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Temperature dependent vibrational lifetimes in supercritical fluids near the critical point

1998; American Institute of Physics; Volume: 109; Issue: 14 Linguagem: Inglês

10.1063/1.477222

1520-9032

D. J. Myers, Shirley Chen, Motoyuki Shigeiwa, Binny J. Cherayil, M. D. Fayer,

Ionic liquids properties and applications

Vibrational relaxation measurements on the CO asymmetric stretching mode (∼1980 cm−1) of tungsten hexacarbonyl (W(CO)6) as a function of temperature at constant density in several supercritical solvents in the vicinity of the critical point are presented. In supercritical ethane, at the critical density, there is a region above the critical temperature (Tc) in which the lifetime increases with increasing temperature. When the temperature is raised sufficiently (∼Tc+70 °C), the lifetime decreases with further increase in temperature. A recent hydrodynamic/thermodynamic theory of vibrational relaxation in supercritical fluids reproduces this behavior semiquantitatively. The temperature dependent data for fixed densities somewhat above and below the critical density is in better agreement with the theory. In fluoroform solvent at the critical density, the vibrational lifetime also initially increases with increasing temperature. However, in supercritical CO2 at the critical density, the temperature dependent vibrational lifetime decreases approximately linearly with temperature beginning almost immediately above Tc. The theory does not reproduce this behavior. A comparison between the absolute lifetimes in the three solvents and the temperature trends is made.