Role of Cation–Water Disorder during Cation Exchange in Small-Pore Zeolite Sodium Natrolite

Abstract

By combining X-ray diffraction with oxygen K-edge absorption spectroscopy we track changes occurring during the K<sup>+</sup>–Na<sup>+</sup> cation exchange of Na-natrolite (Na-NAT) as tightly bonded Na<sup>+</sup> cations and H<sub>2</sub>O molecules convert into a disordered K<sup>+</sup>–H<sub>2</sub>O substructure and the unit cell expands by ca. 10% after 50% cation exchange. The coordination of the confined H<sub>2</sub>O and nonframework cations change from a tetrahedral configuration, similar in ice <i>I</i><sub><i>h</i></sub>, with Na<sup>+</sup> near the middle of the channels in Na-NAT to two-bonded configuration, similar in bulk water, and K<sup>+</sup> located near the walls of the framework in K-NAT. This is related to the enhanced ion-exchange properties of K-NAT, which, in marked contrast to Na-NAT, permits the exchange of K<sup>+</sup> by a variety of uni-, di-, and trivalent cations

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