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DC Field | Value | Language |
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dc.contributor.author | Jubsilp C. | |
dc.contributor.author | Takeichi T. | |
dc.contributor.author | Rimdusit S. | |
dc.date.accessioned | 2021-04-05T03:35:24Z | - |
dc.date.available | 2021-04-05T03:35:24Z | - |
dc.date.issued | 2011 | |
dc.identifier.issn | 1413910 | |
dc.identifier.other | 2-s2.0-79955577362 | |
dc.identifier.uri | https://ir.swu.ac.th/jspui/handle/123456789/14527 | - |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-79955577362&doi=10.1016%2fj.polymdegradstab.2011.03.021&partnerID=40&md5=54e00ccb9d38daaef43706927ae751c2 | |
dc.description.abstract | A novel bisphenol-A-aniline type polybenzoxazine (PBA-a) modified with dianhydride was successfully prepared by reacting bisphenol-A-aniline based benzoxazine (BA-a) resin with 3,3′,4,4′-benzophenonetetracarboxylic dianhydride (BTDA) in 1-methyl-2-pyrrolidone (NMP) solvent. The miscible monomer mixture was easily transformed into transparent PBA-a/BTDA copolymers by thermal cure. Fourier-transform infrared spectroscopy reveals the formation of ester linkage which is a covalent interaction between hydroxyl group of the PBA-a and the carbonyl group in the dianhydride. The PBA-a/BTDA copolymers show only one glass transition temperature (Tg) with the value as high as 263 °C at BA-a:BTDA = 1.5:1 mol ratio. The value is remarkably higher than that of the unmodified PBA-a, i.e. 160 °C. In addition, the resulting PBA-a/BTDA copolymers display relatively high degradation temperature up to 364 °C and substantial enhancement in char yield with a value of up to 61% by weight. Moreover, flexibility of the PBA-a/BTDA copolymer samples is also significantly enhanced compared to the unmodified PBA-a. The obtained copolymer demonstrates high potential for those applications that require high thermal and mechanical properties with fire resistant characteristics. © 2011 Elsevier Ltd. All rights reserved. | |
dc.subject | 1-methyl-2-pyrrolidone | |
dc.subject | Benzophenonetetracarboxylic dianhydride | |
dc.subject | Benzoxazine | |
dc.subject | Bisphenol A | |
dc.subject | Carbonyl groups | |
dc.subject | Char yield | |
dc.subject | Covalent interactions | |
dc.subject | Degradation temperatures | |
dc.subject | Ester linkages | |
dc.subject | Fire resistant | |
dc.subject | Glass transition temperature | |
dc.subject | High potential | |
dc.subject | High thermal | |
dc.subject | Hydroxyl groups | |
dc.subject | Monomer mixtures | |
dc.subject | Polybenzoxazine | |
dc.subject | Thermal property | |
dc.subject | Thermosetting polymers | |
dc.subject | Aniline | |
dc.subject | Copolymers | |
dc.subject | Esters | |
dc.subject | Glass transition | |
dc.subject | Infrared spectroscopy | |
dc.subject | Mechanical properties | |
dc.subject | Organic polymers | |
dc.subject | Phenols | |
dc.subject | Plastic products | |
dc.subject | Resins | |
dc.subject | Thermodynamic properties | |
dc.subject | Thermosets | |
dc.subject | Copolymerization | |
dc.title | Property enhancement of polybenzoxazine modified with dianhydride | |
dc.type | Article | |
dc.rights.holder | Scopus | |
dc.identifier.bibliograpycitation | Polymer Degradation and Stability. Vol 96, No.6 (2011), p.1047-1053 | |
dc.identifier.doi | 10.1016/j.polymdegradstab.2011.03.021 | |
Appears in Collections: | Scopus 1983-2021 |
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