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首页> 外文期刊>Nanomaterials >Removal of Phenolic Compounds from Water Using Copper Ferrite Nanosphere Composites as Fenton Catalysts
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Removal of Phenolic Compounds from Water Using Copper Ferrite Nanosphere Composites as Fenton Catalysts

机译:铁酸铜纳米球复合材料作为Fenton催化剂去除水中的酚类化合物

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Copper ferrites containing Cu + ions can be highly active heterogeneous Fenton catalysts due to synergic effects between Fe and Cu ions. Therefore, a method of copper ferrite nanosphere (CFNS) synthesis was selected that also permits the formation of cuprite, obtaining a CFNS composite that was subsequently calcined up to 400 °C. Composites were tested as Fenton catalysts in the mineralization of phenol (PHE), p -nitrophenol (PNP) and p -aminophenol (PAP). Catalysts were characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS) and magnetic measurements. Degradation of all phenols was practically complete at 95% total organic carbon (TOC) removal. Catalytic activity increased in the order PHE PNP PAP and decreased when the calcination temperature was raised; this order depended on the electronic effects of the substituents of phenols. The as-prepared CFNS showed the highest catalytic activity due to the presence of cubic copper ferrite and cuprite. The Cu + surface concentration decreased after calcination at 200 °C, diminishing the catalytic activity. Cuprite alone showed a lower activity than the CFNS composite and the homogeneous Fenton reaction had almost no influence on its overall activity. CFNS activity decreased with its reutilization due to the disappearance of the cuprite phase. Degradation pathways are proposed for the phenols.
机译:由于Fe和Cu离子之间的协同作用,含Cu +离子的铜铁氧体可以成为高活性的非均相Fenton催化剂。因此,选择了一种铜铁氧体纳米球(CFNS)合成方法,该方法还允许形成铜矿,从而获得CFNS复合材料,随后将其煅烧至400°C。在苯酚(PHE),对硝基苯酚(PNP)和对氨基苯酚(PAP)的矿化中,将复合材料作为Fenton催化剂进行了测试。催化剂通过透射电子显微镜(TEM),扫描电子显微镜(SEM),X射线衍射(XRD),傅里叶变换红外光谱(FTIR),X射线光电子光谱(XPS)和磁测量进行表征。在去除总有机碳(TOC)95%的情况下,所有苯酚的降解实际上都已完成。催化活性按PHE

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