Biocatalyst Based on Magnetic Nanoparticles with Cu(II), Mn(II), Zn(II) and Immobilised Catalase

1Citations
Citations of this article
5Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

This article described a process for the preparation of a Fe3O4 nanocatalyst modified with Mn(II), Cu(II) and Zn(II) ions immobilised with catalase. The effectiveness of the description of the ion sorption process was compared with four equilibrium models: Langmuir, Freundlich, Redlich–Peterson and Sips. The proposed models allow the description of both single- and multi-component sorption. The results were also verified by DFT analysis. The Langmuir model describing single-component sorption and the extended Langmuir model for multi-component systems with the best fit represented the sorption of metal ions on Fe3O4. The maximum sorption capacity values in the pseudo-second-order kinetic model were 10.76, 12.87 and 10.52 mg/g for Cu(II), Zn(II) and Mn(II) in the single-component systems and 11.79, 8.54 and 2.03 mg/g for Cu(II), Zn(II) and Mn(II) in the multi-component system, respectively. The kinetics parameters were described most accurately by a pseudo-second-order model, which suggested, along with the Extended Langmuir model, the chemical nature of the sorption. After preparation of the Fe3O4/Mn–Zn–Cu material, catalase was immobilised on the surface of the material. The final material was able to decompose hydrogen peroxide with an activity of 7130 units/g of material. Modification of the material with Mn(II), Cu(II) and Zn(II) resulted in an increase in H2O2 removal efficiency exceeding 99.9%.

Cite

CITATION STYLE

APA

Długosz, O., Matyjasik, W., Matysik, J., Szostak, K., Śliwa, P., & Banach, M. (2024). Biocatalyst Based on Magnetic Nanoparticles with Cu(II), Mn(II), Zn(II) and Immobilised Catalase. Journal of Cluster Science, 35(1), 143–158. https://doi.org/10.1007/s10876-023-02465-0

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free