This report embodies recommendations on zeolite nomenclature approved by the International Mineralogical Association, Commission on New Minerals and Mineral Names. In a working definition of a zeolite mineral used for this review, structures containing an interrupted framework of tetrahedra are accepted where other zeolitic properties prevail, and complete substitution by elements other than Si and Al is allowed. Separate species are recognized in topologically distinctive compositional series in which different extra-framework cations are the most abundant in atomic proportions. To name these, the appropriate chemical symbol is attached by a hyphen to the series name as a suffix, except for the names harmotome, pollucite and wairakite in the phillipsite and analcime series. Differences in space-group symmetry and in order-disorder relationships in zeolites having the same topologically distinctive framework do not in general provide adequate grounds for recognition of separate species. Zeolite species are not to be distinguished solely on the ratio Si : Al except for heulandite (Si : Al < 4.0) and clinoptilolite (Si : Al ≥ 4.0). Dehydration, partial hydration, and overhydration are not sufficient grounds for the recognition of separate species of zeolites. Use of the term "ideal formula" should be avoided in referring to a simplified or averaged formula of a zeolite. Newly recognized species in compositional series are as follows: brewsterite-Sr, -Ba, chabazite-Ca, -Na, -K, clinoptilolite-K, -Na, -Ca, dachiardite-Ca, -Na, erionite-Na, -K, -Ca, faujasite-Na, -Ca, -Mg, ferrierite-Mg, -K, -Na, gmelinite-Na, -Ca, -K, heulandite-Ca, -Na, -K, -Sr, levyne-Ca, -Na, paulingite-K, -Ca, phillipsite-Na, -Ca, -K, and stilbite-Ca, -Na. Key references, type locality, origin of name, chemical data, IZA structure-type symbols, space-group symmetry, unit-cell dimensions, and comments on structure are listed for 13 compositional series, 82 accepted zeolite mineral species, and three of doubtful status. Herschelite, leonhardite, svetlozarite, and wellsite are discredited as mineral species names. Obsolete and discredited names are listed.Keywords: zeolite nomenclature, herschelite, leonhardite, svetlozarite, wellsite, brewsterite, chabazite, clinoptilolite, dachiardite, erionite, faujasite, ferrierite, gmelinite, heulandite, levyne, paulingite, phillipsite, stilbite. SOMMAIRECe rapport contient les recommandations à propos de la nomenclature des zéolites, telles qu'approuvées par l'Association minéralogique internationale, commission des nouveaux minéraux et des noms de minéraux. Dans la définition d'une zéolite retenue ici, les structures contenant une trame interrompue de tétraèdres sont acceptées dans les cas où les autres propriétés satisfont les critères de cette famille de minéraux. De plus, il peut y avoir remplacement complet de Si et Al par d'autres éléments. Des espèces distinctes font partie de séries de compositions dont l'agencement topologique est le même, le cation dominant ne faisant pas partie de la trame ...

This report embodies recommendations on zeolite nomenclature approved by the International Mineralogical Association Commission on New Minerals and Mineral Names. In a working definition of a zeolite mineral used for this review, interrupted tetrahedral framework structures are accepted where other zeolitic properties prevail, and complete substitution by elements other than Si and Al is allowed. Separate species are recognized in topologically distinctive compositional series in which different extra-framework cations are the most abundant in atomic proportions. To name these, the appropriate chemical symbol is attached by a hyphen to the series name as a suffix except for the names harmotome, pollucite and wairakite in the phillipsite and analcime series. Differences in space-group symmetry and in order-disorder relationships in zeolites having the same topologically distinctive framework do not in general provide adequate grounds for recognition of separate species. Zeolite species are not to be distinguished solely on Si : Al ratio except for the heulandite (Si : Al < 4.0) and clinoptilolite (Si : Al ≥ 4.0) series. Dehydration, partial hydration, and over-hydration are not sufficient grounds for the recognition of separate species of zeolites. Use of the term "ideal formula" should be avoided in referring to a simplified or averaged formula of a zeolite. Newly recognized species in compositional series are as follows:

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A tough challenge in nanomaterials chemistry is the determination of the structure of multicomponent nanosystems. Dye-zeolite L composites are building blocks of hierarchically organized multifunctional materials for technological applications. Supramolecular organization inside zeolite L nanochannels, which governs electronic properties, is barely understood. This is especially true for confined close-packed dye molecules, a regime not investigated in applications yet and that might have great potential for future development in this field. Here we realize for the first time composites of zeolite L with maximally-packed fluorenone molecules and elucidate their structure by integrated multi-technique analyses. By IR, thermogravimetric and X-ray diffraction we establish the maximum degree of dye loading obtained (1.5 molecules per unit cell) and by modeling we reveal that at these conditions fluorenone molecules form quasi 1-D supramolecular nanoladders running along the zeolite channels. Spatial and morphological control provided by the nanoporous matrix combined with a complex blend of strong dye-zeolite and weaker dye-dye van der Walls interactions lie at the origin of this unique architecture, which is also stabilized by the hydrogen bond network of co-adsorbed water molecules surrounding the dye nanoladder and penetrating between its rungs.

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The static and dynamical properties of one-dimensional water chains confined in zeolitic channels are studied by means of the Car Parrinello method. The properties of such an unusual water structure, present in zeolites Li−ABW and bikitaite, are reported and compared. Differences in the zeolitic frameworks are responsible for the different properties of the water chains. A more rigid chain structure is found in bikitaite, whereas our calculations predict that in Li−ABW water molecules are allowed some rotational degrees of freedom. We interpret such a finding on the basis of the different strengths of host−guest dipolar interactions. Weaker interactions in Li−ABW allow for rotation of water molecules.