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