TY - JOUR
T1 - Colloidal activated carbon as a highly efficient bifunctional catalyst for phenol degradation
AU - Septian, Ardie
AU - Kumar, Alam Venugopal Narendra
AU - Sivasankar, Annamalai
AU - Choi, Jiyeon
AU - Hwang, Inseong
AU - Shin, Won Sik
N1 - Publisher Copyright:
© 2021 Elsevier B.V.
PY - 2021/7/15
Y1 - 2021/7/15
N2 - A preparation of colloidal activated carbon (CAC) for phenol remediation from groundwater was introduced. The CAC prepared by a simple pulverization technique was an excellent metal-free catalyst for persulfate (PS) activation due to high contact surface area. The removal efficiency of phenol in the PS/CAC system (~100%) was higher than that in the PS/activated carbon (AC) system (90.1%) and was superior to the conventional PS/Fe2+ system (27.9%) within 30 min. The phenol removal reaction occurred both in bulk solution and at the surface of the CAC, as confirmed by Langmuir–Hinshelwood (L–H) kinetic model fitting, FT−IR, and electron spin resonance (ESR) analyses. The downsizing of particle size from AC to CAC played a critical role in the radical oxidation mechanism by leading to the formation of predominant superoxide radical (O2•–) species in the PS/CAC system. Anions NO3–, SO42−, and Cl– slightly inhibited the phenol removal efficiency, whereas CO32−, HCO3− and PO43− did not. Ferulic acid (C10H10O4) was detected as an organic byproduct of phenol oxidation. The use of CAC as a metal-free bifunctional catalyst has an important implication in the PS activation for phenol degradation in groundwater.
AB - A preparation of colloidal activated carbon (CAC) for phenol remediation from groundwater was introduced. The CAC prepared by a simple pulverization technique was an excellent metal-free catalyst for persulfate (PS) activation due to high contact surface area. The removal efficiency of phenol in the PS/CAC system (~100%) was higher than that in the PS/activated carbon (AC) system (90.1%) and was superior to the conventional PS/Fe2+ system (27.9%) within 30 min. The phenol removal reaction occurred both in bulk solution and at the surface of the CAC, as confirmed by Langmuir–Hinshelwood (L–H) kinetic model fitting, FT−IR, and electron spin resonance (ESR) analyses. The downsizing of particle size from AC to CAC played a critical role in the radical oxidation mechanism by leading to the formation of predominant superoxide radical (O2•–) species in the PS/CAC system. Anions NO3–, SO42−, and Cl– slightly inhibited the phenol removal efficiency, whereas CO32−, HCO3− and PO43− did not. Ferulic acid (C10H10O4) was detected as an organic byproduct of phenol oxidation. The use of CAC as a metal-free bifunctional catalyst has an important implication in the PS activation for phenol degradation in groundwater.
KW - Colloidal activated carbon
KW - Persulfate
KW - Phenol degradation
KW - Radical
UR - http://www.scopus.com/inward/record.url?scp=85101519847&partnerID=8YFLogxK
U2 - 10.1016/j.jhazmat.2021.125474
DO - 10.1016/j.jhazmat.2021.125474
M3 - Article
C2 - 33647616
AN - SCOPUS:85101519847
SN - 0304-3894
VL - 414
JO - Journal of Hazardous Materials
JF - Journal of Hazardous Materials
M1 - 125474
ER -