SSC/Stability/BiPolytropes/HeadScratching

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Broader Examination of Bipolytrope Stability

Our
Broader
Analysis

Overview

file = Dropbox/WorkFolder/Wiki edits/EmbeddedPolytropes/CombinedSequences.xlsx --- worksheet = EqSeqCombined2
file = Dropbox/WorkFolder/Wiki edits/EmbeddedPolytropes/CombinedSequences.xlsx --- worksheet = EqSeqCombined2
Figure 1:  Equilibrium Sequences
of Pressure-Truncated Polytropes

Equilibrium sequences of Pressure-Truncated Polytropes

We expect the content of this chapter — which examines the relative stability of bipolytropes — to parallel in many ways the content of an accompanying chapter in which we have successfully analyzed the relative stability of pressure-truncated polytopes. Figure 1, shown here on the right, has been copied from a closely related discussion. The curves show the mass-radius relationship for pressure-truncated model sequences having a variety of polytropic indexes, as labeled, over the range 1n6. (Another version of this figure includes the isothermal sequence.) On each sequence for which n3, the green filled circle identifies the model with the largest mass. We have shown analytically that the oscillation frequency of the fundamental-mode of radial oscillation is precisely zero for each one of these maximum-mass models. As a consequence, we know that each green circular marker identifies the point along its associated sequence that separates dynamically stable (larger radii) from dynamically unstable (smaller radii) models.


In each case, the fundamental-mode oscillation frequency is precisely zero if, and only if, the adiabatic index governing expansions/contractions is related to the underlying structural polytropic index via the relation, γg=(n+1)/n, and if a constant surface-pressure boundary condition is imposed.



In another accompanying chapter, we have used purely analytic techniques to construct equilibrium sequences of spherically symmetric bipolytropes that have, (nc,ne)=(5,1). For a given choice of μe/μc — the ratio of the mean-molecular weight of envelope material to the mean-molecular weight of material in the core — a physically relevant sequence of models can be constructed by steadily increasing the value of the dimensionless radius at the core/envelope interface, ξi, from zero to infinity. Figure 2, whose content is essentially the same as Figure 1 of this separate chapter, shows how the fractional core mass, νMcore/Mtot, varies with the fractional core radius, qrcore/R, along sequences having seven different values of μe/μc, as labeled: 1 (black), ½ (dark blue), 0.345 (brown), ⅓ (dark green), 0.316943 (purple), 0.309 (orange), and ¼ (light blue).

When modeling bipolytropes, the default expectation is that an increase in ξi along a given sequence will correspond to an increase in the relative size — both the radius and the mass — of the core. This expectation is realized along the Figure 2 sequences that have the largest mean-molecular weight ratios: μe/μc = 1 and ½. But the behavior is different along the other five illustrated sequences. For sufficiently large ξi, the relative radius of the core begins to decrease; along each sequence, a solid purple circular marker identifies the location of this turning point in radius. Furthermore, along sequences for which μe/μc<13, eventually the fractional mass of the core reaches a maximum and, thereafter, decreases even as the value of ξi continues to increase; a solid green circular marker identifies the location of this maximum mass turning point along each of these sequences. (Additional properties of these equilibrium sequences are discussed in yet another accompanying chapter.)

The principal question is: Along bipolytropic sequences, are maximum-mass models associated with the onset of dynamical instabilities?

Planned Approach

file = Dropbox/WorkFolder/Wiki edits/BiPolytrope/qAndNuMaxAug21.xlsx --- worksheet = PlotSigma0
file = Dropbox/WorkFolder/Wiki edits/BiPolytrope/qAndNuMaxAug21.xlsx --- worksheet = PlotSigma0
Figure 2: Equilibrium Sequences of Bipolytropes
with (nc,ne)=(5,1) and Various μe/μc

Ideally we would like to answer the just-stated "principal question" using purely analytic techniques. But, to date, we have been unable to fully address the relevant issues analytically, even in what would be expected to be the simplest case:   bipolytropic models that have (nc,ne)=(0,0). Instead, we will streamline the investigation a bit and proceed — at least initially — using a blend of techniques. We will investigate the relative stability of bipolytropic models having (nc,ne)=(5,1) whose equilibrium structures are completely defined analytically; then the eigenvectors describing radial modes of oscillation will be determined, one at a time, by solving the relevant LAWE(s) numerically. We are optimistic that this can be successfully accomplished because we have had experience numerically integrating the LAWE that governs the oscillation of:

A key reference throughout this investigation will be the paper by 📚 J. O. Murphy & R. Fiedler (1985b, Proc. Astron. Soc. Australia, Vol. 6, no. 2, pp. 222 - 226). They studied Radial Pulsations and Vibrational Stability of a Sequence of Two Zone Polytropic Stellar Models. Specifically, their underlying equilibrium models were bipolytropes that have (nc,ne)=(1,5). In an accompanying chapter, we describe in detail how 📚 Murphy & Fiedler (1985b) obtained these equilibrium bipolytropic structures and detail some of their equilibrium properties.

Here are the steps we initially plan to take:

  • Governing LAWEs:
  • Determine what surface boundary condition should be imposed on physically relevant LAWE solutions, i.e., on the physically relevant radial-oscillation eigenvectors.
  • Initial Analysis:
    • Choose a maximum-mass model along the bipolytropic sequence that has, for example, μe/μc=1/4. Hopefully, we will be able to identify precisely (analytically) where this maximum-mass model lies along the sequence. Yes! Our earlier analysis does provide an analytic prescription of the model that sits at the maximum-mass location along the chosen sequence.
    • Solve the relevant eigenvalue problem for this specific model, initially for (γc,γe)=(6/5,2) and initially for the fundamental mode of oscillation.

Summary of (Inadequate) Detailed Analyses

Key Models Along the μe/μc=1/4 Equilibrium Sequence
ξi q ν R* Mtot* Significance Figure Marker
4.9379 0.0482 0.1394 40.945 43.437 νmax Dark-green circular marker in Figs. 2, 4, & 5
2.766 0.1189 0.1107 16.13 39.14 (inadequate) LAWE analysis Orange triangular marker in Figs. 3, 4, & 5
2.2805 0.1246 0.0931 12.648 38.970 Mtot*|min Light-blue diamond marker in Figs. 4 & 5
1.9139 0.1265 0.0749 10.452 39.058 qmax Purple circular marker in Figs. 2, 4, & 5

Attempts to Identify Marginally Unstable (nc, ne) = (5, 1) Bipolytropes

file = Dropbox/WorkFolder/Wiki edits/BiPolytrope/qAndNuMax.xlsx --- worksheet = PlotSigma0
file = Dropbox/WorkFolder/Wiki edits/BiPolytrope/qAndNuMax.xlsx --- worksheet = PlotSigma0
Figure 3:  Conflicting Instability Regions
Conflicting Instability Regions
  • Virial Analysis
  • Solving the Relevant LAWE:
  • K-BK74 Conjecture
    Through this analysis, we were quite successful at generating a reasonably shaped radial-oscillation eigenfunction for the equilibrium model that lies along the sequence at the maximum mass fraction, νmax. We obtained the eigenfunction by subtracting the structural profile of one model (immediately to the left of this maximum) from the structural profile of a separate model (immediately to the right of this maximum). But, after doing so, we realized that the result could not be physically justified. Although we had been careful to ensure that the core mass fraction (ν) was identical in the two separate models, we had not paid attention to the total mass; it had not been held fixed. Hence, we cannot claim to have performed a valid dynamical perturbation of models in the vicinity of νmax.
     
    The eigenfunction that was constructed in this manner was nevertheless eye-opening! It appears to contain a sizable step function at the interface; that is to say, it appears as though the radial-displacement function at the surface of the core is offset (discontinuously) from the radial-displacement function at the base of the envelope. We had not allowed this to happen in our separate investigation of Radial Oscillations of 51 Models.

We will attempt to incorporate these new insights into our analyses that follow.  

Rethink Evolution and Stability

file = Dropbox/WorkFolder/Wiki edits/BiPolytrope/qAndNuMaxAug21.xlsx --- worksheet = muratio0.25
file = Dropbox/WorkFolder/Wiki edits/BiPolytrope/qAndNuMaxAug21.xlsx --- worksheet = muratio0.25
Figure 4:   Mass vs. Radius
Figure 5:   ν vs. q
Mass versus Radius m_e = 0.93
Mass versus Radius m_e = 0.93
Mass versus Radius m_e = 0.93
Mass versus Radius m_e = 0.93

Consider a system that has m3=(3μe/μc)=0.75 and that slowly evolves along the appropriate (light blue), m3= constant equilibrium sequence shown in Figure 3. It begins its evolution with a very small core — that is, with ξi nearly zero, and with q and ν both very small. The location of the core-envelope interface, ξi, moves slowly outward (in Lagrangian mass space) as the ashes left from hydrogen burning build up the mass of the core at the expense of the envelope. This means that (slow) evolution proceeds along the qν equilibrium sequence in a counter-clockwise direction.

Schwarzschild and his collaborators noticed that, as an evolution proceeds along an equilibrium sequence for which (in our example case) m31, the fractional core mass increases only up to a limiting value, νmax; in our case, νmax0.139. As the core-envelope interface location, ξi, attempts to increase to a value larger than the value associated with the model at νmax, something rather drastic must happen — at least on a secular time scale associated with nuclear burning. We have wondered whether a dynamical instability is also encountered at this "turning point" along the equilibrium sequence. Up to now, all of our (inadequate) detailed analyses have been focused on securing an answer to this question.

As Figure 4 illustrates, along this same sequence, the normalized radius (R*) starts off small and it steadily grows as the evolution proceeds, but the normalized total mass (Mtot*) starts off large and initially decreases. In reality, we expect the system to conserve its total mass throughout the evolution. Given that the mass has been normalized via the expression,

Mtot*=Mtot[G3/2ρc1/5Kc3/2],

we appreciate that a decrease in the dimensionless mass (as depicted in Fig. 4) can quite naturally be attributed to a steady increase in the specific entropy of the core material, Kc. This evolution along the equilibrium sequence will happen on a secular, rather than dynamical, time scale that is set by the rate at which Kc increases — that is, at a rate set by nuclear burning. But at each point along the sequence, we can check to see whether the equilibrium configuration is dynamically stable. We expect that the turning point along the M*(R*) sequence is an indication of transition from a (dynamically) stable to (dynamically) unstable state. We should be able to apply the B-KB74 conjecture to get a good idea of what the unstable eigenfunction looks like at this turning point.

Differentiate M* With Respect to ℓi

In an accompanying discussion titled, New Derivation, we examined how the core mass-fraction (ν) varies with iξi/3. Here, we want to examine how the total mass (Mtot*) varies with i. In what follows, we borrow heavily from various analytic expressions that have been obtained via this separate New Derivation; and, as in this earlier analysis, numerical evaluations (in parentheses) come from Example #1 for which, μe/μc=0.25 and ξi=0.5, which implies that m3=0.75 and i=(12)1/2.

Mtot*

=

(μeμc)2(2π)1/2[ηs2θi(dϕdη)s]

 

=

(μeμc)2(2π)1/2[Aηsθi]=40.09338625,

where,

θi

=

(1+i2)1/2=0.960768923,

ηi

=

m3i(1+i2)=0.199852016,

Λi

=

1m3i[1+(1m3)i2]=4963=4.715027199,

ηs

=

(π2+tan1Λi)+m3i(1+i2)=3.132453649,

A

=

ηi(1+Λi2)1/2=m3i(1+i2){1+1m32i2[1+(1m3)i2]2}1/2=0.963267676.

Now, the differentiation:

dθidi

=

i(1+i2)3/2=12(13)3/2=0.256015475(7);

dΛidi

=

2(1m3)im3i1m3i2[1+(1m3)i2]=1m3i2{2(1m3)i2[1+(1m3)i2]}

 

=

483{1244948}=473=15.66666666;

dηsdi

=

ddi[m3i(1+i2)]+ddi(tan1Λi)=[m3(1+i2)][2m3i2(1+i2)2]+[1+Λi2]1dΛidi

 

=

913232132+[25092233]1(473)=1132{913232[22321347193]}=32132193{11193221347}=0.088573443

 

=

[m3(1+i2)][2m3i2(1+i2)2]+{[1+(1m3)i2]2+m32i2}1{2m3(1m3)i2m3[1+(1m3)i2]};

dAdi

=

(1+Λi2)1/2ddi[m3i(1+i2)]+[m3i(1+i2)]ddi(1+Λi2)1/2

 

=

(1+Λi2)1/2[m3(1+i2)2m3i2(1+i2)2]+[m3i(1+i2)]Λi(1+Λi2)1/2dΛidi=4.819904715(4)[0.585798817(5)]+0.195503386(6)(473)=0.239391902

 

=

(131932233)1/2[3213232]1132+49233/2[3213]1231/2(223313193)1/2(473)

 

=

(311219322133)1/2(37447222133193)1/2=31/22133/21931/2[111937247]=[223552133193]1/2=0.239391901

 

=

1(1+Λi2)1/2{(1+Λi2)[m3(1+i2)2m3i2(1+i2)2]+Λii[1(1+i2)][2(1m3)i2[1+(1m3)i2]]}.

Hence,

(μeμc)2(π2)1/2dMtot*di

=

ddi[Aηsθi]

 

=

ηsθidAdi+AθidηsdiAηsθi2dθidi

 

[(3.132453649)(0.960768923)]0.239391901[(0.963267676)(0.960768923)]0.088573443+[(0.963267676)(3.132453649)(0.960768923)2]0.256015475

 

0.78050(8)0.088803+0.836874=0.032426.

Selected Models

Via a crude iterative technique, we have determined that the derivative, dMtot*/di, goes to zero when ξi=2.27276626 (to eight significant digits); this is therefore the minimum-mass model — identified by the light-blue diamond-shaped marker — along the Mtot*(R*) sequence shown above in Figure 4. A few other properties of this model "A" are recorded in Table 2. For example, (Mtot*,R*)=(38.97032951,12.598233); and its position (also marked by a light-blue diamond) along the Figure 5 (q,ν)=(0.1246568,0.0927131). The lower-left figure in Table 2 shows how (r*) varies with enclosed mass-fraction for this minimum-mass model "A"; the core-envelope interface — where the blue and red segments of the plotted curve meet — is located at (Mr/Mtot,r*)=(0.092713145,1.5704549).

file = Dropbox/WorkFolder/Wiki edits/Bipolytrope/Stability/qAndNuMax.xlsx --- worksheet = K-BK74 thru MinuPreparation
file = Dropbox/WorkFolder/Wiki edits/Bipolytrope/Stability/qAndNuMax.xlsx --- worksheet = K-BK74 thru MinuPreparation
Table 2
Bipolytrope with (nc,ne)=(5,1)
Selected Pairings along the μe/μc=0.25 Sequence
Pairing (ξi)+ Λi Mtot* dMtot*di R* q ν
Example #1 0.5 4.715027199 40.09338625 0.413955 -- -- --
A (degenerate) 2.27276626 1.4535131 38.97032951 6.20×109 12.598233 0.1246568 0.0927131
B1 2.0653386 1.5156453 39.00000000 0.491175 11.31459 0.1261314 0.082829
B2 2.4782510 1.4088069 39.00000000 +0.500086 13.987375 0.1224277 0.1013938
C1 1.83343536 1.612448 39.10000000 0.990185582 10.019034 0.1264476 0.0705448
C2 2.70235958 1.3746562 39.10000000 +1.042782519 15.637446 0.119412 0.1095988

Radius vs. Mass for Minimum-Mass Bipoltrope having μ-ratio = 0.250

Eigenfunction Obtained Via B-KB74 Conjecture
Eigenfunction for Minimum-Mass Bipoltrope having μ-ratio = 0.250


In the context of our analysis of the stability of pressure-truncated n = 5 polytropes, we showed how the B-KB74 conjecture can be used to illustrate the approximate shape of the radial eigenfunction of the marginally unstable mode. Proceeding along the lines of this independent discussion, here we have identified two equilibrium models — labeled "B1" and "B2" in Table 2 — that lie near to, but on either side of, the minimum-mass model along the equilibrium sequence and that have identical total masses: in this case, Mtot*=39.00000000 (identical, to nine significant digits). Using the mass-fraction, mrMr/Mtot, as the Lagrangian coordinate for both models, we subtracted the profile of model "B1" from the profile of model "B2" and divided this difference by the average profile, we obtained the approximate neutral-mode eigenfunction, x(mr), displayed in the lower-right figure of Table 2.

Things to note about this iteratively derived, approximate neutral-mode eigenfunction:

  1. The radial-displacement function, x(mr), has been normalized to unity at the surface.
  2. The location of the model "A" core-envelope interface (mr=νA=0.0927131) has been marked by the vertical, red-dashed line segment.
  3. Throughout the core, x is very small; consistent with being zero throughout.
  4. Moving inward through the envelope, x appears to drop smoothly from "plus" one (at the surface) to approximately "minus" one (at the interface).
  5. Because x passes through zero one time inside the envelope, this cannot be the eigenfunction of the fundamental mode of radial oscillation; instead, it is likely associated with the 1st overtone, as discussed for example in connection with Schwarzschild's modeling of radial eigenfunctions of n = 3 polytropes.

With regard to the second itemized note, we should point out that, although models "B1" and "B2" have identical total masses, their core mass-fraction — that is, the location of the core-envelope interface as defined by the Lagrangian mass marker — is different: νB1=0.082829 and νB2=0.101394. As a result, the B-KB74 conjecture should not be expected to apply in the immediate vicinity of the core-envelope interface.

LAWE

Let's perform the LAWE integration in two parts: (1) Integrate from the center (where the derivative of the displacement function must be zero), through the core, up to the core-envelope interface; and (2) integrate from the surface (where the logarithmic derivative of the displacement function is negative one), through the envelope, down to the core-envelope interface. Examine the discontinuity that results and see whether it makes sense in terms of the required "matching conditions" at the interface.

Throughout the Configuration

From the last couple of lines of an accompanying Foundation presentation, the relevant LAWE may be written as,

0

=

d2xdr*2+{4r*(ρ*P*)Mr*(r*)2}dxdr*+(ρ*P*){ω2γgGρc+(4γg3)Mr*(r*)3}x

 

=

d2xdr*2+{4(ρ*P*)Mr*(r*)}1r*dxdr*+(ρ*P*){2πσc23γgαgMr*(r*)3}x

 

=

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).

 

From a related discussion of interior structural profiles, we appreciate that throughout the core we have,

αg

=

13;

ρ*P*

=

(1+13ξ2)1/2;

Mr*r*

=

(23π)1/2[ξ3(1+13ξ2)3/2](2π3)1/21ξ=2ξ2(1+13ξ2)3/2;

1(r*)2

=

(2π3)ξ2;

and, throughout the envelope we have,

αg

=

+1;

ρ*P*

=

(μeμc)θi1ϕ(η)1;

Mr*r*

=

(μeμc)2θi1(2π)1/2(η2dϕdη)[(μeμc)1θi2(2π)1/2η]1=2(μeμc)1θiη(η2dϕdη);

1(r*)2

=

2π(μeμc)2θi4η2.

Surface Boundary Condition

In an effort to ensure finite-amplitude fluctuations at the surface, we will enforce the condition,

r0dlnxdr0

=

1γg(43γg+ω2R3GMtot)        at         r0=R,

that is,

r*dlnxdr*

=

[(2π3)σc2(R*)3γgMtot*αg]        at         r*=R*,

where the asterisks (*) signal that we have employed the same variable normalizations as have been adopted in our accompanying Foundations discussion. Since our analysis, here, is focused on the marginally unstable (minimum-mass) configuration in which we expect σc2=0, the surface (envelope) constraint becomes,

dlnxdlnη

=

αg=1        at         η=ηs.

Interface

Drawing from an accompanying discussion, the matching condition at the interface is given by the expression,

0

=

[γcxcore(3+dlnxcoredlnr*)γexenv(3+dlnxenvdlnr*)]i.

Given that γc=6/5 and γe=2, this becomes,

[xcore(3+dlnxcoredlnr*)]i

=

53[xenv(3+dlnxenvdlnr*)]i.

Central Boundary Condition

The central boundary condition is,

dxcoredr*

=

0.

In order to kick-start the integration outward from the center of the configuration, we will following the procedure that has been detailed in an accompanying discussion. At the center of the configuration (ξ1=0), we label the fractional displacement function as x1 — value to be set later, perhaps in an effort to help secure the proper matching conditions at the interface — then we will draw on the derived power-series expression to determine the value of the displacement function at the first radial grid line, ξ2=Δξ, away from the center. Specifically, given that n=5,γg=6/5, and αg=1/3 in the core, we will set,

x2

=

x1[1(n+1)𝔉Δξ260]=x1[1𝔉Δξ210],

where,

𝔉

[σc2γg2αg]=16[5σc2+4].

Numerical Integration

Through the Core

Throughout the core, the governing LAWE is,

0

=

d2xdξ2+ξdxdξ+(14π)[5σc2𝒦1+2𝒦2]x,

where,

𝒦1

=

2π3(1+13ξ2)1/2,

(ρ*P*)Mr*(r*)

=

2ξ2(1+13ξ2)1,

=

42ξ2(1+13ξ2)1,

𝒦2

=

(4π3)(1+13ξ2)1.

Now, using the general finite-difference approach described separately, we make the pair of substitutions,

xi=dxdξ

x+x2Δξ;

xi=d2xdξ2

x+2xi+xΔξ2,

which will provide an approximate expression for x+xi+1, given the values of xxi1 and xi. Specifically, if the center of the configuration is denoted by the grid index, i=1, then for zones, i=2N,

[x+2xi+xΔξ2]

=

ξ[x+x2Δξ](14π)[5σc2𝒦1+2𝒦2]x

[x+Δξ2]+ξ[x+2Δξ]

=

[2xixΔξ2]+ξ[x2Δξ](14π)[5σc2𝒦1+2𝒦2]xi

x+{1+ξ[Δξ2]}

=

xi{2(Δξ24π)[5σc2𝒦1+2𝒦2]}x{1ξ[Δξ2]}.

Check Against Independent Derivation

We have dealt with this identical LAWE in connection with our analysis of the stability of pressure-truncated n = 5 Polytropic configurations. Let's see whether that derivation matches our current one. In that case, we found,

x+{2θ+4ΔξθξΔξ(n+1)(θ')}

=

xi{4θΔξ2(n+1)3[σc2γg2α(3θ'ξ)]}x[2θ4Δξθξ+Δξ(n+1)(θ')]

x+{1+Δξ2ξ[46ξ(θ')θ]}2θ

=

xi{2Δξ2θ[5σc26+23(3θ'ξ)]}2θx{1Δξ2ξ[46ξ(θ')θ]}2θ

x+{1+Δξ2ξ[]}2θ

=

xi{2Δξ24π[5σc24π6θ+8π3(3θ'ξθ)]}2θx{1Δξ2ξ[]}2θ.

Given that,

4π6θ

=

2π3(1+13ξ2)1/2𝒦1

      and     

4π3(3θξθ)

=

4π3(1+13ξ2)1𝒦2,

we can confirm that the two expressions are identical.

Through the Envelope

Throughout the envelope — that is, for ηiηηs — the governing LAWE is,

0

=

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

where,

{4(ρ*P*)Mr*(r*)}

      ,      

𝒦1

2π3(ρ*P*)

      and      

𝒦2

(ρ*P*)Mr*(r*)3.

Keep in mind that, once μe/μc and ξi have been specified, other parameter values at the interface are:

θi

=

(1+13ξi2)1/2,

ηi

=

(μeμc)3θi2ξi,

Λi

=

1ηi+(dϕdη)i=(μeμc)113ξiθi2ξi3,

A

=

ηi(1+Λi2)1/2,

B

=

ηiπ2+tan1(Λi),

ηs

=

B+π.

From a related discussion of interior structural profiles, we appreciate that throughout the envelope we have,

αg

=

+1;

ρ*P*

=

(μeμc)θi1ϕ(η)1;

Mr*r*

=

(μeμc)2θi1(2π)1/2(η2dϕdη)[(μeμc)1θi2(2π)1/2η]1=2(μeμc)1θiη(η2dϕdη);

1(r*)2

=

2π(μeμc)2θi4η2.

Hence,

𝒦1

=

2π3(μeμc)θi1ϕ(η)1=2π3(μeμc)θi1[ηAsin(ηB)],

(ρ*P*)Mr*r*

=

2dlnϕdlnη=2[1ηtan(ηB)],

=

4(ρ*P*)Mr*(r*)=42[1ηtan(ηB)]=2[1+ηtan(ηB)],

𝒦2

=

4π(μeμc)2θi4[1ηtan(ηB)]1η2.

Finally, restructuring the radially dependent coefficient of the linear term in the LAWE, we have,

d2xdη2+ηdxdη

=

{12πθi4(μeμc)2𝒦2(σc22)12πθi4(μeμc)2𝒦1}x

 

=

{12πθi4(μeμc)24π(μeμc)2θi4[1ηtan(ηB)]1η2(σc22)12πθi4(μeμc)22π3(μeμc)θi1[ηAsin(ηB)]}x

 

=

{[1ηtan(ηB)]2η2(σc26)1θi5(μeμc)1[ηAsin(ηB)]}x

 

=

{[4]1η2(σc26)1θi5(μeμc)1[ηAsin(ηB)]}x.

Again, using the general finite-difference approach described separately, we make the pair of substitutions,

xi=dxdη

x+x2Δη;

xi=d2xdη2

x+2xi+xΔη2.

For the envelope, we will integrate from the surface, into the core-envelope interface. So, this time these "finite-difference" expressions will provide an approximate expression for xxi1, given the values of x+xi+1 and xi. If the surface of the configuration is denoted by the grid index, i=N, then for zones, i=(N1)??,

x+2xi+xΔη2

=

η[x+x2Δη]+{[4]1η2(σc26)1θi5(μeμc)1[ηAsin(ηB)]}xi

[xΔη2]η[x2Δη]

=

[x+2xiΔη2]η[x+2Δη]+{[4]1η2(σc26)1θi5(μeμc)1[ηAsin(ηB)]}xi

x{1Δη2η}

=

{2+[4]Δη2η2(σc26)Δη2θi5(μeμc)1[ηAsin(ηB)]}xi[1+Δη2η]x+.

dlnxdlnη

=

1

      at,       η=ηs.

Hence,

[x+x2Δη]s

[dxdη]s=xsηs

[xN+1xN12Δη]

xNηs

xN+1

xN12ΔηxNηs.

Inserting this expression for "x+" in the finite-difference representation of the envelope's LAWE allows us to determine the value for x=xN1. Specifically,

xN1{1Δη2η}

=

{2+[4]Δη2η2(σc26)Δη2θi5(μeμc)1[ηAsin(ηB)]}sxN[1+Δη2η][xN12ΔηxNηs]

xN1{1Δη2η}+[1+Δη2η]xN1

=

{2+[4]Δη2η2(σc26)Δη2θi5(μeμc)1[ηAsin(ηB)]}sxN+[1+Δη2η]s[2Δηηs]xN

xN1

=

{1+[Δηηs]+2[Δη2ηs2]+(σc2223)Δη2θi5(μeμc)1[ηsA]}xN.

Note that, in the last term of this last expression, we have acknowledged that, (ηsB)=πsin(ηsB)=1.


Slope at the Interface

We will need to determine the slope that is associated with the envelope's eigenfunction, [dx/dη]env, precisely at the interface. While the envelope's eigenfunction does not actually exist on the "core" side of the interface, we can project what its value at x would be if the envelope's eigenfunction were to continue smoothly just one small step beyond the interface, then use this projected value to determine the function's slope at the interface location. Labeling the interface at i=J, first we have,

[1Δη2η]J[x]project

=

{2+[4]Δη2η2(σc26)Δη2θi5(μeμc)1[ηAsin(ηB)]}JxJ[1+Δη2η]JxJ+1.

Then we conclude that,

[xenv']J[dxenvdη]J

=

xJ+12Δη12Δη[x]project.

Feeble Analytic Attempt

Noice that if we assume σc2=0, the governing envelope LAWE is,

0

=

d2xdη2+[1+ηtan(ηB)]2ηdxdη{[1ηtan(ηB)]2η2}x.

Let's try …

x

=

ηm[tan(ηB)]k

dxdη

=

mηm1[tan(ηB)]k+kηm[tan(ηB)]k1[cos(ηB)]2

d2xdη2

=

m(m1)ηm2[tan(ηB)]k+mηm1k[tan(ηB)]k1[cos(ηB)]2

 

 

+kmηm1[tan(ηB)]k1[cos(ηB)]2+k(k1)ηm[tan(ηB)]k2[cos(ηB)]4+2kηm[tan(ηB)]k1[cos(ηB)]3sin(ηB)

 

=

m(m1)ηm2[tan(ηB)]k+2mηm1k[tan(ηB)]k1[cos(ηB)]2

 

 

+k(k1)ηm[tan(ηB)]k2[cos(ηB)]4+2kηm[tan(ηB)]k[cos(ηB)]2

Hence,

RHS

=

m(m1)ηm2[tan(ηB)]k+2mηm1k[tan(ηB)]k1[cos(ηB)]2

 

 

+k(k1)ηm[tan(ηB)]k2[cos(ηB)]4+2kηm[tan(ηB)]k[cos(ηB)]2

 

 

+[2η+2tan(ηB)]{mηm1[tan(ηB)]k+kηm[tan(ηB)]k1[cos(ηB)]2}

 

 

2[1ηtan(ηB)]ηm2[tan(ηB)]k

 

=

m(m1)ηm2[tan(ηB)]k+2mηm1k[tan(ηB)]k1[cos(ηB)]2

 

 

+k(k1)ηm[tan(ηB)]k2[cos(ηB)]4+2kηm[tan(ηB)]k[cos(ηB)]2

 

 

+2mηm2[tan(ηB)]k+2kηm1[tan(ηB)]k1[cos(ηB)]2

 

 

+2mηm1[tan(ηB)]k1+2kηm[tan(ηB)]k2[cos(ηB)]2

 

 

2ηm2[tan(ηB)]k+2ηm1[tan(ηB)]k1

 

=

m(m1)ηm2[tan(ηB)]k+2kηm[tan(ηB)]k[cos(ηB)]2+2mηm2[tan(ηB)]k2ηm2[tan(ηB)]k

 

 

+2mηm1k[tan(ηB)]k1[cos(ηB)]2+2kηm1[tan(ηB)]k1[cos(ηB)]2+2mηm1[tan(ηB)]k1+2ηm1[tan(ηB)]k1

 

 

+k(k1)ηm[tan(ηB)]k2[cos(ηB)]4+2kηm[tan(ηB)]k2[cos(ηB)]2

 

=

[tan(ηB)]kηm2[cos(ηB)]2{[m(m1)+2m2][cos(ηB)]2+2kη2}

 

 

+[tan(ηB)]k12(m+1)ηm1[cos(ηB)]2{k+[cos(ηB)]2}

 

 

+k[tan(ηB)]k2[cos(ηB)]4ηm{(k1)+2[cos(ηB)]2}

If m=1, the second group of terms disappears and we have,

RHS

=

[tan(ηB)]k[cos(ηB)]2η3{[2kη22[cos(ηB)]2]+k[sin(ηB)]2η2[(k1)+2[cos(ηB)]2]}

 

=

[tan(ηB)]k[cos(ηB)]2η3[sin(ηB)]2{[2kη2][sin(ηB)]2[2[cos(ηB)]2][sin(ηB)]2+kη2(k1)+2kη2[cos(ηB)]2}

 

=

[tan(ηB)]k[cos(ηB)]2η3[sin(ηB)]2{k(k+1)η22[cos(ηB)]2[sin(ηB)]2}

See Also


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