Recycling of Rare Earth Elements: From E‐Waste to Stereoselective Catalytic Reactions

Raw mixtures of Rare Earths Elements, REE, recovered by E-waste, were used as catalysts to promote the (stereoselective) synthesis of highly valuable compounds. Y<sub>2</sub>O<sub>3</sub>, the major species that is recovered by the E-waste, can be easily converted into the catalytically active Y(OTf)<sub>3</sub> that is able to efficiently promote the Michael addition of indoles to benzylidene malonates and the stereoselective Diels-Alder cycloaddition between cyclopentadiene and 4-(S)-3 acryloyl 4-tert-butyl 2-oxazolidinone. Additionally, the raw mixtures were immobilissed onto silica and used to construct packed reactors, resulting in values for Productivity and Space-Time Yields that were significantly higher than those of the corresponding batch conversions. Notably, the prepared cartridge employed in the model Michael reaction maintained its catalytic efficiency for more than 4 days of continuous running.

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Publication Details

Journal
ChemSusChem
Published
2024-09-09
DOI
https://doi.org/10.1002/cssc.202401787
Citations
1
Primary Topic
Catalysis for Biomass Conversion
Type
article
Field-Weighted Citation Impact
0.18

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article

Recycling of Rare Earth Elements: From E‐Waste to Stereoselective Catalytic Reactions

Giuseppe Zanoni, Martin Bertau, Peter J. Fröhlich, Emanuela Donato et al.
1 citations
ChemSusChem
Catalysis for Biomass Conversion
0.18
article

Recycling of Rare Earth Elements: From E‐Waste to Stereoselective Catalytic Reactions

Giuseppe Zanoni, Martin Bertau, Peter J. Fröhlich, Emanuela Donato, Maurizio Benaglia, Alessandra Puglisi, Valerio Chiroli, Fabrizio Medici, Clemens Rogoli
article en
1 citations

Abstract

Raw mixtures of Rare Earths Elements, REE, recovered by E-waste, were used as catalysts to promote the (stereoselective) synthesis of highly valuable compounds. Y<sub>2</sub>O<sub>3</sub>, the major species that is recovered by the E-waste, can be easily converted into the catalytically active Y(OTf)<sub>3</sub> that is able to efficiently promote the Michael addition of indoles to benzylidene malonates and the stereoselective Diels-Alder cycloaddition between cyclopentadiene and 4-(S)-3 acryloyl 4-tert-butyl 2-oxazolidinone. Additionally, the raw mixtures were immobilissed onto silica and used to construct packed reactors, resulting in values for Productivity and Space-Time Yields that were significantly higher than those of the corresponding batch conversions. Notably, the prepared cartridge employed in the model Michael reaction maintained its catalytic efficiency for more than 4 days of continuous running.

ChemSusChemVol. 18(3)
University of Milan (IT), University of Pavia (IT), TU Bergakademie Freiberg (DE)
Università degli Studi di Milano, European Commission, Fondazione Cariplo, Papua New Guinea University of Technology
Responsible consumption and production
Openalex Percentile: Top 53%
Catalysis for Biomass Conversion
0.18
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Recycling of Rare Earth Elements: From E‐Waste to Stereoselective Catalytic Reactions — Giuseppe Zanoni, Martin Bertau, et al. · ChemSusChem (2024) | TGRS Research Map | TGRS