• 분석과학
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• 제9권3호
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• pp.235-243
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• 1996

${\alpha}$-Cyclodextrin을 사용하여 carbon paste 전극을 화학수식하였다. 화학수식전극의 특성은 P-니트로페놀과 ${\alpha}$-cyclodextrin과의 포함복합체형성을 기초로 연구하였다. 화학수식효과를 보기 위해 순환전압전류법과 시차펄스전압전류법을 사용하였다. ${\alpha}$-Cyclodextrin과 탄소분말을 2:1 의 비율로 섞은 전극에서 환원에 의한 봉우리 전류는 o-니트로페놀이나 히드로퀴논의 경우에 비해 p-니트로페놀의 경우 거의 완전히 사라졌다. 이는 p-니트로페놀과 ${\alpha}$-cyclodextrin간의 강한 포함복합체형성에 의한 것이다. 이 전극을 이용하여 p-니트로페놀 존재하에서 o-니트로페놀을 정량할 수 있었다.

• Bulletin of the Korean Chemical Society
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• 제17권11호
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• pp.995-999
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• 1996

A method for the determination of cobalt(Ⅱ) by differential pulse voltammetry using a carbon paste electrode constructed by incorporating 1-(2-pyridylazo)-2-naphthol(PAN) into a conventional carbon paste mixture composed of graphite powder and Nujol oil has been developed. Several influencing factors for the determination of cobalt(Ⅱ) were studied in detail and the optimum analytical conditions were found to be as follows: pH, 4.6; composition of electrode, 20%; temperature of deposition, 43 ℃; time of preconcentration, 15 min. Regeneration of the electrode surface for the continuous uses of the electrode was achieved by exposing the carbon paste electrode to an acidic solution. Response of the electrode was reproducible for the uses of five times and the relative standard deviations were 6.7 and 4.6% for 2.0×10-5 M and 4.0×10-6 M cobalt(Ⅱ), respectively. The calibration curve for cobalt(Ⅱ) obtained by differential pulse voltammetry was divided into two linear ranges of 1.7× 10-6-1.3×10-4 M and 2.0×10-7-8.0×10-7 M. The detection limit was estimated to be 1.3×10-7 M. The effects of coexisting ions were also investigated to test the applicability of the proposed method to the determination of cobalt(Ⅱ) in real samples.

• 폴리머
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• 제33권5호
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• pp.397-406
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• 2009

유기 박막 트랜지스터 (OTFTs)의 소스-드레인 전극을 스크린 인쇄를 통해 제작하였고, 전극용 페이스트로써 전도성 카본블랙 페이스트를 사용하였다. 전도성 카본블랙 페이스트를 제조하기 위해 서로 다른 분자량 및 고분자 사슬 구조를 갖는 2종류의 분산제(DB-2150, DB-9077)를 사용하여 분산제 함량(SOF; solid on powder, 10-40%)에 따른 카본블랙 밀베이스의 분산 특성을 검토한 결과, 분산제 함량이 증가함에 따라 분산 특성이 더 우수해 짐을 알 수 있었다. 전도성 카본블랙 페이스트를 제조하여 레올로지 측정을 통해 카본블랙의 분산상태 및 응집구조에 대해 검토한 결과, 분산제로 DB-2150을 사용한 페이스트들은 분산제 함량이 증가함에 따라 페이스트의 분산 특성이 향상되어 저장 탄성률(G')이 감소하였지만, DB-9077을 사용한 페이스트들은 카본블랙 사이의 상호작용에 의해 망목구조가 존재하였고, 분산제 함량이 증가함에 따라 카본블랙과 분산제간 또는 분산제간의 상호작용에 의해 페이스트의 저장 탄성률(G')은 더욱 증가하였다. 이러한 응집구조는 페이스트의 내부 저항력 (tacky)을 발생시켜 DB-9077을 사용한 페이스트들은 분산제 함량이 증가함에 따라 스크린 인쇄 적성이 좋지 못하였다. 하지만, 스크린 인쇄된 OTFTs용 소스-드레인 전극의 전기적 특성은 카본블랙 사이에 형성된 망목구조에 의해 카본블랙의 도전 경로(conduction Path)가 형성됨에 따라 DB-2150을 사용한 페이스트들의 OTFTs에 비해 더 우수하였다. 그러나, 2종류의 분산제를 사용한 페이스트 모두, 분산제의 함량이 증가함에 따라 카본블랙 표면을 감싸는 분산제 함량 또한 증가하게 되어 이로 인해 카본블랙간의 도전 경로 형성은 어렵게 되고 전극의 특성은 점점 열화되었다.

• Bulletin of the Korean Chemical Society
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• 제31권6호
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• pp.1583-1588
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• 2010

A single step fabrication process of carbon nanotube/Prussian Blue (CNT/PB) paste electrodes based on screen printing technology has been studied as an amperometric sensor for the determination of hydrogen peroxide and free chlorine. Compared to the classical carbon paste (CP) electrode, the CNT paste electrode greatly enhanced the response in the presence of hydrogen peroxide due to the electrocatalytic activity of the CNT. Based on the CNT/binder paste, PB was also incorporated into a network of CNT paste and characterized. The best electroanalytical properties of PB-mixed sensors to hydrogen peroxide were obtained with PB ratio of 10 wt % composition, which showed fast response time ($t_{90}{\leq}5$ s; 0.2 - 0.3 mM), low detection limit of 1.0 ${\mu}M$, good linear response in the range from $5.0{\times}10^{-5}$ - $1.0{\times}10^{-3}$ mol $L^{-1}$ ($r^2$ = 0.9998), and high sensitivity of -8.21 ${\mu}AmM^{-1}$. In order to confirm the enhanced electrochemical properties of CNT/PB electrode, the sensor was further applied for the determination of chlorine in water, which exhibited a linear response behavior in the range of 50 - 2000 ppb for chlorine with a slope of 1.10 ${\mu}Appm^{-1}$ ($r^2$ = 9971).

• 전기화학회지
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• 제7권1호
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• pp.38-43
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• 2004

전기화학적으로 이온을 흡착시켜 제거시키는 capacitive deionization(CDI) 공정용 전극으로 탄소에어로젤에 실리카젤이 첨가된 다공성 탄소에어로젤 복합전극을 사유하여 1,000ppm NaCl수용액에서 10회와 100회 동안 싸이클을 변화시켜 탈염과 재생 특성에 대한 충전과 방전 시 시간에 따른 전류변화, 싸이클에 대한 전하량 변화, 그리고 CDI효율을 조사하였다. Paste rolling법으로 제조된 탄소에어로젤 복합전극은 CDI반응진행에 대한 전극 활물질의 탈락이 없이 전극의 성형성이 크게 향상되었고, 전극시트 제조시간을 $50\%$ 이상 단축시킬 수 있었다. 10분동안 충전과 방전으로 10회 싸이클까지의 전하량 결과를 살펴보면, $50wt.\%$의 실리카젤이 첨가된 C복합전극의 평균 충전 전하량이 실리카젤이 첨가되지 않은 A전극에 비해 $3\%$ 증가하였으며, 평균 방전 전하량은 $7\%$증가하였다. 5분동안 충전과 방전으로 100회 싸이클까지 평균 충전 전하량을 보면 $25w1.\%$와 $50wt.\%$의 실리카젤이 첨가된 B복합전극과 C복합전극은 A전극에 비해 각각 $6\%,\;14\%$증가하였으며, 또한 평균 방전 전하량도 각각 $9\%,\;21\%$증가하여 복합전극의 전하량 특성이 매우 우수하였다. 100회 싸이클까지의 CDI효율은 싸이클이 진행되면서 $70\%$ 이상으로 안정하게 유지하였고, 100회 싸이클에서는 B 복합전극이 $72.3\%$, C 복합전극이 $74.0\%$로 A 전극$(63.1\%)$보다 $10\%$이상 우수한 CDI 효율을 나타내었다.

• Bulletin of the Korean Chemical Society
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• 제25권10호
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• pp.1499-1502
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• 2004

An amperometric biosensor based on carbon paste electrodes (CPEs) for the determination of urea was constructed by enzyme (urease/GL-DH)-modified method. Urea was hydrolyzed to ${NH_4}^+$ by catalyzing urease onto the enzyme-modified electrode surface in sample solution. In the presence of ${\alpha}$-ketoglutarate and reduced nicotinamide adenine dinucleotide(NADH), a liberated ${NH_4}^+$ produce to L-glutamate and $NAD^+$ by Lglutamate dehydrogenase (GL-DH). After the chemical reaction was proceeded, the electrochemical reaction was occurred that an excess of the NADH was oxidized to $NAD^+$. The oxidation current of NADH was monitored at +1.10 volt vs. Ag/AgCl. An optimum conditions of biosensor were investigated: The optimum pH range for catalyzed hydrolysis reaction of urea was pH 7.0-7.4. The linear response range and detection limit were $2.0\;{\times}\;10^{-5}{\sim}2.0\;{\times}\;10^{-4}M\;and\;5.0\;{\times}\;10^{-6}M$, respectively. Another physiological species did not interfere, except L-ascorbic acid.

• 한국응용과학기술학회지
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• 제29권2호
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• pp.302-310
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• 2012

Bio assay of mercury and cadmium ions were searched using voltammetric analysis using DNA doped carbon nanotube paste electrodes (DCP). The square-wave stripping voltammetryic optimized results indicated working ranges of 1-10.0 $ngL^{-1}$ and 20-100 $ugL^{-1}$, Hg(II) Cd(II) within an accumulation time of 120 seconds, in 0.1-M phosphate buffer solutions of pH 6.3. The relative standard deviations of 5 $ngL^{-1}$ Hg(II) and Cd(II) that observed were 0.14 and 0.22% (n=12), respectively, using optimum conditions. The low detection limit (S/N) was pegged at 0.1 $ngL^{-1}$ ($4.9{\times}10^{-11}M$) Hg(II) and 0.2 $ngL^{-1}$ ($1.77{\times}10^{-10}M$) Cd(II). The developed methods can be applied to assays in biological fish kidneys and water samples.

• Bulletin of the Korean Chemical Society
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• 제31권10호
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• pp.2913-2917
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• 2010

When rubber dissolved in toluene was used as a binding material of graphite powder, the mechanical robustness of the carbon paste was guaranteed by the fast volatility of the solvent immediately after electrode construction. This characteristic of the rubber solution met qualifications for practical use of carbon paste electrodes and enabled the design of a new enzyme electrode bound with EPDM. In order to confirm whether the electrode shows quantitative electrochemical behaviors or not, its kinetic parameters, e. g. the symmetry factor (0.2), the exchange current density ($3.66\;{\mu}A/cm^2$), the capacity of the double layer ($2.0{\times}10^{-5}\;F$), the Michaelis constant ($4.39{\times}10^{-3}\;M$), the diffusion coefficient of substrate ($2.58{\times}10^{-12}\;cm^2/sec$), the time constant (0.018 sec) and other factors were investigated.

• Toxicological Research
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• 제24권1호
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• pp.23-28
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• 2008

Voltammetric analysis of mercury ions was developed using paste electrodes (PEs) with DNA and carbon nanotube mixed electrodes. The optimized analytical results of the cyclic voltammetry (CV) of the $1{\sim}14ng\;L^{-1}Hg(II)$ concentration and the square wave (SW) stripping voltammetry of the $1{\sim}12ng\;L^{-1}Hg(II)$ working range within an accumulation time of 400 seconds were obtained in 0.1 M $NH_4H_2PO_4$ electrolyte solutions of pH 4.0. For the relative standard deviations of the $1ng\;L^{-1}Hg(II)$, which were observed at 0.078% (n = 15) at the optimum conditions, the low detection limit (S/N) was pegged at $0.2ng\;L^{-1}(7.37{\times}10^{-13}M)$ for Hg(II). The results can be applied to assays in biological fish kidneys and wastewater samples.

• Toxicological Research
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• 제30권4호
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• pp.311-316
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• 2014

For the detection of trace copper to be used in medical diagnosis, a sensitive handmade carbon nanotube paste electrode (PE) was developed using voltammetry. Analytical optimized conditions were found at 0.05 V anodic peak current. In the same conditions, various common electrodes were compared using stripping voltammetry, and the PE was found to be more sharply sensitive than other common electrodes. At optimum conditions, the working ranges of $3{\sim}19{\mu}gL^{-1}$ were obtained. The relative standard deviation of $70.0{\mu}gL^{-1}$ was determined to be 0.117% (n = 15), and the detection limit (S/N) was found to be $0.6{\mu}gL^{-1}$ ($9.4{\times}10^{-9}M$). The results were applied in detecting copper traces in the kidney and the brain cells of fish.