• 제목/요약/키워드: Nano solution

검색결과 1,208건 처리시간 0.032초

고분자 젤 농도변화에 의한 실리카 나노분말의 합성 (Synthesis of Silica Nanopowder via Change in Polymer Gel Concentration)

  • 김지경;이상근;권재율;서금석;박성수;박희찬
    • 한국세라믹학회지
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    • 제42권3호
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    • pp.205-210
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    • 2005
  • Tetraethyl Orthosilicate(TEOS)를 $SiO_2$ 전구체 용액으로 사용하여 Polyacrlamide gel 방법으로 나노 실리카 분말을 합성하였다. 이 gel 공정법은 비교적 간단한 중합법이며, 고분자 망상구조가 $SiO_2$의 응집을 억제하므로 비교적 낮은 하소온도에서 나노입자를 합성할수 있었다. $SiO_2$ 분말입자의 크기는 gel 전구체중의 ammonium persulphate와 N,N'-methylene-bis-acryamide(BIS)의 농도에 영향을 받았다. 실리카 입자의 크기는 ammonium persulphate의 농도가 증가할수록 작아졌으며 그 농도가 0.01M일때 가장 작은 10nm크기의 입자를 얻었다. 또한 그 입자의 크기는 BIS의 농도가 증가할수록 작아졌으며 그 높도가 0.05M일때 입자의 크기는 5nm였다.

파일럿 규모의 흐름반응기에서 유기 및 무기 첨가제가 질소산화물의 선택적 무촉매 환원반응에 미치는 영향 (Effects of Organic and Inorganic Additives on Selective Non Catalytic Reduction Reaction of NOx in a Pilot Scale Flow Reactor)

  • 박수엽;유경선;이중기;박영권
    • Korean Chemical Engineering Research
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    • 제44권5호
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    • pp.540-546
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    • 2006
  • 파일럿 크기의 흐름반응기에서 유기와 무기 첨가제가 질소산화물의 선택적 무촉매 환원반응에 미치는 영향을 공정변수 변화에 따라 고찰하였다. 질소산화물 저감효율은 반응기의 체류시간과 초기 NOx 농도 증가에 따라 증가하였다. 요소용액에 의한 NOx 환원반응은 $850^{\circ}C$에서 시작되어 $970^{\circ}C$에서는 최대값을 나타내었으며, NSR = 2.0까지 증가 하였다. 유기첨가제로서 에탄올과 페놀의 첨가는 온도창을 저온 영역으로 이동시켰으며, 에탄올 구조내의 탄화수소에 의한 부반응으로 최대의 NOx 저감효율이 감소하였다. NaOH 첨가는 NaOH의 연쇄반응과 $N_2O$ 저감으로 인하여 온도창을 확대시키고, 최대 NOx 저감효율을 10% 정도 향상시켰다.

PET 나노복합재료의 제조 및 특성분석 (The preparation and characterization of poly(ethylene terephthalate)(PET)/layered silicate nanocomposite)

  • 천상욱;손세범;곽승엽
    • 한국복합재료학회:학술대회논문집
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    • 한국복합재료학회 2003년도 추계학술발표대회 논문집
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    • pp.21-24
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    • 2003
  • In general, to enhance physical properties of PET-layered silicate nanocomposites $(P_{et}LSNs)$, it has been well known that the organic modifiers should introduce into gallery regions. However, the organic modifiers in$(P_{et}LSNs)$ may result in thermal decomposition by melt processing at high temperature, and it necessarily lead to deteriorate various physical properties of final products. Therefore, in this study, $(P_{et}LSNs)$ excluding and including organic modifiers were prepared by solution method $(S-P_{et}LSNs_{eom} and S-P_{et}LSNs_{iom})$ and we (focused on the effects of the organic modifiers in $P_{et}$ LSNs with exfoliation structure on the crystallization behaviors, the optical transparency, the thermal stability and the mechanical property. The absence and existence of organic modifiers in $S-P_{et}LSNs_{eom} and S-P_{et}LSNs_{iom}$ were investigated by EA and TGA, and nano-structure of silicate layers in $S-P_{et}LSNs$ was evaluated by using WXRD, SAXS and TEM. $S-P_{et}LSNs_{eom} and S-P_{et}LSNs_{iom}$ were mixed with neat PET as masterbatches by melt method $(M-P_{et}LSNs_{eom} and M-P_{et}LSNs_{iom})$, and also neat PET was mixed with organically modified layered silicates (OLS) by conventional direct melt method $(D-P_{et}LSNs) at 270^{\circ}C$. As results, it was found that $M-P_{et}LSNs_{eom}, M-P_{et}LSNs_{iom}, and D-P_{et}LSN$ showed a exfoliated structure and exhibited faster crystallization rate, better thermal stability and mechanical property than those of neat PET due to the dispersed and detaminated silicate layers in PET matrix. Whereas, considering organic modifiers effect, $M-P_{et}LSNs_{eom} and D-P_{et}LSN$ exhibited slower crystallization rate, poorer optical, thermal and mechanical properties, in comparison to $M-P_{et}LSNs_{eom}> due to the thermal decomposition of organic modifier in $D-P_{et}LSNs$ during melt method.

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Hologram based Internet of Signage Design Using Raspberry Pi

  • Timur, Khudaybergenov;Han, Jungdo;Cha, Jae-Sang
    • 한국컴퓨터정보학회논문지
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    • 제24권12호
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    • pp.35-41
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    • 2019
  • 본 논문에서는 원격 제어 홀로그램 기반 인터랙티브 사이니지 디자인에 대해 제안한다. 제안한 방식은 Raspberry Pi 하드웨어 플랫폼 및 Intel realsense r200 카메라를 사용하여 인터랙션이 가능한 홀로그램 사이니지 구조를 구성하였으며, 소프트웨어 파트는 원격 콘텐츠 관리를 위한 Screenly 솔루션과 콘텐츠 제어를 위한 Open CV 기반 솔루션을 기반으로 구성된다. 3D 게임 기술 Unity 5를 기반으로 한 3D 콘텐츠 렌더링 알고리즘을 사용하여 테스트를 진행하였으며, 홀로그램 피라미드 사이니지 구조를 사용한 모델 테스트를 통해 IoS 설계를 위한 3D 데이터 시각화 및 표출이 가능한 새로운 방식을 실험하였다. 본 논문에서는 해당 홀로그램 사이니지 모델에 대하여 기술하였다.

횡 초음파를 이용한 차세대 플렉시블 디스플레이 모듈 저온 접합 공정 연구 (Study of a Low-Temperature Bonding Process for a Next-Generation Flexible Display Module Using Transverse Ultrasound)

  • 지명구;송춘삼;김주현;김종형
    • 대한기계학회논문집A
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    • 제36권4호
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    • pp.395-403
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    • 2012
  • 오늘날 접합시 열에 의한 재료 손상과 접착제(ACA, NCA) 이용으로 부품간의 정렬이 문제가 되고있다. 따라서, 본 논문은 FPCB 와 HPCB 금속(Au) PAD를 직접 접합하였다. 이때 박막인 재료에 손상을 입히는 열, 부품간의 정렬에 문제가 되는 접착제(ACA, NCA)를 사용하지 않고 상온에서 접합을 하였다. 접합시 초음파 혼을 이용하여 접합을 하였으며, 초음파혼은 40kHz이다. 공정 조건은 접합압력 0.60MPa, 접합시간 0.5, 1.0, 1.5, 2.0sec이다. 또한, 산업에서 요구하는 접합강도는 필강도 테스트 결과값으로 0.60Kgf 이상이며, 본 실험에서는 접합강도가 0.80MPa 이상이 나왔다. 이로서, 열에 의한 재료 손상과, 접 착제(ACA, NCA)에 의한 정렬 문제를 해결하였다. 그리고 산업산업에서 바로 적용하고 생산할 수 있는 FPCB, HPCB 시료 제작을 하였다.

EPD를 이용한 IT-SOFC용 SDC 전해질 필름의 제조 (Preparation of SDC electrolyte film for IT-SOFCs by electrophoretic deposition)

  • 이경섭;김영순;조철기;신형식
    • 한국신재생에너지학회:학술대회논문집
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    • 한국신재생에너지학회 2009년도 추계학술대회 논문집
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    • pp.158-158
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    • 2009
  • The electrophoretic deposition(EPD) technique with a wide range of novel applications in the processing of advanced ceramic materials and coatings, has recently gained increasing interest both in academic and industrial sector not only because of the high versatility of its use with different materials and their combinations but also because of its cost-effectiveness requiring simple apparatus. Compared to other advanced shaping techniques, the EPD process is very versatile since it can be modified easily for a specific application. For example, deposition can be made on flat, cylinderical or any other shaped substrate with only minor charge in electrode design and positioning[1]. The synthesis of the nano-sized Ce0.2Sm0.8O1.9(SDC)particles prepared by aurea based low temperature hydrothermal process was investigated in this study[2].When we made the SDC nanoparticles, changed the time of synthesis of the SDC. The SDC nanoparticles were characterized with field-emission scanning electron microscope(FESEM), energy dispersive X-ray analysis(EDX), and X-ray diffraction(XRD). And also we researched the results of our investigation on electrophoretic deposition(EPD) of the SDC particles from its suspension in acetone solution onto a non-conducting NiO-SDC substrate. In principle, it is possible to carry out electrophoretic deposition on non-conducting substrates. In this case, the EPD of SDC particles on a NiO-SDC substrate was made possible through the use of a adequately porous substrate. The continuous pores in the substrates, when saturated with the solvent, helped in establishing a "conductive path" between the electrode and the particles in suspension[3-4]. Deposition rate was found to increase its increasing deposition time and voltage. After annealing the samples $1400^{\circ}C$, we observed that deposited substrate.

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Novel Water-Soluble Polyfluorenes as an Interfacial layer leading to Cathodes-Independent High Performance of Organic Solar Cells

  • 오승환;심희상;박동원;정연길;이재광;문승현;김동유
    • 한국신재생에너지학회:학술대회논문집
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    • 한국신재생에너지학회 2009년도 추계학술대회 논문집
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    • pp.394-394
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    • 2009
  • Water solubility of conjugated polymers may offer many applications. Potential applications of water-soluble conjugated polymers include the polymer light-emitting diode and new materials for nano and micro hollow-capsules, and bio- or chemo-sensors. We synthesized neutral polyfluorenes containing bromo-alkyl groups by the palladium catalyzed Suzuki coupling reaction. Bromo-alkyl side groups in neutral polyfluorenes were quaternized by tri-methyl amine solution. The electrochemical and optical properties of water-soluble conjugated polymers are discussed. This novel synthesized water-soluble conjugated polymers were used as a interfacial dipole layer between active layer and metal cathode in polymer solar cell for enhancement of open-circuit voltage (Voc), which is one of the most critical factors in determining device characteristics. We also investigated the device performance of polymer solar cell with different metal cathode such as Al, Ag, Au and Cu. In polymer solar cell, novel cationic water-soluble conjugated polymers were inserted between active layer and high-work function cathode (Al, Ag, Au and Cu).

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Bio-Inspired Surface Modification of 3-Dimensional Polycaprolactone Scaffold for Enhanced Cellular Behaviors

  • 조선애;강성민;박수아;이해신
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2011년도 제41회 하계 정기 학술대회 초록집
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    • pp.202-202
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    • 2011
  • The research of 3-dimensional (3-D) scaffold for tissue engineering has been widely investigated as the importance of the 3-D scaffold increased. 3-D scaffold is needed to support for cells to proliferate and maintain their biological functions. Furthermore, its architecture defines the shape of the new bone and cartilage growth. Polycaprolactone (PCL) has been one of the most promising materials for fabricating 3-D scaffold owing to its excellent mechanical property and biocompatibility. However, there are practical problems for using it, in vitro and in vivo; extracellular matrix components and nutrients cannot penetrate into the inner space of scaffold, due to its hydrophobic property, and thus cell seeding and attachment onto the inner surface remain as a challenge. Thus, the surface modification strategy of 3-D PCL scaffold is prerequisite for successful tissue engineering. Herein, we utilized a mussel-inspired approach for surface modification of 3-D PCL scaffold. Modification of 3-D PCL scaffolds was carried out by simple immersion of scaffolds into the dopamine solution and stimulated body fluid, and as a result, hydroxyapatite-immobilized 3-D PCL scaffolds were obtained. After surface modification, the wettability of 3-D PCL scaffold was considerably changed, and infiltration of the pre-osteoblastic cells into the 3-D scaffold followed by the attachment onto the surface was successfully achieved.

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Syntheses and Properties of Quaternary Cr-Ti-B-N Coatings by a High Power Impulse Magnetron Sputtering Technique

  • Myoung, Hee-Bok;Zhang, Teng Fei;Park, Jong-Keuk;Kim, Doo-In;Kim, Kwang Ho
    • 한국표면공학회지
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    • 제45권6호
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    • pp.232-241
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    • 2012
  • Cr-Ti-B-N coatings were synthesized by a hybrid coating system combining high power impulse magnetron sputtering (HIPIMS) and DC pulse magnetron sputtering from a $TiB_2$ and a Cr target in argon-nitrogen environment, respectively. By changing the power applied on the Cr and $TiB_2$ cathodes, the Cr-Ti-B-N coatings with various Ti/Cr ratio and B content were deposited. The phase structure, microstructure and chemical compositions of the Cr-Ti-B-N coatings were studied by X-ray diffraction (XRD), transmission scanning electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). With increase of Cr element in the coatings, the nanocomposite microstructure consisting of nano-sized (Cr, Ti) N crystallites and amorphous BN phase were obtained in the coatings. The microhardness of the Cr-Ti-B-N coatings exhibited a peak value of ~41 GPa for the $CrTi_{0.1}B_{0.4}N_{1.3}$, and then decreased with further increase of Cr content in the coatings, and all the coatings exhibited low friction coefficient. The oxidation and corrosion behavior of the Cr-Ti-B-N coatings revealed better properties due to the formation of a nanocomposite microstructure.

연성 이종 재료 시료의 상온 절편 제작법 (Sample Preparation of Ductile Heterogeneity Materials by Ultramicrotomy)

  • 채희수;권희석;제아름;이석훈;김진규
    • Applied Microscopy
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    • 제42권1호
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    • pp.49-52
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    • 2012
  • For TEM study of biological samples or polymers that are contained in organic structure, it is often required that the sample is prepared by using ultramicrotome and stained with proper agents to increase the contrast of organic structure. In this study, we investigated an efficient TEM sample preparation method for ductile heterogeneity material by using ultramicrotomy. Cryo-ultramicrotomy is a suitable method that is capable of rendering sample hardness for various ductile materials. However, it has several factors to consider, such as experimental cost, working time and finding the optimal staining conditions. To satisfy these considerations, we prepared TEM sample by using ultramicrotome without cryofunction, and secured the sample hardness by applying the staining process prior to ultrathin sectioning. The cross-linked polyethylene structure in the sample was stained with the 2% $RuO_4$ solution in a sealed test tube for 24 hours at $4^{\circ}C$. After the sample staining, ultrathin sections of sample were prepared using ultramicrotome. As a result, it was revealed that the difficulties associated with staining of ultrathin sections prepared by low-temperature conditions were improved. In addition, appropriate staining depth of sample could be selected for sectioning process. The quality of TEM sample obtained by using this method was better than that of cryo-ultramicroscopy. Finally, it is expected that our method could be effectively applied in TEM sample preparation for a variety of nano-bio convergence materials.