亚甲蓝
分解
催化作用
化学
降级(电信)
磷化物
催化循环
亚甲基
电子转移
无机化学
光化学
核化学
药物化学
有机化学
电信
光催化
计算机科学
作者
Can Ma,Shuo Feng,Jinming Zhou,Rufen Chen,Yu Wei,Hui Liu,Sen Wang
标识
DOI:10.1016/j.apcatb.2019.118015
摘要
The greatest problem in the homogeneous Fenton reaction is the low production of HO owing to the slow FeIII/FeII cycle. In this study, we demonstrate a new co-catalyst of FeP and trace Fe2+ that can greatly enhance the decomposition efficiency of H2O2 and accelerate the degradation of methylene blue (MB). This co-catalyst is applicable in a broad pH range (pH = 3.0−9.0) and capable of degrading 95.74% and 89.01% of MB with 100 ppm in concentration within 30 s at pH 3 and 5, and 99.65% and 90.06% within 3 min at pH 7 and 9. The coexistence of FeP with FeII accelerates the FeIII/FeII cycle by electron transfer between Feδ+ in FeP and FeIII. Mössbauer spectra and density functional theory calculations indicate that the unique structure of FeP plays an important role in accelerating the FeIII/FeII cycle.
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