• 제목/요약/키워드: Low Temperature Reaction

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INFRARED ABSORPTION MEASUREMENT DURING LOW-TEMPERATURE PECVD OF SILICON-OXIDE FILMS

  • Inoue, Yasushi;Sugimura, Hiroyuki;Takai, Osamu
    • 한국표면공학회지
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    • 제32권3호
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    • pp.297-302
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    • 1999
  • In situ measurement of infrared absorption spectra has been performed during low-temperature plasma-enhanced chemical vapor depositiion of silicon-oxide films using tetramethoxysilane as a silicon source. Several absorption bands due to the reactant molecules are clearly observed before deposition. In the plasma, these bands completely disappear at any oxygen mixing ratio. This result shows that most of the tetramethoxysilane molecules are dissociated in the rf plasma, even C-H bonds. Existence of Si-H bonds in vapor phase and/or on the film surface during deposition has been found by infrared diagnostics. We observed both a decrease in Si-OH absorption and an increase in Si-O-Si after plasma off, which means the dehydration condensation reaction continues after deposition. The rate of this reaction is much slower than the deposition ratio of the films.

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이산화탄소 농도에 따른 드레이톤 탄의 저온 차-이산화탄소 가스화반응 모델링 비교 (Comparative Modeling of Low Temperature Char-CO2 Gasification Reaction of Drayton Coal by Carbon Dioxide Concentration)

  • 박지윤;이도균;황순철;김상겸;이상헌;윤수경;유지호;이시훈;이영우
    • 청정기술
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    • 제19권3호
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    • pp.306-312
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    • 2013
  • 드레이톤 탄으로부터 제조된 차(char)의 $850^{\circ}C$ 등온조건 가스화 반응에서 반응기체인 이산화탄소-질소 혼합기체의 이산화탄소 농도가 반응속도에 미치는 영향에 대해 알아보았다. 저온 가스화 반응성을 높이기 위해 탄산칼륨을 사용하였다. 이산화탄소의 농도가 증가할수록 차-이산화탄소(char-$CO_2$) 가스화 반응성은 좋으며 전환율 증가 속도는 고농도에서는 일정하게 유지되었다. 가스화 반응성은 증가하였으며, 70% 이상의 고농도 조건에서는 일정하게 유지되었다. 기-고체 반응모델 중에서 shrinking core model (SCM)과 shrinking core model (SCM), modified volumetric reaction model (MVRM)을 비교하였다. 선형 회귀를 통해 얻은 상관계수 값은 저농도에서는 SCM이 VRM보다 높은 반면, 고농도에서는 VRM이 SCM보다 높은 값을 보였다. 모든 농도에서 MVRM의 상관계수 값은 다른 모델들 보다 가장 높은 값을 보였다.

바나디움 산화물의 환원 및 질화반응으로부터 얻어진 바나디움 산화질화물의 제조, 특성분석 및 암모니아 분해반응에서의 촉매 활성 (Synthesis, Characterization and Ammonia Decomposition Reaction Activity of Vanadium Oxynitride Obtained from the Reduction/Nitridation of Vanadium Oxide)

  • 윤경희;신채호
    • Korean Chemical Engineering Research
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    • 제60권4호
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    • pp.620-629
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    • 2022
  • 가열 속도, 몰 공간속도, 질화반응온도 등 다양한 실험 조건을 변화하며 바나디움 산화물과 암모니아와의 승온 질화반응을 통하여 바나디움 산화질화물을 제조하여 특성분석을 수행하였으며 제조된 바나디움 산화질화물 상에서 암모니아 분해반응의 촉매 활성을 검토하였다. 제조된 촉매의 물리·화학적 특성을 알아보기 위하여 N2 흡착분석, X-선 회절분석(XRD), 수소 승온환원(H2-TPR), 산소 존재 하 승온산화 (TPO), 암모니아 탈착 (NH3-TPD), 투과전자현미경(TEM) 분석을 수행하였다. 340 ℃에서 5 m2 g-1의 낮은 비표면적을 갖는 V2O5의 환원에 의하여 V2O3 으로의 변환은 미세 기공 형성에 의해 115 m2 g-1 높은 비표면적 값을 보여주었으며 그 이상의 질화반응 온도가 증가함에 따라 소결현상에 의해 지속적인 비표면적의 감소를 초래하였다. 비표면적에 가장 큰 영향을 미치는 질화반응 변수는 반응온도였으며, 단일 상의 VNxOy의 x + y 값은 질화반응온도가 증가함에 따라 1.5에서 1.0으로 근접하였으며 680 ℃의 높은 반응온도에서 입방 격자상수 a는 VN 값에 근접하였다. 본 실험 조건 중에 질화반응온도가 가장 높았던 680 ℃에서 암모니아 전환율은 93%로 나타났으며 비활성화는 관찰되지 않았다.

Oxalate 침전을 이용한 Li-과량 LiMn$_2$O$_4$ Spinel의 습식합성가 분말 특성 (Wet Chemical Preparation of Li-rich LiMn$_2$O$_4$ Spinel by Oxalate Precipitation)

  • 이병우;김세호
    • 한국세라믹학회지
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    • 제36권7호
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    • pp.698-704
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    • 1999
  • Li rich Li1+xMn2-xO4(x=0.07) spinel powders were prepared by an oxalate precipitation of wet chemical methods at temperature lower than $600^{\circ}C$. The FTIR results showed that the powders prepared at $600^{\circ}C$ had high degree of crystal quality comparing with the spinel powders prepared by solid state reaction at 75$0^{\circ}C$ which was the lowest synthesis temperature of the solid state reaction method. The particle size of powders prepared by the oxalate precipitation at $600^{\circ}C$ was smaller than 0.2${\mu}{\textrm}{m}$ and the specific surface area was 11.01 m2/g A heat treatment over 90$0^{\circ}C$ formed second phase in the precipitates. It was shown that there were phase transitions at temperatures. T1,T2 and T2. The transitions involved weight loss and gain during heating and cooling. The low temperature synthesis below $600^{\circ}C$ avoided the second phase formation and the prepared powders showed improved compositional and physical properties for secondary lithium battery applications.

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귀금속계열 WGS 촉매 연구 (Noble metal catalysts for Water Gas Shift reaction)

  • 임성광;배중면;김선영
    • 대한기계학회:학술대회논문집
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    • 대한기계학회 2007년도 춘계학술대회B
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    • pp.2228-2231
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    • 2007
  • Water gas shift reactor in fuel processing is an important part that converts carbon monoxide into hydrogen. Fuel processing system for PEMFC usually has two stages of WGS reactors, which are high temperature and low temperature shifter. In this study we prepared noble metal catalysts and compared their performances with that of a commercial iron chromium oxide catalyst. Noble metal catalysts and the commercial catalyst showed quite different temperature dependence of carbon monoxide conversion. The conversion of carbon monoxide at the commercial catalyst was very low at medium temperature(${\sim}300^{\circ}C$) and increased rapidly as temperature increased while the conversion at noble metal catalysts was high in the medium temperature range and decreased as temperature increased, which is thermodynamically expected. Their characteristics agreed well with the literature published, and we are accomplishing further study for improvement of the noble metal catalysts.

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MgO-$Al_2O_3$-$SiO_2$계 요업원료의 제조 및 소결특성 -에멜젼법에 의한 Spinel 분체의 저온합성- (Low-Temperature Synthesis of Spinel Powders by the Emulsion Technique)

  • 현상훈;이희수;김의수
    • 한국세라믹학회지
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    • 제27권5호
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    • pp.661-667
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    • 1990
  • Spinel powders were synthesized at the comparatively low-temperature range(800~90$0^{\circ}C$) by the emulsion-hot kerosene drying method and the effects of kerosene-evaporative conditions on powder characteristics were investigated. In emulsion drying, more unagglomerated and sinterable powders could be synthesized through rapid evaporation of emulsion at the higher kerosene temperature. The completion of formation reaction of spinel observed at the low-temperature range confirmed the high reactivity of powders. The relative theoretical density and the fracture toughness of spinel pellets sintered at 1$650^{\circ}C$ for 4hrs. were 98% and 2.1MN/m3/2, respectively.

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Spin-on Glass를 이용한 실리콘과 유리의 저온 접합 공정 (Low Temperature Bonding Process of Silicon and Glass using Spin-on Glass)

  • 이재학;유중돈
    • Journal of Welding and Joining
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    • 제23권6호
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    • pp.77-86
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    • 2005
  • Low temperature bonding of the silicon and glass using the Spin-on Glass (SOG) has been conducted experimentally to figure out the effects of the SOG solution composition and process variables on bond strength using the Design of Experiment method. In order to achieve the high quality bond interface without rack, sufficient reaction time of the optimal SOG solution composition is needed along with proper pressure and annealing temperature. The shear strength under the optimal SOG solution composition and process condition was higher than that of conventional anodic bonding and similar to that of wafer direct bonding.

Zinc Aluminate 촉매를 이용한 고압연속식 고정층 반응기에서의 바이오디젤 제조 (Biodiesel Production with Zinc Aluminate Catalysts in a High-Pressure-Fixed-Bed-Reactor)

  • ;;김선욱;신은우
    • Korean Chemical Engineering Research
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    • 제46권1호
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    • pp.189-193
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    • 2008
  • 본 연구는 zinc aluminate 촉매를 사용한 고압연속식 고정층 반응시스템에서의 대두유와 메탄올의 transesterification에 관한 것이다. 바이오디젤 제조를 위한 고압 연속식 고정층 촉매 반응에서 반응 조건이 메틸에스터 생성에 미치는 영향이 주로 조사되었다. 촉매가 없는 경우, 거의 모든 반응 조건에서 메틸에스터의 수율이 4.5% 이하로 매우 낮았지만, $300^{\circ}C$, 1,200 psi 조건에서는 19%의 메틸에스터 수율을 보여 주었다. 이는 반응 조건이 메탄올의 초임계점에 근접하였기 때문으로 보인다. 촉매 반응에서는 무촉매 반응과 비교하여 비교적 낮은 온도와 압력에서도 높은 메틸에스터 수율을 보여주었다. 또한 수율에 미치는 반응 조건의 영향을 살펴본 결과, 반응온도, 압력, 반응물에서 메탄올 몰비가 높을수록 높은 메틸에스터 수율을 보여주었다. 반응 변수 중에서도 반응온도가 메틸에스터 수율에 가장 큰 영향을 미치는 것으로 확인되었다.

디젤 자열개질 가스 내 포함된 $C_2H_4$ 제거를 위한 후개질기 촉매 활성 실험 (Activity test of post-reforming catalyst for removing the ethylene in diesel ATR reformate)

  • 윤상호;배중면;이상호
    • 한국신재생에너지학회:학술대회논문집
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    • 한국신재생에너지학회 2009년도 추계학술대회 논문집
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    • pp.218-221
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    • 2009
  • Solid oxide fuel cells (SOFCs), as high-temperature fuel cells, have various advantages. In some merits of SOFCs, high temperature operation can lead to the capability for internal reforming, providing fuel flexibility. SOFCs can directly use CH4 and CO as fuels with sufficient steam feeds. However, hydrocarbons heavier than CH4, such as ethylene, ethane, and propane, induce carbon deposition on the Ni-based anodes of SOFCs. In the case of the ethylene steam reforming reaction on a Ni-based catalyst, the rate of carbon deposition is faster than among other hydrocarbons, even aromatics. In the reformates of heavy hydrocarbons (diesel, gasoline, kerosene and JP-8), the concentration of ethylene is usually higher than other low hydrocarbons such as methane, propane and butane. It is importatnt that ethylene in the reformate is removed for stlable operation of SOFCs. A new methodology, termed post-reforming was introduced for removing low hydrocarbons from the reformate gas stream. In this work, activity tests of some post-reforming catalysts, such as CGO-Ru, CGO-Ni, and CGO-Pt, are investigated. CGO-Pt catalyst is not good for removing ethylene due to low conversion of ethylene and low selectivity of ethylene dehydrogenation. The other hand, CGO-Ru and CGO-Ni catalysts show good ethylene conversion, and CGO-Ni catalyst shows the best reaction selectivity of ethylene dehydrogenation.

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