• 분석과학
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• 제8권4호
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• pp.611-615
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• 1995

The design of appropriate chemically modified electrodes should allow development of new voltammetric measurement schemes with enhanced selectivity and sensitivity. Microorganism like algae has high ability to trap toxic and heavy metal ions and different affinities for metal ions. A copper(II) ion-selective carbon paste electrode was constructed by incorporating alga Anabaena into a conventional carbon paste mixture, and then the film of 10% Nafion was coated to avoid the swelling of the electrode surface. Copper ion could be deposited at the 25% algamodified electrode for 15 min without the applied potential while stirring the solution by only immersing the electrode in a buffer (pH 4.0) cot1taining copper(II). Temperature was controlled at $35^{\circ}C$. After preconcentration was carried out the electrode was transferred to a 0.1 M potassium chloride solution and was reduced at -0.6 volt at $25^{\circ}C$. The differential pulse anodic stripping voltammetry was employed. A well-defined oxidation peak could be obtained at -0.1 volt (vs SCE). In five deposition / measurement / regeneration cycles, the responses were reproducible and relative standard deviations were 3.3% for $8.0{\times}10^{-4}M$ copper(II). Calibration curve for copper was linear over the range from $2.0{\times}10^{-4}M$ to $1.0{\times}10^{-3}M$. The detection limit was $7.5{\times}10^{-5}M$. Studies of the effect of diverse ions showed that the coexisting metal ions had little or no effect for the determination of copper. But anions such as cyanide. oxalate and EDTA seriously interfered.

• 대한화학회지
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• 제41권10호
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• pp.557-560
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• 1997

• Journal of Electrochemical Science and Technology
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• 제9권2호
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• pp.109-117
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• 2018

A novel carbon paste electrode modified with $Cu-TiO_2$ nanocomposite, 2-(ferrocenylethynyl)fluoren-9-one (2FF) and ionic liquid (IL) (2FF/$Cu-TiO_2$/IL/CPE) was fabricated and employed to study the electrocatalytic oxidation of droxidopa, using cyclic voltammetry (CV), chronoamperometry (CHA) and differential pulse voltammetry (DPV) as diagnostic techniques. It has been found that the oxidation of droxidopa at the surface of modified electrode occurs at a potential of about 295 mV less positive than that of an unmodified CPE. DPV exhibits a linear dynamic range from $5.0{\times}10^{-8}$ to $4.0{\times}10^{-4}M$ and a detection limit of 30.0 nM for droxidopa. Finally this modified electrode was used for simultaneous determination of droxidopa and tryptophan. Also the 2FF/$Cu-TiO_2$/IL/CPE shows excellent ability to determination of droxidopa and tryptophan in real samples.

• Environmental Engineering Research
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• 제22권2호
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• pp.186-192
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• 2017

The carbon paste electrode (CPE) was modified with the pristine bentonite and hybrid material (HDTMA-modified bentonite). The modified-CPEs are then employed as working electrode in an electrochemical detection of As(V) from aqueous solutions using the cyclic voltammetric measurements. Cyclic voltammograms revealed that As(V) showed reversible behavior onto the working electrode. The hybrid material-modified carbon paste electrode showed significantly enhanced electrochemical signal which was then utilized in the low level detection of As(V). Moreover, the studies were conducted at neutral pH conditions. The electrochemical studies were conducted with scan rates (20 to 200 mV/s) to deduce the mechanism of redox processes involved at the electrode surface. The anodic current was linearly increased, increasing the concentration of As(V) from 5.0 to $35.0{\mu}g/g$ using the hybrid material-modified electrode. This provided fairly a good calibration line for As(V) detection. The presence of varied concentrations of As(III) in the determination of total arsenic was studied. The influence of several cations and anions viz., Cu(II), Mn(II), Zn(II), Pb(II), Cd(II), Fe(III), $Cl^-$, $NO_3{^-}$, $PO_4{^{3-}}$, EDTA and glycine in the detection of As(V) from aqueous solution was also studied. Further, in an attempt to simulate the real matrix analysis, the tap water sample was spiked with As(V) and subjected for As(V) detection using the modified-CPE.

• Bulletin of the Korean Chemical Society
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• 제24권7호
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• pp.948-952
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• 2003

New approach for the determination of Ag(I) ion was performed by using a carbon paste electrode (CPE) containing N,N'-Diphenyl oxamide (DPO) with anodic stripping voltammetry. The CMEs have been prepared by making carbon paste mixtures containing an appropriate amount of DPO salt coated onto graphite particles to analyze trace metal ions via complexation followed by stripping voltammetry. Various experimental parameters affecting the response, such as pH, deposition time, temperature, and electrode composition, were carefully optimized. Using differential pulse anodic stripping voltammetry, the logarithmic linear response range for the Ag(I) ion was 1.0 × $10^{-7}$ - 5.0 × $10^{-9}$ M at the deposition time of 10 min, with the detection limit was 7.0 × $10^{-10}$ M. The detection limit adopted from anodic stripping differential pulse voltammetry was 7.0 × $10^{-10}$ M for silver and the relative standard deviation was ± 3.2% at a 5.0 × $10^{-8}$ M of Ag(I) ion (n = 7). The proposed electrode shows a very good selectivity for Ag(I) in a standard solution containing several metals at optimized conditions.

• 대한화학회지
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• 제38권10호
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• pp.734-740
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• 1994

Ag(I) 이온의 정량을 위해 cinchonidine으로 변성된 탄소 반죽전극(carbon paste electrode : CPE)을 제작하여 순환 전압-전류법 및 시차펄스 전압-전류법(differential pulse voltammetry:DPV)을 사용하여 정량하였다. Ag(Ⅰ)이온의 검출한계는 순환 전압-전류법으로는 $1.0 {\times}10^{-6}$ M, 시차펄스 전압-전류법에서는 $8.0{\times}10^{-9}$ M (${\pm}$0.6%)이었다. Ag(I)이온의 최적 분석조건은 pH 7, 담그는 시간은 20분, 그리고 탄소 분말에 대한 cinchonidine의 함량은 50% (w/w)였다. 방해 작용이 예상되는 다른 여러 종류의 금속 이온에 대하여 실험한 결과 Hg(II)이온을 제외한 다른 금속 이온 용액에서는 25% Ag(I) 이온 전류 크기가 감소하였다. 또한 Mn(II)이온이 존재할 때 pH 9에서 큰 방해 작용을 나타내었다.

• 전기화학회지
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• 제7권4호
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• pp.206-210
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• 2004

금속산화물 $(TiO_2,\;RuO_2,\;PbO_2,\;Ni(OH)_2)$과 Prussian blue (PB)를 각각 탄소반죽에 혼합한 후 스크린 프린팅 기법으로 6종의 탄소반죽 전극들을 제작하였다. 제작된 탄소반죽 전극들로 전자혀 시스템을 제작하여 다양한 음료수와 식품에 대한 감응을 0.1M carbonate buffer, pH 9.6완충 용액에 묽힌 후 대시간전류법의 방법으로 측정하였다 얻어진 자료를 주성분 분석법 (principal component analysis; PCA)으로 처리한 후 식음료의 맛을 평가할 수 있도록 2차원 좌표계에 표시하였으며, 그 결과 본 실험에서 제작한 시스템 및 분석법은 다양한 식음료의 종류를 뚜렷이 구분해 낼 수 있음을 확인하였다.

• Bulletin of the Korean Chemical Society
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• 제30권3호
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• pp.582-588
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• 2009

Direct electron transfer of hemoglobin (Hb) in the chitosan (CTS) and $TiO_2$ nanoparticles (nano-$TiO_2$) composite films was achieved by using a room temperature ionic liquid of 1-butyl-3-methylimidazolium hexafluorophosphate ($BMIMPF_6$) modified carbon paste electrode (CILE) as the basal electrode. UV-Vis and FT-IR spectroscopy indicated that Hb in the film retained the native structure. Electrochemical investigation indicated that a pair of well-defined quasi-reversible redox peaks of Hb heme Fe(III)/Fe(II) was obtained with the formal potential located at -0.340 V (νs. SCE) in pH 7.0 phosphate buffer solution (PBS). The electrochemical parameters such as the electron transfer coefficient (α), the electron transfer number (n) and the standard electron transfer rate constant ($k_s$) were got as 0.422, 0.93 and 0.117 $s^{-1}$, respectively. The fabricated CTS/nano-$TiO_2$/Hb/CILE showed good electrocatalytic ability to the reduction of trichloroacetic acid (TCA) and hydrogen peroxide ($H_2O_2$), which exhibited a potential application in fabricating a new kind of third generation biosensor.

• 전기화학회지
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• 제4권3호
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• pp.109-112
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• 2001

활성화된 탄소반죽전극 표면을 N피드록시숙신이미드(NHS)층으로 수식한 후, 이 전극을 이용하여 square-wave voltammetry방법으로 과량의 아스코빅산 존재 하에서 도파민을 측정하였다. 수식된 전극의 특성은 도파민과 아스코빅산 혼합용액에서 순한전압전류법을 이용하여 조사하였다. 도파민과 아스코빅산의 산화 피크의 분리는 시료용액의 pH에 큰 영향을 받았으며, pH 4.0에서 최대의 피크분리(172mv)를 보였다. 따라서 도파민을 정량하기 위한 square-wave voltammeoy는 140 mM NaCl을 포함하는 100 mM phosphate buffered saline (PBS)의 pH 4.0 조건에서 수행하였다. NHS로 수식된 전극은 0.2mM 아스코빅 산의 존재 하에서 도파민의 농도 $5.0\times10^{-2}$까지 검출한계와 감응기울기 $6.1{\mu}A/{\mu}M$의 감도를 나타내었다. 반면 수식되지 않은 전극은 $1.0{\mu}M$의 검출한계와 $0.93{\mu}A/{\mu}M$ 기울기를 나타내어 표면에 수식된 N-히드록시숙신이미드가 도파민의 감응을 촉진함을 보여주었다.

• Bulletin of the Korean Chemical Society
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• 제17권4호
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• pp.342-347
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• 1996

Voltammetric determination of phenol derivatives, such as phenol, o-, m-, and p-cresols was studied with a β-Cyclodextrin (β-CD) modified-carbon paste electrode composing of the graphite powder and Nujol oil. Phenol derivatives were chemically deposited via the complex formation with β-CD by immersing the CME into a sample solution. The resulting surfaces were characterized with cyclic and differential pulse voltammetry. Treating the CME with 1 M nitric acid for five sec after a measurement could regenerate the electrode surface. Linear sweep and differential pulse voltammograms were recorded for the above system to optimize the experimental parameters for analysing the phenol derivatives. In this case, the detection limit for phenols was 5.0×10-7M for 25 min of the deposition time with differential pulse voltammetry. The relative standard deviation was ±5.2% of 3.0×10-6M (four repetitions). The interference effect of the following organic compounds was also investigated; Bezoic acid, hippuric acid, o-, m-, and p-methylhippuric acid. Adding the organic compounds into the sample solution reduces the peak current of the phenols to about 25%.