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  • Title: Visible-light-driven photodegradation of methylene blue and doxycycline hydrochloride by waste-based S-scheme heterojunction photocatalyst Bi5O7I/PCN/tea waste biochar.
    Author: Soni V, Sonu, Sudhaik A, Singh P, Thakur S, Ahamad T, Nguyen VH, Thi LP, Quang HHP, Chaudhary V, Raizada P.
    Journal: Chemosphere; 2024 Jan; 347():140694. PubMed ID: 37972865.
    Abstract:
    Herein, we have reported a photocatalytic Bi5O7I, protonated g-C3N4 heterojunction with directional charge transfer channels provided by tea waste biochar to achieve effective e-/h+ pair isolation for the improved degradation of Methylene blue (MB) and Doxycycline hydrochloride (DCHCl). An S-scheme heterojunction was fabricated via the novel method that combined hydrothermal and ultrasonic dispersion, followed by an electrostatic self-assembly route. The as-fabricated Bi5O7I/protonated g-C3N4/Tea waste biochar heterojunction formed a strong contact at the interface, as supported by the electron microscopic results. As per the adsorption and photocatalytic degradation kinetics study, Bi5O7I/Tea waste biochar/protonated g-C3N4 (40 wt%) heterojunction showed a higher adsorption rate of 41.56% and 32% for MB and DCHCl within 30 min in the dark. Also, 92.02% MB and 90.21% DCHCl degradation rates in 60 and 90 min, respectively, are approximately 43 and 32 times higher than bare Bi5O7I and protonated g-C3N4 photocatalysts. The highest adsorption and degradation rate was achieved owing to the addition of Tea waste biochar and protonated g-C3N4 in a controlled ratio, and the sufficient interfacial contact between Bi5O7I and protonated g-C3N4 is for the improved isolation rate of e-/h+ pairs as evidenced by zeta potential values photoluminescence spectra as well as from scanning and transmission electron microscopy. Moreover, Bi5O7I/Tea waste biochar/protonated g-C3N4 (40 wt%) possessed high stability and recyclability after four consecutive cycles without much altering the degradation ability. Therefore, we believe that the as-fabricated Bi5O7I/Tea waste biochar/protonated g-C3N4 (40 wt%) provides new insight into the highly efficient S-scheme mechanisms significant for accelerating multicomponent photocatalytic redox reactions; while forming an effective visible light responsive candidate for treating wastewater.
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