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Gas-phase O-methylation of catechol with dimethyl carbonate over SBA-15-supported aluminum phosphate catalyst
Gas-phase O-methylation of catechol with dimethyl carbonate over SBA-15-supported aluminum phosphate catalyst
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Gas-phase O-methylation of catechol with dimethyl carbonate over SBA-15-supported aluminum phosphate catalyst
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Gas-phase O-methylation of catechol with dimethyl carbonate over SBA-15-supported aluminum phosphate catalyst
Gas-phase O-methylation of catechol with dimethyl carbonate over SBA-15-supported aluminum phosphate catalyst

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Gas-phase O-methylation of catechol with dimethyl carbonate over SBA-15-supported aluminum phosphate catalyst
Gas-phase O-methylation of catechol with dimethyl carbonate over SBA-15-supported aluminum phosphate catalyst
Journal Article

Gas-phase O-methylation of catechol with dimethyl carbonate over SBA-15-supported aluminum phosphate catalyst

2024
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Overview
SBA-15-supported Al 2 O 3 -P 2 O 5 with 10 wt% Al 2 O 3 and different P 2 O 5 mass percentages (10Al 2 O 3 - x P 2 O 5 /SBA-15) were prepared by simple impregnation method and used for gas-phase selective O-methylation of catechol to guaiacol with dimethyl carbonate. The 10Al 2 O 3 - x P 2 O 5 /SBA-15 catalysts maintained ordered mesoporous structures, but their specific surface areas, pore volumes, and pores decreased with the addition of Al and P oxides. The addition of P 2 O 5 decreased the strength of weak acid, but with the P 2 O 5 content increasing, the additional pseudo-bridging bonds that are similar to amorphous silica-alumina were formed, which enhanced the acidity of weak acid. Brønsted acid sites introduced by P 2 O 5 promoted more acid sites and lower the strength of acid sites. The basic sites increased with the increase of P 2 O 5 content. Acidic sites are the key to control the catalytic activity, and basic sites are the key to control the catalytic selectivity. 10Al 2 O 3 -5P 2 O 5 /SBA-15 exhibited excellent catalytic activities and high selectivity to guaiacol for the O-methylation of catechol, due to the synergistic effect of acid and base sites.

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