Nanoscale Catalytic Materials by Swelling, Pillaring and Exfoliation of a Zeolite Precursor

Friday, November 21, 2008: 9:15 AM
Room 102-A (Pennsylvania Convention Center)

Sudeep Maheshwari, Department of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, MN
Edgar Jordan, Department of Chemical Engineering, Texas A&M University, College Station, TX
Sandeep Kumar, Department of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, MN
Frank S. Bates, Department of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, MN
R. Lee Penn, Department of Chemistry, University of Minnesota, Minneapolis, MN
Daniel F. Shantz, Department of Chemical Engineering, Texas A&M University, College Station, TX
Michael Tsapatsis, Department of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, MN

The zeolite MCM-22 is formed by calcination of a layered precursor, MCM-22(P)[1]. The layered structure of the precursor allows swelling, pillaring and exfoliation to single layers to produce a host of nanomaterials[2,3]. However, these procedures result in significant degradation of the structure of the layers with partial loss of crystallinity[4,5]. In this work, we describe a modified approach to swell, pillar and exfoliate the MCM-22 layered precursor with improved preservation of crystal morphology and alumino-silicate layer structure. XRD reveals that the swollen derivative evolves to a new ordered layer structure upon washing with water. Solid state NMR spectroscopy indicates preservation of framework connectivity. This ordered material can act as starting material to form inorganic/organic hybrid catalysts with specific guest-host interactions. Interestingly, the swollen derivative can be restored back to the precursor structure by acidification. It can be successfully pillared to produce an MCM-36[2] analogue or exfoliated to produce a high surface area material analogous to ITQ-2[3] but with improved crystallinity. The resulting materials are expected to exhibit distinct catalytic behavior compared to the pre-existing analogues, due to the improved preservation of the pore structure and catalytic sites.

[1] Leonowicz, M. E.; Lawton, J. A.; Lawton, S. L.; Rubin, M. K. , Science, 1994, 264, 1910-13.

[2] Kresge, C. T.; Roth, W. J., US Patent 5278115, 1994.

[3] Corma, A.; Fornes, V.; Pergher, S. B.; Maesen, T. L. M.; Buglass, J. G., Nature, 1998, 396, 353-356.

[4] Schenkel, R.; Barth, J. O.; Kornatowski, J.; Lercher, J. A., Studies in Surface Science and Catalysis, 2002, 142A, 69-76.

[5] Wu, P.; Nuntasri, D.; Ruan, J.; Liu, Y.; He, M.; Fan, W.; Terasaki, O.; Tatsumi, T., Journal of Physical Chemistry B, 2004, 108, 19126-19131.

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