Dysprosium-doped zinc tungstate nanospheres as highly efficient heterogeneous catalysts in green oxidation of terpenic alcohols with hydrogen peroxide

A green route to oxidize terpenic alcohols (nerol and geraniol) with H 2 O 2 over a solid catalyst was developed. The Dy-doped ZnWO 4 catalyst was synthesized by coprecipitation and microwave-assisted hydrothermal heating, containing different dysprosium loads. All the catalysts were characterized t...

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Veröffentlicht in:New journal of chemistry 2021-04, Vol.45 (15), p.6661-667
Hauptverfasser: Batalha, Daniel Carreira, Mesquita Borges, Kellen Cristina, de Fátima Gonçalves, Rosana, de Matos Rodrigues, Murillo Henrique, Godinho, Mário Júnior, Fajardo, Humberto Vieira, de Oliveira Bruziquesi, Carlos Giovani, da Silva, Márcio José
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Sprache:eng
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Zusammenfassung:A green route to oxidize terpenic alcohols (nerol and geraniol) with H 2 O 2 over a solid catalyst was developed. The Dy-doped ZnWO 4 catalyst was synthesized by coprecipitation and microwave-assisted hydrothermal heating, containing different dysprosium loads. All the catalysts were characterized through infrared spectroscopy, powder X-ray diffraction, surface area and porosimetry, transmission electronic microscopy image, and n -butylamine potentiometric titration analyses. The influence of main reaction parameters such as temperature, the stoichiometry of reactants, loads, and catalyst nature was assessed. ZnWO 4 2.0 mol% Dy was the most active catalyst achieving the highest conversion (98%) and epoxide selectivity (78%) in nerol oxidation. The reaction scope was extended to other terpenic alcohols ( i.e. , geraniol, borneol, and α-terpineol). The highest activity of ZnWO 4 2.0 mol% Dy was assigned to the lower crystallite size, higher surface area and pore volume, higher acidity strength and the greatest dysprosium load. Dysprosium-doped zinc tungstate nanospheres efficiently catalyzed the epoxidation of terpenic alcohols using hydrogen peroxide, an inexpensive and environmentally benign oxidant.
ISSN:1144-0546
1369-9261
DOI:10.1039/d0nj05623e