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Ultraviolet absorption cross-section measurements of shock-heated O2 from 2,000a??8,400 K using a tunable laser

DOI:10.1016/j.jqsrt.2020.106959 期刊:Journal of Quantitative Spectroscopy and Radiative Transfer 出版年份:2020 更新时间:2025-09-23 15:19:57
摘要: Accurate spectroscopic modeling is critical when measuring time-resolved, state-specific chemical kinetics of diatomic molecules. Here, a spectroscopic model (Stanford model) was developed to accurately simulate oxygen absorption cross-sections in the Schumann-Runge system for non-equilibrium conditions. Cross-sections of shock-heated oxygen (O2) have been measured using a picosecond pulsed ultraviolet (UV) laser, and the viability of two spectroscopic models has been demonstrated. Measurements were taken behind reflected shocks in 2% and 5% O2 in argon (Ar) mixtures around 211.2 nm and 236.9 nm up to initial post-reflected shock temperatures of 10,700 K. Cross-sections were plotted against vibrational temperature and compared to calculated cross-sections from the Stanford model and the Adjusted Spectrum model. Vibrational temperatures for cross-section measurements were calculated for plateaus and peaks in experimental absorbances using a Bethe-Teller relaxation model up to 6,000 K and a steady-state approach above 6,000 K. Vibrational temperatures calculated using the steady-state approach were 3–5% higher than coupled vibration-dissociation (CVD) calculations. The experimental cross-sections agree to within 15% of the Stanford model for both wavelength regimes.
作者: Ajay Krish,Jesse W. Streicher,Ronald K. Hanson
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Investigating the spectroscopic modeling of oxygen absorption cross-sections in the Schumann-Runge system for non-equilibrium conditions using a tunable, pulsed UV laser.

The study demonstrated the efficacy of using a tunable, pulsed UV laser diagnostic with a spectroscopic model to measure oxygen absorption cross-sections in non-equilibrium conditions. The experimental cross-sections agreed within 15% of the Stanford model predictions, validating the model's accuracy. This approach can be extended to extract vibrational state-specific population time histories of oxygen in hypersonic environments.

The study is limited by the assumption of vibrational temperature reaching the post-shock translational temperature for conditions below 6,000 K and the steady-state approach for higher temperatures. The effects of dissociation on cross-section measurements were mitigated but not entirely eliminated.

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