• Nuclear Engineering and Technology
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• 제32권4호
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• pp.309-315
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• 2000

The changes of Np oxidation state in nitric acid and the effect of nitrous acid on the oxidation state were analyzed by spectrophotometry, solvent extraction, and electrochemical methods. An enhancement of Np extraction to 30 vol.% TBP was carried out through adjustment of Np oxidation state by using a glassy carbon fiber column electrode system. The information of electrolytic behavior of nitric acid was important because the nitrous acid affecting the Np redox reaction was generated during the electrolytic adjustment of the Np oxidation state. The Np solution used in this work consisted of Np（V) and Np（Ⅵ）without （IV）. The composition of Np（V) in the range of 0.5M -5.5 M nitric acid was 32% ~ 19%. The electrolytic oxidation of Np（V) to Np（Ⅵ）in the solution enhanced Np extraction efficiency about five times higher than the case without the electrolytic oxidation. It was confirmed that the nitrous acid of less than about 10-5 M acted as a catalyst to accelerate the chemical oxidation reaction of Np（V) to Np（Ⅵ）.

• Bulletin of the Korean Chemical Society
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• 제24권9호
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• pp.1329-1332
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• 2003

Stepwise dechlorination of 1,2,4-trichlorobenzene was observed at a glassy carbon electrode in dimethylformamide containing 0.1 M tetraethylammonium perchlorate. Especially, dechlorination to dichlorobenzene and further to monochlorobenzene or benzene was successfully demonstrated with a porous reticulated vitreous carbon electrode. Electrochemical dechlorination of polychlorobenzenes employing a flow cell with a reticulated vitreous carbon working electrode is also described. Preliminary experiments with a flow cell showed that dechlorination of trichlorobenzene to dichlorobenzene was partially completed while dechlorination to benzene or monochlorobenzene was not successful, suggesting that a flow rate and electrolysis time should be further optimized for the complete electrolysis.

• 한국환경보건학회:학술대회논문집
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• 한국환경보건학회 2003년도 Challenges and Achievements in Environmental Health
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• pp.177-180
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• 2003

A glassy carbon electrode(GCE) modified with nafion-DTPA-glycerol was used for the highly selective and sensitive determination of a trace amount of Cu$\^$2+/. Various experimental parameters, which influenced the response of nafion-DTPA-glycerol modified electrode to Cu$\^$2+/, were optimized. The copper(II) was accumulated on the electrode surface by the formation of the complex in an open circuit, and the resulting surface was characterized by medium exchange, electrochemical reduction, and differential pulse voltammetry, A linear range was obtained in the concentration range 1.0${\times}$10$\^$-8/M∼1.0${\times}$10$\^$-6/M Cu(II) with 7 min preconcentration. Further, when an approximate amount of lead(II) is added to the test solution, nafion-DTPA-glycerol modified glassy carbon electrode has a dynamic range of 2 orders magnitude(1.0${\times}$10$\^$-9/M∼1.0${\times}$10$\^$-7/M). The detection limit(3 $\sigma$) was as low as 5.0${\times}$10$\^$-6/M(0.032ppb). The interferences from other metal ions could be reduced by adding KCN into the sample solutions. This method was applied to the determination of coppe,(II) in certified reference material(3.23${\times}$10$\^$-7/M, 21ppb), sea water(9.50${\times}$10/sup-7/M, 60ppb). The result agrees satisfactorily with the value measured by Korea Research Institute of Standard and Science.

• 공업화학
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• 제9권4호
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• pp.475-480
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• 1998

본 연구에서는 고밀집 glassy carbon (GC) 섬유 다발체 전극 전해계를 사용하여 우라늄 (VI)를 함유한 유기상과 질산 수용상의 혼합상에서 전해 역추출시 우라늄 (VI) 환원 전해특성 연구가 수행되었고, 이에 관한 전해 역추출 모델을 제시하였다 우라늄 (VI) 전해환원 반응은 혼합상 내의 수용상에서 보다 혼합상 내의 유기상에서 빨리 일어났다. 유기상의 유속이 증가하는 경우 역추출 과정에서 유기상 내 우라늄 이온의 확산 저항 증가에 의해서 수용상으로의 역추출은 증가하다 일정하게 되었으며, 수용상 유속 변화는 총 우라늄 (VI) 환원전류에는 영향을 주지 않았다. 전해반응이 없는 경우보다 전해 반응이 동반되는 경우 우라늄 역추출이 보다 효과적으로 이루어 짐을 알 수 있었다.

• 한국환경보건학회지
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• 제28권5호
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• pp.53-58
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• 2002

A method for the determination of lead(II) ion using a nafion-EDTA(ethylene diamine tetraacetic acid)-glycerol modified glassy carbon electrode was proposed. Lead(II) ion is accumulated at the electrode by complexation and electrostatic attraction with nafion-EDTA-glycerol and detected at -0.560$\pm$0.015V (vs. Ag/AgCl) by differential pulse voltammetry. For the determination of lead(II) ion, a standard calibration curve if obtained from 10$^{-9}$ M lead(II) ion to 10$^{-7}$ M, and the detection limit(3s) is as low as 5.0$\times$10$^{-10}$ M.

• 생약학회지
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• 제17권1호
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• pp.1-6
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• 1986

A cardiac principle of Aconiti tuber, higenamine was analyzed with a differential pluse voltammetry employing a glassy carbon electrode. The peak potentials for the oxidation of higenamine were varied depending on the pH of the media. Higenamine at the concentration of $5.4{\times}10^{-7}M$ (0.146ppm) was easily determined using a pH 7.0 phosphate buffer. The amounts of higenamine in the crude Aconiti tuber and tablets containing A. tuber were determined by a standard addition method after extracting with methanol, partitioning with a mixture of $H_2O$ and $CHCl_3$, and freeze-drying the aqueous layer.

• 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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• 제17권3호
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• pp.223-227
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• 1996

Catalytic effects of transition metal (Co2+, Ni2+) complexes of N,N-bis(salicylaldehyde)-o-phenylenediimine (SOPD), N,N-bis(salicylaldehyde)-m-phenylenediimine (SMPD), and N,N-bis(salicylaldehyde)-p-phenylenediimine (SPPD), on the reduction of thionyl chloride at glassy carbon electrode, are evaluated by determining the kinetic parameters with cyclic voltammetric technique. The charge transfer process for the reduction of thionyl chloride is strongly affected by the concentration of the catalysts. Some quadridentate Schiff base-M(Ⅱ) complexes show sizable catalytic activities for the reduction of thionyl chloride. Catalytic effects of [M(Ⅱ)(SOPD)] complexes are slightly larger compared to [M(Ⅱ)2(SMPD)2] and [M(Ⅱ)2(SPPD)2] complexes. On those electrodes deposited with the catalysts, the observed exchange rate constants (ko) are in the range of 0.89-2.28 × 10-7 cm/s, while it is 1.24 × 10-7 cm/s on the bare glassy carbon electrode.

• Bulletin of the Korean Chemical Society
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• 제30권6호
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• pp.1341-1348
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• 2009

Electrocatalytic oxidation of two anti-inflammatory drugs (Mefenamic acid and Indomethacin) was investigated on a cobalt hydroxide modified glassy carbon (CHM-GC) electrode in alkaline solution. The process of oxidation and its kinetics were established by using cyclic voltammetry and chronoamperometry techniques as well as steady state polarization measurements. Voltammetric studies indicated that in the presence of under study drugs, the anodic peak current of low-valence cobalt species increased, followed by a decrease in the corresponding cathodic current. This result indicates that the drugs were oxidized via cobalt hydroxide species immobilized on the electrode surface via an E$\acute{C}$ mechanism. A mechanism based on the electrochemical generation of Co (IV) active sites and their subsequent consumption by the drugs in question was also investigated. The constants rate of the catalytic oxidation of the drugs and the electron-transfer coefficients reported.

• 대한화학회지
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• 제55권1호
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• pp.50-56
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• 2011

(2, 4-difluoro-phenyl)-(2-phenyl-1H-quinolin-4-ylidene)-amine의 전기화학적 환원에 대하여 실온에서 순환전압전류 기술을 사용한 유리탄소전극(GCE)에서 N,N-dimethylformamide 하에서 0.1 M tetrabutylammoniumbromide로 조사하였다. 이민의 환원은 각각 한 전자를 포함하면서 2단계의 성공적인 단계로 일어난다. 이 매개물에서 처음 피크는 유리탄소전극 표면에서 약 -0.793 V(vs Ag/$Ag^+$)로 관측되었다. 그리고 그것은 더욱 안정하고 2번째 피크와 비교하여 명확하게 설명된다. 연구된 용매 매개물에서 이민의 확산계수($D_0$)는 수정된 Randles-Sevcik 식을 이용해 계산되었다. 반응 종들의 전자 이동 계수($\alpha$) 또한 계산되었다.