• 자원리싸이클링
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• 제10권3호
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• pp.29-36
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• 2001

전기화학적 환원 반응을 이용하는 전기 분해에 의한 방법으로 중금속 폐수를 처리하여 금속성분을 회수하는데 있어 cyclic voltammetry를 적용하였다. 아연용액에서의 아연전극과 탄소전극에 대한 전기적 반응 특성은 voltammogram으로 확인할 수 있었으며 수중 아연이온 환원은 전위가 -0.76V 이하에서 반응이 일어나는 것을 알 수 있었다. 용액 중 아연이온의 산화와 환원으로 인해 형성되는 금속 특성은 X선 회절분석 결과를 통해서 확인할 수 있었으며, AFM 이용하여 구리판에 환원된 아연을 관찰할 수 있었다. 본 연구의 결과는 전기분해에 의한 폐수 중 중금속의 처리 및 회수에 있어 기초자료로 활용죌 수 있을 것으로 사료된다.

• Bulletin of the Korean Chemical Society
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• 제17권2호
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• pp.162-167
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• 1996

Two redox processes of methyl viologen (+2/+, +/0) in acetonitrile were investigated by using channel electrode voltammetric and in situ electrochemical ESR methods. Two separated unequal plateau currents of the first (+2/+) and second (+/0) redox processes of the viologen were observed in the channel electrode voltammograms and showed a cube-root depedndence on the electrolyte flow rate, respectively. The simple Levich analysis resulted in two different diffusion coefficients of $D_{+2}=2.2{\times}10^{-5}\;cm^2/s$ and $D_+=3.0{\times}10^{-5}cm^2/s$ from the limiting currents. In situ electrochemical ESR studies were performed for the monocation radicals generated at the potentials of the two plateau currents in the electrolyte flow range $1.3{\times}10^{-1}{\geq}v_f{\geq}2.7{\times}10^{-3}\;cm^3/s$. Backward implicitfinite difference method was employed to simulate the electrochemical kinetic problem of two sequential electron transfers ($MV^{+2}+e{\leftrightarrows}MV^+,\;MV^{+}+e{\leftrightarrows}MV^0$) coupled with reversible comproportionation ($MV^{2+}+MV^0{{\leftrightarrows}^{k_f}_{k_b}}2MV^+$). $k_f$ was found to be greater than ($10^6M^{-1}s^{-1}.

• 전기화학회지
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• 제22권1호
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• pp.43-52
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• 2019

리튬이차전지(Lithium Secondary Batteries)를 에너지원으로 채용하는 분야가 다양해짐에 따라, 기존 요구 특성뿐만 아니라 각 분야에 특화된 성능 평가 결과까지 요구하고 있다. 이에 대응하기 위해 각 전지 제조사는 연구 인력을 충원하고 고가의 장비를 지속적으로 도입해서 다수의 전지를 오랜 기간 평가해야 하는 어려움을 겪고 있다. 이를 해소하기 위해, 전지 모델링(Modeling)을 기반으로 한 모사(Simulation) 기법을 도입하여, 실험 횟수를 최소화하고 실험 시간도 단축하려는 시도를 지속하고 있다. 현재까지 다양한 리튬이차전지 모델링 기법이 보고되고 있으며, 목적에 따라 최적 기법이 선택 및 활용되어 왔다. 본 리뷰 논문에서는 뉴만(Newman) 모델을 기반으로 한 전기화학적 모델링(Electrochemical Modeling) 기법을 상세히 설명한다. 특히, 전극 반응속도를 나타내는 버틀러-볼머식(Butler-Volmer Equation), 각 상(Phase)에서 전자와 이온의 균형 방정식 (Material and Charge Balance Equations), 그리고 전지의 온도 변화를 설명할 수 있는 에너지 균형 방정식 (Energy Balance Equation)의 물리적 의미를 쉽게 설명하고, COMSOL Multiphysics를 이용한 간단한 해석 과정과 결과를 제시한다.

• 대한화학회지
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• 제37권1호
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• pp.168-171
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• 1993

• Bulletin of the Korean Chemical Society
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• 제9권1호
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• pp.64-66
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• 1988

• 공업화학
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• 제18권6호
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• pp.599-602
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• 2007

결정성 그린 코크스 상의 메조카본 마이크로비즈를 이용하여 약품 및 전기화학 부활 법을 적용하여 23 F/cc 급의 신형 고밀도 활성탄을 합성하였다. 전기화학 부활과정 중에 고성능을 발현하기 위한 전기화학 거동을 순차적인 전압인가법을 이용하여 검토하였다. 전기화학 부활의 유효전압은 높은 비표면적 활성탄의 표면활성 저하에 의해 적용전압에 무관하게 2.7~3.2 V로 확인되었다.

• Corrosion Science and Technology
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• 제17권6호
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• pp.310-316
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• 2018

The effect of passive film on corrosion of metals and alloys in a static corrosive environment has been studied by many researchers and is well known, however few studies have been conducted on the electrochemical measurement of metals and alloys during cavitation corrosion conditions, and there are no test standards for electrochemical measurements 'During cavitation' conditions. This study used commercially additive manufactured(AM) pure titanium in tests of anodic polarization, corrosion potential measurements, AC impedance measurements, and repassivation. Tests were performed in 3.5% NaCl solution under three conditions, 'No cavitation', 'After cavitation', and 'During cavitation' condition. When cavitation corrosion occurred, the passive current density was greatly increased, the corrosion potential largely lowered, and the passive film revealed a small polarization resistance. The current fluctuation by the passivation and repassivation phenomena was measured first, and this behavior was repeatedly generated at a very high speed. The electrochemical corrosion mechanism that occurred during cavitation corrosion was based on result of the electrochemical properties 'No cavitation', 'After cavitation', and 'During cavitation' conditions.

• Bulletin of the Korean Chemical Society
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• 제32권5호
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• pp.1669-1678
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• 2011

Six new binuclear copper(II) complexes have been prepared by template condensation of the dialdehydes 1,8-[bis(3-formyl-2-hydroxy-5-methyl)benzyl]-l,4,8,11-tetraazacyclotetradecane (PC-a) and 1,8-[bis(3-formyl-2-hydroxy-5-bromo)benzyl]-l,4,8,11-tetraazacyclotetradecane (PC-b) with appropriate aliphatic diamines, and copper(II) perchlorate. The structural features of the complexes have been confirmed by elemental analysis, IR, UV-vis and mass spectra etc. The electrochemical behavior of all the copper(II) complexes show two irreversible one electron reduction process. The room temperature magnetic moment studies depict the presence of an antiferromagnetic interaction in the binuclear complexes. The catechol oxidation and hydrolysis of 4-nitrophenylphosphate were carried out by using the complexes as catalyst. The antimicrobial screening data show good results. The binding of the complexes to calf thymus DNA (CT DNA) has been investigated with absorption and emission spectroscopy. The complex [$Cu_2L^{1a}$] displays significant cleavage property of circular plasmid pBR322 DNA in to linear form. Spectral, electrochemical, magnetic and catalytic studies support the distortion of the copper ion geometry that arises as the macrocyclic ring size increases.

• 대한화학회지
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• 제58권2호
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• pp.160-168
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• 2014

The electrochemical behavior and corrosion inhibition of zinc in 0.5 M $H_2SO_4$ in the absence and presence of some chromones has been investigated using weight loss, potentiodynamic polarization, electrochemical impedance spectroscopy (EIS) and electrochemical frequency modulation (EFM) techniques. The presence of these investigated compounds in the corrosive solutions decrease the weight loss, the corrosion current density, and double layer capacitance but increases the charge transfer resistance. Polarization studies were carried out at room temperature, and showed that all the studied compounds act as mixed type inhibitors with a slight predominance of cathodic character. The effect of temperature on corrosion inhibition has been studied and the thermodynamic activation and adsorption parameters were determined and discussed. The adsorption of the investigated compounds on zinc was found to obey Langmuir adsorption isotherm.

• Bulletin of the Korean Chemical Society
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• 제28권10호
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• pp.1729-1734
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• 2007

The electrochemical behaviors of estrone in the presence of various surfactants were examined with great details. It is found that a cationic surfactant, cetyltrimethylammonium bromide (CTAB), obviously facilitates the electro-oxidation of estrone at carbon paste electrode (CPE) from the significant peak current enhancement and the negative shift of peak potential. Additionally, chronocoulometry and electrochemical impedance spectroscopy (EIS) were also used for further investigation of the electrode process of estrone, indicating that low concentration of CTAB exhibits excellent enhancement effects on the electrochemical oxidation of estrone, greatly enhances the diffusion coefficient and the electron transfer rate. Based on this, an electrochemical method was proposed for the determination of estrone. The oxidation peak current is proportional to the concentration of estrone in the ranges over 9.0 × 10?8 - 8.0 × 10?6 mol/L, and a low detection limit of 4.0 × 10?8 mol/L was obtained for 180s accumulation at open circuit (S/N = 3). Finally, this proposed method was demonstrated using estrone tablets with good satisfaction.