Abstract

Summary form only given. It is well known that CO laser can be used to produce low translational temperature, non-equilibrium plasmas in high (/spl sim/1 bar) pressure mixtures of CO and common buffer species, such as nitrogen, argon, and/or helium. In this paper, we will present a new Laser Induced Fluorescence (LIF) thermometry technique, based on strong single photon allowed absorption from vibrationally excited (/spl nu/>7) levels of the ground electronic state of carbon monoxide. Optical pumping is a two-step process which combines resonant absorption of continuous wave CO laser radiation with anharmonic Vibration-Vibration energy exchange, producing non-equilibrium plasmas in the steady state. These plasmas are characterized by exceedingly high (and non-Boltzmann) vibrational mode disequilibrium, and low (/spl sim/400 K) to moderate (/spl sim/1000 K) rotational/translational. temperature. Electron production occurs by means of vibrational pooling collisions in which the sum of the vibrational energies of the colliding partners exceeds the threshold for ionization (/spl sim/33 quanta). In this highly vibrationally excited environment, strong single photon optical resonances exist to both the A and D' excited electronic states. In this paper we present proof-of-concept LIF temperature measurements in CO/Ar optically pumped mixtures. Rotational temperature determined by X/spl rarr/D' LIF is found to agree well (+/- 50 K) with temperature determined by FT-IR emission spectroscopy. Preliminary data employing X/spl rarr/A (4th positive system) LIF will also be presented as will modeling results illustrating the potential of two-dimensional (PLIF) temperature imaging.

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