Photodegradation Studies on Orange G and Acid Blue 113: New Doped Rare Earth Nanometal Oxides as Visible Light Active Photo Catalyst

2014 ◽  
Vol 938 ◽  
pp. 257-262
Author(s):  
G.A. Suganya Josephine ◽  
Arumugam Sivasamy

Dyes are a source of serious pollutants from different industrial outlets and show a major contribution in polluting the environment. In the present study two dyes namely Orange G and Acid Blue 113 were compared for their photodegradation efficiency employing rare earth nanometal oxide as a visible active photocatalyst. The prepared catalyst was nanocrystalline form with particle size 70 nm and the surface of the catalyst was highly porous and rough which facilitates the absorption of the dye further enhance the photo degradation which were confirmed by various characterization techniques. Effect of pH, variation of catalyst dosage, variation of initial dye concentration and kinetic studies were conducted for both the dyes. The reaction followed a pseudo first order kinetics. The activity of the prepared catalyst was higher when compared to a commercially used metal oxide. Reusability studies proved that the catalyst prepared was very active even upto the third cycle. The degradation process was initiated by the attack of the OH radical generated in the in-situ process via visible light irradiation. EPR spin trapping technique was employed to confirm the presence of OH radicals. The prepared catalyst degraded the dye molecules of interest in lesser time duration by absorption of visible light, thereby reducing the cost of photodegradation.

2014 ◽  
Vol 21 (5) ◽  
pp. 1675-1681 ◽  
Author(s):  
Panneerselvam Sathishkumar ◽  
Ramalinga Viswanathan Mangalaraja ◽  
Oscar Rozas ◽  
Héctor D. Mansilla ◽  
M.A. Gracia-Pinilla ◽  
...  

2021 ◽  
Author(s):  
Shiva Chahardahmasoumi ◽  
Seyed Amir Hossein Jalali ◽  
Mehdi Nasiri Sarvi

Abstract The adsorption and photo-Fenton degradation of tetracycline (TC) over Fe saturated nanoporous montmorillonite was analyzed. The synthesized samples were characterized using XRD, FTIR, SEM, and XRF analysis, and the adsorption and desorption of TC onto these samples as well as the antimicrobial activity of TC during these processes were analyzed at different pH. The results indicated that the montmorillonite is a great adsorbent for the separation of the TC from aqueous solutions, however, after increasing the amount of TC adsorbed, the desorption process started, and up to 50% of TC adsorbed onto non-modified montmorillonite was released back to the solution with almost no changes in its antimicrobial activity. After acid treatment (for creation of nanoporous layers) and Fe saturation of the montmorillonite, almost similar great separation was achieved compared to non-modified montmorillonite. In addition, the desorption of TC from modified montmorillonite was still high up to 40% of adsorbed TC. However, simultaneous adsorption and photodegradation of TC were detected and almost no antimicrobial activity was detected after 180 min of visible light irradiation, which could be due to the photo-Fenton degradation of TC on the modified montmorillonite surface. In the porous structures of modified montmorillonite high ˙OH radicals were created in the photo-Fenton reaction and were measured using the Coumarin technique. The ˙OH radicals help the degradation of TC as proposed in an oxidation process. Surprisingly, more than 90 % of antimicrobial activity of the TC decreased under visible light (after 180 min) when desorbed from nanoporous Fe-saturated montmorillonite compared to natural montmorillonite. To the best of our knowledge, this is the first time that such a high TC desorption rate from an adsorbent with the least remained antimicrobial activity is reported which makes nanoporous Fe-saturated montmorillonite a perfect separation substance of TC from the environment.


2014 ◽  
Vol 133 ◽  
pp. 407-414 ◽  
Author(s):  
Panneerselvam Sathishkumar ◽  
Ramalinga Viswanathan Mangalaraja ◽  
Oscar Rozas ◽  
Héctor D. Mansilla ◽  
M.A. Gracia-Pinilla ◽  
...  
Keyword(s):  

Polymers ◽  
2021 ◽  
Vol 13 (22) ◽  
pp. 3991
Author(s):  
Nicoleta Mirela Marin ◽  
Ioana Stanculescu

Despite Acid Blue 113 (AB 113)’s extensive use and negative environmental impact, very few studies have focused on its efficient and environmentally friendly removal. This research aims the removal of AB 113 from environmental aqueous media and its consequent enzymatic biodegradation. A strongly basic anion exchange resin in Cl− form, Amberlite IRA 402 (IRA 402(Cl−)) was used for AB 113 adsorption and a laccase was used to further biodegrade it. For the first time, two novel, efficient and environmentally friendly physical–chemical and biological assays for AB 113 wastewater removal and subsequent biodegradation were combined. The adsorption of AB 113 onto IRA 402(Cl−) was tested in batch and continuous flux modes. Influence of contact time, concentration and desorption in acidic media were evaluated. The kinetic data were best modulated by the Lagergren model with R2 = 0.9275. The Langmuir isotherm model best fitted the experimental data, and the maximum adsorption capacity was 130 mg/g. Dye, resin and AB113 loaded resin were characterized by thermogravimetry and FTIR to evaluate their physical chemical properties modification. Based on the performed studies, a consecutive methodology is proposed, incorporating the ion exchange process in the first stage and the biodegradation process in the second. Thus, in the second stage the residual concentration of AB 113 is reduced by an efficient bio-degradation process produced by the laccase at pH = 4.


2021 ◽  
Author(s):  
Tariq Al–Musawi ◽  
Murat Yilmaz ◽  
Amir Mahvi ◽  
Samaneh Mohebi ◽  
davoud balarak

Abstract This study offers a comprehensive investigation into the efficiency of degradation of acid blue 80 (AB80) dye using a system using ultraviolet (UV) radiation combined with hydrogen peroxide (H2O2) and persulphate (PS) oxidants (UV/PS/H2O2). The degradation reactions were performed under different values of PS and H2O2 concentrations, initial AB80 dye concentration, pH, UV intensity, and contact time. The results revealed that the UV/H2O2 provided the best performance at pH of 5, while the best performance for the UV/PS and UV/PS/H2O2 systems was obtained at pH of 7. Besides, 15 mmol was found to be the optimum concentration for both oxidants. The efficiency of the combined process of the UV/PS/H2O2 was higher than that of the other two processes i.e., UV/PS and UV/H2O2, which was 98.2% for a dye concentration of 25 mg/L. Further, the BOD5/COD ratios at the beginning and end of the UV/PS/H2O2 process were 0.19 and 0.52, respectively, indicative of the conversion of the non-biodegradable dye molecules to biodegradable compounds. The toxicity test was performed using the bioassay method with Daphnia magna, and 90% reduction in toxicity was observed in the effluent. The lethal concentration 50 (LC50) indicator was found to be 4.7 mg/L for the dye solution. The results also revealed that the degradation data followed the pseudo-first-order kinetics, and the reaction rate constant was higher for the UV/PS/H2O2 system than for the other systems. The rate of mineralisation by this process was 0.92. Scavenging studies also showed that both the sulphate (SO°-4) and hydroxyl (OH°) radicals play an important role in the degradation process. Energy consumption in the UV/H2O2, UV/PS, and UV/PS/H2O2 processes was 61, 47.8, and 20.8 kWh/m3, respectively. On conclusion, the UV/PS/H2O2 is an effective and applicable process for the treatment of dye in wastewater, particularly when the medium is neutral.


Nanomaterials ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 1325
Author(s):  
Chiing-Chang Chen ◽  
Janah Shaya ◽  
Kyriaki Polychronopoulou ◽  
Vladimir B. Golovko ◽  
Siriluck Tesana ◽  
...  

This work reports the preparation and detailed characterization of stannum indium sulfide (SnIn4S8) semiconductor photocatalyst for degradation of ethiofencarb (toxic insecticide) under visible-light irradiation. The as-prepared SnIn4S8 showed catalytic efficiency of 98% in 24 h under optimal operating conditions (pH = 3, catalyst dosage of 0.5 g L−1). The photodegradation reaction followed pseudo-first-order kinetics. The major intermediates have been identified using gas chromatography/mass spectrometry. •O2− and •OH radicals appeared to be the primary active species in the degradation process as revealed by scavenger and electronic spin resonance studies, while photogenerated holes had a secondary role in this process. A plausible mechanism involving two routes was proposed for ethiofencarb degradation by SnIn4S8 after identifying the major intermediate species: oxidative cleavage of the CH2-S and the amide bonds of the carbamate moiety. Lastly, SnIn4S8 was found to be efficient, stable, and reusable in treating real water samples in three successive photodegradation experiments. This study demonstrates the prospect of SnIn4S8 photocatalysis in treatment of natural and contaminated water from extremely toxic organic carbamates as ethiofencarb.


2020 ◽  
Vol 10 (6) ◽  
pp. 849-859
Author(s):  
Radwa A. El-Salamony ◽  
Abeer A. Emam ◽  
Nagwa A. Badawy ◽  
Sara F. El-Morsi

Objective: ZnO nanoparticles were synthesized using wet impregnation method, and activated carbon from rice straw (RS) prepared through chemical route. Methods: The nano-composites ZnO-AC series were prepared with different ZnO:AC ratio of 10, 20, 50, and 70% to optimize the zinc oxide nanoparticles used. The obtained composites were characterized by FE-SEM, XRD, SBET, and optical techniques then used for the photo-degradation of Malachite green dye (MG) under visible light. Results: It was found that 10ZnO-AC exhibited excellent visible light photo-catalytic performance. The ·OH radicals’ formation is matching with photo-activity of the prepared composites. The photo-degradation efficiency of MG increased from 63% to 93%, when the 10ZnO-AC photocatalyst amount was increased from 0.5 to 6 g/L. Conclusion: The GC-MS technique was used to analyze the intermediates formed; up to 15 kinds of chemicals were identified as the degradation products.


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