This work reports initial results on the effect of low concentrations (ppm level) of a stabilizing agent (2,6-di-tert-butyl-4-methylphenol, BHT) present in an off-the-shelf solvent on the catalyst performance for the hydrogenolysis of γ-butyrolactone over Cu-ZnO-based catalysts. Tetrahydrofuran (THF) was employed as an alternative solvent in the hydrogenolysis of γ-butyrolactone. It was found that the Cu-ZnO catalyst performance using a reference solvent (1,4-dioxane) was good, meaning that the equilibrium conversion was achieved in 240 min, while a zero conversion was found when employing tetrahydrofuran. The deactivation was studied in more detail, arriving at the preliminary conclusion that one phenomenon seems to play a role: the poisoning effect of a solvent additive present at the ppm level (BHT) that appears to inhibit the reaction completely over a Cu-ZnO catalyst. The BHT effect was also visible over a commercial Cu-ZnO-MgO-Al2O3 catalyst but less severe than that over the Cu-ZnO catalyst. Hence, the commercial catalyst is more tolerant to the solvent additive, probably due to the higher surface area. The study illustrates the importance of solvent choice and purification for applications such as three-phase-catalyzed reactions to achieve optimal performance.

Mesoporous materials are of vital importance for use in separation, adsorption, and catalysis. The first step in their preparation consists of synthesizing an organic-inorganic hybrid in which a structuring directing agent (SDA, normally a surfactant) is used to provide the desired porosity. The most common method to eliminate the SDA, and generate the porosity, is high-Temperature calcination. Such a process is energy-intensive and slow. In this study, we investigated alternative nonthermal surfactant removal methods on a soft MCM-41 material, aiming at reducing the processing time and temperature, while maximizing the material's properties. The choice of a soft MCM-41 is critical since it is hydrothermally unstable, whereas the SDA removal is troublesome. Microwave processing yielded outstanding performance in terms of surfactant removal, structural preservation, and textural features; the surfactant was fully removed, the hexagonal structure was preserved, and the surface was highly rich in Si-OH groups. It is suggested that H2O2 is the dominant oxidant. In terms of the process features, the processing time is significantly reduced, 14 h (calcination) versus 5 min (microwaves), and the applied temperature is much lower. The energy savings were estimated to be 72% lower as compared to calcination; therefore, this approach contributes to the process intensification of a very relevant material's production.