Azomethine-based Phenol Polymer: Synthesis, Characterization and Thermal Study
Abstract
Azomethine-based phenol polymer, poly-2-{[(6-aminopyridin-2-yl)imino]methyl}-phenol (PAPIMP), was synthesized through the combination of condensation reaction and oxidative polymerization. Polymer isolated from aqueous solution was characterized by UV-vis, FT-IR, NMR and TG, SEC analysis. According to the SEC chromatograms, the number-average molecular weight (Mn), weight-average molecular weight (Mw) and polydispersity index (PDI) values of PAPIMP were determined to be 33,550, 78,900 g mol−1 and 2.352, respectively. Also, optical band gaps (Eg) of APIMP and PAPIMP calculated from cyclic voltammetry (CV) measurements. Also, electrical conductivities of each component measured with four-point probe technique. TG analysis showed that PAPIMP was stable up to 300 °C. The thermal decomposition kinetics of PAPIMP was investigated by means of thermogravimetric analysis in dynamic nitrogen atmosphere at four different heating rates: 5, 10, 15 and 20 °C min−1. The apparent activation energies for thermal decomposition of PAPIMP were obtained by Tang, Flynn-Wall-Ozawa (FWO), Kissenger-Akahira-Sunose (KAS) and Coats-Redfern methods (CR) were 96.97, 105.33, 97.28 and 88.60 kJ mol−1, respectively; the mechanism function and pre-exponential factor were determined by master plots method. The most likely decomposition process was a Dn Deceleration type in terms of the Coats-Redfern and master plots results.
Recommended Citation
F. Dogan et al., "Azomethine-based Phenol Polymer: Synthesis, Characterization and Thermal Study," Synthetic Metals, Elsevier, Jan 2011.
The definitive version is available at https://doi.org/10.1016/j.synthmet.2010.11.001
Department(s)
Materials Science and Engineering
Keywords and Phrases
Oxidative Polymerization; Schiff Base Polymer; Kinetic Parameter
International Standard Serial Number (ISSN)
0379-6779
Document Type
Article - Journal
Document Version
Citation
File Type
text
Language(s)
English
Rights
© 2011 Elsevier, All rights reserved.
Publication Date
01 Jan 2011