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Synthesis of sulfonic acid-functionalized Fe3O4@C nanoparticles as magnetically recyclable solid acid catalysts for acetalization reaction

机译:磺酸官能化的Fe3O4 @ C纳米颗粒的合成作为可磁回收的固体酸催化剂,用于缩醛化反应

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摘要

The Fe_3O_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_3O_4@C magnetic nanoparticles were obtained by grafting the sulfonic groups on the surface of Fe_3O_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.
机译:使用二茂铁作为单一反应物,通过一锅溶剂热法合成了平均粒径约为190 nm的Fe_3O_4 @ C核壳磁性纳米粒子。磺酸官能化的Fe_3O_4 @ C磁性纳米粒子是通过将Fe_3O_4 @ C纳米粒子的表面上的磺酸基团接枝得到可磁循环的固体酸催化剂而得到的。通过X射线衍射和透射电子显微镜表征所制备的产物。通过苯甲醛和乙二醇的缩合反应检查了制备的催化剂的催化性能。结果表明,该催化剂在温和条件下具有较高的催化活性,转化率为88.3%。此外,通过使用0.2 T永磁体,易于将室温下磁化饱和度为53.5 emu g(-1)的催化剂从反应混合物中分离出来,并重复使用8次,而催化活性没有明显降低。

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