High-Active Metallic-Activated Carbon Catalysts for Selective Hydrogenation
Please use this identifier to cite or link to this item:
http://hdl.handle.net/10045/77967
Title: | High-Active Metallic-Activated Carbon Catalysts for Selective Hydrogenation |
---|---|
Authors: | Carrara, Nicolas | Betti, Carolina P. | Coloma, Fernando | Almansa Carrascosa, María Cristina | Gutierrez, Laura | Miranda, Cristian | Quiroga, Mónica E. | Lederhos, Cecilia R. |
Research Group/s: | Materiales Avanzados |
Center, Department or Service: | Universidad de Alicante. Servicios Técnicos de Investigación |
Keywords: | Metallic-activated | Carbon catalysts | Selective hydrogenation |
Knowledge Area: | Ingeniería Química |
Issue Date: | 5-Jul-2018 |
Publisher: | Hindawi Publishing Corporation |
Citation: | Nicolás Carrara, Carolina Betti, Fernando Coloma-Pascual, et al., “High-Active Metallic-Activated Carbon Catalysts for Selective Hydrogenation,” International Journal of Chemical Engineering, vol. 2018, Article ID 4307308, 11 pages, 2018. https://doi.org/10.1155/2018/4307308 |
Abstract: | A series of low-loaded metallic-activated carbon catalysts were evaluated during the selective hydrogenation of a medium-chain alkyne under mild conditions. The catalysts and support were characterized by ICP, hydrogen chemisorption, Raman spectroscopy, temperature-programmed desorption (TPD), temperature-programmed reduction (TPR), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR micro-ATR), transmission electronic microscopy (TEM), and X-ray photoelectronic spectroscopy (XPS). When studying the effect of the metallic phase, the catalysts were active and selective to the alkene synthesis. NiCl/C was the most active and selective catalytic system. Besides, when the precursor salt was evaluated, PdN/C was more active and selective than PdCl/C. Meanwhile, alkyne is present in the reaction media, and geometrical and electronic effects favor alkene desorption and so avoid their overhydrogenation to the alkane. Under mild conditions, nickel catalysts are considerably more active and selective than the Lindlar catalyst. |
Sponsor: | The financial assistance of UNL (CAI+D), CONICET (PIP 457), and ANPCyT (PICT-2013-2021 and PICT-2016-1453) is greatly acknowledged. |
URI: | http://hdl.handle.net/10045/77967 |
ISSN: | 1687-806X (Print) | 1687-8078 (Online) |
DOI: | 10.1155/2018/4307308 |
Language: | eng |
Type: | info:eu-repo/semantics/article |
Rights: | © 2018 Nicolás Carrara et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
Peer Review: | si |
Publisher version: | https://doi.org/10.1155/2018/4307308 |
Appears in Collections: | INV - LMA - Artículos de Revistas |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
2018_Carrara_etal_IntJChemEng.pdf | 3,44 MB | Adobe PDF | Open Preview | |
This item is licensed under a Creative Commons License