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Synthesis, characterization and thermal degradation of poly[(2-phenyl-1,3-dioxolane-4-yl)methyl methacrylate]

(2-Phenyl-1,3-dioxolane-4-yl)methyl methacrylate prepared from glycidyl methacrylate and benzaldehyde has been polymerized by benzoyl peroxide. Spectroscopic characterization of the monomer and the polymer has been done by means of Fourier transform infra-red (FTIR) and 1H and 13C nuclear magnetic r...

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Bibliographic Details
Published in:Polymer degradation and stability 1998-01, Vol.60 (1), p.185-193
Main Authors: Coşkun, Mehmet, Ilter, Zülfiye, Özdemir, Eyüp, Demirelli, Kadir, Ahmedzade, Misir
Format: Article
Language:English
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Summary:(2-Phenyl-1,3-dioxolane-4-yl)methyl methacrylate prepared from glycidyl methacrylate and benzaldehyde has been polymerized by benzoyl peroxide. Spectroscopic characterization of the monomer and the polymer has been done by means of Fourier transform infra-red (FTIR) and 1H and 13C nuclear magnetic resonance (NMR) spectroscopies. Also, the techniques of gel permeation chromatography and differential scanning calorimetry have been used in the polymer characterization. Thermal degradation of poly[2-phenyl-1,3-dioxolane-4-yl)methyl methacrylate] has been studied by thermogravimetric analysis and FTIR. Volatile products of the degradation have been investigated by FTIR, 1H and 13C-NMR and gas chromatography-mass spectrometry techniques. The degradation to 270 °C of this polymer gives only the monomer. Side-chain decompositions mainly occur in degradation above 270 °C, including decomposition of the 1,3-dioxolane ring. Total degradation to 500 °C produces many volatile product such as the monomer, benzaldehyde, acrolein, acetone, 2-phenyl-4-hydroxymethyl-1, 3-dioxolane, 4-methylene-2-phenyl-1,3-dioxolane, propene, carbon dioxide and others. A mechanism of degradation showing the formation of some of these products is discussed.
ISSN:0141-3910
1873-2321
DOI:10.1016/S0141-3910(97)00065-7