Excited oxygen kinetics at electronvolt temperatures via 5-MHz RF-diplexed laser absorption spectroscopy.

A multi-MHz laser absorption sensor at 777.2 nm (12,863c m -1) is developed for simultaneous sensing of (1) O(5 S 0) number density, (2) electron number density, and (3) translational temperature at conditions relevant to high-speed entry conditions and molecular dissociation. This sensor leverages a bias tee circuit with a distributed feedback diode laser and an optimization of the laser current modulation waveform to enable temporal resolution of sub-microsecond kinetics at electronvolt temperatures. In shock-heated O 2, the precision of the temperature measurement is tested at 5 MHz and is found to be within ±5% from 6000 to 12,000 K at pressures from 0.1 to 1 atm. The present sensor is also demonstrated in a CO:Ar mixture, in parallel with a diagnostic for CO rovibrational temperature, providing an additional validation across 7500-9700 K during molecular dissociation. A demonstration of the electron number density measurement near 11,000 K is performed and compared to a simplified model of ionization. Finally, as an illustration of the utility of this high-speed diagnostic, the measurement of the heavy particle excitation rate of O(5 S 0) is extended beyond the temperatures available in the literature and is found to be well represented by k(3 P→5 S 0)=2.7×10-14 T 0.5 exp⁡(-1.428×104/T)c m 3⋅s -1 from 5400 to 12,200 K.

High-speed mid-infrared laser absorption spectroscopy of CO 2 for shock-induced thermal non-equilibrium studies of planetary entry.

A high-speed laser absorption technique is employed to resolve spectral transitions of CO 2 in the mid-infrared at MHz rates to infer non-equilibrium populations/temperatures of translation, rotation and vibration in shock-heated CO 2 - Ar mixtures. An interband cascade laser (DFB-ICL) resolves 4 transitions within the CO 2 asymmetric stretch fundamental bands ( Δ v 3 = 1) near 4.19 µ m . The sensor probes a wide range of rotational energies as well as two vibrational states (00 0 0 and 01 1 0). The sensor is demonstrated on the UCLA high enthalpy shock tube, targeting temperatures between 1250 and 3100 K and sub-atmospheric pressures (up to 0.2 atm). The sensor is sensitive to multiple temperatures over a wide range of conditions relevant to Mars entry radiation. Vibrational relaxation times are resolved and compared to existing models of thermal non-equilibrium. Select conditions highlight the shortcomings of modeling CO 2 non-equilibrium with a single vibrational temperature.

Chemical kinetics in an atmospheric pressure helium plasma containing humidity.

Atmospheric pressure plasmas are sources of biologically active oxygen and nitrogen species, which makes them potentially suitable for the use as biomedical devices. Here, experiments and simulations are combined to investigate the formation of the key reactive oxygen species, atomic oxygen (O) and hydroxyl radicals (OH), in a radio-frequency driven atmospheric pressure plasma jet operated in humidified helium. Vacuum ultra-violet high-resolution Fourier-transform absorption spectroscopy and ultra-violet broad-band absorption spectroscopy are used to measure absolute densities of O and OH. These densities increase with increasing H2O content in the feed gas, and approach saturation values at higher admixtures on the order of 3 × 1014 cm-3 for OH and 3 × 1013 cm-3 for O. Experimental results are used to benchmark densities obtained from zero-dimensional plasma chemical kinetics simulations, which reveal the dominant formation pathways. At low humidity content, O is formed from OH+ by proton transfer to H2O, which also initiates the formation of large cluster ions. At higher humidity content, O is created by reactions between OH radicals, and lost by recombination with OH. OH is produced mainly from H2O+ by proton transfer to H2O and by electron impact dissociation of H2O. It is lost by reactions with other OH molecules to form either H2O + O or H2O2. Formation pathways change as a function of humidity content and position in the plasma channel. The understanding of the chemical kinetics of O and OH gained in this work will help in the development of plasma tailoring strategies to optimise their densities in applications.