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The relation between the intrinsic mechanism of various N2O conversions over FeMFI catalysts and the nature of the active iron site(s) has been analyzed. To this end, direct N2O decomposition and N2O reduction with CO in the absence or presence of NO were investigated using a combination of transient pulse and steady-state techniques over steam-activated FeMFI zeolites with a similar iron content (0.6–0.7 wt% Fe) and different framework compositions (Si–Al, Si–Ga, Si–Ge, and Si). The forms of iron in the catalysts were characterized by UV/vis and HRTEM. The intrinsic reaction mechanism determines the optimal iron site distribution, which can be modulated by tuning the steaming temperature during activation. Oligonuclear iron oxo clusters in the zeolite channels are essential in direct N2O decomposition due to a faster desorption of O2 as compared to isolated ions. Such forms of active iron can be achieved at a lower steam-activation temperature over FeAlMFI and FeGaMFI (900 K) than over FeGeMFI and FeMFI (1150 K). Contrarily, zeolites with a more uniform distribution of isolated iron species lead to higher activities in N2O reduction with CO as compared to highly clustered catalysts. In this case, O-removal as CO2 is strongly accelerated vis-à-vis O2 desorption in direct N2O decomposition. The dual role of NO as a promotor in N2O decomposition and as an inhibitor in N2O reduction also supports the participation of different sites in both types of conversions. NO selectively inhibits N2O reduction over isolated iron ions, further evidencing the essential role of oligonuclear iron clusters in the NO-assisted N2O decomposition. [Copyright &y& Elsevier]

Steam-activated Fe-zeolites (MFI and BEA) are efficient catalysts for the N2O-mediated oxidative dehydrogenation of propane, with initial propylene yields up to 25% at 723 K, but deactivate as a result of coke formation. A tapered element oscillating microbalance (TEOM) coupled to GC analysis has been applied to correlate activity and deactivation by simultaneous measurements of reaction and coking. The presence of extraframework iron species, generated during steam treatment, is essential for producing active catalysts. The nature and distribution of extraframework iron species, the zeolite host, and the catalyst acidity have no significant effect on the initial propene yield, but strongly influence the deactivation behavior. FeZSM-5 shows a remarkable resistance against deactivation, while a very rapid and complete deactivation occurred in FeBEA. The initial propene yield over FeZSM-5 and FeBEA was remarkably higher than over commercial H-ZSM-5 and H-BEA (with 30–40 times lower iron content), although the residual activities after 400 min on stream were very similar. [Copyright &y& Elsevier]

The reduction of N2O by CO was investigated over FeMFI zeolites prepared by different methods including sublimation, liquid ion exchange, and hydrothermal synthesis followed by steam activation. This leads to catalysts with different nature and distribution of iron species, as characterized by HRTEM, UV/vis, and EPR techniques. A common denominator in the FeZSM-5 samples is the heterogeneous iron constitution, with a significant degree of clustering in the form of iron oxide particles. Iron clustering was suppressed in steam-activated Fe-silicalite, presenting a remarkable uniform distribution of isolated iron species. In the presence of CO, the conversion of N2O over the catalysts is strongly accelerated with respect to direct N2O decomposition. The reaction rate increases linearly with the molar CO/N2O feed ratio and strongly depends on the preparation method applied. A correlation was found between the fraction of isolated Fe(III) species in the as-prepared catalysts and the activity for N2O reduction with CO. Steam-activated Fe-silicalite, containing mostly isolated iron ions in extraframework positions, shows the highest activity per mole of iron, while the highly clustered liquid-ion-exchanged catalyst presents the lowest activity. In situ UV/vis and EPR studies evidence the participation of mononuclear iron ions in the N2O–CO reaction, and also support the involvement of oligonuclear FexOy species. The reaction mechanism is iron site dependent. Over isolated sites, the reduction of N2O with CO occurs via coordinated CO species on Fe3+ ions. The reaction over oligonuclear sites proceeds via a redox Fe3+/Fe2+ process with intermediate formation of O− radicals. [Copyright &y& Elsevier]

Preparation of steam-activated Fe-silicalite containing mainly isolated iron species in extraframework positions was essential for deriving structure-activity relationships in various N2O conversion reactions over iron zeolite catalysts. Characterization by UV–Vis/DRS revealed that any significant clustering of iron did not occur in this sample. Other steam-activated FeMFI zeolites, with different framework compositions or treated at higher temperatures, showed various degrees of clustering. The activity of the cluster-free Fe-silicalite was significantly higher in N2O reduction with C3H8 and CO. However, some level of association of iron species leads to higher activities in direct N2O decomposition. Due to the intrinsic reaction mechanism, this result demonstrates the sensitivity of reactions for the form of the iron species in Fe-zeolites, rather than the existence of a unique active site. [Copyright &y& Elsevier]

[Display omitted] • Prins cyclisation from isovaleraldehyde and isoprenol to tetrahydropyranol. • Zeolites with varying acidity and hierarchical materials as catalysts. • H-Beta-300 zeolite giving 72% selectivity to the desired product at 99% conversion. • The cis/trans ratio of tetrahydropyranols depends on porous structure. • Parallel formation of tetrahydropyranol and dihydropyran confirmed by DFT. In this work, several heterogeneous micro- and mesoporous, acidic catalysts were tested for the selective synthesis of Florol®, an industrial product formed via condensation and rehydration starting from isoprenol and isovaleraldehyde in dimethylcarbonate as a solvent. The results showed that a mildly acidic, microporous H-Beta-300 with SiO 2 /Al 2 O 3 ratio of 300 was the best catalyst, giving 72% selectivity with 99% conversion at 40 °C when using the molar ratio isoprenol to isovaleraldehyde of 1:5. More acidic zeolites gave slightly lower selectivity, while the lowest selectivity (up to 52%) was obtained with mesoporous catalysts exhibiting mild acidity and no strong Brønsted acid sites. Selectivity to pyranols was nearly constant when changing temperature, while a larger excess of isovaleraldehyde promoted formation of tetrahydropyranol. H-Beta-300 catalyst was successfully after calcination at 400 °C. DFT calculations pointed out on the parallel formation of tetrahydro pyranols and dihydropyrans, which are the corresponding dehydration products. [ABSTRACT FROM AUTHOR]

Abstract: The N2O-mediated oxidative dehydrogenation of propane over iron-containing MFI zeolites was studied by in situ diffuse reflectance Fourier transform infrared spectroscopy, complemented by analyses in a tapered element oscillating microbalance coupled with gas chromatography and characterization by X-ray diffraction, transmission electron microscopy, and N2 adsorption. Samples with different iron speciation and acidic properties, induced by the preparation method (ion-exchange and steam activation) and the framework composition (Fe–Al–Si, Fe–Ga–Si, and Fe–Ge–Si) were analyzed. Real-time monitoring of the reaction under operando conditions allowed us to gain insight into the mechanism and kinetics of deactivation and coke formation, as well as zeolite regeneration in air. Deactivation of iron zeolites in the oxidative dehydrogenation of propane is caused by coke deposition on active extra-framework iron species. The mechanism of coke formation and the nature of the deposits were similar over the samples, independent of the catalytic performance and deactivation pattern. Regeneration in air led to the disappearance of coke-related bands and the practically complete recovery of the original porosity, while the zeolite crystallinity remained intact. The initial propylene yield over the fresh and regenerated Fe–Ga–Si zeolites was the same, but the latter sample exhibited faster deactivation. This is attributed to a change of iron constitution in the first reaction–regeneration cycle. The alteration of the local environment of the iron species was indirectly concluded from the appearance of a band associated with Lewis centers in the infrared spectra of the regenerated zeolite. In support of this, TEM studies demonstrated an extensive degree of iron clustering as FeO x nanoparticles in the regenerated catalyst compared with the fresh and coked catalysts. [Copyright &y& Elsevier]

The hydrolytic hydrogenation of hemicellulose arabinogalactan was investigated in the presence of protonic and Ru (1–5 wt.%)-modified USY zeolites (Si/Al ratio = 15 and 30). The use of the purely acidic materials was effective in depolymerizing the macromolecule into free sugars. While the latter partly dehydrated into 5-hydroxymethylfurfural and furfural, the generation of high molecular-weight compounds (aggregates of sugars and humins) was not favored, in contrast to previous evidences over beta zeolites. Application of the bifunctional Ru/USY catalyst, comprising well-dispersed metallic nanoparticles on the aluminosilicate support, resulted in the formation of galactitol and arabitol, in the suppression of dehydration side products, and further inhibition of polymerization reactions, which only yielded low molecular-weight oligomers. Detailed analysis of the reaction pathways as well as kinetic modeling of hydrolytic hydrogenation was performed with an advanced reaction mechanism. [ABSTRACT FROM AUTHOR]

An accessibility index (ACI) was derived from infrared spectroscopy of substituted alkylpyridines with different size (pyridine: 0.57nm, 2,6-lutidine: 0.67nm, and 2,4,6-collidine: 0.74nm) over hierarchical porous ZSM-5 crystals. The samples were prepared by selective silicon extraction of a commercial sample in NaOH (desilication), and they contained different degrees of intracrystalline mesoporosity. Our results demonstrate the enhanced accessibility of Brønsted acid sites in the hierarchical zeolites. For example, a relatively bulky molecule such as collidine, which probes practically no acid site of the parent medium-pore MFI structure, can access up to 40% of the acid sites in the mesoporous sample. The ACI is a powerful tool to standardize acid site accessibility in zeolites, and can be used to rank the effectiveness of synthetic strategies to prepare hierarchical zeolites. [Copyright &y& Elsevier]

A temporal analysis of products (TAP) reactor was used to study relationships between the mechanism of direct N2O decomposition over metal-loaded zeolites and their resulting activity. Rh-ZSM-5 (prepared by incipient wetness) and Fe-ZSM-5 (prepared by liquid-ion exchange) were chosen as prototypic catalysts displaying low (<550 K) and high (>650 K) temperature activity, respectively. Transient studies at the same contact time revealed the higher activity of Rh-ZSM-5 below 623 K and significantly stronger N2O adsorption over Rh species than over Fe species in the zeolites. Several microkinetic models were applied for simultaneous fitting the transient responses of N2O, N2, and O2. Classical reaction schemes failed to describe the experimental data. The preferred models of N2O decomposition over Rh-ZSM-5 and Fe-ZSM-5 differ in the reaction pathways of O2 formation. For both catalysts, free active metal sites (*) and those occupied by monoatomic oxygen species (*-O) from N2O participate in the decomposition of gas-phase N2O. Gas-phase O2 is formed directly on N2O interaction with *-O over Rh-ZSM-5, whereas the latter reaction over Fe-ZSM-5 leads to a surface bi-atomic oxygen species (O-*-O), followed by its transformation to *-O2. The latter species desorbs as molecular oxygen. Comparison of ion-exchanged and steam-activated Fe-ZSM-5 [J. Phys. Chem. B 110 (2006) 22586] revealed that the reaction mechanism is independent of the iron constitution induced by the preparation and activation routes, despite important differences in catalytic activity. Our quantitative microkinetic analysis demonstrated that both the stronger reversible N2O adsorption and, most importantly, the faster desorption of O2 are distinctive mechanistic features of Rh-ZSM-5, likely indicating its high de-N2O activity. [Copyright &y& Elsevier]

Abstract: The preparation of mesoporous mordenite zeolite and its subsequent application in the liquid-phase alkylation of benzene with ethylene is discussed. Mesoporous mordenite was obtained by controlled silicon extraction on alkaline treatment of successfully synthesized high-silica mordenite zeolites with molar Si/Al ratios in the range of 20–30. Besides substantial mesoporosity development, the combined microporous and mesoporous zeolites show preserved Brønsted acidic properties, which are highly attractive when acid-catalyzed reactions are targeted. Catalytic testing of the mesoporous mordenite found superior performance in benzene alkylation due to the unique interplay between improved physical transport in the shortened micropores and the preserved high density of acid sites. [Copyright &y& Elsevier]