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Bismuthonium‐ and pyrylium‐based radical induced cationic frontal polymerization of epoxides
Author(s) -
Taschner Roland,
Knaack Patrick,
Liska Robert
Publication year - 2021
Publication title -
journal of polymer science
Language(s) - English
Resource type - Journals
eISSN - 2642-4169
pISSN - 2642-4150
DOI - 10.1002/pol.20210196
Subject(s) - cationic polymerization , polymerization , polymer chemistry , chemistry , monomer , radical polymerization , epoxy , organic chemistry , polymer
Cationic polymerization is a powerful tool when it comes to adhesive, coating, composite, and bulk material production. A variety of monomers is suitable for this technique, however epoxy‐based systems are used in many applications, due to their high reactivity and versatility. With the introduction of the radical induced cationic frontal polymerization (RICFP), an even more efficient pathway to cure epoxides and with it a variety of new applications was obtained. The prevailing initiator class for RICFP applications is the iodonium salt. Decades of research and fine‐tuning of the formulations lead to a highly effective and versatile initiator system. With the introduction of bismuth‐ and oxygen‐based onium salts for frontal polymerization, the well‐known iodonium salt is challenged. Bismuthonium hexafluoroantimonates shows high rate of polymerization and conversions of 84% in an epoxy system. The advantage of bismuthonium‐based systems is the pot life of the formulations, which can be cured at the press of a button. In this study, iodonium salts last around 3 days before a significant viscosity increase is measured, while the bismuthonium initiator lasts over 10 times as long with no significant drop in reactivity or frontal velocity.