• Journal of the Korean Applied Science and Technology
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• v.37 no.5
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• pp.1100-1105
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• 2020

We investigated the driving force and the required charges for spontaneous reduction of metal nanoparticles (NPs) on a scotch tape induced by mechanochemical activation. The charges were analyzed based on anodic stripping voltammetry (ASV) of silver, which is proportional to the number of charge identities on the tape. The results supported that the driving force is mechanochemical radicals rather than ions in the light of the high charge density on the tape.

• Journal of the Korean Chemical Society
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• v.17 no.2
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• pp.126-129
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• 1973

An amperometric method has been developed for the titration of silver with 2,5-dimercapto-1,3,4,-thiadiazole in ammonical solution (1N) using rotating platinum electrode as an indicator electrode and the mercury-mercury (II) iodide as reference electrode. Direct titration of milligram amount of silver (0.05-1.0mg) is possible in the presence of a number of foreign ions in ammonical solution containing ethylenediaminetetraacetic acid as masking agent under atmosphere. The interfering elements are gold and platinum. The milligram amount of silver can be determined by the proposed method within an error ${\pm}3{\%}$.

• Resources Recycling
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• v.26 no.2
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• pp.39-45
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• 2017

In order to exclude the effect of uneven distribution of gold in anode slime, the dissolution of gold and silver from the metal mixture was investigated in different systems, such as the mixture of hydrochloric acid and oxidizing reagents ($H_2O_2$, NaClO and $HNO_3$), thiosulfate and thiourea. In the mixture of HCl and either $HNO_3$ or $H_2O_2$, Au was completely dissolved but the leaching percentage of Ag was around 1%. In both thiosulfate and thiourea solution, gold was not dissolved at all. The presence of ferric ion in acidic thiourea solution showed a favorable effect on the leaching of silver but further study is necessary to elucidate the combined effect of ferric ion and sulfuric acid.

• Horticultural Science & Technology
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• v.33 no.6
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• pp.854-859
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• 2015

This experiment was performed to develop a model for nutrition ion concentration and EC in regard to change in pH from 4.0 to 8.0 in nutrient solution. The pH changes according to the variation of $HPO_4{^{-2}}$ and $H_2PO_4{^-}$ in the nutrient solution while variation of EC increased from pH 4.0 to 5.0, stabilized from pH 5.0 to 7.0 and increased again from pH 7.0 to 8.0. For the variance of major elements in the nutrient solution, K, Ca, N and P increased while pH was higher, especially the variables for K and P were increased largely. On the other hand, variables of Mg and S were stable. Based on analysis of the ion balance model of nutrient solution, the cation increased than anion over rising the variation of pH while balance point of ion moved from a-side to d-side. In addition, the imbalance increased while it moved away from the EC centerline as variance of pH increased. It was larger than effect of EC variance to correction values of equivalence ratios of K and Ca about variation of $HPO_4{^{-2}}$ and $H_2PO_4{^-}$ while as variance of pH increased, K decreased but Ca increased. These showed the result that variance of pH about correction values of equivalence ratios of K and Ca gave a second-degree polynomial model rating of 0.97. Through this research, it was identified the pH variable model about variance among pH, ion and EC according to gradient of phosphate.

• Proceedings of the Korean Institute of Surface Engineering Conference
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• 2016.11a
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• pp.113-113
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• 2016

반도체 웨이퍼 패키지 공정에는 솔더 범프용으로 주석-은 합금 도금액이 사용되어 왔다. 최근, 주석-은 도금 피막중의 은 함량의 불균일성, 불용성 양극의 사용에 의한 전압 상승. 은의 도금 치구에의 석출, 리플로 후의 보이드의 형성 등의 문제로 인하여 주석 단독 금속 도금에 의한 범프 형성이 실용화되었다. 본 연구에서는, 범프용 주석 도금액에서의 전류밀도, 금속이온의 농도, 유리산의 농도 및 첨가제의 농도가 범프 두께 균일성에 미치는 영향을 조사하였다.

• Proceedings of the Korean Vacuum Society Conference
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• 2012.08a
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• pp.132-132
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• 2012

압력 $10^{-9}$ Torr 이하의 초고진공(ultrahigh vacuum) 영역에서의 압력 측정에는 수 mA의 열전자로 잔류 가스를 이온화시켜 그 이온 전류를 측정하는 이온게이지를 주로 사용한다. 압력이 $10^{-12}$ Torr영역 이하인 극고진공(extreme high vacuum: XHV) 영역에 진입하면, ESD (electron stimulated desorption) 효과 등에 의한 이온 게이지 자체의 가스방출률이 커져 정확한 압력 측정이 곤란해 진다. 극고진공 영역에서 이온 게이지는 수 와트(W) 이상의 전력을 사용하여 수 mA의 열전자를 방출시키나, 신호인 이온 전류의 양은 1pA 이하이기 때문에 열전자에 의해 발생되는 백그라운드 전류에 묻혀 신호 전류가 측정되지 않는다고 할 수 있다. 100 nm 이하의 곡률을 가진 뾰족한 금속 탐침에 강한 전기장을 걸어주면 고체 내부의 전자가 터널링 효과에 의해 진공 중으로 방출되며, 이를 전계방출(Field Electron Emission) 효과라 부른다. 전계 방출 전류량은 탐침 표면의 일함수에 의존하며, 일함수가 클수록 지수함수 적으로 감소한다. 금속 표면에 진공 중의 잔류 가스가 부착하면 일함수가 증가한다. 가열에 의해 전계방출 탐침의 표면을 세정한 후에 전자 빔을 방출 시키면, 표면에 가스 분자가 흡착하여 방출 전류량은 점점 감소한다. 감소 속도는 압력에 비례하며, W(310) 탐침의 경우 $10^{-10}$ Torr 영역에서는 수분만에 최초 전류값의 1% 이하로 감소한다. 전계방출 전류의 감소속도가 압력에 비례하는 현상을 이용하여 압력을 측정하였다. Extractor Ionization Gauge 측정값 $5{\times}10^{-12}-3{\times}10^{-10}$ Torr의 범위에서 (111) 방향으로 정렬된 텅스텐 단결정 탐침을 사용하여 방출전류의 로그값을 시간의 함수로 semilog그래프를 그리면, 그래프는 직선을 그리며 그 기울기가 압력에 비례함을 알 수 있었다. 기울기 값과 게이지 측정값은 $10^{-11}{\sim}10^{-10}$ Torr 영역에서 거의 완벽한 비례관계를 보여주었으나, $10^{-12}$ Torr 영역에서 게이지 측정값은 기울기 값에서 추출한 압력치보다 높은 값을 보여주었으며, 이는 게이지 백그라운드 전류에 의한 차이라고 생각된다. W (310) 탐침의 방출전류는 그 감소속도가 W (111) 탐침과 마찬가지로 압력에 비례하였으나, 전류-시간 그래프는 가열 세정 직후에 전류가 거의 감소하지 않는 $2{\times}10^{-10}$ Torr에서 약 10분간 지속되는 '안정 영역'이 존재함을 보여주었다. '안정 영역'은 $10^{-11}$ Torr 영역에서는 수십분, $10^{-12}$ Torr 영역에서는 수시간 이상으로 증가하였다. 초-극고진공 영역에서의 잔류가스 주성분인 수소에서 물, 일산화탄소등의 가스로 바뀌면 '안정 영역'은 사라졌고, 이는 '안정 영역'이 수소 흡착에 의해서만 나타나는 고유 현상임을 말해준다.

• Journal of Life Science
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• v.14 no.5
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• pp.882-890
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• 2004

Gap junction is a membrane structure facilitating the direct transmission of several ions and small molecules between two cells. It is also called an 'intercellular channel' to distinguish it from other well-known cellular channels (e.g. sodium and potassium channels). Gap junction channels are not passive conduits, rather the ion channels modulated by several stimuli including pH, calcium ion, voltage, and a chemical modification (mainly known as phosphorylation). Among them, the effects of voltage on the gating of gap junction channels have been well studied. Gap junction channels are more sensitive to the transjunctional potential ($V_j$) between two cells rather than the membrane potential($V_m$) between inside and outside the cell. In this review, I will summarize the general properties of gap junction channel and discuss the gating mechanism for the gap channels.

• Journal of the Korean Chemical Society
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• v.20 no.4
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• pp.280-289
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• 1976

The silver selenide electrode has been prepared and its properties as an indicating electrode for silver ion have been investigated. Epoxy resin was used as a filler of silver selenide electrode. Silver metal plate was directly connected with the membrane of the electrode and the silver paste was used as its binder. The sintered electrode was more sensitive and stable than the pressed electrode, and the silver selenide electrode more sensitive than the silver sulfide electrode to silver ion. The linear relationship between the electrode potential and logarithmic concentration of silver ion has been observed down to 10-6 M for the electrode. Several heavy metal ions except mercuric ion did not interfere this linearity, but halide, cyanide, and thiocyanate ions did intensively interfere owing to the formation of silver compounds and complexes. This electrode has been applied to the potentiometric titration for determining halide ion. It is concluded that interferences from ,$CN^-, SCN^-, S^-, I^-, Br^-, Cl^- and Hg^{2+}$ ions are detrimental to the practical use of the electrodes for measuring pAg.

• Journal of the Mineralogical Society of Korea
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• v.20 no.2 s.52
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• pp.125-134
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• 2007

This study has been carried out in order to examine the precipitation characteristics of Fe, Mn and Al ions in coal mine drainage before removing heavy metals by using the froth flotation method. The removal rate of Fe(III), Mn(II) and Al(III) within 1 h accounted for over 99% in pH 5.0, 10.0, and $6.0{\sim}9.0$ respectively, and residual concentrations of which were under $1mgL^{-1}$. When sodium oleate as a collector was added to the solution of Fe, Mn, and Al ions, insoluble salts was not formed by the reaction of heavy metal and sodium oleate. So, we must remove the metals from coal mine drainage by using not the ion flotation method, but the precipitation flotation method

• Korean Chemical Engineering Research
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• v.48 no.1
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• pp.33-38
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• 2010

A microfluidic system has been developed using biomaterial for the measurement of cupric ion concentration. The cell-membrane-mimicking bilayer lipid membrane(BLM)-coated silver electrode was used for the sensing of cupric ion concentration. The silver-supported BLM could increase its stability. A silver-supported bilayer lipid membrane(s-BLM) was easily obtained using its self-assembling characteristics by immersing silver wire into lipid(phosphatidylcholine; PC) solution and then dipping into aqueous KCl solution. These s-BLMs were used to determine the relationship between $Cu^{2+}$ concentration and current crossing s-BLM. Their relationship showed high linearity and reproducibility. The calibration curve was constructed to express the relationship between $Cu^{2+}$ concentration and current in the $Cu^{2+}$ concentration range of 10 and $130{\mu}M$. This calibration curve was used to measure $Cu^{2+}$ concentration in an unknown sample. Microfluidic system with s-BLM was made of PDMS(polydimethyl siloxane) using typical soft photolithography and molding technique. This integrated system has various functions such as activation of the silver surface without cutting silver wire, coating of BLM on silver surface, injection of KCl buffer solution, injection of $Cu^{2+}$ sample and measurement of $Cu^{2+}$ concentration in the sample.