Origin of enhanced Brønsted acidity of NiF-modified synthetic mica-montmorillonite clay

The Brønsted acidity of synthetic mica-montmorillonite (SMM) clay was studied by periodic DFT calculations. Different structural models were compared to determine the Brønsted acidity of protons of the SMM clay based on (i) isomorphous substitution of Si4+ by Al3+ in the tetrahedral silicate layer and additional NiF-doping (ii) in the platelets and (iii) at the edge terminations of the clay platelets. The acid strength was judged from the computed adsorption energies of ammonia and pyridine. The SMM acidity is mainly determined by the composition of the clay platelets. The strongest acidity is found in structures in which octahedral [AlO]+ is replaced by [NiF]+ adjacent to tetrahedral [Si-(OH)-Al] moieties in the tetrahedral layer. For the Brønsted acid sites in the interlayer of SMM, modification with either Ni2+ or F- in the octahedral layers has only a minor influence on the acidity. Our data indicate that Brønsted acid sites, properly modified in the second coordination shell by electron-withdrawing F, in the interlayer and at defect sites at the edges of clay platelets (intralayer sites) can contribute to the enhanced acidity in NiF-modified SMM. Although the predicted acidity of SMM by ammonia adsorption is higher than that of faujasite zeolite, the reactivity judged from propene protonation demonstrates that zeolites are more reactive than clays. This difference seems to be the result of the curved nature of the micropores of zeolites, which stabilizes the transition states for an acid-catalyzed reaction more than flat surfaces of clays do.ChemE/Inorganic Systems EngineeringChemE/Algemee

Engineering of Transition Metal Catalysts Confined in Zeolites

Transition metal-zeolite composites are versatile catalytic materials for a wide range of industrial and lab-scale processes. Significant advances in fabrication and characterization of well-defined metal centers confined in zeolite matrixes have greatly expanded the library of available materials and, accordingly, their catalytic utility. In this review, we summarize recent developments in the field from the perspective of materials chemistry, focusing on synthesis, postsynthesis modification, (operando) spectroscopy characterization, and computational modeling of transition metal-zeolite catalysts.ChemE/Inorganic Systems EngineeringChemE/Algemee

Catalytic (de)hydrogenation promoted by non-precious metals-Co, Fe and Mn: Recent advances in an emerging field

Catalytic hydrogenation and dehydrogenation reactions form the core of the modern chemical industry. This vast class of reactions is found in any part of chemical synthesis starting from the milligram-scale exploratory organic chemistry to the multi-ton base chemicals production. Noble metal catalysis has long been the key driving force in enabling these transformations with carbonyl substrates and their nitrogen-containing counterparts. This review is aimed at introducing the reader to the remarkable progress made in the last three years in the development of base metal catalysts for hydrogenations and dehydrogenative transformations.ChemE/Inorganic Systems Engineerin

Electronic Structure Analysis of the Diels-Alder Cycloaddition Catalyzed by Alkali-Exchanged Faujasites

The Diels-Alder cycloaddition (DAC) reaction is a commonly employed reaction for the formation of C-C bonds. DAC catalysis can be achieved by using Lewis acids and via reactant confinement in aqueous nanocages. Low-silica alkali-exchanged faujasite catalysts combine these two factors in one material. They can be used in the tandem DAC/dehydration reaction of biomass-derived 2,5-dimethylfuran (DMF) with ethylene toward p-xylene, in which the DAC reaction step initiates the overall reaction cycle. In this work, we performed periodic density functional theory (DFT) calculations on the DAC reaction between DMF and C2H4 in low-silica alkali(M)-exchanged faujasites (MY; Si/Al = 2.4; M = Li+, Na+, K+, Rb+, Cs+). The aim was to investigate how confinement of reactants in MY catalysts changed their electronic structure and the DAC-reactivity trend among the evaluated MY zeolites. The conventional high-silica alkali-exchanged isolated site model (MFAU; Si/Al = 47) served as a reference. The results show that confinement leads to initial-state (IS) destabilization and transition-state (TS) stabilization. Among the tested MY, most significant IS destabilization is found in RbY. Only antibonding orbital interactions between the reactants/reactive complex and cations were found, indicating that TS stabilization arises from ionic interactions. Additionally, in RbY the geometry of the transition state is geometrically most similar to that of the initial and final state. RbY also exhibits an optimal combination of the confinement-effects, resulting in having the lowest computed DAC-activation energy. The overall effect is a DAC-reactivity trend inversion in MY as compared to the trend found in MFAU where the activation energy correlates with the Lewis acidity of the exchangeable cations.ChemE/Algemee

Tuning stability of titania-supported Fischer-Tropsch catalysts: Impact of surface area and noble metal promotion

Cobalt oxidation is a relevant deactivation pathway of titania-supported cobalt catalysts used in Fischer-Tropsch synthesis (FTS). To work towards more stable catalysts, we studied the effect of the surface area of the titania support and noble metal promotion on cobalt oxidation under simulated high conversion conditions. Mössbauer spectroscopy was used to follow the evolution of cobalt during reduction and FTS operation as a function of the steam pressure. The reduction of the oxidic cobalt precursor becomes more difficult due to stronger metal-support interactions when the titania surface area is increased. The reducibility was so low for cobalt on GP350 titania (surface area 283 m2/g) that the catalytical activity was negligible. Although cobalt was more difficult to reduce on P90 titania (94 m2/g) than on commonly used P25 titania (50 m2/g), the Co/P90 catalyst showed increased resistance against cobalt sintering and higher FTS performance than Co/P25. The addition of platinum to Co/P90 led to a higher reduction degree of cobalt and a higher cobalt dispersion, representing a catalyst with promising performance at relatively low steam pressure. Nevertheless, the stronger cobalt-titania interactions result in more extensive deactivation at high steam pressure due to oxidation.RST/Fundamental Aspects of Materials and EnergyRID/TS/Instrumenten groe

Manganese as a structural promoter in silica-supported cobalt Fischer-Tropsch catalysts under simulated high conversion conditions

Understanding the deactivation mechanism of cobalt-based Fischer-Tropsch catalysts is of significant practical importance. Herein, we explored the role of manganese as a structural promoter on silica-supported cobalt nanoparticles under simulated high CO conversion conditions, i.e., high relative humidity. The structural changes in cobalt dispersion and oxidation state were followed by in situ Mössbauer emission spectroscopy. Adding manganese oxide to silica-supported cobalt enhanced the dispersion of metallic cobalt in the reduced catalysts. This higher cobalt dispersion, however, led to a stronger tendency of cobalt silicate formation under humid conditions. Without manganese, the cobalt particles sintered, and the larger ones were prone to transformation into cobalt carbide under high conversion conditions. As such, silica is not preferred as a support for practical FTS.RST/Fundamental Aspects of Materials and EnergyRID/TS/Instrumenten groe

Sintering and carbidization under simulated high conversion on a cobalt-based Fischer-Tropsch catalyst; manganese oxide as a structural promotor

The commercial application of cobalt-based Fischer-Tropsch synthesis (FTS) suffers from catalyst deactivation. One of the main deactivation mechanisms under industrial conditions is sintering. In this work, we explored the role of manganese oxide as a structural promoter against sintering in a carbon nanofiber supported cobalt model catalyst. We employed in situ Mössbauer emission spectroscopy to study cobalt sintering in synthesis gas as a function of the steam partial pressure, which mimics high CO conversion during FTS. Steam accelerates the sintering of non-promoted metallic cobalt particles. Model experiments point to a synergistic effect between carbon monoxide and steam on cobalt sintering. In the mangense-promoted case, sintering is significantly reduced, indicative of the structural stabilization of small cobalt particles by manganese oxide. Nevertheless, a fraction of cobalt particles in close interaction with manganese oxide carburized under these conditions, resulting in a lower catalytic activity.RST/Fundamental Aspects of Materials and EnergyInstrumenten groe

Co-Aromatization of Furan and Methanol over ZSM-5 - A Pathway to Bio-Aromatics

Aromatization of furan and substituted furans over zeolite catalysts is a promising reaction to convert cellulose-derived compounds into valuable aromatic hydrocarbons and light olefins. A lack of understanding of the reaction mechanism however hinders further development of this process. Here, we propose the reaction mechanism, underlying the chemistry of furan and methanol co-aromatization over HZSM-5 zeolite catalyst. Applying 13C isotope labeling in a combination with NMR spectroscopy and high temporal resolution gas chromatography-mass spectrometry analysis, we demonstrate that aromatization of furan and methanol are not mechanistically separated and can be described within the dual-cycle hydrocarbon pool mechanism. Cofeeding furan with methanol leads to a significant enhancement of light aromatics selectivity and increased catalyst lifetime.Accepted Author ManuscriptChemE/Inorganic Systems EngineeringChemE/Algemee

Electronic Structure of the [Cu₃(μ-O)₃]²⁺ Cluster in Mordenite Zeolite and Its Effects on the Methane to Methanol Oxidation

Identifying Cu-exchanged zeolites able to activate C-H bonds and selectively convert methane to methanol is a challenge in the field of biomimetic heterogeneous catalysis. Recent experiments point to the importance of trinuclear [Cu3(μ-O)3]2+ complexes inside the micropores of mordenite (MOR) zeolite for selective oxo-functionalization of methane. The electronic structures of these species, namely, the oxidation state of Cu ions and the reactive character of the oxygen centers, are not yet fully understood. In this study, we performed a detailed analysis of the electronic structure of the [Cu3(μ-O)3]2+ site using multiconfigurational wave-function-based methods and density functional theory. The calculations reveal that all Cu sites in the cluster are predominantly present in the Cu(II) formal oxidation state with a minor contribution from Cu(III), whereas two out of three oxygen anions possess a radical character. These electronic properties, along with the high accessibility of the out-of-plane oxygen center, make this oxygen the preferred site for the homolytic C-H activation of methane by [Cu3(μ-O)3]2+. These new insights aid in the construction of a theoretical framework for the design of novel catalysts for oxyfunctionalization of natural gas and suggest further spectroscopic examination.ChemE/Catalysis EngineeringChemE/Algemee

Instability of NiMoS₂ and CoMoS₂ Hydrodesulfurization Catalysts at Ambient Conditions: A Quasi in Situ High-Resolution Transmission Electron Microscopy and X-ray Photoelectron Spectroscopy Study

The effect of exposure to ambient air of MoS2-based, γ-Al2O3-supported, hydrodesulfurization (HDS) catalysts has been studied using high-resolution transmission electron microscopy (HRTEM). Analysis of unpromoted as well as Ni- and Co-promoted MoS2 samples showed that the number of MoS2 slabs and the average slab length decreased as a function of air exposure time. A parallel X-ray photoelectron spectroscopy (XPS) study showed this effect to be due to oxidation. During the first 24 h of exposure to air, all 1 bar sulfided (Ni/Co)MoS2 samples showed an initial slab length decrease of approximately 20%. After an additional month in air, the slabs had deteriorated significantly further. A sample of CoMoS2 sulfided at 30 bar showed a slightly enhanced effect of oxidation, particularly after the first 5 min in air. The combined HRTEM and XPS results lead to the proposal of the formation of a protective oxide ring around the remaining sulfidic species inside the MoS2 slabs to explain the mechanism of this oxidation process. The data obtained in this study emphasize the general necessity of shielding vulnerable catalyst samples from air during preparation and characterization, a message relevant in all fields of research related to catalysis.Accepted Author ManuscriptChemE/Catalysis Engineerin