Chemistry Reference
In-Depth Information
describe the reaction between the neutral particle C and the molecule DE with
threshold energy ε CD
thres to produce the particle CD. By use of the cross section σ CD
thres
1
ε CDE
thres
ε
σ CDE
thres
σ CDE
eff
=
·
(3.157)
for ε
ε CDE
thres and σ CDE
=
0forε
<
ε CDE
thres , the calculation of the reaction rate coefficient
thres
k CD
thres results in
2
3 / 2
exp
1
π
2 ·
·
m red
ε T
k B T
2
ε T
m red ·
·
ε CDE
thres
ε T
k CDE
thres
σ CDE
eff
=
·
·
·
·
d ε T
π
·
k B T
ε CDE
thres
8
exp
exp
.
T
·
k B T
ε CDE
thres
k B T
ε CDE
thres
k B T
=
σ CDE
eff
·
m red ·
·
(3.158)
π
·
This corresponds to an expression like the Arrhenius function typically for many
chemical reactions with activation energy in thermochemistry.
3.5.4 R ATE C OEFFICIENT FOR E LECTRON I MPACT I ONIZATION
The production rate of single charged positive ions due to direct electron impact
ionization of neutral atoms A in ground state
A k A +
A + +
e
+
A
e
+
e
(3.159)
is calculated by use of the specific electron impact ionization cross section and
the electron velocity distribution function (nonthermal plasma conditions), and the
particle densities of electrons n e and neutrals n A .
dn e
dt
dn A A
dt
+ = σ A A
v r ·
n A
τ eA . (3.160)
+ =
·
n e ·
n A =
k A +
A
·
n e ·
n A =
ν e A ·
n A =
The corresponding electron ionization rate coefficient k A A results in:
σ A A
v r
k A +
A
=
·
=
f e (
v r ) ·
v r ·
σ A A
(
v r ) ·
d v r .
(3.161)
thres .
Generally, the electron velocity distribution function in (3.161) has to be calculated
by a kinetic equation (Boltzmann equation). The necessary collision cross section in
dependence on the relative velocity is mostly taken from experimental data approxi-
mated by analytical functions, or if available by quantum mechanical calculation or
semiclassical formulas, see Section 3.8.
 
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