Temperature dependence of orientation polarization in polyatomic gases If μp denotes the permanent dipole moment (in coulomb–metre) and T is the absolute temperature, how does the orientation polarization of a dilute polyatomic gas vary with μp and T (qualitative proportionality)?

Difficulty: Easy

Correct Answer: Proportional to μp^2 / T

Explanation:


Introduction / Context:
In polar gases, an external electric field tends to align permanent molecular dipoles. Thermal agitation randomizes orientations. The resulting “orientation polarization” is a key contribution to the dielectric constant of gases and many liquids at low frequencies. Understanding its temperature and dipole-moment dependence is fundamental in dielectrics.


Given Data / Assumptions:

  • Dilute gas of non-interacting polar molecules with permanent dipole μp.
  • Low fields such that linear response (Langevin–Debye approximation) applies.
  • Absolute temperature T.


Concept / Approach:

From Debye theory, the mean alignment of dipoles in a weak field gives an orientation polarization term: Porient ≈ N μp^2 E / (3 k T), where N is number density, k is Boltzmann’s constant, and E is field strength. Thus, at fixed E and N, the polarization varies directly with μp^2 and inversely with T. Physically, larger permanent dipoles align more readily; higher temperature increases randomizing thermal energy, reducing net alignment.


Step-by-Step Solution:

Write Debye result for small x = μp E / (k T): Porient ≈ N μp^2 E / (3 k T).Identify proportionality: Porient ∝ μp^2 / T.Thus, doubling μp increases Porient by 4; doubling T halves Porient.


Verification / Alternative check:

Measured dielectric constants of polar gases and liquids typically decrease with rising temperature at low frequencies, consistent with the 1/T dependence of the orientation contribution.


Why Other Options Are Wrong:

  • μp^2 * T or μp * T: predict increase with T, opposite to physical behavior.
  • Independent of temperature: contradicts theory and experiment for polar media.
  • 1/(μp^2 T): incorrectly inverts μp dependence.


Common Pitfalls:

Confusing permanent dipole orientation with electronic polarization (which is nearly temperature independent); forgetting that only the orientation term carries the strong 1/T dependence.


Final Answer:

Proportional to μp^2 / T

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