• 분석과학
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• 제14권6호
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• pp.540-544
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• 2001

Determination of cyanide ion has been studied by adsorptive stripping voltammetry using hanging mercury electrode. Cyanide ion complexed with copper ion is adsorpbed on the electrode and oxidised at the positive potential scan. Optimal conditions of CN determination were found to be ; supporting electrolyte solution ; 0.1 M NaCl of ammonium buffer at pH 10, accumulation potential; -800 mV vs Ag/AgCl, accumulation time ; 300 s, scan rate ; 50mV/s. The linear concentration of cyanide ion was observed in the range $1{\times}10^{-8}$, $1{\times}10^{-7}M$. The detection limit(n/s=3) was $0.13{\mu}g/L$($5{\times}10^{-9}M$) with 3.5% RSD.

• 한국표면공학회:학술대회논문집
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• 한국표면공학회 2015년도 춘계학술대회 논문집
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• pp.31-31
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• 2015

본 연구는, TAB(Tape Automated Bonding)접속이나 Flip Chip 접속에 의한 패캐징을 실현시키기 위해, 실리콘 웨이퍼 표면에 구리 필러 및 주석 합금을 전기 도금법으로 형성하는 전기 접점용 범프에 관한 것이다. 본 연구에서는, 균일 범프 두께, 범프 표면의 균일화, 범프 내의 보이드 발생 문제 해결, 균일한 합금 조성 및 도금 속도의 고속화를 위해, Cu 도금액 및 Sn-Ag 도금액의 첨가제에 의한 표면 형상의 제어를 중심으로 그 성능에 대해 보고한다.

• 한국표면공학회지
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• 제15권4호
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• pp.192-207
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• 1982

A study has been made of the interaction parameters of Zn other elements in dilute solutesd solution of molten cadmium alloys over the temperature range of 450 to 570$^{\circ}C$. The experi-mental measurementss were made in a touch instant cell using a fusedd Licl-KCl electrolyte. The activity of zinc in binary and ternary solutions sexhibiteds a strong positive deviation from Raoult's law. The addition of silver, indium or lead increased the activity of zinc whereas addition of copper, bismuth or tin decreased the zinc activity slightly. The results for all the metallic solutions showed a linear dependence of reciprocal of ab-solute temperature over the experimental range. The interaction parameters obtained are as follows.

• 한국응용과학기술학회지
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• 제18권1호
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• pp.12-19
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• 2001

Eu(III) exhibits one electron-transfer reduction at $E_{1/2}$ = -0.564 V(vs. Ag/AgCl) and the hypersensitive peak at 615 ㎚ corresponding to $^{5}D_{0}{\rightarrow}^{7}F_{2}$ transition in 0.1 M $LiClO_{4}$ aqueous solution. Upon the addition of 2,6-pyridine dicarboxylic acid(PDA) to the Eu(III) aqueous soultion, the reduction potential shifts negatively and the PDA, and the Eu(III)-PDA complex emits great fluorescence than free-Eu(III) ion at 615 nm. The results are interpreted in term of the electrochemical and spectrofluorometric studies.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2004년도 하계학술대회 논문집 Vol.5 No.2
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• pp.920-923
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• 2004

We have investgated on the monolayer LB film of BASH-DMPC mixture on an ITO for the photoisomerization by light irradiation. We measured electrochemical properties by using cyclic voltammetry with a three-electrode system, An Ag/AgCl reference electrode, a platinum wire counter electrode and LB film-coated ITO working electrode in $NaClO_4$ solution at a variable concentration and monolayer LB films. A measuring range was reduced from initial potential to -1350mV, continuously oxidized to 1650 mV and measured to the initial point. The scan rate were 50, 100, 150 and 200 mV/s. As a results, LB films of 8A5H-DMPC appeared reversible process caused by the reduction-oxidation current from the cyclic voltammogram.

• Bulletin of the Korean Chemical Society
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• 제15권12호
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• pp.1035-1037
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• 1994

An ultrasensitive and selective stripping voltammetric scheme for the determination of rhodium is described. By the use of combined accumulation and catalytic effects in formaldehyde-hydrochloric acid medium, substantial improvement in the limit of detection can be obtained. Optimal experimental conditions were found to be 0.42 M hydrochloric acid solution containing 0.008${\%}$ formaldehyde, an accumulation potential of -0.70 V (vs. Ag/AgCl) and an accumulation time of 20 s. The stripping mode was differential pulse voltammetry. In these conditions the limit of detection lies at 2 ${\times}$ l0$^{-12}$ M (0.21 ppt). The relative standard deviation at 5 ${\times}$ l0$^{-11}$ M was 4.9${\%}$ (n=5). There were no serious interferences from other platinum group metal ions being the tolerable amounts more than 500 times that of rhodium.

• Bulletin of the Korean Chemical Society
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• 제15권12호
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• pp.1050-1054
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• 1994

Eu(Ⅲ) exhibits one electron-transfer reduction at E$_{1/2}$ =-0.617 V vs. Ag/AgCl and the hypersensitive peak at 618 nm corresponding to $^5D_0$ ${\leftrightarro}$ $^7F_2$ transition in 0.10 M LiClO$_4$ aqueous solutions. Upon the addition of carboxylate or sulfonate anions to the Eu(Ⅲ) aqueous solutions, the reduction potential shifts negatively and the reduction current decreases because of the complex formation between Eu(Ⅲ) ions and the anions. However, for the case of carboxylate anion (acetate or propionate) the shift of reduction peak potential and the emission intensity at 618 nm are greater. The results are interpreted in terms of the differences in the formation constants and the hypersensitivity.

• Bulletin of the Korean Chemical Society
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• 제18권5호
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• pp.496-500
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• 1997

Electrochemical behavior of mer-tris(2-pyridinethiolato)cobalt(Ⅲ) in dimethylformamide was studied on a platinum electrode by means of cyclic voltammetry, chronoamperometry, and chronocoulometry. It was found that the neutral complex molecule was electroactive between the potential region of 1.0 and - 1.2 V vs. a nonaqueous Ag/Ag+ electrode. The Co(Ⅲ) complex was reversibly reduced to Co(Ⅱ) species by one-electron transfer at about - 1.1 V, followed by an irreversible dissociation reaction. However, the oxidation process at around 0.8 V, was responsible for an irreversible two-electron transfer that occurred at a ligand site.

• Bulletin of the Korean Chemical Society
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• 제18권11호
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• pp.1149-1152
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• 1997

An enzyme electrode for the amperometric measurement of urea was prepared by co-immobilizing L-glutamate dehydrogenase and urease onto an Immobilon-AV affinity membrane attached to a glassy carbon electrode. The reduced nicotinamide adenine dinucleotide(NADH) was used as the electroactive species. The electrochemical oxidation of NADH was monitored at +1.0 volt vs. Ag/AgCl. The enzyme-immobilized electrode was linear over the range of 2.0 × 10-5 to 2 × 10-4 M. The response time of the electrode was approximately 3 min. and the optimum pH of the enzyme immobilized membrane was pH 7.4-7.6 (Dulbcco's buffer solution). It was stable for at least two weeks or 50 assays. There was no interference from other physiological species, except from high levels of ascorbic acid.

• Bulletin of the Korean Chemical Society
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• 제32권10호
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• pp.3687-3691
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• 2011

Ion exchange experiments of molybdenum(VI) from strong HCl and $H_2SO_4$ solution have been done to investigate the existence of anionic complexes. The concentration of HCl and $H_2SO_4$was changed from 1 to 9 M. From the data on the complex formation of molybdenum in aqueous solution, a new distribution diagram of Mo(VI) was constructed in the pH range from zero to 10. AG 1 X-8, an anion exchange resin, and Diphonix, a cation exchange resin were used in the loading experiments. Ion exchange results indicate that anionic complexes of Mo(VI) begins to form from 3 M HCl and 1 M $H_2SO_4$ solution and the tendency to form anionic complexes is stronger in HCl than in $H_2SO_4$ solution. Our results can be utilized in the analysis of Mo(VI) in strong acid solution and in the design of a process to separate Mo(VI).