Visible Light Activated Photocatalytic Degradation of 2,4-dichlorophenol Using Silver Halide Photocatalysts (2024)

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photocatalytic degradation of chlorophenol in water

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This work aims to study the photocatalytic degradation of chlorophenols. They belong to a notable group of pollutants because of their high toxicity, and hardly biodegradable, and are difficult to remove from the environment. Photocatalytic degradation of chlorophenols using UV light was investigated over mesoporous catalysts. Ti-MCM-41(20), Ti-MCM-41(10), TiO2/MCM-41, Fe-Ti-MCM-41, TiO2/Fe-MCM-41 and TiO2/SBA-15 catalysts were prepared from the corresponding metal salts by the sol-gel technique. The catalyst were investigated using X-ray diffraction (XRD), FT-IR spectroscopes, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and BET surface areas of the samples were determined using the nitrogen adsorption and desorption isotherms. 100 ppm was used as model pollutants. High purity 2,4,6-trichlorophenol and 4-chlorophenol solutions individually and 0.1 g/L of each catalyst was tested at different irradiation times. At each interval time 10 ml of irradiated solution was taken and analyzed by High Performance Liquid Chromatography (HPLC), Ion Chromatography (IC). Aromatic intermediates, organic acid and chloride ions were detected. The reaction mechanism has been proposed.

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Silver Doped TiO 2 Nanoparticles: Preparation, Characterization and Efficient Degradation of 2,4-dichlorophenol Under Visible Light

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Hydrothermally synthesized TiO 2 nanoparticles containing different amounts of silver were characterized by X-Ray diffraction (XRD), Fourier transform infrared (FT-IR) and scanning electron microscopy equipped with energy dispersive X-ray microanalysis (SEM/EDX) techniques. XRD results showed prepared samples include 100% anatase phase. The presence of silver in TiO 2 nanoparticle network was established by XRD, SEM/EDX and FT-IR techniques. The photocatalytic performance of the prepared catalysts was tested for the degradation of 2,4-dichlorophenol (2,4-DCP) under visible light.. The experiments demonstrated that 2,4-DCP was effectively degraded in the presence of Ag/TiO 2 samples. It was confirmed that the presence of Ag on TiO 2 catalysts could enhance the photocatalytic degradation of 2,4-DCP in aqueous suspension. It was found that an optimal dosage of 1.68 wt% Ag in TiO 2 achieved the fastest 2,4-DCP degradation (95% after 180 min irradiation) under the experimental conditions. On the basis of various characterizations of the photocatalysts, the reactions involved to explain the photocatalytic activity enhancement due to Ag doping include a better separation of photogenerated charge carriers. GC-MS analysis showed the major intermediates of 2,4-DCP degradation are simple acids like oxalic acid, acetic acid, etc. as the final products. How to cite this article

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Visible Light Activated Photocatalytic Degradation of 2,4-dichlorophenol Using Silver Halide Photocatalysts (2024)

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