<p>Green synthesis is an important route in the preparation of bare metals and metal oxides that provides cost-effective, eco-friendly, and highly efficient catalysts for catalyzing various reactions. In this paper we report, for the first time, the green synthesis of Co<sub>3</sub>O<sub>4</sub> employing jasmine flower extract as a green precursor for the application as catalyst during NaBH<sub>4</sub> hydrolysis. Moreover, the role of calcination temperature (300–900&#xa0;°C) on stability, morphology, texture, and catalytic performance of the formed Co<sub>3</sub>O<sub>4</sub> have been addressed too. Co<sub>3</sub>O<sub>4</sub> was found to be the major formed phase together with trace quantities of graphitic carbon over the 300–700&#xa0;°C range. Pushing the calcination temperature to 900&#xa0;°C was associated with a thermal reduction of Co<sub>3</sub>O<sub>4</sub> to CoO and the elimination of the graphitic carbon. The highest activity was obtained using the 700&#xa0;°C calcined catalyst (4449 ml g<sup>− 1</sup> min<sup>− 1</sup> at 45&#xa0;°C).</p> Graphical Abstract <p></p>

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Green Synthesis of Co3O4 Catalysts Using Jasmine Flower Extract for the Effective Hydrolysis of NaBH4

  • Ebtesam Hassan,
  • Tarek T. Ali,
  • Bahaa M. Abu-Zied

摘要

Green synthesis is an important route in the preparation of bare metals and metal oxides that provides cost-effective, eco-friendly, and highly efficient catalysts for catalyzing various reactions. In this paper we report, for the first time, the green synthesis of Co3O4 employing jasmine flower extract as a green precursor for the application as catalyst during NaBH4 hydrolysis. Moreover, the role of calcination temperature (300–900 °C) on stability, morphology, texture, and catalytic performance of the formed Co3O4 have been addressed too. Co3O4 was found to be the major formed phase together with trace quantities of graphitic carbon over the 300–700 °C range. Pushing the calcination temperature to 900 °C was associated with a thermal reduction of Co3O4 to CoO and the elimination of the graphitic carbon. The highest activity was obtained using the 700 °C calcined catalyst (4449 ml g− 1 min− 1 at 45 °C).

Graphical Abstract