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Research Article

The first and low cost copper Schiff base/manganese oxide bio nanocomposite from unwanted plants as a robust industrial catalyst

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Pages 560-571 | Received 15 Sep 2019, Accepted 28 Dec 2019, Published online: 11 Feb 2020

Figures & data

Figure 1. XRD of synthesized product from manganese salt in the presence of plant at pH = 7 (a), at pH = 9 (b) and XRD of Mn3O4/CuL bio-nanocolloid (c).

Figure 1. XRD of synthesized product from manganese salt in the presence of plant at pH = 7 (a), at pH = 9 (b) and XRD of Mn3O4/CuL bio-nanocolloid (c).

Scheme 1. Synthesis of Mn3O4/CuL bio-nanocolloid under ultrasonic irradiation.

Scheme 1. Synthesis of Mn3O4/CuL bio-nanocolloid under ultrasonic irradiation.

Figure 2. 1H NMR (top) and 13C (down) spectra of L ligand.

Figure 2. 1H NMR (top) and 13C (down) spectra of L ligand.

Figure 3. FT-IR of L ligand, CuL nanocomplex, and Mn3O4/CuL bio-nanocolloid.

Figure 3. FT-IR of L ligand, CuL nanocomplex, and Mn3O4/CuL bio-nanocolloid.

Figure 4. The EDAX (a), elemental analysis (a), SEM (b) and TEM (c) of Mn3O4/CuL bio-nanocolloid.

Figure 4. The EDAX (a), elemental analysis (a), SEM (b) and TEM (c) of Mn3O4/CuL bio-nanocolloid.

Figure 5. (a–h) Optimization of oxidation of benzyl alcohol.

Figure 5. (a–h) Optimization of oxidation of benzyl alcohol.

Scheme 2. The oxidation of primary and secondary alcohols catalysed by Mn3O4/CuL bio-nanocolloid using H2O2 to have O2 and water as byproducts under ultrasonic irradiation.

Scheme 2. The oxidation of primary and secondary alcohols catalysed by Mn3O4/CuL bio-nanocolloid using H2O2 to have O2 and water as byproducts under ultrasonic irradiation.

Figure 6. Proposed mechanism for the catalytic oxidation of benzyl alcohol by Mn3O4/CuL bio-nanocolloid.

Figure 6. Proposed mechanism for the catalytic oxidation of benzyl alcohol by Mn3O4/CuL bio-nanocolloid.

Table 1. Oxidation of alcohols catalysed by Mn3O4/CuL bio-nanocolloid using hydrogen peroxide.

Table 2. Comparison of the result of this study with that of related references.

Figure 7. (a) The FT-IR of fresh catalyst (top) and reused catalyst after six times (down) and (b) recycling of catalyst.

Figure 7. (a) The FT-IR of fresh catalyst (top) and reused catalyst after six times (down) and (b) recycling of catalyst.