Laboratory Scale Unit for Photocatalytic Removal of Organic Micropollutants from Water and Wastewater. Methyl Orange Degradation

2013 ◽  
Vol 52 (6) ◽  
pp. 2201-2208 ◽  
Author(s):  
Andrea Petrella ◽  
Mario Petrella ◽  
Giancarlo Boghetich ◽  
Piero Mastrorilli ◽  
Valentina Petruzzelli ◽  
...  
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.


2020 ◽  
Vol 598 ◽  
pp. 117672 ◽  
Author(s):  
Noman Khalid Khanzada ◽  
Muhammad Usman Farid ◽  
Jehad A. Kharraz ◽  
Jungwon Choi ◽  
Chuyang Y. Tang ◽  
...  

2020 ◽  
Vol 18 (1) ◽  
pp. 129-137
Author(s):  
Yayuk Astuti ◽  
Rizka Andianingrum ◽  
Abdul Haris ◽  
Adi Darmawan ◽  

AbstractSynthesis of bismuth oxide synthesis through the precipitation method using H2C2O4 and Na2CO3 precipitating agents, identification of physicochemical properties and its photocatalysis activity for methyl orange degradation were conducted. The bismuth oxide synthesis was undertaken by dissolving Bi(NO3)3.5H2O in HNO3, then added precipitating agents to form precipitate. The results showed that bismuth oxide produced by H2C2O4 precipitating agent was a yellow powder containing a mixture of α-Bi2O3 (monoclinic) and β-Bi2O3 (tetragonal), porous with size of 28-85 μm. Meanwhile, the use of Na2CO3 as precipitating agent resulted in bismuth oxide consisting of α-Bi2O3 and β-Bi2O3 and Bi2O4, irregular shape without pore being 40-115 μm in size. Bismuth oxide synthesized with H2C2O4 precipitating agent showed higher photocatalytic activity compared to bismuth oxide synthesized using Na2CO3 on degrading methyl orange dye with degradation rate constants of 2.35x10-5 s-1 for H2C2O4 and 1.81x10-5 s-1 for Na2CO3.


2018 ◽  
Vol 79 (5) ◽  
pp. 947-957 ◽  
Author(s):  
Mahabubur Chowdhury ◽  
Sarah Kapinga ◽  
Franscious Cummings ◽  
Veruscha Fester

Abstract Advanced oxidation processes based on sulphate radical generated by peroxymonosulphate (PMS) activation is a promising area for environmental remediation. One of the biggest drawbacks of heterogeneous PMS activation is catalyst instability and metal ion leaching. In this study, a simple organic binder mediated route was explored to substitute Ti4+ ions into the Co3O4 host lattice structure to create a Co-O-Ti bond to minimise cobalt leaching during methyl orange degradation. The catalyst was characterised by X-ray diffraction, and scanning and transmission electron microscopy. The as-prepared catalysts with Co3O4:TiO2 ratio of 70:30 exhibited minimal leaching (0.9 mg/L) compared to other ratios studied. However, the pristine Co3O4 exhibited highest catalytic activity (rate constant = 0.41 min−1) and leaching (26.7 mg/L) compared to composite material (70:30 Co3O4:TiO2). Interestingly, the morphology of the composite and leaching of Co2+ ions were found to be temperature dependent, as an optimum temperature ensured strong Co-O-Ti bond for prevention of Co2+ leaching. The classical quenching test was utilised to determine the presence and role of radical species on methyl orange degradation. The fabricated catalyst also exhibited good catalytic activity in degrading mixed dyes and good recyclability, making it a potential candidate for commercial application.


Author(s):  
Srimala Sreekantan ◽  
Roshasnorlyza Hazan ◽  
Zainovia Lockman ◽  
Ishak Mat

The present study is directed to clarify the influence of carbon doping on the degradation of methyl orange. TiO2 nanotubes were prepared by anodizing titanium foils in a two electrode configuration bath with titanium foil as the anode and platinum as the counter electrode. The electrochemical bathconsists of 1 M Na2SO4 with 0.7 g ammonium fluoride, NH4F. The nanotubes obtained were further doped with carbon via in-situ and ex-situ method. Incorporation of carbon on TiO2 via in-situ method is accomplished during the anodization process by introducing oxalic acid into electrolyte while theex-situ doping involves carbon incorporation into pre-fabricated TiO2 nanotube via flame annealing using carbon blackN330. Characterization such as Scanning Electron Microscope (SEM), Energy Dispersive X-ray Analysis (EDX), and X-Ray Diffraction (XRD) are used to determine the surfacemorphology, composition of dopants, and phases exists. Well ordered nanotube with good adherence and smooth surface was obtained for both methods. When the oxide was annealed, X-ray diffraction analysis revealed the presence of anatase and rutile phase. The photocatalytic properties of thepure TiO2 and carbon doped TiO2 were tested for methyl orange degradation and the result indicated that the in-situ doped TiO2 has much better degradation than the ex-situ and pure TiO2. The percentage of methyl orange degradation for in-situ was 20% and 41% higher than ex-situ doped TiO2 and pure TiO2, respectively.


Author(s):  
Nguyen Quang Long

For a few decades, Titanium Dioxide (TiO2) has been the most studied photocatalyst due to its significant optical property. In the paper, TiO2 pigment powder (Anatase form) was selected as a precursor to prepare a variety of Black-TiO2 samples, and the typical material was then evaluated for its photocatalytic activity in organic pollutant treatment. Some properties of Black-TiO2 were determined via common methods such as sensory analysis, X-Ray diffraction, and bandgap measurement obtained from UV-Vis spectroscopy. As a result, the material was successfully converted to more than 40% organic pollutant as Methyl Orange (C14H14N3NaO3S) for an hour, as two times higher than that of the amount converted by pristine TiO2. In addition, Black-TiO2 performed much better photocatalytic activity in an acidic medium in comparison with a neutral one, and the material also remained its activity as more than 90% after three time-continuous recycling operations.


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