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Copper/silica nanocomposite catalysts prove efficient for the direct hydrocyclization of biomass‐derived levulinic acid to cyclic 2‐methyltetrahydrofuran in the vapor phase, at moderate hydrogen pressures. A nickel‐promoted copper/silica catalyst with a high copper loading (72 wt %) is particularly effective for the direct hydrocyclization (89 % selectivity). The catalysts are stable during long‐term experiments, showing little sign of leaching or sintering.

Large-pore hexagonal SBA-15 molecular sieves partially substituted with iron(III) have been synthesized for the first time in highly acidic media. The degree of iron(III) incorporation into SBA-15 can easily be controlled by a simple adjustment of the molar ratio of water and hydrochloric acid. All the materials have been characterized by XRD, N 2 adsorption, UV-Vis DRS, ESR, and XANES spectroscopy. The characterization of the FeSBA-15 materials by UV-Vis DRS, ESR, and XANES spectroscopies suggests that the iron atoms are highly dispersed and mostly occupy isolated tetrahedral sites. XANES studies revealed that the proportion of tetrahedrally coordinated Fe atoms decreases with decreasing n Si /n Fe ratios. Benzylation of benzene (or substituted benzenes) using benzyl chloride as the alkylating agent over FeSBA-15 with different n Si /n Fe ratios was investigated as was the same reaction using AlSBA-15 as catalyst. The influence of parameters such as reaction temperature, reactant feed ratio, and the presence of electrondonating substituents on the activity and selectivity of AlSBA-15 was studied. Under optimized reaction conditions, the FeSBA-15 catalyst showed a superior catalytic performance in the benzylation of benzene and other aromatics using benzyl chloride, with a clean conversion of benzyl chloride to the monoalkylated product (100% selectivity) with a very high rate constant when compared to other mesoporous materials such as AlSBA-15 and FeHMS. Interestingly, use of FeSBA-15(21) resulted in quantitative conversion of benzyl chloride with a high rate constant of 2420.5 × 10 -4 min -1 under the optimized reaction conditions.

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Novel three dimensional cubic Fm3m mesoporous aluminosilicates (AlKIT‐5) with very high structural order and unprecedented loadings of Al in the silica framework have been successfully prepared for the first time by using non ionic surfactant as a template in a highly acidic medium. The obtained materials have been unambiguously characterized in detail by several sophisticated techniques such as XRD, N2 adsorption, HRTEM, HRSEM, EDS, elemental mapping, 27Al MAS NMR, and NH3‐TPD. We also demonstrate that the nature, and the amount of Al incorporation in the silica framework can easily be controlled by simply varying the nH2O/nHCl and the nSi/nAl ratios, and the Al sources in the synthesis gel. Among the Al sources examined, the Al isopropoxide (AiPr) is superior over other Al sources. 27Al MAS NMR results reveal that the amount of tetrahedral Al in the framework can be controlled by simply adjusting the nSi/nAl ratio in the synthesis gel, which increases with increasing the Al incorporation. One of the interesting findings in the work is the increase of the specific surface area, specific pore volume and the pore diameter of AlKIT‐5 with increasing the Al incorporation in the silica framework (up to nSi/nAl ratio of 10) while retaining the well‐ordered three dimensional cage type porous structure, and the mechanism for the unusual behavior has been discussed in detail. Finally, the acidity and the catalytic activity in the acetylation of veratrole of the AlKIT‐5 catalysts have been studied and the results have been compared with the several zeolites catalysts. Among the catalysts examined, AlKIT‐5(10) is found to be superior over the zeolites catalysts such as mordenite, zeolite H‐Y, zeolite H‐β, and ZSM‐5.

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