The thermal polymerization of clean styrene has been studied through Rayleigh-Brillouin light scattering. The frequency shifts, Rayleigh to Brillouin intensity ratios, Rayleigh depolarization ratios, and depolarized intensities were measured as the polymerization proceeded to completion at 90°C. The depolarized intensities decreased and the frequency shifts increased smoothly from the monomer to the polymer values. The Vv intensities and Rayleigh to Brillouin intensity ratios increase dramatically during the first stages of polymerization then decrease systematically to their final values. There is a large increase in the Rayleigh to Brillouin intensity ratio from the monomer to the final polymer value. The vertical depolarization ratio pv and the horizontal depolarization ratio pV were found to be respectively 0.4 and 1 for the polymer. Our observations are explained in terms of light being scattered from concentration fluctuations in the early stages of polymerization and from spherically symmetric strain fields in the polymer. We believe that the background, which we observed to embrace a wide range of frequencies, was due to rotational Raman transitions.
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Coakley et al. (1976) studied this question.
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