• Title/Summary/Keyword: Polarography

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Determination of Frequency for decision of heavy metal ion concentration in Square Wave Voltammetry with FPGA SoC (FPGA SoC를 이용한 네모파 전압전류법의 주파수 변화에 따른 계측 분석)

  • Lee, Jaechoon
    • Journal of Korea Society of Digital Industry and Information Management
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    • v.14 no.4
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    • pp.101-107
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    • 2018
  • In the stripping scan square wave voltammetry (SV+SWV) polarography that is often used to analyze the concentration of heavy metals in water, we must measure the point where the faradic current that flows by the pure oxidation-reduction reaction at the electrode is greater than the capacitive current, the frequency cannot be too high. Therefore we wanted to find the frequency range that can be measured. In order to do this, we came up with a method to analyze the signal using FPGA Soc. With this method, the frequency of the square wave was increased from 10Hz to 400Hz by 10Hz, and the measuring time of the square wave was changed from 96.695% to 96.765% by 0.005% while 1600 experiments were conducted. As a result, the frequency of the square wave maintained a stable area of potential-current within 320Hz and it was possible to measure the potential-current signal when calculating the measuring time within the frequency range of 96.7155%.

Studies on the Determinations of Dissolved Oxygen in Beverages (음료중 산소분석법에 관한 연구)

  • Lee, Tal-Soo;Lee, Young-Ja;Kwon, Yong-Kwan;Park, Jae-Seok;Hwang, Jung-Yun;Lee, Ju-Yeun;Song, Jee-Won;Chung, Bo-Yong;Lee, Chul-Won
    • Korean Journal of Food Science and Technology
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    • v.34 no.3
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    • pp.361-364
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    • 2002
  • This study was performed to establish a simple and accurate method for the determination of oxygen that is a processing aid in various beverage. The quantitative determination of dissolved oxygen (DO) contents in 30 cases of samples were performed by traditional titration method and polarography. As a result of the study, the analysis of DO contents in fruit-extract beverages containing oxygen by titration method was time consuming and large sample volumes were needed. Besides, serious interferences with compounds such as hydroxylamine and nitric oxide were observed, leading to false response. Although the polarography is easily affected by $H_2S$, proteins, and various organic compounds, it is a simple and practical method that provides inexpensive and relatively rapid analysis. The polarography is best suited to the routine determination of DO in a large number of samples and it is expected that the polarography can directly be applied to the quality control of the beverages containing added oxygen. The analysis results of DO contents in various fruit-extract beverages with oxygen and without oxygen were as follows: 23.10 ppm to 32.60 ppm for various frutis extract beverages with oxygen, 0.70 pp to 2.54 ppm for mixed beverages without oxygen, 7.63 ppm to 8.28 ppm for drinking water.

Electrochemical Studies on the Heavy Lanthanide Complexes (무거운 란탄족 이온 착물의 전기화학적 연구)

  • Pak, Chong Min;Kim, Chae Kyun;Son, Byung Chan
    • Analytical Science and Technology
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    • v.5 no.3
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    • pp.249-261
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    • 1992
  • Electrochemical behavior of the heavy lanthanide complexes of alizarin red S(ARS) has been investigated by d. c. polarography, differential pulse polarography and cyclic voltammetry. The reduction mechanism at a mercury electrode of alizarin red S as a complexing ligand showed a one step of two-electron transfer and the electron process is found to be reversible. Alizarin red S forms a 3:1 adsorptive complexes with lanthanides and the complexes are reduced via one step of two-elctron. The reduction potential of complex wave($P_2$) shifted more negatively than the ligand wave($P_1$). The linear calibration curves of the decreacing $P_1$ and increasing $P_2$ is obtained when the lanthanide concentration varies from $2.0{\times}10^{-6}M$ to $6.4{\times}10^{-5}M$ under the condition of pH 9.5, 0.1M LiCl and $1{\times}10^{-3}M$ ARS.

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Analytical Techniques for Sulfur Compounds by the Combination of GC/PFPD. (GC/PFPD를 이용한 악취성 황화합물의 분석기법에서의 회수율에 대한 연구)

  • 김기현;최여진;오상인
    • Proceedings of the Korea Air Pollution Research Association Conference
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    • 2003.11a
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    • pp.283-284
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    • 2003
  • 환원황 성분들은 사람들이 일상적으로 생활하는 환경권역에서 고농도 (ppb 수준 이상)로 존재할 경우, 악취의 주요원인물질로 작용한다는 점에서 상당한 주목을 받고 있다. 국내의 경우, 환경부에서는 이미 '92년 8월 대기환경보전 법을 개정하여, 황화수소를 위시한 4개의 황화합물과 트리메틸아민, 암모니아, 아세트알데히드, 스티렌을 포함하는 총 8개 화합물을 악취물질로 지정하여 관리하고 있다. 이러한 황화합물을 분석하는데 spectrophotometry, polarography, fluorescence, coulometry, impregnated filter 방식 등이 활용되고 있다 (Blank et al., 1978). (중략)

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Reaction Conditions and Mechanism of Electrolytic Reduction of Dibenzoylmethane$^\dag$

  • Kang, Sung-Chul;Chon, Jung-Kyoon
    • Bulletin of the Korean Chemical Society
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    • v.8 no.5
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    • pp.414-418
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    • 1987
  • Electrochemical reduction of dibenzoylmethane was studied on mercury electrode by means of cyclic voltammetry, polarography and potentiostatic measurements in ethanol-water system. In acidic solutions monomeric pinacol was produced by irreversible two-electron process while monomeric and dimeric pinacol were competitively produced by the same process in neutral solution. However, in basic solution the dimeric pinacol was mostly produced through radical by irreversible one-electron transfer process. Mechanisms of the reduction of dibenzoylmethane are deduced from Tafel slope, pH dependance and reaction order with respect to the concentration of dibenzoylmethane in the solution of various pH.

New Micro Rotating Mercury Electrode for Voltammetry (전류전압법을 위한 미크로 회전수은 전극)

  • Choe, Gyu-Won
    • Journal of the Korean Chemical Society
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    • v.11 no.3
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    • pp.81-84
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    • 1967
  • A simple rotating micro mercury electrode is constructed in such a way that the mercury surface can be renewed quite easily with reasonable reproducibility. It consists of a glass capillary of about 1mm diameter connected to a mercury filled tube by means of a ground joint that allows mercury flow at a particular relative position only, and the electrical connection between the two parts is made by a platinum wire fused in the bottom of the latter. Thus the mercury surface exposed at the tip of the capillary replaces the platinum tip of the usual platinum micro electrode; however, the capillary has to be bent so that the tip directs upwards. It has been found to be a convenient electrode in the amperometric titration in strongly acidic media. Furthermore, it has been advantageously used in the alternating-current polarography because of its smaller electrical resistance than the ordinary dropping mercury electrodes. It also can be used as a stationary mercury electrode in fast scanning polarography.

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Redox Reaction Mechanisms of Thorium (IV) Complexes with Crown Ethers in Dimethylsulfoxide (디메틸술폭시드용매중에서 Thorium (IV)-Crown Ether 착물의 산화-환원 반응메카니즘)

  • Jung, Hak-Jin;Jung, Oh-Jin;Suh, Hyouck-Choon
    • Journal of the Korean Chemical Society
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    • v.31 no.3
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    • pp.250-257
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    • 1987
  • The electrical conductances for the thorium (IV) complexes with crown ethers have been measured in DMSO, and water solvents, and the oxidation-reduction reaction mechanisms, electron number and diffusion coefficients in the reversible reduction process have been examined by polarography and cyclic voltammography. The dissociation mole ratio of $Th^{4+}$ and nitrate ion are 1:1 and in aprotic solvent, and 1:4 in protic solvent like as water. The limiting molar conductances of all complexes in aprotic solvent have been found to be in the range of $92.2{\times}159$ $ohm^{-1}cm^2mol^{-1}$. In aprotic solvent, DMSO, the reduction of each complex is reversible by one electron reduction of one step, and the range of diffusion coefficients is obserbed to be $5.83\;10^{-6}{\sim}6.90{\times}10^{-6}$. The complexes which have reduction step were hydrolyzed above at 1.8volt with reference saturated calomel electrode, generating the hydrogen gas. The reaction mechanisms of thorium (IV)-crown ether complexes appear as follows. ${Th_m(IV)L_n(H_2O)_x(NO_3)_{4y}}_=^{DMSO} {\overline{{Th_m(IV)L_n(H_2O)_x(NO_3)_{4y-1}}}^+ + NO_3-$

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Electrochemical Reduction on the -S-N= Bond of N-Oxyldiethylenebenzothiazole-2-sulfenamide (N-Oxyldiethylenebenzothiazole-2-sulfenamide의 -S-N= 결합에 대한 전기화학적 환원)

  • Kim, Hae-Jin;Jung , Keun-Ho;Choi, Qw-Won;Kim, Il-Kwang;Leem, Sun-Young
    • Journal of the Korean Chemical Society
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    • v.35 no.6
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    • pp.680-688
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    • 1991
  • The electrochemical reduction of N-oxyldiethylenebenzothiazole-2-sulfenamide (ODBS; vulcanization accelerator) was investigated by direct current polarography, differential pulse polarography, cyclic voltammetry and controlled potential coulometry. The irreversible electrode reduction of ODBS proceeded E-C-E-C reaction mechanism by three electrons transfer with irreversible one wave (-1.86 volts vs. Ag/0.1 M AgN$O_3$ in AN). As the results of controlled potential electrolysis, mercaptobenzothiazole (MBT), benzothiazole disulfide (MBT dimer) and extricated sulfur were products which followed by cleavage of the sulfenamide (-S-N=) bond. Upo the basis of products analysis and polarogram interpretation witli pH variable, electrochemical reaction mechanism was suggested.

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Electrochemical Reduction Behavior of Bilirubin (Bilirubin의 전기화학적 환원거동)

  • Bae Zun Ung;Lee Heung Lark;Jung Mi Sik;Park Tae Myung
    • Journal of the Korean Chemical Society
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    • v.35 no.4
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    • pp.374-378
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    • 1991
  • The electrochemical reduction behavior of Bilirubin (BR) in phosphate buffer (pH 7.8) solution was studied by DC polarography, differential pulse polarography, cyclic voltammetry and controlled potential coulometry. In DC polarogram, two reduction waves of BR were found. The half wave potentials of two reduction waves were -1.32 and -1.51 volts vs. Ag/AaCl respectively. The current type of 1st reduction wave was diffusion-controlled and the 2$^{nd}$ reduction wave was diffusion current containing a little kinetic current. The electrochemical reduction process of BR at each reduction step was all irreversible. The prewave appeared at lower concentration than 3.4 ${\times}$ 10$^{-4}$M, this prewave was identified as adsorption prewave. And the number of electron transfered in reduction steps, n$_{app}$ was two for the 1st reduction step and one for the 2$^{nd}$ reduction step.

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Electrochemical Behaviors and Analytical Application of Copper-1,5,9,13-Tetrathiacyclohexadecane Complex in Acetonitrile (아세토니트릴 용매 중에서 Copper-1,5,9,13-Tetrathiacyclohexadecane착물의 전기화학적 거동과 그 분석적 응용)

  • Moo-Lyong Seo;Bu-Yong Lee;Myung-Ja Choi;Bae Jun Ung;Park Tae Myeong
    • Journal of the Korean Chemical Society
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    • v.36 no.3
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    • pp.412-418
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    • 1992
  • The electrochemical behaviors and analytical application of copper-1,5,9,13-tetrathiacyclohexadecane[16-ane-$S_4$] complex in acetonitrile(AN) solution have been investigated by the use of DC polarography and differential pulse polarography. Thus the formation constant of copper complex was $10^{3.51}$. Copper (Ⅱ) ion was found to form complex of 1-to-1 composition with [16-ane-$S_4$]. In addition, reduction step was irreversible and the reduction current was diffusion controlled. And the effect of concentration of the salting-out reagent and chelating agent and pH of aqueous phase on the determination of copper (Ⅱ) was investigated and diverse ion effect was discussed. By salting-out extraction technique, we can be determined until the concentration of copper (Ⅱ) of 60 ppb.

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