Non-aqueous potentiometry using zeolites.

Potentiometric investigations using pressed zeolite discs are reported. Potential measurements have been performed in non-aqueous solutions--this is the first report, to our knowledge, of potentiometric detection of ions in non-aqueous media with zeolite materials. Nernstian behaviour is also displayed in aqueous solutions for ions that are only able to penetrate a fraction of the internal volume of the zeolite employed.     

Solvate-supported proton transport in zeolites.

Solvate-supported proton transport in zeolite H-ZSM-5 was studied by means of complex impedance spectroscopy. The zeolite shows enhanced proton mobility in the presence of NH3 and H2O that depends on the concentration of the solvate molecule, temperature (298-773 K), and the SiO2/Al2O3 ratio of the zeolite (30-1000). In general, proton conductivity in H-ZSM-5 is most effectively supported in the presence of NH3 and H2O at high concentrations, low temperatures, and low SiO2/Al2O3 ratios (< or = 80). For the aluminum-rich samples desorption measurements reflect different transport mechanisms that depend on the respective temperature range. Up to about 393 K a Grotthus-like proton transport mechanism is assumed, whereas at higher temperatures (393-473 K) vehiclelike transport seems to dominate. The activation energies for NH4+ and H3O+ vehicle conductivity depend on the SiO2/Al2O3 ratio, and the values are in the range of 49-59 and 39-49 kJ mol-1, respectively, and thus significantly lower than those for "pure" proton conduction in solvate-free samples.     

Heck reaction catalyzed by PD-modified zeolites.

[Pd]-exchanged NaY zeolites have been prepared, characterized, and applied for the first time for catalytic carbon-carbon coupling reactions. The catalysts exhibit a high activity and selectivity toward the Heck reaction of aryl bromides with olefins for small palladium concentrations (< or =0.1 mol % of Pd). The catalysts can easily be separated from the reaction mixture and reused after washing without loss in activity. No limitation to the diffusion of adducts in the zeolite cages was observed (for linear alkenes). The electronic nature of the aryl bromides and the olefins has a dominating effect on the reaction yield and selectivity. The heterogeneous catalysts quantitatively convert all types of all aryl bromide (complete conversion of bromobenzene within 30 min) and activated aryl chlorides under standard reaction conditions. Product form selectivity is observed in the Heck reaction with cyclic olefins.     

Studies on the conversion of isopentane over shape selective zeolites, I. H-ZSM-5 and H-ZSM-11 zeolites

H-ZSM-5 and H-ZSM-11 efficiently catalyze the conversion of isopentane into aromatic hydrocarbons.n-Pentane produces more aromatic hydrocarbons than isopentane, but at low conversion levels (high space velocity) isopentane was about two times more reactive thann-pentane in terms of the first order rate constant for the cracking of the pentane isomers.     

Stabilized zeolites of Y-type. Their adsorption and catalytic properties

The stabilized decationized form of a Y-type zeolite has been prepared by the self-steaming calcination method. The temperature of the stabilization process influenced the nature of the interaction with ethylene.

---

Y . .

     

Flash vacuum pyrolysis over solid catalysts. 1. Pyrazoles over zeolites

Flash vacuum pyrolysis (fvp) reactions of 1H-pyrazole (1), 3,5-dimethylpyrazole (2), and 3,5-diphenylpyrazole (3) were carried out over zeolites. Reactions were performed using ZCOY-7, NH(4)-Y, and Na-Y zeolites. Reaction temperatures of heterogeneous reactions were lower than the corresponding temperatures in the homogeneous system, showing a catalytic effect of the zeolites. Compounds 1-3 afforded nitrogen extrusion in homogeneous fvp reactions while in the heterogeneous ones different reactions were present. Compounds 1 and 2 also afforded nitrogen extrusion; products arising from ring fragmentation were found in reactions of 2 and 3 while an isomeric imidazole was isolated in reactions of 3. Isomerization of 3 is attributed to a transition-state selectivity by the catalyst due to the relation between the size of the molecule and the cavity of the zeolite. This isomerization reaction was present only when zeolites with active Br?nsted sites were used.     

Isomerization of dimethylnaphthalenes over zeolites

A dimethylnaphthalene (DMN) isomer mixture from a reforming unit was reacted at 350°C and atmospheric pressure over H-mordenites (Si/Al ranging from 5 to 100), a partially decationated NaY (Si/Al=2.4) and a slightly dealuminated HY (Si/Al=5), with the aim of increasing the 2,6- and 2,7-DMN content by isomerization. The best results were obtained on H-mordenite with Si/Al=10, where shape selective effects made possible to double the amount of the valuable isomers while limiting to a negligible extent the side reactions of disproportionation and dealkylation.     

Intracrystalline diffusion in zeolites

Conclusions A technique for measuring diffusion coefficients for rapid sorption processes has been proposed and applied for studying intracrystalline mass transfer in zeolites.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 6, pp. 1217–1219, June, 1981.     

Adsorption characteristics of some zeolites

Attempts have been made to correlate the Si/Al atom ratio, the degree of crystallinity, crystallite dimensions and the mean diameter of crystalline particles with the relative adsorption affinity index (RAI). Differences in molecular sieving effect and in some diffusional aspects between traditional zeolites and the new shape-selective ZSM are revealed by the adsorption characteristics of cyclohexane, benzene, toluene, neopentane and xylenes.

---

Si/Al , , , (RAI). - ZSM , , , .

     

Confined space synthesis. A novel route to nanosized zeolites

Confined space synthesis is a novel method in zeolite synthesis. It involves crystallization of the zeolite inside the pore system of an inert mesoporous matrix. In this way it is possible to prepare nanosized zeolites with a controlled size distribution by proper choice of the inert matrix. Here, confined space synthesis was adopted to prepare nanosized ZSM-5, zeolite Beta, zeolite X, and zeolite A with tailored crystal size distributions using mesoporous carbon blacks as inert matrices. All zeolites were characterized by X-ray powder diffraction, transmission electron microscopy, and nitrogen adsorption/desorption prior to and after removal of the carbon matrix. ZSM-5 with Si/Al ratios of 50, 100, and infinity (silicalite-1) were synthesized with controlled average crystal sizes in the range 20-75 nm. Nanosized zeolite Beta (7-30 nm), zeolite X (22-60 nm), and zeolite A (25-37 nm) were prepared similarly. Removal of the carbon matrix by controlled combustion allows a convenient method for isolation of the pure and highly crystalline zeolites. Therefore, confined space synthesis appears to be an attractive method for preparation of zeolites with a controlled size distribution.     

Spectroscopic signatures of nitrogen-substituted zeolites

Nanoporous acid catalysts such as zeolites form the backbone of catalytic technologies for refining petroleum. With the promise of a biomass economy, new catalyst systems will have to be discovered, making shape-selective base catalysts especially important because of the high oxygen content in biomass-derived feedstocks. Strongly basic zeolites are attractive candidates, but such materials are notoriously difficult to make due to the strong inherent acidity of aluminosilicates. Several research groups have endeavored to produce strongly basic zeolites by treating zeolites with amines, but to date there is no compelling evidence that nitrogen is incorporated into zeolite frameworks. In this communication, we detail synthesis, NMR spectroscopy, and quantum mechanical calculations showing that nitrogen adds onto both surface and interior sites while preserving the framework structure of zeolites. This finding is crucial for the rational design of new biomass-refinement catalysts, allowing 50 years of zeolite science to be brought to bear on the catalytic synthesis of biofuels.     

FTIR characterization of metal-loaded zeolites

FTIR transmission spectra of self-supporting zeolite wafers of Na₁₂A (Linde 4A), Na_3.6Ca_4.2A (Linde 5A) and Ag_11.8Na_0.2A in the range of 20 to 13 500 cm^–1 are reported. Reduction of Ag⁺ by H₂ is probed directly in the FAR IR and indirectly by adsorption of CO and CO₂.     

Thermal analysis of NaMgA zeolites

Water desorption from NaMgA zeolites was investigated as a function of magnesium ion content with the help of thermal analytical methods such as combined TG-DTG-DTA, TMA and X-ray heating technique. At least five partly overlapping desorption effects of water were observed from DTA and DTG features. The amount of water corresponding to individual desorption peaks was determined by experimental methods of separation. An assignment of the desorption effects to the related adsorbed forms of water is suggested.     

Raman spectroscopy on zeolites

The zeolite Raman literature is reviewed, with an emphasis on zeolite structure and synthesis, adsorption and metal complex formation in zeolites