Journal Article FZJ-2022-03231

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Vibrational relaxation and triggering of the non-equilibrium vibrational decomposition of CO 2 in gas discharges



2022
IOP Publ. Bristol

Plasma sources science and technology 31(9), 094002 - () [10.1088/1361-6595/ac882f]

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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.

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Contributing Institute(s):
  1. Plasmaphysik (IEK-4)
Research Program(s):
  1. 1232 - Power-based Fuels and Chemicals (POF4-123) (POF4-123)

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Open Access

 Datensatz erzeugt am 2022-09-05, letzte Änderung am 2024-07-11


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