Key Laboratory of Environmental Materials and Pollution Control, The Education Department of Jilin Province, Jilin Normal University, Siping, 136000, China.
School of Environmental Science and Engineering, Jilin Normal University, Siping, 136000, China.
Environ Sci Pollut Res Int. 2020 May;27(15):18773-18783. doi: 10.1007/s11356-020-08364-5. Epub 2020 Mar 23.
To improve the electrocatalytic efficiency of the cathode and provide a wider pH range in the electro-Fenton process, N-doped multi-walled carbon nanotubes (NCNTs) and ferrous ion complexed with carboxylated carbon nanotubes (CNT-COOFe) were used to fabricate the diffusion layer and catalyst layer of a membrane cathode, respectively. The morphology, structure, and composition of CNT-COOFe were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), Raman spectroscopy, and X-ray photoelectron spectroscopy (XPS). The oxygen reduction performance of NCNT was evaluated using cyclic voltammetry (CV) and the rotating disk electrode technique (RDE). In addition, a potential application of the cathode in sequential electro-Fenton degradation of p-nitrophenol (p-NP) was investigated. The results revealed that iron was successfully doped on the carboxylated carbon nanotubes in ionic complexation form and the content of iron atoms in CNT-COOFe was 2.65%. Furthermore, the defects on the tube walls provided more reactive sites for the electro-Fenton process. A combination of CV and RDE data indicated that NCNT had better electrocatalytic HO generation activity with a more positive onset potential and higher cathodic peak current response than CNT. A p-NP removal rate of 96.04% was achieved within 120 min, and a mineralization efficiency of 80.26% was obtained at 180 min in the sequential electro-Fenton process at a cathodic potential of - 0.7 V vs SCE and neutral pH. The activity of the used cathode was restored simply through electro-reduction at - 1.0 V vs SCE, and a p-NP removal rate of more than 70% was obtained at 60 min after six regeneration cycles.
为提高阴极的电催化效率并拓宽电芬顿过程的 pH 适用范围,分别采用氮掺杂多壁碳纳米管(NCNT)和与羧基化碳纳米管(CNT-COOFe)配位的亚铁离子制备了膜阴极的扩散层和催化剂层。采用扫描电子显微镜(SEM)、X 射线衍射(XRD)、拉曼光谱和 X 射线光电子能谱(XPS)对 CNT-COOFe 的形貌、结构和组成进行了表征。采用循环伏安法(CV)和旋转圆盘电极技术(RDE)评价了 NCNT 的氧还原性能。此外,还研究了该阴极在顺序电芬顿降解对硝基苯酚(p-NP)中的潜在应用。结果表明,铁以离子络合的形式成功掺杂到羧基化碳纳米管中,并且 CNT-COOFe 中铁原子的含量为 2.65%。此外,管壁上的缺陷为电芬顿过程提供了更多的活性位点。CV 和 RDE 数据的组合表明,NCNT 具有更好的电催化 HO 生成活性,其起始电位更正,阴极峰电流响应更高。在 -0.7 V vs SCE 的阴极电位和中性 pH 条件下,顺序电芬顿过程中 120 min 内可实现 96.04%的 p-NP 去除率,180 min 时可获得 80.26%的矿化效率。通过 -1.0 V vs SCE 的电还原可简单地恢复使用后的阴极的活性,经过六次再生循环后,在 60 min 内可获得超过 70%的 p-NP 去除率。