Appendix/Ramblings/51BiPolytropeStability/BetterInterface

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Better Interface for 51BiPolytrope Stability Study

Content Pointing to Previous Work

Tilded Menu Pointers

  1. Murphy & Fiedler (1985b): SSC/Stability/MurphyFiedler85
    1. Interface Conditions as promoted by Ledoux & Walraven (1958)
    2. Numerical Integration
      1. General Approach
      2. Special Handling at the Center
      3. Special Handling at the Interface
    3. Reconcile Approaches
  2. Excellent Foundation (no pointer from Tiled Menu): SSC/Stability/Biipolytropes
  3. Our Broader Analysis: SSC/Stability/BiPolytropes/HeadScratching
  4. Succinct Discussion: SSC/Stability/BiPolytropes/SuccinctDiscussion

Ramblings: Analyzing Five-One Bipolytropes

  1. Assessing the Stability of Spherical, BiPolytropic Configurations
  2. Searching for Analytic EigenVector for (5,1) Bipolytropes
  3. See (below) Discussing Patrick Motl's 2019 BiPolytrope Simulations
  4. Continue Search
  5. Renormalize Structure
  6. Renormalize Structure (Part 2)
  7. More Carefully Exam Step Function Behavior
  8. More Focused Search for Analytic EigenVector if (5,1) Bipolytropes
  9. Do Not Confine Search to Analytic Eigenvector
  10. Clean, Methodical Examination
  11. Rethink Handling of n = 1 Envelope
  12. Improved Treatment of Core-Envelope Interface

Solid Foundation

Here we pull primarily from the chapters labeled II and III, above.

Entire Configuration

Beginning with the familiar,

Adiabatic Wave (or Radial Pulsation) Equation

d2xdr02+[4r0(g0ρ0P0)]dxdr0+(ρ0γgP0)[ω2+(43γg)g0r0]x=0

where,

g0

=

GMr*(r*)2[ρc3/5(KcG)1/2],

if we adopt the variable normalizations,

ρ*

ρ0ρc

;    

r*

r0[Kc1/2/(G1/2ρc2/5)]

P*

P0Kcρc6/5

;    

Mr*

Mr[Kc3/2/(G3/2ρc1/5)]

the LAWE takes the form,

0

=

d2xdr*2+r*dxdr*+[(σc2γg)𝒦1αg𝒦2]x,

where,

{4(ρ*P*)Mr*(r*)}

      ,      

𝒦1

2π3(ρ*P*)

      and      

𝒦2

(ρ*P*)Mr*(r*)3,

σc2

3ω22πGρc

      ,      

αg

(34γg).

 

Core

Given that, in the core, γg=6/5 and,

r*

=

(32π)1/2ξ,

we can rewrite the LAWE to read,

0

=

d2xdξ2+ξdxdξ+(14π)[5σc2𝒦1+2𝒦2]x,

where,

𝒦1

=

2π3(1+13ξ2)1/2,

=

42ξ2(1+13ξ2)1,

𝒦2

=

(4π3)(1+13ξ2)1.

Structure at the Interface

Once μe/μc and ξi have been specified, other parameter values at the interface are:

θi

=

(1+13ξi2)1/2,

ηi

=

(μeμc)3θi2ξi,

Λi

=

1ηiξi3,

A

=

ηi(1+Λi2)1/2,

B

=

ηiπ2+tan1(Λi),

ηs

=

B+π.

Linearized Perturbation at the Interface

At all radial locations throughout the equilibrium configuration, the three spatially dependent quantities — pδp/P*,dδρ/ρ*, and xδr/r* — are related to one another via the set of linearized governing relations, namely,

Linearized
Equation of Continuity
r0dxdr0=3xd,

Linearized
Euler + Poisson Equations
P0ρ0dpdr0=(4x+p)g0+ω2r0x,

Linearized
Adiabatic Form of the
First Law of Thermodynamics

p=γgd.

Combining the 2nd and 3rd equations, we find,

(4x+γgd)g0+ω2r0x = P0ρ0d(γgd)dr0



At the interface, presumably the dimensional structural variables, P* and r* have the same values, whether viewed from the perspective of the core or from the perspective of the envelope. But ρ* has a different value, depending on the point of view. Specifically,

ρ*|env = (μeμc)ρ*|core.

Hence, from the perspective of the core, the linearized equation of continuity may be written as,

[r0dxdr0+3x]core = δρ[ρ*]core;

while, from the perspective of the envelope, the linearized equation of continuity may be written as,

[r0dxdr0+3x]env = δρ[ρ*]core(μeμc)1

Try again

From here, we know …

Pργg

=

exp[s(γg1)/μ¯].

And, from my discussions with Patrick Motl, we find …

CORE:   Throughout the core,

P*

=

(1+ξ23)3

    and    

ρ*

=

(1+ξ23)5/2

    and    

γg

=

65.

Hence, independent of the radial location, ξ, throughout the core,

s/μ¯|core

=

5ln(5).

ENVELOPE:   Throughout the envelope,

P*

=

θi6[ϕ(η)]2

    and    

ρ*

=

(μeμc)θi5[ϕ(η)]

    and    

γg

=

2.

Hence, independent of the radial location, η, throughout the envelope,

s/μ¯|env

=

ln[(μeμc)2θi4]

=

ln[(μeμc)2(1+ξi23)2].

Envelope

Given that, throughout the envelope γg=2 and,

r*

=

(μeμc)1θi2(2π)1/2η,

we can rewrite the LAWE to read,

0

=

d2xdη2+ηdxdη+12πθi4(μeμc)2[(σc22)𝒦1𝒦2]x,

where,

𝒦1

=

2π3(μeμc)θi1[ηAsin(ηB)],

=

2[1+ηtan(ηB)],

𝒦2

=

4π(μeμc)2θi4[1ηtan(ηB)]1η2.

Entropy as a Step Function

Useful Chapters:

Review

The unit — or, Heaviside — step function, H(x), is defined such that,

H(x)={0;x<01;x>0


[MF53], Part I, §2.1 (p. 123), Eq. (2.1.6)

Heaviside Function

In evaluating this function at x=0, we will adopt the half-maximum convention and set H(0)=12. As has been pointed out in, for example, a relevant Wikipedia discussion, the derivative of the unit step function is,

dH(x)dx

=

δ(x),

where, δ(x) is the Dirac Delta function.

Density

Let,

ζ

rri1

ρ(r)

H(ζ)ρenv+H(ζ)ρcore

See Also

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