• 제목/요약/키워드: Catalyst generation

검색결과 196건 처리시간 0.036초

차세대 반도체용 유-무기 나노 복합재료의 에폭시 수지변화에 따른 흡습특성 (Moisture Absorption Properties of Organic-Inorganic Nano Composites According to the Change of Epoxy Resins for Next Generation Semiconductor Packaging Materials)

  • 김환건;김동민
    • 반도체디스플레이기술학회지
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    • 제12권1호
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    • pp.23-28
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    • 2013
  • Epoxy resins are widely used in microelectronics packaging such as printed circuit board and encapsulating for semiconductor manufacturing. Water can diffuse into and through the epoxy matrix systems and moisture absorption at boarding interfaces of matrix resin systems can lead to a hydrolysis at the interfaces resulting in delamination of encapsulating materials. In the study, the changes of diffusion coefficient and moisture content ratio of epoxy resin systems with nano-sized fillers according to the change of liquid type epoxy resins were investigated. RE-304S, RE-310S, RE-810NM and HP-4032D as a epoxy resin, Kayahard AA as a hardener, and 1B2MI as a catalyst were used in these epoxy resin systems. After curing, moisture content ratios were measured with time under the 85 and 85% relative humidity condition using a thermo-hydrostat. The maximum moisture absorption ratio and diffusion coefficient of EMC decrease with the filler content. It can be seen that these decreases are due to the increase of filler surface area and the decrease of moisture through channel with the content of nano-sized filler.

Effective α-Helix Stabilization via Hexenyl Propionate Cross-Link

  • Yoo, Jiyeon;Kim, Young-Woo
    • Bulletin of the Korean Chemical Society
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    • 제35권12호
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    • pp.3627-3631
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    • 2014
  • In this study we examined two ester-containing cross-links, hex-2-enyl acetate and hex-2-enyl propionate, as new cross-linking systems for helix stabilization of short peptides. We demonstrated that these hexenyl ester cross-links can be readily installed via a ruthenium-mediated ring-closing metathesis reaction of L-aspartic acid 4-allyl ester or L-glutamic acid 5-allyl ester at position i and (S)-2-(4'-pentenyl)alanine at position i+4 using second generation Hoveyda-Grubbs catalyst at $60^{\circ}C$. Between these two cross-links, we found that the hex-2-enyl propionate significantly stabilizes the ${\alpha}$-helical conformations of short model peptides. The helix-stabilizing effects of the hex-2-enyl propionate tether appear to be as powerful as Verdine's i,i+4 all-hydrocarbon stapling system, which is one of the most widely used and the most potent helix-stabilizing cross-linking systems. Furthermore, the hex-2-enyl propionate bridge is reasonably robust against non-enzymatic hydrolytic cleavage at a physiological pH. While extended studies for probing its chemical scopes and biological applications are needed, we believe that this new helix-stabilizing system could serve as a useful chemical tool for understanding protein folding and designing conformationally-constrained peptide drugs.

고정입자패드를 이용한 텅스텐 CMP 개발 및 평가 (Development and Evaluation of Fixed Abrasive Pad in Tungsten CMP)

  • 박범영;김호윤;김구연;정해도
    • 한국기계가공학회지
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    • 제2권4호
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    • pp.17-24
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    • 2003
  • Chemical mechanical polishing(CMP) has been applied for planarization of topography after patterning process in semiconductor fabrication process. Tungsten CMP is necessary to build up interconnects of semiconductor device. But the tungsten dishing and the oxide erosion defects appear at end-point during tungsten CMP. It has been known that the generation of dishing and erosion is based on the over-polishing time, which is determined by pattern selectivity. Fixed abrasive pad takes advantage of decreasing the defects resulting flam reducing pattern selectivity because of the lower abrasive concentration. The manufacturing technique of fixed abrasive pad using hydrophilic polymers is introduced in this paper. For application to tungsten CMP, chemicals composed of oxidizer, catalyst, and acid were developed. In comparison of the general pad and slurry for tungsten CMP, the fixed abrasive pad and the chemicals resulted in appropriate performance in point of removal rate, uniformity, material selectivity and roughness.

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연료전지 자동차용 수소센서의 히터 조건에 따른 열전달 특성에 관한 연구 (Study on Heat Transfer Characteristics by Heater Conditions of Hydrogen Sensor for Fuel Cell Electric Vehicle)

  • 서호철;박경석
    • 한국자동차공학회논문집
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    • 제21권1호
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    • pp.23-29
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    • 2013
  • In recent years, development of energy conversion systems using hydrogen as an energy source has been accelerated globally. Even though hydrogen is an environment-friendly energy source, safety and effectiveness issues in storage, transportation, and usage of hydrogen should be clearly resolved in every application. Therefore, sensors for detecting hydrogen leakage, especially for fuel cell electric vehicles, should be designed to have much higher resolution and accuracy in comparison with conventional gas sensors. In this study, we conducted to determine the design parameters for the semiconductor hydrogen sensor with optimized sensing conditions under the thermal distribution characteristic and thermal transfer characteristic. The heat generation study on power supply voltage was studied for correlation analysis of thermal energy according to the power supply voltage variation from 1.0 voltage to 10.0 voltage every 0.5 voltage. And we studied for the temperature coefficient of resistance with hydrogen sensor.

Effects of Polyamidoamine Dendrimers on the Catalytic Layers of a Membrane Electrode Assembly in Fuel Cells

  • Lee Jin Hwa;Won Jongok;Oh In Hwan;Ha Heung Yong;Cho Eun Ae;Kang Yong Soo
    • Macromolecular Research
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    • 제14권1호
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    • pp.101-106
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    • 2006
  • The transport of reactant gas, electrons and protons at the three phase interfaces in the catalytic layers of membrane electrode assemblies (MEAs) in proton exchange, membrane fuel cells (PEMFCs) must be optimized to provide efficient transport to and from the electrochemical reactions in the solid polymer electrolyte. The aim of reducing proton transport loss in the catalytic layer by increasing the volume of the conducting medium can be achieved by filling the voids in the layer with small-sized electrolytes, such as dendrimers. Generation 1.5 and 3.5 polyamidoamine (PAMAM) dendrimer electrolytes are well-controlled, nanometer-sized materials with many peripheral ionic exchange, -COOH groups and were used for this purpose in this study. The electrochemically active surface area of the deposited catalyst material was also investigated using cyclic voltammetry, and by analyzing the Pt-H oxidation peak. The performances of the fuel cells with added PAMAM dendrimers were found to be comparable to that of a fuel cell using MEA, although the Pt utilization was reduced by the adsorption of the dendrimers to the catalytic layer.

The effect of dynamic operating conditions on nano-particle emissions from a light-duty diesel engine applicable to prime and auxiliary machines on marine vessels

  • Lee, Hyungmin;Jeong, Yeonhwan
    • International Journal of Naval Architecture and Ocean Engineering
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    • 제4권4호
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    • pp.403-411
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    • 2012
  • This study presents the nano-sized particle emission characteristics from a small turbocharged common rail diesel engine applicable to prime and auxiliary machines on marine vessels. The experiments were conducted under dynamic engine operating conditions, such as steady-state, cold start, and transient conditions. The particle number and size distributions were analyzed with a high resolution PM analyzer. The diesel oxidation catalyst (DOC) had an insignificant effect on the reduction in particle number, but particle number emissions were drastically reduced by 3 to 4 orders of magnitude downstream of the diesel particulate filter (DPF) at various steady conditions. Under high speed and load conditions, the particle filtering efficiency was decreased by the partial combustion of trapped particles inside the DPF because of the high exhaust temperature caused by the increased particle number concentration. Retarded fuel injection timing and higher EGR rates led to increased particle number emissions. As the temperature inside the DPF increased from $25^{\circ}C$ to $300^{\circ}C$, the peak particle number level was reduced by 70% compared to cold start conditions. High levels of nucleation mode particle generation were found in the deceleration phases during the transient tests.

기상 공정에 의한 나노 미립자 제조 (Preparation of Nanoparticles by Gas Phase Processes)

  • 김동주;김교선
    • Korean Chemical Engineering Research
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    • 제45권6호
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    • pp.536-546
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    • 2007
  • 나노 미립자는 부피대비 높은 표면적을 가지고 있기 때문에 벌크 상태에서는 볼 수 없는 여러 흥미로운 성질들을 가지고 있다. 나노 미립자들은 나노 구조체 재료, 산업용 재료 혹은 촉매 재료 등을 제조하는데 사용될 수 있다. 기상공정에 의해 높은 단분산성을 갖는 다양한 크기의 나노 미립자를 제조할 수 있으며 제조된 미립자는 각종 첨단 기능성 재료의 원료로 이용될 수 있다. 본고에서는 기상공정을 통하여 나노 미립자 제조에 이용되는 에어로솔 반응기들을 소개하였으며 각 반응기의 특성을 분석하였고 기상 공정에 의한 미립자 제조에 관련된 최근 흥미 있는 연구들을 소개하도록 하였다.

One-Pot 합성공정으로 만든 Aluminum이 doping된 폴리카보실란으로부터 제조된 치밀한 결정화 탄화규소 섬유 (Dense Polycrystalline SiC Fiber Derived from Aluminum-doped Polycarbosilane by One-Pot Synthesis)

  • 신동근;공은배;류도형;김영희;박홍식;김현이
    • 한국세라믹학회지
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    • 제44권7호
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    • pp.393-402
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    • 2007
  • Polyaluminocarbosilane was synthesized by direct reaction of polydimethylsilane with aluminum(III)-acetylacetonate in the presence of zeolite catalyst. A fraction of higher molecular weight polycarbosilane was formed due to the binding of aluminium acetylacetonate radicals with the polycarbosilane backbone. Small amount of Si-O-Si bond was observed in the as-prepared polyaluminocarbosilane as the result. Polyaluminocarbosilane fiber was obtained through a melt spinning and was pyrolyzed and sintered into SiC fiber from $1200{\sim}2000^{\circ}C$ under a controlled atmosphere. The nucleation and growth of ${\beta}-SiC$ grains between $1400{\sim}1600^{\circ}C$ are accompanied with nano pores formation and residual carbon generation. Above $1800^{\circ}C$, SiC fiber could be sintered to give a fully crystallized ${\beta}-SiC$ with some ${\alpha}-SiC$.

Non-gaseous Plasma Immersion Ion Implantation and Its Applications

  • Han, Seung-Hee;Kim, En-Kyeom;Park, Won-Woong;Moon, Sun-Woo;Kim, Kyung-Hun;Kim, Sung-Min
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2012년도 제43회 하계 정기 학술대회 초록집
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    • pp.151-151
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    • 2012
  • A new plasma process, i.e., the combination of PIII&D and HIPIMS, was developed to implant non-gaseous ions into materials surface. HIPIMS is a special mode of operation of pulsed-DC magnetron sputtering, in which high pulsed DC power exceeding ~1 kW/$cm^2$ of its peak power density is applied to the magnetron sputtering target while the average power density remains manageable to the cooling capacity of the equipment by using a very small duty ratio of operation. Due to the high peak power density applied to the sputtering target, a large fraction of sputtered atoms is ionized. If the negative high voltage pulse applied to the sample stage in PIII&D system is synchronized with the pulsed plasma of sputtered target material by HIPIMS operation, the implantation of non-gaseous ions can be successfully accomplished. The new process has great advantage that thin film deposition and non-gaseous ion implantation along with in-situ film modification can be achieved in a single plasma chamber. Even broader application areas of PIII&D technology are believed to be envisaged by this newly developed process. In one application of non-gaseous plasma immersion ion implantation, Ge ions were implanted into SiO2 thin film at 60 keV to form Ge quantum dots embedded in SiO2 dielectric material. The crystalline Ge quantum dots were shown to be 5~10 nm in size and well dispersed in SiO2 matrix. In another application, Ag ions were implanted into SS-304 substrate to endow the anti-microbial property of the surface. Yet another bio-application was Mg ion implantation into Ti to improve its osteointegration property for bone implants. Catalyst is another promising application field of nongaseous plasma immersion ion implantation because ion implantation results in atomically dispersed catalytic agents with high surface to volume ratio. Pt ions were implanted into the surface of Al2O3 catalytic supporter and its H2 generation property was measured for DME reforming catalyst. In this talk, a newly developed, non-gaseous plasma immersion ion implantation technique and its applications would be shown and discussed.

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이온성 액체 촉매를 이용한 Tricyclopentadiene 합성에 관한 연구 (A Study on the Synthesis of Tricyclopentadiene Using Ionic Liquid Catalysts)

  • 김수정;한정식;전종기;임진형
    • 공업화학
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    • 제26권5호
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    • pp.593-597
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    • 2015
  • 차세대 고밀도 연료인 tricyclopentadiene (TCPD)는 dicyclopentadiene (DCPD)를 Diels-Alder 소중합 반응을 통하여 제조하여 왔다. 이에 본 연구에서는 다양한 음이온 전구체와 양이온 전구체의 조합으로 만들어진 이온성 액체 촉매를 이용한 tricyclopentadiene (TCPD) 합성에 관한 연구를 수행하였다. 본 연구에 사용된 2가지 음이온 전구체는 copper(I) chloride (CuCl), iron(III) chloride ($FeCl_3$)이며 양이온 전구체는 triethylamine hydrochloride (TEAC), 1-butyl-3-methylimidazolium chloride (BMIC)이다. 이온성 액체 촉매의 소중합을 통한 TCPD의 제조는 기존 Diels-Alder 반응보다 DCPD의 전환율과 TCPD의 수율 측면에서 우수하였다. 또한, 음이온/양이온 전구체의 조합으로 제조된 이온성 액체 촉매의 산도와 TCPD 수율과의 상관관계가 있었다. 이온성 액체 촉매의 루이스 산도가 낮은 음이온 전구체로 CuCl를 이용하였을 때가 $FeCl_3$를 사용하였을 때보다 TCPD 수율이 좋았다. $FeCl_3$를 음이온 전구체로 하고 양이온 전구체로 BMIC를 사용하여 두 전구체의 몰 비를 조절하여 루이스 산도를 낮추면 TCPD 수율을 증가시킬 수 있었다.