催化作用
降级(电信)
化学
聚丙烯腈
介孔材料
化学工程
核化学
4-硝基苯酚
傅里叶变换红外光谱
聚合物
有机化学
工程类
计算机科学
电信
作者
Xiong Li,Chang Li,Guanyu Gao,Bosheng Lv,Lusheng Xu,Yin Lu,Guoliang Zhang
标识
DOI:10.1016/j.scitotenv.2019.134910
摘要
Abstract From the view of channel confinement and functional site capture, we develop an in-situ self-assembly strategy to fabricate the carboxyl functionalized Fe-HPAN bead catalyst with highly stable and uniformly dispersed metallic sites for efficient photo-Fenton oxidation of p-nitrophenol (p-NP). BET and FTIR analysis reveal that numerous carboxyl groups and mesopores exist in Fe-HPAN beads, which acts to capture and immobilize iron ions. Catalytic results show that the degradation rate and TOC removal for p-NP were up to 99.78 and 91.68% under the optimal condition. Even at near neutral pH, the degradation rate almost keep the same and the TOC removal can still reach 73.05%. Due to the autocatalytic cycle of FeIII/FeII, the apparent rate constant of Fe-HPAN (0.2247 min−1) was 5.4 times as high as unmodified Fe-PAN (0.0415 min−1) in the presence of H2O2 and visible light irradiation, which was 2–3 orders of magnitude larger than that of other reaction systems. More importantly, Fe-HPAN bead catalyst exhibited little loss of activity even after 20 cycles of re-utilization. The possible degradation pathway of p-NP was also proposed based on GC/MS analysis. The present work may provide a new perspective for the use of synthetic polymer to prepare low-cost, efficient and robust photo-Fenton oxidation catalysts.
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