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Graphene oxide and cobalt oxide nanocomposites (Co3O4/GO) are fabricated in situ as heterogeneous catalysts by the decomposition of cobalt nitrate through heat and crystal growth of Co3O4 on the surface of GO sheets in 1-hexanol solvent. The Co3O4/GO catalyst is characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), energy dispersive X-ray spectroscopy (EDS), scanning electron microscopy (SEM), and high-resolution transmission electron microscopy (HRTEM). Results show that the Co3O4/GO catalysts are large GO sheets decorated homogenously with well-dispersed Co3O4 nanoparticles. Although Co3O4 or GO alone exhibit little catalytic activity, their hybrid (Co3O4/GO) exhibits an unexpectedly high catalytic activity in the degradation of Orange II in water by advanced oxidation technology based on sulfate radicals, and 100% decomposition can be achieved in 6 min. These phenomena suggest a synergistic catalytic activity of Co3O4 and GO in the hybrid.

The current paper investigated the removal of the azo dye Orange II from water using advanced oxidation processes based on sulfate radicals. The cobalt oxide catalyst immobilized on graphene oxide (GO) can activate peroxymonosulfate (PMS) for the degradation of Orange II in water. The Co 3 O 4 /GO catalyst system was characterized via X-ray diffraction, Fourier transform infrared spectroscopy, Raman spectroscopy, scanning electron microscopy, and X-ray spectroscopy. Results showed that Co 3 O 4 was distributed on GO. The Co 3 O 4 /GO catalyst system exhibited high activity in Orange II oxidation when the Co 3 O 4 /GO catalyst has an optimum Co 3 O 4 loading. In addition, 100% decomposition could be achieved within 6 min with 0.2 mM Orange II, 0.1 g L −1 catalyst, and 2 mM PMS. Meanwhile, inductively coupled plasma analysis revealed that the leach of cobalt ions was low. The catalyst also exhibited stable performance after several rounds of regeneration. Several operational parameters, such as catalyst amount, oxidant amount, pH, temperature, and oxidation rate, affected the degradation of Orange II.

Graphene oxide (GO) nanosheets as functional material have a unique planar structure and intriguing mechanical that have attracted intensive interests recently. A method was developed for the immobilization protease on GO sheets using glutaraldehyde as cross-linking reagent. The results showed that the thermostability and reusability of immobilized protease have been obviously improved compared to the free enzyme. However, there was no significant change in optimum pH value between the free and immobilized protease. The immobilized protease exhibited good operational stability. The apparent K m and V max for free and immobilized alkaline protease were determined, and the bio-catalytic activity was not impaired by immobilization.