energy Eint of an

The Work done at constant volume,

The change in internal energy of the system,

The change in internal energy of the system,

Thus Cp is greater than the molar specific heat at

The change in internal energy,

Figure 19-13 shows common models of helium (a monatomic molecule,

James Clerk Maxwell introduced the theorem of the

Every kind of molecule has a certain number f of degrees of

However, experiment shows this is true only for the polyatomic

(a) W = pΔV = p(0) = 0

(b) Q = nCVΔT = n ( ΔT = 2.00 (15) = 373.95 J [CV = (

(d) ΔK = (ΔT = (15 = 31.05 J

p = 1.00 atm = 1x105 Pa

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