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
同种类的
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
热力学
物理
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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