Hidrólise enzimática do óleo de macaúba (Acrocomia aculeata)

Detalhes bibliográficos
Ano de defesa: 2014
Autor(a) principal: Raspe, Djéssica Tatiane
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 Estadual de Maringá
Brasil
Departamento de Engenharia Química
Programa de Pós-Graduação em Bioenergia
UEM
Maringá, PR
Centro de Tecnologia
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://repositorio.uem.br:8080/jspui/handle/1/4355
Resumo: Modification of vegetable oils and fats for biodiesel production have been widely studied, where the incentive to search for alternative raw materials for the production of this biofuel has been the focus of interest. Aiming to use an oleaginous without food purposes, with availability and low cost matrix, oil Macaúba (Acrocomia aculeata) has been reported, with its large production potential. In this context, the aim of this study was to investigate the production of free fatty acids (FFA) through the enzymatic hydrolysis process, the initial reaction hidroesterificação. Front to yield free fatty acids (FFAs) were evaluated different commercial enzymatic catalysts (Lipozyme® RM IM, Lipozyme® TL IM and Novozyme® 435), addition of sodium phosphate buffer at different pHs (5.7-8.0), salts (CuCl2, CaCl2, KCl, NH4Cl, NaCl, MgCl2), surfactants (Triton X-100, Tween 80) and organic (n-hexane, n-heptane, isopropanol, tert-butanol) solvent, as well as process variables: agitation (400-2000 rpm), temperature (30-60 °C), weight ratio of substrates (1:20-1:1 oil:water) and percentage of catalyst (1-20% by mass of oil). The results show that the addition of a buffer solution (pH 8.0) and organic solvent n-hexane contributed significantly to the increase in free fatty acids in the hydrolysis yield being obtained approximately 82% at 55 °C oil weight ratio: Buffer 1:2, 100% n-hexane solvent relative to the weight of oil and 400 rpm for 6 hours reaction, 15% Lipozyme® RM IM. The reaction conditions of the process were explored in the presence of n-hexane organic solvent by means of experimental design, in order to maximize the yield FFAs in the process, as well as obtaining the kinetics of production of FFAs. Given the variables, it can be seen that no increase in yields of FFA by increasing the weight ratio of oil:solvent n-hexane, temperature, buffer and percentage of catalyst variables that influence the process significantly. In reaction kinetics, about 88% free fatty acids were produced in reaction medium consisting of 70% buffer, 100% of n-hexane solvent and 15% of catalyst, reaction for 8 hours. The reuse of the enzyme catalyst has been reported before 20 reaction cycles, where it was detected decrease of approximately 50% of revenue in the initial FFA process.
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spelling Hidrólise enzimática do óleo de macaúba (Acrocomia aculeata)Enzymatic hydrolysis from the Macaúba oil (Acrocomia aculeata).Tecnologia industrialÓleos e gordurasHidróliseCatálise enzimáticaÓleo de macaúba (Acrocomia aculeata).HydrolysisMacauba kernel oil (Acrocomia aculeata)Enzymatic catalysisBrazil.EngenhariasEngenharia BiomédicaModification of vegetable oils and fats for biodiesel production have been widely studied, where the incentive to search for alternative raw materials for the production of this biofuel has been the focus of interest. Aiming to use an oleaginous without food purposes, with availability and low cost matrix, oil Macaúba (Acrocomia aculeata) has been reported, with its large production potential. In this context, the aim of this study was to investigate the production of free fatty acids (FFA) through the enzymatic hydrolysis process, the initial reaction hidroesterificação. Front to yield free fatty acids (FFAs) were evaluated different commercial enzymatic catalysts (Lipozyme® RM IM, Lipozyme® TL IM and Novozyme® 435), addition of sodium phosphate buffer at different pHs (5.7-8.0), salts (CuCl2, CaCl2, KCl, NH4Cl, NaCl, MgCl2), surfactants (Triton X-100, Tween 80) and organic (n-hexane, n-heptane, isopropanol, tert-butanol) solvent, as well as process variables: agitation (400-2000 rpm), temperature (30-60 °C), weight ratio of substrates (1:20-1:1 oil:water) and percentage of catalyst (1-20% by mass of oil). The results show that the addition of a buffer solution (pH 8.0) and organic solvent n-hexane contributed significantly to the increase in free fatty acids in the hydrolysis yield being obtained approximately 82% at 55 °C oil weight ratio: Buffer 1:2, 100% n-hexane solvent relative to the weight of oil and 400 rpm for 6 hours reaction, 15% Lipozyme® RM IM. The reaction conditions of the process were explored in the presence of n-hexane organic solvent by means of experimental design, in order to maximize the yield FFAs in the process, as well as obtaining the kinetics of production of FFAs. Given the variables, it can be seen that no increase in yields of FFA by increasing the weight ratio of oil:solvent n-hexane, temperature, buffer and percentage of catalyst variables that influence the process significantly. In reaction kinetics, about 88% free fatty acids were produced in reaction medium consisting of 70% buffer, 100% of n-hexane solvent and 15% of catalyst, reaction for 8 hours. The reuse of the enzyme catalyst has been reported before 20 reaction cycles, where it was detected decrease of approximately 50% of revenue in the initial FFA process.A modificação de óleos vegetais e gorduras para a produção de biodiesel têm sido amplamente estudada, onde o incentivo à pesquisa de matérias-primas alternativas para a produção deste biocombustível tem sido foco de interesse. Visando a utilização de uma matriz oleaginosa sem fins alimentícios, com disponibilidade e baixo custo, tem sido reportado o óleo de Macaúba (Acrocomia aculeata), com seu grande potencial de produção. Neste contexto, o objetivo deste trabalho foi investigar a produção de ácidos graxos livres (AGL) através do processo de hidrolise enzimática, reação inicial da hidroesterificação. Frente ao rendimento em ácidos graxos livres (AGLs), foram avaliados diferentes catalisadores enzimáticos comerciais (Lipozyme® RM IM, Lipozyme® TL IM e Novozyme® 435), adição de solução tampão fosfato de sódio em diferentes pHs (5,7-8,0), sais (CuCl2, CaCl2, KCl, NH4Cl, NaCl, MgCl2), surfactantes (Triton X-100, Tween 80) e solventes orgânicos (n-hexano, n-heptano, Isopropanol, terc-Butanol), bem como as variáveis do processo: agitação (400-2000 rpm), temperatura (30-60 ºC), razão mássica dos substratos (1:20-1:1 óleo:água) e percentual de catalisador (1-20% em relação à massa de óleo). Os resultados obtidos demonstram que a adição de solução tampão (pH 8,0) e solvente orgânico n-hexano contribuíram significativamente para o aumento no rendimento em AGLs da hidrólise, sendo obtidos aproximadamente 82% à 55 ºC, razão mássica óleo:solução tampão 1:2, 100% de solvente n-hexano em relação à massa de óleo e 400 rpm, durante 6 horas de reação e 15% de Lipozyme® RM IM. As condições reacionais deste processo foram exploradas na presença de solvente orgânico n-hexano por meio de planejamentos experimentais, visando a maximização no rendimento em AGLs do processo, bem como a obtenção da cinética de produção de AGLs. Perante as variáveis, pode-se verificar que não houve aumento nos rendimentos em AGLs, ao aumentar a razão mássica de óleo:solvente n-hexano, sendo a temperatura, percentual de solução tampão e catalisador as variáveis que influenciaram significativamente o processo. Na cinética eacional, cerca de 88% em AGLs foram produzidos em meio reacional composto por 70% de solução tampão, 100% de solvente n-hexano e 15% de catalisador, durante 8 horas reacionais. A reutilização do catalisador enzimático foi avaliado perante 20 ciclos reacionais, onde foi verificada diminuição de aproximadamente 50% do rendimento em AGLs inicial do processo.110 fUniversidade Estadual de MaringáBrasilDepartamento de Engenharia QuímicaPrograma de Pós-Graduação em BioenergiaUEMMaringá, PRCentro de TecnologiaCamila da SilvaMara Heloisa Neves Olsen Scaliante - UEMPedro Augusto Arroyo - UEMRaspe, Djéssica Tatiane2018-04-18T19:57:35Z2018-04-18T19:57:35Z2014info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesishttp://repositorio.uem.br:8080/jspui/handle/1/4355porinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da Universidade Estadual de Maringá (RI-UEM)instname:Universidade Estadual de Maringá (UEM)instacron:UEM2018-10-15T17:31:16Zoai:localhost:1/4355Repositório InstitucionalPUBhttp://repositorio.uem.br:8080/oai/requestrepositorio@uem.bropendoar:2018-10-15T17:31:16Repositório Institucional da Universidade Estadual de Maringá (RI-UEM) - Universidade Estadual de Maringá (UEM)false
dc.title.none.fl_str_mv Hidrólise enzimática do óleo de macaúba (Acrocomia aculeata)
Enzymatic hydrolysis from the Macaúba oil (Acrocomia aculeata).
title Hidrólise enzimática do óleo de macaúba (Acrocomia aculeata)
spellingShingle Hidrólise enzimática do óleo de macaúba (Acrocomia aculeata)
Raspe, Djéssica Tatiane
Tecnologia industrial
Óleos e gorduras
Hidrólise
Catálise enzimática
Óleo de macaúba (Acrocomia aculeata).
Hydrolysis
Macauba kernel oil (Acrocomia aculeata)
Enzymatic catalysis
Brazil.
Engenharias
Engenharia Biomédica
title_short Hidrólise enzimática do óleo de macaúba (Acrocomia aculeata)
title_full Hidrólise enzimática do óleo de macaúba (Acrocomia aculeata)
title_fullStr Hidrólise enzimática do óleo de macaúba (Acrocomia aculeata)
title_full_unstemmed Hidrólise enzimática do óleo de macaúba (Acrocomia aculeata)
title_sort Hidrólise enzimática do óleo de macaúba (Acrocomia aculeata)
author Raspe, Djéssica Tatiane
author_facet Raspe, Djéssica Tatiane
author_role author
dc.contributor.none.fl_str_mv Camila da Silva
Mara Heloisa Neves Olsen Scaliante - UEM
Pedro Augusto Arroyo - UEM
dc.contributor.author.fl_str_mv Raspe, Djéssica Tatiane
dc.subject.por.fl_str_mv Tecnologia industrial
Óleos e gorduras
Hidrólise
Catálise enzimática
Óleo de macaúba (Acrocomia aculeata).
Hydrolysis
Macauba kernel oil (Acrocomia aculeata)
Enzymatic catalysis
Brazil.
Engenharias
Engenharia Biomédica
topic Tecnologia industrial
Óleos e gorduras
Hidrólise
Catálise enzimática
Óleo de macaúba (Acrocomia aculeata).
Hydrolysis
Macauba kernel oil (Acrocomia aculeata)
Enzymatic catalysis
Brazil.
Engenharias
Engenharia Biomédica
description Modification of vegetable oils and fats for biodiesel production have been widely studied, where the incentive to search for alternative raw materials for the production of this biofuel has been the focus of interest. Aiming to use an oleaginous without food purposes, with availability and low cost matrix, oil Macaúba (Acrocomia aculeata) has been reported, with its large production potential. In this context, the aim of this study was to investigate the production of free fatty acids (FFA) through the enzymatic hydrolysis process, the initial reaction hidroesterificação. Front to yield free fatty acids (FFAs) were evaluated different commercial enzymatic catalysts (Lipozyme® RM IM, Lipozyme® TL IM and Novozyme® 435), addition of sodium phosphate buffer at different pHs (5.7-8.0), salts (CuCl2, CaCl2, KCl, NH4Cl, NaCl, MgCl2), surfactants (Triton X-100, Tween 80) and organic (n-hexane, n-heptane, isopropanol, tert-butanol) solvent, as well as process variables: agitation (400-2000 rpm), temperature (30-60 °C), weight ratio of substrates (1:20-1:1 oil:water) and percentage of catalyst (1-20% by mass of oil). The results show that the addition of a buffer solution (pH 8.0) and organic solvent n-hexane contributed significantly to the increase in free fatty acids in the hydrolysis yield being obtained approximately 82% at 55 °C oil weight ratio: Buffer 1:2, 100% n-hexane solvent relative to the weight of oil and 400 rpm for 6 hours reaction, 15% Lipozyme® RM IM. The reaction conditions of the process were explored in the presence of n-hexane organic solvent by means of experimental design, in order to maximize the yield FFAs in the process, as well as obtaining the kinetics of production of FFAs. Given the variables, it can be seen that no increase in yields of FFA by increasing the weight ratio of oil:solvent n-hexane, temperature, buffer and percentage of catalyst variables that influence the process significantly. In reaction kinetics, about 88% free fatty acids were produced in reaction medium consisting of 70% buffer, 100% of n-hexane solvent and 15% of catalyst, reaction for 8 hours. The reuse of the enzyme catalyst has been reported before 20 reaction cycles, where it was detected decrease of approximately 50% of revenue in the initial FFA process.
publishDate 2014
dc.date.none.fl_str_mv 2014
2018-04-18T19:57:35Z
2018-04-18T19:57:35Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
format doctoralThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://repositorio.uem.br:8080/jspui/handle/1/4355
url http://repositorio.uem.br:8080/jspui/handle/1/4355
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv Universidade Estadual de Maringá
Brasil
Departamento de Engenharia Química
Programa de Pós-Graduação em Bioenergia
UEM
Maringá, PR
Centro de Tecnologia
publisher.none.fl_str_mv Universidade Estadual de Maringá
Brasil
Departamento de Engenharia Química
Programa de Pós-Graduação em Bioenergia
UEM
Maringá, PR
Centro de Tecnologia
dc.source.none.fl_str_mv reponame:Repositório Institucional da Universidade Estadual de Maringá (RI-UEM)
instname:Universidade Estadual de Maringá (UEM)
instacron:UEM
instname_str Universidade Estadual de Maringá (UEM)
instacron_str UEM
institution UEM
reponame_str Repositório Institucional da Universidade Estadual de Maringá (RI-UEM)
collection Repositório Institucional da Universidade Estadual de Maringá (RI-UEM)
repository.name.fl_str_mv Repositório Institucional da Universidade Estadual de Maringá (RI-UEM) - Universidade Estadual de Maringá (UEM)
repository.mail.fl_str_mv repositorio@uem.br
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