Physics:Gibbs rotational ensemble

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Short description: Statistical ensemble


The Gibbs rotational ensemble represents the possible states of a mechanical system in thermal and rotational equilibrium at temperature T and angular velocity ω.[1] The Jaynes procedure can be used to obtain this ensemble.[2] An ensemble is the set of microstates corresponding to a given macrostate.

The Gibbs rotational ensemble assigns a probability pi to a given microstate characterized by energy Ei and angular momentum 𝐉i for a given temperature T and rotational velocity ω.[1][3]

pi=1Ze−β(Ei−ω⋅𝐉i)

where Z is the partition function

Z=∑ie−β(Ei−ω⋅𝐉i)

Derivation

The Gibbs rotational ensemble can be derived using the same general method as to derive any ensemble, as given by E.T. Jaynes in his 1956 paper Information Theory and Statistical Mechanics.[3] Let f(x) be a function with expectation value

⟨f(x)⟩=∑ipif(xi)

where pi is the probability of xi, which is not known a priori. The probabilities pi obey normalization

∑ipi=1

To find pi, the Shannon entropy H is maximized, where the Shannon entropy goes as

H∼∑ipiln⁡(pi)

The method of Lagrange multipliers is used to maximize H under the constraints ⟨f(x)⟩ and the normalization condition, using Lagrange multipliers λ and μ to find

pi=e−λ−μf(xi)

λ is found via normalization:

λ=ln⁡(∑ie−μf(xi))=ln⁡(Z(μ))

and ⟨f(x)⟩ can be written as

⟨f(x)⟩=−∂∂μln⁡(∑ie−μf(xi))=−∂∂μln⁡(Z(μ))

where Z is the partition function

Z(μ)=∑ie−μf(xi)

This is easily generalized to any number of equations f(x) via the incorporation of more Lagrange multipliers.[3]

Now investigating the Gibbs rotational ensemble, the method of Lagrange multipliers is again used to maximize the Shannon entropy H, but this time under the constraints of energy expectation value ⟨E⟩ and angular momentum expectation value ⟨J⟩,[3] which gives pi as

pi=e−λ0Ei−λ1⋅𝐉i−λ3

Via normalization, λ3 is found to be

λ3=ln⁡(∑ie−λ0Ei−λ1⋅𝐉i)=ln⁡(Z)

Like before, ⟨E⟩ and ⟨J⟩ are given by

⟨E⟩=−∂∂λ0ln⁡(∑ie−λ0Ei−λ1⋅𝐉i)=−∂∂λ0ln⁡(Z)

⟨J⟩=−∂∂λ1ln⁡(∑ie−λ0Ei−λ1⋅𝐉i)=−∂∂λ1ln⁡(Z)

The entropy S of the system is given by

S=−k∑ipiln⁡(pi)=k(λ0⟨E⟩+λ1⋅⟨𝐉⟩+ln⁡(Z))

such that

dS=k(λ0d⟨E⟩+λ1d⟨𝐉⟩+dln⁡(Z))

where k is the Boltzmann constant. The system is assumed to be in equilibrium, follow the laws of thermodynamics, and have fixed uniform temperature T and angular velocity ω. The first law of thermodynamics as applied to this system is

dE=dQ+ω⋅d⟨𝐉⟩

Recalling the entropy differential dS=dQT

Combining the first law of thermodynamics with the entropy differential gives

dS=dET−ω⋅d⟨𝐉⟩T

Comparing this result with the entropy differential given by entropy maximization allows determination of λ0 and λ1

λ0=β

λ1=−βω

which allows the probability of a given state pi to be written as

pi=1Ze−β(Ei−ω→⋅𝐉i)

which is recognized as the probability of some microstate given a prescribed macrostate using the Gibbs rotational ensemble.[1][3][2] The term Ei−ω⋅𝐉i can be recognized as the effective Hamiltonian ℋ for the system, which then simplifies the Gibbs rotational partition function to that of a normal canonical system

Z=∑ie−βℋi

Applicability

The Gibbs rotational ensemble is useful for calculations regarding rotating systems. It is commonly used for describing particle distribution in centrifuges. For example, take a rotating cylinder (height Z, radius R) with fixed particle number N, fixed volume V, fixed average energy ⟨E⟩, and average angular momentum ⟨𝐉⟩. The expectation value of number density of particles ⟨n(r)⟩ at radius r can be written as

⟨n(r)⟩=1Z∫n(r)d3pd3qh3e−β(E−ω⋅𝐉)

Using the Gibbs rotational partition function, Z can be calculated to be

Z=π5/2Zβm(e12βmR2ω2−1)2β3h3ω2

Density of a particle at a given point can be thought of as unity divided by an infinitesimal volume, which can be represented as a delta function.

n(r)=1drrdθdz→δ(r′−r)δ(θ′−θ)δ(z′−z)r′

which finally gives ⟨n(r)⟩ as

⟨n(r)⟩=βmω22πZe12βmr2ω2e12βmR2ω2−1

which is the expected result.

Difference between Grand canonical ensemble and Gibbs canonical ensemble

The Grand canonical ensemble and the Gibbs canonical ensemble are two different statistical ensembles used in statistical mechanics to describe systems with different constraints.

The grand canonical ensemble describes a system that can exchange both energy and particles with a reservoir. It is characterized by three variables: the temperature (T), chemical potential (μ), and volume (V) of the system.[4] The chemical potential determines the average particle number in this ensemble, which allows for some variation in the number of particles. The grand canonical ensemble is commonly used to study systems with a fixed temperature and chemical potential, but a variable particle number, such as gases in contact with a particle reservoir.[5]

On the other hand, the Gibbs canonical ensemble describes a system that can exchange energy but has a fixed number of particles. It is characterized by two variables: the temperature (T) and volume (V) of the system. In this ensemble, the energy of the system can fluctuate, but the number of particles remains fixed. The Gibbs canonical ensemble is commonly used to study systems with a fixed temperature and particle number, but variable energy, such as systems in thermal equilibrium.[6]

References

  1. ↑ 1.0 1.1 1.2 Gibbs, Josiah Willard (2010). Elementary Principles in Statistical Mechanics. doi:10.1017/CBO9780511686948. ISBN 978-1-108-01702-2. 
  2. ↑ 2.0 2.1 Thomson, Mitchell; Dyer, Charles C. (2012). Black Hole Statistical Mechanics and the Angular Velocity Ensemble (Preprint). 
  3. ↑ 3.0 3.1 3.2 3.3 3.4 Heims, S. P.; Jaynes, E. T. (April 1962). "Theory of Gyromagnetic Effects and Some Related Magnetic Phenomena". Reviews of Modern Physics 34 (2): 143–165. doi:10.1103/RevModPhys.34.143. Bibcode: 1962RvMP...34..143H. 
  4. ↑ Satoh, A. (2003). "Statistical Ensembles". Introduction to Molecular-Microsimulation of Colloidal Dispersions. Studies in Interface Science. 17. pp. 7–18. doi:10.1016/S1383-7303(03)80030-3. ISBN 978-0-444-51424-0. "The grand canonical ensemble is a statistical ensemble which is specified by the system volume V, temperature T, and chemical potential μ; the chemical potential is the energy which is necessary for adding one particle to the system adiabatically, and the detailed definition will be shown later. This statistical ensemble is highly appropriate for treating a physical system in which particles and energies can be transported across the walls of the system." 
  5. ↑ "LECTURE 9 Statistical Mechanics". https://ps.uci.edu/~cyu/p115A/LectureNotes/Lecture9/html_version/lecture9.html. [self-published source?]
  6. ↑ Emch, Gérard G.; Liu, Chuang (2002). "The Gibbs Canonical Ensembles". The Logic of Thermostatistical Physics. pp. 331–372. doi:10.1007/978-3-662-04886-3_10. ISBN 978-3-642-07462-2.