• 한국자동차공학회논문집
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• 제15권5호
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• pp.105-111
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• 2007

In this study, we investigated the conversion performance of de-NOx catalyst for lean-burn natural gas engine. As a de-NOx catalyst, NOx storage reduction catalyst was composed of Pt, Pd and Rh with washcoat including Ba and Ni, Ru-ZSM-5. Ni, Ru-ZSM-5, which was regarded as a NOx direct decomposition catalyst, was made up of ion exchanged ZSM-5 by 5wt.% Ni or Ru. The performance of de-NOx catalyst was evaluated by NOx storage capacity and catalytic reduction in air/fuel, $\lambda=1.6$. The catalytic reaction was also observed when the added fuel was supplied to fuel rich atmosphere by fuel spike period of 5 seconds. The NOx conversion of the catalysts with Ni-ZSM-5 or Ru-ZSM-5 was mainly caused by the effect of NOx adsorption of Ba rather than the catalytic reduction of Ni, Ru-ZSM-5. Ni, Ru-ZSM-5 catalysts can not use for the NSR catalyst because they have quick process in thermal deactivation.

• Carbon letters
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• 제6권1호
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• pp.31-40
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• 2005

The carbon nanofibers (CNFs) were synthesized through the catalytic decomposition of hydrocarbons in a quartz tube reactor. The CNFs prepared from $C_3H_8$ at $550^{\circ}C$ was selected as the purification sample due to the higher content of impurity than that prepared from other conditions. In this study, we carried out the purification of CNFs by oxidation in air or carbon dioxide after acid treatment, and investigated the influence of purification parameters such as kind of acid, concentration, oxidation time, and oxidation temperature on the structure of CNFs. The metal catalysts could be easily eliminated from the prepared CNFs by liquid phase purification with various acids and it was verified by ICP analysis, in which, for example, Ni content decreased from 2.51% to 0.18% with 8% nitric acid. However, the particulate carbon and heterogeneous fibers were not removed from the prepared CNFs by thermal oxidation in air and carbon dioxide. This result can be explained by that the direction of graphene sheet in CNFs is vertical to the fiber axis and the CNFs are oxidized at about the similar rate with the impurity carbon.

• 대한화학회지
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• 제59권3호
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• pp.215-224
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• 2015

Unsymmetrical tetradentate Schiff base N-(2-hydroxy-5-methylacetophenone)-N'-(2-hydroxy acetophenone) ethylene diamine (H₂L) and its complexes with Cr(III), Mn(II), Fe(III), Co(II), Ni(II) and Cu(II) have been synthesized and characterized by elemental analyses, magnetic susceptibility measurements, IR, electronic spectra and thermogravimetric analyses. ¹H, ¹³C-NMR and FAB Mass spectra of ligand clearly indicate the presence of OH and azomethine groups. Elemental analyses of the complexes indicate that the metal to ligand ratio is 1:1 in all complexes. Infrared spectra of complexes indicate a dibasic quadridentate nature of the ligand and its coordination to metal ions through phenolic oxygen and azomethine nitrogen atoms. The thermal behavior of these complexes showed the loss of lattice water in the first step followed by decomposition of the ligand in subsequent steps. The thermal data have also been analyzed for the kinetic parameters by using Horowitz-Metzger method. The dependence of the electrical conductivity on the temperature has been studied over the temperature range 313-403 K and the complexes are found to show semiconducting behavior. XRD and SEM images of some representative complexes have been recorded. The antimicrobial activity of the ligand and its complexes has been screened against various microorganisms and all of them were found to be active against the test organisms. The Fe(III) and Ni(II) complex have been tested for the catalytic oxidation of styrene.

• 한국대기환경학회지
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• 제30권6호
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• pp.577-585
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• 2014

A series of experiments using atmospheric-pressure non-thermal plasma coupled with transition metal catalysts were performed to remove ethylene from agricultural storage facilities. The non-thermal plasma was created by dielectric barrier discharge, which was in direct contact with the catalyst pellets. The transition metals such as Ag and $V_2O_5$ were supported on ${\gamma}-Al_2O_3$. The effect of catalyst type, specific input energy (SIE) and oxygen content on the removal of ethylene was examined to understand the behavior of the hybrid plasma-catalytic reactor system. With the other parameters kept constant, the plasma-catalytic activity for the removal of ethylene was in order of $V_2O_5/{\gamma}-Al_2O_3$ > $Ag/{\gamma}-Al_2O_3$ > ${\gamma}-Al_2O_3$ from high to low. Interestingly, the rate of plasma-catalytic ozone generation was in order of $V_2O_5/{\gamma}-Al_2O_3$ > ${\gamma}-Al_2O_3$ > $Ag/{\gamma}-Al_2O_3$, implying that the catalyst activation mechanisms by plasma are different for different catalysts. The results obtained by varying the oxygen content indicated that nitrogen-derived reactive species dominated the removal of ethylene under oxygen-lean condition, while ozone and oxygen atoms were mainly involved in the removal under oxygen-rich condition. When the plasma was coupled with $V_2O_5/{\gamma}-Al_2O_3$, nearly complete removal of ethylene was achieved at oxygen contents higher than 5% by volume (inlet ethylene: 250 ppm; gas flow rate: $1.0Lmin^{-1}$; SIE: ${\sim}355JL^{-1}$).

• 한국진공학회지
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• 제20권1호
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• pp.70-76
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• 2011

전자 방출원 및 디스플레이 응용분야에서 우수한 가능성을 보이고 있는 이중벽 탄소나노튜브를 Tetrahydrofuran (THF) 열분해 방법으로 대량 합성하였다. 합성된 이중벽 탄소나노튜브는 불순물로 비정질 탄소와 금속촉매를 포함하고 있어, 이를 제거하기 위해 열처리와 과산화수소, 질산, 염산을 이용한 산 처리를 하였다. 정제된 이중벽 탄소나노튜브를 계면 활성제인 Sodium dodecylbenzenesulfonate (SDBS)를 사용하여 잉크를 제작하였고, 잉크를 스프레이 방법으로 Indium Tin Oxide (ITO)기판에 분무하여 전계방출을 위한 에미터를 제작하였다. 본 연구에서는 염산 처리 시간에 따른 이중벽 탄소나노튜브의 특성을 X-ray diffraction, Thermal Gravity Analysis (TGA) 측정을 통해 평가하였고, 염산 처리 시간이 증가할수록 전계방출 특성이 향상되는 것을 FE-current 측정으로 확인하였다.

• 대한기계학회논문집B
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• 제28권1호
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• pp.24-30
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• 2004

Analysis model for the two-phase catalytic reactor is presented. With the progress in development of micro thermofluidic devices, needs fur understanding of the phenomena in two phase reaction in cm scale has been arisen. To investigate thermal and reactive performance of down scaled two phase reactor simple analysis model that is a kind of lumped flow model is proposed. Analysis model presented is based on the experiment on mm scale model reactor. Target experiment is catalytic decomposition of 70wt％ hydrogen peroxide with existence of perovskite L $a_{0.8}$S $r_{0.2}$Co $O_3$ catalyst. It is composed of balance equations of mass and energy. Each phase is considered to be a species fur the simplicity. Axial diffusion and transversal distribution of properties are neglected. Two phase catalytic reaction is modeled as successive gasification of liquid lump around catalyst and reaction in gas phase. Heat transfer is modeled by model function ofNu number. Modeled Nu is expressed as Nu=N $u_{0}$ (1＋ $a_1$( $a_2$ $T^{-}$ $a_3$)exp( $a_4$ $T^{-1}$)exp( $a_{5}$ z). Transfer coefficients are determined by the comparison of experimental results. With the model, heat transfer characteristics are investigated. Also by the mass transfer coefficient, characteristics in mass transfer is investigated. With the result basic understanding on design and analysis of mm scale two-phase reactive device is obtained. Also it can be further applied to micro scale reactive device fabricated by micromachining.ing..

• 공업화학
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• 제19권1호
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• pp.17-26
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• 2008

기후변화협약에 이은 교토의정서가 발효되면서 온실가스 저감은 세계적인 당면 문제가 되어 있는 가운데 청정개발체제(CDM) 및 공동이행(JI) 등을 통한 배출권 확보가 국가적인 경쟁이 되고 있다. 이산화탄소($CO_2$) 및 메탄가스($CH_4$)와 더불어 대표적인 온실가스의 하나인 $N_2O$는 온난화효과가 $CO_2$에 비해 310배에 이르며 120년의 분해기간이 소요될 만큼 대기 중에서 매우 안정하여 성층권에서 오존층을 파괴하는 물질로 알려져 있다. 또한 $N_2O$는 분해하기가 쉽지 않아 고온 열분해 시키는 방법 외에 $400^{\circ}C$ 이상에서 촉매에 의해 선택적으로 분해시키는 방법이 알려져 있으나 대개 NOx가 같이 존재하여 $N_2O$ 분해를 방해하는 역할을 한다. 본 보문은 국내외의 $N_2O$ 발생원에 대한 내역과 더불어 각종 온실가스 저감사업에 의한 배출권 거래현황과 탄소시장의 성장 및 $N_2O$ 저감사업의 위치, $N_2O$ 촉매 분해에 관한 기술개발의 현황과 방향, 그리고 CDM 사업으로서의 전망 등을 분석 집약하였다.

• Bulletin of the Korean Chemical Society
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• 제29권6호
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• pp.1217-1223
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• 2008

A series of Zr,S co-doped $TiO_2$ were synthesized by a modified sol-gel method and characterized by various spectroscopic and analytical techniques. The presence of sulfur caused a red-shift in the absorption band of $TiO_2$. Co-doping of sulfur and zirconium (Zr-$TiO_2$-S) improves the surface properties such as surface area, pore volume, and pore diameter and also enhances the thermal stability of the anatase phase. The Zr-$TiO_2$-S systems are very effective visible-light active catalysts for the degradation of toluene. All reactions follow pseudo firstorder kinetics with the decomposition rate reaching as high as 77% within 4 h. The catalytic activity decreases in the following order: Zr-$TiO_2$-S >$TiO_2$-S >Zr-$TiO_2$>$TiO_2$$\approx$ P-25, demonstrating the synergic effect of codoping with zirconium and sulfur. When the comparison is made within the series of Zr-$TiO_2$-S, the catalytic performance is found to be a function of Zr-contents as follows: 3 wt % Zr-TiO2-S >0.5 wt % Zr-$TiO_2$-S> 5 wt % Zr-$TiO_2$-S >1 wt % Zr-$TiO_2$-S. Higher calcination temperature decreases the reactivity of Zr-$TiO_2$-S.

• 한국추진공학회지
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• 제25권2호
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• pp.98-109
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• 2021

극초음속 비행체용 능동냉각시스템의 전체적인 운용 성능을 결정하는 주요 요소는 크게 탄화수소흡열연료, 재생냉각 채널, 시스템 소재 및 구조로 구분되며, 그 중에서도 효율적인 재생냉각시스템 개발을 위한 일련의 연구는 탄화수소 항공유의 흡열반응 성능 향상으로부터 시작된다. 따라서 이전 연구에서는 탄화수소 항공유 자체의 흡열분해 특성에 대한 광범위한 연구 동향을 정리하였으며, 본 연구에서는 그에 대한 후속 연구로서 효과적인 흡열분해 특성 개선 및 성능 향상 방안으로 다양하게 시도되고 있는 촉매 분해와 수증기 개질 연구들에 대한 세부기술 분석을 수행하였다.

• 한국추진공학회:학술대회논문집
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• 한국추진공학회 2009년도 제33회 추계학술대회논문집
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• pp.93-96
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• 2009

고속 비행기술의 발전과 엔진효율의 향상은 비행체와 엔진의 열적부하를 증가시킨다. 극초음속까지 비행체의 속도가 빨라지면 공기흐름을 이용한 냉각이 어렵기 때문에 항공유를 주요 냉각제로서 사용하게 된다. 연료가 열 흡수원(Heat sink)으로서 사용될 때 열분해반응 또는 촉매분해반응과 같은 흡열반응(Endothermic reaction)을 거쳐 분해가 되는데 이러한 특성을 지닌 연료를 흡열연료(Endothermic fuels)라고 한다. 흡열반응은 촉매를 통해 개선될 수 있지만, 코킹침적이 형성되기 이전까지의 온도로 제한된다. 본 연구에서는 흡열연료에 관련된 주요 기술을 조사하여 기초연구에 활용하고자 하였다.