STUDY OF POLYMER GELATION BY FLUORESCENCE SPECTROSCOPY

A fluorescence technique is used to study the mechanism and dynamics of thermoreversible gel formation in concentrated polymer solutions. Two examples of these ordered structures were studied: isotactic polystyrene (iPS) in decalin and syndiotactic poly(methyl methacrylate) (sPMMA) in toluene. iPS can form two types of gels in decalin solutions. Turbid suspensions are formed between 60-degrees-C and 130-degrees-C. When the solution is quenched beneath 20-degrees-C, transparent gels are formed. In the former solution the polymer has a 3, helix structure; in the latter a 12(1) helix is formed. These structures formed by iPS in decalin solution have different fluorescence spectra. The ratio (I(m)/I(e)) of the intensity of the monomer fluorescence band in the spectrum over the intensity of the excimer emission band is higher in the spectra of transparent gels. The formation of the transparent gels from a solution can be followed by plotting I(m)/I(e) as a function of temperature. The kinetics of the gel formation are studied by following I(m)/I(e) as a function of time at a fixed temperature. sPMMA forms gels in toluene by a mechanism called "conformational gelation." This mechanism consists of two steps: a fast conformational change followed by a slower aggregation of polymer chains. Both steps were followed by measuring fluorescence of a pyrene label attached to the polymer. The fluorescence lifetime of this probe is sensitive to the polarity of the environment. When the polymer conformation goes from a random coil to an all trans conformation, the environment of the fluorescent label becomes increasingly richer in solvent. This change in polarity is reflected in a change in fluorescence lifetime. The change in fluorescence anisotropy of the label reflects the second step of the mechanism and correlates with the occurrence of chain aggregation.