• Applied Biological Chemistry
• /
• v.1
• /
• pp.26-33
• /
• 1960

Organic mercurial fungicides, for seed treatments and dust formulations, has been increasingly used by farmers. Evaluation of the purity of organic mercurial fungicides has been performed by precipitation method at this laboratory. There are several methods for the an alyses of organic mercuric formulation, among which are (1) Precipitation met hod, (2) Volatilization method, (3) Volumetric method, and (4) Dithizon method. These methods, however, show some deffects in specificity (differentiation of organic form) and quantitativity. Polarography applied for the estimation of phenyl mercuric acetate was found to be simple, rapid and accurate. Tile fundamental method of polarography arid accuracy of analysis are discussed statistically and a satisfactory results was obtained.

• Analytical Science and Technology
• /
• v.5 no.1
• /
• pp.17-24
• /
• 1992

Germanium(IV) was determinated in perchloric acid supporting electrolyte solution containing catechol derivates 3.4-dihydroxy benzoic acid, 3.4-dihydroxy benzaldehyde, adrenaline by hanging mercury electrode(HMDE) of anodic stripping polarography. And then to apply this experimental method for determination of germanium(IV) in natural samples. Germanium(IV) was determinated $300{\mu}g/L$ in ginseng and $210{\mu}g/L$ in mineral water.

• Archives of Pharmacal Research
• /
• v.23 no.3
• /
• pp.197-201
• /
• 2000

In an aqueous piperacillin sodium solution, a well-defined single wave or single peak was observed by direct current(DC) polarography or differential pulse polarography(DPP). The peak potential change per pH unit was -54 mV in the phosphate buffer at $18^{\circ}C$, which indicated that protons were involved in the electrochemical reduction of the 2,3-dioxopiperazine moiety of piperacillin sodium with a $H^{+}e^{-}$ ratio of one. Using a phosphate buffer of pH 4.3, the $1.0{times}10^{-7}$ M piperacillin sodium single peak could be determined by DPP with relative standard deviation of 1.6 %(n=3). Piperacillin sodium could be analyzed with-out interference from penicillin G-potassium, which enabled the employment of DPP as a fast and simple technique for monitoring the synthetic process of the antibiotic.

• Journal of Korea Society of Digital Industry and Information Management
• /
• v.5 no.4
• /
• pp.11-17
• /
• 2009

Polarography is a subclass of voltammetry where the working electrode is a dropping mercury electrode. More, I developed the experiment for raising up mercury electrode. In Voltammetry, information about an analyte is obtained by measuring the current as the potential is varied at oxidation-reduction reaction. A plot of current vs. potential in a polarography experiment shows the current oscillations correspoding to the drops of Hg falling from the capillary. The drops growth causes capacitive and faradic current. These changing current effects combined with experiments where the potential is continuously changed can result in noisy traces. The raising up type improved upon the method of dropping in hardware. In reduction of the noise, moving average smoothing method have been used. But the other procedure is introduced based on Fourier transformation. So FFT and IFFT engine was implemented and installed in my experiment. However, after experimentation, peak height as the measuring parameter gave a good linear relationship to concentration. The resolution of potential peaks of various kinds, using Zn and Cu as the example, was improved using the smoothing method.

• Journal of the Korean Chemical Society
• /
• v.10 no.4
• /
• pp.175-180
• /
• 1966

The electrode reduction velocity constants of Calcium, Nickel and Manganese (Zinc) ions in various supporting electrolyte solutions and temperatures were measured by polarography. The rate constants of those ions calculated by Delahay's graphimetric method and Koutecky's method were matched in 50% of experimental error. This error would be accountable because of the application of thier approximate method. But there are magnificent differences between those values and Randles and Sentioomerton's. We, also, have attempted to deduce the simplified relation between velocity constant and electrocappilary characteristics, computing the velocity constant simply and rapidly, on which Kambara, lshii and Imai, Adachi had studied and established thier related equations using parameter x, y and z, for some limited range of x. And we have extended the equation to the wider range of y value than they did for the above mentioned ions.

• Journal of Environmental Health Sciences
• /
• v.12 no.2
• /
• pp.11-15
• /
• 1986

Hydroxlamine effect on the determination of dissolved oxygen by the azide-modified Winkder method and polarography has been studied. It was found that hydroxylamine interference on the dissolved oxygen by the azide-modified Winklet method can be eliminated completely by using permanganate. An inexpensive and convenient polarograph device was constructed. Dissolved oxygen in an air-saturated 0.1 F KCl solution undergoes, independent of hydroxylamine concentrations a two-step irreversible reduction at the dropping electrode the $H_2O_2$ produced in the first step is reduced to $H_2$O in the second. Two waves of equal size result, the first with a half-wave potential (E1/2) at about -0.13 V and the second at about -0.91 V (vs. SCE).

• Analytical Science and Technology
• /
• v.8 no.4
• /
• pp.691-698
• /
• 1995

The complexation of platinum and palladium with synthetic polyelectrolytes was studied. The successive and overall stability constants of Pd(II) with PEI and 2PVP were obtained by potentiometric titration. Because of the slow equilibrium time, the potentiometric titrations were performed using the home-made automatic titrator in order to analyze the complexations according to the modified Bjerrum method. The complex formation constant of Pt(IV) with 2PVP, measured by differential pulse polarography, was calculated from the peak currents that were obtained in non-complexing media and in solution containing 2PVP.

• Analytical Science and Technology
• /
• v.8 no.4
• /
• pp.655-661
• /
• 1995

The electrochemical reduction of coumarin derivatives in 0.1M TEAP acetonitrile solution was investigated by the direct current, differential pulse polarography, cyclic voltammetry and controlled potential coulometry. The electrochemical reduction of 7-acetoxy-4-bromomethyl-coumarin(ABMC) was proceeded as an irreversible three steps(-0.58, -1.63 and -2.25 volts) of electrochemical transfer before chemical reaction. The solution color turned to yellow after the carboxyl group was reduced at 2nd step(-1.63 volts vs. Ag-AgCl) and the change in color was independant to the bromo group. Upon the basis of the results on the products analysis and the interpretaton of polarograms, a possible electrochemical reaction mechanism was suggested.

• Journal of the Korean Chemical Society
• /
• v.11 no.4
• /
• pp.138-142
• /
• 1967

The electrode reduction velocities of Zn, Ni and Co ions at DME in various supporting electrolytes and temperatures were measured by Randles' method. The values for Zn ions agreed with Randles' values within 20%. As mentioned in the auther's previous paper, the observed values of Ni and Co ions were considered to be reasonable. In the present work the curves log y vs. log z for the various metals in the range of 20~35$^{\circ}C$ were obtained.

• Journal of the Korean Chemical Society
• /
• v.18 no.5
• /
• pp.341-353
• /
• 1974

The electrochemical reduction of triphenylphosphine penylimide in nonaqueous media has been examined by polarography, cyclic voltammetry, controlled-potential coulometry and electron spin resonance spectroscopy. The reduction of triphenylphosphine phenylimide proceeds by a one-electron transfer to form anion radical which undergoes both protonation and a second one-electron reduction followed by cleavage of the phosphorus-nitrogen double bond. Aniline is a major product. The cleavage of a phosphorus-phenyl bond was also observed after reduction of triphenylphosphine oxide which is one of the major products of the chemical reaction which follow the primary process.