Preparation of nZVI embedded modified mesoporous carbon for catalytic persulfate to degradation of reactive black 5

Highlights

• The MCNZVI is prepared as an interesting material for PS activation.

• Graphitized carbon shells facilitate electron transfer from Fe⁰.

• The MCNZVI exhibits excellent performance to degrade RB5 by ¹O₂.

• The MCNZVI has high stability and reusability in the oxidation system.

Abstract

High-efficiency and cost-effective catalysts with available strategies for persulfate (PS) activation are critical for the complete mineralization of organic contaminants in the environmental remediation and protection fields. A nanoscale zero-valent iron-embedded modified mesoporous carbon (MCNZVI) with a core-shell structure is synthesized using the hydrothermal synthesis method and high-temperature pyrolysis. The results showed that nZVI could be impregnated within mesoporous carbon frameworks with a comparatively high graphitization degree, rich nitrogen doping content, and a large surface area and pore volume. This material was used as a persulfate activator for the oxidation removal of Reactive Black 5 (RB5). The effects of the material dosage, PS concentration, pH, and some inorganic anions (i.e., Cl⁻, SO₄²⁻) on RB5 degradation were then investigated. The highest degradation efficiency (97.3%) of RB5 was achieved via PS (20 mmol/L) activation by the MCNZVI (0.5 g/L). The pseudo-first-order kinetics (k = 2.11 × 10⁻² min⁻¹) in the MCNZVI/PS (0.5 g/L, 20 mmol/L) was greater than 100 times than that in the MCNZVI and PS. The reactive oxygen species (ROS), including ¹O₂, SO₄^·−, HO^·, and ·O₂⁻, were generated by PS activation with the MCNZVI. Singlet oxygen was demonstrated to be the primary ROS responsible for the RB5 degradation. The MCNZVI could be reused and regenerated for recycling. This work provides new insights into PS activation to remove organic contamination.

Graphical abstract

Keywords

MCNZVI / Core-shell structure / Reactive Black 5 / Persulfate / Mechanism

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Acknowledgements

This work was financially supported by the National Natural Science Foundation of China (Grant No. 41907168).

Electronic Supplementary Material

Supplementary material is available in the online version of this article at https://doi.org/10.1007/s11783-020-1372-4 and is accessible for authorized users.

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