• YAKHAK HOEJI
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• v.16 no.2
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• pp.73-84
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• 1972

단백질과 전이금속 이온들과의 상호작용을 연구하는데 있어서 단백질중의 이미다졸기 및 아미노산의 반응성은 중요하다. Cd(II)-2-메틸이미다졸 착물들의 경우 이미다졸 분자중의 결합측은 "피로올"형 보다 오히려 "피리딘" 질소임을 알 수 있다. 이 착물들의 환원파는 가역적이며 2전자반응으로 나타난다. 그리고 이미다졸 존재하의 Ni(II) 이온은 촉매파를 나타내며 Ni(II) 이온만의 환원파는 불가역성인 것에 비해 가역성을 보여주었다. 또한 그 반파전위는 Ni(II) 이온만의 반파전위보다 수백 mV 양전위로 이동된다. 이러한 성질은 전극 반응에 관여한 주물질이 전극 표면에서 흡착되어 환원되기 때문이다. 이미다졸 농도의 대수값에 대해 반파전위를 도시했을 때 그 기울기가 30mV로써 이론치와 일치한다. 한편 $Cd(II)-2CH_{3}Im$의 단계적 생성항수 $pK_{1},pK_{2},pK_{3},pK_{4}$는 각각 2.68, 4.01, 4.90, 5.36이었다.4.01, 4.90, 5.36이었다.

• Journal of Advanced Navigation Technology
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• v.19 no.3
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• pp.230-236
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• 2015

In this paper, the electric potential of electrode surface is investigated by assuming them as two dimensional sets of point current sources. And, the simulated water tank is manufactured as a reduced scale of the earth. Henceforth, the adequate model electrode for test is decided to decrease experimental errors relevant to the limitation of the size of the water tank. The one of important things of this work, the deduction method of the potential interference factor is proposed, which used as the criterion of the potential interference according to the shape of conductors and the laying conditions, when multiple grounding conductors are situated at the same resistance grounding area. Also, the validity of this theory is verified from a numerical simulation of the grounding electrode to be used in experiments, and this study is realized by the verified theory and the simulated experiments.

• Journal of the Korean Chemical Society
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• v.61 no.6
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• pp.320-327
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• 2017

In a borate buffer solution, the growth kinetics and the electronic properties of passive film on cobalt were investigated, using the potentiodynamic method, chronoamperometry, and single-frequency electrochemical impedance spectroscopy. It was found out that the unstable passive film ($Co(OH)_2$) and CoO of Co formed in the low electrode potential changes to $Co_3O_4$ and CoOOH while the electrode potential increases. And the composition of the passive films was varied against the applied potential and oxidation time. The oxide film formed during the passivation process of cobalt has showed the electronic properties of p-type semiconductor, which follow from the Mott-Schottky equation.

• Proceedings of the Korean Institute of Surface Engineering Conference
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• 2016.11a
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• pp.145-145
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• 2016

해양환경용 구조물은 극심한 부식 환경에 노출되어 있고 부식손상으로 인한 직간접적 경제적 손실이 발생하고 있는 상황이다. 이에 대한 방식대책으로써 음극방식법이 선박, 교량, 각종 화학장비에 널리 이용되고 있으며, 이러한 산업분야에 가장 흔히 적용되고 있는 음극방식 중 하나가 피방식체에 일정 전류 또는 음극 전위를 인가하는 외부전원법이다. 이는 전도성 부식환경인 해수환경 하에서 철강 및 해양환경용 구조 재료의 내식성을 월등히 향상시킬 수 있기 때문에 설계에 있어서 고급 내식재료 대신 경제적인 상용 재료를 적용할 수 있어 비용 절감효과를 가질 수 있다. 한편 적정 방식전위에서는 부식손상으로부터 강재를 보호하지만, 과방식 전위에서는 취성이 발생함으로써 내구성 감소의 역효과가 나타날 수도 있기 때문에 최적 방식전위의 규명은 반드시 필요하다. 따라서, 본 연구에서는 S355ML강에 대하여 천연해수 용액에서 다양한 정전위를 조건으로 전기화학실험을 실시하여 최적 방식전위를 규명하고자 하였다. 시험편은 에머리 페이퍼로 2000번까지 연마하였고, 아세톤과 증류수로 세척하여 실험하였다. 전기화학(정전위) 실험은 천연해수 속에서 $1.28cm^2$의 면적만을 노출시켜 진행하였으며, OCP로부터 -2.0V까지의 음극분극 곡선을 분석하여 정전위 조건들을 선정하였다. 그리고 외부 직류전원장치를 이용하여 1,200초 동안 다양한 정전위를 인가하였으며, 기준전극은 Ag/AgCl 전극을 이용하였다. 실험 후에는 주사전자현미경과 3D 현미경을 통해 시험편 표면을 관찰하였으며, 그 결과 일부 음극분극 구간에서 강재 표면에 전착물에 의한 뷸균일한 피막이 형성되었다. 또한, 일정 전위구간에서 용해 및 과전압에 대하여 표면손상 정도를 관찰하여, 해수환경 하에서 S355ML강의 최적 방식전위를 규명하였다.

• Journal of the Korean Chemical Society
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• v.28 no.2
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• pp.86-94
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• 1984

The single crystal ion-selective electrode,$ {\beta}-Ag_3SI/PVC-THF $membrane electrode has showed a linear potential response to the activities of iodide ion (10-1${\sim}$10-7M). The $ {\beta}-Ag_3SI$ membrane electrode was compared with AgI/PVC-THF membrane and copper metal plate membrane electrodes. In order to measure the selectivity coefficient of the electrodes toward $Cl^-$ and $Br^-$, the separation and mixed solution method were employed. The potential-time curve was obtained by the usual immersion technique and pH effect was also examined. The orders of selectivity for $Br^-$, $Cl^-$ and stability of response time are ${\beta}-Ag_3SI/PVC-THF $membrane > AgI/PVC-THF membrane > copper metal plate membrane. These electrodes could be used as indicating electrodes in the potentiometric titration of a single halide and mixed halides with the standard solution of silver nitrate.

• Journal of the Korean Chemical Society
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• v.29 no.2
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• pp.137-143
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• 1985

Construction of a liquid membrane type of cupric ion selective electrode and its application to the potentiometric titration have been studied. A liquid ion-exchange membrance was prepared by extracting Cu(II) in aqueous solution into 1-(2-pyridylazo)-2-naphthol/nitrobenzene. A Ag/AgCl internal reference electrode was dipped into the aqueous reference solution of $1.00 {\times} 10^{-3}M\;Cu(NO_3)_2$ buffered with HAc-NaAc buffer solution, which was in contact with the nitrobenzene extract. The electrode showed the nernstian response to Cu(II) in the concentration range from $1.00{\times} 10^{-6}$ to $1.00{\times} 10^{-3}$M. The most suitable ion-exchanger concentration in the liquid membrane was $1.00{\times} 10^{-4}$M. The selectivity coefficients of the electrode for the various metal cations were investigated. The electrode was applied to the potentiometric titration of Cu(II) with EDTA.

• Journal of the Korean Chemical Society
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• v.56 no.6
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• pp.731-738
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• 2012

The purpose of this study is to analyze the understandings of science high school students on the conception of chemical cell in relation to chemical equilibrium from the microscopic viewpoint at molecular level through questionnaires and follow-up interviews. The results show that they have high understandings on the chemical equilibrium states in the electrochemical cell and on the redox reaction taking place simultaneously when a metal electrode is immersed in the metal ion solution. However, they do not fully comprehend the development of electrical potential difference, electron movement, electrode potential measurement in the half-cells, and calculation of the net cell voltage between anode and cathode in the chemical cell because of difficulties in the microscopic understanding the interaction on the interface at the electrode and the electrolyte solution.

• Applied Chemistry for Engineering
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• v.27 no.1
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• pp.74-79
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• 2016

The effects of scale formation of hardness material caused by electrode reactions on the desalination performance of the membrane capacitive deionization (MCDI) were investigated. During the repeated adsorption and desorption process for the influent containing $Ca^{2+}$ ion, changes in effluent concentration and cell potential with respect to the number of adsorption were analyzed. It was found that $OH^-$ generation at the cathode was initiated at about 0.8 V or more of cell potential. In addition, the scale of $Ca(OH)_2$ was formed on the surface of cathode carbon electrode by combining adsorbed $Ca^{2+}$ ions and $OH^-$ ions generated from electrode reaction. As the scale was forming, the electrical resistance of carbon electrode was increasing, which resulted in the decrease of the adsorption amount. In the case of the operation at 1.5 V cell potential, the adsorption was reduced to 58% of the initial adsorption amount due to the scale formation.

• Journal of the Korean Institute of Illuminating and Electrical Installation Engineers
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• v.23 no.8
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• pp.86-92
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• 2009

In order to minimize ac mutual coupling, the auxiliary electrode are located at a right angle in measuring ground impedance. In case that the measurement space is limited, the alternative method is employed. At that time, it is necessary to investigate the measurement errors due to ac mutual coupling and earth mutual resistance in measuring the ground impedances. 'This paper presents the measurement accuracy according to the location of the current and potential auxiliary electrodes in measuring ground impedance of vertically or horizontally buried ground electrode. The measurement errors due to ac mutual coupling were evaluated Consequently, the effect of ac mutual coupling on the measurement accuracy for horizontally buried ground electrode is greater than that for vertically buried ground electrode. Measurement errors due to ac mutual coupling is the largest when the current and potential auxiliary electrodes are located in parallel. The 61.8[%] rule is inappropriate in measuring ground measurement. Theoretically, in case that the angle between the current and potential auxiliary electrodes is 90$[^{\circ}]$, there is no ac mutual coupling. If it is not possible to route the current and potential auxiliary electrodes at a right angle with limitation of measurement space, the location of these electrodes with an obtuse angle is preferred to that with an acute angle in reducing the measurement errors due to ac mutual coupling.

• Proceedings of the Korea Society for Energy Engineering kosee Conference
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• 1994.05a
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• pp.114-117
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• 1994

아연-산화은 전지는 높은 에너지 및 전력밀도를 가지고 있으나 비싼 제작비용 때문에 우주항공, 군사무기 등 특수한 분야에서 주로 이용되며, 특히 전해액이 별도의 용기에 보관되어 있다가 외부 신호에 의해 충전된 dry상태의 전지에 주입되어 활성화되는 1차 또는 비축형 아연산화은 전지는 우수한 고율방전 특성, 장시간의 저장기간 및 활성화와 동시에 부하를 인가 할 수 있는 특성 때문에 많은 무기체계에서 이용하고 있다. 이러한 아연-산화은 전지의 아연전극은 높은 다공도와 반응 면적을 가져야 하며, 특히 방전중 아연전극의 전위는 가역 수소전위 보다 더 음전위이기 때문에 수소가스가 다량 발생하게 되므로 수은과 같은 높은 과전압을 갖는 물질을 첨가하여 가스 발생량을 줄이고 부동태화(passivation)를 억제하게 된다. 그러나 국내 여건상 수은을 사용하여 전지를 제작하는 것은 환경문제 등으로 인하여 어렵기 때문에 본 연구에서는 수은을 사용하지 않고 비축형 아연-산화은 전지의 음극판을 제작하기 위하여 전착법(electro deposit)과 mesh 제작방법을 혼합하여 아연전극을 제작하였으며, 기판에 석출된 아연과 아연 mesh의 질량비율에 따른 전지의 성능을 평가하였다.