• 제목/요약/키워드: catalytic application

검색결과 244건 처리시간 0.03초

알루미나 나노산화물이 Nitrendipine 제조 공정에 미치는 영향 (Effect of Alumina Nanooxide Application on Nitrendipine Manufacturing Process)

  • 채은진;엄영랑;한병선;이창규;박상언
    • 한국분말재료학회지
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    • 제14권2호
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    • pp.127-131
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    • 2007
  • The alumina nano powders synthesized by levitational gas condensation (LGC) method were applied to catalyst in manufacturing process of Hanzsch reaction for Nitrendipine. The L-tartaric acid on the surface is carried out with participation of carbonyl fragments, O-H, C-H bonds which affects stereo selectivity, yield on the reagents positively. From the analysis of the IR-spectroscopy, the carbonyl fragments, O-H, and C-H bond were created by the catalytic reaction. From the analysis of the rR-spectroscopy, the carbonyl fragments, O-H, and C-H bond were created by the catalytic reaction. The newly created bonds made a chiral center on the final product.

Comparison of Removal Efficiency of Mn-loaded Natural Zeolites and Red Mud for the Catalytic Ozonation of 2-Butanone

  • Park, Youna;Lee, Jung Eun;Park, Young-Kwon
    • 공업화학
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    • 제33권3호
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    • pp.328-334
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    • 2022
  • For the study of environmental application of natural zeolites (NZ) and red mud (RM), which are discharged from various industrial fields, the catalytic ozonation of 2-butaone (methyl ethyl ketone, MEK) was performed using the Mn-loaded NZ prepared according to the Mn content of 1, 3, 5, 7, and 10 wt%. By the addition of Mn to NZ, the BET (Brunaure-Emmett-Teller) specific surface area of Mn/NZ catalysts decreased while the ratio of Mn3+/[Mn3++Mn4+] intensively increased. Besides, the addition of Mn component to NZ increased the ratio of adsorbed oxygen (Oadsorbed) toward lattice oxygen (Olattice), Oadsorbed/Olattice from 0.076 of NZ to 0.465 of 10 wt% Mn/NZ according to the amount of Mn. It is known that the proportion of two species, Mn3+ and Oadsorbed, would greatly affect the catalytic activity. However, the balancing between the paired species, Mn3+ vs. Mn4+ and Oadsorbed vs. Olattice might be more essential for the catalytic ozonation of MEK at room temperature. Among the Mn-loaded NZ catalysts, the 3 wt% Mn/NZ showed the best activity for the removal of MEK and ozone. The 5, 7, and 10 wt% Mn/NZ catalysts are slightly inferior to the 3 wt% Mn/NZ. Compared to the pristine NZ, the Mn/NZ catalysts showed better activity for the catalytic ozonation of MEK. In addition, the 3 wt% Mn/NZ was confirmed to have the most available acid sites among them by the analysis of NH3-TPD (temperature programmed desorption). This might be the major reason for the best catalytic activity of 3 wt% Mn/NZ together with the adjusted distribution ratios of Mn3+/Mn4+ and Oadsorbed/Olattice. Considering the result of 3 wt% Mn/NZ, the 3 wt% Mn/RM was prepared to perform the catalytic activity for the removal of MEK and ozone, but the efficiency of 3 wt% Mn/RM was significantly lower than that of the 3 wt% Mn/NZ.

Preparation of Alumino-silicate Membrane and Its Application to a Gas Separation

  • 김태환
    • 한국막학회:학술대회논문집
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    • 한국막학회 2002년도 제15회 심포지움
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    • pp.23-46
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    • 2002
  • The cryogenic, pressure swing adsorption and membrane methods have been used to separate air into nitrogen and oxygen. The air separation membrane is made of the polymers, of which manufacturing process is complicate and it causes a little high production cost. Polymer membrane has temperature limit in usage and low durability even at moderate temperature. Therefore, inorganic membranes have been studied for years. As formation of unit alumino-silicate membrane, unit cells of membrane were made with a few coating methods. In this study the dipping of substrate into sols, application of vacuum to the opposite side of substrate with coating and rotating of the substrate in the sols were found as good coating memthods to make a uniform coating and to control the thickness of membrane. The membrane coats were examined by SEM and XRD. The sample ESZl-1 was compared with those of samples that prepared by another method. The present developed coating methods could be applied to the various types of zeolite membrane formation, that is A- X-, Y- ZSM- and MCM-types of membranes. Also these membrane forming methods could be applied to formation of catalyst absorbed zeolite membrane, of which zeolite absorb the catalytic metals. The product obtained from these coating methods could be applied to the industrial gas and liquid phase catalytic reaction and separation processes.

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프로톤 전도성 세라믹 멤브레인 촉매 반응기를 이용한 수소 분리 및 제조 기술 (Hydrogen Separation and Production using Proton-Conducting Ceramic Membrane Catalytic Reactors)

  • 서민혜;박은덕
    • Korean Chemical Engineering Research
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    • 제57권5호
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    • pp.596-605
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    • 2019
  • 프로톤 전도성 세라믹인 페로브스카이트 구조의 산화물은 고온 환경에서 고체 전해질 및 촉매로써 동시에 활용이 가능하여, 반응과 분리기능을 동시에 갖춘 멤브레인 반응기로 적용하기에 우수한 소재이다. 특히 수소 제조 촉매와 분리, 이를 결합한 멤브레인 반응기 개발에 관한 연구는 전해질 내 도핑 금속의 종류 및 온도, 반응물의 조성 등에 따라 다양한 연구 결과가 제시되고 있다. 이에 본 총설에서는 프로톤 전도성 세라믹반응기에서 메탄을 활용하여 수소 제조촉매와 멤브레인 반응기로 응용해 온 연구 동향을 살펴보고, 차세대 수소의 제조와 분리 기술로서의 응용분야 및 전망에 관해 고찰하고자 한다.

Preparation and Catalytic Application of Pd Loaded Titanate Nanotube: Highly Selective α Alkylation of Ketones with Alcohols

  • Jang, Jum-Suk;Kwon, Min-Serk;Kim, Hyun-Gyu;Park, Jae-Wook;Lee, Jae-Sung
    • Bulletin of the Korean Chemical Society
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    • 제33권5호
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    • pp.1617-1621
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    • 2012
  • The titanate nanotube (TNT) was hydrothermally synthesized in 10 M NaOH aqueous solution at $150^{\circ}C$ for 72 h. Titanate nanotube with high surface area (292 $m^2$/g) is a good candidate as a support for catalytic reaction or organic synthesis. Palladium nanoparticles with an average size of $ca$. 3 nm were well dispersed onto the surface of TNT nanotubes. Palladium loaded catalyst with high surface area shows a highly efficient ${\alpha}$ alkylation of ketones with primary alcohols.

Formation Fe2O3 Nanowalls through Solvent-Assisted Hydrothermal Process and Their Application for Titan Yellow GR Dye Degradation

  • Ahmed, Khalid Abdelazez Mohamed
    • 대한화학회지
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    • 제58권2호
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    • pp.205-209
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    • 2014
  • Hematite iron oxide (${\alpha}$-$Fe_2O_3$) nanowalls were fabricated on aluminum substrate by a facile solvent-assisted hydrothermal oxidation process. The XRD and EDS patterns indicate that the sample has a rhombohedral phase of hematite $Fe_2O_3$. FE-SEM, TEM, HR-TEM, SA-ED were employed to characterize the resulting materials. $N_2$ adsorption-desorption isotherms was used to study a BET surface area. Their capability of catalytic degradation of titan yellow GR azo dye with air oxygen in aqueous solution over $Fe_2O_3$ catalysts was studied. The result indicates that the as-prepared product has a high catalytic activity, because it has a larger surface area. Langmuir and Freundlich isotherms of adsorption dye on the catalysts surface were investigated and the decomposition of titan yellow GR follows pseudo-first order kinetic.

The Enhanced Physico-Chemical and Electrochemical Properties for Surface Modified NiO Cathode for Molten Carbonate Fuel Cells (MCFCs)

  • Choi, Hee Seon;Kim, Keon;Yi, Cheol-Woo
    • Bulletin of the Korean Chemical Society
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    • 제35권5호
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    • pp.1305-1311
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    • 2014
  • The nickel oxide, the most widely used cathode material for the molten carbonate fuel cell (MCFC), has several disadvantages including NiO dissolution, poor mechanical strength, and corrosion phenomena during MCFC operation. The surface modification of NiO with lanthanum maintains the advantages, such as performance and stability, and suppresses the disadvantages of NiO cathode because the modification results in the formation of $LaNiO_3$ phase which has high conductivity, stability, and catalytic activity. As a result, La-modified NiO cathode shows low NiO dissolution, high degree of lithiation, and mechanical strength, and high cell performance and catalytic activity in comparison with the pristine NiO. These enhanced physico-chemical and electrochemical properties and the durability in marine environment allow MCFC to marine application as a auxiliary propulsion system.

백금 핀서 화합물의 합성 및 Silylcyanation 촉매반응에 대한 응용 (Synthesis of a Platinum-Pincer Complex and Application to Catalytic Silylcyanation)

  • 김윤태;윤명식
    • 공업화학
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    • 제27권4호
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    • pp.366-370
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    • 2016
  • 본 연구에서는 1,3-bis(2-pyridyloxy)benzene과 $K_2PtCl_4$를 이용하여 백금을 중심으로 2개의 6원환을 이루는 백금 핀서 화합물을 합성하였다. NMR과 X-ray를 이용하여 구조를 규명하였고 백금원자를 중심으로 이루는 6원환 구조는 angle strain을 감소시켜 안정한 화합물을 형성하였다. 이 화합물을 알데하이드와 이민의 silylcyanation 반응에 적용하여 본 결과 수율 99%까지 나타내는 효과적인 촉매작용을 보여주었다.

Synthesis of Graphene Oxide Based CuOx Nanocomposites and Application for C-N Cross Coupling Reaction

  • Choi, Jong Hoon;Park, Joon B.
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2014년도 제46회 동계 정기학술대회 초록집
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    • pp.176.1-176.1
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    • 2014
  • Graphene has attracted an increasing attention due to its extraordinary electronic, mechanical, and thermal properties. Especially, the two dimensional (2D) sheet of graphene with an extremely high surface to volume ratio has a great potential in the preparation of multifunctional nanomaterials, as 2D supports to host metal nanoparticles (NPs). Copper oxide is widely used in various areas as antifouling paint, p-type semiconductor, dry cell batteries, and catalysts. Although the copper oxide(II) has been well known for efficient catalyst in C-N cross-coupling reaction, copper oxide(I) has not been highlighted. In this research, CuO and Cu2O nanoparticles (NPs) dispersed on the surface of grapehene oxide (GO) have been synthesized by impregnation method and their morphological and electronic structures have been systemically investigated using TEM, XRD, and XAFS. We demonstrate that both CuO and Cu2O on graphene presents efficient catalytic performance toward C-N cross coupling reaction. The detailed structural difference between CuO and Cu2O NPs and their effect on catalytic performance are discussed.

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Pt@Cu/C Core-Shell Catalysts for Hydrogen Production Through Catalytic Dehydrogenation of Decalin

  • Kang, Ji Yeon;Lee, Gihoon;Jeong, Yeojin;Na, Hyon Bin;Jung, Ji Chul
    • 한국재료학회지
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    • 제26권1호
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    • pp.17-21
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    • 2016
  • Pt@Cu/C core-shell catalysts were successfully prepared by impregnation of a carbon support with copper precursor, followed by transmetallation between platinum and copper. The Pt@Cu/C core-shell catalysts retained a core of copper with a platinum surface. The prepared catalysts were used for hydrogen production through catalytic dehydrogenation of decalin for eventual application to an onboard hydrogen supply system. Pt@Cu/C core-shell catalysts were more efficient at producing hydrogen via decalin dehydrogenation than Pt/C catalysts containing the same amount of platinum. Supported core-shell catalysts utilized platinum highly efficiently, and accordingly, are lower-cost than existing platinum catalysts. The combination of impregnation and transmetallation is a promising approach for preparation of Pt@Cu/C core-shell catalysts.