• Analytical Science and Technology
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• v.5 no.4
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• pp.417-423
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• 1992

The effects of metal ions on the arsenic(III) stripping peak were examined by the cathodic stripping voltammetry. The reduction stripping peak potential and current of arsenic(III) value were -0.79V(vs. Ag/AgCl). $0.86{\mu}A$ by using 0.1N-hydrochloric acid solution. When 10 times of Cu(II) was added to the solution, the reduction stripping peak potential of arsenic(III) was the value of -0.84V(vs. Ag/Cl), which showed a good agreement with theoretical value -0.84V(vs. Ag/Cl) by using 0.1N hydrochloric acid solution. Lead(II) and copper(II) increased the stripping peak heigh of arsenic(III), Among them, the copper(II) extremely enhanced it.

• Food Engineering Progress
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• v.21 no.2
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• pp.180-186
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• 2017

Salt, as food, is the most essential element for human survival due to its significant physiological functions. Here, we report the simultaneous detection of Pb and Cd in sea salt by square wave anodic stripping voltammetry (SWASV). Stripping voltammetric measurements were conducted using a manufactured rotating disk electrode system (MRDES). The detection limit was $3.6{\pm}0.18{\mu}gL^{-1}$ for Pb and $3.9{\pm}0.37{\mu}gL^{-1}$ Cd in NaCl solution. When the pH increased from 5.5 to 8.5, the peak currents of Pb and Cd decreased. At a pH of 8.3, the ratio of the current drop compared with that at a pH of 5.5 was 0.6 for Pb and 0.73 for Cd. The concentrations corrected by the current drop are in agreement with the concentrations obtained with ICP (inductively coupled plasma). This system demonstrates the reliable detection of heavy metals in aqueous media and, at a high $Na^+$ concentration, the successful application for the determination of Pb and Cd in sea salts.

• YAKHAK HOEJI
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• v.27 no.1
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• pp.1-10
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• 1983

Voltammetric deposition and differential pulse anodic stripping (DPASV) of Ge(IV)at a gold electrode was investigated. Germanium (IV) exhibits two stripping peaks by DPASV in sodium borate solution, the first peak at about -1.1v. vs SCE and the second one, in the range of -0.6 to -0.2v. vs SCE. Factors affecting the sensitivity and precision included the nature of working electrode, supporting electrolytes, deposition potential, deposition time, pH, pulse height, voltage scan rate. The relative standard deviation of the measurements of the peak currents, for 100ng/ml Ge(IV), was less than ${\pm}3%$. The detection limit of Ge(IV) was 0.01ng/ml. Percent recovery in the extraction procedure of Ge(IV) from matrices by benzene in c-HCl, followed by back extraction with saturated borax solution, ranged from 96 to 104%.

• Journal of the Korean Applied Science and Technology
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• v.28 no.1
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• pp.15-21
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• 2011

Threelectrodes systems were used in stripping voltammetry (SW) and cyclic voltammetry (CV) instead of the expensive platinum and Ag/AgCl reference electrodes. Moreover, the electrolyte solution was used with deep seawater, which can reduce water pollution, is more eco-friendly, and has a lower cost. The analytical optimum parameters measured via CV and SW and with working ranges were obtained from 10 to 80 ug/L using fluorine immobilized on a graphite pencil electrode (FE). Under the optimum conditions, the analytical detection limit of 6.30 ug/LAu was obtained. The results of the study can be applied to diagnostic assay for natural minerals and human finger tissue.

• Bulletin of the Korean Chemical Society
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• v.32 no.9
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• pp.3501-3504
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• 2011

• Korean Chemical Engineering Research
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• v.50 no.5
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• pp.933-937
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• 2012

In the present study, we evaluate the sensitivity and optimal stripping voltammetry (SV) conditions of copper (Cu), which is one of the main trace heavy metals inducing the environmental contamination, using carbon nanotube (CNT) electrode. In addition, the reaction mechanism of stripping reaction of Cu is investigated. The electrochemical analyses such as squarewave stripping voltammetry (SWSV) and linear scan voltammetry (LSV) are used for the evaluations. As a result of that, the best SWSV conditions like squarewave amplitude of 15 mV, frequency of 60 Hz, deposition potential of -1.0V vs. Ag/AgCl and deposition time of 200s are determined with the measured Cu sensitivity of $1.824{\mu}A/{\mu}M$. As a driving force affecting the stripping reaction of Cu, surface reaction is more dominant one than diffusion. These results are compared with other reference results and it is confirmed that our suggested CNT electrode gives rise to better Cu sensitivity result than other references.

• Analytical Science and Technology
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• v.11 no.5
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• pp.400-403
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• 1998

The germanium content of the cultivated Korean medicinal herbs in several growing district was determined by adsorption stripping voltammetry. The optimum conditions in germanium determination were as following: deposition time; 120 sec, deposition potential; -0.9 volts vs. Ag/AgCl, and frequency; 100 Hz in $5.0{\times}10^{-2}M$ perchloric acid supporting electrolyte solution containing $8.0{\times}10^{-2}M$ catechol. Calibration curve was shown a good lineality in the range of 0.4 ppb to 2.0 ppm and the detection limit was 0.08 ppb. There was a large difference in content of the cultivated hermit leaf according to growing district such as 29.7~385.7 ppm and the content of nontreated hermit leaf was higher than the processed health foodstuffs. The content of the Korean ginseng (5 years) was 83 ppm while the Korean herb of life was 214 ppm.

• Analytical Science and Technology
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• v.8 no.1
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• pp.25-32
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• 1995

Determination method of trace thioglycolate has been studied by adsorptive stripping voltammetry. Copper(II)-thioglycolate complex is adsorbed at the hanging mercury drop electrode and stripped during cathodic scan. Electrolyte was used pH 6.5 phosphate and pH 9.5 borate buffer solutions. Optimal conditions were a copper(II) concentration $1{\times}10^{-4}M$, an adsorption accumulation potential -0.2V, an adsorption accumulation time 60 sec and a scan rate 20mV/sec. A detection limit of $1{\times}10^{-9}M$ thioglycolate was obtained. The method was applied to the determination of thioglycolate in cold wave fluids and depilating creams.

• Analytical Science and Technology
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• v.6 no.1
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• pp.47-55
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• 1993

The quantitative determination of trace cyanide ion in the presence of sulfide ion has been studied by addition of cupric ion using differential pulse Cathodic Stripping Voltammetry. The detection limit of cyanide ion in the presence of $5.0*10^{-5}M$ sulfide ion and $1.0*10^{-3}M$ cupric ion was $2.0*10^{-7}M$ in KCI-Phosphate buffer(pH=7.0) at accumulation potential -0.30V and accumulation time 3.0 min.

• Bulletin of the Korean Chemical Society
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• v.31 no.11
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• pp.3077-3083
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• 2010

The electrochemical detection of As(III) was investigated on a platinum-iron(III) nanoparticles modified multiwalled carbon nanotube on glassy carbon electrode(nanoPt-Fe(III)/MWCNT/GCE) in 0.1 M $H_2SO_4$. The nanoPt-Fe(III)/MWCNT/GCE was prepared via continuous potential cycling in the range from -0.8 to 0.7 V (vs. Ag/AgCl), in 0.1 M KCl solution containing 0.9 mM $K_2PtCl_6$ and 0.6 mM $FeCl_3$. The Pt nanoparticles and iron oxide were co-electrodeposited into the MWCNT-Nafion composite film on GCE. The resulting electrode was examined by cyclic voltammetry (CV), scanning electron microscopy (SEM), and anodic stripping voltammetry (ASV). For the detection of As(III), the nanoPt-Fe(III)/MWCNT/GCE showed low detection limit of 10 nM (0.75 ppb) and high sensitivity of $4.76\;{\mu}A{\mu}M^{-1}$, while the World Health Organization's guideline value of arsenic for drinking water is 10 ppb. It is worth to note that the electrode presents no interference from copper ion, which is the most serious interfering species in arsenic detection.