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Effects of the Addition of Amino-Terminated Highly Branched Polyurea on Curing Properties of Phenol-Formaldehyde Resin

In this work, a highly branched polyurea (HBP-NH(2)) similar to urea structure was introduced to phenol-formaldehyde (PF) resin to accelerate itscuring speed The results of gel time and bonding strength were combined to obtain a good modified additional stage and amount of HBP-NH(2). The relative mo...

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Detalles Bibliográficos
Autores principales: Lian, Shiguan, Lin, Huali, Zhang, Wenbin, Lei, Hong, Cao, Ming, Mao, Jianrong, Li, Taohong, Chen, Shi, Yang, Long
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10224463/
https://www.ncbi.nlm.nih.gov/pubmed/37241247
http://dx.doi.org/10.3390/ma16103620
Descripción
Sumario:In this work, a highly branched polyurea (HBP-NH(2)) similar to urea structure was introduced to phenol-formaldehyde (PF) resin to accelerate itscuring speed The results of gel time and bonding strength were combined to obtain a good modified additional stage and amount of HBP-NH(2). The relative molar mass changes of HBP-NH(2)-modified PF resin were investigated by gel permeation chromatography (GPC). The effects of HBP-NH(2) on the curing of PF resin were investigated by differential scanning calorimetry (DSC) and dynamic mechanical analysis (DMA). The effect of HBP-NH(2) on the structure of PF resin was also investigated by nuclear magnetic resonance carbon spectroscopy ((13)C-NMR). The test results show that the gel time of the modified PF resin was reduced by 32% and 51% at 110 °C and 130 °C, respectively. Meanwhile, the addition of HBP-NH(2) increased the relative molar mass of PF resin. The bonding strength test showed that the bonding strength of modified PF resin increased by 22% after soaking in boiling water (93 °C ± 2) for 3 h. The DSC and DMA analysis indicated that the curing peak temperature decreased from 137 °C to 102 °C, and the curing rate of the modified PF resin was also faster than that of the pure PF resin. The (13)C-NMR results showed that HBP-NH(2) in the PF resin reacted to produce a co-condensation structure. Finally, the possible reaction mechanism of HBP-NH(2) for the modification of PF resin was given.