Abstract
Microporous structures not only continue to raise great scientific interest, but, in addition, several representatives bear high technical importance and have commercial value as functional materials. Their functionality depends on both, particular features of their structure and their actual chemical composition. Many micro-porous structure types with a wide variety of chemical compositions are currently known, and new ones are discovered in short intervals, see (Baerlocher and McCusker, http://www.iza-structure.org/databases/). Various experimental parameters are at the disposal of the experimentalist when he attempts to find synthesis methods for the preparation of materials with new topological or geometrical features, e.g. heteropolyhedral topology, larger pores, wider rings, ... or having superior physical or chemical properties. An obvious strategy to follow is variation of the chemical composition. A particular case which is in the focus of the present contribution is constituted by the aluminosilicate frameworks, i.e. three-dimensional frameworks built from corner-connected [SiO4]- and [AlO4]-tetrahedra. The development in this field has been given impetus by real technical demands. Many natural, and also many as-synthesized, aluminosilicate zeolites have a Si:Al ratio close to 1. However, one of the most important technical applications of zeolites is their use as catalysts in crude oil refining. The underlying chemical processes necessitate high degrees of thermal stability, hydrophobicity and resistivity to low pH. This can be achieved by pushing the Si:Al ratio to values much higher than 1.0, up to the compositions of highly siliceous or even pure silica zeolites.
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References
Baerlocher Ch, McCusker LB Database of Zeolite Structures: http://www.iza-structure.org/databases/
Baur WH (1992) Self-limiting distortion by antirotating hinges is the principle of flexible but noncollapsible frameworks. J Solid State Chem 97:243–247
Baur WH (1995) Why the open framework of zeolite A does not collapse, while the dense framework of natrolite is collapsible. In: Rozwadowski M (ed) Proceedings of the 2nd Polish-German Zeolite Colloquim. Nicholas Copernicus University Press, Toruń, pp 171–185
Bosenick A, Dove MT, Myers ER, Palin EJ, Sainz-Diaz CI, Guiton BS, Warren MC, Craig MS, Redfern SAT (2001) Computational methods for the study of energies of cation distributions: applications to cation-ordering phase transitions and solid solutions. Mineral Mag 65:193–219
Dent Glasser LS, Henderson AP, Howie RA (1982) Refinement of the structure of a framework aluminate. Acta Crystallogr B38:24–27
Depmeier W (1988a) Structure of cubic aluminate sodalite Ca8[Al12O24](WO4) in comparison with its orthorhombic phase and with cubic Sr8[Al12O24](CrO4). Acta Crystallogr B44:204–207
Depmeier W (1988b) Aluminate Sodalites-A family with strained structures and ferroic phase transitions. Phys Chem Miner 15:419–426
Dove MT, Cool T, Palmer DC, Putnis A, Salje EKH, Winkler B (1993) On the role of Al-Si ordering in the cubic-tetragonal phase transition of leucite. Am Mineral 78:486–492
Dove MT, Heine V, Hammonds KD (1995) Rigid unit modes in framework silicates. Mineral Mag 59:629–639
Dove MT, Thayaparam S, Heine V, Hammonds KD (1996) The phenomenon of low Al-Si ordering temperatures in aluminosilicate framework structures. Am Mineral 81:349–362
Gupta AK, Chatterjee ND (1978) Synthesis, composition, thermal stability, and thermodynamic properties of bicchulite, Ca2[Al2SiO6](OH)2. Am Mineral 63:58–65
Höche T (2004) Incommensurate structural modulations in fresnoite framework structures. Habilitation Thesis, University of Leipzig
Jones JB (1968) Al-O and Si-O Tetrahedral distances in aluminosilicate framework structures. Acta Crystallogr B 24:355–358
Loewenstein W (1954) The distribution of aluminium in the tetrahedra of silicates and aluminates. Am Mineral 39:92–98
McCusker LB, Baerlocher Ch (1984) The effect of dehydration upon the crystal structure of zeolite rho. Proceedings of the 6th International Zeolite Conference 812–822
Meier WM (1960) The crystal structure of natrolite. Zeitschrift fuer Kristallographie 113:430–444
Myers ER, Heine V, Dove MT (1998) Thermodynamics of Al/Al avoidance in the ordering of Al/Si tetrahedral framework structures. Phys Chem Miner 25:457–464
Peters L (2005) Gekoppelte Substitutionen im Melilith-und Sodalith-Strukturtyp. PhD Thesis, University of Kiel, http://e-diss.uni-kiel.de/diss 1519/
Peters L, Knorr K, Knapp M, Depmeier W(2005) Thermal expansion of gehlenite, Ca2Al[AlSiO7], and the related aluminates LnCaAl[Al2O7] with Ln = Tb, Sm. Phys Chem Miner 32:460–465
Peters L, Knorr K, Depmeier W (2006a) Structural variations in the solid-solution series LnxCa2−x Al[Al1+x Si1−x O7], with 0 ≤ x ≤ 1 and Ln = La, Eu, Er. Z Anorg Allg Chem 632:301–306
Peters L, Knorr K, Fechtelkord M, Appel P, Depmeier W (2006b) Structural variations in the solid solution series of sodalite-type |(EuxCa2−x )4(OH)8|[(Al2+x Si1−x )4O24]-SOD with Δx = 0.125, determined by X-ray powder diffraction and 27Al MAS NMR spectroscopy. Z Kristallogr 221:643–648
Peters L, Knorr K, Katzke H, Knapp M, Depmeier W (2006c) The transformation mechanism of the sodalite-to the melilite-topology: Thermal expansion and decomposition of bicchulite-type to melilite-type compounds. Z Kristallogr 221:198–205
Rietveld H (1967) Line profiles of neutron powder-diffraction peaks for structure refinements. Acta Crystallogr 22:151–152
Roth G, Pentinghaus H, Wanklyn BM (1989) Eine neue Variante in der Sodalith-Strukturfamilie: Dy2Al4Si2O12·MoO4, mit dreiwertigen groβen Kationen. Z Kristallogr 186:251–252
Sahl K (1980) Refinement of the crystal structure of bicchulite, Ca2[Al2SiO6](OH)2. Z Kristallogr 152:13–21
Sahl K, Chatterjee ND (1977) The crystal structure of bicchulite, Ca2[Al2SiO6](OH)2. Z Kristallogr 146:35–41
Thayaparam S, Dove MT, Heine V (1994) A Computer simulation study of Al/Si ordering in gehlenite and the paradox of the low transition temperature. Phys Chem Miner 21:110–116
Vegard L, Dale H (1928) Untersuchungen über Mischkristalle und Legierungen. Z Kristallogr 67:148–162
Warren BE (1930) The structure of melilite (Ca,Na)2(Mg,Al)1(Si,Al)2O7. Z Kristallogr 74:131–138
Winkler B, Dove MT, Leslie M (1991) Static lattice energy minimization and lattice dynamics calculations on aluminosilicate minerals. Am Mineral 76:313–331
Winkler B, Milman V, Pickard CJ (2004) Quantum mechanical study of Al/Si disorder in leucite and bicchulite. Mineral Mag 68:819–824
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Peters, L., Rahmoun, NS., Knorr, K., Depmeier, W. (2008). Why Do Super-Aluminous Sodalites and Melilites Exist, but Not so Feldspars?. In: Krivovichev, S.V. (eds) Minerals as Advanced Materials I. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-77123-4_3
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DOI: https://doi.org/10.1007/978-3-540-77123-4_3
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