scholarly journals Polyaniline-Grafted RuO2-TiO2 Heterostructure for the Catalysed Degradation of Methyl Orange in Darkness

Catalysts ◽  
2019 ◽  
Vol 9 (7) ◽  
pp. 578 ◽  
Author(s):  
Mousli ◽  
Chaouchi ◽  
Jouini ◽  
Maurel ◽  
Kadri ◽  
...  

Massive industrial and agricultural developments have led to adverse effects of environmental pollution resisting conventional treatment processes. The issue can be addressed via heterogeneous photocatalysis as witnessed recently. Herein, we have developed novel metal/semi-conductor/polymer nanocomposite for the catalyzed degradation and mineralization of model organic dye pollutants in darkness. RuO2-TiO2 mixed oxide nanoparticles (NPs) were modified with diphenyl amino (DPA) groups from the 4-diphenylamine diazonium salt precursor. The latter was reduced with ascorbic acid to provide radicals that modified the NPs and further served for in situ synthesis of polyaniline (PANI) that resulted in RuO2/TiO2-DPA-PANI nanocomposite catalyst. Excellent adhesion of PANI to RuO2/TiO2-DPA was noted but not in the case of the bare mixed oxide. This stresses the central role of diazonium compounds to tether PANI to the underlying mixed oxide. RuO2-TiO2/DPA/PANI nanocomposite revealed superior catalytic properties in the degradation of Methyl Orange (MO) compared to RuO2-TiO2/PANI and RuO2-TiO2. Interestingly, it is active even in the darkness due to high PANI mass loading. In addition, PANI constitutes a protective layer of RuO2-TiO2 NPs that permitted us to reuse the RuO2-TiO2/DPA/PANI nanocomposite nine times, whereas RuO2-TiO2/PANI and RuO2-TiO2 were reused seven and five times only, respectively. The electronic displacements at the interface of the heterojunction metal/semi-conductor under visible light and the synergistic effects between PANI and RuO2 result in the separation of electron-hole pairs and a reduction of its recombination rate as well as a significant catalytic activity of RuO2-TiO2/DPA/PANI under simulated sunlight and in the dark, respectively.

RSC Advances ◽  
2015 ◽  
Vol 5 (69) ◽  
pp. 55704-55712 ◽  
Author(s):  
Hong Zhang ◽  
Aiju Lv ◽  
Jinsheng Liang ◽  
Junping Meng

The synergistic effects of tourmaline and Ce on the degradation of methyl orange by a TiO2 composite photocatalyst are described.


2020 ◽  
Vol 16 ◽  
Author(s):  
Nimisha Jadon ◽  
Gulzar Ahmad Bhat ◽  
Manoharmayum Vishwanath Sharma ◽  
Harendra Kumar Sharma

Background: The study focuses on the synthesis of chitosan/ Fe2O3 nanocomposite, its characterization and application in methyl orange dye degradation. Methods: The synthesized chitosan/ Fe2O3 nanocomposite was characterized with Powder X-Ray Diffraction, Fourier Transformation Infrared Spectroscopy (FTIR), Transmission Electron Microscopy (TEM) and UV-Vis Spectroscopy. Results: The characterization showed that the Fe2O3nanoparticles were embedded in the polymer matrix of chitosan. The size of the Fe2O3nanoparticles were less than 10nm and the crystallite size was 1.22 nm.The synthesized chitosan/ Fe2O3nanocomposite was tested for methyl orange degradation using different parameters such as effect of contact time, effect of dose, effect of concentration and effect of pH for the degradation of methyl orange dye in aqueous solution.The Fruendlich, Langmuir and Temkin isotherm studies were also conducted for adsoption of methyl orange on Chitosan/ Fe2O3nanocomposite. Conclusion: The study indicated that the synthesized chitosan/Fe2O3 nanocomposite had the potential of degrading methyl orange dye up to 75.04% under the set condition in this experiment which indicate that Chitosan/ Fe2O3 nanocomposite is a viable option that can be used for the degradation of methyl orange dye.


2019 ◽  
Vol 95 ◽  
pp. 105933
Author(s):  
Guohui Wang ◽  
Ruiqi Huang ◽  
Annan Zhou ◽  
Qinghong Xu

Catalysts ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 117
Author(s):  
Zahir Muhammad ◽  
Farman Ali ◽  
Muhammad Sajjad ◽  
Nisar Ali ◽  
Muhammad Bilal ◽  
...  

Degradation of organic dyes and their byproducts by heterogeneous photocatalysts is an essential process, as these dyes can be potentially discharged in wastewater and threaten aquatic and xerophyte life. Therefore, their complete mineralization into nontoxic components (water and salt) is necessary through the process of heterogeneous photocatalysis. In this study, Zr/CrO2 (Zirconium-doped chromium IV oxide) nanocomposite-based photocatalysts with different compositions (1, 3, 5, 7 & 9 wt.%) were prepared by an environmentally friendly, solid-state reaction at room temperature. The as-prepared samples were calcined under air at 450 °C in a furnace for a specific period of time. The synthesis of Zr/CrO2 photocatalysts was confirmed by various techniques, including XRD, SEM, EDX, FT-IR, UV-Vis, and BET. The photocatalytic properties of all samples were tested towards the degradation of methylene blue and methyl orange organic dyes under UV light. The results revealed a concentration-dependent photocatalytic activity of photocatalysts, which increased the amount of dopant (up to 5 wt.%). However, the degradation efficiency of the catalysts decreased upon further increasing the amount of dopant due to the recombination of holes and photoexcited electrons.


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