Policondensação de monômeros oriundos de fontes renováveis

Detalhes bibliográficos
Ano de defesa: 2018
Autor(a) principal: Gomes, Frederico Wegenast.
Orientador(a): Não Informado pela instituição
Banca de defesa: Não Informado pela instituição
Tipo de documento: Tese
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal do Rio de Janeiro
Brasil
Instituto Alberto Luiz Coimbra de Pós-Graduação e Pesquisa de Engenharia
Programa de Pós-Graduação em Engenharia Química
UFRJ
Programa de Pós-Graduação: Não Informado pela instituição
Departamento: Não Informado pela instituição
País: Não Informado pela instituição
Palavras-chave em Português:
Link de acesso: http://hdl.handle.net/11422/12803
Resumo: The present study evaluated the use of poly(ethylene-2,5-furandicarboxylate) - PEF – copolymers modified with succinic acid and glycerol as possible substitutes for poly(ethylene terephthalate) - PET, with emphasis on the production and processing. The present study also sought to elucidate the polymerization behavior in relation to the mass transfer rates between the molten and gaseous phases, as well as to develop a mathematical model capable of describing the evolution of the reaction based on the masses of by-products and molar masses distributions over time. It was observed that although the synthesis of furanic copolymers by an environment friendly route is feasible, the lower thermal stability of the furanic polyesters under processing conditions (227 ± 12 °C) hinders the direct substitution of PET in several commercial applications. The developed models showed good reproducibility of the experimental data and allowed to observe that the polycondensation is highly affected by the mass transfer rates of the byproducts, especially during the esterification. Finally, the synthesis of polyesters derived from succinic acid and the manipulation of the structure of such polymers were also studied. Aided by functionalization techniques it was possible to insert specific groups in the polymer chain (6 to 100%) in different steps of the polymerization, allowing the synthesis of polymers that would not be easily obtained by conventional polymerization techniques.