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)?
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AProportional to μp^2 / T
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BProportional to μp^2 * T
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CProportional to μp * T
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DIndependent of temperature
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EProportional to 1 / (μp^2 T)
Answer
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