dc.contributorCinthia de Castro Oliveira
dc.contributorhttp://lattes.cnpq.br/5735402062329725
dc.contributorLuiz Carlos Alves de Oliveira
dc.contributorMaraisa Gonçalves
dc.contributorRenata Diniz
dc.creatorIzabela Diniz Padula
dc.date.accessioned2021-11-11T00:29:03Z
dc.date.accessioned2022-10-03T22:14:16Z
dc.date.available2021-11-11T00:29:03Z
dc.date.available2022-10-03T22:14:16Z
dc.date.created2021-11-11T00:29:03Z
dc.date.issued2020-02-17
dc.identifierhttp://hdl.handle.net/1843/38639
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3796716
dc.description.abstractThe purpose this research was synthesis of niobium-modified hydrotalcite (HT) catalysts for crude glycerin conversion to value-added products. For this, the synthesis of the precursor (HT) was performed by the coprecipitation method and the Nb addition was performed by wet impregnation and ion exchange methods. The Nb precursor employed in catalyst synthesis was a synthesized niobium oligomer with high negative charge. Thus, five catalysts were obtained: HT, Nb@HT, MgAl, Nb@MgAl and Nb/MgAl, and the last three were obtained after heat treatment at 600 °C. The characterization of the materials proved the lamellar structure of HT and that the ion exchange process (Nb@HT) was efficient in the carbonate ion exchange (CO32-) present in the interlamellar space by the niobium polyoxometalate clusters. In addition, the MgAl mixed oxide was verified in the calcined materials (i.e., MgAl, Nb@MgAl and Nb/MgAl). The Nb2O5 was observed for all the Nb modified catalysts whereas a new phase identified as Mg5Nb4O15 was observed only for Nb/MgAl (synthesized by impregnation). EDX and FRX analyzes confirmed the presence of Nb in the catalysts (16, 18 and 19% Nb for Nb@HT, Nb@MgAl and Nb/MgAl, respectively). The Nb addition further increased the specific surface area of the catalysts (HT = 65, Nb@HT = 89, MgAl = 88, Nb@MgAl = 229 and Nb/MgAl = 123 m2 g-1), increased the amount of acid sites and decreased the basicity of the materials. The catalytic tests were performed in reflux (batch) and in a continuous flow process in a fixed bed reactor (PBR). High conversions were obtained, reaching ~70% for reflux and 90% for continuous flow. In all reactions, the main products formed in the liquid phase were diglycerol (DG) and formic acid (FA). In all catalytic tests, the Nb/MgAl catalyst generated higher FA due to higher acidity and basicity and the Nb@MgAl showed higher DG yield. Finally, the fractional distillation of the products formed in continuous flow of the reaction with Nb/MgAl allowed to concentrate the FA fraction generating 45% (v/v) yield. Thus, the work presents promising catalysts for generation of chemicals of high industrial interest from a renewable source of biomass (residual glycerol), contributing to the increased sustainability of biodiesel production.
dc.publisherUniversidade Federal de Minas Gerais
dc.publisherBrasil
dc.publisherICX - DEPARTAMENTO DE QUÍMICA
dc.publisherPrograma de Pós-Graduação em Química
dc.publisherUFMG
dc.rightshttp://creativecommons.org/licenses/by-nd/3.0/pt/
dc.rightsAcesso Aberto
dc.subjectHidróxido duplo lamelar
dc.subjectÓxidos mistos
dc.subjectGlicerol
dc.subjectÁcido fórmico
dc.subjectDiglicerol
dc.subjectNióbio
dc.subjectCatálise heterogênea
dc.subjectLayered double hydroxide
dc.subjectMixed oxides
dc.subjectGlycerol
dc.subjectFormic acid
dc.subjectDiglycerol
dc.subjectNiobium
dc.subjectHeterogeneous catalysis
dc.titleÓxidos mistos de MgAl modificados com nióbio como catalisadores para a conversão da glicerina residual
dc.typeDissertação


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