Free-radical crosslinking copolymerization of styrene and divinylbenzene: Real time monitoring of the gel effect using fluorescence probe

Oguz Okay, Demet Kaya, Onder Pekcan*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

74 Citations (Scopus)

Abstract

The steady-state fluorescence and dilatometric techniques were used to study the free-radical crosslinking copolymerization of styrene (S) and commercial divinylbenzene (DVB) in bulk. Pyrene (Py) was used as a fluorescence probe for the in situ polymerization experiments. The time required for a sudden increase in the fluorescence intensity of Py was recorded for various DVB content and temperature. The monomer conversions and the gel points were recorded by dilatometry. To interpret the experimental data, a kinetic model was developed for the S-DVB copolymerization system. It was shown that both the pendant vinyl groups and Py molecules are affected by the reaction medium in a similar way, their mobility decreases as the DVB concentration increases or the temperature decreases. The reaction time at which the Py intensity in the fluorescence spectra exhibits a sudden increase corresponds to the reaction time at which the rate of polymerization becomes maximum resulting from the gel effect. The results show that the fluorescence technique can be used to follow the onset of the gel effect in S-DVB copolymerization.

Original languageEnglish
Pages (from-to)6179-6187
Number of pages9
JournalPolymer
Volume40
Issue number22
DOIs
Publication statusPublished - Oct 1999

Keywords

  • Free-radical crosslinking copolymerization
  • Gel effect
  • Steady-state fluorescence technique

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