The reaction kinetics in the dark of photopolymerized mono-and dimethacrylates in a polymeric binder has been studied. Electron spin resonance spectroscopy (ESR) provided useful information regarding the nature of the radicals involved in postpolymerization reactions. Computer simulations were perfo
Kinetic investigations on the photopolymerization of di- and tetrafunctional (meth)acrylic monomers in polymeric matrices. ESR and calorimetric studies. I. Reactions under irradiation
✍ Scribed by P. Bosch; J. Serrano; J. L. Mateo; P. Calle; C. Sieiro
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 194 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0887-624X
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✦ Synopsis
The photopolymerization of several di-and tetrafunctional (meth)acrylic monomers in the presence of a styrene-butadiene-styrene polymeric matrix (SBS) has been studied. Electron spin resonance spectroscopy (ESR) and differential scanning photocalorimetry (photo-DSC) were used as monitoring techniques to identify the photogenerated radicals and analyze photopolymerization profiles, radical environments, and radical secondary reactions. The study of the photopolymerization and/or photocrosslinking reactions of these monomers in the solid media was carried out by taking into consideration different factors, such as the influence of both monomer and photoinitiator structures on the hydrogen abstraction in the binder with formation of benzylic and allylic radicals, the polymerization of the monomers itself and the hydrogen abstraction reaction in the polymerized acrylic chains. Finally, irradiation of the system SBS/photoinitiator in the absence of monomer was also accomplished.
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