중성과 산성의 전해질내에서 여러 탄소전극의 전기화학적 특성과 전극재료의 중요함수인 이중층 축전용량에 대하여 조사 하였다. 이를 위해 임피던스 스펙트로스코피를 이용하였으며, 0.5M K2SO4용액과 0.1M H2SO4용액내에서 electrographite와 박판상 흑연의 경우 이중층 축전용량은 다른 두 전극재료에 비하여 높게 나타났으며, 0.1M H2SO4용액에서 탄소재료의 전하이동저항 R1은 유리상 탄소와 PVDF graphite의 경우 140 ㏀과 31.9㏀로 나타났으며 electropraphite와 박판상 흑연의 경우 2.0㏀과 5.7㏀의 적은 값을 나타냈다. 이는 재료의 표면이나 내부의 기공에 의해 생기는 커다란 비 표면적 때문이며, 이것에 의해 재료의 상경계에서 측정된 임피던스량은 저주파영역에서 낮게 나타났다. 특히 electrographite는 전극계면에서 흡착의 영향이 현저하게 나타났으며, 4종류 전극재료의 전기화학적 특성과 이중층 축전용량은 전극표면 조직에 의해 차이가 나타났다.

Laser ablation기술에 의해 Pt와 YBacu3O7-x(YBCO)전극위에 epitaxially성장된 BST박막의 조성과 전기적 특성이 연구되었다. RBS분석으로부터 Pt전극 위에 증착된 BST박막의 결정성이 YBCO전극 위에 증착된 것보다도 더 우수하였다. 600˚C에서 Pt 전극위에 증착된 BST박막은 100kHz의 주파수에서 유전상수가 320, 유전손실이 0.023이었다. Pt전극위에 증착된 BST박막의 누설전류 밀도가 TBCO전극위에 증착된 것 보다도 더 작았다. 0.15MV/cm의 전기장 하에서 누설전류밀도는 약 0.8 μ A/ cm2이었다.

In this study, we evaluated the treatment efficiency of livestock wastewater by altering the current density using boron-doped diamond (BDD) electrodes. As the current density was adjusted from 10 to 35 mA/cm2, the removal efficiency of organic matter increased from 22.2 to 71.5%. Similar to that of organic matter, the removal efficiency of color increased with increasing current density up to 85.7%, indicating a higher removal efficiency for color than that of organic matter. The removal efficiency of ammonia nitrogen increased from 14.6 to 53.3% as the current density increased, but it was lower than that of organic matter. In addition, the removal of organic matter, color, and ammonia nitrogen followed first-order reactions, according to the reaction rate analysis. The energy consumption ranged from 4.87 to 8.33 kWh/kg COD, and it was found that the organic matter removal efficiency was more efficient at high current densities. Based on various analyses, the optimal current density was 20 mA/cm2, and the corresponding energy consumption was 6.824 kWh/kg COD.

In this study, the relation between the direction of the reinforcing bars and the arrangement of the electrodes in the concrete resistivity measurement was experimentally examined. The results showed that the apparent resistivity was lower in the parallel measurement with the reinforced concrete bars, and the value of the apparent resistivity was higher as the measurement direction is closer to perpendicularity against the rebar.

Soluble cutting fluids (SCFs) have been used in metal machining processes to improve the quality of metal processing equipment and products in modern society. Because the characteristics among metal machining processes differ, various types of cutting fluids are manufactured to enhance the cutting efficiency of different metals. Although SCFs are useful and essential materials, particular treatment is required attributable to the high concentration of nitrogen materials and chemical oxygen demand (COD). In this study, the removal efficiency of total nitrogen (T-N) contained in SCFs was analyzed using electrochemical treatment. The electrode was made of 316 stainless steel, which had been perforated to prevent an imbalanced sample concentration in the reactor. Cathodic and anodic electrodes were alternately inserted into an acrylic reactor. The removal efficiency of T-N in SCFs using 40 A/m2, 60 A/m2, and 80 A/m2 current density, was 48.2%, 61.5% and 69.3%, respectively. The removal efficiency of T-N in SCFs with the addition of 0, 5 mM, and 10 mM NaCl was 69.3%, 74.6%, 77.6%, respectively.

몇 가지 점토광물과 메틸바이올로젠 또는 메틸렌블루를 함유시킨 점토수식전극을 이용하여 산소환원에 대한 전기화학적 촉매성을 검토하였다. 점토광물로는 Na-몬모릴로나이트, Ca-몬모릴로나이트, 카오리나이트를 사용하였다. 점토수식전극은 유리탄소전극 표면에 점토 현탁액을 입히고 메틸바이올로젠을 흡착시킨 것을 사용하였으며, 전기화학적 산소환원의 정도는 순환 전압전류법(cyclic voltammetry)으로 측정하였다. 실험결과, 다른 점토시료에 비하여 Na-몬모릴로나이트가 메틸바이올로젠의 흡착효과가 가장 크게 나타났고, 메틸바이올로젠을 흡착시킨 점토수식전극이 산소환원에 대한 촉매성이 월등히 우수하였다. 즉 촉매산소환원 피크가 242.6 mV 만큼 +방향으로 이동하였다. 메틸바이올로젠을 흡착시킨 점토수식전극이 메틸렌블루를 흡착시킨 점토수식전극보다 산소환원에 대한 촉매성이 더 높게 나타났다. Ca-몬모릴로나이트의 경우는 변화가 없었으나 Na-몬모릴로나이트의 구조는 메틸바이올로젠의 흡착으로 변화되었다. 메틸바이올로젠- Na-몬모릴로나이트 점토수식전극은 현탁액의 점토 농도가 약 0.87 g/10 mL이고. 메틸바이올로젠의 수용액의 농도가 대략 2.5 mM일 때 산소환원 촉매 효과가 가장 탁월하였다. 지지전해질의 pH에 따른 점토수식 전극의 산소 환원 촉매성은 중성의 pH 범위(6.3과 8.3)에서보다 산성인 pH 3.7과 알칼리성인 pH 12.7에서 월등히 크게 나타났다.

Laboratory experiments were performed to investigate the effects of various factors on the phosphorus removal by electrolysis with aluminium electrodes. The efficiency of phosphorus removal increased with increasing of voltage applied, surface area of electrodes and electrolyte concentration, and decreasing of electrode distance. The phosphorus removal was not affected by the connection number of an electric circuit. The amount of aluminium ion eluted from electrodes according to Faraday's law was 4.47 ㎎ and the Al/P mole ratio was 2.14 at the electric current value of 20 ㎃.

The electrochemical carbon dioxide reduction to produce acetaldehyde, methanol and ethanol is investigated by using perovskite type electrode (La0.9Sr0.1CuO3). The experiments were performed under 100 mA/㎠ and -2 to -2.5 V vs. Ag/AgCl. The highest faradaic efficiencies for methanol, ethanol, acetaldehyde were 11.6, 15.3, and 6.2%, respectively. The experimental data demonstrated that the capability of the perovskite type oxide for the electrode of electrochemical carbon dioxide reduction to produce alcohols was superior to other metal electrode.

New thia-and diselena-crown ethers containing two suffer and selenium donor atoms have been prepared. And then, mercury (Hg^2+) ion-selective electrodes with PVC-plasticizer (STPB) based on some macrocycles as neutral carriers were also made. The electrochemical selectivities for various ions, and the effects for macrocycles, matrix of membranes, ratio of plasticizer to macrocycles, concentration and pH of test solution were investigated on the Hg^2+ ion selective electrodes. The 1,10-diselena-l8-crown-6-PVC-STPB (sodium tetraphenylborate) exhibited good linear responses of 28.2 ± 0.6 decade^-1 for Hg^2+ ion in the concentration ranges of 10^-2∼10^-6 M Hg^2+ ion. This electrode exhibited comparatively good selectivities for Hg^2+ ion in comparison with alkali and alkaline earth metal ions, some heavy metal ions and rare earth metal ion in the range of pH 2.5∼6.0. In addition, this electrode was applied as a sensor in the titration of Hg^2+ ion with I^- ion in water.