In Situ Transesterification of Microbial Biomass for Biolubricant Production Catalyzed by Heteropolyacid Supported on Niobium

dc.contributor.authorZorn, Savienne M. F. E.
dc.contributor.authorda Silva, Ana Paula T.
dc.contributor.authorBredda, Eduardo H. [UNESP]
dc.contributor.authorBento, Heitor B. S. [UNESP]
dc.contributor.authorPedro, Guilherme A.
dc.contributor.authorCarvalho, Ana Karine F.
dc.contributor.authorSilva, Messias Borges [UNESP]
dc.contributor.authorDa Rós, Patrícia C. M.
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionFederal University of Alfenas
dc.date.accessioned2022-05-01T13:57:33Z
dc.date.available2022-05-01T13:57:33Z
dc.date.issued2022-02-01
dc.description.abstractLubricants are substances of the foremost importance in the modern world, as they are essential to the proper functioning of various mechanisms. Most lubricants, however, are still made from petroleum fractions. I light of this, and due to various environmental problems, the search for feasible biolubricants has become essential. This study obtained biolubricants through the in situ transesterification of microbial biomass, containing at least 20 wt% of lipids. The following two distinct biomasses were evaluated: the marine microalgae, Dunaliella salina, and the consortium of microalgae-fungi, Scenedesmus obliquus and Mucor circinelloides. Microbial oil from both biomasses presented a fatty acid profile with high amounts of oleic acid. The oil of D. salina had a lower content of polyunsaturated fatty acids relative to the microbial consortium profile, which indicates that this is a good configuration for increasing biolubricant oxidation resistance. The catalyst used was a Keggin-structure heteropolyacid supported on niobium, H3 PMo12 O40 /Nb2 O5, activated at 150◦ C, which had high transesterification yields, notwithstanding the feedstocks, which were rich in free fatty acids. The performed transesterification reactions resulted in excellent yields, up to 97.58% and 96.80%, for marine microalgae and the consortium, respectively, after 6 h at 250◦ C, with 10 wt% of catalyst (related to the lipid amount). As such, the (H3 PMo12 O40 /Nb2 O5 ) catalyst could become an attractive option for producing biolubricants from microbial biomass.en
dc.description.affiliationEngineering School of Lorena University of São Paulo
dc.description.affiliationEngineering Faculty of Guaratinguetá São Paulo State University (UNESP)
dc.description.affiliationBioprocess Engineering and Biotechnology Faculty of Pharmaceutical Sciences São Paulo State University (UNESP)
dc.description.affiliationPostgraduate Program in Biotechnology Chemistry Institute Federal University of Alfenas
dc.description.affiliationUnespEngineering Faculty of Guaratinguetá São Paulo State University (UNESP)
dc.description.affiliationUnespBioprocess Engineering and Biotechnology Faculty of Pharmaceutical Sciences São Paulo State University (UNESP)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdCNPq: 165390/2017-4
dc.description.sponsorshipIdFAPESP: 2016/10636-8
dc.description.sponsorshipIdFAPESP: 2016/18909-3
dc.description.sponsorshipIdFAPESP: 2018/01386-3
dc.description.sponsorshipIdFAPESP: 2020/15513-7
dc.identifierhttp://dx.doi.org/10.3390/en15041591
dc.identifier.citationEnergies, v. 15, n. 4, 2022.
dc.identifier.doi10.3390/en15041591
dc.identifier.issn1996-1073
dc.identifier.scopus2-s2.0-85125197157
dc.identifier.urihttp://hdl.handle.net/11449/234195
dc.language.isoeng
dc.relation.ispartofEnergies
dc.sourceScopus
dc.subjectBiolubricant
dc.subjectConsortium
dc.subjectDunaliella salina
dc.subjectFusel oil
dc.subjectH3 PMo12 O40
dc.subjectMicroalgae
dc.subjectMicrobial biomass
dc.subjectMucor circinelloides
dc.subjectScenedesmus obliquus
dc.titleIn Situ Transesterification of Microbial Biomass for Biolubricant Production Catalyzed by Heteropolyacid Supported on Niobiumen
dc.typeArtigo
unesp.departmentProdução - FEGpt

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