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@ARTICLE{Kotov:909542,
author = {Kotov, Vladislav},
title = {{V}ibrational relaxation and triggering of the
non-equilibrium vibrational decomposition of {CO} 2 in gas
discharges},
journal = {Plasma sources science and technology},
volume = {31},
number = {9},
issn = {0963-0252},
address = {Bristol},
publisher = {IOP Publ.},
reportid = {FZJ-2022-03231},
pages = {094002 -},
year = {2022},
abstract = {Non-equilibrium vibrational dissociation CO2 → CO + O at
translational–rotational temperatures T ⩽ 1200 K is
investigated with semi-empiric and computational models. The
governing parameter $Q/{n}_{0}^{2}$ has been introduced,
where Q is the specific volumetric power coupled into
vibrational states and n0 is the initial number density of
CO2. It has been shown that the non-equilibrium vibrational
process can only be triggered when $Q/{n}_{0}^{2}$ exceeds
some critical value determined by the speed of vibrational
relaxation. Simple semi-empiric calculations are backed by
the state-to-state simulations of the CO2 vibrational
kinetics in two-modes approximation performed for conditions
of microwave sustained gas discharges. The vibrational
kinetics model is benchmarked against the experimental
vibrational relaxation times as well as the shock tube data
on the rate of the process CO2 + M → CO + O + M for M = Ar
and literature data for M = CO2. At T = 300 K the estimated
${\left(Q/{n}_{0}^{2}\right)}_{\text{crit}}\eqsim 6\times
1{0}^{-40}$ W m3 or
${\left(Q/{p}^{2}\right)}_{\text{crit}}\eqsim $ 35 W (m−3
Pa−2) (p is the gas pressure).
${\left(Q/{p}^{2}\right)}_{\text{crit}}$ is found to always
increase with increased T.},
cin = {IEK-4},
ddc = {530},
cid = {I:(DE-Juel1)IEK-4-20101013},
pnm = {1232 - Power-based Fuels and Chemicals (POF4-123)},
pid = {G:(DE-HGF)POF4-1232},
typ = {PUB:(DE-HGF)16},
doi = {10.1088/1361-6595/ac882f},
url = {https://juser.fz-juelich.de/record/909542},
}