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Natural and Modified Montmorillonite Clays as Catalysts for Synthesis of Biolubricants

In this study, natural and modified clays were evaluated as catalysts in an esterification reaction to obtain bio-based lubricants. The biolubricants are environmentally preferred to petroleum-based lubricants because they are biodegradable and non-toxic. Other advantages include very low volatility...

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Detalles Bibliográficos
Autores principales: Luna, Francisco Murilo Tavares, Cecilia, Juan Antonio, Saboya, Rosana Maria Alves, Barrera, Deicy, Sapag, Karim, Rodríguez-Castellón, Enrique, Cavalcante, Célio Loureiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6163643/
https://www.ncbi.nlm.nih.gov/pubmed/30231539
http://dx.doi.org/10.3390/ma11091764
Descripción
Sumario:In this study, natural and modified clays were evaluated as catalysts in an esterification reaction to obtain bio-based lubricants. The biolubricants are environmentally preferred to petroleum-based lubricants because they are biodegradable and non-toxic. Other advantages include very low volatility due to the high molecular weight and excellent viscosity properties with temperature variations. Modifications in natural clay were performed intending to obtain materials with different textural properties that could improve the reaction under study. The modified clays were obtained in two ways: by pillarization using Al(13) Keggin polyoxocations or by acid treatments with H(2)SO(4), HCl and HNO(3). All samples were evaluated for the esterification reaction of fatty acids from castor oil (FACO) using 2-ethyl-hexanol. During the reaction step, a zeolite-based adsorbent was used for water removal to increase the reaction equilibrium conversion. Gas chromatography and nuclear magnetic resonance were performed to ensure the formation of the products. The highest conversion of fatty acids to esters was obtained using pillared clays. Adding adsorbent in the reaction medium (10 g of 3A zeolite to 100 g of FACO), the conversion improved from 74–88 wt % after 6 h at 50 °C.