• Journal of Electrochemical Science and Technology
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• v.10 no.2
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• pp.104-114
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• 2019

Energy is an essential driving force for modern society. In particular, electricity has become the standard source of power for almost every aspect of life. Electric power runs lights, televisions, cell phones, laptops, etc. However, it has become apparent that the current methods of producing this most valuable commodity combustion of fossil fuels are of limited supply and has become detrimental for the Earth's environment. It is also self-evident, given the fact that these resources are non-renewable, that these sources of energy will eventually run out. One of the most promising alternatives to the burning of fossil fuel in the production of electric power is the proton exchange membrane (PEM) fuel cell. The PEM fuel cell is environmentally friendly and achieves much higher efficiencies than a combustion engine. Water management is an important issue of PEM fuel cell operation. Water is the product of the electrochemical reactions inside fuel cell. If liquid water accumulation becomes excessive in a fuel cell, water columns will clog the gas flow channel. This condition is referred to as flooding. A number of researchers have examined the water removal methods in order to improve the performance. In this paper, a new water removal method that investigates the use of vibro-acoustic methods is presented. Piezo-actuators are devices to generate the flexural wave and are attached at end of a cathode bipolar plate. The "flexural wave" is used to impart energy to resting droplets and thus cause movement of the droplets in the direction of the traveling wave.

• 한국전기화학회:학술대회논문집
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• 2000.04a
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• pp.17-17
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• 2000

• Journal of Korean Society of Water and Wastewater
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• v.33 no.1
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• pp.31-41
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• 2019

Volatile organic compounds(VOCs) are toxic carcinogenic compounds found in wastewater. VOCs require rapid removal because they are easily volatilized during wastewater treatment. Electrochemical advanced oxidation processes(EAOPs) are considered efficient for VOC removal, based on their fast and versatile anodic electrochemical oxidation of pollutants. Many studies have reported the efficiency of removal of various types of pollutants using different anodes, but few studies have examined volatilization of VOCs during EAOPs. This study examined the removal efficiency for VOCs (chloroform, benzene, trichloroethylene and toluene) by oxidization and volatilization under a static stirred, aerated condition and an EAOP to compare the volatility of each compound. The removal efficiency of the optimum anode was determined by comparing the smallest volatilization ratio and the largest oxidization ratio for four different dimensionally stable anodes(DSA): Pt/Ti, $IrO_2/Ti$, $IrO_2/Ti$, and $IrO_2-Ru-Pd/Ti$. EAOP was operated under same current density ($25mA/cm^2$) and electrolyte concentration (0.05 M, as NaCl). The high volatility of the VOCs resulted in removal of more than 90% within 30 min under aerated conditions. For EAOP, the $IrO_2-Ru/Ti$ anode exhibited the highest VOC removal efficiency, at over 98% in 1 h, and the lowest VOC volatilization (less than 5%). Chloroform was the most recalcitrant VOC due to its high volatility and chemical stability, but it was oxidized 99.2% by $IrO_2-Ru/Ti$, 90.2% by $IrO_2-Ru-Pd/Ti$, 78% by $IrO_2/Ti$, and 75.4% by Pt/Ti anodes The oxidation and volatilization ratios of the VOCs indicate that the $IrO_2-Ru/Ti$ anode has superior electrochemical properties for VOC treatment due to its rapid oxidation process and its prevention of bubbling and volatilization of VOCs.

• Journal of environmental and Sanitary engineering
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• v.11 no.3
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• pp.37-46
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• 1996

In this study, the effect of pH, Temp, dye concentration, distance of electrode, and the potential on the removal efficiency of dye-wastewater using electrochemical reaction were investigated. Optimum conditions for the electrochemical treatment of dye-wastewater were obtained that pH;7, 8V, electrode distance; 1cm and the reaction time for obtaining above 99% removal efficiency were 10 - 40min at each conditions, From this result, we can determine the instantaneous current efficiency and specific energy consumption, and we can provide the effective data for economical treatment of industrial dye-wastewater.

• Journal of Environmental Health Sciences
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• v.34 no.6
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• pp.439-445
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• 2008

The feasibility study for the application of the removal and mineralization of Rhodamine B (RhB) was performed in a batch electrochemical reactor. The electro/UV process was consisted of DSA (dimensionally stable anode) electrode and UV-C or ozone lamp. The experimental results showed that RhB removal by the ozone lamp was higher than that of the UV-C lamp. Optimum current of the electro/UV process was 1 A. The electrochemical, UV and electro/UV process could completely degrade RhB, while a prolonged treatment was necessary to reach a high level RhB mineralization. It was observed that RhB removal in electro/UV process is similar to the sum of the UV and electrolytic decolorization. However, it was found that the COD of RhB could be degraded more efficiently by the electro/UV process (90.2 %) than the sum of the two individual oxidation processes [UV (19.7%) and electrolytic process (50.8%)]. A synergetic effect was demonstrated between the UV and electrolysis.

• Analytical Science and Technology
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• v.19 no.4
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• pp.316-322
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• 2006

The removal efficiencies of silver-ACFs were associated with their surface properties such as surface area, porosity, and the electro-chemical reaction time for the silver treatments. X-ray diffraction patterns of fibers electrochemically treated with silver display diffraction peaks for metallic silver and kinds of silver chloride complexes on the fiber surface after electrochemical adsorption. The results of SEM and EDX indicate that surface reaction motive of silver-ACF prepared by electrochemical reaction are depend on time function for the chloride ion removal efficiency. Finally, Cl ion adsorbed by the silver-ACFs from the ICP analysis seems to show an excellent removal effect.

• Journal of Electrochemical Science and Technology
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• v.8 no.2
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• pp.124-132
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• 2017

The performance of electrolytic processes using copper and catalyzed electrodes for enhanced nutrient removal with various catalyzers and combinations of electrodes was evaluated. The catalyzed electrodes removed more ammonia nitrogen than the copper electrode, but higher ammonia removal was achieved using a Pt/Ti anode. On the other hand, electrolysis using the Pt/Cu anode consumed less energy and cost less. During electroreduction, nitrate was better removed by a pair of copper electrodes than by the catalyzed electrodes. During electrolysis of synthetic wastewater, ammonia removal not only increased owing to direct oxidation at the anode, but was also influenced by indirect oxidation at the cathode. Platinum-coated copper and titanium cathodes actively produced oxidizers and thus removed more ammonia than a pure metal cathode. Although phosphorus was removable irrespective of the type of catalyzer, electrocoagulation using the copper electrode achieved complete removal of phosphorus in a period of less than 10 min.

• Korean Journal of Environmental Agriculture
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• v.19 no.2
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• pp.134-141
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• 2000

For electrochemical treatment of industrial wastewater, the effects of voltage, distance between electrodes, initial pH and NaCl concentrations on removal of pollutants were investigated in a batch electrolysis system. Temperature and pH in electrochemical reactor increased with increase in supplied voltage, but no significant change in EC was found. Removal of COD, turbidity, T-N and T-P were also enhanced with increase in the voltage. On the conditions of short distances between electrodes and long electrochemical reaction times, it was found that COD and T-N were very effectively removed in the system. Regardless of the distances, more than 80% of turbidity and T-P were removed at the beginning of reaction. When initial pH of the wastewater was about 7, the highest efficiency of COD removal was found in the system. On the other hand, removal efficiency of turbidity was unlikely affected by initial pH of the wastewater. T-N removal was increased with increase in initial pH. T-P was successfully removed in the pH range of 5 to 9 with varying removal efficiency of 79 to 96% after 2 minutes of electrochemical reaction time. Addition of NaCl into the electrochemical reactor increased removal efficiency of electrochemical treatment. The highest removal efficiency of COD and T-P, turbidity and T-N was obtained at NaCl concentrations of 500mg/L, 1,000 mg/L and 500mg/L, respectively.

• Applied Chemistry for Engineering
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• v.16 no.2
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• pp.206-211
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• 2005

Mediated electrochemical oxidation (MEO) of polyethylene glycols (PEGs) of molecular weight of 1000, 4000 and 20000, was carried out on both platinum (Pt) and titanium-iridium electrodes in 8.0 M nitric acid solution containing 0.5 M Fe(II) and Co(II) ion. The electrochemical parameters such as current densities, kinds of electrode, electrolyte concentration and removal efficiency were investigated in both Fe(III)/Fe(II) and Co(III)/Co(II) redox systems. The PEGs was decomposed into carbon dioxide by MEO in Fe(III)/Fe(II) and Co(III)/Co(II) redox system during 180 min and 210 min at the current density of $0.67A/cm^2$ on the Pt electrode. Removal efficiency of PEGs by MEO was better in Co(III)/Co(II) redox system than Fe(III)/Fe(II) redox system, indicating mediated electrochemical removal efficiency was 100%.

• Advances in nano research
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• v.13 no.6
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• pp.513-525
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• 2022

In this study, it was aimed to evaluate direct oxidation of aqueous solution containing cefalexin antibiotic with new generation Sn/Sb/Ni: 500/8/1 anode. The fact that there is no such a study on treatment of cefalexin with these new anode made this study unique. According to the operating parameters evaluation COD graphs showed clearer results compared to TOC and CLX and thus, it was it was chosen as major parameter. Furthermore, pseudo-first degree kd values were calculated from CLX results to show more accurate and specific results. Experimental results showed that after 60 min of electrochemical oxidation, complete removal of COD and TOC was accomplished with 750 mg L^-1 KCl, at pH 7, 50 mA cm^-2 current density and 1 cm anode-cathode distance. Also, the stability of the Sn/Sb/Ni anode was evaluated by taking SEM and AFM images and XRD analysis before and after of electrochemical oxidation processes. According to the results, it was not occurred too much change on the anode surface even after 300 h of electrolysis. Thus, it was thought that the anode material was not corroded to a large extent. Furthermore, the removal efficiencies were very high for almost all the time and conditions. According to the results of the study, electrochemical oxidation with new generation Sn/Sb/Ni anodes for the removal of cefalexin antibiotic was found very successful and applicable due to require less reaction time complete mineralization and doesn't require pH adjustment step compared to other studies in literature. In future studies, different antibiotic types should be studied with this anode and maybe with real wastewaters to test applicability of the process in treatment of pharmaceutical wastewaters containing antibiotics, in a better way.