Enhanced tetracycline degradation using carbonized PEI-grafted lignin microspheres supported Fe-loading catalyst
Jiubing Zhang1, Hongye Wu2, Zhili Li3
1School of Chemistry & Chemical Engineering, Guangxi Key Laboratory of Petrochemical Resource Processing and Process Intensification Technology, Guangxi University, 100 Daxuedong Road, Nanning 530004, China; Key Laboratory of Green Building Materials, Henan Building Materials Research and Design Institute Co., Ltd, Henan Academy of Sciences, 228 Chongshi Lane, Zhengdong New District, Zhengzhou 450046, China.
Abstract:
Traditional homogeneous Fenton systems face limitations, including a narrow pH range, potential secondary pollution, and poor repeatability. In this study, these bottlenecks in tetracycline wastewater treatment were addressed with using carbonized porous polyethyleneimine-grafted lignin microspheres (PLMs) supported Fe-loading catalysts (PLMs/Fe-C). An optimized PLMs/Fe-C catalyst under specific conditions (carbonization temperature: 350 °C, PLMs: Fe = 1:1, and alkali lignin: PEI = 1:4) was developed, which proved to be an efficient Fenton-like catalyst for tetracycline (TC) degradation. TC degradation results showed that the PLMs/Fe-C + H2O2 system achieved a high removal efficiency of 100 % within 150 min (50 mL TC with an initial concentration of 50 mg/L, 0.015 g catalyst, 0.5 mL H2O2), demonstrating its applicability over a wide pH range (3-10) and the capability to remove multiple pollutants (2,4-D, BPA, Lev, etc.). This efficiency was attributed to the stronger electron-donating ability and mass transfer properties derived from the porous structure and functional groups. Arrhenius fitting analysis revealed a lower activation energy (E = 52.98 kJ/mol) for the PLMs/Fe-C, indicating a more accessible reaction. Additionally, the removal efficiency marginally decreased from 100 % to 98.32 % after five cycles, demonstrating excellent reusability. Mechanistic investigations indicated that the PLMs/Fe-C can activate H2O2 to produce reactive oxygen species •OH, 1O2, effectively degrading TC.
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