4.7 Article

Cu(I)-doped Fe3O4 nanoparticles/porous C composite for enhanced H2O2 oxidation of carbamazepine

期刊

JOURNAL OF COLLOID AND INTERFACE SCIENCE
卷 551, 期 -, 页码 16-25

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2019.04.083

关键词

Heterogeneous Fenton; Fe-Cu bimetal oxide; Ordered porous carbon; Interface mechanism

资金

  1. National Natural Science Foundation of China [21577160, 51338010, 51290282]
  2. National Water Pollution Control and Treatment Science and Technology Major Project [2015ZX07406005-002]
  3. International Postdoctoral Exchange Fellowship Program [20160010, Cu+/2+-H2O]

向作者/读者索取更多资源

Cu(I) doped nano-Fe3O4 were synthesized and loaded on ordered porous carbon materials using a facile co-precipitated. The synthesized catalysts were characterized by XRD, XPS, HRTEM, FESEM-EDX mapping and N-2 adsorption-desorption. The results showed that the crystal unit cell of Fe3O4 was enlarged due to the implantation of small amount of Cu(I) into the Fe3O4 structure (Fe2.85Cu0.15O4). With increased Cu content, the catalyst was dominated with Cu2O and the Fe3O4 phase disappeared, the catalytic performance of Fe-Cu bimetal oxide became worse. The Cu(I)-Fe3O4/C composite was enriched with Fe(II), Fe(III) and Cu(I) sites. The prepared Cu-Fe bimetal oxide/C composite exhibited higher specific TOF and oxidation efficiency E on carbamazepine oxidation than Fe2.85Cu0.15O4 and Fe3O4. The enhanced catalytic reactivity was attributed to the synergetic effect of surface Fe and Cu species on the H2O2 activation. The dissolved metals induced catalytic reaction at pH 4.5-8.1 was ignorable. Thus, the catalytic decomposition of H2O2 by Cu-Fe3O4/C at near neutral pH was controlled by interface reactions. The CBZ in the close proximity to the interface was attacked by the generated ROS and formed urea, 2-hydroxybenzyl alcohol and other oxidative products. (C) 2019 Elsevier Inc. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据