• Journal of Nuclear Fuel Cycle and Waste Technology(JNFCWT)
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• v.5 no.3
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• pp.221-227
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• 2007

Fenton's reagent is applied to directly decompose the ion-exchange resins, IRN-78 and the mixed resin with IRN-77. The newly applied procedures is to dry the resin first and the catalyst solution is completely absorbed into the resin, then a limited dose of $H_2O_2$ is introduced for an effective reaction between the reagents within the resin. As a characteristic on the decomposition of IRN-78, the resin mixture should be heated to $40^{\circ}C$ to induce the initial reaction and lag time is also needed for about 20 minutes until the main reaction occurs. The effectiveness of the decomposition is investigated using $CuSO_4,\;Cu(NO_3)_2\;and\;FeSO_4$ as a catalyst and the decomposition rate is compared depending on the concentration of each catalyst and the amount of $H_2O_2$. The most effective catalyst was found to be $FeSO_4$ for IRN-78 alone and the mixed resin with IRN-77, and $FeSO_4$ showed a special effect that the reaction was initiated without heating and a lag time. Furthermore, the optimum concentration of the catalyst for each resin and the mixed one is suggested in the view point of the amount of $H_2O_2$ needed and the stability of the decomposition reaction.

• Journal of Korean Society of Environmental Engineers
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• v.32 no.7
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• pp.706-713
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• 2010

The research seeks to find the optimal conditions for sonodegradation of naphthalene and phenol as exemplary organic pollutants to be subjected to ultrasound in varying frequencies (28 kHz, 580 kHz, and 1,000 kHz) and in the presence of different kinds of additive (T$TiO_2$, $H_2O_2$, $FeSO_4$, Zeolite, and Cu). In cases of both naphthalene and phenol, 580 kHz of ultrasound has proven to be the most effective among others at sonodegradation. Based on the observation that OH radicals are also produced in maximum under exposure of 580 kHz of ultrasound, we concluded that this frequency of ultrasound creates hospitable condition for the combined process of degradation by pyrolysis and oxidization. $FeSO_4's$ degradation rate and k1 value have increased by approximately 1.8 times compared with the results of the solutions without any additives. This seems to be the result of ultrasound reaction which, accompanied by Fenton's reaction, increased the oxidative degradation and the production of OH radicals. However, application of ultrasound and Fenton's reaction is limited to the batch type conditions, as its use in continuous system can cause loss of iron or decay of the cistern, thereby creating additional pollutants. When the additive is replaced with $TiO_2$, on the contrary, the rate of sonodegradation has increased up to 20% compared to when there was no additive. We therefore conclude that $TiO_2$ could prove to be an effective additive for ultrasound degradation in continuous treatment system.

• Journal of Korean Society of Environmental Engineers
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• v.31 no.5
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• pp.352-357
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• 2009

Due to rapid consumption of hydrogen peroxide, large amount of hydrogen peroxide is required when Fenton reaction is applied to the contaminated soil. In this study, acetate was employed as a ligand of $Fe^{2+}$ to enhance the efficiency of removal of phenanthrene by securing the stability of hydrogen peroxide. 0.5 ${\sim}$ 3 times of acetate (2${\sim}$12mM) was added to compare with molar concentration of $Fe^{2+}$. Low initial concentration of hydrogen peroxide was 0.7% to eliminate side effect of removal efficiency. The results showed that hydrogen peroxide lifetime was lasted up to 72 hours, or more than 50 times of normal lifetime. Phenanthrene removal efficiency was improved up to 70% due to stabilized hydrogen peroxide. Ferrous ion was oxidized to ferric ion and oxidation-reduction was repeated during the reaction. Finally ferric ion was reduced to ferrous by $HO_2$. It was confirmed that, due to the influence of hydrogen peroxide, pH was acid region and it remained at the range of 4 ${\sim}$ 5 when 8 mM or more of acetate was added. Acetate which was used as the ligand of Fe was also decomposed by Fenton reaction. The decomposition time of acetate was slower than phenanthrene. Therefore, it was able to come to the conclusion that phenanthrene was superior to acetate at the competition for decomposition. Through the results of this study, it was able to identify the possibilities to improve the efficiency of Fenton reaction in the contaminated soil and its economic feasibility, and to move to more realistic technique through research expanded to neutral pH region.

• Applied Chemistry for Engineering
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• v.29 no.1
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• pp.117-121
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• 2018

A stainless steel mesh was applied to the cathode of an electro-Fenton system. Methylene blue (MB) solution was chosen as the model waste water with non-biodegradable pollutants. For the model waste water, the degradation efficiency was compared among various SUS mesh cathodes with different surface treatments and magnetite coatings on them. With increasing amount of the magnetite coating on SUS mesh, the degradation efficiency also increased. The improved electro-catalytic characteristic was explained by the increased amount of in situ generated hydrogen peroxide near the cathode surface. Cyclic voltammetry data also showed improved electro-catalytic performance for SUS mesh with more magnetite coatings on them.

• Journal of Korean Society of Water and Wastewater
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• v.21 no.1
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• pp.123-130
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• 2007

The effects of hydrogen peroxide treatment on the reduction of waterworks sludge were investigated in this study. Sludge treated by peroxidation $H_2O_2$ oxidation) was dewatered using a pressure filter at 3atm. It was observed that $H_2O_2$ treatment at the acidic condition significantly reduce both cake water content and specific resistance to filtration (SRF), indicating the enhancement of dewaterability and filterability. The filterability by hydrogen peroxide treatment at pH 3.5 was better than acidic treatment and became comparable with polymer conditioning. The sludge filterability evaluated by SRF was optimal at a dose 2ml $H_2O_2$/sludge($0.02g\;H_2O_2/gTS$) after adjusting of pH to 3.5. The $H_2O_2$ oxidation at pH 3.5 also produced even more dewatered cake when compared with polymer conditioning. The reduction rate of sludge mass at an optimal condition showed 34% compared with untreated sludge. The effects of peroxidation on sludge properties including zeta potential, bound water and particle size were also evaluated. Peroxidation at the acidic condition reduced both bound water and zeta potential. By $H_2O_2$ combined with sulfuric acid leached iron caused Fenton's reaction, which showed a potential to significantly reduce the amount of solids mass and to produce more compact cake with higher filterability.

• Journal of Korea Soil Environment Society
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• v.2 no.3
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• pp.49-57
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• 1997

Naturally-occurring iron minerals, goethite and magnetite, were used to catalyze hydrogen peroxide and initiate Fenton-like oxidation of silica sand contaminated with diesel, kerosene in batch systems. Reaction conditions were investigated by varying H$_2$0$_2$concentration(0%, 1%, 15%), initial contaminant concentration(0.2, 0.5, 1.0g diesel and kerosene/kg soil), and iron minerals(1, 5wt% magnetite or goethite). Contaminant degradations in silica sand-iron mineral-$H_2O$$_2$ systems were identified by determining total petroleum hydrocarbon(TPH) concentration. In case of silica sand contaminated with diesel(1g contaminan/kg soil with 5wt% magnetite) addition of 0%, 1%, 15% of $H_2O$$_2$showed 0%, 25%, and 60% of TPH reduction in 8 days, respectively When the mineral contents were varied from 1 to 5wt%, removal of contaminants increased by 16% for magnetite and 13.1% for goethite. The results from system contaminated by kerosene were similar to those of the diesel. Reaction of magnetite system was more aggressive than that of goethite system due to dissolution of iron and presence of iron(II) and iron(III); however, dissolved iron precipitated on the surface of iron mineral and seemed to cause reducing electron transfer activity on the surface and quenching $H_2$$O_2$. The system used goethite has better treatment efficiency due to less $H_2$$O_2$ consumption. Results of this study showed possible application of catalyzed $H_2$$O_2$ system to petroleum contaminated site without addition of iron source since natural soils generally contain iron minerals such as magnetite and goethite.

• Analytical Science and Technology
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• v.22 no.3
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• pp.254-262
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• 2009

Activated carbon fiber treated with iron compound (Fe-ACF) was employed for preparation of Feactivated carbon fiber/$TiO_2$ (Fe-ACF/$TiO_2$) composite catalysts. Then, the prepared Fe-ACF/$TiO_2$ composite catalysts were characterized by employing BET, SEM, XRD and EDX instruments. It showed that BET surface area was related to adsorption capacity for each composite. The SEM results showed that ferric compound and titanium dioxide were distributed on the surfaces of ACF. The XRD results showed that Fe-ACF/$TiO_2$ composite mostly contained an anatase structure with a Fe mediated compound. EDX results showed the presence of C, O, and Ti with Fe peaks in Fe-ACF/$TiO_2$ composites. From photocataytic degradation effect, it was observed in the organic dye (Methylene blue, MB) degradation by these composites. Different degradation effect can be attributed to the synergetic effects of photo-Fenton reaction of Fe. It was considered that the combined reactions of Fe-ACF/$TiO_2$ produce powerful photo-Fenton process in the MB degradation.

• Journal of Environmental Science International
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• v.17 no.1
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• pp.37-44
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• 2008

The electro-chemical decolorization of Rhodamine B (RhB) in water has been carried out by electro Fenton-like process. The effect of distance, material and shape of electrode, NaCl concentration, current, electric power, $H_2O_2$ and pH have been studied. The results obtained that decrease of RhB concentration of Fe(+)-Fe(-) electrode system was higher than that of other electrode system. The decrease of RhB concentration was not affected electrode distance and shape. Decolorization of electro Fenton-like reaction, which was added $H_2O_2$ onto the electrolysis using electrode was higher than electrolysis. Addition of NaCl decreased the electric consumption. The lower pH is, the faster initial reaction rate and reaction termination time observed.

• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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• 2002.04a
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• pp.127-130
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• 2002

Recently, the contamination with heavy metals in closed mines has been seriously considered since it can disturb human health through the polluted drinking-water and crops. Therefore, the concerns about the remediation of polluted land and treatment technology for hazardous matters have been accelerated. However, any of practical methods for treatment and/or remediation have not been yet suggested. In this research, a novel technology was studied to immobilize arsenic in tailings and soils disturbed by mining. In this technology, Fenton-like reaction were applied to immobilize arsenic in tailings. In the examination of Fenton-like reaction using pure pyrite, $H_2O$$_2$ and arsenic, the concentrations of extracted arsenic and iron were reduced up to 90 and 75%, respectively From the result of SEM-EDS, the Immobilization of arsenic was observed on the surface of pyrite. Thus, it can be said that the coating and/or adsorption prevents the extraction of arsenic.

• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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• 2002.09a
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• pp.231-234
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• 2002

According to recent investigations regarding Fenton-like reaction, it was reported that there was a key factor to decompose organic materials by not only the hydoroxyl radical but also several reductants which were superoxide anion and hydroperoxide anion. This research was focused on an investigation of the decomposition of carbon tetrachloride(CT) by reductants which were generated by pyrolusite with hydrogen peroxide. Generally, CT decomposition rate increased with raising pH values. Especially,, CT was decomposed over 60 percent by 10,000 ppm of hydrogen peroxide within 10 minutes in neutral condition. In addition, the decomposition of chlorinated compounds would be accelerated in alkaline condition, even with low concentration of hydrogen peroxide.