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One-pot preparation of Ni-Cu nanoparticles supported on γ-Al2O3 as selective and stable catalyst for the Guerbet reaction of 1-octanol
This paper reports on the “in-situ” preparation-deposition and reduction of Ni-Cu nanoparticles (NPs) on γ-Al2O3 as support, using a green and elegant one-pot synthesis approach. Pristine and supported Ni-Cu NPs were evaluated as (de)hydrogenation catalysts for the Guerbet reaction of 1-octanol and...
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Published in: | Catalysis communications 2017-07, Vol.98, p.94-97 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | This paper reports on the “in-situ” preparation-deposition and reduction of Ni-Cu nanoparticles (NPs) on γ-Al2O3 as support, using a green and elegant one-pot synthesis approach. Pristine and supported Ni-Cu NPs were evaluated as (de)hydrogenation catalysts for the Guerbet reaction of 1-octanol and compared with a classic impregnated and “ex-situ” reduced NiCu on γ-Al2O3 catalyst. XRD reavealed that the degree of Ni-Cu nano-alloying was insignificant in the one-pot preparation method, resulting in Ni-Cu nanocomposites, while the degree of nano-alloying was resp. low and very high in the pristine nanoparticles (NPs) and the classic impregnated catalyst. The degree of reduction was very similar for both the in-situ and ex-situ reduction treatments of the supported catalysts as demonstrated by H2 chemisorption. The “in-situ” prepared supported Ni-Cu NPs showed an enhanced kinetics when compared to the unsupported pristine Ni-Cu NPs, showing a beneficial effect of the metal-support interaction, however the classic impregnated catalyst showed overall the best kinetics, selectivity and stability for the Guerbet reaction of 1-octanol.
•Easy preparation of supported Ni-Cu NPs using a one-pot synthesis methodology•Upon alumina support Ni-Cu NPs were more active and stable for Guerbet reaction.•One-pot synthesis method favored disaggregation and stability of the supported catalyst. |
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ISSN: | 1566-7367 1873-3905 |
DOI: | 10.1016/j.catcom.2017.05.005 |