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Controlling the selectivity of the hydrogenolysis of polyamides catalysed by ceria-supported metal nanoparticles

XinBang Wu, Wei-Tse Lee, Roland C. Turnell-Ritson, Pauline C. L. Delannoi, Kun-Han Lin () and Paul J. Dyson ()
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XinBang Wu: Swiss Federal Institute of Technology Lausanne (EPFL)
Wei-Tse Lee: Swiss Federal Institute of Technology Lausanne (EPFL)
Roland C. Turnell-Ritson: Swiss Federal Institute of Technology Lausanne (EPFL)
Pauline C. L. Delannoi: Swiss Federal Institute of Technology Lausanne (EPFL)
Kun-Han Lin: National Tsing Hua University (NTHU)
Paul J. Dyson: Swiss Federal Institute of Technology Lausanne (EPFL)

Nature Communications, 2023, vol. 14, issue 1, 1-11

Abstract: Abstract Catalytic hydrogenolysis is a promising approach to transform waste plastic into valuable chemicals. However, the transformation of N-containing polymers, such as polyamides (i.e. nylon), remains under-investigated, particularly by heterogeneous catalysis. Here, we demonstrate the hydrogenolysis of various polyamides catalysed by platinum-group metal nanoparticles supported on CeO2. Ru/CeO2 and Pt/CeO2 are both highly active but display different selectivity; Ru/CeO2 is selective for the conversion of all polyamides into water, ammonia, and methane, whereas Pt/CeO2 yields hydrocarbons retaining the carbon backbone of the parent polyamide. Density functional theory computations illustrate that Pt nanoparticles require higher activation energy for carbon−carbon bond cleavage than Ru nanoparticles, rationalising the observed selectivity. The high activity and product selectivity of both catalysts was maintained when converting real-world polyamide products, such as fishing net. This study provides a mechanistic basis for heterogeneously catalysed polyamide hydrogenolysis, and a new approach to the valorisation of polyamide containing waste.

Date: 2023
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DOI: 10.1038/s41467-023-42246-x

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