Research Article
Tuning of Activated Carbon for Solvent-Free Oxidation of Cyclohexane
Table 1
AC-catalyzed organic substrates, with productivity and reaction conditions.
| S. number | Oxidation reaction | Productivity | Reaction condition | Ref |
| 1 | Aerobic benzylic oxidation of 2-benzylbenzo[d]imidazoles | 0.35 | Reactant: 2 mmol; AC: 60 mg; time: 12 hours; temp: 80°C | [24] | 2 | Aerobic oxidation of benzyl alcohol | 0.11 | Reactant: 0.184 mmol; AC: 0.1 g; time: 3 hours; temp: 80°C | [25] | 3 | Oxidation of cyclohexane | 28.8 | Reactant: 59 mmol; acetonitrile: 10 mL; TBHP: 5 mL; O2: 30 mL/min, 70°C, 2 hours | [26] | 4 | Oxidation of benzyl alcohol | 0.506 | Reactant: 1.1 mmol; AC: 100 mg; ethanol: 5 cm3; temp: 120°C; time: 5 hours | [27] | 5 | Oxidation of cinnamyl alcohol | 0.15 | Reactant: 1.1 mmol; AC: 100 mg; ethanol: 5 cm3; temp: 80°C; time: 15 hours | 6
| Oxidation of cyclohexane | 2.14 | Reactant: 115.56 mmol; AC: 0.4 g; temp: 75; time: 14 hours; pO2: 760 Torr | Current study | 4.85 | Reactant: 115.56 mmol; AC: 0.4 g; temp: 75; time: 14 hours; pO2: 760 Torr; NaOH: 0.2 mmol |
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Productivity (mmol g−1 h−1) = mmol of product/catalyst (g) × time (h).
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