N-Benzylmaleimide (NBMI) was synthesized and subsequently copolymerized with methyl methacrylate (MMA) through free-radical polymerization in tetrahydrofuran (THF), using azobisisobutyronitrile (AIBN) and benzoyl peroxide (BPO) as initiators. The synthesized NBMI homopolymer and NBMI-MMA copolymer (CBMI) were characterized by Fourier-transform infrared (FT-IR) spectroscopy, proton nuclear magnetic resonance (1H NMR) spectroscopy, solubility studies, intrinsic-viscosity measurements, gel permeation chromatography (GPC), and thermogravimetric analysis (TGA). The NBMI homopolymer and CBMI copolymer were obtained in yields of 39.5% and 44.0%, respectively, with intrinsic-viscosity values of 0.031 and 0.060 dL/g. FT-IR and 1H NMR analyses confirmed the consumption of the maleimide carbon–carbon double bond during polymerization, while the characteristic imide-ring structure remained intact. Solubility studies revealed that the CBMI copolymer exhibited favourable solubility in several organic solvents. GPC analysis showed that the copolymer possessed a molecular weight of 25,881 g mol−1. Furthermore, TGA demonstrated a predominantly single-stage degradation pattern and satisfactory thermal stability. The higher yield and intrinsic viscosity of CBMI compared with the NBMI homopolymer indicate the successful incorporation of MMA into the polymer system. Overall, the results demonstrate that NBMI-MMA copolymer exhibits favourable structural, physicochemical, and thermal characteristics, making it a promising material for potential advanced polymer applications.
| Published in | American Journal of Polymer Science and Technology (Volume 12, Issue 3) |
| DOI | 10.11648/j.ajpst.20261203.12 |
| Page(s) | 82-89 |
| Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
| Copyright |
Copyright © The Author(s), 2026. Published by Science Publishing Group |
N-Benzylmaleimide, Methyl Methacrylate, NBMI-MMA Copolymer, Free-radical Copolymerization, Thermogravimetric Analysis, Thermal Stability
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APA Style
Bansal, S., Mehta, P., Jain, D., Mehta, R., Sen, P. (2026). Comparative Study of Synthesis Characterization and Thermal Properties of Homomer and Copolymers of N-Benzylmaleimide. American Journal of Polymer Science and Technology, 12(3), 82-89. https://doi.org/10.11648/j.ajpst.20261203.12
ACS Style
Bansal, S.; Mehta, P.; Jain, D.; Mehta, R.; Sen, P. Comparative Study of Synthesis Characterization and Thermal Properties of Homomer and Copolymers of N-Benzylmaleimide. Am. J. Polym. Sci. Technol. 2026, 12(3), 82-89. doi: 10.11648/j.ajpst.20261203.12
AMA Style
Bansal S, Mehta P, Jain D, Mehta R, Sen P. Comparative Study of Synthesis Characterization and Thermal Properties of Homomer and Copolymers of N-Benzylmaleimide. Am J Polym Sci Technol. 2026;12(3):82-89. doi: 10.11648/j.ajpst.20261203.12
@article{10.11648/j.ajpst.20261203.12,
author = {Sameeksha Bansal and Preeti Mehta and Deepika Jain and Rajeev Mehta and Pankaj Sen},
title = {Comparative Study of Synthesis Characterization and Thermal Properties of Homomer and Copolymers of
N-Benzylmaleimide},
journal = {American Journal of Polymer Science and Technology},
volume = {12},
number = {3},
pages = {82-89},
doi = {10.11648/j.ajpst.20261203.12},
url = {https://doi.org/10.11648/j.ajpst.20261203.12},
eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ajpst.20261203.12},
abstract = {N-Benzylmaleimide (NBMI) was synthesized and subsequently copolymerized with methyl methacrylate (MMA) through free-radical polymerization in tetrahydrofuran (THF), using azobisisobutyronitrile (AIBN) and benzoyl peroxide (BPO) as initiators. The synthesized NBMI homopolymer and NBMI-MMA copolymer (CBMI) were characterized by Fourier-transform infrared (FT-IR) spectroscopy, proton nuclear magnetic resonance (1H NMR) spectroscopy, solubility studies, intrinsic-viscosity measurements, gel permeation chromatography (GPC), and thermogravimetric analysis (TGA). The NBMI homopolymer and CBMI copolymer were obtained in yields of 39.5% and 44.0%, respectively, with intrinsic-viscosity values of 0.031 and 0.060 dL/g. FT-IR and 1H NMR analyses confirmed the consumption of the maleimide carbon–carbon double bond during polymerization, while the characteristic imide-ring structure remained intact. Solubility studies revealed that the CBMI copolymer exhibited favourable solubility in several organic solvents. GPC analysis showed that the copolymer possessed a molecular weight of 25,881 g mol−1. Furthermore, TGA demonstrated a predominantly single-stage degradation pattern and satisfactory thermal stability. The higher yield and intrinsic viscosity of CBMI compared with the NBMI homopolymer indicate the successful incorporation of MMA into the polymer system. Overall, the results demonstrate that NBMI-MMA copolymer exhibits favourable structural, physicochemical, and thermal characteristics, making it a promising material for potential advanced polymer applications.},
year = {2026}
}
TY - JOUR T1 - Comparative Study of Synthesis Characterization and Thermal Properties of Homomer and Copolymers of N-Benzylmaleimide AU - Sameeksha Bansal AU - Preeti Mehta AU - Deepika Jain AU - Rajeev Mehta AU - Pankaj Sen Y1 - 2026/10/26 PY - 2026 N1 - https://doi.org/10.11648/j.ajpst.20261203.12 DO - 10.11648/j.ajpst.20261203.12 T2 - American Journal of Polymer Science and Technology JF - American Journal of Polymer Science and Technology JO - American Journal of Polymer Science and Technology SP - 82 EP - 89 PB - Science Publishing Group SN - 2575-5986 UR - https://doi.org/10.11648/j.ajpst.20261203.12 AB - N-Benzylmaleimide (NBMI) was synthesized and subsequently copolymerized with methyl methacrylate (MMA) through free-radical polymerization in tetrahydrofuran (THF), using azobisisobutyronitrile (AIBN) and benzoyl peroxide (BPO) as initiators. The synthesized NBMI homopolymer and NBMI-MMA copolymer (CBMI) were characterized by Fourier-transform infrared (FT-IR) spectroscopy, proton nuclear magnetic resonance (1H NMR) spectroscopy, solubility studies, intrinsic-viscosity measurements, gel permeation chromatography (GPC), and thermogravimetric analysis (TGA). The NBMI homopolymer and CBMI copolymer were obtained in yields of 39.5% and 44.0%, respectively, with intrinsic-viscosity values of 0.031 and 0.060 dL/g. FT-IR and 1H NMR analyses confirmed the consumption of the maleimide carbon–carbon double bond during polymerization, while the characteristic imide-ring structure remained intact. Solubility studies revealed that the CBMI copolymer exhibited favourable solubility in several organic solvents. GPC analysis showed that the copolymer possessed a molecular weight of 25,881 g mol−1. Furthermore, TGA demonstrated a predominantly single-stage degradation pattern and satisfactory thermal stability. The higher yield and intrinsic viscosity of CBMI compared with the NBMI homopolymer indicate the successful incorporation of MMA into the polymer system. Overall, the results demonstrate that NBMI-MMA copolymer exhibits favourable structural, physicochemical, and thermal characteristics, making it a promising material for potential advanced polymer applications. VL - 12 IS - 3 ER -