过氧二硫酸盐
催化作用
硼
煅烧
化学
电子顺磁共振
无机化学
碳纤维
浸出(土壤学)
电子转移
钴
降级(电信)
核化学
光化学
材料科学
复合数
有机化学
环境科学
土壤科学
土壤水分
物理
核磁共振
复合材料
电信
计算机科学
作者
Yanting Jiang,Zhendong Yu,Yuancai Lv,Xiaojuan Li,Chunxiang Lin,Xiaoxia Ye,Guifang Yang,Yifan Liu,Leilei Dai,Minghua Liu,Roger Ruan
标识
DOI:10.1016/j.jcis.2023.08.198
摘要
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.
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