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Published on: August 17, 2019
Mechanochemically Engineered CaO-CeO2 Dual-Function Catalysts for Sustainable Glycerol Carbonate Production without
Patcharaporn Inrirai1, Runzhe Yu1, Daniel Goma Jiménez1
1School of Chemistry and Chemical Engineering, Queen's University Belfast, David-Keir Building, Belfast BT9 5AG, U.K.
This study developed a green mechanochemical method to create calcium oxide-cerium oxide (CaO-CeO2) catalysts for converting glycerol waste into valuable glycerol carbonate. The optimized catalyst achieved 95% conversion, enhancing biorefinery circularity and sustainability.
Area of Science:
- Catalysis
- Materials Science
- Green Chemistry
Background:
- Biorefinery waste, like glycerol, requires upgrading for sustainability and circular economy.
- Glycerol carbonate is a valuable product with applications in fuel additives and chemical synthesis.
- Developing efficient and sustainable catalytic processes is crucial for biorefinery valorization.
Purpose of the Study:
- To explore the catalytic conversion of glycerol into glycerol carbonate using calcium oxide-cerium oxide (CaO-CeO2) dual-function catalytic materials.
- To develop a clean, efficient, and solvent-free synthesis method for glycerol carbonate.
- To enhance the circular economy and reduce the carbon footprint of biorefineries.
Main Methods:
- Synthesis of CaO-CeO2 catalysts via a green mechanochemical method.
- Comprehensive catalyst characterization using XRD, FTIR, ICP, N2 sorption, CO2-TPD, and SEM/EDS.
- Evaluation of catalytic activity in the solvent-free transesterification of glycerol with dimethyl carbonate (DMC).
Main Results:
- The 40 wt% CaO-CeO2 catalyst demonstrated superior performance, achieving 95% glycerol conversion and 99% selectivity to glycerol carbonate.
- Optimized conditions included 10 wt% catalyst loading, 90 °C, 60 min reaction time, and a glycerol/DMC molar ratio of 1:3.
- The catalyst exhibited excellent reusability over four cycles, maintaining high conversion rates.
- Reaction kinetics followed irreversible second-order kinetics with an activation energy of 46.9 kJ mol-1.
Conclusions:
- A highly efficient, cost-effective, and environmentally friendly approach for sustainable glycerol carbonate production from glycerol was developed.
- The synergistic interaction between CaO and CeO2 at the interface significantly enhances catalytic activity.
- This method contributes to the valorization of biorefinery waste, promoting a circular economy and net-zero goals.
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