Intensification of advanced oxidation processes (AOPs) for the degradation of bisphenol-A

Author(s):  
Mahendra Chinthala ◽  
Badrinarayana K. Ashwathanarayanaiah ◽  
Soundarya Kulkarni ◽  
Yajnesh Udayakishore ◽  
Aishwarya Halyal ◽  
...  

Abstract Bisphenol-A (BPA), a precursor for many polymers, is a harmful compound for living organisms if present beyond permissible limits in aqueous streams. The combinations of oxidation processes like Hydrodynamic Cavitation (HC), hydrogen peroxide (H2O2), and Fenton’s reagent (H2O2 + FeSO4) were examined for the degradation of BPA in the present study. The effects of operating parameters like inlet pressure, initial concentration of BPA, orifice geometry were investigated on BPA degradation. The degradation rates of BPA increased with inlet pressure up to 0.5 MPa and then showed a decreasing trend beyond 0.5 MPa. The initial concentration of BPA had an inverse relation with the degradation percentage. The multiple hole orifice plate showed better degradation of BPA compared to the single hole orifice plate. In the intensification studies, the addition of hydrogen peroxide to BPA in the cavitation reactor favored BPA degradation. A combination of HC + Fenton’s reagent (0.1 M H2O2 + 0.01 M FeSO4) significantly degraded BPA present in the aqueous streams.

2013 ◽  
Vol 39 (2) ◽  
pp. 107-115 ◽  
Author(s):  
Barbara Pieczykolan ◽  
Izabela Płonka ◽  
Krzysztof Barbusiński ◽  
Magdalena Amalio-Kosel

Abstract Treatment of leachate from an exploited since 2004 landfill by using two methods of advanced oxidation processes was performed. Fenton’s reagent with two different doses of hydrogen peroxide and iron and UV/H2O2 process was applied. The removal efficiency of biochemically oxidizable organic compounds (BOD5), chemically oxidizable compounds using potassium dichromate (CODCr) and nutrient (nitrogen and phosphorus) was examined. Studies have shown that the greatest degree of organic compounds removal expressed as a BOD5 index and CODCr index were obtained when Fenton’s reagent with greater dose of hydrogen peroxide was used - efficiency was respectively 72.0% and 69.8%. Moreover, in this case there was observed an increase in the value of ratio of BOD5/CODCr in treated leachate in comparison with raw leachate. Application of Fenton’s reagent for leachate treatment also allowed for more effective removal of nutrients in comparison with the UV/H2O2 process.


1997 ◽  
Vol 36 (12) ◽  
pp. 215-222 ◽  
Author(s):  
Shyh-Fang Kang ◽  
Huey-Min Chang

This study was designed to use both artificial and real textile secondary effluents to evaluate (1) the COD and color removal efficiencies for ferrous coagulation and Fenton's coagulation, and (2) the feasibility of using hydrogen peroxide to improve ferrous coagulation to meet more stringent effluent standards. The results indicate that the optimum pHs for both ferrous coagulation and Fenton's preoxidation processes range between 8.0–10 and 3.0–5.0, respectively. The rate for color removal is faster than that for COD removal in the Fenton's preoxidation process. The removals of COD and color are mainly accomplished during Fenton's preoxidation step. The ratio of COD removal for Fenton's coagulation versus ferrous coagulation, given the same ferrous dosage, ranges from 1.4 to 2.3, and it ranges from 1.1 to 1.9 for color removal, using two effluent samples. Therefore, using hydrogen peroxide can enhance the ferrous coagulation, and this ensures more stringent effluent standards of COD and color are met.


2004 ◽  
Vol 4 (4) ◽  
pp. 113-119 ◽  
Author(s):  
C.A. Murray ◽  
S.A. Parsons

Advanced oxidation processes have been reported to have the potential to remove natural organic matter from source waters. Of these Fenton's reagent, photo-Fenton's reagent and titanium dioxide photocatalysis are the three most promising processes. Compared to conventional coagulation/flocculation processes they have higher removal efficiencies in terms of both dissolved organic carbon and UV254 absorbance. Under optimum reaction conditions all three remove over 80% dissolved organic carbon and 0% UV254 absorbance. In addition the enhanced removal of natural organic matter leads to a corresponding reduction in the formation of disinfection by-products following chlorination of the treated water. Advanced oxidation processes give enhanced removal of organic species ranging from low to high molecular weight while coagulation/flocculation is inefficient at removing low molecular weight species. One additional benefit is all three processes produce less residuals compared to conventional coagulation, which is advantageous as the disposal of such residuals normally contributes a large proportion of the costs at water treatment works.


Author(s):  
Richard J. Watts ◽  
Tanya M. Haeri-McCarroll ◽  
Amy L. Teel

AbstractThe effect of contaminant hydrophobicity on hydrogen peroxide dosage requirements in the treatment of contaminated soils using catalyzed H


2003 ◽  
Vol 17 (3) ◽  
pp. 321-326 ◽  
Author(s):  
Asgar Farahnaky ◽  
David A Gray ◽  
John R Mitchell ◽  
Sandra E Hill

1997 ◽  
Vol 69 (5) ◽  
pp. 1052-1056 ◽  
Author(s):  
Brian K. Aldershof ◽  
Ronald M. Dennis ◽  
Craig J. Kunitsky

Author(s):  
Phalguni Banerjee ◽  
Sunando DasGupta ◽  
Sirshendu De

An advanced oxidation study using Fenton's reagent, i.e., ferrous sulfate and hydrogen peroxide was carried out for studying oxidation of eosin dye. Effects of concentration of various reagents on the degradation of dye were explored during an advanced oxidation process. It was found that ferrous concentration plays a major role in dye decomposition. Rate of dye decomposition is faster with an increase in ferrous sulfate concentration compared to the increase in hydrogen peroxide concentration. A detailed kinetic model was proposed. Profiles for eosin, hydrogen peroxide and various intermediates were also generated. The rate constant of the reaction of eosin with a hydroxyl radical was found to be of the order of 109 l/mol.s.


2003 ◽  
Vol 47 (9) ◽  
pp. 165-171 ◽  
Author(s):  
A. Burbano ◽  
D. Dionysiou ◽  
M. Suidan ◽  
T. Richardson

In previous laboratory experiments Fenton's Reagent (FR) was successfully used as the source of hydroxyl radicals (OH•) for chemical treatment of low concentrations of methyl tert-butyl ether (MTBE) in water. Although under certain conditions MTBE degradation levels as high as 99.99% were achieved, none of these experiments resulted in complete MTBE mineralization. In all cases, these experiments applied FR as an equimolar concentration of ferrous iron (Fe2+) and hydrogen peroxide (H2O2). The present study investigates the effect of H2O2/Fe2+ molar ratio on the extent of degradation of MTBE and intermediate products in water at pH = 3.0. The initial concentration of MTBE studied was 0.0227 mM (approximately 2 mg/L). Initially, the dose of Fe2+ was kept constant at a Fe2+/MTBE molar ratio of 10:1 and the dose of H2O2 was varied to achieve different H2O2/Fe2+ molar ratios. The results revealed that higher degradation efficiency was achieved when FR was used as an equimolar mixture (H2O2/Fe2+ molar ratio = 1.0). The extent of MTBE degradation decreased when the H2O2/Fe2+ molar ratio was changed to values higher or lower than 1.0. These results suggest that a stoichiometric relationship (1:1) between the FR components optimizes the degradation process for this reactant system. It is hypothesized that an excess of H2O2 enhances the effect of reactions that scavenge OH•, while a decreased amount of H2O2 would be a limiting factor for the Fenton Reaction.


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