Journal
ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
Volume 28, Issue 21, Pages 27398-27410Publisher
SPRINGER HEIDELBERG
DOI: 10.1007/s11356-021-12640-3
Keywords
Adsorption; Porous carbons; Sodium lignosulfonate; One-step method; Chloramphenicol
Categories
Funding
- National Postdoctoral Science Foundation [2017M610618]
- Postdoctoral Science Foundation Funded Project of Shaanxi Province [2017BSHEDZZ64]
- Fundamental Research Funds for the Central Universities of Chang' an University [300102290104]
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This study successfully developed an effective adsorbent for the removal of chloramphenicol in water by converting waste lignin into porous carbon materials, demonstrating high efficiency, wide application potential, and good stability.
This work explored the use of porous carbon (PC) materials converted from waste lignin as raw materials for the removal of chloramphenicol (CAP) in water. The PC with controllable pores was prepared through a facile, cost-effective one-step method. The physical and chemical properties of the material were characterized by BET, SEM, FT-IR, and XRD, and the best conditions for preparation were selected based on the results of adsorption experiments. The PC, which was prepared at reaction temperature of 800 degrees C and the K2CO3/sodium lignosulfonate mass ratio of 4, namely PC-800-4, had a high specific surface area (1305.5 m(2) g(-1)) and pore volume (0.758 cm(3) g(-1)). At a lower initial concentration of CAP (C-0 = 120 mg L-1), the maximum adsorption capacity of this adsorbent was 534.0 mg g(-1) at 303 K. In addition, PC-800-4 maintained good adsorption performance in a wide pH range and strongly resisted the interference of ions and humic acid. The results showed that the adsorption removal CAP was based on physical adsorption and chemical adsorption as a process supplement. The advantages of wide sources, high efficiency and speed, wide application, and rich oxygen-containing functional groups made the adsorbent have great application potential for removal chloramphenicol from water.
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