Analysis of Primary Degradation and Decolourization of Dyes in Water by an H2O2/UV Advanced Oxidation Process

Author(s):  
Amaia Menendez ◽  
Jose Ignacio Lombraña ◽  
Ana de Luis

AbstractSynthetic dyes are extensively used in textile dyeing, paper printing, colour photography, pharmaceuticals, food, cosmetics and other industries. In spite of their diversity there are a certain number of properties common to many dye compounds, such as aromatic constitution, chromophore groups and others. Similarly to other dyes and due to the formation of colour intermediates, in the case of Rhodamine 6G colour capacity is maintained in the initial steps of dye degradation. For this reason in the degradation of a dye it is necessary to distinguish between two processes that take place simultaneously: dye removal and decolourization. This study was conducted by using a water solution of 50 mg/L of Rhodamine 6G (Rh-6G), as a model of a dye wastewater, in the hydrogen peroxide/UV system. The kinetic model proposed in this paper for the removing of Rh- 6G is a sequential first-order reaction. This model describes acceptably the changes in two kinds of compound for a wide interval of H

Author(s):  
Natalija Koprivanac ◽  
Dinko Vujevic

Organic synthetic dyes are widely produced and used today. Significant losses of organic and inorganic content occurs during the manufacturing and application of dyes and its discharge in the effluent presents a threat to the eco-systems due to general toxicity and resistance to destruction by biological treatment methods. Particularly azo dyes are of special environmental concern due to their degradation products such as aromatic amines, which are considered highly carcinogenic. So, dyes have to be removed from coloured wastewater before discharge. However, traditional treatment methods (adsorption, coagulation/flocculation) mainly transfer the contaminants from wastewater to secondary waste. Therefore, advanced oxidation processes seem to be sustainable and clean technology to decolorize and minimize organic dyes content from wastewater. In this paper, degradation of an azo dye C.I. Direct Orange 39 (DO39) using Fenton type processes (Fe2+/H2O2, Fe3+/H2O2and Fe0/H2O2) has been performed. The molar ratio of Fenton’s type reagents has been varied in the range of 1 : 5 up to 1 : 50 at 0.5 and 1.0 mM concentrations of iron salts and iron powder. Experiments have been conducted for two hours in a batch reactor with magnetic stirring, ambient conditions and pH 3. The process efficiency and formation of degradation by-products have been determined on the basis of results obtained by UV/VIS spectrophotometric, total organic carbon (TOC) and high performance liquid chromatography (HPLC) analyses. The optimal Fenton and Fenton ``like" processes parameters have been applied in the photo reactor, too. It has been observed that simultaneous utilization of UV irradiation with Fenton's and Fenton ``like" reagents increases the degradation of DO39 dye. Degradation of the dye in dilute aqueous solution follows pseudo-first order kinetics. The maximal decolourization of 20 mg L-1 DO39 in water of 93.2% and TOC degradation of 76.9% were obtained using Fe3+/H2O2= 1 : 5 molar ratio. The results indicate that the treatment of DO39 dye wastewater with UV/Fe3 +/H2O2 system was found to be the most efficient.


2021 ◽  
Author(s):  
Bijoli Mondal ◽  
Shib Sankar Basak ◽  
Arnab Das ◽  
Sananda Sarkar ◽  
Asok Adak

Abstract In the photochemical UV-H2O2 advanced oxidation process, H2O2 absorbs UV light and is decomposed to form hydroxyl radicals (OH·), which are highly excited and reactive for electron-rich organic compounds and hence can degrade organic compounds. In the present work, the UV-H2O2 process was investigated to degrade ciprofloxacin (CIP), one of India's widely used antibiotics, from aqueous solutions using a batch type UV reactor having photon flux = 1.9 (± 0.1) ×10-4 Einstein L-1 min-1. The effects of UV irradiation time on CIP degradation were investigated for both UV and UV-H2O2 processes. It was found that about 75% degradation of CIP was achieved within 60 s with initial CIP concentration and peroxide concentration of 10 mg L-1 and 1 mol H2O2/ mol CIP, respectively, at pH of 7(±0.1) and fluence dose of 113 mJ cm-2. The experimental data were analyzed by the first-order kinetics model to find out the time- and fluence-based degradation rate constants. Under optimized experimental conditions (initial CIP concentration, pH and H2O2 dose of 10 mg L-1, 7(±0.1) and 1.0 mol H2O2 / mol CIP, respectively), the fluence-based pseudo-first-order rate constant for the UV and UV-H2O2 processes were determined to be 1.28(±0.0) ×10-4 and 1.20(±0.04) ×10-2 cm2 mJ-1 respectively. The quantum yields at various pH under direct UV were calculated. The impacts of different process parameters such as H2O2 concentration, solution pH, initial CIP concentration, and wastewater matrix on CIP degradation were also investigated in detail. CIP degradation was favorable in acidic conditions. Six degradation products of CIP were identified. Results clearly showed the potentiality of the UV-H2O2 process for the degradation of antibiotics in wastewater.


2019 ◽  
Vol 79 (6) ◽  
pp. 1134-1143 ◽  
Author(s):  
Ada Azevedo Barbosa ◽  
Ramon Vinicius Santos de Aquino ◽  
Naiana Santos da Cruz Santana Neves ◽  
Renato Falcão Dantas ◽  
Marta Maria Menezes Bezerra Duarte ◽  
...  

Abstract This work investigated the efficiency of polyethylene terephthalate (PET) as support material for TiO2 films in the photocatalytic degradation of red Bordeaux and yellow tartrazine dyes. The optimum operating conditions were determined by a factorial design, which resulted after 180 min of treatment in degradations of 99.5% and 99.1% for the UVC/H2O2/TiO2Sup and solar/H2O2/TiO2Sup systems, respectively. For the kinetic study, the experimental data fitted to the pseudo-first-order model and the calculated kinetic constants (k) values were 0.03 min−1 for the UVC/H2O2/TiO2Sup system and 0.0213 min−1 for the system solar/H2O2/TiO2Sup. It was verified that TiO2 supported in the PET remained with high degradation efficiency even after five cycles of reuse, indicating a good stability of the photocatalyst in the support. A significant reduction of TOC content was also observed along the reaction time. The phytotoxicity bioassay with Lactuca sativa demonstrated that after treatment with UVC/H2O2/TiO2Sup and solar/H2O2/TiO2SUP, an increase in IC50 and consequently lower toxicity was observed.


2019 ◽  
Vol 68 (8) ◽  
pp. 666-674 ◽  
Author(s):  
Shiljashree Vijay ◽  
Raj Mohan Balakrishnan ◽  
Eldon R. Rene ◽  
Uddandarao Priyanka

Abstract Nanotechnologies have prominent applications in the field of science and technology owing to their size-tunable properties providing a promising approach for degradation of various pollutants. In this scenario, the present work aims to study the effect of nickel ferrite nanoparticles on the degradation of Irgalite violet dye by Fenton's reaction using oxalic acid as an oxidizing agent in the presence of sunlight. The effect of pH and adsorbent dosage on the rate of dye degradation was monitored. Based on these studies it was observed that 99% dye degradation was achieved for catalyst dosage of 0.2 g, 400 ppm dye concentration and 2.0 mM oxalic acid at pH 3.0 within 60 min. The studies reveal that the degradation follows pseudo-first-order kinetics and the catalyst reusability remained constant almost for five cycles. Further, nickel ferrite nanoparticles are proven to be an efficient alternative for the removal of dyes from coloured solutions.


2021 ◽  
Author(s):  
Deepak Gola ◽  
Pankaj Kumar Tyagi ◽  
Arvind Arya ◽  
Dhriti Gupta ◽  
Jyoti Raghav ◽  
...  

2013 ◽  
Vol 442 ◽  
pp. 26-35 ◽  
Author(s):  
Nahum A. Medellin-Castillo ◽  
Raúl Ocampo-Pérez ◽  
Roberto Leyva-Ramos ◽  
Manuel Sanchez-Polo ◽  
José Rivera-Utrilla ◽  
...  

Catalysts ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 1150
Author(s):  
Muhammad Hamza ◽  
Ataf Ali Altaf ◽  
Samia Kausar ◽  
Shahzad Murtaza ◽  
Nasir Rasool ◽  
...  

Dye removal through photocatalytic degradation employing nanomaterials as catalysts is a growing research area. In current studies, photocatalytic alizarin red (AR) dye degradation has been investigated by designing a series of Cr based manganese oxide nanomaterials (MH1–MH5). Synthesized nanomaterials were characterized by powder X-ray diffraction, scanning electron microscopy/energy dispersive x-ray, Brunauer–Emmett–Teller, and photoluminescence techniques and were utilized for photocatalytic AR dye degradation under UV light. AR dye degradation was monitored by UV–visible spectroscopy and percent degradation was studied for the effect of time, catalyst dose, different dye concentrations, and different pH values of dye solution. All the catalysts have shown more than 80% dye degradation exhibiting good catalytic efficiencies for dye removal. The catalytic pathway was analyzed by applying the kinetic model. A pseudo second-order model was found the best fitted kinetic model indicating a chemically-rate controlled mechanism. Values of constant R2 for all the factors studied were close to unity depicting a good correlation between experimental data.


Polymers ◽  
2019 ◽  
Vol 11 (2) ◽  
pp. 252 ◽  
Author(s):  
José Pellicer ◽  
María Rodríguez-López ◽  
María Fortea ◽  
Carmen Lucas-Abellán ◽  
María Mercader-Ros ◽  
...  

β-cyclodextrin (β-CD) and hydroxypropyl-β-cyclodextrin (HP-β-CD) were used to prepare insoluble polymers using epichlorohydrin as a cross-linking agent and the azo dye Direct Red 83:1 was used as target adsorbate. The preliminary study related to adsorbent dosage, pH, agitation or dye concentration allowed us to select the best conditions to carry out the rest of experiments. The kinetics was evaluated by Elovich, pseudo first order, pseudo second order, and intra-particle diffusion models. The results indicated that the pseudo second order model presented the best fit to the experimental data, indicating that chemisorption is controlling the process. The results were also evaluated by Freundlich, Langmuir and Temkin isotherms. According to the determination coefficient (R2), Freunlich gave the best results, which indicates that the adsorption process is happening on heterogeneous surfaces. One interesting parameter obtained from Langmuir isotherm is qmax (maximum adsorption capacity). This value was six times higher when a β-CDs-EPI polymer was employed. The cross-linked polymers were fully characterized by nuclear magnetic resonance (NMR), Fourier transform infrared spectroscopy (FTIR), thermal gravimetric analysis (TGA). Also, morphology and particle size distribution were both assessed. Under optimized conditions, the β-CDs-EPI polymer seems to be a useful device for removing Direct Red 83:1 (close 90%), from aqueous solutions and industrial effluents. Complementarily, non-adsorbed dye was photolyzed by a pulsed light driven advanced oxidation process. The proposed methodology is environmental and economically advantageous, considering the point of view of a sustainable recycling economy in the textile dyeing process.


Membranes ◽  
2020 ◽  
Vol 10 (5) ◽  
pp. 106 ◽  
Author(s):  
Saranya Rameshkumar ◽  
Rory Henderson ◽  
Ramesh Babu Padamati

The synergistic mechanism of photocatalytic-assisted dye degradation has been demonstrated using a hybrid ZnO-MoS2-deposited photocatalytic membrane (PCM). Few layers of MoS2 sheets were produced using the facile and efficient surfactant-assisted liquid-phase exfoliation method. In this process, hydrophilic moieties of an anionic surfactant were adsorbed on the surface of MoS2, which aided exfoliation and promoted a stable dispersion due to the higher negative zeta potential of the exfoliated MoS2 sheets. Further, the decoration of ZnO on the exfoliated MoS2 sheets offered a bandgap energy reduction to about 2.77 eV, thus achieving an 87.12% degradation of methylene blue (MB) dye within 15 min of near UV-A irradiation (365 nm), as compared with pristine ZnO achieving only 56.89%. The photocatalysis-enhanced membrane filtration studies on the ZnO-MoS2 PCM showed a complete removal of MB dye (~99.95%). The UV-assisted dye degradation on the ZnO-MoS2 PCM offered a reduced membrane resistance, with the permeate flux gradually improving with the increase in the UV-irradiation time. The regeneration of the active ZnO-MoS2 layer also proved to be quite efficient with no compromise in the dye removal efficiency.


2011 ◽  
Vol 239-242 ◽  
pp. 2597-2601
Author(s):  
Wei Ding ◽  
Ming Ke ◽  
Zhao Zheng Song

Anthraquinone dye Reactive Blue (KN-R) is first selected as the model dye to test the treatment of UV-vis/Ferrioxalate/H2O2system. The effect of parameters Fe2+/H2O2, pH and H2C2O4are synthetically assessed. The optimum concentration is obtained at 1:15 of Fe2+/H2O2and 30mg·L-1of H2C2O4 at pH=3.0 in 30min. Under the optimum condition, the removal rate of color, chemical oxygen demand (COD) and total organic carbon (TOC) are more than 99%, 87.7% and 66.8% respectively. The results show that the reaction accorded with a pseudo-first-order and the degeneration velocity of KN-R is 0.2459[dye](mg·L-1/min).


Sign in / Sign up

Export Citation Format

Share Document