Synthesis of sulfonic acid-functionalized Fe3O4@C nanoparticles as magnetically recyclable solid acid catalysts for acetalization reactionElectronic supplementary information (ESI) available. See DOI: 10.1039/c3dt52098f
The Fe 3 O 4 @C core-shell magnetic nanoparticles with an average size of about 190 nm were synthesized via a one-pot solvothermal process using ferrocene as a single reactant. The sulfonic acid-functionalized Fe 3 O 4 @C magnetic nanoparticles were obtained by grafting the sulfonic groups on the su...
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Main Authors | , , , , |
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Format | Journal Article |
Language | English |
Published |
10.12.2013
|
Online Access | Get full text |
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Summary: | The Fe
3
O
4
@C core-shell magnetic nanoparticles with an average size of about 190 nm were synthesized
via
a one-pot solvothermal process using ferrocene as a single reactant. The sulfonic acid-functionalized Fe
3
O
4
@C magnetic nanoparticles were obtained by grafting the sulfonic groups on the surface of Fe
3
O
4
@C nanoparticles to produce magnetically recyclable solid acid catalysts. The as-prepared products were characterized by X-ray diffraction and transmission electron microscopy. The catalytic performance of the as-prepared catalysts was examined through the condensation reaction of benzaldehyde and ethylene glycol. The results showed that the catalysts exhibited high catalytic activity with a conversion rate of 88.3% under mild conditions. Furthermore, catalysts with a magnetization saturation of 53.5 emu g
−1
at room temperature were easily separated from the reaction mixture by using a 0.2 T permanent magnet and were reused 8 times without any significant decrease in catalytic activity.
In this article, we report a route for preparing highly efficient, stable, and magnetically recyclable solid acid catalysts
via
grafting sulfonic groups on the surface of Fe
3
O
4
@C MNPs, showing a high efficiency in the acetalization reaction of benzaldehyde with ethylene glycol. |
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Bibliography: | 10.1039/c3dt52098f Electronic supplementary information (ESI) available. See DOI |
ISSN: | 1477-9226 1477-9234 |
DOI: | 10.1039/c3dt52098f |