Improving the performance of ASA in the DAC of 2,5-DMF and ethylene
A variety of methods are employed to synthesize amorphous silica-alumina (ASA) to resolve the role of Al speciation and surface area in the catalytic performance in the Diels-Alder cycloaddition reaction of 2,5-dimethylfuran and ethylene to p -xylene. ASA was prepared by homogeneous deposition-preci...
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Veröffentlicht in: | Catalysis science & technology 2023-12, Vol.13 (24), p.6959-6967 |
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Sprache: | eng |
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Zusammenfassung: | A variety of methods are employed to synthesize amorphous silica-alumina (ASA) to resolve the role of Al speciation and surface area in the catalytic performance in the Diels-Alder cycloaddition reaction of 2,5-dimethylfuran and ethylene to
p
-xylene. ASA was prepared by homogeneous deposition-precipitation (HDP) of Al
3+
on ordered mesoporous silica,
i.e.
, SBA-15 and OMS prepared under hydrothermal synthesis conditions using an imidazole-based template, and one-step flame spray pyrolysis (FSP). IR spectroscopy and
27
Al MAS NMR showed that the resulting ASA represented a set of materials with distinct textural and acidic properties. ASA prepared by grafting Al to ordered mesoporous silica led to a much higher concentration of Brønsted acid sites (BAS). These samples performed much better in the DAC reaction, with
p
-xylene yields higher than those obtained with a HBeta zeolite benchmark. Materials with Al partially in the bulk of silica (OMS, FSP) and containing significant alumina domains are less acidic and exhibit much lower
p
-xylene yields. These findings point to the importance of Brønsted acidity for
p
-xylene formation. This study shows that careful design of the Al speciation can lead to amorphous silica-alumina with similar DAC performance to microporous zeolites.
A variety of methods are employed to synthesize amorphous silica-alumina (ASA) to resolve the role of Al speciation and surface area in the catalytic performance in the Diels-Alder cycloaddition reaction of 2,5-dimethylfuran and ethylene to
p
-xylene. |
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ISSN: | 2044-4753 2044-4761 |
DOI: | 10.1039/d3cy01224g |