Enhanced 1,2-Propanediol Production from Glycerol using Bimetallic NiCu Catalysts on Different Supports

Abstract

The activity of NiCu bimetallic catalysts on various commercial supports (SiO2-Al2O3 and SiO2) and synthesized pristine supports (AlO(OH), Al-TUD-1 and meso-TiO2) in glycerol dehydration-hydrogenation for making 1,2-propanediol (1,2-PD) was investigated. The catalytic performance of bimetallic NiCu on various supports was evaluated, with the NiCu/AlO(OH) catalyst exhibiting superior activity, achieving 79.5% selectivity for 1,2-propanediol at 90.2% glycerol conversion. The results were promising, revealing that the bimetallic 25 wt% Ni-10 wt% Cu incorporated Lewis acidity, significantly enhancing the selectivity for 1,2-propanediol in glycerol dehydration-hydrogenation process. This high performance could be attributed to the well-dispersed Ni and Cu nanoparticles on AlO(OH), mesoporous structure of AlO(OH) with large pore structure, and the presence of sufficient acid sites on catalyst. Acid site analysis revealed that metal loading generally reduced Lewis acidity, while Brønsted acidity showed a slight increase, suggesting a shift in catalytic mechanism influenced by metal-support interactions. Comparative analysis exhibited that synthesized supports like meso-TiO2 and Al-TUD-1 offered high Lewis acid sites due to their mesoporous frameworks. However, AlO(OH) stood out due to its unique surface hydroxyl groups and moderate acidity, promoting metal-support interactions and catalyst stability. The findings suggest the importance of support selection in the design of bimetallic catalysts for maximizing glycerol conversion and production of 1,2-PD.

Article information

Article type
Paper
Submitted
05 Apr 2025
Accepted
23 Jul 2025
First published
09 Aug 2025

Sustainable Energy Fuels, 2025, Accepted Manuscript

Enhanced 1,2-Propanediol Production from Glycerol using Bimetallic NiCu Catalysts on Different Supports

A. Ghorbani, P. Boahene and A. K. Dalai, Sustainable Energy Fuels, 2025, Accepted Manuscript , DOI: 10.1039/D5SE00480B

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