• 유기물자원화
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• 제30권2호
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• pp.5-15
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• 2022

본 연구에서는 궐련형 담배의 담뱃잎 바이오매스 폐기물을 수거하여 슈퍼커패시터용 활물질로 제조 및 응용하였다. 수거한 담뱃잎 폐기물을 질소 환경에서 다양한 온도(800/850/950℃)로 탄화하였으며, 탄소/산소 성분비(C/O ratio) 분석을 통해 850℃에서 가장 우수한 품질의 탄소 물질이 제조되었음을 확인하였다. 추가적으로 담뱃잎 기반의 탄소 물질에 폴리피롤(Polypyrrole)을 저온중합법을 통해 코팅하여 전기화학적 성능을 향상시켰다. 탄소 물질(CTL-850)과 폴리피롤을 코팅한 탄소 물질(CTL-850/PPy)을 기반으로 한 전극의 전기화학적 성능을 측정한 결과, -1.0-0.0V와 0.0-1.0V의 전위창에서 각각 100.2F g^-1@1 A g^-1과 155.3F g^-1@1 A g^-1의 우수한 비정전용량(Specific capacitance)를 나타내었다. 두 개의 전극을 활용하여 비대칭형 슈퍼커패시터 소자(Asymmetric supercapacitor device)를 제작하였으며, 제조한 비대칭형 CTL-850//CTL-850/PPy 소자는 2.0V의 구동전압 범위와 비정전용량(31.1F g^-1@1 A g^-1)을 가지고 있음을 확인하였다. 또한, 제조한 슈퍼커패시터 소자의 방전을 통해 1.8V의 Red Led를 점등할 수 있음을 확인하였다. 본 연구 결과를 통해 바이오매스를 우수한 성능의 친환경 에너지 저장매체로 활용하는 후속 연구에 대한 방향성을 제시할 수 있을 것으로 판단된다.

• Carbon letters
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• 제24권
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• pp.62-72
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• 2017

The aim of this work was to evaluate the dielectric properties of impregnated and activated palm kernel shells (PKSs) samples using two activating agents, potassium carbonate ($K_2CO_3$) and sodium hydroxide (NaOH), at three impregnation ratios. The materials were characterized by moisture content, carbon content, ash content, thermal profile and functional groups. The dielectric properties were examined using an open-ended coaxial probe method at various microwave frequencies (1-6 GHz) and temperatures (25, 35, and $45^{\circ}C$). The results show that the dielectric properties varied with frequency, temperature, moisture content, carbon content and mass ratio of the ionic solids. PKSK1.75 (PKS impregnated with $K_2CO_3$ at a mass ratio of 1.75) and PKSN1.5 (PKS impregnated with NaOH at a mass ratio of 1.5) exhibited a high loss tangent ($tan{\delta}$) indicating the effectiveness of these materials to be heated by microwaves. $K_2CO_3$ and NaOH can act as a microwave absorber to enhance the efficiency of microwave heating for low loss PKSs. Materials with a high moisture content exhibit a high loss tangent but low penetration depth. The interplay of multiple operating frequencies is suggested to promote better microwave heating by considering the changes in the materials characteristics.

• Journal of Welding and Joining
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• 제2권1호
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• pp.4-17
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• 1984

Overlaid weld metals of austenitic stainless steel in a pressure vessel of power reactor are usually post-weld heated for a long period of time after welding. The PWHT is considered as a kind of sensitizing and it is important to check the soundness of the weld metal after PWHT, especially about the precipitation of carbides. The purpose of this report is to obtain information on the relation between the change of microstructure and Post-Weld Heat Treatment in the overlaid weld metals. Metallurgical aspects of the problem on austenitic stainless steel heated at $625^{\circ}C$, $670^{\circ}C$, $720^{\circ}C$ and $760^{\circ}C$ for 3, 10, 30, 100 and 300 hours have been investigated by means of optical-micrography, micro-hardness measurement, scanning electron microscope and electron-probe micro analysis. From the results obtained, the following conclusions are drawn; 1) The PWHT above $625^{\circ}C$ for a long time causes a diffusion of carbon atoms from low alloy steel into stainless steel, and consequently carbon is highly concentrated at the boundary layer of stainless steel. 2) C in ferritic steel migrated to austenitic steel and carbides precipitated in austenitic steel along fusion line. At higher temperatures, the ferrite grains coarsened in the decarburized zone. 3) In the change of microstructure of stainless steel overlaid weld metal, the width of carbides precipitated zone and decarburized zone increased with increase of PWHT temperature and time. 4) At about $625^{\circ}C$ to $760^{\circ}C$, chromium carbides, mainly $M_{23} C_6$, precipitate very closely in the carburized layer with remarkable hardening. 5) Precipitation of delta ferrite from molten weld metal depends on solidification phenomenon. There was a small of ferrite near the bond in which the local solidification time was short, comparing with after parts of weld metal. Shape and amount of ferrite were not changed by Post-Weld Heat Treatment after solidification.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2014년도 제46회 동계 정기학술대회 초록집
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• pp.181.2-181.2
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• 2014

A single-layer graphene has been uniformly grown on a Cu surface at elevated temperatures by thermally processing a poly (methyl methacrylate) (PMMA) film in a rapid thermal annealing (RTA) system under vacuum. The detailed chemistry of the transition from solid-state carbon to graphene on the catalytic Cu surface was investigated by performing in-situ residual gas analysis while PMMA/Cu-foil samples being heated, in conjunction with interrupted growth studies to reconstruct ex-situ the heating process. We found that the gas species of mass/charge (m/e) ratio of 15 ($CH_3{^+}$) was mainly originated from the thermal decomposition of PMMA, indicating that the formation of graphene occurs with hydrocarbon molecules vaporized from PMMA, such as methane and/or methyl radicals, as precursors rather than by the direct graphitization of solid-state carbon. We also found that the temperature for dominantly vaporizing hydrocarbon molecules from PMMA and the length of time, the gaseous hydrocarbon atmosphere is maintained, are dependent on both the heating temperature profile and the amount of a solid carbon feedstock. From those results, we strongly suggest that the heating rate and the amount of solid carbon are the dominant factors to determine the crystalline quality of the resulting graphene film. Under optimal growth conditions, the PMMA-derived graphene was found to have a carrier (hole) mobility as high as ${\sim}2,700cm^2V^{-1}s^{-1}$ at room temperature, which is superior to common graphene converted from solid carbon.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2013년도 제45회 하계 정기학술대회 초록집
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• pp.131-131
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• 2013

A single-layer graphene has been uniformly grown on a Cu surface at elevated temperatures by thermally processing a poly(methyl methacrylate) (PMMA) film in a rapid thermal annealing (RTA) system under vacuum. The detailed chemistry of the transition from solid-state carbon to graphene on the catalytic Cu surface was investigated by performing in-situ residual gas analysis while PMMA/Cu-foil samples being heated, in conjunction with interrupted growth studies to reconstruct ex-situ the heating process. The data clearly show that the formation of graphene occurs with hydrocarbon molecules vaporized from PMMA, such as methane and/or methyl radicals, as precursors rather than by the direct graphitization of solid-state carbon. We also found that the temperature for vaporizing hydrocarbon molecules from PMMA and the length of time the gaseous hydrocarbon atmosphere is maintained, which are dependent on both the heating temperature profile and the amount of a solid carbon feedstock are the dominant factors to determine the crystalline quality of the resulting graphene film. Under optimal growth conditions, the PMMA-derived graphene was found to have a carrier (hole) mobility as high as ~2,700 cm2V-1s-1 at room temperature, superior to common graphene converted from solid carbon.

• 대한원격탐사학회지
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• 제27권3호
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• pp.235-258
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• 2011

The purpose of this study is to investigate climatological variations from the temporal and spatial surface particulate organic carbon (POC) estimates based on SeaWiFS spectral radiance, and to determine the physical mechanisms that affect the distribution of pac in the Gulf of Mexico. 7-year monthly mean values of surface pac concentration (Sept. 1997 - Dec. 2004) were estimated from Maximum Normalized Difference Carbon Index (MNDCI) algorithm using SeaWiFS data. Synchronous 7-year monthly mean values of remote sensing data (sea surface temperature (SST), sea surface wind (SSW), sea surface height anomaly (SSHA), precipitation rate (PR)) and recorded river discharge data were used to determine physical forcing factors. The spatial pattern of POC was related to one or more factors such as river runoff, wind-derived current, and stratification of the water column, the energetic Loop Current/Eddies, and buoyancy forcing. The observed seasonal change in the POC plume's response to wind speed in the western delta region resulted from seasonal changes in the upper ocean stratification. During late spring and summer, the low-density river water is heated rapidly at the surface by incoming solar radiation. This lowers the density of the fresh-water plume and increases the near-surface stratification of the water column. In the absence of significant wind forcing, the plume undergoes buoyant spreading and the sediment is maintained at the surface by the shallow pycnocline. However, when the wind speed increases substantially, wind-wave action increases vertical motion, reducing stratification, and the sediment were mixed downward rather than spreading laterally. Maximum particle concentrations over the outer shelf and the upper slope during lower runoff seasons were related to the Loop Current/eddies and buoyancy forcing. Inter-annual differences of POC concentration were related to ENSO cycles. During the El Nino events (1997-1998 and 2002-2004), the higher pac concentrations existed and were related to high runoffs in the eastern Gulf of Mexico, but the opposite conditions in the western Gulf of Mexico. During La Nina conditions (1999-2001), low Poe concentration was related to normal or low river discharge, and low PM/nutrient waters in the eastern Gulf of Mexico, but the opposite conditions in the western Gulf of Mexico.

• 한국인터넷방송통신학회논문지
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• 제20권5호
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• pp.121-126
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• 2020

지구촌 곳곳에서 기후 온난화로 인하여 엄청난 환경적 재난이 매년 되풀이되고 있다. 에너지의 주공급원인 화석연료 과다 사용으로 지구 환경변화에 영향을 끼쳐 지구 생태계를 파괴하고 자원을 고갈시키고 있다. 이를 극복하기 위해서 신재생에너지의 개발을 통하여 탄소 배출량을 줄이려는 노력이 국내외적으로 활발히 연구되고 있는 게 현실이다. 이미 해외에서는 탄소 배출량을 줄이려는 신기술들이 심심치 않게 보도되고 있다. 제로 에너지 하우스는 고단열재 고기밀성 재료사용으로 저탄소 배출 및 에너지 사용량을 줄어들게 하고 최소한의 요구하는 에너지는 신재생에너지를 통해 공급받아 실거주가 가능한 모델이다. 이를 국내에서도 적용하려 노력 중이나 경제성이 떨어지기 때문에 보편화 되기는 어려운 실정이다. 본 연구의 목적은 친환경적 요소인 탄소 배출을 제로화 하고, 환기 시스템과 열교환기 및 에너지 저장장치를 공용으로 사용하여 제로 에너지 하우스의 시공 경제성을 확보하고, 창호 개방/폐쇠에 자동화 시스템을 부착하여 실내 적정온도 유지가 가능한 모델을 연구하고자 한다.

• Journal of the Korean Wood Science and Technology
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• 제33권6호통권134호
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• pp.63-70
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• 2005

$225^{\circ}C$에서 $325^{\circ}C$ 이하의 저온에서 열처리한 셀룰로오스의 물성과 에틸아민 흡착특성을 열처리온도별로 조사하였다. 열처리온도의 증가와 더불어 수율이 감소하고, 탄소함량이 증가하는 반면, 수소나 산소의 함량은 감소하였다. 표면관능기량을 Boehm 법으로 측정한 결과, 열처리온도가 $300^{\circ}C$까지 올라가면 산성관능기량이 증가하였으나 그 이상의 온도에서는 다소 감소하는 경향이 있었다. 염기성관능기는 거의 존재하지 않았으며 열처리온도 $325^{\circ}C$에서 미량 확인할 수 있을 정도였다. 열처리셀룰로오스를 1점법으로 측정한 비표면적은 처리온도가 높으면 다소 증가하는 경향이 있었으나 매우 적었다. 열처리 온도가 증가할수록 셀룰로오스의 에틸아민증기 흡착량이 증가하여 $300^{\circ}C$ 처리 셀룰로오스의 에틸아민흡착에 의한 중량증가가 최대 113%를 나타내었다. $275^{\circ}C$에서 열처리셀룰로오스는 에틸아민 흡착 시, 팽윤이 일어나고 용해현상이 일어났다. $275^{\circ}C$ 이상의 온도에서 열처리한 셀룰로오스는 X선회절도 상에서 무정형화 하는 것으로 나타났다. 에틸아민 흡착한 열처리셀룰로오스의 용해 현상은 셀룰로오스의 결정구조 붕괴와 염기성 가스의 흡착량 증가에 의한 것으로 추측된다.

• 한국재료학회지
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• 제25권6호
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• pp.279-287
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• 2015

In order to prepare anode materials for high power lithium ion secondary batteries, carbon composites were fabricated with a mixture of petroleum pitch and coke (PC) and a mixture of petroleum pitch, coke, and natural graphite (PC-NG). Although natural graphite has a good reversible capacity, it has disadvaantages of a sharp decrease in capacity during high rate charging and potential plateaus. This may cause difficulties in perceiving the capacity variations as a function of electrical potential. The coke anodes have advantages without potential plateaus and a high rate capability, but they have a low reversible capacity. With PC anode composites, the petroleum pitch/cokes mixture at 1:4 with heat treatment at $1000^{\circ}C$ (PC14-1000C) showed relatively high electrochemical properties. With PC-NG anode composites, the proper graphite contents were determined at 10~30 wt.%. The composites with a given content of natural graphite and remaining content of various petroleum pitch/cokes mixtures at 1:4~4:1 mass ratios were heated at $800{\sim}1200^{\circ}C$. By increasing the content of petroleum pitch, reversible capacity increased, but a high rate capability decreased. For a given composition of carbonaceous composite, the discharge rate capability improved but the reversible capacity decreased with an increase in heat treatment temperature. The carbonaceous composites fabricated with a mixture of 30 wt.% natural graphite and 70 wt.% petroleum pitch/cokes mixture at 1:4 mass ratio and heat treated at $1000^{\circ}C$ showed relatively high electrochemical properties, of which the reversible capacity, initial efficiency, discharge rate capability (retention of discharge capacity in 10 C/0.2 C), and charge capacity at 5 C were 330 mAh/g, 79 %, 80 %, and 60 mAh/g, respectively.

• 대한화학회지
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• 제40권2호
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• pp.109-116
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• 1996

물시료 중 존재하는 흔적량 게르마늄을 전열 원자흡수 분광광도법으로 정랑하기 위해 사용되는 매트릭스 개선제의 종류와 사용량, 이에 따를 회화 및 원자화 온도의 변화, 보조제의 사용여부 및 양에 관하여 연구하였다. 게르마늄은 회화단계에서 이산화 게르마늄이 흑연로 성분인 탄소로 인해 휘발성 일산화 게르마늄으로 환원되에 감도 및 재현성을 저하시킨다. 따라서 개선제를 사용하여 게르마늄을 열적 및 화학적으로 안정화시켜야 한다. 이를 위해 단일 개선제를 사용할 경우 파라듐이 가장 좋은 효과를 나타내었다. 이 경우 원자화온도는 변화시키지 않지만, 회화온도는 800.deg.C에서 1, 000.deg.C로 올릴수 있었고 흡광도도 증가하였다. 이런 조건에서 팔라듐의 농도가 게르마늄에 대해 몰비로 14-100인 10-70.mu.g/mL까지 흡광도가 일정하였다. 보조개선제의 사용도 검토하였는데, 1% 수산화암모늄을 가하여 회화온도를 1, 000.deg.C까지 증가시켰다. 이제까지 검토한 최적조건을 바탕으로 광천수 3가지를 분석한 결과 게르마늄이 2.46, 1.60 및 0.020.mu./mL이었다. 끝으로, 시료에 일정량의 게르마늄을 첨가하여 얻은 회수율은 모두 95%이상으로 정량적이라고 할 수 있고, 검출한계는 6.9ng/mL로 흔적량 게르마늄 분석에 유용한 것으로 판단되었다.