scholarly journals An Efficient Strategy for the Fabrication of CuS as a Highly Excellent and Recyclable Photocatalyst for the Degradation of Organic Dyes

Catalysts ◽  
2019 ◽  
Vol 10 (1) ◽  
pp. 40 ◽  
Author(s):  
Na Qin ◽  
Wutao Wei ◽  
Chao Huang ◽  
Liwei Mi

An effective and practical in situ sulfuration approach has been developed in this work, for the fabrication of CuS with a 3D hierarchical network structure under mild preparation conditions. The prepared CuS consists of a primary structure of the multi-structure interchange copper foam precursor, and a secondary structure of nanoplates. The structural characteristics, morphologies, and photocatalytic performances of the prepared photocatalyst were investigated systematically. To evaluate the photocatalytic performance of the prepared CuS samples, we investigated the degradation of MB (methylene blue), RhB (Rhodamine B), and MB/RhB dye solutions over the samples under the irradiation of simulated solar light. Specifically, the degradation of RhB rapidly reached ≈100.0% after simulated solar light irradiation for 25 min, which is higher than those of P25 (83.0%) and bulk CuS (54.8%). For the mixed systems of MB/RhB, both the degradations of MB and RhB reached up to ≈99.0% after simulated solar light irradiation for 25 min. The superior photocatalytic performances of the prepared samples are attributed to the synergistic effects of high optical absorption, large specific surface area, and abundant active sites. The prepared catalysts can retain the photocatalytic activities during the entire reaction process without significant loss after four catalytic cycles, which reveals that the CuS with a stable 3D hierarchical network structure has a promising prospect as an ideal recyclable catalyst.

2019 ◽  
Vol 6 (3) ◽  
pp. 937-947 ◽  
Author(s):  
Feng Liu ◽  
Weifang Zhang ◽  
Le Tao ◽  
Boyuan Hao ◽  
Jing Zhang

The reduction of Cr(vi) and oxidation of As(iii) were markedly accelerated by employing iron oxide encapsulated in hydrothermal carbon sphere under simulated solar light irradiation.


2020 ◽  
Vol 267 ◽  
pp. 118695 ◽  
Author(s):  
Zhao Gao ◽  
Hanpei Yang ◽  
Jingwei Li ◽  
Li Kang ◽  
Lina Wang ◽  
...  

2015 ◽  
Vol 3 (34) ◽  
pp. 17858-17865 ◽  
Author(s):  
Xiaohong Hu ◽  
Qi Zhu ◽  
Xinlong Wang ◽  
Naoki Kawazoe ◽  
Yingnan Yang

P/Ag/Ag2O/Ag3PO4/TiO2 composite photocatalyst has been successfully prepared by a sol–gel method. It shows highly enhanced photocatalytic ability and stability under simulated solar light irradiation.


2012 ◽  
Vol 9 (6) ◽  
pp. 558 ◽  
Author(s):  
Lei Wu ◽  
Xuefeng Hu

Environmental context Aromatic amines are widely used chemicals, which show enhanced toxicity and longer environmental persistence when halogenated. We investigated the chlorination of aniline in seawater and in natural aqueous solutions containing Fe3+ and Cl–, under simulated sunlight irradiation. The results increase our understanding of the transformation pathway of typical nitrogen-containing aromatic contaminants in the environment. Abstract Photochlorination of aniline was observed in aqueous solutions containing dissolved FeIII and chloride ions under simulated solar light irradiation. Effects of O2, Cl–, Fe3+ and pH on the formation of chloroanilines (CAs) were investigated. para-chloroaniline (4CA) was identified as the main chlorinated product. The formation of 4CA is enhanced with increased concentrations of Cl– or Fe3+, and decreased pH, whereas oxygen plays a negligible role in the process. The results indicate that, Cl• is formed mainly by the photodissociation of FeCl2+–FeCl2+ complexes, and reacts with Cl– to produce Cl2•–. Aniline is then oxidised by Cl2•– into an anilino radical cation, which further reacts with Cl2•– to generate CAs. The photochlorination of aniline in natural seawater was also observed. Other phototransformation products of aniline were detected and a transformation pathway was proposed. This work provides evidence for the photochemical chlorination path of aniline-based aromatic amines in aqueous solutions.


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