TG/DSC/FTIR study of porous copolymeric beads based on the dimethacrylate derivative of m-xylene
Autor: | Barbara Gawdzik, Magdalena Rogulska, Małgorzata Maciejewska |
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Rok vydání: | 2019 |
Předmět: |
02 engineering and technology
021001 nanoscience & nanotechnology Condensed Matter Physics Divinylbenzene m-Xylene 01 natural sciences Toluene 010406 physical chemistry 0104 chemical sciences chemistry.chemical_compound Monomer chemistry Polymerization Physical and Theoretical Chemistry Fourier transform infrared spectroscopy 0210 nano-technology Derivative (chemistry) Nuclear chemistry Carbon monoxide |
Zdroj: | Journal of Thermal Analysis and Calorimetry. 141:1351-1360 |
ISSN: | 1588-2926 1388-6150 |
DOI: | 10.1007/s10973-019-09143-2 |
Popis: | The present study describes the thermal properties of a series of porous microspheres synthesised from the dimethacrylate derivative of m-xylene, i.e. (4,6-dimethyl-1,3-phenylene)dimethylene bis(2-methylprop-2-enoate) and divinylbenzene via an aqueous suspension polymerisation in the presence of toluene and decan-1-ol as porogenic diluents. Various molar ratios of monomers were applied in the syntheses (1:4, 1:1, 4:1). The TG/DSC/FTIR analyses were performed in inert (helium) and oxidative (synthetic air) atmospheres. They revealed that the properties of the copolymeric microspheres were dependent on both their chemical composition and the testing atmosphere. The microspheres were stable up to 229–296 °C (in helium) and 302–308 °C (in synthetic air), as determined on the basis of the temperature of 1% mass loss. However, the most thermally stable were those synthesised at the molar ratio of the dimethacrylate derivative of m-xylene to divinylbenzene equal to 1:4. In helium, the copolymeric beads decomposed in one, two or three stages, whereas in synthetic air in two ones. The basic decomposition volatiles were carbon monoxide, carbon dioxide and organic carbonyl products, including esters, carboxylic acids and aldehydes as well as unsaturated and aromatic compounds. |
Databáze: | OpenAIRE |
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