Catalytic performance and deactivation of sulfonated hydrothermal carbon in the esterification of fatty acids: Comparison with sulfonic solids of different nature
Sulfonated hydrothermal carbon is able to catalyze the esterification of palmitic acid with methanol at a higher initial rate per site than other well-known sulfonic solids, including stronger acids such as Nafion-silica. Although the origin of this higher rate per site is not clear, it seems to be...
| Autores: | , , , |
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| Tipo de recurso: | artículo |
| Estado: | Versión aceptada para publicación |
| Fecha de publicación: | 2015 |
| País: | España |
| Institución: | Consejo Superior de Investigaciones Científicas (CSIC) |
| Repositorio: | DIGITAL.CSIC. Repositorio Institucional del CSIC |
| OAI Identifier: | oai:digital.csic.es:10261/154638 |
| Acceso en línea: | http://hdl.handle.net/10261/154638 |
| Access Level: | acceso abierto |
| Palabra clave: | Sulfonated hydrothermal carbon Acid catalysts Esterification Deactivation Sulfonic solids |
| Sumario: | Sulfonated hydrothermal carbon is able to catalyze the esterification of palmitic acid with methanol at a higher initial rate per site than other well-known sulfonic solids, including stronger acids such as Nafion-silica. Although the origin of this higher rate per site is not clear, it seems to be related to high surface density of acid groups (both carboxylic and sulfonic). At the same time, their close proximity makes possible the mutual activation of the surface groups for esterification with methanol. The formation of sulfonate esters on the surface produces irreversible partial deactivation of the solid for a second reaction. Other solids able to bring sulfonic groups close, such as Dowex, show the same deactivation pattern, but their sites are less active than those in sulfonated hydrothermal carbon. As an additional advantage, this solid displays enhanced stability against the presence of water, which enables improvement of the behavior after recovery by minimization of the esterification of the surface acid sites. |
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