• 한국자동차공학회논문집
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• 제19권2호
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• pp.98-104
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• 2011

The introduction of a diesel engine into the passenger car and light duty applications in the United States involves significant technical challenges for the automotive makers. This paper describes the SCR System optimization procedure for such a diesel engine application to meet Tier2 Bin5 emission regulation. A urea SCR system, a representative $NO_x$ reduction after-treatment technique, is applied to a 3.0 liter diesel engine. To achieve the maximum $NO_x$ reduction performance, the exhaust system layout was optimized using series of the computational fluid dynamics and the urea distribution uniformity test. Furthermore a comprehensive simulation model for the key factors influencing $NO_x$ reduction performance was developed and embedded in the Simulink/Matlab environment. This model was then applied to the urea SCR system and played a key role to shorten the time needed for SCR control parameter calibration. The potential of a urea SCR system for reducing diesel $NO_x$ emission is shown for FTP75 and US06 emission standard test cycle.

• 공업화학
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• 제31권3호
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• pp.323-327
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• 2020

이산화탄소 메탄화 공정 적용을 위해 저온에서 우수한 활성을 나타내는 Ni/CeO_2-X의 반응 특성을 조사하였다. 지지체인 CeO_2-X는 Ce(NO₃)₃를 400 ℃에서 열처리하여 획득하였으며, 촉매는 함침법으로 제조되었다. 실험의 운전 변수로써 반응기 내부 압력, 유입가스 중 산소, 메탄, 황화수소의 조성 및 반응 온도에 대하여 수행하였다. Ni/CeO_2-X를 이용한 이산화탄소 메탄화 반응에서 압력이 1 bar에서 3 bar로 증가함에 따라 CO₂ 전환율은 25% 이상 증가하였으며, 낮은 반응 온도에서 증가폭이 크게 나타났다. 유입가스 중 산소와 메탄은 촉매의 CO₂ 전환율을 최대 16, 4%씩 감소시켰으며, 산소와 메탄의 농도가 높아질수록 CO₂ 전환율의 감소율이 증가하는 경향을 나타내었다. 또한 황화수소는 촉매의 CO₂ 전환율을 최대 7% 감소시켰으며 촉매의 비활성화를 야기하였다. 본 연구의 결과들은 이산화탄소의 메탄화 공정 기초 자료로 유용하게 사용될 수 있을 것이다.

• 한국산학기술학회논문지
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• 제12권9호
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• pp.4250-4256
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• 2011

활성증진 물질 Cu가 첨가된 Mn계 촉매를 제조하여 암모니아를 이용하여 질소산화물을 제거하는 SCR공정에서 질소산화물제거능을 측정하였다. 제조된 촉매를 사용하여 반응온도, 유량, 수분함량 그리고 산소농도에 대한 활성변화를 조사하였다. $H_2$-TPR 시스템에서 온도에 따른 촉매의 수소전환특성을 측정하였다. 수분공급유무를 조절함으로써 촉매반응에 대한 수분의 억제효과를 파악하였다. Mn-Cu계 촉매는 $160{\sim}260^{\circ}C$의 온도범위에서 높은 탈질효율을 보였다. 그리고 산소농도의 증가는 촉매활성 증진효과를 가져왔으나 수분함유는 촉매활성을 감소시키는 역할을 함을 알 수 있었다.

• 한국결정성장학회지
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• 제16권5호
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• pp.216-221
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• 2006

Anatase $TiO_2$에 $WO_3$ 및 $V_2O_5$ 촉매를 첨가하여 SCR(selective catalytic reduction)용 분말을 합성하였으며, 촉매 첨가가 합성분말의 미세구조, 상합성 및 SCR 촉매능에 미치는 영향에 대해 연구하였다. 촉매의 지지체로 사용된 상용 anatase-$TiO_2$에서 rutile 단일상으로의 상전이 온도는 $1200^{\circ}C$이었다. 그러나 $WO_3$를 10wt% 첨가하면 이 상전이 온도가 $900^{\circ}C$로 낮아졌으며, $V_2O_5$를 첨가(5와 10wt%)할 경우 $650^{\circ}C$ 이하로 낮아졌다. $450^{\circ}C$에서 제조된 $WO_3(10wt%)/TiO_2$, SCR 분말은 $350^{\circ}C{\sim}400^{\circ}C$에서 100%에 가까운 우수한 $NO_x$ 변환효율을 보였다. $650^{\circ}C$에서 열처리한 경우, 보다 넓은 $300{\sim}400^{\circ}C$온도영역에서 100%가까운 우수한 촉매능을 보였다. $650^{\circ}C$에서 합성된 $V_2O_5(5wt%)/TiO_2$ 촉매분말은 넓은 온도범위($250^{\circ}C{\sim}350^{\circ}C$)에 걸쳐 100%에 달하는 가장 우수한 $NO_x$ 변환효율을 보였다. $650^{\circ}C$ 합성분말의 경우 10wt%의 $V_2O_5$ 첨가는 5wt% $V_2O_5$ 첨가 때 보다 분말물성과 촉매물성이 저하되었으며, 이는 $V_2O_5$의 높은 반응성으로 인한, 촉매의 입자성장에 따른 비표면적감소 때문으로 해석된다.

• 한국자동차공학회논문집
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• 제20권5호
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• pp.71-80
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• 2012

To improve the $NO_X$ conversion over a SCR (selective catalytic reduction) catalyst, the DOC (diesel oxidation catalyst) is usually placed upstream of the SCR catalyst to enhance the fast SCR reaction ($4NH_3+2NO+2NO_2{\rightarrow}4N_2+6H_2O$) using equimolar amounts of NO and $NO_2$. Here, a ratio of $NO_2/NO_X$ above 50% should be avoided, because the reaction with $NO_2$ only ($4NH_3+4NO+O_2{\rightarrow}4N_2+6H_2O$) is slower than the standard SCR reaction ($4NH_3+4NO+O_2{\rightarrow}4N_2+6H_2O$). In order to accurately predict the performance characteristics of SCR catalysts, it is therefore desired to develop a more simple and reliable mathematical and kinetic models on the oxidation kinetics of nitric oxide over a DOC. In the present work, the prediction accuracy and limit of three different chemical reaction kinetics models are presented to describe the chemicophysical characteristics and conversion performance of DOCs. Steady-state experiments with DOCs mounted on a light-duty four-cylinder 2.0-L turbocharged diesel engine then are performed, using an engine-dynamometer system to calibrate the kinetic parameters such as activation energies and preexponential factors of heterogeneous reactions. The reaction kinetics for NO oxidation over Pt-based catalysts is determined in conjunction with a transient one-dimensional (1D) heterogeneous plug flow reactor (PFR) model with diesel exhaust gas temperatures in the range of 115~$525^{\circ}C$ and space velocities in the range of $(0.4{\sim}6.5){\times}10^5\;h^{-1}$.

• 공업화학
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• 제34권5호
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• pp.507-514
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• 2023

촉매(Ag/γ-Al₂O₃) 충진형 유전체 장벽 방전 플라즈마 반응기를 이용한 질소산화물(NO_x)의 선택적 촉매 환원을 조사하였다. 촉매 상에서 간헐적으로 플라즈마를 발생시킬 때 NO_x의 환원제인 탄화수소가 부분 산화되어 알데하이드류를 생성하였으며, 알데하이드류의 높은 환원력으로 인해 촉매를 단독으로 사용한 경우에 비해 높은 NO_x 전환율을 보여주었다. 동일한 운전 조건(온도: 250 ℃; C/N: 8)에서 비교한 NO_x 저감 효율은 탄화수소(n-헵테인), 프로피온알데하이드, 뷰티르알데하이드에 대해 각각 47.5%, 92%, 96%로 나타났으며, 알데하이드류의 높은 질소산화물 환원 성능이 확인되었다. 간헐적 플라즈마 발생시 적정 조건을 파악하기 위하여, 고전압 on/off 주기를 0.5~3 min으로 조절하였고, 연속적인 플라즈마 발생의 경우와 동일한 에너지밀도에서 NO_x 저감 성능을 비교하였다. 고전압을 2 min 간격으로 on/off 하여 간헐적으로 플라즈마를 생성시켰을 때 연속적인 플라즈마 발생 대비 가장 높은 질소산화물 저감 효율이 얻어졌다. 동일한 에너지밀도에서도 간헐적 플라즈마 방전의 경우가 연속 플라즈마에 비해 높은 NO_x 저감 효율을 보이는 것은, 탄화수소가 분해되어 생성되는 알데하이드류 등의 중간생성물들이 NO_x 저감 반응에 보다 효율적으로 이용되었기 때문이다.

• 한국대기환경학회지
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• 제26권1호
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• pp.1-9
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• 2010

In this study, the selective catalytic reduction of $NO_x$ with ammonia was carried out in a filter bag support reactor. The experiments were performed by powder type $MnO_x$ and $V_2O_5$/$TiO_2$ catalyst at low temperature between 130 and $250^{\circ}C$. Also, the effect of $SO_2$ and $H_2O$ on the NO conversion was investigated under our test conditions. The powder type catalysts were analyzed by X-ray photoelectron spectrum (XPS), X-ray diffraction(XRD), scanning electron microscopy (SEM) and thermal gravimetric analysis (TGA). It was observed that NO removal efficiency of the powder type $V_2O_5$/$TiO_2$ catalyst was 85% at low temperature($200^{\circ}C$) under presence of oxygen and that of $MnO_x$ was 50% at the same condition. The powder type $V_2O_5$/$TiO_2$ catalyst, in conclusion, was found to be available for SCR reaction in a filter bag support system.

• International Journal of Naval Architecture and Ocean Engineering
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• 제7권6호
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• pp.1020-1033
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• 2015

In order to design a compact urea selective catalytic reduction system, numerical simulation was conducted by computational fluid dynamics tool. A swirl type static mixer and a mixing chamber were considered as mixing units in the system. It had great influence on flow characteristics and urea decomposition into ammonia. The mixer caused flow recirculation and high level of turbulence intensity, and the chamber increased residence time of urea-water-solution injected. Because of those effects, reaction rates of urea decomposition were enhanced in the region. When those mixing units were combined, it showed the maximum because the recirculation zone was significantly developed. $NH_3$ conversion was maximized in the zone due to widely distributed turbulence intensity and high value of uniformity index. It caused improvement of $NO_x$ reduction efficiency of the system. It was possible to reduce 55% length of the chamber and connecting pipe without decrease of $NO_x$ reduction efficiency.

• Restorative Dentistry and Endodontics
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• 제27권1호
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• pp.16-23
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• 2002

Physical properties of composite resins such as strength, resistance to wear, discoloration, etc depend on the degree of conversion of the resin components. The purpose of this study was to evaluate the degree of conversion of the composite resins according to the thickness of tooth structure penetrated by light and applied light curing time. The coronal portions of extracted human teeth (one anterior tooth, three posterior tooth) was embedded by pink denture material. the mounted teeth were cut into three illumination sections (1mm thickness enamel section, 1mm thickness dentin section, 2mm thicknes dentin section) and one backing section with cutting wheel. Thin resin films were made by using 6kg pressure between slide glass during 5 minutes Thin resin film was light cured on coupled illumination section during 40sec, 80sec and 120sec. each illumination section was coupled as follows; no tooth structure(X), ename section(E), enamel section + 1mm dentin section(ED1), enamel section + 2mm dentin section(ED2), enamel section + 1mm dentin section + 2mm dentin section(EDD). To simulate the clinical situation more closely, thin resin films was cured against a backing section of tooth structure. The degree of conversion of carbon double bonds to single bonds in the resin films were examined by means of Fourier Transform Infrared Spectrometer. The results were obtained as follows ; 1 As curing time was increased, conversion rate was increased and as tooth thickness which was penetrated by curing light was increased, conversion rate was decreased. 2. At all tooth thickness groups, conversion rate between 80sec and 120sec was not significantly increased(P＞0.05). 3. At 40sec group and 80sec, conversion rate between no tooth structure(X) group and 1mm enamel section(E) group was not significantly decreased(P＞0.05). 4. At 80sec group and 120sec, conversion rate between 1mm enamel section(E) group and 1mm enamel section + 1mm dentin section(ED1) group was not significantly decreased(P＞0.05).

• 한국세라믹학회지
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• 제40권11호
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• pp.1058-1061
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• 2003

Gallium Nitride (GaN) powders were synthesized by calcining a gallium(III) sulfate salt in flowing ammonia in the temperature range 500-1100$^{\circ}C$. The process of conversion of the salt to GaN was monitored by X-Ray Diffraction (XRD). The salt decomposed to ${\gamma}$-Ga$_2$O$_3$ and then converted to GaN without ${\gamma}$-${\beta}$Ga$_2$O$_3$ phase transition. Variations in XRD patterns and weight loss of samples with temperature indicate that the conversion of ${\gamma}$-Ga$_2$O$_3$ to GaN does not proceed through Ga$_2$O but stepwise via amorphous gallium oxynitride (GaO$\_$x/N$\_$y/) as intermediates. Room-temperature photoluminescence spectra of GaN powders obtained showed the emission peak at 363 nm and no yellow band.