Sustainable synthesis of vanillin through base-free selective oxidation using synergistic AgPd nanoparticles loaded on ZrO 2

The synergistic effect between bimetallic nanoparticles, as well as the support effect, is particularly important for supported catalysts in heterogeneous catalysis. In this work, an AgPd/ZrO 2 bimetallic catalyst was reported for the base-free aerobic oxidation of vanillyl alcohol to vanillin, a ch...

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Veröffentlicht in:Catalysis science & technology 2021-11, Vol.11 (22), p.7268-7277
Hauptverfasser: Sun, Weixiao, Lin, Peng, Tang, Qinghu, Jing, Fangli, Cao, Qiue, Fang, Wenhao
Format: Artikel
Sprache:eng
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Zusammenfassung:The synergistic effect between bimetallic nanoparticles, as well as the support effect, is particularly important for supported catalysts in heterogeneous catalysis. In this work, an AgPd/ZrO 2 bimetallic catalyst was reported for the base-free aerobic oxidation of vanillyl alcohol to vanillin, a challenging transformation of an aromatic bio-alcohol into a valuable fine chemical. The crystalline structure and textural properties of ZrO 2 were modulated by using different zirconium precursors and precipitants during the precipitation process. The ZrO 2 obtained from zirconium nitrate and trimethylamine was found to be the most suitable support. It displayed abundant reactive oxygen species and the largest specific surface area. Then, an Ag promoter was added to the Pd/ZrO 2 catalyst and the synergy between Ag and Pd was tuned by varying their ratios. The Ag 0.5 Pd 1 /ZrO 2 catalyst showed an enhanced performance, i.e. , 100% conversion of vanillyl alcohol and 95% selectivity to vanillin at 120 °C and 3 bar O 2 within 4 h, in comparison with the Pd/ZrO 2 catalyst (69% and 87%, respectively). Moreover, the vanillin productivity reached 133.0 mol mol −1 h −1 , the best result reported in the literature to date. Various characterization methods demonstrated that the addition of Ag can reduce the mean size of Pd nanoparticles (4.9 nm vs. 3.8 nm), and Ag + species were beneficial to stabilizing Pd 0 species in a high fraction due to electron transfer. The reactive Pd 0 sites closely interacting with the Ag promoter allowed lowering of the apparent activation energy of the reaction (27.3 vs. 37.5 kJ mol −1 ). In addition, the Ag 0.5 Pd 1 /ZrO 2 catalyst exhibited superior stability during consecutive recycling uses owing to the strong metal–support interactions.
ISSN:2044-4753
2044-4761
DOI:10.1039/D1CY01526E