Catalytic Properties of Hierarchical Ti-MFI Zeolites in the Synthesis of Cyclic Carbonates from Styrene Under CO2 Pressure
DOI:
https://doi.org/10.24959/ophcj.26.360726Keywords:
styrene, cyclic carbonate, styrene oxide, hierarchical zeolites, titanosilicatesAbstract
Hierarchical titanosilicate zeolites of the MFI structural type (zeolites with the MFI framework topology according to the classification of the International Zeolite Association) showed a high catalytic activity in the synthesis of cyclic carbonate from styrene in the presence of tert-butyl hydroperoxide as an oxidant. It has been shown that the combination of the redox properties of titanium centers with the acid-base characteristics of the zeolite matrix ensures the efficient implementation of the tandem process within a single reaction medium. The results obtained confirm the potential of titanium-containing zeolites as an effective platform for creating heterogeneous catalysts for the direct conversion of olefins into cyclic carbonates.
Supporting Agency
- The author received no specific funding for this work.
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References
- Aresta, M.; Dibenedetto, A. Utilisation of CO2 as a chemical feedstock: opportunities and challenges. Dalton Trans. 2007, 28, 2975–2992. https://doi.org/10.1039/B700658F.
|
|
- Quadrelli, E. A.; Centi, G.; Duplan, J.-L.; Perathoner, S. Carbon Dioxide Recycling: Emerging Large-Scale Technologies with Industrial Potential. ChemSusChem 2011, 4 (9), 1194–1215. https://doi.org/10.1002/cssc.201100473.
|
|
- Sakakura, T.; Choi, J.-C.; Yasuda, H. Transformation of Carbon Dioxide. Chem. Rev. 2007, 107 (6), 2365–2387. https://doi.org/10.1021/cr068357u.
|
|
- Artz, J.; Müller, T. E.; Thenert, K.; Kleinekorte, J.; Meys, R.; Sternberg, A.; Bardow, A.; Leitner, W. Sustainable Conversion of Carbon Dioxide: An Integrated Review of Catalysis and Life Cycle Assessment. Chem. Rev. 2018, 118 (2), 434–504. https://doi.org/10.1021/acs.chemrev.7b00435.
|
|
- Yu, W.; Maynard, E.; Chiaradia, V.; Arno, M. C.; Dove, A. P. Aliphatic Polycarbonates from Cyclic Carbonate Monomers and Their Application as Biomaterials. Chem. Rev. 2021, 121 (18), 10865–10907. https://doi.org/10.1021/acs.chemrev.0c00883.
|
|
- Watanabe, Y.; Takaoka, S.; Haga, Y.; Kishi, K.; Hakozaki, S.; Narumi, A.; Kato, T.; Tanaka, M.; Fukushima, K. Organic carboxylate salt-enabled alternative synthetic routes for bio-functional cyclic carbonates and aliphatic polycarbonates. Polymer Chemistry 2022, 13 (36), 5193–5199. https://doi.org/10.1039/D2PY00705C.
|
- Rokicki, G.; Parzuchowski, P. G.; Mazurek, M. Non-isocyanate polyurethanes: synthesis, properties, and applications. Polym. Adv. Technol. 2015, 26 (7), 707–761. https://doi.org/10.1002/pat.3522.
|
- Xu, K. Electrolytes and Interphases in Li-Ion Batteries and Beyond. Chem. Rev. 2014, 114 (23), 11503–11618. https://doi.org/10.1021/cr500003w.
|
|
- Schäffner, B.; Schäffner, F.; Verevkin, S. P.; Börner, A. Organic Carbonates as Solvents in Synthesis and Catalysis. Chem. Rev. 2010, 110 (8), 4554–4581. https://doi.org/10.1021/cr900393d.
|
|
- Clegg, W.; Harrington, R. W.; North, M.; Pizzato, F.; Villuendas, P. Cyclic carbonates as sustainable solvents for proline-catalysed aldol reactions. Tetrahedron: Asymmetry 2010, 21 (9), 1262–1271. https://doi.org/10.1016/j.tetasy.2010.03.051.
|
- Shaikh, A.-A. G.; Sivaram, S. Organic Carbonates. Chem. Rev. 1996, 96 (3), 951–976. https://doi.org/10.1021/cr950067i
|
|
- North, M.; Pasquale, R.; Young, C. Synthesis of cyclic carbonates from epoxides and CO2. Green Chem. 2010, 12 (9), 1514–1539. https://doi.org/10.1039/C0GC00065E.
|
- Mishra, V.; Peter, S. C. A comprehensive overview of the catalytic pathway for CO2 utilization with epoxide to cyclic carbonate. Chem Catalysis 2024, 4 (1). https://doi.org/10.1016/j.checat.2023.100796.
|
- Zhang, S.; Xia, Z.; Zou, Y.; Cao, F.; Liu, Y.; Ma, Y.; Qu, Y. Interfacial Frustrated Lewis Pairs of CeO2 Activate CO2 for Selective Tandem Transformation of Olefins and CO2 into Cyclic Carbonates. Journal of the American Chemical Society 2019, 141 (29), 11353–11357. https://doi.org/10.1021/jacs.9b03217.
|
|
- Calmanti, R.; Selva, M.; Perosa, A. Tandem catalysis: one-pot synthesis of cyclic organic carbonates from olefins and carbon dioxide. Green Chem. 2021, 23 (5), 1921–1941. https://doi.org/10.1039/D0GC04168H.
|
- Wang, L.; Que, S.; Ding, Z.; Vessally, E. Oxidative carboxylation of olefins with CO2: environmentally benign access to five-membered cyclic carbonates. RSC Adv. 2020, 10 (15), 9103–9115. https://doi.org/10.1039/C9RA10755J.
|
|
- Honda, M.; Tamura, M.; Nakao, K.; Suzuki, K.; Nakagawa, Y.; Tomishige, K. Direct Cyclic Carbonate Synthesis from CO2 and Diol over Carboxylation/Hydration Cascade Catalyst of CeO2 with 2-Cyanopyridine. ACS Catalysis 2014, 4 (6), 1893–1896. https://doi.org/10.1021/cs500301d.
|
- Tamura, M.; Honda, M.; Nakagawa, Y.; Tomishige, K. Direct conversion of CO2 with diols, aminoalcohols and diamines to cyclic carbonates, cyclic carbamates and cyclic ureas using heterogeneous catalysts. Journal of Chemical Technology & Biotechnology 2014, 89 (1), 19–33. https://doi.org/10.1002/jctb.4209.
|
- Na, K.; Jo, C.; Kim, J.; Ahn, W.-S.; Ryoo, R. MFI Titanosilicate Nanosheets with Single-Unit-Cell Thickness as an Oxidation Catalyst Using Peroxides. ACS Catalysis 2011, 1 (8), 901–907. https://doi.org/10.1021/cs2002143.
|
- Přech, J.; Eliášová, P.; Aldhayan, D.; Kubů, M. Epoxidation of bulky organic molecules over pillared titanosilicates. Catal. Today 2015, 243, 134–140. https://doi.org/10.1016/j.cattod.2014.07.002.
|
- Choi, M.; Na, K.; Kim, J.; Sakamoto, Y.; Terasaki, O.; Ryoo, R. Stable single-unit-cell nanosheets of zeolite MFI as active and long-lived catalysts. Nature 2009, 461 (7261), 246–249. https://doi.org/10.1038/nature08288.
|
|
- Lippens, B. C.; de Boer, J. H. Studies on pore systems in catalysts: V. The t method. J. Catal. 1965, 4 (3), 319–323. https://doi.org/10.1016/0021-9517(65)90307-6.
- Barrett, E. P.; Joyner, L. G.; Halenda, P. P. The Determination of Pore Volume and Area Distributions in Porous Substances. I. Computations from Nitrogen Isotherms. Journal of the American Chemical Society 1951, 73 (1), 373–380. https://doi.org/10.1021/ja01145a126.
- Kubelka, P. New Contributions to the Optics of Intensely Light-Scattering Materials. Part I. J. Opt. Soc. Am. 1948, 38 (5), 448–457. https://doi.org/10.1364/JOSA.38.000448.
|
|
- Emeis, C. A. Determination of Integrated Molar Extinction Coefficients for Infrared Absorption Bands of Pyridine Adsorbed on Solid Acid Catalysts. J. Catal. 1993, 141 (2), 347–354. https://doi.org/10.1006/jcat.1993.1145.
|
- Zhang, W.; Fröba, M.; Wang, J.; Tanev, P. T.; Wong, J.; Pinnavaia, T. J. Mesoporous Titanosilicate Molecular Sieves Prepared at Ambient Temperature by Electrostatic (S+I-, S+X-I+) and Neutral (S°I°) Assembly Pathways: A Comparison of Physical Properties and Catalytic Activity for Peroxide Oxidations. Journal of the American Chemical Society 1996, 118 (38), 9164–9171. https://doi.org/10.1021/ja960594z.
|
- Liu, C.; Huang, J.; Sun, D.; Zhou, Y.; Jing, X.; Du, M.; Wang, H.; Li, Q. Anatase type extra-framework titanium in TS-1: A vital factor influencing the catalytic activity toward styrene epoxidation. Applied Catalysis A: General 2013, 459, 1–7. https://doi.org/10.1016/j.apcata.2013.03.013.
|
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