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Heterogeneous Fenton water purification catalyzed by iron phosphide (FeP)
Water Research ( IF 11.4 ) Pub Date : 2023-05-30 , DOI: 10.1016/j.watres.2023.120151
Shu-Chuan Mei 1 , Liang Li 1 , Gui-Xiang Huang 1 , Xiao-Qiang Pan 1 , Han-Qing Yu 1
Affiliation  

Heterogeneous Fenton reaction has a great application potential in water purification, but efficient catalysts are still lacking. Iron phosphide (FeP) has a higher activity than the conventional Fe-based catalysts for Fenton reactions, but its ability as a Fenton catalyst to directly activate H2O2 remains unreported. Herein, we demonstrate that the fabricated FeP has a lower electron transfer resistance than the typical conventional Fe-based catalysts, i.e., Fe2O3, Fe3O4, and FeOOH, and thus could active H2O2 to produce hydroxyl radicals more efficiently. In the heterogeneous Fenton reactions for sodium benzoate degradation, the FeP catalyst presents a superior activity with a reaction rate constant more than 20 times those of the other catalysts (i.e., Fe2O3, Fe3O4, and FeOOH). Moreover, it also exhibits a great catalytic activity in the treatment of real water samples and has a good stability in the cycling tests. Furthermore, the FeP could be loaded onto a centimeter-sized porous carbon support and the prepared macro-sized catalyst exhibits an excellent water treatment performance and can be well recycled. This work reveals a great potential of FeP as a catalyst for heterogeneous Fenton reactions and may inspire further development and practical application of highly efficient catalysts for water purification.



中文翻译:

磷化铁(FeP)催化多相芬顿水净化

多相芬顿反应在水净化方面具有巨大的应用潜力,但仍缺乏高效的催化剂。磷化铁(FeP)比传统的Fenton反应铁基催化剂具有更高的活性,但其作为Fenton催化剂直接活化H 2 O 2能力尚未报道。在此,我们证明所制备的 FeP 比典型的传统铁基催化剂(即 Fe 2 O 3、Fe 3 O 4和 FeOOH)具有更低的电子转移电阻,因此可以活化 H 2 O 2更有效地产生羟基自由基。在苯甲酸钠降解的非均相芬顿反应中,FeP催化剂表现出优异的活性,反应速率常数是其他催化剂(即Fe 2 O 3、Fe 3 O 4)的20倍以上。和 FeOOH)。此外,它在处理真实水样时也表现出良好的催化活性,并且在循环测试中具有良好的稳定性。此外,FeP可以负载在厘米级的多孔碳载体上,所制备的大尺寸催化剂表现出优异的水处理性能,并且可以很好地回收利用。这项工作揭示了FeP作为非均相芬顿反应催化剂的巨大潜力,并可能激发高效水净化催化剂的进一步开发和实际应用。

更新日期:2023-06-02
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