Thermonuclear Fusion Reactivities for Drifting Tri-Maxwellian Ion Velocity Distributions
Transcript of Thermonuclear Fusion Reactivities for Drifting Tri-Maxwellian Ion Velocity Distributions
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Journal of Fusion Energy ISSN 0164-0313 J Fusion EnergDOI 10.1007/s10894-013-9594-0
Thermonuclear Fusion Reactivities forDrifting Tri-Maxwellian Ion VelocityDistributions
D. Nath, R. Majumdar & M. S. Kalra
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ORIGINAL RESEARCH
Thermonuclear Fusion Reactivities for Drifting Tri-MaxwellianIon Velocity Distributions
D. Nath • R. Majumdar • M. S. Kalra
Received: 28 November 2012 / Accepted: 4 January 2013
� Springer Science+Business Media New York 2013
Abstract The presence of strong magnetic fields in
magnetically confined thermonuclear fusion plasmas
introduces a considerable anisotropy in the ion velocity
distributions. Drifting or streaming of ionic species is
another source of anisotropy in fusion plasmas. To account
for these anisotropies, we consider in the present work a
generalization of the equilibrium Maxwellian distribution
in the form of a drifting tri-Maxwellian distribution func-
tion. It is shown that the calculation of thermonuclear
reactivities for these distributions is best carried out in a
transformed velocity space. Computational results for gy-
rotropic velocity distributions with drifts parallel and per-
pendicular to the magnetic field are presented.
Keywords Plasma � Fusion reactivity � Bi/tri-Maxwellian
distributions � Anisotropy � Drifts
List of symbols
a, A Dimensionless constants
b, B Dimensionless constants
c, C Dimensionless constants
f Distribution function
k, l As in Eq. 12
m Mass
r Vdrift/vrms
R T\/TkT Temperature (in energy units)
u Dimensionless velocity
v V - V0
V Velocity in laboratory frame
V0 Drift velocity
a, b, c Dimensionless constants
r Microscopic fusion cross section
hr vi Fusion reactivity
Subscripts
A, B Species
k Parallel
D Deuterons
\ Perpendicular
T Tritons
i x, y, z
Introduction
Fusion reactivities generally reported in the literature are for
two interacting Maxwellian species at the same temperature
[1–4]. In magnetically confined thermonuclear fusion plas-
mas under reacting conditions, the ion velocity distributions
can, however, deviate considerably from Maxwellian dis-
tributions. Especially the presence of strong magnetic fields
introduces anisotropy because it leads to different particle
velocities parallel and perpendicular to the magnetic field,
characterized by different kinetic temperatures. Another
source of anisotropy is drifting or streaming of ionic species
caused, for example, by neutral-beam-injection (NBI)
plasma heating. The interaction of the energetic charged
particles produced in exothermic nuclear reactions with the
plasma can also lead to deviations from the Maxwellian [5].
These enhance the tail part of the Maxwellian spectrum. On
D. Nath (&) � M. S. Kalra
Nuclear Engineering and Technology Program, Indian Institute
of Technology Kanpur, Kanpur 208 016, India
e-mail: [email protected]
M. S. Kalra
e-mail: [email protected]
R. Majumdar
Department of Nuclear Engineering, North Carolina State
University, Raleigh, NC 27695-7909, USA
123
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DOI 10.1007/s10894-013-9594-0
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the other hand, faster reactions or losses at the high energy
end of the spectrum can result in a tail-depleted Maxwellian
distribution. Impact of these deviations from the isotropic
Maxwellian distributions on fusion reactivities can be con-
siderable and worth investigating in connection with prac-
tical fusion reactors. Such information may play a significant
role in hot thermonuclear plasma diagnostics, characteriza-
tion, power balances, and the physics and engineering gain
factors [4].
The effect on fusion reactivities of Maxwellian tail
depletion and enhancement under isotropic conditions has
been studied earlier both analytically and numerically
[6–9]. A kinetic analysis of non-Maxwellian knock-on ions
in a self-sustained D-T, fusion plasma with an admixture of
other light elements has been used to show a reactivity
enhancement [5]. Some results related to the effect of
anisotropy as well as unequal ion temperatures on reac-
tivity have also been reported [8, 10].
In the present work, we consider a generalization of the
equilibrium Maxwellian distribution in the form of a
streaming tri-Maxwellian distribution function in which
each velocity component of a reacting species is charac-
terized by a different kinetic temperature with an associ-
ated drift. The formulation is very general and can
accommodate arbitrary drifts in the reacting species toge-
ther with the anisotropy resulting from unequal ion tem-
peratures parallel and perpendicular to the magnetic field as
a special case. It is shown that the calculation of fusion
reactivities for these distributions is best carried out in a
transformed velocity space resulting in a reduction of
computational time by two to four orders of magnitude
depending on the accuracy desired. These computations
would be prohibitively time-consuming if carried out in the
laboratory frame of reference. This formulation is then
applied to investigate the effect of bi-Maxwellian gyro-
tropic velocity distributions on fusion reactivities with or
without parallel or perpendicular drift or streaming. The
results of computations are presented for D-T, D-D, and
D-3He fusion reactions in the form of reactivity surfaces as
well as their projections on appropriate planes.
Tri-Maxwellian Distribution with Drifts
A simple generalization of the equilibrium Maxwellian
distribution allows us to represent a streaming anisotropic
plasma characterized by different component temperatures
and drifts. The unit-normalized shifted or drifting Max-
wellian distribution for one component of the velocity of a
species is given as below [11–13]:
fAðVAiÞ ¼mA
2pTAi
� �1=2
� exp �mA VAi � V0
Ai
� �2
2TAi
( ); ð1Þ
where TAi is the kinetic temperature of the component i, VAi0
is the corresponding drift, and other symbols are given in
the Nomenclature. The full streaming tri-Maxwellian
distribution for species A is obtained by multiplying the
three one-dimensional Maxwellians given in Eq. 1:
fAiðVAÞ ¼Y
i¼x;y;z
mA
2pTAi
� �1=2
� exp �mA VAi � V0
Ai
� �2
2TAi
( );
ð2Þ
and similarly for the species B:
fBiðVBÞ ¼Y
i¼x;y;z
mB
2pTBi
� �1=2
� exp �mB VBi � V0
Bi
� �2
2TBi
( ):
ð3Þ
In the present work, A will stand for D (deuterons) and
B will stand for D, T, or 3He, depending upon the fusion
reaction under consideration. In the formulation presented
below, in general, TAi = TBi; TAi = TAj; i = j. Thus the
formulation can accommodate different component
temperatures and drifts for each of reacting species.
In terms of the unit-normalized tri-Maxwellians in
Eqs. 2 and 3, the fusion reactivities or the reaction rate
parameters, rvh i, can be written as the following six-
dimensional integral in velocity space:
rvh i ¼ZZ
d3VAd3VBjVA � VBj
� rAB jVA � VBjð ÞfA VAð ÞfB VBð Þ:ð4Þ
where rAB is the microscopic fusion cross section between
species A and B and depends only on the relative speed
jVA � VBj.
Nondimensionalization and Velocity Space
Transformation
The analytical expressions for rAB for D-T, D-D, and
D-3He reactions are well established [14]. However, evalua-
tion of rvh iwith any reasonable accuracy by direct calculation
of the six-dimensional integral in Eq. 4 is computationally
prohibitive. In this section, we present a velocity space trans-
formation which reduces the six-dimensional integral in Eq. 4
to a three-dimensional integral which can be numerically
evaluated easily. The nondimensionalized velocities uA and
uB are obtained as
uA ¼vA
vN; uB ¼
vB
vN;
where vA ¼ VA � V0A
� �and vB ¼ VB � V0
B
� �, i.e., in
component form, vAi ¼ VAi � V0Ai
� �; i = x, y, z. Rest of
the parameters are given below:
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v2N
� �¼ v2
A
� �þ v2
B
� �
v2A
� �¼ 3TA
mA; v2
B
� �¼ 3TB
mB
TA ¼TAx þ TAy þ TAz
3; TB ¼
TBx þ TBy þ TBz
3:
In terms of the dimensionless velocities uA and uB, the
distribution functions in Eqs. 2 and 3 can be written as
fAiðuAÞ ¼1
2p
� �3=21ffiffiffiffiffiffiffiabcp � exp � u2
Ax
2a�
u2Ay
2b�
u2Az
2c
!;
ð5Þ
fBiðuBÞ ¼1
2p
� �3=21ffiffiffiffiffiffiffiffiffiffi
ABCp � exp � u2
Bx
2A�
u2By
2B�
u2Bz
2C
!;
ð6Þ
where the dimensionless parameters a, b, c and A, B, C are
given below
a ¼ TAx
3 TAþmAmB
TB
; A ¼ TBx
3mBmA
TAþTB
b ¼ TAy
3 TAþmAmB
TB
; B ¼ TBy
3mBmA
TAþTB
c ¼ TAz
3 TAþmAmB
TB
; C ¼ TBz
3mBmA
TAþTB
9>>>>>>>=>>>>>>>;: ð7Þ
We now transform the velocity space uA; uBð Þ to u;Uð Þgiven for each component as
ui ¼ uAi � uBi Ui ¼ kiuAi þ liuBi: ð8Þ
Note that u is simply the dimensionless relative velocity of
the interacting species whereas U is a linear combination of
uA and uB yet to be specified.
The fusion reactivity, in terms of the transformed
velocities u and U, can be written as
rvh i ¼ vN
Zd3uur uð ÞfAB uð Þ; ð9Þ
where
fAB uð Þ ¼ fAB uxð ÞfAB uy
� �fAB uzð Þ; ð10Þ
and
fAB uxð Þ ¼1
2pffiffiffiffiffiffiaAp
Z1
�1
dUx
� exp � Ux � kxuxð Þ2
2A
( )
� exp � Ux þ lxuxð Þ2
2a
( ):
ð11Þ
Similar expressions hold for y and z components. We
now choose kx and lx such that the Jacobian determinant of
the transformation in Eq. 8 has a magnitude of 1 and the
cross-terms containing the product uxUx in the exponent in
Eq. 11 become zero. So both these requirements are
satisfied if and only if
kx ¼A
aþ A; lx ¼
a
aþ A: ð12Þ
The integral in Eq. 11 can then be shown to yield
fAB uxð Þ ¼ffiffiffiap
rexp �au2
x
� �; ð13Þ
where a ¼ 1= 2aþ 2Að Þ. For y and z components, a and A
in Eq. 12 are replaced by b and B, c and C, respectively,
giving the following expressions for y and z components of
the relative velocity.
fAB uy
� �¼
ffiffiffibp
rexp �bu2
y
; ð14Þ
fAB uzð Þ ¼ffiffifficp
rexp �cu2
z
� �; ð15Þ
where b ¼ 1= 2bþ 2Bð Þ; c ¼ 1= 2cþ 2Cð Þ. Thus we finally
have,
fAB uð Þ ¼ffiffiffiffiffiffiffiffiabc
p3=2
rexp �au2
x � bu2y � cu2
z
: ð16Þ
Using this equation (Eq. 16) for the relative velocity
distribution, the reactivity in Eq. 9 can be easily evaluated
by a three-dimensional integral instead of a six-
dimensional integral implied in Eq. 4. We may mention
here that for axisymmetric situations investigated in the
present work, a further reduction is possible by
transforming to cylindrical coordinates. However, we do
not attempt it here to avoid more algebra. Further
reduction for the special case of axisymmetric
distributions loses the generality of Eq. 16, and, since
the computation is already greatly simplified, not much
further is gained by specializing Eq. 16 to specific
cases. The evaluation of the three-dimensional integral
in Eq. 16 is computationally quite acceptable and
straightforward.
Computational Results and Discussion
The general formulation developed in the preceding section
is now applied to fusion reactivity calculations for bi-
Maxwellian gyrotropic distributions with and without drifts
as well as for Maxwellian species with a relative drift.
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Reactivity Surface for Gyrotropic Distributions
Without Drifts
The anisotropic bi-Maxwellian two-temperature gyrotropic
velocity distribution (also referred as two-dimensional
pseudo-Maxwellian or pancake distribution) is given by
Stacey [3, 12]
fA Vð Þ ¼ m
2pT?
� �m
2pTk
� �1=2
� exp �mv2?
2T?�
mv2k
2Tk
( );
ð17Þ
where T\ and Tk denote the kinetic temperatures (in joules)
perpendicular and parallel to the magnetic field. Here we
consider two interacting species with same T\ and Tkwithout drifts. For this case the tri-Maxwellian formulation
presented in nondimensionalization section can be used by
simply substituting
TAx ¼ TAy ¼ TBx ¼ TBy � T?;
TAz ¼ TBz ¼ Tk;
V0Ai ¼ V0
Bi ¼ 0:
and for the above case we may define an effective kinetic
temperature, Tk, and a ratio R as follows:
Tk ¼2T? þ Tk
3; R ¼ T?
Tk:
Due to fast reactivity computations made possible by the
formulation presented in this work, it is possible to calculate
the reactivity surface over a wide range of Tk and R without
much computational effort. These are presented in Fig. 1 for
D-T, D-T, and D-3He, reactions using the microscopic cross
sections given in [14]. The projections of these surfaces for
selected temperatures are shown in Fig. 2. It can be seen
from these figures that for D-T reaction the gyrotropic
velocity distribution can enhance the reactivity considerably
at 5 keV as compared to the Maxwellain distribution
(R ¼ 1). At 15 keV, it has almost no effect on reactivity
while at 30 keV the reactivity for gyrotropic distribution is
less than the corresponding Maxwellian reactivity. For the
D-D and D-3He, reactions also, a similar behavior is
observed, i.e., at lower temperatures, the reactivity is
enhanced by the two-temperature distribution while at
higher temperatures, it is reduced as compared to the
corresponding Maxwellian reactivity.
Effect of Drift on Maxwellian Reactivities
To see the effect of relative drift on the fusion reactivity of
two Maxwellian species, we simply take all temperatures
(a)
(b)
(c)
Fig. 1 Reactivity surfaces for the gyrotropic velocity distributions
a D-T, b D-D, and c D-3He reactions
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same in Eqs. 2 and 3 and all drifts zero except one. Here
we consider deuterons as having drift velocity and define a
ratio
r ¼ Vdrifts
Vrms;
where Vrms ¼ 3T=mDð Þ1=2is the root mean square speed of
the deuterons. The computed reactivities at various tem-
peratures for D� T reaction are shown in Fig. 3 It can be
seen that drift enhances the reactivity considerably, par-
ticularly at lower temperatures.
(a)
(b)
(c)
Fig. 2 Projections of the reactivity surfaces for selected temperatures
a D-T, b D-D, and c D-3He reactions
(a)
(b)
Fig. 3 Effect of drift on Maxwellian reactivities for D� T reaction areactivity surface, b projection on rvh i � r plane at temperatures
5 keV; 15 keV, and 30 keV
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(a)
(b)
(c)
Fig. 4 Effect of parallel drift on bi-Maxwellian reactivities at
tempertures a 10 keV, b 15 keV, and c 20 keV
(a)
(b)
(c)
Fig. 5 Effect of perpendicular drift on bi-Maxwellian reactivities
a 10 keV, b 15 keV, and c 20 keV
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Effect of Parallel and Perpendicular Drifts on Bi-
Maxwellian Reactivities
As mentioned above, for the bi-Maxwellian gyrotropic
distribution, we take temperature x and y direction as T\
and z direction as Tk. The root mean square speed would
now be defined as 3Tk=mDð Þ1=2. The results are shown in
Figs. 4 and 5 for parallel and perpendicular drifts respec-
tively. It can be observed from theses figures that the rel-
ative drift, parallel or perpendicular, between the
interacting species enhances the reactivity. At 15 keV,
when Vdrift is comparable to Vrms r ¼ 1ð Þ, the fusion reac-
tivity almost doubles as compared to no drift ðr ¼ 0Þ.Similar effect is seen at other temperatures shown in these
figures.
Conclusion
A formulation for the calculation of thermonuclear fusion
reactivities for drifting/streaming tri-Maxwellian ion
velocity distributions is presented based on a transformed
velocity space. The velocity transformations proposed in
the present work reduce the six-dimensional reactivity
integral in the laboratory frame of reference into a three-
dimensional integral in the transformed velocity space. The
later can be evaluated very fast, resulting in a reduction of
computation time by two to four orders of magnitude,
depending on the accuracy desired. This formulation is
applied in evaluating the fusion reactivities for bi-Max-
wellian gyrotropic distributions with and without parallel
or perpendicular drift between two interacting species. The
effect of drift between two interacting Maxwellian species
is also investigated using the same formulation. It is found
that the relative drift increases the fusion reactivity at all
temperatures of interest in thermonuclear fusion. The
anisotropy introduced by the bi-Maxwellian distribution
increases the reactivity at lower temperatures and decreases
the same at higher temperatures as compared to the Max-
wellian reactivities.
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