Efficient co-templating roles of amines and amides admixed with alkylammonium salts for the stabilisation of new AlPO4-n topologies

Two different aluminophosphate structures were synthesised in aqueous media using as main template methylamine (MA), directly added, or generated in situ from methylformamide (MF). Both involve novel AlPO4-n topologies that undergo structural transformations upon template removal, yielding above 350°C microporous thermostable materials with interesting properties. Tetraalkylammonium (TEA) cations were used optionally as co-templates along with MA. Only non protonated MA was found incorporated into the pore volume of both structures, in relatively strong interaction with the framework oxygens. TEA appeared to stabilise one of the phases at defined stages of nucleation and/or growth processes, without playing any specific structure-directing role

Synthesis, characterization, and catalytic properties of AlPO4-40, CoAPO-40, and ZnAPO-40

The experimental conditions leading to the synthesis of pure and highly crystalline AlPO,-40, CoAPO-40, and ZnAPO-40 have been optimized. Although the preparation of these phases is favored by the presence of TMA+ in the synthesis gel, these ions have not been found incorporated in the final AFR structures. All materials have been characterized by powder XRD, t.g./d.s.c., SEM, EDX, 13C, 27AI, and 3’P solid-state n.m.r., diffuse reflectance u.v.-vis spectroscopy, FTi.r., and catalytic tests using the n-t-xylene isomerization as a model reaction. This multitechnique approach provides strong evidence for the framework incorporation of cobalt and zinc. The acid sites generated by the framework insertion of cobalt and zinc are stronger than those generated by the incorporation of silicon

Disproportionation of ethylbenzene over SAPO-40

SAPO-40 exhibits strong acid sites, which catalyse the reaction of disproportionation of ethylbenzene. The distribution of diethylbenzene isomers suggests a high void volume in the structure of this molecular sieve

Metal-Substituted Microporous Aluminophosphates

This chapter aims to present the zeotypes aluminophosphates (AlPOs) as a complementary alternative to zeolites in the isomorphic incorporation of metal ions within all-inorganic microporous frameworks as well as to discuss didactically the catalytic consequences derived from the distinctive features of both frameworks. It does not intend to be a compilation of either all or the most significant publications involving metal-substituted microporous aluminophosphates. Families of AlPOs and zeolites, which include metal ion-substituted variants, are the dominant microporous materials. Both these systems are widely used as catalysts, in particular through aliovalent metal ions substitution. Here, some general description of the synthesis procedures and characterization techniques of the MeAPOs (metal-contained aluminophosphates) is given along with catalytic properties. Next, some illustrative examples of the catalytic possibilities of MeAPOs as catalysts in the transformation of the organic molecules are given. The oxidation of the hardly activated hydrocarbons has probably been the most successful use of AlPOs doped with the divalent transition metal ions Co2+, Mn2+, and Fe2+, whose incorporation in zeolites is disfavoured. The catalytic role of these MeAPOs is rationalized based on the knowledge acquired from a combination of the most advanced characterization techniques. Finally, the importance of the high specificity of the structure-directing agents employed in the preparation of MeAPOs is discussed taking N,N-methyldicyclohexylamine in the synthesis of AFI-structured materials as a driving force. It is shown how such a high specificity could be predicted and how it can open great possibilities in the control of parameters as critical in catalysis as crystal size, inter-and intracrystalline mesoporosity, acidity, redox properties, incorporation of a great variety of heteroatom ions or final environment of the metal site (surrounding it by either P or Al)