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Hydrogen Borrowing: towards Aliphatic Tertiary Amines from Lignin Model Compounds Using a Supported Copper Catalyst.
Dieter Ruijten1, Thomas Narmon1, Hanne De Weer1
1Center for Sustainable Catalysis and Engineering, KU Leuven, Celestijnenlaan 200F, Leuven, 3001, Belgium.
A new catalytic method converts lignin-derived alcohols into valuable tertiary amines using a copper-zirconium dioxide (Cu-ZrO2) catalyst. This process offers a sustainable route to producing renewable aromatic chemicals.
Area of Science:
- Chemical Engineering
- Catalysis
- Renewable Energy
Background:
- Biorefineries are emerging to produce renewable chemicals from biomass.
- Lignin valorization yields aromatic compounds with aliphatic alcohols.
- Sustainable synthesis of amines from these alcohols is crucial.
Purpose of the Study:
- To develop a catalytic hydrogen borrowing method for synthesizing tertiary amines.
- To utilize lignin-derived monomers and dimethylamine as reactants.
- To identify an effective and reusable catalyst system.
Main Methods:
- Screening of various industrial metal catalysts.
- Hydrogen borrowing reaction using lignin model and actual monomers with dimethylamine.
- Kinetic studies to elucidate reaction networks.
- Catalyst characterization using ToF-SIMS, N2O chemisorption, TGA, and XPS.
Main Results:
- Cu-ZrO2 demonstrated high alcohol conversion and good tertiary amine selectivity.
- Low H2 pressure favored catalyst activity and selectivity by preventing side reactions.
- Catalyst deactivation was linked to product desorption and copper species loss.
- Thermal reduction successfully restored catalyst performance.
Conclusions:
- Cu-ZrO2 is a suitable catalyst for producing tertiary amines from lignin-derived alcohols.
- The catalytic system is robust and reusable after thermal regeneration.
- This method provides a sustainable pathway for renewable aromatic amine production.
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