• 센서학회지
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• 제33권2호
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• pp.63-69
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• 2024

A novel method for measuring hydrogen concentration is introduced, along with its working principle and a novel detection algorithm. This configuration requires no additional reference compartment for potentiometric electrochemical measurements; therefore, it is the most suitable for measuring dissolved hydrogen in the liquid phase. The sensor's electromotive force saturates at a certain point, depending on the hydrogen concentration during the heating process of the sensor operation. This dynamic temperature scanning method provides higher sensitivity than the constant temperature measurement method.

• The Korean Journal of Ceramics
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• 제4권1호
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• pp.15-19
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• 1998

Defects formation of Chemical Vapor Deposition (CVD) diamond on $^4He^{2+}$ irradiation and after remote hydrogen plasma treatment(RHPT) were investigated by cathodoluminescence(CL). As calculated in the TRIM simulation, the light elements of $^4He^{2-}$ can be penetrated into the diamond bulk structure at 3~4 $\mu\textrm{m}$ depth. The effects of the implantation region were observed when 5 keV~20 keV electron energy (insight 0.3~4.0$\mu\textrm{m}$) of CL measurement was irradiated to diamond at temperature 80 K. After the RHPT, rehybridization of irradiation damaged diamond was studied. The intensity of 5RL center(intrinsic defect of C) was diminished. The 2.16 eV center (N-V center) occurring usually by annealing could not be seen after RHPT. The diamond was rehybridized by hydrogen radicals without etching and thermal degradation by the RHPT.

• 한국재료학회:학술대회논문집
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• 한국재료학회 1997년도 한국재료학회 춘계학술발표회
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• pp.113-113
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• 1997

• 한국진공학회:학술대회논문집
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• 한국진공학회 2012년도 제43회 하계 정기 학술대회 초록집
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• pp.269-269
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• 2012

A new ion source has been designed, fabricated, and installed at the NBTS (Neutral Beam Test Stand) at the KAERI (Korea Atomic Energy Research Institute) site. The goalis to provide a 100 keV, 2MW deuterium neutral beam injection as an auxiliary heating of KSTAR (Korea Super Tokamak Advanced Research). To cope with power demand, an ion current of 50 A is required considering the beam power loss and neutralization efficiency. The new ion source consists of a magnetic cusp bucket plasma generator and a set of tetrode accelerators with circular copper apertures. The plasma generator for the new ion source has the same design concept as the modified JAEA multi-cusp plasma generator for the KSTAR prototype ion source. The dimensions of the plasma generator are a cross section of $59{\times}25cm^2$ with a 32.5 cm depth. The anode has azimuthal arrays of Nd-Fe permanent magnets (3.4 kG at surface) in the bucket and an electron dump, which makes 9 cusp lines including the electron dump. The discharge properties were investigated preliminarily to enhance the efficiency of the beam extraction. The discharge of the new ion source was mainly controlled by a constant power mode of operation. The discharge of the plasma generator was initiated by the support of primary electrons emitted from the cathode, consisting of 12 tungsten filaments with a hair-pin type (diameter = 2.0 mm). The arc discharge of the new ion source was achieved easily up to an arc power of 80 kW (80 V/1000 A) with hydrogen gas. The 80 kW capacity seems sufficient for the arc power supply to attain the goal of arc efficiency (beam extracted current/discharge input power = 0.8 A/kW). The accelerator of the new ion source consists of four grids: plasma grid (G1), gradient grid (G2), suppressor grid (G3), and ground grid (G4). Each grid has 280 EA circular apertures. The performance tests of the new ion source accelerator were also finished including accelerator conditioning. A hydrogen ion beam was successfully extracted up to 100 keV /60 A. The optimum perveance is defined where the beam divergence is at a minimum was also investigated experimentally. The optimum hydrogen beam perveance is over $2.3{\mu}P$ at 60 keV, and the beam divergence angle is below $1.0^{\circ}$. Thus, the new ion source is expected to be capable of extracting more than a 5 MW deuterium ion beam power at 100 keV. This ion source can deliver ~2 MW of neutral beam power to KSTAR tokamak plasma for the 2012 campaign.

• 상하수도학회지
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• 제21권4호
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• pp.375-383
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• 2007

Treatment efficiency research was performed using Fenton process and the electrochemical process in the presence of ferrous ion and hydrogen peroxide for the industrial wastewater including 1,4-Dioxane produced during polymerization of polyester. The Fenton process and the electrochemical Iron Redox Reaction (IRR) process were applied for this research to use hydroxyl radical as the powerful oxidant which is continuously produced during the redox reaction with iron ion and hydrogen peroxide. The results of $COD_{Cr}$ and the concentration of 1,4-Dioxane were compared with time interval during the both processes. The rapid removal efficiency was obtained for Fenton process whereas the slow removal efficiency was occurred for the electrochemical IRR process. The removal efficiency of $COD_{Cr}$ for 310 minutes was 84% in the electrochemical IRR process with 1,000 mg/L of iron ion concentration, whereas it was 91% with 2,000 mg/L of iron ion concentration. The lap time to remove all of 1,4-Dioxane, 330 mg/L in the wastewater took 150 minutes with 1,000 mg/L of iron ion concentration, however it took 120 minutes with 2,000 mg/L of iron ion concentration in the electrochemical IRR process.

• 한국환경과학회지
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• 제13권11호
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• pp.987-991
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• 2004

The purpose of this research is to evaluate the removal efficiencies of COD$\_$Cr/ and color for the dyeing wastewater by the different dosages of ferrous solution and H$_2$O$_2$ in Fenton process. In the case of H$_2$O$_2$ divided dosage for the Fenton's reagent 7:3 of H$_2$O$_2$ was more effective than 3:7 to remove COD$\_$Cr/ and color. The results showed that COD$\_$Cr/ was mainly removed by Fenton coagulation, where the ferric ions are formed in the initial step of Fenton reaction. On the other hand color was removed by Fenton oxidation rather than Fenton coagulation. The removal mechanism of COD$\_$Cr/ and color was mainly coagulation by ferrous ion, ferric ion and Fenton oxidation. The removal efficiencies were dependent on the ferric ion amount at the beginning of the reaction. However, the final removal efficiency of COD$\_$Cr/ and color was in the order of Fenton oxidation, ferric ion coagulation and ferrous ion coagulation. The reason of the highest removal efficiency by Fenton oxidation can be explained by the chain reactions with ferrous solution, ferric ion and hydrogen peroxide.

• 한국수소및신에너지학회논문집
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• 제26권1호
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• pp.54-63
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• 2015

The secondary battery using sodium is investigating as one of power storage system and power in electric vehicles. The secondary battery using sodium as a sodium battery and sodium ion battery had merits such as a abundant resources, high energy density and safety. Sodium battery (sodium molten salt battery) is operated at lower temperature ($100^{\circ}C$) compared to NAS and ZEBRA battery ($300{\sim}350^{\circ}C$). Sodium ion battery is investigating as one of the post lithium ion battery. In this paper, it is explained for the principle and recent research trends in sodium molten salt and sodium ion battery.

• 멤브레인
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• 제7권3호
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• pp.136-141
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• 1997

토양 유기물에서 생물학적 난분해성인 부식물질을 알카리에서 추출하고 산성영역에서 침전되는 성분인 부식산을 정제, 추출하였다. 부식산의 주성분인 카르복실기가 이온교환 능력을 가지고 있는 것을 이용하여 PVA와의 불균질한 이온교환막을 제조하여 생리활성 이온인 $K^+$, $Na^＋$의 이동 및 이동속도를 검토하여 보았다. 그 결과 수소이온 농도가 높을수록 이동속도는 빠르게 나타나고, 특히 $10^-1$,$10^0$영역에서 급격한 변화를 보였다. 또한 $K^+$, $Na^＋$의 농도가 증가함에 따라 그 선택성이 나타났으며, 특히 수소이온농도 $10^0$ 일때는$K^+$이 2배정도 빠르게 이동되고 있다. 따라서 이러한 생리활성 이온의 선택성 및 이동속도의 향상으로 부식산이 이온교환막의 새로운 재료로서의 그 가능성을 나타내었다.

• Korean Chemical Engineering Research
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• 제57권3호
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• pp.438-443
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• 2019

본 연구에서는 HT-PEMFC 공기극용 Pt계열 연료극 촉매의 인산이온 피독 특성에 대한 새로운 평가 방법을 제시하였다. 이를 위하여, 기존의 전기화학적 인산이온 피독 측정법인 CV와 ORR RDE 측정법이 갖고 있는 문제점을 저감하기 위하여, 과산화수소를 Pt 촉매와의 반응물로 이용하여 고농도 인산 이온 분위기에서의 내피독성 측정값 오차를 감소시켰다. 그 결과 인산이온 농도 0.1 M 이하의 저농도와 0.5 M 이상의 고농도에서 인산농도 대비 전류밀도의 변화가 직선적으로 나타나, 실제 HT-PEMFC의 구동 환경과 유사한 고농도의 인산이온 분위기에서의 Pt계 인산이온 피독 정량화에 대하여 기존의 측정방법에 비해 우수함을 확인하였다.

• 한국수소및신에너지학회논문집
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• 제28권6호
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• pp.669-674
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• 2017

In this study, the novel electrochemical and colorimetric analysis methods are suggested to estimate the degree of phosphoric acid ion poisoning on Pt based catalyst surface and to confirm the possibility of replacing the expensive and long time consumed conventional methods. As the ways, the electrochemical half cell tests such as cyclic voltammetry (CV) and linear sweep voltammetry (LSV) are used and the change in chemical behavior by absorption of the phosphoric acid ion on Pt based catalyst surface and hydrogen peroxide decomposition reaction are successfully recognized by colorimetric measurements. Conclusively, it is proved that the new methods show superior sensitivity for identifying the degree of phosphoric acid poisoned on Pt based catalyst.