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Previous issue date: 2018-03-05 / Este trabalho investigar a síntese do biodiesel proveniente do óleo de fritura através da reação de hidroesterificação, utilizando como suporte catalítico heterogêneo, a vermiculita. A hidrólise foi efetuada em reator de autoclave numa temperatura de 300 ºC por 3 h, e em seguida, a esterificação foi realizada sob razão molar do álcool etílico/ácido graxo na proporção 6:1, na presença de 5% do catalisador em relação à massa do óleo. Tanto o biodiesel e o óleo de fritura foram caracterizados por meio de parâmetros físico-químico, térmicos e por espectrofotometria de absorção na região do UV-Visível com fins de melhor compreensão. O rendimento reacional em relação à massa do óleo de fritura residual para o biodiesel foi de 66,65%. A curva termogravimétrica referente ao biodiesel apresentou duas etapas de decomposição, sendo a primeira etapa com 83,1% de perda de massa, indicando a conversão em monoacilglicerideos, e a segunda com 14,3% de perda de massa, atribuída a presença de traços de diacilglicerídeos e/ou triacilglicerídeos não convertida em ésteres de ácidos graxos etílicos. Os espectros de absorção na região do infravermelho confirmaram a presença dos ésteres de ácidos graxos etílicos em 1749,7 cm-1, no entanto, também verificou presença de banda vibracional correspondente ao estiramento do grupo OH, em 3600 a 3300 cm-1, confirmando presença de umidade e/ou a não conversão total da hidrólise de glicerídeos. Por fim, este trabalho demonstrou ser satisfatório em termos de conversão, embora requeira um estudo mais aprofundado, manipulando as condições reacionais. / This study aimed to investigate the synthesis of biodiesel from frying oil through the
hydroesterification reaction, using as heterogeneous catalytic support – vermiculite. Both the
biodiesel obtained and the raw material (frying oil) were characterized by physical-chemical,
thermal and absorption spectrophotometry in the UV-Visible region for better understanding.
The synthesis of biodiesel by hydroesterification involved two steps: hydrolysis and
esterification, whereby the residual frying oil was subjected to the step of hydrolysis in an
autoclave reactor at a temperature of 300 ° C for 03 hours. After the hydrolysis, the glycerin
was removed and the fatty acids generated were subjected to the esterification step and
processed under the following conditions: 6: 1 molar ratio of the ethyl alcohol / fatty acid in
the presence of 5% of the catalyst (vermiculite) relative to the mass of the oil. Subsequently,
the mixture was subjected to the stirring process and transferred to the autoclave reactor at
200°C for 01 hour. After that, the mixture was decanted for 2 hours and the phases were
separated. The dense phase – biodiesel – was characterized according to the standards of the
National Agency for Petroleum, Natural Gas and Biofuel. Thus, the reaction yield in relation
to the initial mass of the residual frying oil for biodiesel was 66.65%. It is suggested that this
yield was compromised by the acidity of the obtained biodiesel (0.61mg KOH/g),
contributing to the release of the free fatty acids in the medium. Regarding the thermal study,
the thermogravimetric curves showed that biodiesel is more volatile compared to the frying
oil and presented two stages of decomposition: the first probably corresponding to the ethyl
ester volatilization, with 83.1% of mass loss, indicating the conversion to
monoacylglycerides; and the second stage with 14.3% of mass loss, attributed to the presence
of diacylglyceride and/or triacylglyceride traces not converted to esters of ethyl fatty acids.
The absorption spectra in the infrared region confirmed the presence of the strongly acidic
fatty acid esters of 1749.7 cm-1; however, the presence of medium-sized vibrational band,
corresponding to OH group stretching, is also present at 3600 to 3300cm-1, corroborating the
thermal and physicochemical profile, confirming the presence of moisture and/or total nonconversion
of glyceride hydrolysis. Finally, according to the results presented, this study
proved to be feasible in terms of conversion, although it requires further investigation,
manipulating the reactional conditions.
Identifer | oai:union.ndltd.org:IBICT/oai:localhost:riufcg/664 |
Date | 14 May 2018 |
Creators | LACERDA, José Gorete Pedroza de. |
Contributors | CANDEIA, Roberlúcia Araújo., SALES, Luciano Leal de Morais., ARAÚJO, Alfredina dos Santos., CUNHA, Fernando Antônio Portela da Cunha. |
Publisher | Universidade Federal de Campina Grande, PÓS-GRADUAÇÃO EM SISTEMAS AGROINDUSTRIAIS, UFCG, Brasil, Centro de Ciências e Tecnologia Agroalimentar - CCTA |
Source Sets | IBICT Brazilian ETDs |
Language | Portuguese |
Detected Language | English |
Type | info:eu-repo/semantics/publishedVersion, info:eu-repo/semantics/masterThesis |
Source | reponame:Biblioteca de Teses e Dissertações da UFCG, instname:Universidade Federal de Campina Grande, instacron:UFCG |
Rights | info:eu-repo/semantics/openAccess |
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