TY - JOUR
T1 - β-cyclodextrin-modified cobalt oxide as a heterogeneous catalyst for efficient peroxymonosulfate activation towards the degradation of Ciprofloxacin
T2 - Performance and degradation pathways
AU - Alotaibi, Mshari A.
AU - Khalid, Awais
AU - Alharthi, Abdulrahman I.
N1 - Publisher Copyright:
© 2024 Elsevier B.V.
PY - 2025/2/19
Y1 - 2025/2/19
N2 - In this study, β-cyclodextrin-modified cobalt oxide (Co3O4@β-CD) composites were developed through hydrothermal processes and employed for heterogeneous activation of peroxymonosulfate (PMS) for the removal of ciprofloxacin (CIP) antibiotics. The results revealed that the degradation of CIP by Co3O4@β-CD/PMS was 99.13 %, which was significantly higher than the degradation of CIP by Co3O4/PMS (79.06 %) in a 25-minute period under optimal conditions ([Co3O4@β-CD] = 0.25 g/L, [PMS] = 0.25 mM, pH=7.0). The enhanced degradation of CIP contributed to the greater surface area (162.84 m2/g) of the Co3O4@β-CD to the Co3O4 (121.47 m2/g). Besides, the study assessed the impact of several reaction variables and interrupting anions on the abatement of CIP. A possible degradation procedure for CIP has been established by identifying reaction intermediates. The activation of PMS was achieved by both radical and non-radical routes. Further, Co3O4@β-CD exhibited remarkable stability and maintained its degrading efficiency after five consecutive cycles.
AB - In this study, β-cyclodextrin-modified cobalt oxide (Co3O4@β-CD) composites were developed through hydrothermal processes and employed for heterogeneous activation of peroxymonosulfate (PMS) for the removal of ciprofloxacin (CIP) antibiotics. The results revealed that the degradation of CIP by Co3O4@β-CD/PMS was 99.13 %, which was significantly higher than the degradation of CIP by Co3O4/PMS (79.06 %) in a 25-minute period under optimal conditions ([Co3O4@β-CD] = 0.25 g/L, [PMS] = 0.25 mM, pH=7.0). The enhanced degradation of CIP contributed to the greater surface area (162.84 m2/g) of the Co3O4@β-CD to the Co3O4 (121.47 m2/g). Besides, the study assessed the impact of several reaction variables and interrupting anions on the abatement of CIP. A possible degradation procedure for CIP has been established by identifying reaction intermediates. The activation of PMS was achieved by both radical and non-radical routes. Further, Co3O4@β-CD exhibited remarkable stability and maintained its degrading efficiency after five consecutive cycles.
KW - Catalytic degradation
KW - CIP removal
KW - CoO@β-CD
KW - Degradation pathways
KW - PMS activation
UR - http://www.scopus.com/inward/record.url?scp=85201897255&partnerID=8YFLogxK
U2 - 10.1016/j.seppur.2024.129274
DO - 10.1016/j.seppur.2024.129274
M3 - Article
AN - SCOPUS:85201897255
SN - 1383-5866
VL - 354
JO - Separation and Purification Technology
JF - Separation and Purification Technology
M1 - 129274
ER -