Zeolite Y-based catalysts for efficient epoxidation of R-(+)-Limonene: Insights into the structure-activity relationship
Parent, hierarchical, and metal-modified hierarchical zeolite Y were investigated as heterogeneous catalysts in the R-(+)-limonene epoxidation, a catalytic route for synthesizing precursors of bio-polycarbonates, an alternative to isocyanate polyurethanes. The fresh catalysts underwent detailed char...
- Autores:
-
Gallego Villada, Luis Alfonso
Alarcón Durango, Edwin Alexis
Mäki-Arvela, Päivi
Kumar, Narendra
Vajglová, Zuzana
Tirri, Teija
Angervo, Ilari
Lassfolk, Robert
Lastusaari, Mika
Murzin, Dmitry Yu
- Tipo de recurso:
- Article of investigation
- Fecha de publicación:
- 2024
- Institución:
- Universidad de Antioquia
- Repositorio:
- Repositorio UdeA
- Idioma:
- eng
- OAI Identifier:
- oai:bibliotecadigital.udea.edu.co:10495/46668
- Acceso en línea:
- https://hdl.handle.net/10495/46668
- Palabra clave:
- Limoneno
Limonene
Zeolitas
Zeolites
Catalizadores
Catalysts
https://id.nlm.nih.gov/mesh/D000077222
- Rights
- openAccess
- License
- http://creativecommons.org/licenses/by/4.0/
| Summary: | Parent, hierarchical, and metal-modified hierarchical zeolite Y were investigated as heterogeneous catalysts in the R-(+)-limonene epoxidation, a catalytic route for synthesizing precursors of bio-polycarbonates, an alternative to isocyanate polyurethanes. The fresh catalysts underwent detailed characterization using XRD, N2 physisorption, TEM, SEM-EDX, pyridine-FTIR, NH3-TPD, CO2-TPD, UV–Vis-DRS, and solid-state NMR. Spent materials were investigated by TPO-MS and TGA, confirming low coke formation on the catalytic surface. The most active material was K–Sn-modified dealuminated zeolite Y, reflected in a high turnover frequency (TOF) of 96 h−1. This material exhibited the lowest Brønsted to Lewis acidity ratio (0.1), the highest mesoporosity fraction (43%), and the lowest total surface area (465 m2 g−1). Aprotic polar solvents with high polarity and medium donor capacity appeared suitable for limonene epoxidation. Limonene conversion of ca. 97% was reached at 70 °C, H2O2: limonene molar ratio = 7, and acetonitrile as a solvent, while selectivity to total monoepoxides exhibited values up to 96% under different reaction conditions. Hydration of internal epoxides to limonene diol was favored at high temperatures and high H2O2/limonene molar ratios. The efficiency of H2O2 reached maximum values of about 85% at low H2O2 amounts, while no significant influence was observed for temperature, catalyst amount, and the initial concentration of limonene. A plausible reaction mechanism was proposed for the R-(+)-limonene epoxidation with H2O2 based on the experimental findings. |
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