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Adsorption of emerging pollutants on lignin-based activated carbon: Analysis of adsorption mechanism via characterization, kinetics and equilibrium studies
被引:84
|作者:
Sellaoui, L.
[1
]
Gomez-Aviles, A.
[2
]
Dhaouadi, F.
[1
]
Bedia, J.
[2
]
Bonilla-Petriciolet, A.
[3
]
Rtimi, S.
[4
]
Belver, C.
[2
]
机构:
[1] Monastir Univ, Fac Sci Monastir, Lab Quantum & Stat Phys, LR18ES18, Monastir, Tunisia
[2] Univ Autonoma Madrid, Chem Engn Dept, Campus Cantoblanco, E-28049 Madrid, Spain
[3] Inst Tecnol Aguascalientes, Aguascalientes 20256, Aguascalientes, Mexico
[4] Global Inst Water Environm & Hlth, CH-1201 Geneva, Switzerland
关键词:
Acetaminophen;
Acetamiprid;
Activated carbon;
Adsorption;
PERSONAL CARE PRODUCTS;
AQUEOUS-SOLUTIONS;
REMOVAL;
PHARMACEUTICALS;
WATER;
ACETAMINOPHEN;
PARACETAMOL;
FORMULATION;
PESTICIDES;
DYE;
D O I:
10.1016/j.cej.2022.139399
中图分类号:
X [环境科学、安全科学];
学科分类号:
08 ;
0830 ;
摘要:
Lignin has been employed as a precursor to synthesize activated carbons with the aim of lignin-biomass reva-lorization. The properties of these activated carbons were compared, and the best adsorbent was employed to remove two emerging pollutants from water, acetaminophen and acetamiprid. The adsorption mechanisms of pharmaceutical and pesticide compounds were analyzed, modeled and interpreted via statistical physics models. In particular, adsorption kinetics and isotherms of acetaminophen and acetamiprid at temperatures between 20 and 60 degrees C were quantified experimentally. Equilibrium data were fitted to different statistical physics-based isotherm models to establish the corresponding adsorption mechanism. A double layer adsorption model with one type of functional group was the best to correlate and explain the removal of these organic molecules. Steric parameters for the adsorption of these organic compounds were also calculated thus determining that their adsorption was multi-molecular. At tested operating conditions, acetaminophen adsorption was endothermic, while acetamiprid removal was exothermic. Physical adsorption forces were expected to be responsible for the removal of both compounds. This study reports new insights on the adsorption mechanisms of relevant emerging pollutants commonly found in water worldwide.
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