Heterogeneous co-activation of peroxymonosulfate by CuCoFe calcined layered double hydroxides and ultraviolet irradiation for the efficient removal of p-nitrophenol

被引:30
|
作者
Zhou, Shu [1 ]
Li, Caifeng [1 ]
Zhao, Guoqing [1 ]
Liu, Lukai [1 ]
Yu, Jingang [1 ]
Jiang, Xinyu [1 ]
Jiao, Feipeng [1 ]
机构
[1] Cent S Univ, Sch Chem & Chem Engn, Changsha 410083, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
ACID ORANGE 7; PHOTOCATALYTIC DEGRADATION; ACTIVATED PERSULFATE; ADVANCED OXIDATION; AQUEOUS-SOLUTION; AZO-DYE; SULFATE; CATALYST; CO; HETEROJUNCTION;
D O I
10.1007/s10854-019-02258-0
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
Advanced oxidation processes by the activation of peroxymonosulfate (PMS) have been widely concerned for the enhanced degradation of organic pollutants. In this work, CuCoFe calcined layered double hydroxides (CuCoFe-CLDH) were successfully prepared via a simple method, and its lamellar structure and spinel-like composites were proved by using XRD, SEM and FT-IR. The CuCoFe-CLDH was used to activate PMS to produce many active species for the degradation of p-nitrophenol (PNP) under ultraviolet irradiation (UV). At the optimal conditions of CuCoFe-CLDH dosage 0.3 g/L and PMS dosage 0.3 g/L, it was discovered that the degradation efficiency of 20 mg/L PNP was about 95.11% under UV light within 30 min. In addition, the degraded reaction accorded with the pseudo-first-order kinetic behaviors, and it was found that SO4 center dot- and center dot OH radicals were effective active species in the quenching experiments under the CuCoFe-CLDH/UV/PMS system. The CuCoFe-CLDH could still keep above 93% after five continuous recycles, and also showed remarkable reusability and stability in accord with the characterization analysis of fresh and used materials. Briefly, this work could be a promising method for the treatment of the phenol-bearing wastewater and support theoretical foundation for PMS activation.
引用
收藏
页码:19009 / 19019
页数:11
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