ONLINE TIME-RESOLVED FLUORESCENCE SPECTROSCOPY OF EMULSION POLYMERIZATIONS TO STUDY THE LOCAL DYNAMICS IN THE POLYMERIZING PARTICLES

Citation
S. Rudschuck et al., ONLINE TIME-RESOLVED FLUORESCENCE SPECTROSCOPY OF EMULSION POLYMERIZATIONS TO STUDY THE LOCAL DYNAMICS IN THE POLYMERIZING PARTICLES, Macromolecular chemistry and physics, 199(5), 1998, pp. 771-776
Citations number
17
Categorie Soggetti
Polymer Sciences
ISSN journal
10221352
Volume
199
Issue
5
Year of publication
1998
Pages
771 - 776
Database
ISI
SICI code
1022-1352(1998)199:5<771:OTFSOE>2.0.ZU;2-B
Abstract
An on-line time-resolved fluorescence technique is applied to study lo cal dynamics in polymer particles during an emulsifier-free heterogene ous polymerization. The polymerization of styrene in the aqueous phase , initiated with a polymeric initiator (hydrolyzed propene-maleic acid copolymer with tert-butyl perester groups) was chosen as an illustrat ive system. To analyze the heterogeneous reaction pyrenyl probes were attached to the backbone of the initiator. Within the end phase of the polymerization an increase of fluorescence lifetime and intensity was observed. Fluorescence quenching experiments of the photo excited pyr ene with dibenzoyl peroxide in toluene proved that the perester groups act as quencher. The calculated quenching constant points out that th e quenching reaction is diffusion controlled. The also investigated bu lk polymerization of styrene with dibenzoyl peroxide as initiator and pyrene as fluorophore showed that a change of the quenching probabilit y at the gel point is responsible for a fluorescence lifetime and inte nsity enhancement. The emulsion polymerization showed the gel effect, too, although the macro-initiator forms a shell around the polystyrene core. At the gel point the chain mobility is reduced so that the enco unter probability of pyrenyl and perester groups is limited. Despite t he turbidity of the reaction mixture, fluorescence techniques allow to study the dynamics in the polymerizing particles.