• Proceedings of the KIEE Conference
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• 1988.07a
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• pp.363-366
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• 1988

A new $NH_{3}-O_{2}$ oxidation method was estimated by the electrical properties of the fabricated n-MOS transistor. For the C-V characteristic curves the Qox are almost equal to Qss and no hysteresis phenomena are observed. The Id-Vds characteristics show that $NH_{3}-O_{2}$ oxidation method is superior to Dry oxidation.

• Journal of Soil and Groundwater Environment
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• v.26 no.1
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• pp.45-53
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• 2021

The removal of 2,4-dichlorophenoxyacetic acid (2,4-D) in aqueous solution by coupled electro-oxidation and Fe(II) activated persulfate oxidation process was investigated. The electrochemical oxidation was performed using carbon sheet electrode and persulfate using Fe(II) ion as an activator. The oxidation efficiency was investigated by varying current density (2 - 10 mA/㎠), electrolyte (Na2SO4) concentration (10 - 100 mM), persulfate concentration (5 - 20 mM), and Fe(II) concentration (10 - 20 mM). The 2,4-D removal efficiency was in the order of Fe(II) activated persulfate-assisted electrochemical oxidation (Fe(II)/PS/ECO, 91%) > persulfate-electrochemical oxidation (PS/ECO, 51%) > electro-oxidation (EO, 36%). The persulfate can be activated by electron transfer in PS/ECO system, however, the addition of Fe(II) as an activator enhanced 2,4-D degradation in the Fe(II)/PS/ECO system. The 2,4-D removal efficiency was not affected by the initial pHs (3 - 9). The presence of anions (Cl- and HCO3-) inhibited the 2,4-D removal in Fe(II)/PS/ECO system due to scavenging of sulfate radical. Scavenger experiment using tert-butyl alcohol (TBA) and methanol (MeOH) confirmed that although both sulfate (SO4•-) and hydroxyl (•OH) radicals existed in Fe(II)/PS/ECO system, hydroxyl radical (SO4•-) was the predominant radical.

• Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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• 2008.11a
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• pp.412-412
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• 2008

ENIG(Electroless Nickel Immersion Gold)is a surface treatment method that is used most widely at fine pitch's SMT and BGA packaging process. ENIG has good diffusion barrier of Ni against solder and good wettability due to Au finish. But when the discoloration occurred on the Au finish of ENIG, some key characteristics related to the quality and reliability of PCB such as bondability, solderability and electrical flowing of packaging process could be deteriorated. In this paper, we have performed the water dip test ($88^{\circ}C$ purified water) which accelerates the galvanic corrosion of Ni diffused from the Ni-P layer. That is, the excessive oxidation of the Ni layer could result in non-wetting of the solder because the flux may not be able to remove excessive oxides. Though Au discoloration have been reported to be caused by Ni oxides in many literature, it is still open to verify and discuss The microstructures and chemical compositions have been investigated using FE-SEM, TEM, FIB, EDS and XPS. As a result, authors have found that the Au discoloration in ENIG type is severely caused by the oxidation of the Ni and the mechanism of Au discoloration can be confirmed through the experiment result of water dip test.

• Journal of Electrochemical Science and Technology
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• v.7 no.3
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• pp.190-198
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• 2016

Application of fuel cell to produce renewable energy for commercial purpose is limited by the high cost of Pt based electrode materials. Development of inexpensive, high energetic electrode is the need of the hour to produce pollution free energy using bio-fuel through a fuel cell. Ni-Cu and Ni-CeO₂-Cu electrode materials, electro synthesized by pulse current have been developed. The surface morphology of the electrode materials is controlled by different deposition parameters in order to produce a high current from the electro-oxidation of the fuel, the ethanol. The developed materials are electrochemically characterized by Cyclic Voltammetry (CV), Chronoamperometry (CA) and Potentiodynamic polarization tests. The results confirm that the high current is due to their enhanced catalytic properties viz. high exchange current density (i₀), low polarization resistance (R_p) and low impedance. It is worthwhile to mention here that the addition of CeO₂ to Ni-Cu has outperformed Pt as far as the high electro catalytic properties are concerned; the exchange current density is about eight times higher than the same on Pt surface. The morphology of the electrode surface examined by SEM and FESEM exhibits that the grains are narrow and sub spherical with 3D surface, containing vacancies in between the elongated grains. The fact has enhanced more surface area for electro oxidation of the fuel, giving rise to an increase in current. Presence of Ni, CeO₂, and Cu is confirmed by the XRD and EDXS. Fuel cell fabricated with Ni-CeO₂-Cu material electrode is expected to produce clean electrical energy at cheaper rates than conventional one, using bio fuel the derived from biomass.

• 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.

• 한국전기화학회:학술대회논문집
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• 1998.10a
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• pp.43-43
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• 1998

• 한국전기화학회:학술대회논문집
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• 2003.07a
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• pp.221-224
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• 2003

• Bulletin of the Korean Chemical Society
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• v.30 no.8
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• pp.1798-1804
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• 2009

In this study, we have studied on improved performance of carbon nanotubes/titanium (CNT/TiO2) structure electrode for methylene blue (MB). The composite electrodes consisting of CNTs and a titanium oxide matrix with phenol resin binder was fabricated with a mixture method. The chemical and morphological structure of CNT/Ti$O_2$ composites were characterized by means of BET surface area, X-ray diffraction (XRD), scanning electron microscopy (SEM), UV-Vis absorption technique, Raman spectroscopy and energy dispersive X-ray (EDX). The electrode showed a remarkably enhanced performance for MB oxidation under UV illumination with or without electro-chemical reaction (ECR). Such a remarkably improved performance of the CNT/Ti$O_2$ structure electrode might be due to the enhanced MB oxidation by electro- and photo-generated electrons and holes in the CNTs and Ti$O_2$ under UV illumination with or without ECR.

• Journal of the Korean institute of surface engineering
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• v.28 no.2
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• pp.110-118
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• 1995

The effect of reductants (Ti, Si, Al, Mn, Fe) addition into molten Borax has been studied on oxidation resistance and the growth of boronized layer formed during electro-boronizing on the substrate such as carbon steel and STS 430. Experiments have been carried out at the current density of 0.5 A/$\cm^2$ and in temperature range of 600~$1000^{\circ}C$ for 1~5 hours. The penetrated depth of the boron increased with addition of reductants (Ti, Si, Al) and decreased with addition of Mn and Fe. But excessive addition of reductants inhibited the boronizing due to an increase in viscosity of electrolyte. Oxidation resistance of the boronized carbon steel was improved but that of the boronized STS 430 decreased.

• 한국신재생에너지학회:학술대회논문집
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• 2009.11a
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• pp.191-194
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• 2009

PtRu based and PtSn based ternary catalysts were prepared by a conventional impregnation method using NaBH4 as reducing agent. The alloy formation, crystalline size and chemical composition of the in-house catalysts were determined by XRD, TEM and EDX, respectively. The chemical compositions of in-house catalysts were quite similar to the nominal value and good alloy formations were also observed. Further, crystalline sizes of ternary catalysts were comparatively smaller than binary catalysts and were approximately 3.5 ~ 5.5 nm. The electrochemical measurements were carried out in the solution 1 M $H_2SO_4$ with 1 M $C_2H_5OH$ at room temperature. LSV results obtained that ternary catalysts were higher current densities and specific activities. Especially, in case of tungsten addition system, Pt5Sn4W/C have the highest specific activities values and was approximately 21.2 and 3.1 times higher than that of PtRu/C and PtSn/C electrocatalyst.