• 대한화학회지
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• 제49권4호
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• pp.355-362
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• 2005

• 한국환경보건학회:학술대회논문집
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• 한국환경보건학회 2003년도 Challenges and Achievements in Environmental Health
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• pp.204-207
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• 2003

Determination of Lead(II) using nafion-DTPA (diethylene triamine pentaacetic acid)-glycerol-modified glassy carbon electrodes is described. Lead(II) is accumulated at the electrode by complexing with the DTPA, reduced, and detected by differential pulse voltammetry. In this study, we demonstrate that at a preconcentration time of 5min the nafion-DTPA-glycerol-modified glassy carbon electrode has a linear calibration curve at range 1.0${\times}$10$\^$-9/M∼1.0${\times}$10$\^$-7/M in pH 4.0 buffer solution. The detection limit(3$\sigma$) is as low as 5.0${\times}$10$\^$-6/M. This method is applied to the determination of lead(II) in certified reference material and the result agrees satisfactorily with the certified value.

• 한국결정성장학회지
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• 제6권4호
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• pp.648-662
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• 1996

임피던스 스펙트럼을 이용하여 황산 용액에서 glassy carbon과 인조흑연(PVDF 합성 흑연)의 전극표면에 cyclic 분극을 부하 하였을 경우 전극표면에서 나타나는 표면반응에 대하여 조사하여 . 두 재료 표면에서 산소의 산화 혹은 환원과 관련되거나 또는 탄소재료 표면에 화학흡착된 표면작용기(surface functional group)의 변화와 관련되는 것으로 생각되는 산화환원 피크가 potentio-dynamic곡선에서 나타났다. 이러한 전극 표면에서의 표면작용기의 산화환원은 glassy carbon과 PVDF합성 흑연의 임피던스 스펙트럼에도 커다란 영향을 미치는 것으로 나타났다. 또 glassy carbon과 PVDF합성 흑연에서의 임피던스 파라미터는 분극부하에의해 현저한 변화가 나타났다.가 나타났다.

• Bulletin of the Korean Chemical Society
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• 제15권7호
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• pp.563-567
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• 1994

The electroreduction of dioxygen at glassy carbon electrodes with irreversible self-assembly of N-hexadecyl-N'-methyl viologen $(C_{16}VC_1)$ proceeds at potentials more positive than those where the reduction occurs at bare electrodes. The electrocatalyzed reduction takes place at potentials well ahead of those where the catalyst is reduced in the absence of dioxygen and the limiting currents observed at rotating disk electrodes did not deviate from the thoretical Levich line up to 6400 rpm, indicating that the electrocatalysis is extremely rapid. The rate constant for the heterogeneous reaction between $C_{16}V^+C_1$ immobilized on the electrode surface and $O_2$ in solution was estimated to be ca. $10^8\;M^{-1}s^{-1}$. The half-wave potential of dioxygen reduction was independent of solution pH.

• Journal of Electrochemical Science and Technology
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• 제7권4호
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• pp.286-292
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• 2016

Chemically amplified electrochemical detection, redox-active probe being amplified its electrochemical anodic current by a sacrificial electron donor presenting in solution, holds great potential for simple and quantitative bioanalytical analysis. Herein, we report the chemically amplified electrochemical analysis that drastically enhanced a detection of ferrocenemethanol (analyte) by ferrocyanide (chemical amplifier) on 4-nitrophenyl grafted glassy carbon electrodes at $60^{\circ}C$. The glassy carbon electrode grafted with a 4-nitrophenyl group using an electrochemical reduction suppressed the oxidation of ferrocyanide and thus enabled detection of ferrocenemethanol with excellent selectivity. The ferrocenemethanol was detected down to an nM range using a linear sweep voltammetry under kinetically optimized conditions. The detection limit was improved by decreasing the concentration of the ferrocyanide and increasing temperature.

• 한국환경보건학회지
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• 제26권4호
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• pp.110-114
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• 2000

Determination of mercury(II) using Nafion-EDTA-modified glassy carbon electrodes is proposed. it is based on the chemical reactivity of an immobilized modifier, Nafion-EDTA. Differential pulse voltammetry is employed, and the oxidation of complexes, at +0.43V vs. Ag/AgCl, is observed. For a 5-min preconcentration period, a linear calibration curve is obtained for mercury(II) concentrations ranging from 1.0$\times$ 10$^{-8}$ to 1.0$\times$10$^{-6}$ M. Further, when an approximate amount of copper(II) is added to the test solution, We demonstrate that at a preconcentration time of 5 min the Nafion-EDTA-modified glassy carbon electrode has a dynamic range of 2 orders of magnitude(from 10$^{-10}$ to 10$^{-8}$ M) and the detection limit is as low as 0.5$\times$ 10$^{-10}$ M(0.01 ppb). This method is applied to the determination of mercury(II) in sea water(4.0$\times$10$^{-10}$ M, 0.08ppb). The result agrees satisfactorily with the value(below 0.1 ppb) measured by using ICP/MS.

• 대한화학회지
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• 제37권8호
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• pp.702-710
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• 1993

이핵성 네자리 schiff base Co(II), Ni(II), Cu(II) alc Fe(II) 착물들을 촉매로 사용하여 몰리브데늄 전극과 유리질 탄소 전극에서 SOCl2의 전기화학적 환원반응을 조사하였다. 이들 전이금속(II) 착물들은 먼저 전극 표면에 흡착된 후 촉매로 작용하였으며, 각각의 전이금속(II) 착물들의 촉매 화합물은 SOCl$_2$ 를 환원시킬 수 있는 최적 조건의 농도를 나타냈다. SOCl$_2$의 환원반응에 대한 촉매 효과는 몰리브데늄 전극에서보다 유리질 탄소전극에서 더 크게 나타났고, 환원 전류는 최고 120% 정도 증가하였다. 주사속도 증가에 따른 SOCl$_2$의 환원 전류는 증가하였고 환원 전위는 음전위쪽으로 이동되었으며, SOCl$_2$의 환원과정은 확산지배적인 반응으로 진행되었다.

• 대한화학회지
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• 제41권1호
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• pp.1-11
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• 1997

0.5 M $K_2SO_4$ 용액에서 여러 가지 세 탄소전극(glassy carbon, 인조흑연, graphite foil)에 대하여 양극분극에 따른 전극표면반응에 대한 연구를 임피던스 스펙트로스코피를 통하여 실시했다. Graphite foil 전극의 경우 이중츨 capacotance는 다른 두 전극재료에 비하여 높게 나타났으며, 양극분극시 glassy carbon과 인조 흑연(PVDF 혼합 graphite)은 전극계면에서 흡착현상에 의한 capacitance C의 영향이 현저하게 나타남을 알 수 있었다. 3종류 전극재료의 전기화학적 거동은 전극표면 조직의 차이에 의해 glassy carbon의 경우는 분극시 파라데이 임피던스의 영향을 받으며, graphite foil의 경우는 field transport의 지배를 받아 전압의 변화에 의한 임피던스 파라미터의 변화는 거의 나타나지 않았다.

• 분석과학
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• 제8권4호
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• pp.617-622
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• 1995

Electrocatalytic reduction of dioxygen has been investigated by cyclic voltammetry at glassy carbon electrode modified with new Co(II)-Schiff base complexes in aqueous solutions of various pH. The reduction potentials of dioxygen at chemically adsorbed electrodes show the dependence of pH between pH 4 and 14. The catalytic effect is large and the reaction occurs via two or four electron transfer in various pH solution.

• Bulletin of the Korean Chemical Society
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• 제16권5호
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• pp.392-397
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• 1995

o-Phenylenediamine (o-PD) was electropolymerized on glassy carbon electrodes under a potential cycling condition. The resulting polymer films mediated electrons for the reduction of molecular oxygen at pH=1.0. It was found from the RDE, RRDE, and cyclic voltammetry experiments that the modified electrodes reduce oxygen to hydrogen peroxide at about 300 mV lower potential than the bare glassy carbon electrode. The polymer film consisted of more than two components. Among those, only one component was active in oxygen reduction, which was formed mainly in the earlier stage of the electropolymerization. 2,3-Diaminophenazine, a cyclic dimer of o-PD, was also active in the oxygen reduction reaction, from which it was suggested that the active polymeric component has a structural unit similar to the cyclic dimer. Finally, the electropolymerization mechanism for the formation of the active and inactive components has been proposed.