• 대한환경공학회지
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• 제29권12호
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• pp.1329-1336
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• 2007

본 연구에서는 간헐적으로 발생되는 고농도의 NO를 효율적으로 제거할 수 있는 혼합 공정으로 선택적촉매환원(Selective Catalytic Reduction, SCR)과 활성탄소섬유(Activated Carbon Fiber, ACF)흡착이 결합된 신 개념의 공정을 설계하고 특성을 고찰하였다. NO를 흡착한 ACF에 열과 진공을 동시에 가하여 재생 실험을 수행한 결과, $140^{\circ}C$에서 600 mmHg의 진공으로 탈착하였을 때 가장 높은 재생효율을 보였다. SCR공정에는 상용촉매를 사용하였으며, 반응온도 $300^{\circ}C$, $NO/NH_3$몰비 1.0인 조건에서 실험을 수행하였다. ACF 재생공정에서 발생한 NO를 SCR공정으로 처리하였을 경우 98%의 매우 우수한 제거효율을 보였다. 그러나 지속적으로 유입되는 300ppm의 NO와 ACF에서 탈착되는 NO를 기존의 SCR공정에서 동시에 처리하였을 때 약 1분간 고농도의 NO가 배출되었다. 따라서 ACF의 재생시 발생하는 고농도의 NO를 기존의 SCR공정에서 병행처리할 때는 탈착속도를 조절하거나 고농도로 배출되는 짧은 시간 동안 $NH_3$농도를 높여서 주입할 필요가 있으며, 소규모의 SCR공정을 추가로 설치하여야 한다. SCR과 ACF를 결합한 공정을 이용하여 NO를 처리하였을 때, 간헐적으로 2배의 농도를 가지는 NO가 유입되어도 80% 이상의 탈질 효율을 가지는 공정의 구현이 가능하였으며, 반복 사용에도 활성이 유지되어 안정적인 운전이 가능함을 입증하였다.

• 자연과학논문집
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• 제17권1호
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• pp.13-29
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• 2006

산화-환원 활성 단백질중에 하나인 설피레독신과의 결합 단백질을 효모 Two-hybrid 기법을 이용하여 탐색한 결과, 알파-만노시다제가 설피레독신과 특이적으로 결합함을 밝혔다. 알파-만노시다제는 D-만노스 당을 비환원성 말단으로부터 유리시키는 가수분해 효소로서, 세포 원형질에 다량체 형태로 존재한다. 본 연구에서는 설피레독신과 알파-만노시다제간의 단백질결합을 설피레독신의 새로운 생리기능 관점에서 토의했다.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2012년도 제42회 동계 정기 학술대회 초록집
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• pp.556-556
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• 2012

Transition metal-based organometallic complexes have shown great talents as a catalyst in various reactions. Designing organic molecules and coordinating them to such active centers have been a promising route to control the catalytic natures. Metallocene, which has transition metal atoms sandwiched by aromatic rings, is one of the representative systems for organometallic catalysts. Group 4-based metallocene catalysts have been most commonly used for the production of polyolefins, which have great world-wide markets in the real life. Graphenes and carbon nanotubes (CNTs) were composed of extended $sp^2$ carbon networks, showing high electron mobility as well as have extremely large steric bulkiness relative to metal centers. We were inspired by these characteristics of such carbon-based nano-materials and assumed that they could intimately interact with active centers of metallocene catalysts. We examined this hypothesis and, recently, reported that CNTs dramatically changed catalytic natures of group 4-based catalysts when they formed hybrid systems with such catalysts. In conclusion, we produced hybrid materials composed of group-4 based metallocenes, $Cp_2ZrCl_2$ and $Cp_2TiCl_2$, and carbon-based nano-materials such as RGO and MWCNT. Such hybrids were generated via simple adsorption between Cp rings of metallocenes and graphitic surfaces of graphene/CNT. The hybrids showed interesting catalytic behaviors for ethylene polymerizations. Resulting PEs had significantly increased Mw relative to those produced from free metallocene-based catalytic systems, which are not adsorbed on carbon-based nano-materials. UHMWPEs with extremely high Mw were obtained at low Tp.

• 한국추진공학회:학술대회논문집
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• 한국추진공학회 2017년도 제48회 춘계학술대회논문집
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• pp.117-119
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• 2017

본 논문에서는 하이브리드 로켓의 자동점화를 위한 다단 방식의 촉매점화시스템에 관한 연구를 수행하였다. 다단 촉매점화기의 열분해 성능을 평가하기 위해 1단 점화기에 촉매를 충전하여 예열 후, 1단 점화기와 2단 점화기에 각각 저유량과 고유량을 공급하여 실험을 진행하였다. 이때 저유량의 $N_2O$가스를 분해하여 생성된 고온의 가스로 고유량의 $N_2O$가스를 분해하였다. 실험 결과 기존 점화기보다 점화 시간이 감소되었다. 또한 1단 점화기에서 분해된 가스를 이용하여 2단 점화기에 공급된 고유량 $N_2O$가스의 분해 가능성을 확인하였다.

• 대한금속재료학회지
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• 제50권3호
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• pp.201-205
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• 2012

The effects of various manganese precursors for the low-temperature selective catalytic reduction (SCR) of $NO_x$ were investigated in terms of structural, morphological, and physico-chemical analyses. $MnO_x/TiO_2$ catalysts were prepared from three different precursors, manganese nitrate, manganese acetate(II), and manganese acetate(III), by the sol-gel method. The manganese acetate(III)-$MnO_x/TiO_2$ catalyst tended to suppress the phase transition from the anatase structure to the rutile or the brookite after calcination at $500^{\circ}C$ for 2 h. It also had a high specific surface area, which was caused by a smaller particle size and more uniform distribution than the others. The change of catalytic acid sites was confirmed by Raman and FT-IR spectroscopy and the manganese acetate(III)-$MnO_x/TiO_2$ had the strongest Lewis acid sites among them. The highest de-NOx efficiency and structural stability were achieved by using the manganese cetate(III) as a precursor, because of its high specific surface area, a large amount of anatase $TiO_2$, and the strong catalytic acidity.

• Korean Journal of Chemical Engineering
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• 제35권12호
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• pp.2442-2451
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• 2018

Novel highly active visible-light photocatalysts in the form of zinc bismuth oxide ($ZnBi_2O_4$) and graphite hybrid composites were prepared by coupling via a co-precipitation method followed by calcination at $450^{\circ}C$. The asprepared $ZnBi_2O_4$-graphite hybrid composites were tested for the degradation of rhodamine B (RhB) solutions under visible-light irradiation. The existence of strong electronic coupling between the two components within the $ZnBi_2O_4$-graphite heterostructure suppressed the photogenerated recombination of electrons and holes to a remarkable extent. The prepared composite exhibited excellent photocatalytic activity, leading to more than 93% of RhB degradation at an initial concentration of $50mg{\cdot}L^{-1}$ with 1.0 g catalyst per liter in 150 min. The excellent visible-light photocatalytic mineralization of $ZnBi_2O_4-1.0graphite$ in comparison with pristine $ZnBi_2O_4$ could be attributed to synergetic effects, charge transfer between $ZnBi_2O_4$ and graphite, and the separation efficiency of the photogenerated electrons and holes. The photo-induced $h^+$ and the superoxide anion were the major active species responsible for the photodegradation process. The results demonstrate the feasibility of $ZnBi_2O_4-1.0graphite$ as a potential heterogeneous photocatalyst for environmental remediation.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2012년도 제43회 하계 정기 학술대회 초록집
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• pp.169-169
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• 2012

The high-temperature superconductor YBa2Cu3O7-x (YBCO) have attached attentions because of a high superconducting transition temperature, low surface resistance, high superconducting critical current density (Jc), and superior superconducting capability under magnetic field. Moreover, the Jc of YBCO superconductors can be enhanced by adding impurities to the YBCO films for vortex-pinning. Understanding and controlling pinning centers are key factors to realize high Jc superconductors. We synthesized vertically-aligned ZnO nanorods on SrTiO3 (STO) substrates by catalyst-free metal-organic chemical vapor deposition (MOCVD), and subsequently, deposited YBCO films on the ZnO nanorods/STO templates using pulsed laser deposition (PLD). The various techniques were used to analyze the structural and interfacial properties of the YBCO/ZnO nanorods/STO hybrid structures. SEM, TEM, and XRD measurements demonstrated that YBCO films on ZnO nanorods/STO were well crystallized with the (001) orientation. EXAFS measurements from YBCO/ZnO nanorods/STO at Cu K edge demonstrated that the local structural properties around Cu atoms in YBCO were quite similar to those of YBCO/STO.

• 한국수소및신에너지학회논문집
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• 제24권3호
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• pp.193-199
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• 2013

In this work, thin film type Cu/ZnO nanostructure catalysts were fabricated by several synthetic routes in order to maximize the performance of the micro reforming system. For this work, various Cu/ZnO nanostructure catalysts could be synthesized by means of four approaches which are chemical vapor method, wet solution method and their hybrid method. The reforming performance of these as-synthetic catalysts was evaluated as compared to the conventional catalysts. Among the as-synthetic nanostructures, sphere type catalysts with specific surface of $18.6m^2/g$ showed the best performance of hydrogen production rate of 30ml/min at the feed rate of 0.2ml/min. This work will give the first insight on thin film type Cu/ZnO nanostructure catalyst for micro reforming system for hydrogen production of portable electronic systems.

• 폴리머
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• 제30권4호
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• pp.311-317
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• 2006

촉매 $WCl_6$를 사용하여 ROMP에 의한 poly-DCPD (PDCPD)를 제조하였고, 또한 poly-DCPD 내에 실리케이트를 분산시켜 poly-DCPD/실리케이트 나노복합체를 제조하였는데 나노복합재료 제조는 초음파 분산법을 적용하여 제조하였다. 유기화 처리를 하지 않은 $Na^+MMT$ 보다 유기화 처리를 하여 고분자와의 상용성을 증가시킨 CL 15A 가 매트릭스 내에 분산이 더 잘 되고 우수한 열적, 기계적 물성을 보이는 것을 확인하였으며 수분 차단 성도 높음을 확인하였다.

• Bulletin of the Korean Chemical Society
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• 제32권6호
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• pp.1873-1878
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• 2011

Under solvent-free conditions and in one-pot, a series of 2-amino-4-aryl-3-cyano-6-(3,4-dimethoxyphenyl)-pyridines and 4-aryl-3-cyano-6-(3,4-dimethoxyphenyl)-2(1H)-pyridinones were prepared using 3,4-dimethoxyacetophenone, an aldehyde, malononitrile (or ethyl cyanoacetate), and ammonium acetate in the presence of 3-methyl-1-(4-sulfonylbutyl)imidazolium hydrogen sulfate $[HO_3S(CH_2)_4MIM][HSO_4]$ (a Br${\o}$nsted acidic ionic liquid) as the catalyst in very short reaction time. The preference for the formation of more stable tautomers was consistence with the theoretical calculation using the Gaussian 03 program at the B3LYP hybrid density functional level.