dc.creatorBravo Fuchineco, Daiana Antonella
dc.creatorHeredia, Angelica Constanza
dc.creatorMendoza, Sandra Marina
dc.creatorRodríguez Castellón, Enrique
dc.creatorCrivello, Mónica Elsie
dc.date.accessioned2022-07-27T16:00:35Z
dc.date.accessioned2022-10-15T11:19:31Z
dc.date.available2022-07-27T16:00:35Z
dc.date.available2022-10-15T11:19:31Z
dc.date.created2022-07-27T16:00:35Z
dc.date.issued2022-03-25
dc.identifierBravo Fuchineco, Daiana Antonella; Heredia, Angelica Constanza; Mendoza, Sandra Marina; Rodríguez Castellón, Enrique; Crivello, Mónica Elsie; Esterification of Levulinic Acid to Methyl Levulinate over Zr-MOFs Catalysts; MDPI; ChemEngineering; 25-3-2022
dc.identifierhttp://hdl.handle.net/11336/163282
dc.identifier2305-7084
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4380055
dc.description.abstractAt present, the trend towards partial replacement of petroleum‐derived fuels by those from the revaluation of biomass has become of great importance. An effective strategy for pro-cessing complex biomass feedstocks involves prior conversion to simpler compounds (platform molecules) that are more easily transformed in subsequent reactions. This study analyzes the met-al–organic frameworks (MOFs) that contain Zr metal clusters formed by ligands of terephthalic acid (UiO‐66) and aminoterephthalic acid (UiO‐66‐NH2), as active and stable catalysts for the esterification of levulinic acid with methanol. An alternative synthesis is presented by means of ultrasonic stirring at room temperature and 60 °C, in order to improve the structural properties of the catalysts. They were analyzed by X‐ray diffraction, scanning electron microscopy, infrared spectroscopy, X‐ray photoelectron spectroscopy, microwave plasma atomic emission spectroscopy, acidity measurement, and N2 adsorption. The catalytic reaction was carried out in a batch system and under pressure in an autoclave. Its progress was followed by gas chromatography and mass spectrometry. Parameters such as temperature, catalyst mass, and molar ratio of reactants were optimized to improve the catalytic performance. The MOF that presented the highest activity and selectivity to the desired product was obtained by synthesis with ultrasound and 60 °C with ami-noterephthalic acid. The methyl levulinate yield was 67.77% in batch at 5 h and 85.89% in an auto-clave at 1 h. An analysis of the kinetic parameters of the reaction is presented. The spent material can be activated by ethanol washing allowing the catalytic activity to be maintained in the recycles.
dc.languageeng
dc.publisherMDPI
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.3390/chemengineering6020026
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://www.mdpi.com/2305-7084/6/2/26
dc.rightshttps://creativecommons.org/licenses/by/2.5/ar/
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectBATCH AND PRESSURE REACTIONS
dc.subjectESTERIFICATION KINETICS
dc.subjectLEVULINIC ACID
dc.subjectMETHYL LEVULINATE
dc.subjectUIO‐66
dc.subjectUIO‐66‐NH2
dc.titleEsterification of Levulinic Acid to Methyl Levulinate over Zr-MOFs Catalysts
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


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