Polymerization of styrene and methyl methacrylate (MMA) were studied by UV and fluorescence spectroscopic techniques. Using a sharp decrease in the extinction coefficient at 250 nm and the fluorescence quantum yield at 308 nm of styrene following polymerization, styrene conversion in solution polymerization by UV and fluorescence measurements were found to correlate well with IR results monitoring the disappearance of vinyl groups, at three different temperatures (65, 70, and 75 degrees C). The activation energy of about 6 kcal/mol was obtained. Using the decrease in UV absorbance of MMA during polymerization, solution polymerization of MMA was studied and compared with IR results. Due to the solvent absorbance, the UV method underestimates the conversion to a certain extent. When a small amount of styrene is added in MMA polymerization as a reactive extrinsic comonomer, the conversion of styrene measured by fluorescence is found to be faster than MMA, due to the characteristic reactivity ratios of MMA and styrene. The correlation curve could be used to estimate MMA conversion from styrene fluorescence, providing a method more sensitive than the viscosity-dependent fluorescence probe technique. Bulk polymerization of styrene was studied by bifurcated fiber-optic fluorescence. Due to self-quenching, little fluorescence of styrene is observed up to 75% conversion, but increases sharply from 75 to 85% conversion, followed by a drastic decrease during the last 15% conversion. In comparison to other methods of following vinyl polymerization such as refractive index, density, and gel permeation chromatography, these spectroscopic techniques provide real-time in situ capability as well as better sensitivity, especially in the later stages of polymerization.