• 한국산학기술학회논문지
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• 제12권1호
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• pp.537-544
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• 2011

본 연구에서는 탄화수소가스 중에서 가장 발화온도가 높은 메탄을 대상으로 전이금속 촉매의 산화반응 특성을 수행하였다. 망간의 경우 MnO, $MnO_2$, $Mn_2O_3$, $Mn_3O_4$, $Mn_4O_5$와 같이 다양한 산화가를 나타내므로 산화망간을 선택하여 메탄산화반응실험을 실시하였다. 메탄의 산화를 위한 전이금속 촉매중 망간을 산화물형태로 $Al_2O_3$, $TiO_2$에 담지하였으며, 조촉매로는 Ni, Co 등을 이용하여 활성능과 수명의 향상을 연구하였다. 본 연구에서 촉매 제조는 과잉용액 함침법을 사용하였다. 촉매의 활성화에너지, $T_{50}$, $T_{90}$을 계산하기 위하여 온도와 공간속도에 대한 전환율을 측정하였다. Mn-Co, Mn-Ni의 두성분의 전이금속촉매의 수명이 망간촉매에 비하여 10%이상 증가하고 활성은 약간 감소함을 알 수 있었다.

• 한국광학회지
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• 제7권4호
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• pp.348-356
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• 1996

기체의 순간 온도를 측정할 수 있는 펄스 레이저를 사용한 이동형 CARS 분광기를 제작하였다. 이 분광기의 측정 프로그램은 측정한 스펙트럼으로 부터 온도를 얻기 위하여 8가지의 빠른 온도 계산법과 최소제곱법을 포함하고 있다. 빠른 온도 계산법 중 두 가지는 최소제곱법 보다 계산 시간은 훨씬 덜 걸리면서 온도의 분산이 작은 측정 결과를 준다. CARS 온도의 정밀 정확도는 복사온도계를 기준으로 흑연관 흑체로에서 측정하였다. 1000K부터 2400K의 온도 영역에서 정확도는 .+-.2% 이내이고 정밀도는 가장 정밀한 결과를 주는 빠른 온도 계산법을 적용할 때 1600K에서 .+-.35K이다. 순간 온도 측정의 적용 예를 보이기 위하여 이 분광기를 정해진 조건에 있는 난류 연소의 측정에 적용하였다.

• 한국전기전자재료학회논문지
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• 제22권4호
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• pp.342-349
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• 2009

This study investigated the growth characteristics of carbon nanotubes (CNTs) by changing a period of annealing time and a $C_{2}H_{2}/H_2$ flow ratio at temperature as low as $450^{\circ}C$ with inductively coupled plasma chemical vapor deposition. The 1-nm-thick Fe-Ni-Co alloy thin film served as a catalyst layer for the growth of CNTs, which was thermally evaporated on the 15-nm-thick Al underlayer deposited on the 50-nm-thick Ti diffusion barrier. The annealing at low temperature of $450^{\circ}C$ brought about almost no granulation of the catalyst layer, and the CNT growth was not affected by a period of annealing time. A study of changing the flow rate of $C_{2}H_{2}$ and $H_2$ showed that as the ratio of the $C_{2}H_{2}$ flow rate to the $H_2$ flow rate was lowered, the CNTs were grown to be longer With further decreasing the flow ratio, the length of CNTs reached the maximum and then became shorter. Under the optimized gas flow rates, we successfully synthesized CNTs with a uniform length over a 4-inch Si wafer at $450^{\circ}C$.

• 센서학회지
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• 제13권2호
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• pp.96-100
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• 2004

Optical fiber sensors have been used to detect small amounts of chemical species. In this work, a new thin polymer-clad fiber sensor is developed. Polyaniline is chemically synthesized and thin clad layers of the polymer are easily deposited on optical fiber by dip-coating technique. The optical property of polyaniline as a sensing material is analyzed by UV-Vis-NIR. The light source is stabilized He-Ne laser at 635 nm wavelength with 1 mW power. The light power transmitted through the optical fiber is measured with a spectrophotometer. By selecting a fixed incident angle, variation of transmitted light intensity through the optical fiber can be detected as gas molecules absorbed in the polyaniline clad layer. Among the various gases, the fabricated optical fiber sensor shows good sensitivity to $NH_{3}$ gas. The optical fiber sensors was shown more improved properties than polymer based sensors which measure conductivity changes.

• 멤브레인
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• 제19권3호
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• pp.237-243
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• 2009

본 연구는 polyimide (Pl)막에 2,2'-bis(3,4-carboxylphenyl) hexafluoropropane dianhydride (6FDA)과 4,4'-dia-minodiphenylmethane (DAM)을 이용하여 폴리이미드 막을 중합반응을 통해 합성하였고, 합성된 Pl막을 5분에서 20분까지 설폰화 반응을 통해 막에 설폰산기를 도입하였다. 개질된 막에 대한 기체 투과도와 분리요인을 단일 기체인 $N_2$, $O_2$, $CO_2$에 대해 조사하였다. 설폰화 반응을 진행한 모든 범위의 시간에서 bulky한 그룹의 $-{SO_3}H$의 도입으로 인하여 확산도와 용해도는 모두 감소되었다. 설폰화 반응 시간이 20분 경과하였을 때, $N_2$ 가스의 확산도와 용해도는 각각 21%와 26%까지 감소하였다. 결과적으로 설폰화 반응이 20분이 지났을 때 $O_2/N_2$와 $CO_2/N_2$의 분리 효율은 증가하는 것을 알 수 있었다.

• 한국재료학회지
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• 제23권1호
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• pp.47-52
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• 2013

Graphene has been synthesized on 100- and 300-nm-thick Ni/$SiO_2$/Si substrates with $CH_4$ gas (1 SCCM) diluted in mixed gases of 10% $H_2$ and 90% Ar (99 SCCM) at $900^{\circ}C$ by using inductively-coupled plasma chemical vapor deposition (ICP-CVD). The film morphology of 100-nm-thick Ni changed to islands on $SiO_2$/Si substrate after heat treatment at $900^{\circ}C$ for 2 min because of grain growth, whereas 300-nm-thick Ni still maintained a film morphology. Interestingly, suspended graphene was formed among Ni islands on 100-nm-thick Ni/$SiO_2$/Si substrate for the very short growth of 1 sec. In addition, the size of the graphene domains was much larger than that of Ni grains of 300-nm-thick Ni/$SiO_2$/Si substrate. These results suggest that graphene growth is strongly governed by the direct formation of graphene on the Ni surface due to reactive carbon radicals highly activated by ICP, rather than to well-known carbon precipitation from carbon-containing Ni. The D peak intensity of the Raman spectrum of graphene on 300-nm-thick Ni/$SiO_2$/Si was negligible, suggesting that high-quality graphene was formed. The 2D to G peak intensity ratio and the full-width at half maximum of the 2D peak were approximately 2.6 and $47cm^{-1}$, respectively. The several-layer graphene showed a low sheet resistance value of $718{\Omega}/sq$ and a high light transmittance of 87% at 550 nm.

• 한국세라믹학회지
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• 제35권11호
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• pp.1171-1181
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• 1998

$SrZr_{0.95}$$Y_{0.05}$$O_{2.975}$ powder was synthesized by ultrasonic spray pyrolysis using a solution that Sr carbonate and Zr and Y nitrates were dissolved in a citric acid solution. The processes of particle formation were in-vestigated with respect to solution properties and pyrolysis temperature. With changing the solution con-centration form 0.1M to 0.01M there was a tendency that average sizes of droplets and particles were de-creased and their size distributions were narrowed. Citrate functional groups converted the droplets into gel particles which prevented an inhomogeneous precipitation of the metal ions and facilitated the diffusion of gases during thermal decomposition. As a result the powder having spherical particles without hollow par-ticles could be prepared. Low pyrolysis temperature led to amorphous particles due to incomplete pyrolysis and made the particles difficult to maintain spherical shape due to retarded gelation of the droplets. Whereas higher pyrolysis temperature produced hollow and broken particles because the droplets un-derwent rapid gelationand decomposition. The particles obtained at two pyrolysis temperature $500^{\circ}$and $1000^{\circ}C$ consisted of a perovskite phase and a very small amount of $SrCO_3$ However after calcination at $1000^{\circ}C$ the particles contained a single perovskite phase having an average particle size of 0.63${\mu}{\textrm}{m}$ and an apparent density near to the theoretical density.

• 센서학회지
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• 제29권6호
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• pp.388-393
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• 2020

In this study, a PbS quantum dots (QDs)-based H₂ gas sensor with a Pd electrode was proposed. QDs have a size of several nanometers, and they can exhibit a high surface area when forming a thin film. In particular, the NH₂ present in the ligand of PbS QDs and H₂ gas are combined to form NH₃⁺, subsequently the electrical characteristics of the QDs change. In addition to the resistance change owing to the reaction between Pd and H₂ gas, the resistance change owing to the reaction between the NH₂ of PbS QDs and H₂ gas increases the current signal at the sensor output, which can produce a high output signal for the same concentration of H₂ gas. Using the XRD and absorbance properties, the synthesis and particle size of the synthesized PbS QDs were analyzed. Using PbS QDs, the sensitivity was significantly improved by 44%. In addition, the proposed H₂ gas sensor has high selectivity because it has low reactivity with heterogeneous gases such as C₂H₂, CO₂, and CH₄.

• 한국표면공학회지
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• 제37권6호
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• pp.360-365
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• 2004

Ti$_3$SiC$_2$ material was synthesized via the powder metallurgical route, and oxidation tested between 900 and $1200^{\circ}C$ in air for up to 100 hr. The oxidation of $Ti_3$$SiC_2$ material resulted in the formation of $TiO_2$and $SiO_2$, accompanying the evolution of CO or $CO_2$ gases from the initial stage of oxidation. The oxidation resistance of $Ti_3$$SiC_2$ mainly owes the protectiveness of highly stoichiometric $SiO_2$. During the initial stage of oxidation, the dominant reaction was the inward transport of oxygen into the matrix. As the oxidation progressed, an outer $TiO_2$ layer and an inner ( $TiO_2$ + $SiO_2$) mixed layer formed. Between these layers and inside the oxide scale, numerous fine voids formed. Numerous, fine oxide grains formed at $900^{\circ}C$ developed into the outer coarse $TiO_2$ grains and an inner fine ($TiO_2$ + $SiO_2$) mixed grains at the higher temperatures. The oxidation resistance of$ Ti_3$SiC$_2$ progressively deteriorated as the oxidation temperature increased, forming thick scales above $1000^{\circ}C$. The outer coarse $TiO_2$ grains formed above $1100^{\circ}C$ grew rapidly mainly along (211).

• 멤브레인
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• 제25권6호
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• pp.488-495
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• 2015

Trimethylamine과 chloromethyl ethyl ether를 사용하여 PPO를 기반으로 하는 APPO를 제조하여 특성평가를 진행하였다. 전기 물리적 특성을 알아보기 위해 8 wt%의 APPO chloroform 용액으로 APPO막을 제막하여 특성평가를 진행하였다. 접촉각은 $44.4^{\circ}$, 함수율은 37.9%의 결과값을 얻을 수 있었다. 전기적 특성인 이온교환용량과 이온전도도는 각각 2.3 meq/g, 0.027 S/cm로 측정되었다. 또 time-lag 장치를 이용하여 단일기체(질소, 산소, 메탄, 이산화탄소, 이산화황)에 대한 확산도 및 용해도를 알아보았다. 산성가스인 이산화탄소와 황산의 경우, 투과도는 각각 20.7, 511.5 barrer로 측정되었다. 선택도의 경우, 이산화탄소/메탄은 39.8, 이산화탄소/질소는 42.2, 이산화황/이산화탄소는 24.7로 측정되었다.