Metathesis of 1-hexene over rhenium oxide supported on ordered mesoporous aluminas: comparison with Re 2O 7/γ-Al 2O 3

Abstract

Self-metathesis of 1-hexene was carried out at 40 °C over Re 2O 7 supported on two micelle templated aluminas (sol–gel mesoporous alumina (SGAL) and MSU), prepared with cationic and neutral surfactant, respectively, and a reference Re 2O 7/γ-Al 2O 3 catalyst with the same rhenium oxide content (∼9 wt%). Both mesostructured catalysts (Re 2O 7/MSU and Re 2O 7/SGAL) showed similar activity and far higher than that of the reference Re 2O 7/γ-Al 2O 3 catalyst, with a selectivity towards the self-metathesis products above 99%. Among the tested solvents, dodecane yielded the highest conversion likely because of its low polarity and better product removal. Similar TOF values were obtained for Re 2O 7/SGAL catalysts with mesopore diameter within the 5.0–12.0 nm range. In relation with the rhenium content, an optimum in TOF values was detected for rhenium oxide loadings within 6–10 wt%. The increase in activation temperature within 550–700 °C led towards a greater rise in activity over Re 2O 7/SGAL catalysts than over Re 2O 7/γ-Al 2O 3. DRIFT chemisorbed pyridine spectra disclosed only Lewis acid sites over the activated catalysts and in higher amounts over both mesostructured catalysts. 31P MAS NMR spectra of chemisorbed triethylphosphine oxide (TEPO) indicated the presence of three kind of acid sites ( δ ∼58, 68 and 80 ppm), with a higher content of strong Lewis acid sites (80 ppm) over both mesostructured catalysts. The remarkable performance of both ordered mesoporous catalysts was ascribed to the presence of these strong Lewis acid sites, likely stemming from the interaction of linked rhenium species with the weak Lewis acid sites of the support.