Highly mesoporous single-crystalline zeolite beta synthesized using a nonsurfactant cationic polymer as a dual-function template
Rigutto, Marcello S.
Van Der Made, Alexander W.
KAUST DepartmentAdvanced Membranes and Porous Materials Research Center
Chemical Science Program
Nanostructured Functional Materials (NFM) laboratory
Physical Science and Engineering (PSE) Division
Online Publication Date2014-02-04
Print Publication Date2014-02-12
Permanent link to this recordhttp://hdl.handle.net/10754/563391
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AbstractMesoporous zeolites are useful solid catalysts for conversion of bulky molecules because they offer fast mass transfer along with size and shape selectivity. We report here the successful synthesis of mesoporous aluminosilicate zeolite Beta from a commercial cationic polymer that acts as a dual-function template to generate zeolitic micropores and mesopores simultaneously. This is the first demonstration of a single nonsurfactant polymer acting as such a template. Using high-resolution electron microscopy and tomography, we discovered that the resulting material (Beta-MS) has abundant and highly interconnected mesopores. More importantly, we demonstrated using a three-dimensional electron diffraction technique that each Beta-MS particle is a single crystal, whereas most previously reported mesoporous zeolites are comprised of nanosized zeolitic grains with random orientations. The use of nonsurfactant templates is essential to gaining single-crystalline mesoporous zeolites. The single-crystalline nature endows Beta-MS with better hydrothermal stability compared with surfactant-derived mesoporous zeolite Beta. Beta-MS also exhibited remarkably higher catalytic activity than did conventional zeolite Beta in acid-catalyzed reactions involving large molecules. © 2014 American Chemical Society.
CitationZhu, J., Zhu, Y., Zhu, L., Rigutto, M., van der Made, A., Yang, C., … Xiao, F.-S. (2014). Highly Mesoporous Single-Crystalline Zeolite Beta Synthesized Using a Nonsurfactant Cationic Polymer as a Dual-Function Template. Journal of the American Chemical Society, 136(6), 2503–2510. doi:10.1021/ja411117y
SponsorsThis research was supported by the National Natural Science Foundation of China (Grants 11227403, 21201076, 91022030, 21333009), Fundamental Research Funds for the Central Universities (2013XZZX001), Shell Company, and the Competitive Research Grant to Y.H. from King Abdullah University of Science and Technology. Y.H.Z. is supported by the Sabic Post-doc Fellowship.
PublisherAmerican Chemical Society (ACS)