• Journal of Advanced Marine Engineering and Technology
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• 제37권8호
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• pp.877-885
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• 2013

선박 기관실의 해수 배관은 염소이온 농도와 전기 전도성이 높은 해수가 빠른 속도로 유동하는 환경에 놓여 있게 된다. 따라서 부식성이 강한 염소 이온으로 인해 배관 내부에 국부 부식이 발생하여 해수가 누설되는 경우가 종종 발생하고 있다. 그래서 해수 배관의 누설 부위에 대해 일반적으로 선박 내에서 여러 가지 피복아크용접봉을 사용하여 교류 아크용접기로 보수용접을 한다. 본 연구에서는 해수파이프 등에 E4301, E4311, E4313 및 E4316과 같은 피복아크용접봉으로 용접한 경우, 용접부위에 대해 영역별로 내식성 차이를 전기화학적 방법으로 비교 분석하고, 각각의 용접부위에 대한 미세조직 관찰 및 미소 비커스 경도를 측정하였다. E4313의 용접봉을 사용한 용접부가 다른 용접봉을 사용한 용접부에 비해 가장 낮은 경도 값을 나타내었으나 내식성은 가장 우수하게 나타나고 있다. 그리고 용접봉의 종류에 관계없이 용접부는 모재보다 상대적으로 내식성이 더 우수하였고, 경도도 더 높은 값을 나타내었다.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2011년도 제40회 동계학술대회 초록집
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• pp.204-205
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• 2011

In thin film silicon solar cells, p-i-n structure is adopted instead of p/n junction structure as in wafer-based Si solar cells. PECVD is a most widely used thin film deposition process for a-Si:H or ${\mu}c$-Si:H solar cells. For best performance of thin film silicon solar cell, the dopant profiles at p/i and i/n interfaces need to be as sharp as possible. The sharpness of dopant profiles can easily achieved when using multi-chamber PECVD equipment, in which each layer is deposited in separate chamber. However, in a single-chamber PECVD system, doped and intrinsic layers are deposited in one plasma chamber, which inevitably impedes sharp dopant profiles at the interfaces due to the contamination from previous deposition process. The cross-contamination between layers is a serious drawback of a single-chamber PECVD system in spite of the advantage of lower initial investment cost for the equipment. In order to resolve the cross-contamination problem in single-chamber PECVD systems, flushing method of the chamber with NH3 gas or water vapor after doped layer deposition process has been used. In this study, a new plasma process to solve the cross-contamination problem in a single-chamber PECVD system was suggested. A single-chamber VHF-PECVD system was used for superstrate type p-i-n a-Si:H solar cell manufacturing on Asahi-type U FTO glass. A 80 MHz and 20 watts of pulsed RF power was applied to the parallel plate RF cathode at the frequency of 10 kHz and 80% duty ratio. A mixture gas of Ar, H2 and SiH4 was used for i-layer deposition and the deposition pressure was 0.4 Torr. For p and n layer deposition, B2H6 and PH3 was used as doping gas, respectively. The deposition temperature was $250^{\circ}C$ and the total p-i-n layer thickness was about $3500{\AA}$. In order to remove the deposited B inside of the vacuum chamber during p-layer deposition, a high pulsed RF power of about 80 W was applied right after p-layer deposition without SiH4 gas, which is followed by i-layer and n-layer deposition. Finally, Ag was deposited as top electrode. The best initial solar cell efficiency of 9.5 % for test cell area of 0.2 $cm^2$ could be achieved by applying the in-situ plasma cleaning method. The dependence on RF power and treatment time was investigated along with the SIMS analysis of the p-i interface for boron profiles.

• 공업화학
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• 제23권1호
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• pp.47-52
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• 2012

다공성 탄소나노섬유의 아민 작용기에 따른 $CO_2$ 가스 감응특성을 고찰하고자, 아민작용기가 도입된 다공성 탄소나노섬유 기반 $CO_2$ 가스센서를 제조하였다. Polyacrylonitrile를 전구체로 하여 전기방사법을 통해 나노섬유를 제조하였으며, 열처리 및 화학적 활성화 공정, 그리고 Diethylenetriamine 액상처리법을 통하여 아민작용기가 도입된 다공성 탄소나노섬유를 제조하였다. BET 비표면적 분석결과, 화학적 활성화법에 의해 최대 $2000m^2/g$까지 탄소나노섬유의 비표면적이 향상됨을 확인하였으며, FT-IR 분광법을 통해 아민 작용기의 도입을 확인하였다. 아민 작용기가 도입된 가스센서의 $CO_2$ 가스 감응특성은 다공성 탄소섬유 기반 가스센서에 비해 약 4배 향상됨을 확인하였다. 결과적으로 화학적 활성화법에 의해 발달된 기공특성과 아민작용기 도입에 따른 화학흡착 유도에 의하여 감응특성이 향상되었음을 확인하였다.

• 공업화학
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• 제7권6호
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• pp.1125-1131
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• 1996

고체전해질형 연료전지의 산소극 재료로서 페롭스카이트 구조를 갖는 $PrMnO_3$에 Ca과 Sr을 도핑시켜 도핑량에 따른 전기전도도, 산소환원과전압 등의 전기화학적 특성과, 전해질인 yttria stabilized zirconia와의 반응성 그리고 열 팽창률 등을 살펴 보았다. 합성된 페롭스카이트 분말은 대략 $2{\sim}5{\mu}m$의 평균입자 크기를 나타내었는데 이때 입자크기 및 비표면적은 도핑량과 무관하였다. Ca이 30mo1% 도핑되었을 때 전기전도도는 $1000^{\circ}C$에서 $266S{\cdot}cm^{-1}$로 가장 높은 값을 나타내었고, 분극을 통해 살펴 본 산소환원특성도 Ca이 30mol% 도핑되었을 때 가장 우수한 특성을 나타내었다. 전극물질과 전해질인 YSZ를 $1200^{\circ}C$에서 100시간 동안 반응시킨 결과 $PrMnO_3$에 Sr을 도핑시켰을 때보다 Ca을 도핑시킨 것이 반응성이 훨씬 약한 결과를 나타내었다. $Pr_{0.7}Ca_{0.3}MnO_3$의 열팽창계수는 $300{\sim}1000^{\circ}C$의 영역에서 $1.19{\times}10^{-5}K^{-1}$로 측정되었고 이 값은 YSZ의 열팽창계수 $1.15{\times}10^{-5}K^{-1}$과 유사한 값이었다.

• Bulletin of the Korean Chemical Society
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• 제34권4호
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• pp.1081-1088
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• 2013

Two new metal-free organic dyes bridged by anthracene-mediated ${\pi}$-conjugated moieties were successfully synthesized for use in a dye-sensitized solar cell (DSSC). A N,N-diphenylthiophen-2-amine unit in these dyes acts as an electron donor, while a (E)-2-cyano-3-(thiophen-2-yl)acrylic acid group acts as an electron acceptor and an anchoring group to the $TiO_2$ electrode. The photovoltaic properties of (E)-2-cyano-3-(5-((10-(5-(diphenylamino)thiophen-2-yl)anthracen-9-yl)ethynyl)thiophen-2-yl)acrylic acid (DPATAT) and (E)-2-cyano-3-(5'-((10-(5-(diphenylamino)thiophen-2-yl)anthracen-9-yl)ethynyl)-2,2'-bithiophen-5-yl)acrylic acid (DPATABT) were investigated to identify the effect of conjugation length between electron donor and acceptor on the DSSC performance. By introducing an anthracene moiety into the dye structure, together with a triple bond and thiophene moieties for fine-tuning of molecular configurations and for broadening the absorption spectra, the short-circuit photocurrent densities ($J_{sc}$), and open-circuit photovoltages ($V_{oc}$) of DSSCs were improved. The improvement of $J_{sc}$ in DSSC made of DPATABT might be attributed to much broader absorption spectrum and higher molecular extinction coefficient (${\varepsilon}$) in the visible wavelength range. The DPATABT-based DSSC showed the highest power conversion efficiency (PCE) of 3.34% (${\eta}_{max}$ = 3.70%) under AM 1.5 illumination ($100mWcm^{-2}$) in a photoactive area of $0.41cm^2$, with the $J_{sc}$ of $7.89mAcm^{-2}$, the $V_{oc}$ of 0.59 V, and the fill factor (FF) of 72%. In brief, the solar cell performance with DPATABT was found to be better than that of DPATAT-based DSSC.

• 대한한의학회지
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• 제20권3호
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• pp.36-44
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• 1999

Objectives: It has been well known that electroacupuncture(EA) has an analgesic effect and there is a pain control system in the central nervous system(CNS). The pain control system is composed of three major nuclei, which are periaqueductal gray(PAG), raphe nuclei, and the pain inhibitory complex located in the spinal cord. It has been suggested that the analgesic effect of EA might be the result of activation of the pain control system in the CNS. However, there may be a possibility that other nuclei are also involved in this pain modulation. Thus, we investigated whether the posterior intralaminar thalamic nuclei (PTIN) are involved in the pain modulation. Methods: To measure the level of pain, the jaw opening reflex (JOR) was used as a pain index. The magnitude of JOR is estimated by averaging the area of 10 successive responses. JOR was evoked by tooth-pulp stimulation with bipolar electrode carrying stimulus with the following parameters: intensity ranging from 420uA to 680ulA, 0.3ms duration of square pulse, and 0.5 Hz. Hapkog($LI_4$) and Taechung ($LR_3$) were the chosen acupoints. The Hapkog point was stimulated ipsilaterally at 5V, 3 Hz, for 15min in total, and the Taechung was stimulated at 2-3 V, 3 Hz, and for a total of 15 or 30 minutes. Different intensities of stimulation were given the PITN; one was given at $300{\mu}A$ and the other was at 500uA. The position stimulated in these nuclei by Paxinos Atlas was AP; from bregma $-4.0{\sim}-4.3mm,\;L; 0.5{\sim}1.8mm,\;D;\;4.8{\sim}6.3mm$. Results: The Hapkog point had a significant analgesic effect (P<0.05). However, the Taechung point had no effect. Both types of stimulation in the PITN did not reveal any analgesic effects. Conclusions: From these results, it was suggested that the posterior intralaminar thalamic nuclei are not involved in the modulation of pain.

• Restorative Dentistry and Endodontics
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• 제16권1호
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• pp.6-15
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• 1991

The purpose of this study was to observe in vitro chloride corrosion behavior from 5 kinds of amalgam (Caulk spheracal, Amalcap, Dispersalloy, Tytin, Sybralloy) as a function of time after tritruration by using potentiostat. After each amalgam alloy and Hg was triturated as the direction of the manufacturer by the mechanical amalgamator, the triturated mass was inserted the cyrindrical matal mold ($12{\times}10mm$) and was condensed by using routine manner. The specimen was removed from the mold and was stored at room temperature for 1 week, 1 month and 3 months, and standard surface preparation was routine carried out. The 0.9% saline solution was used as electrolyte in pH 6.8~7.0 at $30{\pm}0.5.^{\circ}C$. The open circuit potential was determined after 30 minutes' immersion of 1 week, 1 month and 3 month old specimens. The scan rate was 1 mV/sec and the surface area of amalgam exposed to the solution was $0.65\;Cm^2$ for each specimen. All potentials reported are with respect to a silver / silver chloride electrode (SSE). The following result was obtained. 1. All amalgam specimens became more noble corrosion potentials which represent the improved corrosion resistance as the time elapsed. 2. Three kinds of high copper amalgam always exhibited more noble potential than low copper amalgam at 1 week, 1 month and 3 months. 3. Two kinds of low copper amalgam had the similar polarization curve pattern with 3 current peaks at each time period and current densities associated with these peaks were decreased as aging especially in caulk spherical amalgam. 4. All kinds of high copper amalgam had the similar polarization curve pattern with absence of prominent current peak at each time period, but the polarization curve of D amalgam had one apparent current peak at 1 week.

• Restorative Dentistry and Endodontics
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• 제13권2호
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• pp.221-235
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• 1988

The purpose of this study was to observe characteristic properties through the polarization curves and EMPA images from 4 different types of amalgam obtained by using the potentiostats (EG & G PARC) & EPMA (Jeol JSM-35), to investigate the degree of corrosion of each phase of amalgam on the oxidation peak, and to identify corrosion products from the corroded amalgam by use of X-ray diffractometer(Rigaku). After each amlgam alloy and Hg were triturated as the direction of the manufacturer by means of the mechanical amalgamator(Shofu), the triturated mass was inserted into the cylindrical metal mold which was 12mm in diameter and 10mm in height and was condensed by means of routine manner. The specimen was removed from the mold and stored at room temperature for about 7 days. The standard surface preparation was routinely carried out. Anodic polarization measurement was employed to compare the corrosion behaviours of the amalgams in 0.9% saline solution(pH6.8~7.0) and artificial saliva (pH6.8~7.0) at $37^{\circ}C$. The open circuit potential was determined after 30 minutes' immersion of specimen in electrolyte and the potential scan was begun at the potential of 100mV cathodic from the corrosion potential. The scan rate was 1mV/sec and the surface area of amalgam exposed to the solution was 0.64$cm^2$ for each specimen. All the potentials reported are with respect to a saturated calomel electrode (SCE). EPMA images on the determined oxidation peaks of each amalgam in artificial saliva were observed. X-ray diffraction patterns of each sample were recorded before and after polarization in artificial saliva (Aristaloy, Caulk Spherical, Dispersalloy and Tytin: at +770mV, +585mV, +8.10m V and +680m V respectively) by use of a recording diffractometer. Nickel filtered Cu $K_{{\alpha}_1}$ radiation was used and sample was scanned at $4^{\circ}(2{\theta})/min.$ from $25^{\circ}$ to $80^{\circ}$. The following results were obtained. 1. Oxidation peak potential in artificial saliva shifted to more anodic direction than that in saline solution. 2. The corrosion potential of high copper amalgam was more anodic than the potential of low copper amalgam. 3. The current density was lower in artificial saliva than in saline solution. 4. One of the corrosion products, AgCl was identified by X-ray diffraction analysis. 5. ${\gamma}_2$ phase was the most susceptible to corrosion and e phase was stable in low copper amalgam and ${\eta}$' phase and Ag-Cu eutectic were susceptible to corrosion in high copper amalgam.

• 전기화학회지
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• 제23권4호
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• pp.97-104
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• 2020

전기 물 분해 기술 중 주요 과제 중 하나는 귀금속의 Ir과 Ru 기반의 촉매를 대체할 수 있는 고성능, 저비용의 산소 발생 반응 (OER) 촉매를 개발하는 것이다. 본 연구에서는 CoSO₄와 Fe(NO₃)₃ 수용액을 1차 가열 후 KNO₃와 NaOH 추가 반응을 이용한 침전법을 이용하여 OER 촉매로 사용 가능한 역스피넬 구조의 약 44 nm 크기를 갖는 CoFe₂O₄ 나노 입자를 합성하였다. CoFe₂O₄ 나노 입자의 합성 시간을 조절하여 입자 및 결정립 크기를 제어하였다. CoFe₂O₄ 나노 입자의 합성 시간이 6시간일 때, 높은 전도성과 전기 화학 표면적을 가졌다. 이 CoFe₂O₄ (6 h)는 전류 밀도 10 mA/㎠의 과전압 및 Tafel slope는 각각 395 mV 및 52 mV/dec으로 나타났다. 또한, 이 촉매는 10 mA/㎠에서 18시간 동안 우수한 내구성을 나타냈다.

• 태양에너지
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• 제17권4호
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• pp.3-11
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• 1997

다결정 실리콘에서 결정입계는 광생성된 반송자들의 재결합 중심으로 작용할 뿐 아니라 전위장벽으로 작용하여 태양전지의 변환효율을 감소시킨다. 결정입계의 영향을 줄이기 위해 열처리, 결정입계에 대한 선택적 식각, 결정입계로 함몰전극을 형성하는 방법, 다양한 전극 구조, 초박막 금속 형성 후 전극형성 등 여러가지 요소들을 조사하였다. 질소 분위기에서 $900^{\circ}C$ 전열처리, $POCl_3$ 확산을 통한 게터링, 후면전계 형성을 위한 Al 처리로 다결정 실리콘의 결함밀도를 감소시켰다. 결정입계에서의 반송자 손실을 감소시키기 위한 기판 처리로 Schimmel 식각액을 사용하였다. 이는 texturing 효과와 함께 결정입계를 선택적으로 $10{\mu}m$ 깊이로 식각하였다. 결점입계를 우선적으로 식각한 후면으로 Al을 확산하여 후면에서의 재결합 손실을 감소시켰다. 전극 핑거(grid finger) 간격이 0.4mm인 세밀한 전극 구조에 결정입계로 $0.4{\mu}m$ 깊이로 함몰전극을 추가로 형성하여 태양전지의 단락 전류 밀도가 개선되었다. 80% 이상의 광투과율을 보인 20nm 두께의 크롬 박막 형성으로 직렬 저항을 감소시켰다. 본 논문은 저가의 고효율, 지상 전력용 태양진지를 위해 결정입계에 대한 연구를 하였다.