An extensive CO2 plasma model is presented that is relevant for the production of “solar fuels.” It is based on reaction rate coefficients from rigorously reviewed literature, and is augmented with reaction rate coefficients that are obtained from scaling laws. The input data set, which is suitable for usage with the plasma simulation software Plasimo (https://plasimo.phys.tue.nl/), is available via the Plasimo and publisher's websites. The correctness of this model implementation has been established by independent ZDPlasKin implementation (http://www.zdplaskin.laplace.univ-tlse.fr/), to verify that the results agree. Results of these “global models” are presented for a DBD plasma reactor.
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AbstractAn inductively coupled radio-frequency plasma in chlorine is investigated via a global (volume-averaged) model, both in continuous and square wave modulated power input modes. After the power is switched off (in a pulsed mode) an ion-ion plasma appears. In order to model this phenomenon, a novel quasi-neutrality implementation is proposed. Several distinct Cl wall recombination probability measurements exist in the literature, and their effect on the simulation data is compared. We also investigated the effect of the gas temperature that was imposed over the range 300-1500 K, not calculated self-consistently. Comparison with published experimental data from several sources for both continuous and pulsed modes shows good agreement with the simulation results.
The reaction kinetics in the excitation space of Ar and the conversion space of Armolecule mixtures are explored using a combination of high rep-rate YAG-Dye laser systems with a well defined and easily controllable Surfatron Induced Plasma set-up. Applying the method of Saturation Time Resolved Laser Induced Fluorescence (SaTiRe-LIF), we could trace excitation and conversion channels and determine rates of electron and heavy particle excitation kinetics. The time resolved density disturbances observed in the Ar excitation space, which are initiated by the laser, reveal the excitation channels and corresponding rates; responses of the molecular radiation in Ar-molecule mixtures corresponds to the presence of conversion processes induced by heavy particle excitation kinetics.
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