The use of lanthanide triflates in the preparation of poly(thiourethane) covalent adaptable networks

Covalent adaptable networks (CANs) are new polymeric materials with the mechanical properties of thermosets and the possibility of being recycled like thermoplastics. Poly(thiourethane) networks have demonstrated vitrimeric-like behavior at high temperatures due to the trans-thiocarbamoylation proce...

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Detalles Bibliográficos
Autores: Guerrero Ruiz, Federico, Gamardella, Francesco, Ramis Juan, Xavier|||0000-0003-2550-7185, De la Flor López, Silvia, Serra Albet, Maria Àngels|||0000-0003-1387-0358
Tipo de recurso: artículo
Fecha de publicación:2023
País:España
Institución:Universitat Politècnica de Catalunya (UPC)
Repositorio:UPCommons. Portal del coneixement obert de la UPC
Idioma:inglés
OAI Identifier:oai:upcommons.upc.edu:2117/394777
Acceso en línea:https://hdl.handle.net/2117/394777
https://dx.doi.org/10.1016/j.polymer.2023.126262
Access Level:acceso abierto
Palabra clave:Polymers
Polymeric composites
Chemistry, Inorganic
Poly(thiourethanes)
Lanthanide triflates
Covalent adaptable networks
Recyclability
Reshapability
Polímers
Compostos polimèrics
Química inorgànica
Àrees temàtiques de la UPC::Enginyeria dels materials::Materials plàstics i polímers
Descripción
Sumario:Covalent adaptable networks (CANs) are new polymeric materials with the mechanical properties of thermosets and the possibility of being recycled like thermoplastics. Poly(thiourethane) networks have demonstrated vitrimeric-like behavior at high temperatures due to the trans-thiocarbamoylation process, which Lewis acids and bases can accelerate. In this study, we report the use of lanthanide triflates (La, Sm, Dy, Er, and Yb) as Lewis acid catalysts, a greener alternative to other metallic catalysts as dibutyltin dilaurate (DBTDL) widely used in poly (urethane) and poly(thiourethane) networks. Moreover, they are not as reactive as DBTDL, and the curing mixture can be manipulated for a longer time at room temperature. As monomers, trimethylolpropane tris(3- mercapto propionate) (S3), hexamethylene diisocyanate (HDI), and isophorone diisocyanate (IPDI) have been used. We have demonstrated that the materials prepared with lanthanum triflate present the lowest relaxation times than those prepared with other lanthanide triflates or DBTDL. Calorimetry (DSC) and infrared spectroscopy (FTIR) were applied to study the curing process. The materials obtained were fully characterized by thermog- ravimetric analysis (TGA) and thermomechanical tests (DMA).