Estudo da adsorção de saxitoxina e geosmina em carbono ativado através de simulação molecular

Detalhes bibliográficos
Ano de defesa: 2018
Autor(a) principal: Paiva, Carlos Adller Saraiva
Orientador(a): Não Informado pela instituição
Banca de defesa: Não Informado pela instituição
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Não Informado pela instituição
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://www.repositorio.ufc.br/handle/riufc/57353
Resumo: Human activities have been causing negative impacts towards the available water for human consumption regarding both its quality and quantity, being important to mention eutrophication of water sources and the occurrence of cyanobacterial blooms. Such microorganisms, in addition to producing substances that cause the odor and taste of mold and earth to water (2-methylisoborneol and geosmin), also produce metabolites, associated with various intoxications in animals and man, called cyanotoxins (cyanobacterial toxins) and which include hepatoxins acting on the liver, neurotoxins acting on the nervous system and dermatoxinscausing skin irritation. Sinceconventional water treatment plants (coagulation, flocculation, sedimentation and filtration) are not able to remove cyanotoxins and other dissolved extracellular metabolites, the two main forms of removal are the use of activated carbons (GAC) and post-chlorination. Aiming to establish a theoretical approachregarding the selection of suitable activated carbon for cyanobacteria metabolite removal, in particular saxitoxin (STX), a number of molecular simulations targeting to study both STX and GSM adsorptionin activated carbon pores and graphitic surfaces were performed. Before, however, simulation parameters (force field type, force field parameters, molecular loads) were validated based on experimental studies with biphenyl (BPH), phenylcyclohexane (PCH) and bicyclohexyl (BCH)