Selvi, M and Devaraju, S and Vengatesan, M. R and Alagar, M Synthesis and characterization of heterocyclic core-based polybenzoxazine matrices. Journal of Applied Polymer Science, 136 (9). p. 47134. ISSN 1097-4628
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Abstract
ABSTRACT: In the present work, four types of heterocyclic core-based polybenzoxazine matrices (HC-PBZ) developed based on
pyridine, thiophene, and thiazole and their molecular structure, thermal, flame-retardant and luminescent properties were studied
and discussed. The heterocyclic core-based benzoxazine monomers (HC-BZ) were synthesized using two types of phenols (phenol,
and 4-hydroxyphenylacetonitrile), and two types of heterocyclic diamines [2,6-Bis-(4-aminophenyl)-4-thiophen-2-yl-pyridine (BATP)
and 4-(2-methylthiazol-5-yl)-2,6-bis-(4-aminophenyl)-pyridine (BAMTP)] with formaldehyde through Mannich reaction. The structure of the four HC-BZ monomers was confirmed by various spectral analysis such as Fourier-transform infrared spectroscopy (FTIR), and Nuclear magnetic resonance spectroscopy (1
HNMR and 13CNMR). All the four HC-BZ monomers have the maximum range of curing temperature (Tp) between 252 and 267 �C. Data resulted from the thermal studies indicate that the HC-PBZ exhibits better Tg, thermal stability and flame-retardant properties. Among the four HC-PBZ systems the thiazole based system possesses the higher value of Tg of 268 �C and thermal stability when compared to those of other matrices. It was also observed that the HC-BZ monomers and HC-PBZ polymers exhibit a photoluminescent (PL) emission range between 441–445 and 414–417 nm, respectively. Overall, it seems that the thiazole and thiophene based HC-PBZ can be considered as competitive materials for luminescent applications with high thermal and
flame-retardant properties. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019, 136, 47134
Item Type: | Article |
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Subjects: | AC Rearch Cluster |
Depositing User: | Unnamed user with email techsupport@mosys.org |
Date Deposited: | 02 Nov 2023 07:01 |
Last Modified: | 02 Nov 2023 11:48 |
URI: | https://ir.vignan.ac.in/id/eprint/254 |