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Updated: Jan 11, 2026

Fabrication of a Functionalized Magnetic Bacterial Nanocellulose with Iron Oxide Nanoparticles
Published on: May 26, 2016
Porous cellulose microfibrils functionalized with magnetite nanostructures: Morphology controlled efficiency in
Amel El Ghali1, Laroussi Chaabane2, Meriem Ben Daoud3
1Physico-Chemistry Laboratory of Innovative Materials (LR24ES16), Preparatory Institute for Engineering Studies of Monastir, University of Monastir, Tunisia.
Abstract:
As the demand for effective methods to remove organic dyes from water bodies continues to rise, addressing the dual challenges of biomass valorization and sustainable catalysis has become critical for the future of wastewater treatment. Despite notable advancements, the influence of the different morphologies of sono-Fenton-driven Fe3O4 nanoparticles (NPs) and nanorods (NRs) supported on porous cellulose microfibrils (PCMs) remain insufficiently explored. In this pioneering study, we present a novel approach to synthesizing PCMs derived from coffee pulp, a renewable biomass, thereby offering an innovative pathway to transform agricultural waste into high-value, sustainable materials. Through alkali treatment and bleaching, non-cellulosic impurities were effectively removed, yielding hydrophilic PCMs with a highly intricate macro- and microporous structure. To enhance their catalytic efficiency, Fe3O4NPs and NRs were successfully integrated into the PCM framework through co-precipitation and hydrothermal techniques. This process resulted in a uniform distribution of Fe3O4NPs (10-30 nm) and Fe3O4NRs (∼150 nm length and ∼ 53 nm width), significantly increasing the surface roughness and porosity of the PCMs. When tested for the degradation of Acid Blue 25 (AB 25) dye in aqueous solution, the sono-Fenton catalytic performance of PCMs@Fe3O4NPs and PCMs@Fe3O4NRs demonstrated exceptional efficiency. The combination of ultrasound, hydrogen peroxide, and PCMs@Fe3O4NRs achieved complete dye degradation (100 %) in 12 min, surpassing the performance of PCMs@Fe3O4NPs, which achieved 97 % ± 0.4 % degradation in 15 min. Kinetic studies confirmed that the degradation followed pseudo-first-order (PFO) reaction kinetics, while radical scavenging experiments identified hydroxyl radicals (•OH) as the dominant reactive species. Furthermore, the PCMs@Fe3O4NRs catalyst demonstrated excellent reusability, maintaining a degradation efficiency above 98 % ± 0.3 % after five consecutive cycles, underscoring its potential as a sustainable and high-performance material for advanced wastewater treatment applications.
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