Kinetic Theory Of Gases Assumptions

Kinetic Theory Of Gases Assumptions

Vishal kumarUpdated on 02 Jul 2025, 07:49 PM IST

The Kinetic Theory of Gases provides a microscopic understanding of how gases behave, focusing on the motion of individual gas molecules. It rests on several assumptions that simplify the complex nature of gases, making it easier to predict their properties like pressure, temperature, and volume. The theory assumes that gas molecules are in constant, random motion, have negligible volume compared to the container, and experience perfectly elastic collisions. These molecules do not exert attractive or repulsive forces on one another, except during collisions.

This Story also Contains

  1. Assumption of Ideal Gases
  2. Solved Examples Based on the Assumption of Ideal Gases
  3. Summary
Kinetic Theory Of Gases Assumptions
Kinetic Theory Of Gases Assumptions

In real life, the assumptions of kinetic theory explain common experiences. For example, when you inflate a balloon, the gas molecules inside are constantly moving and colliding with the balloon’s walls, creating pressure that keeps it inflated. Similarly, when you heat a pot of water, the temperature rises and increases the speed of gas molecules, which explains why heated air rises. These assumptions allow us to understand and predict the behaviour of gases in everyday situations like weather patterns, vehicle engines, and even respiration.

Assumption of Ideal Gases

The assumptions of ideal gases are foundational to the kinetic theory of gases and simplify the behaviour of gases to make calculations easier. These assumptions describe an "ideal" gas that perfectly follows the gas laws.

What is Ideal gas?

It is a hypothetical gas (which is not real gas), whose molecules occupy negligible space and have no interactions (Force of interaction is much less), and which consequently obeys the gas laws exactly.

So, the ideal gas does not exist in real, but for study, we take some assumptions to make the gas ideal and we can apply some laws which are only valid for ideal gases. These assumptions are

  1. The size of the molecules is negligible in comparison to intermolecular distance (10-9m)
  2. The molecules of a gas are identical, spherical, rigid and perfectly elastic point masses (It means that when they collide with each other, then there is no loss of energy during collision).
  3. The molecules of a given gas are all identical but these molecules are different than those of another gas.
  4. The volume of molecules is negligible in comparison to the volume of gas.
  5. Molecules of a gas move randomly in all possible directions with all possible velocities.
  6. The speed of gas molecules varies from zero and infinity.
  7. The gas molecules keep on colliding among themselves as well as with the walls of the containing vessel. These collisions are perfectly elastic (no loss of energy).
  8. The time spent in a collision between two molecules is negligible in comparison to time between two successive collisions (i.e., time required to travel means free path).
  9. The number of collisions per unit volume in a gas remains constant.
  10. No attractive or repulsive force acts between gas molecules.
  11. Gravitational attraction among the molecules is negligible due to extremely small masses and the very high speed of molecules.
  12. Molecules constantly collide with the walls of the container due to which their momentum changes. The change in momentum is transferred to the walls of the container and due to this Pressure is exerted by gas molecules on the walls of the container.
  13. The density of gas does not change at any point in the container.

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Solved Examples Based on the Assumption of Ideal Gases

Example 1: Which is true for an ideal gas?

(1) Molecule of gas is identical spherical rigid and perfectly elastic point mass.

(2) There is always some attractive and repulsive force acting between gas molecules.

(3) The density of a gas is constant at all points of the container molecules

1) only 1

2) 1 and 3

3) 2 and 3

4) only 3

Solution:

True: For an ideal gas, the molecules are considered to be identical, spherical, rigid, and perfectly elastic point masses. This is a fundamental assumption of the ideal gas model.

False: An ideal gas assumes no intermolecular forces (no attractive or repulsive forces) between gas molecules. This is key to the ideal gas behaviour.

False: The density of an ideal gas can vary within the container depending on temperature and pressure. It is not necessarily constant at all points in the container.

Hence, the answer is the option (1)

Example 2: For an ideal gas which statement is not true?

1) It obeys Boyle's Law

2) It follows PV = RT

3) Molecules of gas are identical spherical rigid and perfectly elastic point masses.

4) It follows Vander Waal's equation.

Solution:

Rest all the statements are correct and till now you have learned all those statements. But ideal gas does not obey the Van der Waals equation. Let us understand this in brief.

Van der Waals equation:

$ \left(P+\frac{a}{V^2}\right)(V-b)=R T$

To account for the volume that a real gas molecule takes up, the van der Waals equation replaces V in the ideal gas law with (V-b), where v is the molar volume of the gas and b is the volume that is occupied by one mole of the molecules.

Here a and b depend on the gas and unlike an ideal gas, the real gas molecules do interact among themselves (attraction or repulsion)

$\therefore$ It does not follow Vander Waal's equation.

Hence, the answer is the option (4).

Example 3: According to the kinetic theory of gases,
A. The motion of the gas molecules freezes at $0^{\circ} \mathrm{C}$.
B. The mean free path of gas molecules decreases if the density of molecules is increased.
C. The mean free path of gas molecules increases if the temperature is increased keeping pressure constant.

D. Average kinetic energy per molecule per degree of freedom is $\frac{3}{2} \mathrm{k}_{\mathrm{B}} \mathrm{T}$ (for monoatomic gases).
Choose the most appropriate answer from the options given below:

1) $A$ and $C$ only
2) $B$ and C only
3) A and B only
4) C and D only

Solution:

Mean free path, $\lambda=\frac{\mathrm{kT}}{\sqrt{2} \pi \mathrm{d}^2 \rho}$

The mean free path is directly proportional to temperature $(\mathrm{T})$ and inversely proportional to the density $(\rho)$

Hence, the answer is the option (2).

Example 4:

There are two identical chambers, completely thermally insulated from the surroundings. Both chambers have a partition wall dividing the chambers into two compartments. Compartment 1 is filled with an ideal gas and compartment 3 is filled with a real gas. Compartments 2 and 4 are vacuum. A small hole (orifice) is made in the partition walls and the gases are allowed to expand in a vacuum.

Statement 1: No change in the temperature of the gas takes place when the ideal gas expands in a vacuum. However, the temperature of real gas goes down (cooling) when it expands in a vacuum.

Statement 2: The internal energy of an ideal gas is only kinetic. The internal energy of a real gas is kinetic as well as potential.

1) Statement 1 is false and statement 2 is true

2) Statement 1 and statement 2 both are true statement 2 is the correct explation of statement 1.

3) Statement 1 is true and statement 2 is false.

4) Statement 1 and statement 2 both are true. But statement 2 is not the correct explanation of statement 1.

Solution:

In ideal gases, the molecules are considered point particles and for point particles, there is no internal excitation, no vibration and no rotation. For an ideal gas, the internal energy can only be translational kinetic energy, and for real gas, both kinetic and potential energy.

Example 5: For an ideal gas relation between pressure and volume is $P=K V$,, the coefficient of pressure expansion is

1) T

2) 1/T

3) 2T

4) 1/2T

Solution:

Co-efficient of Pressure Expansion
$
\beta=\frac{\Delta P}{P_0} \frac{1}{\Delta \theta}
$

wherein

$
\begin{aligned}
& P^{\prime}=P(1+\beta \Delta \theta) \\
& P^{\prime}=\text { Final pressure } \\
& P=K V \\
& P V=n R T \Rightarrow V=\frac{n R T}{P} \\
& \text { or } P=K \cdot \frac{n R T}{P} \Rightarrow P^2=(K n R) T
\end{aligned}
$

on differentiating we get

$
2 P \cdot \frac{d P}{d T}=k n R
$
Coefficient of pressure expansion $=\frac{1}{P} \frac{d P}{d T}=\frac{1}{P} \frac{K n R}{2 P}=\frac{K n R}{2(k n R) T}=\frac{1}{2 T}$

Hence, the answer is the option (4).

Summary

The Kinetic Theory of Gases explains gas behaviour through assumptions like constant molecular motion, negligible volume, and no intermolecular forces, forming the basis for the ideal gas model. An ideal gas is hypothetical, following laws like Boyle's law and PV = RT, with assumptions such as perfectly elastic collisions and no intermolecular attraction. However, real gases deviate under specific conditions, requiring corrections like the Van der Waals equation to account for molecular interactions and volume.

Frequently Asked Questions (FAQs)

Q: How does the Kinetic Theory explain the phenomenon of Joule-Thomson cooling?
A:
The Joule-Thomson effect, where a real gas cools upon expansion, is explained by the
Q: What role does the concept of degrees of freedom play in the Kinetic Theory of Gases?
A:
Degrees of freedom in the Kinetic Theory refer to the independent ways a molecule can store energy. For monatomic gases, there are three translational degrees of freedom. Diatomic and polyatomic molecules have additional rotational and vibrational degrees of freedom. This concept is crucial for understanding gas heat capacities, energy distribution, and the equipartition theorem, which states that energy is equally distributed among all available degrees of freedom at thermal equilibrium.
Q: How does the Kinetic Theory account for deviations from ideal gas behavior?
A:
While the basic Kinetic Theory assumes ideal gas behavior, it can be modified to account for real gas behavior. Deviations occur when the assumptions of negligible particle volume and no intermolecular forces break down. The theory can be adjusted by including terms for particle volume (as in the Van der Waals equation) and attractive/repulsive forces between particles, explaining behaviors like gas condensation at high pressures or low temperatures.
Q: What does the Kinetic Theory say about the relationship between particle collisions and gas pressure?
A:
The Kinetic Theory directly relates gas pressure to particle collisions with container walls. Pressure is the result of the force exerted by these collisions per unit area. The theory shows that pressure increases with the number of collisions (more particles or higher temperature) and the force of each collision (higher particle speed or mass). This microscopic view provides a physical basis for macroscopic gas laws.
Q: How does the Kinetic Theory explain the phenomenon of gas diffusion through membranes?
A:
The Kinetic Theory explains gas diffusion through membranes as a result of the random motion of gas particles and their size relative to membrane pores. Smaller molecules can pass through pores more easily than larger ones. The rate of diffusion depends on factors like temperature (affecting particle speed), pressure difference, and the concentration gradient. This explanation is crucial for understanding processes like respiration and gas separation techniques.
Q: What does the Kinetic Theory predict about the relationship between temperature and particle speed?
A:
The Kinetic Theory predicts a direct relationship between temperature and the root-mean-square speed of gas particles. As temperature increases, the average kinetic energy of particles increases, resulting in higher average speeds. Specifically, the root-mean-square speed is proportional to the square root of the absolute temperature. This relationship is crucial for understanding how temperature affects gas behavior and properties.
Q: How does the Kinetic Theory explain the concept of equipartition of energy?
A:
The equipartition theorem, a key concept in the Kinetic Theory, states that energy is equally distributed among all accessible degrees of freedom in a system at thermal equilibrium. For an ideal gas, this means that each degree of freedom (e.g., each direction of motion) contributes equally to the total energy. This principle helps explain the specific heat capacities of gases and their temperature-dependent behavior.
Q: What does the Kinetic Theory say about the internal energy of a gas?
A:
According to the Kinetic Theory, the internal energy of an ideal gas is solely due to the kinetic energy of its particles. For monatomic gases, this is entirely translational kinetic energy. For polyatomic gases, rotational and vibrational energies also contribute. The theory relates the average kinetic energy per particle to temperature, providing a microscopic explanation for the macroscopic concept of internal energy.
Q: What does the Kinetic Theory say about the frequency of collisions in gases?
A:
The Kinetic Theory predicts that the frequency of collisions in gases depends on factors like temperature, pressure, and particle size. Higher temperatures increase particle speeds, leading to more frequent collisions. Higher pressures mean more particles in a given volume, also increasing collision frequency. This concept is crucial for understanding reaction rates, mean free path, and energy transfer in gases.
Q: How does the Kinetic Theory account for gas viscosity?
A:
Gas viscosity, though much lower than liquid viscosity, is explained by the Kinetic Theory through momentum transfer between gas layers moving at different velocities. As particles move between layers, they carry momentum, creating a drag force. The theory predicts that gas viscosity increases with temperature (unlike liquids) because faster-moving particles transfer momentum more effectively between layers.