No abstract

A kinetic model describing the time evolution of ∼70 individual CO 2 (X 1 Σ + ) vibrational levels during the afterglow of a pulsed DC glow discharge is developed in order to contribute to the understanding of vibrational energy transfer in CO 2 plasmas. The results of the simulations are compared against in situ Fourier transform infrared spectroscopy data obtained in a pulsed DC glow discharge and its afterglow at pressures of a few Torr and discharge currents of around 50 mA. The very good agreement between the model predictions and the experimental results validates the kinetic scheme considered here and the corresponding vibration-vibration and vibration-translation rate coefficients. In this sense, it establishes a reaction mechanism for the vibrational kinetics of these CO 2 energy levels and offers a firm basis to understand the vibrational relaxation in CO 2 plasmas. It is shown that first-order perturbation theories, namely, the Schwartz-Slawsky-Herzfeld and Sharma-Brau methods, provide a good description of CO 2 vibrations under low excitation regimes.

This is the second of two papers presenting the study of vibrational energy exchanges in nonequilibrium CO 2 plasmas in low-excitation conditions. The companion paper addresses a theoretical and experimental investigation of the time relaxation of ∼70 individual vibrational levels of ground-state CO X 2 1 S + ( )molecules during the afterglow of a pulsed DC glow discharge, operating at pressures of a few Torr and discharge currents around 50mA, where the rate coefficients for vibration-translation (V-T) and vibration-vibration (V-V) energy transfers among these levels are validated (Silva et al 2018 Plasma Sources Sci. Technol. 27 015019). Herein, the investigation is focused on the active discharge, by extending the model with the inclusion of electron impact processes for vibrational excitation and de-excitation (e-V). The time-dependent calculated densities of the different vibrational levels are compared with experimental data obtained from time-resolved in situ Fourier transform infrared spectroscopy. It is shown that the vibrational temperature of the asymmetric stretching mode is always larger than the vibrational temperatures of the bending and symmetric stretching modes along the discharge pulse-the latter two remaining very nearly the same and close to the gas temperature. The general good agreement between the model predictions and the experimental results validates the e-V rate coefficients used and provides assurance that the proposed kinetic scheme provides a solid basis to understand the vibrational energy exchanges occurring in CO 2 plasmas.

The excitation and relaxation of the vibrations of CO 2 as well as the reduction of CO 2 to CO are studied in a pulsed glow discharge. Two diagnostics are employed: (1) time-resolved in situ Fourier transform infrared spectroscopy and (2) spatiotemporally resolved in situ rotational Raman spectroscopy. Experiments are conducted within a pressure range of 1.3-6.7mbar and a current range of 10-50mA. In the afterglow, the rate of exponential decay from the asymmetric stretch temperature (T 3 ) to the rotational temperature (T rot ) is found to be only dependent on T rot , in the conditions under study. The decay rate r -

A rotational Raman study under non-thermal conditions in a pulsed CO 2 glow discharge. Plasma Sources Science and Technology, 27(4), [045009].