4.5 Article

In situ fabrication of layered double hydroxide film immobilizing gold nanoparticles in capillary microreactor for efficient catalytic carbonylation of glycerol

Journal

MOLECULAR CATALYSIS
Volume 513, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.mcat.2021.111825

Keywords

Capillary microreactor; LDH film; Glycerol; Urea; Au nanoparticles; Catalytic carbonylation

Funding

  1. National Natural Science Foundation of China [22072136, 41701334]
  2. State Key Laboratory Breeding Base of Green Chemistry-Synthesis Technology, The Zhejiang University of Technology [GCTKF2014006]
  3. Research Foundation of Education Bureau of Anhui Province, China [KJHS2016B09]
  4. Engineering Research Center of Non-metallic Minerals of Zhejiang Province, Zhejiang Institute of Geology and Mineral Resource, China [ZD2020K07]

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A facile method for in situ fabrication of LDH film immobilizing gold nanoparticles in a capillary microreactor is reported in this study, showing good catalytic performance in glycerol carbonylation with urea. Adjusting the reaction conditions allows precise control of film thickness, morphology, and Au loading, demonstrating high stability and productivity in heterogeneous catalysis.
Microreactor is capable of intensifying catalytic reaction processes. The fabricating of catalytic film inside microchannels for catalytic reaction remains a challenge. Here we report a facile method for in situ fabrication of layered double hydroxide (LDH) film immobilizing gold nanoparticles in capillary microreactor. Through adjusting the reaction condition of in situ hydrothermal crystallization process and flow deposition process inside microchannel, film thickness, film morphology and Au loading of Au/LDH coating can be finely controlled. Such Au/LDH film inside microchannel exhibited good performance in catalytic carbonylation of glycerol with urea. The yield of glycerol carbonate reached 31.9% at flow rate of 10 mu l/min, residence time of 6.62 min and reaction temperature of 413 K under atmospheric pressure. The maximum productivity of 3.78 g.h- 1.g 1 was obtained at flow rate of 40 mu l/min and residence time of 1.65 min under same reaction temperature and pressure. Continuously running the microreactor for 30 h proved the high stability of this catalytic film inside microchannels. This approach could be extended to fabricate other diatomic and triatomic metal LDH films immobilizing metal nanoparticles inside microchannels for heterogeneous catalysis.

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