TY - JOUR
T1 - Insights to PFOS elimination with peroxydisulfate activation mediated by boron modified Fe/C catalysts
T2 - Enhancing mechanism of boron and PFOS degradation pathway
AU - Jiang, Yanting
AU - Yu, Zhendong
AU - Lv, Yuancai
AU - Li, Xiaojuan
AU - Lin, Chunxiang
AU - Ye, Xiaoxia
AU - Yang, Guifang
AU - Liu, Yifan
AU - Dai, Leilei
AU - Liu, Minghua
AU - Ruan, Roger
N1 - Publisher Copyright:
© 2023
PY - 2023/12/15
Y1 - 2023/12/15
N2 - In this study, the boron-doped iron-carbon composite (Fe@B/C-2) was prepared via a simple solvothermal and secondary calcination process by using iron metal–organic frameworks (Fe-MOFs) as precursor. The obtained Fe@B/C-2 possessed abundant active sites and low iron ion leaching, and exhibited excellent performance on peroxydisulfate (PDS) activation for efficient PFOS (10 mg/L) degradation (94 %) in 60 min, with 0.2 g/L of catalyst dosage, 1.0 g/L of PDS dosage and at 5.0 of initial pH. The radical scavenging and electron paramagnetic resonance (EPR) tests demonstrated that SO4·− and ·OH were the primary active species during PFOS elimination. Under the attack of these species, PFOS was first transformed into PFOA, followed by a sequential defluorination process, and lastly mineralized into CO2 and F−. Notably, DFT results revealed that Fe species, -BC3/-BC2O structures on the carbon matrix performed crucial roles in PDS activation. The extraordinary catalytic activity of Fe@B/C-2 was attributable to the synergistic effects of Fe nanoparticles and the B-doped on carbon matrix. The doped B not only could activate the inert carbon skeleton and provided more catalytic centers, but also could accelerate the electron transfer efficiency, leading to a boost in PDS decomposition.
AB - In this study, the boron-doped iron-carbon composite (Fe@B/C-2) was prepared via a simple solvothermal and secondary calcination process by using iron metal–organic frameworks (Fe-MOFs) as precursor. The obtained Fe@B/C-2 possessed abundant active sites and low iron ion leaching, and exhibited excellent performance on peroxydisulfate (PDS) activation for efficient PFOS (10 mg/L) degradation (94 %) in 60 min, with 0.2 g/L of catalyst dosage, 1.0 g/L of PDS dosage and at 5.0 of initial pH. The radical scavenging and electron paramagnetic resonance (EPR) tests demonstrated that SO4·− and ·OH were the primary active species during PFOS elimination. Under the attack of these species, PFOS was first transformed into PFOA, followed by a sequential defluorination process, and lastly mineralized into CO2 and F−. Notably, DFT results revealed that Fe species, -BC3/-BC2O structures on the carbon matrix performed crucial roles in PDS activation. The extraordinary catalytic activity of Fe@B/C-2 was attributable to the synergistic effects of Fe nanoparticles and the B-doped on carbon matrix. The doped B not only could activate the inert carbon skeleton and provided more catalytic centers, but also could accelerate the electron transfer efficiency, leading to a boost in PDS decomposition.
KW - Boron-doping
KW - Degradation
KW - Fe-based catalyst
KW - Perfluorooctane sulfonic acid
KW - Peroxydisulfate activation
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U2 - 10.1016/j.jcis.2023.08.198
DO - 10.1016/j.jcis.2023.08.198
M3 - Article
C2 - 37672977
AN - SCOPUS:85169816957
SN - 0021-9797
VL - 652
SP - 1743
EP - 1755
JO - Journal of Colloid And Interface Science
JF - Journal of Colloid And Interface Science
ER -