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Controlling the selectivity of the hydrogenolysis of polyamides catalysed by ceria-supported metal nanoparticles
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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 LinPaul J. Dyson
Nature Communications, 卷.14(1), 6524
12/2023
PMID: 37845260

摘要

Chemistry (all) Biochemistry Genetics and Molecular Biology (all) Physics and Astronomy (all)
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 CeO 2 . Ru/CeO 2 and Pt/CeO 2 are both highly active but display different selectivity; Ru/CeO 2 is selective for the conversion of all polyamides into water, ammonia, and methane, whereas Pt/CeO 2 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.

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