Study of poly (ethylene oxide)/Carbopol blends through thermal analysis and infrared spectroscopy

LA Kanis, FC Viel, JS Crespo, JR Bertolino, ATN Pires… - Polymer, 2000 - Elsevier
LA Kanis, FC Viel, JS Crespo, JR Bertolino, ATN Pires, V Soldi
Polymer, 2000Elsevier
Properties such as miscibillity, interaction and the thermal degradation behavior of blends of
poly (ethylene oxide)(PEO) with Carbopol were studied by thermal analysis (DSC, TGA) and
infrared spectroscopy (FTIR). The miscibility of PEO/Carbopol blends in all composition
ranges was confirmed, and the interaction is favored by hydrogen bonding between the
carboxylic acid group of Carbopol and the PEO ether oxygen. TGA analysis showed that,
with temperature increase, anhydride formation occurred first, confirmed by the FTIR bands …
Properties such as miscibillity, interaction and the thermal degradation behavior of blends of poly(ethylene oxide) (PEO) with Carbopol were studied by thermal analysis (DSC, TGA) and infrared spectroscopy (FTIR). The miscibility of PEO/Carbopol blends in all composition ranges was confirmed, and the interaction is favored by hydrogen bonding between the carboxylic acid group of Carbopol and the PEO ether oxygen. TGA analysis showed that, with temperature increase, anhydride formation occurred first, confirmed by the FTIR bands in 1806, 1756 and 1047cm−1. Thermal degradation products such as carbon dioxide appear as a result of fragmentation of the anhydride ring structures and decarboxylation of the Carbopol acid groups. Bands related with unsaturated structures (1605cm−1) were observed at 310°C and 470°C, presumably as a result of scissions of the main carbon–carbon chain. The activation energy of PEO/Carbopol blends increased with the Carbopol content in the blend, indicating that the thermal degradation is delayed with the presence of Carbopol.
Elsevier
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