• Journal of the Korea Academia-Industrial cooperation Society
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• v.18 no.3
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• pp.681-686
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• 2017

Degradation is commonly observed in field-aged PV modules due to corrosion of the photovoltaic ribbon. The reduced performance is caused by a loss of fill factor due to the high series resistance in the PV ribbon. This study aimed to mitigate the degradation by corrosion using five sacrificial anodes - Al, Zn and their alloys - to identify the most effective material to mitigate the corrosion of the PV ribbon. The corrosion behavior of the five sacrificial anode materials were examined by open circuit potential measurements, potentiodynamic polarization tests, and galvanic current density and potential measurements using a zero resistance ammeter. Immersion tests for 120 hours were also conducted using materials and damp heat test tests were performed for 1500 hours using 4 cell mini modules. The Al-3Mg and Al-3Zn-1Mg sacrificial anodes had a low corrosion rate and reduced drop in power, making then suitable for long-term use.

• Journal of the Korean Chemical Society
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• v.25 no.5
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• pp.325-330
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• 1981

The electrochemical behavior of cadmium electrode for the nickel-cadmium battery system has been studied by cyclic voltammetry, controlled potential electrolysis and X-ray diffraction method. Cathodic polarization curve for cadmium hydroxide electrode prepared by electrochemical pretreatment of metallic cadmium showed two peaks. It has been found that cadmium hydroxide was reduced to cadmium metal at the first peak potential, whereas very activated metal of cadmium which was strongly oriented (002) rather than (101) was formed at the second peak potential. It was also found that the cadmium formed at the second peak potential reacted rapidly with oxygen. Therefore, it could be presumed that the cadmium recombination reaction with the oxygen was chemical, and could be represented as $2Cd + O_2 + 2H_2O\;{\longrightarrow}\;2Cd(OH)_2$.

• Corrosion Science and Technology
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• v.14 no.1
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• pp.19-24
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• 2015

Flow Accelerated Corrosion (FAC) causes unexpected accidents in a secondary side of a nuclear power plant. The secondary side pipes are mainly carbon steel tubes that have a protective magnetite ($Fe_3O_4$) layer on the inner surface. The stability of the protective magnetite layer depends on the parameters related to the FAC phenomena such as pH, temperature, flow rate, surface roughness etc. The dissolution of magnetite is basically the electrochemical reaction, but the most of the experiments of magnetite dissolution were carried out thermodynamically to determine the solubility of magnetite. The knowledge of the electrochemical properties of magnetite is required to understand the dissolution process of magnetite. This paper reviews the manufacture of the magnetite ($Fe_3O_4$) electrode, and summaries the electrochemical properties of the magnetite.

• Journal of the Korea Concrete Institute
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• v.21 no.4
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• pp.409-417
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• 2009

In this study, autogenous crack healing and artificial crack healing using electrochemical electro deposition method were conducted to compare in the aspects of corrosion monitoring. Furthermore, the analysis of impressed voltage characteristics, galvanic current and linear polarization resistance comparison, and photo image processing technique were performed for quantitative comparisons of healing ratio. As a result, it was found that, in view of impressed voltage of artificial crack healing, the measured voltage was increased as time goes by. From the galvanic test results of artificial crack healing, the current vs. potential distribution value were formed widely in comparison with autogenous crack healing. In this point, it was shown that artificial crack healing has more eleatic resistance capacity than autogenous crack healing technique. Finally, it was found that artificial crack healing was 1.63 times higher than autogenous healing in view of crack healing ratio.

• Journal of the Korean Ceramic Society
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• v.38 no.6
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• pp.558-567
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• 2001

본 연구에서는 알콕사이드를 전구물질로 하는 졸겔공정을 이용하여 Bi 과잉 12 mol%의 조성인 B $i_4$ $Ti_3$ $O_{12}$ 박막과 B $i_4$ $Ti_{3-x}$T $a_{x}$ $O_{12}$(x=0.1, 0.2, 0.3) 박막을 제조하였다. XPS 분석에 따르면 Ta 치환 x=0.2에서 Bi 4f의 photoemission 곡선이 낮은 결합에너지로 이동하였고 피크 강도가 감소하는 현상이 관측되었다. 이는 x=0.1과 0.2 사이에서 Bi-O 결합이 길어져 인장상태 하에 있었음을 나타내었다. B $i_4$ $Ti_3$ $O_{12}$(BIT) 박막의 유전상수와 유전손실은 100 kHz에서 340, 0.05이었고, B $i_4$ $Ti_{3-x}$T $a_{x}$ $O_{12}$ 박막에서 이들 값은 x=0.1에서 가장 높았으며, 각각 480, 0.13이었다. B $i_4$ $Ti_3$ $O_{12}$ 박막의 잔류분극과 항전계는 1.24$\mu$C/$ extrm{cm}^2$, 31.4 kV/cm 이었으나, Ta 치환 x=0.2에서 이들 값은 각각 19.7$\mu$C/$\textrm{cm}^2$, 49.5 kV/cm 에 이르렀다. 또한, B $i_4$ $Ti_3$ $O_{12}$ 박막의 누설전류 밀도는 ~$10^{-6}$ A/$\textrm{cm}^2$ 정도이었으며, Ta 치환은 누설전류를 감소시켜 Ta 치환 x=0.2 이상에서 BIT 박막에 비해 한 차수 정도 낮아졌다. Ta 치환에 따른 B $i_4$ $Ti_3$ $O_{12}$ 전기 물성에서 변화는 Bi-O 결합에서 관측된 인장상태로의 전이와 연관성이 있었으며, 덧붙여 치환에서 생성된 전자에 의한 정공보상이 이에 영향을 끼쳤다. 정공보상이 이에 영향을 끼쳤다.끼쳤다.

• Journal of the Korean Electrochemical Society
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• v.2 no.2
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• pp.106-111
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• 1999

The effect of the MG on the electrochemical charge-discharge properties of $CaNi_5$ hydrogen storage alloys was investigated under Ar and $H_2$ atmosphere. $CaNi_5$ alloy was partially decomposed to CaO and Ni phase during the MG process. The decomposition of $CaNi_5$ alloy was enhanced by the MG process which leads to crash and reformation of oxide layer on the alloy surface. As the MG process time increased, initial discharge capacity of the electrode was reduced, but the decay rate of the capacity compared to $CaNi_5$ alloys was slower. It may be described that the degradation of $MG-CaNi_5$ electrode was caused by the reduction of the reversible hydrogen reaction sites and increasing polarization resistance of hydrogen adsorption resulted from phase decomposition and disorder during the MG process, and/or by hydroxide formation during the electrochemical charge-discharge cycles.

• Journal of the Korean Chemical Society
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• v.21 no.4
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• pp.276-283
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• 1977

Reduction of dichromate at a platinum cathode in acid solution was studied by cyclic voltammetry and controlled potential electrolysis. Cathodic polarization curve consisted of three waves in unbuffered solution of potassium dichromate having initial pH ranges 1.5∼4.0, with sodium sulfate as the supporting electrolyte. Relative heights of the first and the second waves were, respectively, a function of chromium (Ⅵ) concentration and activity of hydrogen ion, but that of the third wave was not proportional to both of them. The current of the first two peaks were proportional to the sweep rate of potential (${\nu}$), while that of the last peak vs. ${\nu}^{1/2}$ was linear at the sweep rate of less than 50mV/sec. By the controlled potential electrolysis, the reduction of chromium (Ⅵ) was almost completely suppressed at potentials more negative than the last peak and at initial pH's above ca. 2.3 of unbuffered solution. Therefore, these peaks represented, respectively, $Cr_2O_7^{2-}{\to}Cr^{3+},\;2H^+{\to}H_2$ and the formation of a cathodic film.

• Journal of the Korean Electrochemical Society
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• v.5 no.2
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• pp.62-67
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• 2002

The corrosion of the metallic cell components is blown to be one of the major reason f3r the performance degradation and subsequently the life-time limitation of the MCFC. To elucidate the corrosion phenomena, a corrosion study with the AISI-type 316L stainless steel, the most widely used separator material, in 621Li/38K carbonate eutectic melt was carried out. Corrosion phenomena in an MCFC were observed to differ from one location to another due to different environmental condition. The stability of passive film was found to be responsible fur the variations in corrosion phenomena. According to the potentiodynamic analysis, the passive film formed in anode-gas environment was less stable than in cathode-gas environment. The potentiostatic method combined with XRD analysis in addition to the cyclicvoltammetry was conducted to get an insight on variety corrosion reaction of AISI-type 316L stainless steel in a carbonate melt.

• The Journal of Engineering Geology
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• v.10 no.2
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• pp.172-188
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• 2000

This paper presents the state of art and the role of geophysical exploration techniques with evaluating the trend of domestic and worldwide seawater intrusion research, and illustrates advanced techniques obtained through the project of 'Development of the techniques for estimation, prediction, and prevention of seawater intrusion' funded by the Ministry of Science and Technology of Korea. The advanced geophysical interpretation was achieved by adding the digital geophysical logging data. DC resistivity and TEM monitorings were applied to determine whether or not the seawater intrusion was in progress. Induced Polarization technique using electric current monitoring channel was introduced to discriminate seawater contaminated zone from highly conductive layer caused by clay minerals. A conceptual model was suggested with spatial visualization of the study area to predict the diffusion of seawater contamination. Finally, the future work of the development of geophysical techniques was suggested with the base of the present level of them.

• Journal of the Korean Chemical Society
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• v.17 no.5
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• pp.378-384
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• 1973

To investigate the mechanism of the reaction of electrolytic oxidation of iodide to iodate ions, polarization curves are determined in various kinds of solution using electrodeposited lead peroxide and platinum anodes. It was observed from the polarization curves that the limiting current is exists at concentration 1.5 M of potassium iodide, and these limiting current disappeared as potassium hydroxide was added up to concentration of 0.1 M. while in case of platinum anode, limiting current did not appear in dilute potassium iodide solution. These results are owing to the chemical reaction, $PbO_2+2I^{-}+2H^+{\to}PbO+I_2+H_{2}O$ ocurring at the surface of lead peroxide anode. Also, we studied to obtain the optimum conditions of electrolytic preparation of iodate from iodide solution using a cell without the diaphragm. The results are that; (a) addition of potassium dichromate at the anti-reducing agent is proper in concentration of 0.1 g/l, (b) electrolytic temperature is not so much effective in raising the current efficiency, (c) current efficiency is increased with current density, and (d) electrolysis is the most effective in weak alkaline solutions.