Activity of Gallium and Aluminum SBA-15 materials in the Friedel–Crafts alkylation of toluene with benzyl chloride and benzyl alcohol

Ga-, Al- and AlGa-SBA-15 mesoporous materials synthesized via a direct sol–gel hydrothermal protocol were found active and selective in the Friedel–Crafts alkylation of toluene with benzyl chloride (promoted by Lewis acidity) and benzyl alcohol (promoted by Brönsted acidity). The solid acids were al...

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Veröffentlicht in:Applied catalysis. A, General General, 2008-10, Vol.349 (1), p.148-155
Hauptverfasser: Gracia, Maria J., Losada, Elia, Luque, Rafael, Campelo, Juan M., Luna, Diego, Marinas, Jose M., Romero, Antonio A.
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Sprache:eng
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Zusammenfassung:Ga-, Al- and AlGa-SBA-15 mesoporous materials synthesized via a direct sol–gel hydrothermal protocol were found active and selective in the Friedel–Crafts alkylation of toluene with benzyl chloride (promoted by Lewis acidity) and benzyl alcohol (promoted by Brönsted acidity). The solid acids were also highly reusable preserving almost their initial catalytic activity after five reuses. ▪ Ga-, Al- and AlGa-SBA-15 mesoporous materials were synthesized via a direct sol–gel hydrothermal protocol. The SBA-15 materials were characterized using X-ray fluorescence (XRF), X-ray diffraction (XRD), N 2 physisorption, transmission electron microscopy (TEM) and pyridine and 2,6-dimethylpyridine titration. The activity of the Ga- and AlGa-SBA-15 was investigated in the Friedel–Crafts alkylation of toluene with benzyl chloride (promoted by Lewis acidity) and benzyl alcohol (promoted by Brönsted acidity). Quantitative conversion of the starting material was found for all Ga- and AlGa-SBA-15 after a few hours of reaction at 110 °C in the alkylation of toluene with benzyl chloride. The mesoporous acidic materials provided very poor activities in the alkylation of toluene with benzyl alcohol, with the exception of the Al-SBA-15. The activities of the Ga- and AlGa-SBA-15 were correlated to the higher proportion of Lewis compared to Brönsted acid sites. The solid acids were also highly reusable preserving almost their initial catalytic activity after five reuses.
ISSN:0926-860X
1873-3875
DOI:10.1016/j.apcata.2008.07.023