Coherent anti-Stokes Raman spectroscopy of shock-compressed liquid carbon monoxide-oxygen and nitrogen-oxygen mixtures

被引:7
作者
Schmidt, SC
Moore, DS
Shaw, MS
机构
[1] Los Alamos National Laboratory, Los Alamos
[2] Fresenius' Jnl. Analytical Chemistry, D-65220 Taunusstein
关键词
D O I
10.1063/1.474393
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A two-stage light gas gun and single-pulse multiplex coherent anti-Stokes Raman scattering (CARS) have been used to obtain carbon monoxide, nitrogen, and oxygen vibrational spectra for several high-pressure/high-temperature, dense fluid, carbon monoxide-oxygen, and nitrogen-oxygen mixtures. The experimental spectra were compared to synthetic spectra calculated with a semiclassical model for CARS intensities and using best fit vibrational frequencies, peak Raman susceptibilities, and Raman linewidths for each mixture component. Up to a maximum shock pressure of 6.75 GPa for carbon monoxide-oxygen mixtures, the CO and O-2 vibrational frequencies were found to increase monotonically with pressure and depended on the carbon monoxide-oxygen mixture ratio. For the nitrogen-oxygen mixtures, the N-2 vibrational frequency increased monotonically with pressure to a maximum experimental pressure of 12.9 GPa, however the O-2 vibrational frequency increased with pressure to about 11 GPa and then appeared to decrease slightly as the pressure increased to the experiment maximum of 12.9 GPa. Empirical fits of the measured Raman frequencies incorporating previously published neat nitrogen, carbon monoxide, and oxygen data and using a functional form dependent on pressure, temperature, and mixture ratio, accurately describe the N-2, CO, and O-2 vibrational frequency shifts for both the carbon monoxide-oxygen and the nitrogen-oxygen mixtures. The transition intensity and linewidth data suggest that thermal equilibrium of the vibrational levels is attained in less than 10 ns at these shock pressures. The vibrational temperatures obtained for the nitrogen-oxygen mixtures were used to improve the oxygen potential function used to calculate equation-of-state pressures and temperatures. The measured linewidths for CO, N-2, and O-2 were different for the different mixtures and did not appear to depended significantly on mixture ratios, The broadening of all spectral lines suggested that the vibrational dephasing time for each species decreased to a few ps at the highest pressure shock states. (C) 1997 American Institute of Physics.
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页码:325 / 336
页数:12
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