期刊
CHEMOSPHERE
卷 262, 期 -, 页码 -出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2020.128322
关键词
Sludge; Activated carbon; Adsorption; Pharmaceuticals; Simulated effluent
This study investigated the use of sludge-derived activated carbons for pharmaceuticals adsorption in aqueous media. The ABSAC showed superior adsorption efficiency compared to BSAC, with higher surface area and total pore volume. The adsorbent proved to be highly efficient in removing pharmaceutical compounds in a simulated drug effluent, making it a promising candidate for treating pharmaceutical contaminants in industrial wastewater.
The presence of emerging contaminants such as pharmaceuticals in aquatic means presents as a serious threat, since their real consequences for the environment and human health are not well known. Therefore, this work consisted of preparing and characterize sludge-derived activated carbons (beverage sludge activated carbon - BSAC and acid-treated beverage sludge activated carbon - ABSAC) to investigate their use in the pharmaceuticals adsorption in aqueous media. The morphology study has demonstrated that ABSAC, unlike BSAC, exhibited an abundant porous structure, with smaller particles and bigger roughness. Adsorption results indicated that the ABSAC was more effective that BSAC, since it presented superior surface area (642 m(2) g(-1)) and total pore volume (0.485 cm(3) g(-1)) values. Pseudosecond-order kinetic model was more suitable to predict experimental data. Sips model best described the equilibrium data, with maximum adsorption capacities of 145, 105, and 57 mg g(-1) for paracetamol, ibuprofen, and ketoprofen, respectively. Besides, the sludge-derived adsorbent was highly efficient in the treatment of a simulated drug effluent, removing 85.16% of the pharmaceutical compounds. Therefore, the material prepared in this work possesses intrinsic characteristics that make it a remarkable adsorbent to be applied in the treatment of pharmaceutical contaminants contained in industrial wastewater. (C) 2020 Elsevier Ltd. All rights reserved.
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