• 제목/요약/키워드: Catalytic Surface Reaction

검색결과 378건 처리시간 0.029초

Novel Fabrication of Designed Silica Structures Inspired by Silicatein-a

  • Park, Ji-Hun;Kwon, Sun-Bum;Lee, Hee-Seung;Choi, In-Sung S.
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2012년도 제42회 동계 정기 학술대회 초록집
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    • pp.557-557
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    • 2012
  • Silicatein-${\alpha}$, the enzyme extracted from silica spicules in glass sponges, has been studied extensively in the way of chemistry from 1999, in which the pioneering work by Morse, D. E. - the discovery of the enzymatic hydrolysis in Silicatein-${\alpha}$ - was published. Since its reaction conditions are physiologically favored, synthesis of various materials, such as gallium oxide, zirconium oxide, and silicon oxide, was achieved without any hazardous wastes. Although some groups synthesized oxide films and particles, they have not achieved yet controlled morphogenesis in the reaction conditions mentioned above. With the knowledge of catalytic triad involved in hydrolysis of silicone alkoxide and oligomerization of silicic acid, we designed the novel peptide amphiphiles to not only form self-assembled structure, but also display similar activities to silicatein-${\alpha}$. Designed templates were able to self-assemble into left-handed helices for the peptide amphiphiles with L-form amino acid, catalyzing polycondensation of silicic acids onto the surface of them. It led to the formation of silica helices with 30-50 nm diameters. These results were characterized by various techniques, including SEM, TEM, and STEM. Given the situation that nano-bio-technology, the bio-applicable technology in nanometer scale, has been attracting considerable attention; this result could be applied to the latest applications in biotechnology, such as biosensors, lab-on-a-chip, biocompatible nanodevices.

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Titanium Containing Solid Core Mesoporous Silica Shell: A Novel Efficient Catalyst for Ammoxidation Reactions

  • Venkatathri, N.;Nookaraju, M.;Rajini, A.;Reddy, I.A.K.
    • Bulletin of the Korean Chemical Society
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    • 제34권1호
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    • pp.143-148
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    • 2013
  • Novel titanium containing solid core mesoporous shell silica has been synthesized by using octadecyltrichloro silane and triethylamine. The synthesized material was characterized by various physicochemical techniques. The mesoporous character of the material has been revealed from PXRD studies. The presence of octadecyltrichloro silane and triethylamine in the sample has been confirmed from EDAX studies. TG/DTA analysis reveals the thermal characteristics of the synthesized material. The presence of titanium in the frame work and its coordination state has been studies by UV-vis DR studies and XPS analysis. Chemical environment of Si in the framework of the material has been studied by $^{29}SiMASNMR$ studies. The surface area of the material is found to be around $550\;m^2g^{-1}$ and pore radius is of nano range from BET analysis. The spherical morphology and particle size of the core as well as shell has been found to be 300 nm and 50 nm respectively from TEM analysis. The catalytic application of this material towards the synthesis of caprolactam from cyclohexanone in presence of hydrogen peroxide through ammoxidation reaction has been investigated. The optimum conditions for the reaction have been established. The plausible mechanism for the formation of core silica and conversion of cyclohexanone has been proposed.

High-valence Mo doping for promoted water splitting of Ni layered double hydroxide microcrystals

  • Kyoungwon Cho;Seungwon Jeong;Je Hong Park;Si Beom Yu;Byeong Jun Kim;Jeong Ho Ryu
    • 한국결정성장학회지
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    • 제33권2호
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    • pp.78-82
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    • 2023
  • The oxygen evolution reaction (OER) is the primary challenge in renewable energy storage technologies, specifically electrochemical water splitting for hydrogen generation. We report effects of Mo doping into Ni layered double hydroxide (Ni-LDH) microcrystal on electrocatalytic activities. In this study, Mo doped Ni-LDH were grown on three-dimensional porous nicekl foam (NF) by a facile solvothermal method. Homogeneous LDH structure on the NF was clearly observed. However, the surface microstructure of the nickel foam began to be irregular and collapsed when Mo precursor is doped. Electrocatalytic OER properties were analyzed by Linear sweep voltammetry (LSV) and Electrochemical impedance spectroscopy (EIS). The amount of Mo doping used in the electrocatalytic reaction was found to play a crucial role in improving catalytic activity. The optimum Mo amount introduced into the Ni LDH was discussed with respect to their OER performance.

기상 TCE 제거반응용 $CrO_x/TiO_2$계 복합 산화물 촉매 디자인 (A Design Approach to $CrO_x/TiO_2$-based Catalysts for Gas-phase TCE Oxidation)

  • 양원호;김문현
    • 대한환경공학회지
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    • 제28권4호
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    • pp.368-375
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    • 2006
  • 순수한 아나타제 구조로 이루어진 DT51D $TiO_2$$CrO_x,\;FeO_x,\;MnO_x,\;LaO_x,\;CoO_x,\;NiO_x,\;CeO_x,\;CuO_x$와 같은 단일 산화물 촉매를 각각 5 wt.% 담지하여 모델반응으로 선택한 기상 TCE 제거반응을 수행하였으며, 이로부터 얻어진 결과를 바탕으로 $CrO_x/TiO_2$-based 복합 산화물 촉매상에서 TCE 산화반응을 연구함으로써 유해 중금속의 사용량을 최소화하기 위한 최적의 촉매 디자인 방법을 도출하고자 하였다. DT51D $TiO_2$에 담지된 여러 단일 금속 산화물들 중에서 기상 TCE 제거반응에 대하여 $CrO_x$가 가장 우수한 촉매활성을 보이는 것으로 나타났으며, 반응온도의 함수로 얻어진 TCE 제거반응의 활성은 $CrO_x$의 담지량에 의존하였다. 5 wt.% $CrO_x$-based 복합 산화물 촉매는 10 wt.% $CrO_x$만으로 이루어진 단일 산화물 촉매와 거의 동일한 수준의 TCE 제거반응 활성을 보였을 뿐만 아니라 이 복합 산화물 촉매들은 10 wt.% $CoO_x,\;MnO_x,\;FeO_x,\;NiO_x$ 등과 같은 단일 산화물 촉매들보다 높은 반응활성을 갖는 것으로 나타났다. 단일 산화물 촉매의 반응활성과 비교하였을 때 5 wt.% $CrO_x$-based 복합 산화물 촉매상에서 TCE 제거반응 동안에 얻어지는 반응활성의 증가 정도는 $420^{\circ}C$ 이하의 반응온도 기준으로 약 $10{\sim}80%$ 이상이었다. 따라서, CVOCs 제거반응을 위하여 널리 사용되고 있는 단일 $CrO_x/Al_2O_3$ 촉매보다는 $CrO_x$의 사용량을 최소화하면서도 우수한 반응활성을 얻을 수 있는 $CrO_x/TiO_2$-based복합 산화물 촉매가 보다 바람직하며 하나의 대안적인 촉매 디자인 방법으로 응용될 수 있을 것으로 생각된다.

Fabrication of CNT/CMK3 Carbon Composites with High Electrical/Thermal Conductive Properties

  • Choi, Seung Dae;Lee, Ju Hyun;Park, Da Min;Kim, Geon-Joong
    • Bulletin of the Korean Chemical Society
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    • 제34권7호
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    • pp.2155-2161
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    • 2013
  • Composite materials of mesoporous carbon and carbon nanotubes were synthesized using Ni, Co and Pd-loaded CMK3 via a catalytic reaction of methane and $CO_2$. The CNTs grew from the pores of the mesoporous carbon supports, and they were attached tightly to the CMK3 surface in a densely tangled shape. The CNT/CMK3 composite showed both non-graphitic mesoporous structures, and graphitic characteristics originating from the MWCNTS grown in the pores of CMK3. The electrochemical properties of the materials were characterized by their electrorheological effects and cyclic voltammetry. The CNTs/CMK3 composites showed high electrical conductivity and current density. The CNT/CMK3 or KOH-modified CNT/CMK3 particles were incorporated in a PMMA matrix to improve the thermal and electrical conductivity. Even higher thermal conductivity was achieved by the addition of KOH-modified CNT/CMK3 particles.

Preparation of the MnO2/Macroporous Carbon for PET Glycolysis

  • Choi, Bong Gill;Yang, MinHo
    • 한국분말재료학회지
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    • 제25권3호
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    • pp.203-207
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    • 2018
  • Plastic pollution is threatening human health and ecosystems, resulting in one of the biggest challenges that humanity has ever faced. Therefore, this study focuses on the preparation of macroporous carbon from biowaste (MC)-supported manganese oxide ($MnO_2$) as an efficient, reusable, and robust catalyst for the recycling of poly(ethylene terephthalate) (PET) waste. As-prepared $MnO_2/MC$ composites have a hierarchical pore network and a large surface area ($376.16m^2/g$) with a narrow size distribution. $MnO_2/MC$ shows a maximum yield (98%) of bis(2-hydroxyethyl)terephthalate (BHET) after glycolysis reaction for 120 min. Furthermore, $MnO_2/MC$ can be reused at least nine times with a negligible decrease in BHET yield. Based on this remarkable catalytic performance, we expect that $MnO_2$-based heterogeneous catalysts have the potential to be introduced into the PET recycling industry.

Dissolved Oxygen Removal in a Column Packed with Catalyst

  • Lee, Han-Soo;Hongsuk Chung;Cho, Young-Hyun;Ahn, Do-Hee;Kim, Eun-Kee
    • Nuclear Engineering and Technology
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    • 제28권5호
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    • pp.482-487
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    • 1996
  • The dissolved oxygen removal by H$_2$-O$_2$ reaction in column packed with various catalysts wes examined. The catalysts employed were the prepared polymeric catalyst platinum on activated carbon, and Lewatit OC-1045 which is available commercially. The column experiments with the prepared polymeric catalyst showed the dissolved oxygen reduced to 35 ppb which is below the limit in feed water of power plants. This implies the likely application of the prepared catalyst for practical use. The activated carbon required the pre-treatment for the removal of dissolved oxygen, since the surface of activated carbon contains much oxygen adsorbed initially. The Lewatit catalyst exposed the best performance, however, the aged one showed the gradual loss of catalytic activity due to degradation of resin catalyst.

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니켈 섬유 매트 촉매를 사용한 바이오가스 수증기개질 반응 (Steam Reforming of Biogas on Nickel Fiber Mat Catalysts)

  • ;김용민;윤창원;남석우
    • 에너지공학
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    • 제20권3호
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    • pp.252-258
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    • 2011
  • Nickel fiber mat was investigated as a potential structured catalyst for steam reforming of biogas in the temperature range of $600-700^{\circ}C$. The activity of as-received catalyst was very low owing to the smooth surface of fibers. Pretreatment of the catalyst by oxidation followed by reduction under methane partial oxidation condition significantly improved the catalytic activity, although degradation of the activity was found during the reaction due to oxidation and sintering. This deactivation was retarded by supplying additional hydrogen in the inlet gases or by coating $CeO_2$ over the catalyst surfaces.

Bioinspired Metal Surfaces by Plasma Treatment

  • 유의선;고태준;오규환;문명운
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2013년도 제44회 동계 정기학술대회 초록집
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    • pp.97-97
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    • 2013
  • The exterior structures of natural organisms have continuously evolved by controlling wettability, such as the Namib Desert beetle, whose back has hydrophilic/hydrophobic contrast for water harvesting by mist condensation in dry desert environments, and some plant leaves that have hierarchical micro/nanostructures to collect or repel liquid water. In this work, we have provided a method for wettability contrast on metals by both nano-flake or needle patterns and tuning of the surface energy. Metals including steel alloys and aluminum were provided with hierarchical micro/nanostructures of metaloxides induced by fluorination and a subsequent catalytic reaction of fluorine ions on metal surfaces in water with various ranges from room to boiling temperature of water. Then, a hydrophobic material was deposited on the structured surfaces, rendering superhydrophobicity. Plasma oxidization induces the formation of superhydrophilic surfaces on selective regions surrounded by superhydrophobic surfaces. We show that wettability contrast surfaces align liquid water within patterned hydrophilic regions during the condensation process. Furthermore, this method could have a greater potential to align other liquids or living cells.

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Degradation of Phenol with Fenton-like Treatment by Using Heterogeneous Catalyst (Modified Iron Oxide) and Hydrogen Peroxide

  • Lee, Si-hoon;Oh, Joo-yub;Park, Yoon-chang
    • Bulletin of the Korean Chemical Society
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    • 제27권4호
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    • pp.489-494
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    • 2006
  • Goethite, hematite, magnetite and synthesized iron oxide are used as catalysts for Fenton-type oxidation of phenol. The synthesized iron oxides were characterized by X-ray diffraction (XRD), BET, X-ray photoelectron spectroscopy (XPS), and electron paramagnetic resonance (EPR). The catalytic activity of these materials is classified according to the observed rate of phenol oxidation. The effectiveness of the catalysts followed the sequence: ferrous ion > synthesized iron oxide >> magnetite hematite > goethite. According to these results, the most effective iron oxide catalyst had the structure similar to natural hematite. The surface oxidation state of the catalyst was between magnetite and hematite (+2.5 ~ +3.0). Phenol degraded completely in 40 min at neutral pH (pH = 7). Soluble ferric and ferrous ions were not detected in the filtrate from Fenton reaction solution by AAS. The formation of hydroxyl radicals was confirmed by EPR.