A titanosilicate molecular sieve with adjustable pores for size-selective adsorption of molecules
Steven M. Kuznicki (),
Valerie A. Bell,
Sankar Nair,
Hugh W. Hillhouse,
Richard M. Jacubinas,
Carola M. Braunbarth,
Brian H. Toby and
Michael Tsapatsis
Additional contact information
Steven M. Kuznicki: Strategic Technology Group, Engelhard Corporation
Valerie A. Bell: Strategic Technology Group, Engelhard Corporation
Sankar Nair: 159 Goessmann Laboratory, University of Massachusetts
Hugh W. Hillhouse: 159 Goessmann Laboratory, University of Massachusetts
Richard M. Jacubinas: Strategic Technology Group, Engelhard Corporation
Carola M. Braunbarth: 159 Goessmann Laboratory, University of Massachusetts
Brian H. Toby: NIST Center for Neutron Research, National Institute of Standards and Technology
Michael Tsapatsis: 159 Goessmann Laboratory, University of Massachusetts
Nature, 2001, vol. 412, issue 6848, 720-724
Abstract:
Abstract Zeolites and related crystalline microporous oxides—tetrahedrally coordinated atoms covalently linked into a porous framework—are of interest for applications ranging from catalysis to adsorption and ion-exchange1. In some of these materials (such as zeolite rho) adsorbates2, ion-exchange, and dehydration and cation relocation3,4 can induce strong framework deformations. Similar framework flexibility has to date not been seen in mixed octahedral/tetrahedral microporous framework materials, a newer and rapidly expanding class of molecular sieves5,6,7,8,9,10,11,12,13,14,15,16. Here we show that the framework of the titanium silicate ETS-4, the first member of this class of materials8, can be systematically contracted through dehydration at elevated temperatures to ‘tune’ the effective size of the pores giving access to the interior of the crystal. We show that this so-called ‘molecular gate’ effect can be used to tailor the adsorption properties of the materials to give size-selective adsorbents17 suitable for commercially important separations of gas mixtures of molecules with similar size in the 4.0 to 3.0 Å range, such as that of N2/CH4, Ar/O2 and N2/O2.
Date: 2001
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DOI: 10.1038/35089052
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