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Thermal analysis characterization of PAAm-co-MC hydrogels
Authors:Taís Vanessa Gabbay Alves  Eraldo José Madureira Tavares  Fauze Ahmad Aouada  Charles Alberto Brito Negrão  Marcos Enê Chaves Oliveira  Anivaldo Pereira Duarte Júnior  Carlos Emmerson Ferreira da Costa  José Otávio Carréra Silva Júnior  Roseane Maria Ribeiro Costa
Affiliation:1.Federal University of Pará,Belém,Brazil;2.Embrapa Eastern Amazon,Laboratory of Agrobusiness,Belém,Brazil;3.Chemistry Institute,S?o Paulo State University,Araraquara,Brazil;4.Faculty of Chemical Engineering,Federal University of Pará,Belém,Brazil;5.Federal University of Pará,Belém,Brazil
Abstract:This paper reports the thermal characterization of polyacrylamide-co-methylcellulose hydrogels and the constituent monomers (acrylamide and methylcellulose). Polymeric materials can be used to produce hydrogels, which can be natural, synthetic, or a mixture. The hydrogels described here were obtained by free radical polymerization, in the presence of N,N′-methylene-bis-acrylamide as a cross-linker agent. Four acrylamide concentrations were used for the synthesis of hydrogels: 3.6, 7.2, 14.7, and 21.7% (w/v). The materials so obtained were analyzed by TG, DTG, DSC, and FT-IR. The TG curves of acrylamide and methylcellulose showed three mass loss events. In DSC curves, the acrylamide exhibited one melting peak at 84.5 °C, and methylcellulose indicated one exothermic event. Nevertheless, acrylamide was considered more stable than methylcellulose. The TG curves of the hydrogels exhibited three mass loss events, and on the DSC curves, three endothermic events were observed. It was verified that the different acrylamide proportions influenced the thermic behavior of hydrogels, and that the authors considered the 7.2% hydrogel a promising drug carrier system. The absorption bands were well defined, confirming the presence of the functional groups in the samples.
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