TY - JOUR
T1 - Clarifying the mechanism of peroxydisulfate and sulfite activated by Fe2+ for waste activated sludge pretreatment
T2 - Enhancement of dewaterabiliy, removal of antibiotic resistance genes and pathogenic microorganisms
AU - Zhang, Ruiliang
AU - Han, Yule
AU - Cai, Teng
AU - Dai, Qicai
AU - Liu, Zhaobin
AU - Gao, Yijing
AU - Lu, Xueqin
AU - Zhen, Guangyin
N1 - Publisher Copyright:
© 2024
PY - 2024/11/15
Y1 - 2024/11/15
N2 - The remarkable performance of SO4-• based advanced oxidation processes in improving waste activated sludge (WAS) dewatering has recently received considerable attention. However, its potential effect on the removal of emerging pollutants is often overlooked. In this study, two types of pretreatment methods (S2O82-/Fe2+ and SO32-/Fe2+) were employed to comprehensively evaluate their performance in improving the dewatering of WAS and the removal of antibiotic resistance genes (ARGs) and pathogenic microorganisms. At the optimal dosage of 1.2/1.5 mmol-S2O82-/Fe2+/g-VS, the capillary suction time reduction rate of WAS after S2O82-/Fe2+ was 1.8 times than that of SO32-/Fe2+. Notably, both S2O82-/Fe2+ and SO32-/Fe2+ could remove the 12 types of ARGs identified in WAS. Nonetheless, S2O82-/Fe2+ was more effective in removing ARGs, with a range of removal rate (0.96–2.17 log-units), and reduced the propagation and proliferation potential of residual ARGs. Furthermore, the coliforms content in WAS after S2O82-/Fe2+ decreased significantly with a minimum of 1.84 ± 0.24 log (MPN/g-TS) compared to SO32-/Fe2+. Further analysis indicated that the redistribution of bound extracellular polymeric substances (EPS) in WAS, especially the variations in protein, was the key factor affecting the dewaterability. In contrast to SO32-/Fe2+, the S2O82-/Fe2+ could quickly destroy the EPS structure to release bound water, accelerate the dissociation of WAS flocs, and cause cell lysis and DNA dissolution because of the continuous production and accumulation of SO4-• in the hostile conditions inside. Therefore, S2O82-/Fe2+ is an efficient, economical, and green method to improve WAS dewatering and the removal of pollutants.
AB - The remarkable performance of SO4-• based advanced oxidation processes in improving waste activated sludge (WAS) dewatering has recently received considerable attention. However, its potential effect on the removal of emerging pollutants is often overlooked. In this study, two types of pretreatment methods (S2O82-/Fe2+ and SO32-/Fe2+) were employed to comprehensively evaluate their performance in improving the dewatering of WAS and the removal of antibiotic resistance genes (ARGs) and pathogenic microorganisms. At the optimal dosage of 1.2/1.5 mmol-S2O82-/Fe2+/g-VS, the capillary suction time reduction rate of WAS after S2O82-/Fe2+ was 1.8 times than that of SO32-/Fe2+. Notably, both S2O82-/Fe2+ and SO32-/Fe2+ could remove the 12 types of ARGs identified in WAS. Nonetheless, S2O82-/Fe2+ was more effective in removing ARGs, with a range of removal rate (0.96–2.17 log-units), and reduced the propagation and proliferation potential of residual ARGs. Furthermore, the coliforms content in WAS after S2O82-/Fe2+ decreased significantly with a minimum of 1.84 ± 0.24 log (MPN/g-TS) compared to SO32-/Fe2+. Further analysis indicated that the redistribution of bound extracellular polymeric substances (EPS) in WAS, especially the variations in protein, was the key factor affecting the dewaterability. In contrast to SO32-/Fe2+, the S2O82-/Fe2+ could quickly destroy the EPS structure to release bound water, accelerate the dissociation of WAS flocs, and cause cell lysis and DNA dissolution because of the continuous production and accumulation of SO4-• in the hostile conditions inside. Therefore, S2O82-/Fe2+ is an efficient, economical, and green method to improve WAS dewatering and the removal of pollutants.
KW - Antibiotics resistance genes
KW - Peroxydisulfate
KW - Sludge dewaterability
KW - Sulfite
KW - Waste activated sludge
UR - https://www.scopus.com/pages/publications/85206613740
U2 - 10.1016/j.cej.2024.156759
DO - 10.1016/j.cej.2024.156759
M3 - 文章
AN - SCOPUS:85206613740
SN - 1385-8947
VL - 500
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 156759
ER -