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A Facile Synthetic Method to Obtain Bismuth Oxyiodide Microspheres Highly Functional for the Photocatalytic Processes of Water Depuration
Published on: March 29, 2019
Bi5O7I supported chitosan nanocomposite a robust, highly efficient, and sustainable catalyst for methyl orange pand
Abdelmalik Brik1, Mustapha El Kadiri2, Taha El Assimi2
1IMED-Lab, Faculty of Sciences and Techniques, CadiAyyad University, Avenue Abdelkrim Elkhattabi, B.P. 549, 40000 Marrakech, Morocco; High Throughput Multidisciplinary Research (HTMR), Mohammed VI Polytechnic University (UM6P), Lot 660 Hay Moulay Rachid, Ben Guerir, Morocco.
Abstract:
Chitosan (CS) has garnered significant attention as catalyst support due to its abundance, eco-friendliness, and renewable nature, making it a highly sustainable option in catalytic applications. We report herein a new simple and eco-friendly strategy to stabilize Bi5O7I nanosheets within CS-hydrogel and their immobilization in catalytic applications. The Bi5O7I nanosheets were firstly prepared through a solvothermal process and then stabilized within CS-hydrogel beads through a simple co-precipitation in alkaline media. The prepared Bi5O7I nanosheets and Bi5O7I@CSb composite were fully characterized by X-ray diffraction, XPS, SEM, EDS, TGA, FTIR, Raman, and Zeta-potential. Photodegradation experiments of methyl orange (MO) over Bi5O7I@CSb in aqueous media exhibit a high performance with a removal efficiency of up to 97 % within 120 min. Likewise, the Bi5O7I@CSb composite demonstrated a high reduction efficiency toward 4-nitrophenol (4-NP) reduction up total conversion within only 3 min using NaBH4 as a reducing agent. More importantly, the Bi5O7I@CSb composite could easily be recovered from the reaction mixture by simple filtration with no significant loss of their activity and stability even after 7 and 10 successive uses for both MO and 4-NP, respectively. Thus, this contribution may offer a great opportunity for the use of CS bismuth-based materials in catalytic and photocatalytic wastewater treatment.

