4.7 Article

Understanding of the key properties of supported Cu-based catalysts and their influence on ester hydrogenolysis

Journal

CATALYSIS TODAY
Volume 397, Issue -, Pages 173-181

Publisher

ELSEVIER
DOI: 10.1016/j.cattod.2021.09.039

Keywords

Supported copper catalyst; Ester hydrogenolysis; Dimethyl adipate; Reaction pathway

Funding

  1. Czech Science Foundation [GA20-28093S]
  2. Ministry of Education, Youth and Sports of the Czech Republic [LM2018098]

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The application of Cr-free Cu-based catalysts in ester hydrogenolysis is an environmentally-friendly research approach. This study investigated the performance of four different supported Cu-based catalysts on various supports. The results showed that Al2O3 support provided the best dispersion of nanoparticles, while Cu-TiO2 nanoparticles were prone to sintering. Cu-ZrO2 exhibited the best performance in the dimethyl adipate hydrogenolysis. Furthermore, the study revealed a correlation between the number of acid-base sites and catalyst selectivity.
The application of Cr-free Cu-based catalysts in ester hydrogenolysis is a modern environmentally-friendly research approach. The comprehensive study of four supported Cu-based catalysts was performed using 8 wt % of Cu loaded on Al2O3, ZnO, TiO2 and ZrO2 supports by an impregnation method. Using XRD, H2-TPR, BET, pyridine-TPD, CO2-TPD and N2O-RFC methods, the effect of the support on the formation of Cu-nanoparticles was described. Al2O3 was evaluated as the support ensuring the highest nanoparticles dispersion, while Cu nanoparticles in Cu-TiO2 were liable to sintering. The catalysts were tested in dimethyl adipate hydrogenolysis, where the catalyst performance and activity (TOF) were evaluated and Cu-ZrO2 showed the best results. A correlation between the number of acid-base sites and the catalyst selectivity was revealed and the catalyst effect on the formation of various by-products was described. The intrinsic selectivity to hydrogenolysis products was found to decrease with the increasing acid-base character of the supports whereas the selectivity to transesterification and cyclization products increased. The hydrogenolysis activity was not a simple function of the number of the surface copper atoms, but it was affected by the support nature and its properties.

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