催化作用
化学
金属
2,4-二氯苯氧基乙酸
氧化还原
反应条件
无机化学
核化学
钯
有机化学
植物
生物
作者
Xin Zhou,Haopeng Luo,Quanyuan Chen,Xin Cao,Chensi Shen,Juan Zhou
标识
DOI:10.1016/j.cej.2020.126175
摘要
The eliminate of 2,4-dichlorophenoxyacetic acid (2,4-D) was achieved via individual and combination of catalytic hydrodechlorination (HDC) and AOPs involved peroxymonosulfate activation. The CMK-3 supported monometallic Pd catalysts with varied Pd loadings were prepared and applied in the reactions. The results showed that Pd/CMK-3 were highly active and competitive in both the HDC and AOPs of 2,4-D, and the removal efficiencies were 91.6 and 95.2% over Pd3/CMK-3 respectively after reaction for 90 min. The dechlorination of 2,4-D was completed via both the stepwise and concerted pathways while the reactant experienced free radical oxidation processes in the AOPs. For the combined HDC-AOPs reaction, Pd/CMK-3 reflected a good advanced oxidation ability after the effective HDC of 2,4-D. Additionally, the catalysts exhibited higher Pdn+/Pd0 ratios after reactions and metal Pd was more stable after the reductive dechlorination than that of advanced oxidation.
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