The crystal structures of vacuum-dehydrated, fully Mg 2+ -, Ca 2+ -, and Ba 2+ -exchanged zeolite X (Mg 46 (H 2 O) 4 −X, Ca 46 −X, and Ba 46 −X; X = Si 100 Al 92 O 384 ) have been determined by single-crystal X-ray diffraction techniques in the cubic space group Fd 3̄ at 21 °C ( a = 24.671(5), 25.024(4), and 25.266(5) Å, respectively). Their structures were refined to the final error indices R w = 0.046 with 439 reflections, 0.037 with 434 reflections, and 0.049 with 485 reflections, respectively, for which I > 3σ( I ). In Mg 46 (H 2 O) 4 −X, Mg 2+ ions are found at four crystallographic sites: 14 per unit cell are located at site I at the center of the hexagonal prism (Mg−O = 2.262(6) Å), only four are at site I‘ in the sodalite cavity near the hexagonal prism (Mg−O = 2.221(5) Å), four, each coordinated to an H 2 O molecule, are located at site II‘ in the sodalite cavity (Mg−O = 2.223(12) Å), and the remaining 24 are at site II near single six-oxygen rings in the supercage (Mg−O = 2.184(5) Å). In Ca 46 −X, Ca 2+ ions are found at only two sites: 16 per unit cell fill site I (Ca−O = 2.429(8) Å) and the remaining 30 at site II (Ca−O = 2.276(5) Å). In Ba 46 −X, Ba 2+ ions are again found at three sites: 14.5 per unit cell are at site I (Ba−O = 2.778(11) Å), only 1.5 are at site I‘ (Ba−O = 2.44(3) Å), and 30 are at site II (Ba−O = 2.667(8) Å). In the three crystals, sites I and II are the most populated; sites I‘ and II‘, if they were used, are only sparsely occupied. Ca 2+ appears to fit the octahedral site I best. No cations are found at sites III or III‘, all of which are clearly less favorable for alkaline-earth cations in dehydrated zeolite X.
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Yeom et al. (1997) studied this question.
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