Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/14011
Title: Enhanced film forming ability of benzoxazine-urethane hybrid polymer network by sequential cure method
Authors: Rimdusit S.
Sudjidjune M.
Jubsilp C.
Tiptipakorn S.
Keywords: Benzene
Copolymers
Crosslinking
Esters
Glass
Glass transition
Moisture
Polymer blends
Resins
Thermosets
Benzoxazine resin
Dynamic mechanical analysis (DMA)
Film-forming abilities
Fourier transform infrared
Hybrid polymer network
Isocyanate group
Network formation
Phenolic hydroxyl group
Curing
Issue Date: 2014
Abstract: Uniform copolymer films of benzoxazine resin (BA-a) and urethane prepolymer (PU) were prepared at various BA-a/PU mass ratios (100/0, 80/20, 60/40, 40/60, 20/80, and 0/100) via sequential cure method comprising of moisture cure and thermal cure steps. In the moisture cure step, Fourier Transform Infrared (FT-IR) spectra revealed the network formation between NCO-terminated group and moisture to firstly produce PU solid film. Then in the thermal cure step, the change of tri-substituted benzene ring to tetra-substituted benzene ring was observed suggesting polybenzoxazine network formation in this step. Moreover, the spectra reveal that isocyanate groups in polyurethane structure could react with phenolic hydroxyl groups of BA-a to form biuret and allophanate groups. Dynamic mechanical analysis (DMA) confirms a synergistic behavior in glass transition temperature (Tg) of the alloys with the highest T g value of 275°C which is uniquely observed in these alloys obtained from traditionally thermal cure method. The proposed sequential cure method above is found to be highly useful for uniform coating or film casting process which lacks in traditional, low A-stage viscosity, benzoxazine resin. Copyright © 2014 Wiley Periodicals, Inc.
URI: https://ir.swu.ac.th/jspui/handle/123456789/14011
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84897978339&doi=10.1002%2fapp.40502&partnerID=40&md5=7a497b9d97301252d61d322fdb849a1f
ISSN: 218995
Appears in Collections:Scopus 1983-2021

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