Publication: Effects of aromatic carboxylic dianhydrides on thermomechanical properties of polybenzoxazine-dianhydride copolymers
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Issued Date
2012
Resource Type
File Type
application/pdf
ISSN
323888
Other identifier(s)
2-s2.0-84863721716
Rights Holder(s)
มหาวิทยาลัยศรีนครินทรวิโรฒ
Bibliographic Citation
Polymer Engineering and Science. Vol 52, No.8 (2012), p.1640-1648
Suggested Citation
Jubsilp C., Ramsiri B., Rimdusit S. Effects of aromatic carboxylic dianhydrides on thermomechanical properties of polybenzoxazine-dianhydride copolymers. Polymer Engineering and Science. Vol 52, No.8 (2012), p.1640-1648. doi:10.1002/pen.23107 Retrieved from: https://hdl.handle.net/20.500.14740/6995
Author(s)
Abstract
Enhanced thermomechanical properties of bisphenol-A based polybenzoxazine (PBA-a) copolymers obtained by reacting bisphenol-A-aniline-type benzoxazine (BA-a) resin with three different aromatic carboxylic dianhydrides, i.e., pyromellitic dianhydride (PMDA), 3,3',4,4' biphenyltetracarboxylic dianhydride (s-BPDA), or 3,3',4,4' benzophenonetetracarboxylic dianhydride (BTDA) were reported. Glass transition temperature (T g), of the copolymers was found to be in the order of PBA-a:PMDA>PBA-a:s-BPDA>PBA-a:-BTDA. The difference in the T g of the copolymers is related to the rigidity of the dianhydride components. Furthermore, the T g of PBA-a:BTDA, PBA-a:s-BPDA, and PBA-a:BTDA films was observed to be significantly higher than that of the neat PBA-a owing to the enhanced crosslink density by the dianhydride addition. This greater crosslink density results from additional ester linkage formation between the hydroxyl group of PBA-a and the anhydride group of dianhydrides formed by thermal curing. Moreover, the copolymers exhibit enhanced thermal stability with thermal degradation temperature (T d) ranging from 410°C to 426°C under nitrogen atmosphere. The char yield at 800°C of the copolymers was found to be remarkably greater than that of the neat PBA-a with a value up to 60% vs. that of about 38% of the PBA-a. Toughness of the copolymer films was greatly improved compared to that of the neat PBA-a. POLYM. ENG. SCI., 2012. © 2012 Society of Plastics Engineers Copyright © 2012 Society of Plastics Engineers.
Subject(s)
Benzophenonetetracarboxylic dianhydride
Benzoxazine
Bisphenol A
Char yield
Copolymer films
Cross-link densities
Dianhydrides
Ester linkages
Hydroxyl groups
Nitrogen atmospheres
Polybenzoxazine
Pyromellitic dianhydride
Thermal curing
Thermal degradation temperatures
Thermomechanical properties
Phenols
Copolymers
Benzoxazine
Bisphenol A
Char yield
Copolymer films
Cross-link densities
Dianhydrides
Ester linkages
Hydroxyl groups
Nitrogen atmospheres
Polybenzoxazine
Pyromellitic dianhydride
Thermal curing
Thermal degradation temperatures
Thermomechanical properties
Phenols
Copolymers