• 선박안전
• /
• 통권21호
• /
• pp.66-77
• /
• 2006

Stainless steel has been stably used closed by passivity oxidation films(Cr₂O₃) is made by neutral atmospheric environment. However, passivity oxidaton films of the surface of stainless steel occasionally comes to be destroyed in seawater which is influenced by an environment having galogen ion like Cl‾, then, localization corrosion comes to occur Stainless steel 304 for shaft system material of the small-size FRP fishing boat on seawater environments made an experiment on simulation of sacrifical anode(Al, Zn). Through these experiment and study, following results have been obtained ; According to the field inspection and corrosion simulation, the corrosion on the 2nd class stainless steel shaft(STS304) in FRP fishing boat has been verified to occur by crevice corrosion and galvanic corrosion etc., According to the comparison and analysis of Stainless steel 304 was severely corroded, but, protected shaft specimen was not totallay corroded. This result is assumed to be made by the facts that anodic reaction, Fe → fe²+＋ 2e¯, has been restricted by the cathodic protection current of sacrificial anode material.

• 한국재료학회지
• /
• 제22권1호
• /
• pp.8-15
• /
• 2012

Silicon-based thin film was prepared at room temperature by an electrochemical deposition method and a feasibility study was conducted for its use as an anode material in a rechargeable lithium battery. The growth of the electrodeposits was mainly concentrated on the surface defects of the Cu substrate while that growth was trivial on the defect-free surface region. Intentional formation of random defects on the substrate by chemical etching led to uniform formation of deposits throughout the surface. The morphology of the electrodeposits reflected first the roughened surface of the substrate, but it became flattened as the deposition time increased, due primarily to the concentration of reduction current on the convex region of the deposits. The electrodeposits proved to be amorphous and to contain chlorine and carbon, together with silicon, indicating that the electrolyte is captured in the deposits during the fabrication process. The silicon in the deposits readily reacted with lithium, but thick deposits resulted in significant reaction overvoltage. The charge efficiency of oxidation (lithiation) to reduction (delithiation) was higher in the relatively thick deposit. This abnormal behavior needs to clarified in view of the thickness dependence of the internal residual stress and the relaxation tendency of the reaction-induced stress due to the porous structure of the deposits and the deposit components other than silicon.

• Journal of Electrochemical Science and Technology
• /
• 제7권1호
• /
• pp.76-81
• /
• 2016

An anatase TiO₂ nanotube array (NTA) was fabricated by anodization and successive heat treatments. When the anatase TiO₂ NTA was cathodically polarized, its color changed to blue, and it could be used as an electrochemically active anode for an oxygen evolution reaction (OER) in alkaline water electrolysis. The structure of the blue anatase TiO₂ NTA was controlled by the anodization conditions and its catalytic activity increased with an increase of the surface area. The activity of the blue anatase TiO₂ NTA gradually reduced with the continued OER because of the partial oxidation of Ti³⁺ to Ti⁴⁺. However, an intermittent cathodic regeneration process could significantly slow its reduction rate. The blue anatase TiO₂ NTA could be an alternative anode for alkaline water electrolysis.

• Journal of Korean Vacuum Science & Technology
• /
• 제3권1호
• /
• pp.38-42
• /
• 1999

Using the LOCOS process, we have fabricated the lateral type polysilicon field emission triodes with poly-Si/oxide/Si structure and investigated their current-voltage characteristics for three biasing modes of operation. The fabricated devices exhibit excellent electrical performances such as a relatively low turn-on anode voltage of 14 V at VGC = 0V, a stable and high emission current of 92${\mu}$A/triode over 90 hours, a small gate leakage current of 0.23 ${\mu}$A/triode and an outstanding transconductance of 57${\mu}$S/5triodes at VGC = 5V and VAC = 26V. these superior electrical operation is believed to be due to a large field enhancement effect, which is related to the sharp cathode tips produced by the LOCOS process as well as the high aspect ratio (height /radius ) of the cathode tip end.

• 한국세라믹학회지
• /
• 제40권1호
• /
• pp.69-76
• /
• 2003

리튬이차 박막전지로서, 실리콘 첨가(0, 2, 6, 10, 20㏖%)에 따른 주석 산화물 박막을 기판온도 30$0^{\circ}C$, Ar:O$_2$=7:3으로 R.F. magnetron sputtering법으로 제조하였다. 실리콘의 함량이 증가함에 따라, Si-O 결합량이 증가하고 Sn-O 결합량은 감소하였다. 적정량의 실리콘 첨가는 주석의 산화상태를 감소시켜 비가역성을 줄이고 충방전 동안 주석의 부피변화를 막아 사이클 특성이 향상되는 결과를 보여주었다. 6㏖% Si를 첨가한 주석 산화물 박막은 100사이클동안 700mAh/g의 용량을 가지는 가장 좋은 사이클 특성을 나타내었다.

• Environmental Engineering Research
• /
• 제24권3호
• /
• pp.443-448
• /
• 2019

The present study was conducted to compare the voltage generation in two-chamber microbial fuel cells (MFCs) with a biocathode where nitrate and oxygen are used as a terminal electron acceptors (TEA) and to investigate the nitrogen removal and the electrochemical characteristics depending on the separators of the MFCs for denitrification. The maximum power density in a biocathode MFC using an anion exchange membrane (AEM) was approximately 40% lower with the use of nitrate as a TEA than when using oxygen. The MFC for denitrification using an AEM allows acetate ($CH_3COO^-$) as a substrate and nitrate ($NO_3{^-}$) as a TEA to be transported to the opposite sides of the chamber through the AEM. Therefore, heterotrophic denitrification and electrochemical denitrification occurred simultaneously at the anode and the cathode, resulting in a higher COD and nitrate removal rate and a lower maximum power density. The MFC for the denitrification using a cation exchange membrane (CEM) does not allow the transport of acetate and nitrate. Therefore, as oxidation of organics and electrochemical denitrification occurred at the anode and at the cathode, respectively, the MFC using a CEM showed a higher coulomb efficiency, a lower COD and nitrate removal rate in comparison with the MFC using an AEM.

• 청정기술
• /
• 제7권3호
• /
• pp.215-223
• /
• 2001

A present semiconductor cleaning technology is based upon RCA cleaning technology which consumes vast amounts of chemicals and ultra pure water(UPW) and is the high temperature process. Therefore, this technology gives rise to the many environmental issues, and some alternatives such as electrolyzed water(EW) are being studied. In this work, intentionally contaminated Si wafers were cleaned using the electrolyzed water. The electrolyzed water was generated by an electrolysis system which consists of three anode, cathode, and middle chambers. Oxidative water and reductive water were obtained in anode and cathode chambers, respectively. In case of NH4Cl electrolyte, the oxidation-reduction potential and pH for anode water(AW) and cathode water(CW) were measured to be +1050mV and 4.8, and -750mV and 10.0, respectively. AW and CW were deteriorated after electrolyzed, but maintained their characteristics for more than 40 minutes sufficiently enough for cleaning. Their deterioration was correlated with CO2 concentration changes dissolved from air. Contact angles of UPW, AW, and CW on DHF treated Si wafer surfaces were measured to be $65.9^{\circ}$, $66.5^{\circ}$ and $56.8^{\circ}$, respectively, which characterizes clearly the eletrolyzed water. To analyze the amount of metallic impurities on Si wafer surface, ICP-MS was introduced. It was known that AW was effective for Cu removal, while CW was more effective for Fe removal. To analyze the number of particles on Si wafer surfaces, Tencor 6220 were introduced. The particle distributions after various particle removal processes maintained the same pattern. In this work, RCA consumed about $9{\ell}$ chemicals, while EW did only $400m{\ell}$ HCl electrolyte or $600m{\ell}$ NH4Cl electrolyte. It was hence concluded that EW cleaning technology would be very effective for promoting environment, safety, and health(ESH) issues in the next generation semiconductor manufacturing.

• Ecology and Resilient Infrastructure
• /
• 제3권4호
• /
• pp.279-284
• /
• 2016

선광 및 제련과 같은 광산활동 과정에 발생하는 광미는 고농도의 중금속을 함유하고 있고, 그 중 황철석을 함유한 광미는 광산주변 수계 및 토양 오염의 주요 원인이다. 이러한 황철석을 함유한 광미의 무해화를 위해 화학전지 (연료전지)의 개념을 활용할 수 있다. 화학전지에서 황철석의 자발적인 산화, 즉, 갈바닉 산화를 통해 황철석이 용해되면서 $Fe^{3+}$와 황산이 생성되어 pH가 감소하게 된다. 이는 황철석 함유 광미 내 중금속의 용출 촉진 효과를 가져올 수 있다. 본 연구에서는 $23^{\circ}C$ 조건에서 4주 간 산성용액과 갈바닉 반응기를 이용해 황철석을 처리하며 총 용존 철 농도와 용액의 pH를 확인하였다. 또한 주사전자현미경을 이용해 처리 후 황철석 표면을 관찰하였다. 갈바닉 반응기를 이용한 황철석의 용해가 산성용액을 이용한 황철석의 용해에 비해 약 2.9배 높은 총 철을 용출시킨 것을 확인하였고, pH 저감 효과도 더 큰 것을 확인하였다. 또한 표면 분석 결과 갈바닉 반응기 내에서 반응한 황철석의 표면에서 더 많은 홈을 발견되었다. 본 연구를 통해 갈바닉 산화에 의해 황철석의 용해가 촉진된 것을 확인하였으며, 갈바닉 산화가 황철석 함유 광미의 무해화 기술로 사용될 수 있는 가능성을 확인하였다.

• 한국생산제조학회지
• /
• 제21권4호
• /
• pp.575-581
• /
• 2012

The electrochemical oxygen demand (ECOD) is an additional sum parameter, which has not yet found the attention it deserves. It is defined as the oxygen equivalent of the charge consumed during an electrochemical oxidation of the solution. Only one company has yet developed an instrument to determine the ECOD. This instrument uses $PbO_2$-electrodes for the oxidation and has been successfully implemented in an automatic on-line monitor. A general problem of the ECOD determination is the high overpotential of electrochemical oxidations of most organic compounds at conventional electrodes. Here we present a new approach for the ECOD determination, which is based on the use of a solid composite electrodes with highly efficient electro-catalysts for the oxidation of a broad spectrum of different organic compounds. Lead dioxide as an anode material has found commercial application in processes such as the manufacture of sodium per chlorate and chromium regeneration where adsorbed hydroxyl radicals from the electro-oxidation of water are believed to serve as the oxidizing agent. The ECOD sensors based on the Au/$PbO_2$ electrode were operated at an optimized applied potential, +1.6 V vs. Ag/AgCl/sat. KCl, in 0.01 M $Na_2SO_4$ solution, and reduced the effect of interference ($Cl^-$ and $Fe^{2-}$) and an expended lifetime (more than 6 months). The ECOD sensors were installed in on-line auto-analyzers, and used to analyze real samples.

• 대한화학회지
• /
• 제46권5호
• /
• pp.444-456
• /
• 2002

차체의 산화를 방지하기 위하여 희생적 양극을 사용한 산화방지 장치를 개발하였다. 희생적 양극은 철보다 산화 전위가 높은 Mg, Al, Zn으로 만들어 졌고 이것은 차체의 철이나 철합금보다 먼저 산화되어 차체의 부식을 방지한다. 차체 산화방지 장치를 제작하여 철시편을 염산, 질산 및 황산에 대한 방식효과를 시간에 따라 측정하였고 SEM과 XPS를 이용하여 철시편 표면의 방식효과를 분석하였다. 철시편을 산화 방지 장치에 연결하면 산화되어 산성용액 속으로 녹아 들어가는 철의 양이 현저하게 감소하고 철시편 표면의 산화가 방지되며 산화된 철은 $Fe_2O_3$의 산화형태를 가짐을 확인하였다. 따라서 차체 산화방지를 차체에 직접 부착한다면 차체의 부식 및 산화를 효과적으로 방지할 것으로 기대된다.