Your browser doesn't support javascript.
loading
Magnetic-responsive solid acid catalysts for esterification.
Xue, Dan; Jiang, Yun; Zheng, Fangxia.
Afiliação
  • Xue D; School of Chemical Engineering, University of Science and Technology Liaoning Anshan 114051 China.
  • Jiang Y; Key Lab of Eco-restoration of Regional Contaminated Environment (Shenyang University), Ministry of Education Shenyang 110036 China danxue@ustl.edu.cn.
  • Zheng F; School of Chemical Engineering, University of Science and Technology Liaoning Anshan 114051 China.
RSC Adv ; 13(39): 27579-27588, 2023 Sep 08.
Article em En | MEDLINE | ID: mdl-37720832
Two kinds of magnetic-responsive solid acid catalysts were designed and prepared via an in situ polymerization of poly(ionic liquid)s (PILs) on the surface of Fe3O4@SiO2 NPs for the catalyzed esterification of palmitic acid and methanol. They were characterized using XRD, TGA, VSM, NMR spectroscopy, FTIR spectroscopy, XPS, SEM, and GC techniques. The results confirmed the preparation of solid acid catalysts. Meanwhile, they possessed excellent catalytic activity and recyclability. The effect of the reaction conditions on the esterification was investigated through single-factor analyses, and the proposed catalytic mechanism of the prepared solid acid catalysts in the esterification are also discussed. Under the optimal reaction conditions (10 wt% catalyst, 6 h, 70 °C, and molar ratio (MR) of methanol to palmitic acid of 12 : 1), the conversion rate of palmitic acid could reach 94% and 79% with Fe3O4@SiO2-poly(1-vinyl-3-ethylimidazolium phosphotungstate) (Fe3O4@SiO2-P([VLIM]PW)) and Fe3O4@SiO2-poly(1-vinylimidazole-3-propyl sulfonate) (Fe3O4@SiO2-P([VLIM]SO3)) NPs serving as catalysts, respectively. Furthermore, the Fe3O4@SiO2-P([VLIM]PW) NPs could still maintain a high catalytic activity even after being reused 5 times without significant deactivation.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article