Plasma and Fusion Research
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Approximate Formulae Representing Effective-Charge-Number Dependence of Collisional Relaxation Coefficients for Electron Fluid Moment Equations in Open Magnetic Field System
Tomonori TAKIZUKASatoshi TOGO
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2026 年 21 巻 論文ID: 1403040

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Abstract

We study the collisional relaxation processes of electron fluid moments in open magnetic field systems, such as scrape-off layer and divertor plasmas, by using a simplified Fokker-Planck equation. Anisotropies in temperature and heat flux in directions parallel and perpendicular to the magnetic field are taken into account. The thermal force is not given by the temperature gradient but by the heat flux damping. The relaxation of heat-flux anisotropy is found to play a role in the heat flux transport. For the convenience of plasma fluid simulations, approximate formulae are devised to represent the dependence of relaxation coefficients on the effective charge number.

1.  Introduction

Heat transports in peripheral plasmas of magnetic confinement systems have been investigated by using plasma fluid models [13]. Magnetic field lines in the scrape-off layer (SOL) plasma hit directly plasma facing components, such as divertor plates. The outflowing power from a core plasma is transported mainly along the open magnetic field B in the SOL-divertor plasma. Major channel of the heat transport along B is the electron heat conduction, which is governed by Coulomb collisions. In the general electron fluid equations, the parallel conductive heat flux is given by qe=κeTe. The thermal conductivity is defined as κe=γ0neTeτe0/me, where the subscript denotes the parallel to B, Te is the electron temperature, ne the electron density and me the electron mass. The electron collision time τe0 is proportional to Te3/2 and inversely proportional to the effective charge number of background ions Zeff as well as to ne; τe0 = 3.5 × 1011 TE3/2/neZeffΛ (τe0: s, TE: eV, ne: m−3, Λ: Coulomb logarithm) [4]. A constant called “thermal-conductivity coefficient” is γ0 = 3.16 for Zeff = 1, and is increased gradually with Zeff.

The friction force, Ffr=α0nemeU/τe0, and the thermal force, Fth=β0neTe, are also dependent on Zeff nonlinearly (U: electron mean flow velocity relative to ion flow). A constant called “friction-force coefficient” α0 = 0.51 for Zeff = 1 is decreased gradually with Zeff, while another constant called “thermal-force coefficient” β0 = 0.71 for Zeff = 1 is increased gradually with Zeff [4]. For the convenience of simulation studies, we devise approximate formulae representing the Zeff dependence of these relaxation coefficients.

In Sec. 2, a simplified Fokker-Planck equation is applied to study the collisional relaxation processes of an electron fluid in an open magnetic field system, such as SOL-divertor plasma. The anisotropy in Te and qe in directions parallel and perpendicular to B is taken into account. Relaxation terms for fluid moment equations are derived in Sec. 3. Approximate formulae representing the Zeff dependence of relaxation coefficients are devised. Summary and discussion are given in Sec. 4.

2.  Basics of Fluid Moment Equations

We derive electron fluid moment equations in an open magnetic field system, where the transport along B is dominant. Five fluid moments are taken into account in this paper, a mean flow (or electric current), two anisotropic temperatures (or effective isotropic temperature and temperature anisotropy), and two anisotropic heat fluxes (or total heat flux and heat flux anisotropy). Relaxation terms are derived by taking account of a simplified Fokker-Planck equation.

2.1  Distortion of velocity distribution function

Consider a plasma in a uniform magnetic field B. Electrons are perturbed from a thermal equilibrium state. Mean flow, anisotropic temperature and heat flux are the results of the perturbation. The velocity distribution function of electrons is distorted a little from a Maxwellian, fM=ne(me/2πTe)3/2exp(mev2/2Te), and is expressed as

  
f e = f M + δ f e = f M + ( δ f U + δ f Δ T + δ f q ) . (1)

The “mean-flow (MF) distortion” δfU and the “anisotropic-temperature (AT) distortion” δfΔT are derived by expanding a shifted bi-Maxwellian distribution, fSBMexp{me(vU)2/2Te}×exp{mev2/2Te},

  
δ f U = ( z v U / v te 2 ) G U f M , (2)
  
δ f Δ T = Δ T ( 3 z 2 1 ) ( v 2 / 4 v te 2 ) f M , (3)

where v is the absolute velocity, z=cosθ is a pitch angle variable (θ = 0 is at the direction of B) and vte(Te/me)1/2 is the electron thermal speed. The parallel velocity is v=vz, and the perpendicular velocity v=v(1z2)1/2 (subscripts and denote the components parallel and perpendicular to B, respectively).

Fluid moments are obtained by integrating fe in the velocity space, M(n)=vn=(1/ne)dv(vnfe)=(2π/ne)∫∫dzv2dv(vnfe). The 1st order moment is the electron mean flow velocity U relative to the ion flow velocity, which comes from a MF distortion δfU; U=v=(1/ne)dv(vδfU). In the parallel direction to B, a shifted Maxwellian distribution is further deformed by the competitive relaxation due to electron-ion (e/i) and electron-electron (e/e) collisions. We conveniently put an adjustment function in Eq. (2), GU=GU(ξ,Zeff) with ξv/vte, so that the friction force agrees with that given in [4] (see next Sec. 3 and Appendix). The 2nd order moment is the electron temperature, which is anisotropic in the parallel and perpendicular to B directions; Te=mev2, and Te=mev2/2. The effective isotropic temperature is given by Te=(Te+2Te)/3, and the anisotropy in the temperature, ΔT=2(TeTe)/3Te, is generated by an AT distortion δfΔT. Kinetic simulations for SOL-divertor plasmas by a particle modeling (PARASOL) showed a remarkable discrepancy between Te and Te (ΔT ~ −0.5) for low collisionality [5, 6]. The 4th order moments can be expressed with the square of the 2nd order moment including ΔT effect as,

  
m e v 4 / 2 = ( 3 / 2 + 3 Δ T ) T e 2 / m e ( 3 / 2 ) T e 2 / m e , (4)
  
m e v 2 v 2 / 2 = ( 1 + Δ T / 2 ) T e 2 / m e T e T e / m e , (5)

which are necessary for the transport equation of the heat flux qe [7].

The conductive heat flux qe is generated by the asymmetry in the velocity spread, i.e., skewness. One of major sources of the velocity-spread asymmetry (VSA) is the temperature gradient, Te. At first, we assume a skewed Maxwellian distribution for an isotropic VSA, fSkMexp{mev2/2(1+εzv/vt)Te}. The isotropic VSA is in proportion to zv (ε is a small parameter). The “heat-flux (HF) distortion”, δfq, is derived by expanding fSkM; δfqz(v3/5vte3v/vte)fM. It is noted that the HF distortion is set not to generate the mean flow; v=(1/ne)dv(vδfq)=0. A function, (v3/5vte3v/vte), makes v=0 by dv integration. The total heat flux can be divided into parallel component and perpendicular component, qe=qe+qe; qe=dv(mevv2/2)δfq and qe=dv(mev3/2)δfq. For the case of isotropic VSA, their percentages are fixed as qe/qe = 3/5 and qe/qe = 2/5.

Next, we consider the anisotropic VSA; fSkBexp{mev2/2(1+εzv/vte)Te}×exp{mev2/2(1+εzv/vte)Te}. The above percentages are varied by the anisotropic VSA as qe/qe=3/5+rq and qe/qe=2/5rq, where rq=(2qe3qe)/5qe is the “HF anisotropy” in the range of −3/5 < rq < 2/5. An HF distortion function consists of two parts, δfq=δfq1+δfq2, total flux part δfq1 and anisotropic flux part δfq2;

  
δ f q 1 = ( q e / q e FS ) z ( v 3 / 5 v te 3 v / v te ) G q 1 f M , (6)
  
δ f q 2 = r q ( q e / q e FS ) ( 5 z 3 3 z ) ( v 3 / 6 v te 3 ) G q 2 f M . (7)

The magnitude of qe is based on the free-streaming-energy flux, qeFS=vteneTe. A skewed Maxwellian distribution is further deformed by collisions. Similarly to the MF dissipation for reasonable convenience, we put functions in Eqs. (6) and (7), Gq1,2=Gq1,2(ξ,Zeff), so that the heat conductivity and the thermal force agree with those given in [4]. As noted above, the HF distortion does not create the mean flow. A function, (5z33z), for δfq2 promises v = 0 by dz integration.

On the other hand, the current-carrying heat flux qJ comes from δfU, and its components are approximately given by qJ=3UneTe/2 and qJ=UneTe, respectively. The percentages are qJ/qJ = 3/5 and qJ/qJ = 2/5, which coincide with those of conductive heat flux for the isotropic condition, qe/qe = 3/5 and qe/qe = 2/5.

2.2  Simplified Fokker-Planck equation

The above distortions are dissipated by Coulomb collisions. Non-thermal-equilibrium quantities, U, ΔT, qe and rq, are relaxed in the fluid moment equations. In order to evaluate quantitatively the relaxation processes, we apply a Fokker-Planck equation for electron distribution function fe in a one-dimensional system along B.

  
t f e + v s f e ( e E / m e ) v f e = C ( f e ) + S , (8)

where t is the time and s is a coordinate parallel to B. Partial differential operators are t/t, s/s and v=/v, respectively. Variables are the elementary charge e, the electric field E parallel to B and the source/sink term S for particle, momentum, energy and heat flux.

The simplified collision term consists of two terms, C(fe)=Ce/i(fe)+Ce/e(fe),

  
C e / i ( f e ) = ( Z eff / 2 τ e 1 ) z [ ( 1 z 2 ) z δ f e ] , (9)
  
C e / e ( f e ) = ( 1 / c z τ e 1 ) z [ ( 1 z 2 ) z δ f e ] , (10)

where Eq. (9) corresponds to the pitch-angle scattering (PAS) with ions, and Eq. (10) corresponds to the PAS within electrons. The energy diffusion term is ignored. A basic collision time depending on v3, τe1=4πε02me2v3/e4neΛ (ε0: permittivity of free space) [8], is adopted for e/i collision, while an averaged collision time, τe1(2vt2/v2)3/2τe1=(4/3π1/2)Zeffτe0 defined at mev2/2=Te, is used for e/e collision, for simplicity.

The AT distortion δfΔT is dissipated by the PAS. The self-relaxation time for the anisotropic temperature is defined as dTe/dt=2(TeTe)/τrele/e with τrele/e=15(2π)1/2τe1/8=5Zeffτe0/21/2 [8]. The RHS of the above equation is given by the 2nd moment of the e/e collision term; dv(mev2z2)Ce/e(δfΔT)=6neΔTTe/czτe1=4ne(TeTe)/czτe1. The coefficient is then determined as cz=15(2π)1/2/4.

3.  Relaxation Terms for Fluid Moment Equations

3.1  Momentum balance equation

The electron fluid momentum equation is simplified to a generalized Ohm’s law by neglecting the inertia and source terms;

  
en e E = s ( n e T e ) + F fr + F th , (11)

where s(neTe) is the pressure-gradient force. The friction force Ffr parallel to B comes from the e/i collision term as

  
F fr d v ( m e v ) C e / i ( δ f U ) = α 0 n e m e U / τ e 0 . (12)

The “friction-force coefficient” is given by α0. Its value is α0 = 0.51 for Zeff = 1, and is decreased gradually with Zeff. The nonlinear dependence on Zeff comes from the fact that the relaxation process is affected by both the e/e collision, Ce/eZeff0/v0, and the e/i collision, Ce/iZeff/v3 (see Sec. 2.2). The value of α0 was shown in TABLE 2 of [4] by “Braginskii”. Hereafter we denote this listed value as α0BR. For the availability on the continuous Zeff dependence of α0, we devise a simple and convenient expression,

  
α 0 fit = ( 0.77 + 0.35 Z eff ) / ( 1 + 1.2 Z eff ) . (13)

Table 1 compares α0fit and α0BR for several Zeff values (Zeff = 1, 2, 3, 4 and ∞). There are also listed “exact” values at Zeff = 1 and ∞, which were written nearby TABLE 2 of [4]. One sees satisfactory agreement between them. How to construct this fitting function is presented in Appendix.

Table 1. Zeff dependences of α0, β0, γ0, and Aq*=5(1β0)/2γ0.

Zeff 1 2 3 4
α0BR 0.5129 0.441 0.397 0.375 0.2949
exact 0.5063 3π/32
α0fit 0.509 0.432 0.396 0.374 0.292
β0BR 0.7110 0.905 1.016 1.090 1.521
exact 0.7033 3/2
β0fit 0.7083 0.894 1.009 1.087 1.500
γ0BR 3.162 4.890 6.064 6.920 12.47
exact 3.203 128/3π
γ0fit 3.200 4.900 6.114 7.025 13.40
Aq*BR 0.2285 0.0485 −0.007 −0.033 −0.104
exact 0.2316 −0.092
Aq*fit 0.233 0.067 0.011 −0.017 −0.100

The thermal force Fth is generated by the relaxation of HF distortion δfq due to e/i PAS depending on 1/v3. This force is linearly proportional to qe and inversely proportional to τe0,

  
F th d v ( m e v ) C e / i ( δ f q ) = A th q e / v te 2 τ e 0 , (14)

where we call Ath the “basic thermal-force coefficient”. It is noted that the HF anisotropy rq does not appear in Eq. (14) (see Appendix). This formula is explicitly different from the conventional one [4],

  
F th, T = β 0 n e T e , (15)

which is linearly proportional to Te and independent of τe0. Though Eqs. (14) and (15) seem fully different each other, they are equivalent when the conductive heat flux is given by the conventional formula so called “Spitzer-Hahm (SH)” heat flux,

  
q e = q e SH γ 0 n e v te 2 τ e 0 T e . (16)

Equation (14) is rewritten as Fth=Athγ0neTe, and an essential relation is found;

  
A th = β 0 / γ 0 . (17)

In a rare-collision plasma, however, qeSH can become much larger than qeFS unphysically, and some kinetic effects (or flux limiting effects) on qe have been added to the fluid simulation modeling, such as a harmonic average model, 1/qe=1/qeSH+1/αeqeFS (αe: electron heat-flux-limiting factor) [6, 7, 9]. Therefore, it is necessary to use Eq. (14) directly instead of the conventional formula, Eq. (15).

Values of β0 and γ0 were listed in TABLE 2 of [4]. Dependences of β0 and γ0 on Zeff are approximated by the expressions similar to Eq. (13) for α0,

  
β 0 fit = ( 0.36 + 0.66 Z eff ) / ( 1 + 0.44 Z eff ) , (18)
  
γ 0 fit = ( 0.65 + 3.35 Z eff ) / ( 1 + 0.25 Z eff ) . (19)

Figure 1, as well as Table 1, shows that approximate formulae of α0fit, β0fit and γ0fit fit very well those values given in [4]. The approximation of Ath is simply given by Athfit=β0fit/γ0fit.

Fig. 1.  Fitting curves of relaxation coefficients, α0fit, β0fit and γ0fit. Open diamonds are those listed in TABLE 2 of [4], and closed circles are those written as “exact” values in [4].

3.2  Transport equations for temperature

Basing on the above simplified Boltzmann transport equation, the 2nd order moment equation of an electron fluid for the effective isotropic temperature Te is obtained as

  
( 3 / 2 ) n e t T e + s q e = Q , (20)

where Q is the total heating/cooling power density. The current-carrying heat transport is neglected, for simplicity. When taking into account the anisotropic temperatures, two transport equations for Te and Te are treated separately;

  
( 1 / 2 ) n e t T e + s q e = Q A Δ T n e ( T e T e ) / τ e 0 , (21)
  
n e t T e + s q e = Q + A Δ T n e ( T e T e ) / τ e 0 , (22)

where Q heats up Te and Q heats up Te, separately. For the case of isotropic heating/cooling, Q is divided into the parallel component Q=Q/3 and the perpendicular component Q=2Q/3, respectively. The “AT relaxation coefficient” AΔT is given by

  
A Δ T = 2 / 5 + 2 1 / 2 / 5 Z eff , (23)

where the 2nd part is equal to τe0/τrele/e. These set of equations for Te and Te are rewritten to a transport equation of ΔTTe;

  
( 3 / 2 ) n e t ( Δ T T e ) + s ( 2 q e q e ) = ( 2 Q Q ) 9 A Δ T n e Δ T T e / 2 τ e 0 . (24)

Even for the isotropic heating/cooling case (2Q=Q), or no heating/cooling case (Q = Q = 0), the temperature anisotropy ΔTTe can be driven by the 2nd term of LHS; unbalance in the heat flux, 2qeqe=(4/5+3rq)qe. This unbalance exists naturally for the isotropic heat flux, rq = 0. Accordingly, we have to solve the transport of heat fluxes, qe and qe, simultaneously with Eq. (24).

3.3  Transport equations for heat flux

The 3rd order moment equation for the total conductive heat flux qe is obtained as

  
t q e + s ( n e M 4 ) + ( 5 / 2 + Δ T ) e E n e v te 2 = A q * q e / τ e 0 , (25)

where M4mev2v2/2 is a 4th order moment explained below in detail. We neglect the current-carrying heat transport and the source/sink term for qe, for simplicity.

The collision term dv(mevv2/2)C(δfq)=dv(mevv2/2)C(δfq1) is expressed by Aq*qe/τe0 in the RHS. It is interestingly noted that the “HF rate coefficient” Aq* in Eq. (25) is not always the damping one (Aq* > 0) but sometimes the growing one (Aq* < 0) due to the v3 dependence of the e/i collision time τe1. Considering qe > 0, δfq consists of “forward” higher-energy part with v+ > 0 and “backward” lower-energy part with v < 0. The larger scattering of low-energy electrons by ions reduces faster the backward heat flux, while smaller scattering of high-energy electrons reduces slower the forward heat flux. As a result, an increase in the net forward heat flux can arise. When Zeff ≫ 1, the PAS by e/i collision with τe/iv3 is dominant. We evaluate qe(n+v+T++nvT), and obtain qenevte(T+T) under a condition of v = 0. Then we can approximate the temporal change of qe for Zeff ≫ 1 as, (1/nevte)dqe/dtd/dt(T+T)(T+/τ+T/τ)(Te3/2/τe/i)(1/T+1/21/T1/2)(T+T)/τe/i+(1/nevte)(qe/τe/i). When Zeff approaches to unity and the PAS by e/e collision is effective, Aq* becomes positive. The above collisional growth of qe was not clearly mentioned in the previous works, e.g., [7]. It is noted again a well-known fact that the thermal force is generated due to v3 dependence of τe/i; Fth=d/dt(menev)=Athqe/vte2τe/i (see Eq. (14)).

The 4th order moment, neM4nemev2v2/2, in the LHS of Eq. (25) is given from Eqs. (4) and (5) as; neM4=(5/2+7ΔT/2)neTevte2=(5/2)neTevte2+ΔTneTevte2. Its gradient is expanded as; s(neM4)(5/2+ΔT)vte2s(neTe)+(5/2)(1+ΔT)nevte2sTe+(nevte2)s(ΔTTe). Considering the force balance of the generalized Ohm’s law, Eq. (11), the above s(neM4) is rewritten as follows; s(neM4)+(5/2+ΔT)eEnevte2(5/2+ΔT)Athqe/τe0+(5/2)(1+ΔT)nevte2sTe+(nevte2)s(ΔTTe).

Taking into account this thermal-force effect on s(neM4), Eq. (25) is reduced to

  
t q e + ( 5 / 2 ) ( 1 + Δ T ) n e v te 2 s T e + n e v te 2 s ( Δ T T e ) = A q q e / τ e 0 . (26)

A new relaxation coefficient, AqAq*+(5/2+ΔT)Ath, is called “HF relaxation coefficient”. This collision term is always the damping type (Aq > 0). When we force ΔT = 0, we obtain a steady-state relation similar to the SH heat flux; qe=(5/2Aq)nevte2τe0sTe. By comparing with Eq. (16), we immediately find Aq|ΔT=0=5/2γ0. The HF rate coefficient is then determined as Aq*=5/2γ05Ath/2=5(1β0)/2γ0. Although Aq* is approximated by Aq*5(1β0fit)/2γ0fit, we apply a much simpler expression, a linear function of 1/Zeff,

  
A q * fit = ( 1 0.3 Z eff ) / 3 Z eff . (27)

This Zeff dependence agrees fairly well with that of Aq*5(1β0)/2γ0 (see Table 1). The HF relaxation coefficient Aq is approximated by applying the fitting expressions, γ0fit and Athfit=β0fit/γ0fit,

  
A q fit = 5 / 2 γ 0 fit + Δ T A th fit . (28)

In order to calculate s(ΔTTe) in Eq. (26), the transport of anisotropic heat fluxes, qe and qe, have to be solved simultaneously. The transport equations for qe and qe are given separately as follows,

  
t q e + ( 3 / 2 ) ( 1 + Δ T ) n e v te 2 s T e + ( 3 / 2 ) n e v te 2 s ( Δ T T e ) = 3 A q q e / 5 τ e 0 A r ( 2 q e 3 q e ) / 5 τ e 0 , (29)
  
t q e + ( 1 + Δ T ) n e v te 2 s T e ( 1 / 2 ) n e v te 2 s ( Δ T T e ) = 2 A q q e / 5 τ e 0 + A r ( 2 q e 3 q e ) / 5 τ e 0 . (30)

The 1st collision terms in RHS of Eqs. (29) and (30) concern the HF distortion δfq1; dv(mev3/2)C(δfq1)=3Aq*qe/5τe0 with AqAq*+(5/2+ΔT)Ath. On the other hand, the 2nd collision terms concern the anisotropic part δfq2; dv(mev3/2)C(δfq2)=Arrqqe/τe0 with rq(2qe3qe)/5qe. It is interesting that the relaxation processes are fully coupled between qe and qe due to the PAS, (1/τ)z[(1z2)zδfq]. In the previous works, e.g. [7], this coupling was not taken into account. Because we cannot find suitable reference values for the curve fitting on the “HF anisotropy relaxation coefficient” Ar, we create an approximate formula similar to Eq. (27) for Aq*fit.

  
A r cre = ( 2 + 0.8 Z eff ) / Z eff . (31)

To create this linear function of 1/Zeff, we apply two values of Ar=(τe0/rqqe)dv(mev3/2)C(δfq2) with Gq2ξ3 for Zeff ≫ 1 and Gq2ξ2 for Zeff ≈ 2.7 (see Appendix).

Figure 2 shows fitting curves (dashed lines) of the relaxation coefficients, α0fit, Athfit and Aq*fit dependent on 1/Zeff. Open circles are obtained by setting Gξ3 for 1/Zeff = 0 and Gξ2 for 1/Zeff = 1/2.7, which agree well with own fitting curve. A red solid line for Arcre passes through two points at 1/Zeff = 0 and 1/2.7 (red closed circles). The slope 2 of Arcre is set just six times larger than 1/3 of Aq*fit, because Ce/e(δfq1)=(21/2/5Zeffτe0)δfq1 and Ce/e(δfq2)=6×(21/2/5Zeffτe0)δfq2.

Fig. 2.  Fitting curves of relaxation coefficients, α0fit, Athfit=β0fit/γ0fit and Aq*fit. Diamonds are those given in [4]. Circles are analytical ones. HF anisotropy relaxation coefficient Arcre is created so that the line passes through two points (red circles at 1/Zeff = 0 and 1/2.7).

It is noted that a sum of Eqs. (29) and (30) becomes the total heat flux transport equation of Eq. (26). Further, a subtraction, (2/5) × Eq. (29) − (3/5) × Eq. (30), becomes the transport equation for the anisotropic heat flux;

  
t ( r q q e ) + ( 9 / 10 ) ( n e v te 2 ) s ( Δ T T e ) = A r r q q e / τ e 0 . (32)

This equation for rqqe includes s(ΔTTe) term but does not include sTe term, while Eq. (26) for qe includes both sTe and s(ΔTTe) terms.

We complete the five transport equations of electron fluid moments, Eq. (11) of the force balance, Eq. (20) for Te, Eq. (24) for ΔTTe, Eq. (26) for qe and Eq. (32) for rqqe. Anisotropies in Te and qe are taken into account. Another set of five equations is equivalently available; Eqs. (11) and (21) for Te, Eq. (22) for Te, Eq. (29) for qe and Eq. (30) for qe. The electron continuity equation is not always necessary to be solved, but the ion continuity equation is solved under the condition of charge neutrality.

4.  Summary and Discussion

In this paper, we study the collisional relaxation processes of electron fluid moments in open magnetic field systems, such as SOL-divertor plasmas, by using a simplified Fokker-Planck equation. The thermal force is given not by the temperature gradient, Fth=β0neTe, but by the heat flux damping, Fth=Athqe/vte2τe0. We devise approximate formulae representing the Zeff dependence of relaxation coefficients, “friction-force coefficient” α0, “thermal-force coefficient” β0 and “thermal-conductivity coefficient” γ0;

  
α 0 fit = ( 0.77 + 0.35 Z eff ) / ( 1 + 1.2 Z eff ) ,
  
β 0 fit = ( 0.36 + 0.66 Z eff ) / ( 1 + 0.44 Z eff ) ,
  
γ 0 fit = ( 0.65 + 3.35 Z eff ) / ( 1 + 0.25 Z eff ) .

These expressions can be easily utilized in general divertor simulation codes using conventional plasma fluid equations.

Anisotropies in the temperature, ΔT2(TeTe)/3Te, and in the conductive heat flux, rq=(2qe3qe)/5qe, are taken into account. A relaxation between qe and qe is definitely described in the transport equation, t(2qe3qe)Ar(2qe3qe)/τe0. The “heat-flux anisotropy relaxation coefficient” Ar is derived and its approximation formula is created, Arcre=(2+0.8Zeff)/Zeff. We complete a set of five electron fluid moment equations; a force balance equation, and four transport equations of Te, ΔTTe, qe and rqqe. We will study, in the near future, the electron heat transport along B in open magnetic field systems by utilizing these electron fluid moment equations. The conductive heat flux is not simply be expressed as qe=qeSH nor 1/qe=1/qeSH+1/αeqeFS. The flux-limiting effect in a rare-collision plasma, which has been sometimes called kinetic effect, can be described to some extent by solving directly the transport equation of qe.

We have developed the anisotropic-ion-pressure (AIP) fluid model for the SOL-divertor plasma simulation [10, 11]. To simulate more accurately the plasma transport in a rare-collision plasma, we are going to extend the AIP model by adding the heat flux transport equations. The present methodology will be useful. For the ion transport in SOL plasmas, however, the Mach number and temperature anisotropy become remarkably large [5, 6, 10]. Resultantly the present functional forms of δf generate the unacceptably-wide negative f region. Alternative proper forms of δfi should be found out to complete the ion fluid moment equations.

 Acknowledgements

We acknowledge Dr. K. Ibano of Starlight Engine Ltd., Dr. Y. Homma of QST and Prof. M. Sakamoto of University of Tsukuba for their collaborations and encouragements on our research activities. This work is partly supported by the NIFS Collaboration Research Program (NIFS25KFFT001).

Appendix. Relaxation Coefficients

The collision term given by Eqs. (9) and (10) for an MF distortion, δfU=(zvU/vte2)GUfM, is written as C(δfU)=2(Zeff/2τe1+1/czτe1)δfU, because z[(1z2)z(z)]=2z. A stationary Fokker-Planck equation, (eE/me)vfM=C(δfU), is then reduced to a relation, eE/me=(2U/τe1){Zeff(2vte2/v2)3/2+1/cz}GU. We find that the adjustment function has a form of GU(ξ,Zeff)1/(23/2Zeff/ξ3+1/cz), where ξv/vte. The friction force is given by Ffr=dv(mev)Ce/i(δfU)=α0nemeU/τe0. In case of Zeff ≫ 1, GU becomes simply proportional to ξ3 and δfU[G(3)]={(2π)1/2U/32vte}zξ4fM. Brackets [G(3)] denote a quantity calculated by setting Gξ3, and later [G(2)] denote a quantity calculated by setting Gξ2. One obtains analytically Ffr[G(3)]=(3π/32)nemeU/τe0, i.e., α0[G(3)] = 3π/32. This was written nearby TABLE 2 of [4] as an exact value for Zeff = ∞.

The above GU is not enough accurate for Zeff ~ O(1), because the present e/e collision term is a simplified model without taking account of the relative-velocity effect and the energy-relaxation effect. Therefore, we apply an approximate expression of the “friction-force coefficient” α0 representing the Zeff dependence. Considering the form, GU1/{1+g(ξ)Zeff}, we introduce a variable, X(h,Zeff)=1/(1+hZeff), and carry out a linear fitting, α0fit=a+bX(h,Zeff), against 5 points of α0BR values in TABLE 2 of [4]. We obtain 3 coefficients, h = 1.2, a ≈ 0.29 and b ≈ 0.48, i.e., α0fit=(0.77+0.35Zeff)/(1+1.2Zeff). Approximate formulae for β0 and γ0 are also obtained by this linear fitting technique; β0fit=(0.36+0.66Zeff)/(1+0.44Zeff) and γ0fit=(0.65+3.35Zeff)/(1+0.25Zeff), respectively. To obtain values of a and b for γ0fit, an exact value of γ0 = 128/3π at Zeff = ∞ is regarded.

In accordance with the above analysis, we calculate the “basic thermal-force coefficient” Ath. The collision terms for δfq1 and δfq2 are written as C(δfq1)=2(Zeff/2τe1+1/czτe1)δfq1z and C(δfq2)=12(Zeff/2τe1+1/czτe1)δfq2(5z33z), respectively. Because an integration, dz(mev)C(δfq2), is always null, the HF anisotropy rq does not appear in Eq. (14) for Fth. In case of Zeff ≫ 1 and Gq1ξ3, the HF distortion is given by δfq1[G(3)]={(2π)1/2/32}(qe/qeFS)z(ξ6/8ξ4)fM. The thermal force is analytically obtained as Fth[G(3)]=dv(mev)C(δfq1)=(9π/256)qe/vte2τe0, i.e., Ath[G(3)] = 9π/256 ≈ 0.110. This is smaller a little than β0BR/γ0BR ≈ 0.122 based on TABLE 2 of [4], but just the same as one based on exact values, β0 = 3/2 and γ0 = 128/3π, wrote in [4]. The approximation of Ath is simply given by Athfit=β0fit/γ0fit.

The “HF-rate coefficient” Aq* can be approximated as Aq*5(1β0fit)/2γ0fit, but we apply a much simpler expression, a linear function of 1/Zeff, Aq*fit=(10.3Zeff)/3Zeff, by fair agreements. The analytical evaluation, Aq*qe/τe0=dv(mevv2/2)C(δfq1) for Zeff ≫ 1 and Gq1ξ3, gives Aq*[G(3)] = −(15π/512) ≈ −0.092, which agrees with one based on exact values wrote in [4].

Since there was no suitable reference value for the curve fitting on the “HF anisotropy relaxation coefficient” Ar, we create an approximate formula similar to Aq*fit. To create a linear function of 1/Zeff, two points of Ar=(τe0/rqqe)dv(mev3/2)C(δfq2) are necessary. One point is at 1/Zeff = 0, which is calculated by setting Gq2ξ3 and δfq2[G(3)]={7(2π)1/2/3072}rq(qe/qeFS)(5z33z)ξ6fM. The result is Ar[G(3)] = 63π/256 ≈ 0.77. Another point is calculated by setting artificially Gq2ξ2 and δfq2[G(2)]=(1/54)rq(qe/qeFS)(5z33z)ξ5fM. The result is Ar[G(2)]=32/35+6(21/2/5Zeff). In order to select a proper Zeff value corresponding to Gq2ξ2, we calculate former relaxation coefficients for Gξ2; α0[G(2)] = 2/5, Ath[G(2)] = 6/35, and Aq*[G(2)]=4/3521/2/5Zeff. The MF distortion is δfU[G(2)]=(U/5vte)zξ3fM. Each value coincides with each fitting expression at a certain Zeff value; Zeff ≈ 2.9 for α0, Zeff ≈ 2.7 for Ath, and Zeff ≈ 2.7 for Aq*. By putting Ar[G(2)] ≈ 1.54 at Zeff ≈ 2.7, we obtain the slope for 1/Zeff is about 2.7(1.54 − 0.77) ≈ 2, which is six times larger than that of Aq*fit. This magnification is quite reasonable, because e/e collision terms, Eq. (10), are related as Ce/e(δfq1)=(21/2/5Zeffτe0)δfq1 and Ce/e(δfq2)=6×(21/2/5Zeffτe0)δfq2. Finally, we chose a very simple form of Arcre with an intercept 0.8; Arcre=(2+0.8Zeff)/Zeff (see Fig. 2 in Sec. 3.3).

References
 
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