A comparative study on the adsorption of ciprofloxacin (CIP) and sulfamethoxazole (SMX) onto CO2-activated biochars derived from leather tannery waste (ABT) and Sargassum brown macroalgae (ABS) is presented. N2 physisorption revealed that ABS possesses a higher Langmuir surface area (1305 m2/g) and a hierarchical micro–mesoporous structure, whereas ABT exhibits a lower surface area (412 m2/g) and a predominantly microporous texture. CHNS and FTIR analyses confirmed the presence of N-, O-, and S-containing heteroatoms and functional groups on both adsorbents, enhancing surface reactivity. Adsorption isotherms fitted well to the Langmuir model, with ABS showing superior maximum capacities of 256.41 mg/g (CIP) and 256.46 mg/g (SMX) compared to ABT (210.13 and 213.00 mg/g, respectively). Kinetic data followed a pseudo-second-order model (R2 > 0.998), with ABS exhibiting faster uptake due to its mesoporosity. Over eight reuse cycles, ABS retained >75% removal efficiency for both antibiotics, while ABT declined to 60–70%. pH-dependent adsorption behavior was governed by the point of zero charge (pHPZC≈ 9.0 for ABT; ≈7.2 for ABS), influencing electrostatic and non-electrostatic interactions. These findings demonstrate that ABS is a highly effective, sustainable adsorbent for antibiotic removal in water treatment applications.

Sustainable Adsorption of Antibiotics in Water: The Role of Biochar from Leather Tannery Waste and Sargassum Algae in Removing Ciprofloxacin and Sulfamethoxazole

Taghavi, Somayeh
;
Signoretto, Michela
Writing – Review & Editing
2026

Abstract

A comparative study on the adsorption of ciprofloxacin (CIP) and sulfamethoxazole (SMX) onto CO2-activated biochars derived from leather tannery waste (ABT) and Sargassum brown macroalgae (ABS) is presented. N2 physisorption revealed that ABS possesses a higher Langmuir surface area (1305 m2/g) and a hierarchical micro–mesoporous structure, whereas ABT exhibits a lower surface area (412 m2/g) and a predominantly microporous texture. CHNS and FTIR analyses confirmed the presence of N-, O-, and S-containing heteroatoms and functional groups on both adsorbents, enhancing surface reactivity. Adsorption isotherms fitted well to the Langmuir model, with ABS showing superior maximum capacities of 256.41 mg/g (CIP) and 256.46 mg/g (SMX) compared to ABT (210.13 and 213.00 mg/g, respectively). Kinetic data followed a pseudo-second-order model (R2 > 0.998), with ABS exhibiting faster uptake due to its mesoporosity. Over eight reuse cycles, ABS retained >75% removal efficiency for both antibiotics, while ABT declined to 60–70%. pH-dependent adsorption behavior was governed by the point of zero charge (pHPZC≈ 9.0 for ABT; ≈7.2 for ABS), influencing electrostatic and non-electrostatic interactions. These findings demonstrate that ABS is a highly effective, sustainable adsorbent for antibiotic removal in water treatment applications.
2026
18
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10278/5111167
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