• 한국정밀공학회지
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• 제17권8호
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• pp.120-125
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• 2000

This paper proposes a tilt sensor made by MEMS technology. The sensor consists of an electrode glass a small mercury drop a circular channel and a cover glass. The mercury drop is used as medium of a current flow and in contact with two circular chromel electrodes used as an angular-motion resistance When this sensor inclines the mercury drop inside the circular channel moves into the bottom under the influence of gravity. A tilt angle can be measured by changed resistance as tilting this sensor, This sensor has a linear section between +50.$^{\circ}$ and -50.$^{\circ}$ with the accuracy of 2.$^{\circ}$. We are also studying about the enlargement of the linear section and the effect of the size of the mercury drop.

• 전기화학회지
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• 제7권2호
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• pp.80-82
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• 2004

The a.c. technique is employed to evaluate electrochemical characteristics of Naphthalie-1,4,5,8-tetracarboxylic acid bisanilide (NTB). The measurements were carried out in dry and pure propionitrle (PCN) and acetonitrile(CAN) at the hanging mercury drop electrode [HMDE). An A.C. phase sensitive detector using computer controlled lock-in amplifier was employed. Primary goal of this report, was to establish on a firm the rare behavior of the phase angle associated with a.c. polarograms of the compound. Although, not an initial goal of this study, the electron transfer rate parameters attending the electroreduction of the compound under investigation were determined. This because the results shed some light on the electrokinetics in aprotic solvent which until recently negligible data were available. Experimental Results and comparison of data obtained are reported. The good precision of the method makes it suitable for studying electrochemical data with unusual behavior at electrodes in non aqueous media.

• 한국입자에어로졸학회지
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• 제6권4호
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• pp.173-183
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• 2010

The high temperature pleated filter bags which were used during this study were made of pleated nonwoven fabric of heat and acid resistant polysulfonate fibers which can withstand the heat up to $300^{\circ}C$ and have a filtration area which is 3 to 5 times larger than the conventional round filter bags. Cartridge module packed with 3 kind of the sulfur impregnated activated-carbon based sorbents were inserted in the inner of the pleated filter bag. This type of pleated filter bag was designed to remove not only the particulate matter but also the gaseous elemental mercury. The electrostatic precipitator part can enhance the particulate removal efficiency and reduce the pressure drop of the pleated filter bag by agglomerated particles to form a more porous dust layer on the surface of the pleated bag which is increased the filter bag cleaning efficiency. In addition, the most of particles are separated from the flue gas stream through the cyclone and the electrostatic precipitator part which were installed at the lower part and main body part of the convergence particulate collector, respectively. Thus reduce particulate loading of the high temperature pleated filter bags were applied in this study to analyze the removal characteristics of particulate matter and gaseous elemental mercury.

• 분석과학
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• 제6권3호
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• pp.247-254
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• 1993

스트론튬을 비롯한 알칼리 토금속의 전기화학적 분석의 적용은 수용액상에서 DME(Drop Mercury Electrod)에 대한 환원이 어렵기 때문에 그 연구가 많지 않다. 본 연구에서는 지금까지 UV-VIS 흡광광도법에서 스트론튬의 분석에 이용되어 온 o-Cresolphthaleoxon을 가지고 이들 사이의 착물형성에 따른 전자이동을 이용하여 전기화학적 분석에 적용시켰다. 이 때 지지전해질의 선택, Accumulation Potential 등 전기화학적 분석에 영향을 미치는 실험조건 등을 조사하여 정량범위를 결정짓고, 분석시 공존 이온의 영향을 조사하였다. UV-VIS 흡광광도법의 경우 $100{\mu}g/L$로 검출감도가 좋지 못하였으나, 전기화학적 방법을 이용할 경우 $5{\sim}30{\mu}g/L$ 범위까지의 정량이 가능하였다.

• 분석과학
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• 제8권1호
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• pp.25-32
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• 1995

구리이온(II)과 티오글리콜산의 착물인 CuRS를 HMDE(Hanging Mercury Drop Electrode)에 흡착시켜 음극으로 주사하는 흡착벗김 전압전류법으로 미량의 티오글리콜산을 정량하는 방법을 고찰하였다. 지지 전해질로는 pH 6.5 인산염 완충용액과 pH 9.5 붕산염 완충용액을 사용하였고, 최적 조건은 구리이온(II) 농도 $1{\times}10^{-4}M$, 흡착 축적 전위 -0.2V, 흡착 축적 시간 60초, 그리고 주사 속도 20mV/sec이다. 이 때 티오글리콜산의 검출 한계는 $1{\times}10^{-9}M$이다. 이 조건하에서 콜드 파마액과 제모제 속에 포함된 티오글리콜산의 함량을 구하였다.

• 전기화학회지
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• 제7권1호
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• pp.9-15
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• 2004

Cyclic voltammetry and chronocoulometry have been used for characterization of catechol violet (CV) at the hanging mercury drop electrode in acetic acid-sodium acetate buffer solution. At pH 2.94 a nearly symmetric cyclic voltammetric wave due to an irreversible weak adsorption of CV on mercury was obtained at concentration of $0.53{\mu}mol\;dm ^{-3}$. Under these conditions, CV adsorbes in a monolayer. Upon increasing the concentration, the symmetry of the wave decreases; it can be attributed to a mixed diffusion adsorption process. The amount of the adsorbed catechol violet on the HMDE expressed as surface concentration as well as the surface areaf occupied by one molecule$(\sigma)$ were calculated. It was found that the values obtained for f and o utilizing cyclic voltammetric and chrono-coulometry are almost identical. A 1:1 and 1:2 Th (IV)-CV complexes are formed on addition of thorium (IV) to catechol violet. These complexes are adsorbed and reduced on the HMDE at more negative potentials than the peak potential of free CV, Using the square-wave (SW) technique, the adsorptive cathodic stripping voltammetry, ACSV, of these complexes was studied. It was found that the SW-ACSV of Th(IV)-CV can be applied to the determination of thorium at the nanomole level. Optimum conditions and the analytical method of determination were presented and discussed.

• 대한화학회지
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• 제6권1호
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• pp.14-18
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• 1962

Solution to the diffusion layer for the first order reaction at a droping mercury electrode (D.M.E.) is presented. Equations are derived for polarographic currents for the reactions at the D.M.E. A factor which is applicable to the D.M.E. is derived, when we use the equations of the polarographic currents for the reactions at a plane electrode(P.E.), and the rate constants of the backward reactions are negligibly small. Polarographic currents from a combination of diffusions and reactions are obtained at the D.M.E. with special approximation. Rate constant for the reaction of ferrous ion with hydrogen-peroxide is determined at the D.M.E.,using the data of Kolthoff and Perry. The agreement of the equation with the data of Kolthoff and Perry for the kinetic current of ferric ion in the presence of hydrogen-peroxide is good. Ratios of diffusion layer at the D.M.E. to the diffusion layer at the P.E. are discussed and show that, when the rate constants of the backward reactions for the first order reactions are larger than 1/0.05 sec-1. and drop-time about 3 sec., these ratioes are about one.

• 분석과학
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• 제5권1호
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• pp.7-15
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• 1992

게르마늄을 Phenylfluorone과 착물을 만들어 과염소산 지지전해질에서 Linear Sweep Voltammetry에 의해 정량하고, 염산용액 중에서 형성된 착물을 UV-VIS Spectrophotometry로 정량한 결과를 비교하였다. 이때 전기화학적인 방법의 경우 정량범위가 $2.5{\sim}80{\mu}g/L$이었고, 분광광도법의 경우는 $10{\sim}300{\mu}g/L$이었다.

• Journal of the Optical Society of Korea
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• 제10권4호
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• pp.174-177
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• 2006

We propose a new technique to minimize gain-transient time of wavelength-division-multiplexing (WDM) signals in erbium-doped fiber amplifiers (EDFA) in channel add/drop networks. We have dramatically reduced the gain-transient time to less than $3{\mu}sec$ by applying, for the first time to our knowledge, a disturbance observer with a proportional/integral/differential (PID) controller to the control of EDFA gain. The $3{\mu}sec$ gain-transient time is the fastest one ever reported and it is approximately less than 1.5% of $200{\mu}sec$ gain-transient time of commercially available EDFAs for WDM networks. We have demonstrated the superiority of the new technique by performing the simulation with a numerical modeling software package such as the $Optsim^{TM}$.

• 대한화학회지
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• 제38권7호
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• pp.496-501
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• 1994

Tellurium(Ⅳ)에 대한 네모파 전압전류법적 연구를 HMDE를 사용하여 염산 용액에서 수행하였다. 염산 용액중에서 Tellurium(Ⅳ)의 환원반응은 산에 의한 촉매반응의 특징을 나타내는 비가역적인 과정으로 진행됨을 알 수 있었다. 본 연구에서는 또한 네모파 전압전류법에 의한 Tellurium(Ⅳ)의 분석 조건 및 방해이온들에 대하여 검토하였다. 이 방법에 의한 Tellurium(Ⅳ)의 검출한계는 $4.2\;ppb (3.3{\tiems}10^{-8}M)$이었으며, 전극표면에서의 4.2 Tellurium(Ⅳ)의 양은 ${\Gamma}=(7.2{\pm}1.4){\times}10^{-11}\;mol\;cm^{-2}$이었다.