• 제목/요약/키워드: inert materials

검색결과 227건 처리시간 0.024초

라이트의 유소니언 오토매틱 주택 시스템에 나타난 재료 및 공법에 관한 연구 (Materials and Methods in Usonian Automatic House System of Frank Lloyd Wright)

  • 김태영
    • 한국농촌건축학회논문집
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    • 제18권4호
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    • pp.1-8
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    • 2016
  • This study is to investigate the meaning and value of Usonian Automatic House System(UAHS) of Frank Lloyd Wright in his later period, focused on materials, methods, and his thoughts. The results of this study are follows. UAHS was the outcome of moderate cost and prefab house which Wright had successively attempted after the early Prairie period. The construction was simple and comparatively cheap, but subsequent automatics were difficult and expensive to build. Nevertheless, it was sufficiently flexible to support a rather wide range of house designs. Concrete was the inert mass and a plastic material. Wright saw a kind of weaving coming out of it. He also saw a kind of concrete masonry, steel for warp and masonry units for woof in the automatic concrete block. The reinforced bars in hollowed joints of concrete block increased the safety factor and affected the expression of the construction through the stabilization they provided. But they did not give concrete block the capability of structural span. Standardization as the soul of the machine might be seen in UAHS. The concrete blocks were more cheap, lighter, and larger hollowed plain than textile blocks in 1920s. But the variety of pattern and different block types in the UAHS were achieved at some sacrifice of standardization. The repetitive nature of production was compromised for artistic goals. The sense of compromise was not maximized, however, because the units as installed looked far more repetitive than they actually were.

Corrosion and Wear Properties of Cold Rolled 0.087% Gd Lean Duplex Stainless Steels for Neutron Absorbing Material

  • Choi, Yong;Baik, Youl;Moon, Byung-Moon;Sohn, Dong-Seong
    • Nuclear Engineering and Technology
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    • 제48권1호
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    • pp.164-168
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    • 2016
  • Lean duplex stainless steels with 0.087 wt.% gadolinium (Gd) were inert arc-melted and cast in molds of size $10mm{\times}10mm{\times}20mm$. The micro-hardnesses of the rolling direction (RD), transverse direction (TD) and short transverse (ST) direction were $258.5H_V$, $292.3H_V$, and $314.7H_V$, respectively. A 33% cold rolled specimen had the crystallographic texture that (100) pole was mainly concentrated to the normal direction (ND) and (110) pole was concentrated in the center of ND and RD. The corrosion potential and corrosion rate in artificial seawater and $0.1M\;H_2SO_4$ solution were in the range of $105.6-221.6mV_{SHE}$, $0.59-1.06mA/cm^2$, and $4.75-8.25mV_{SHE}$, $0.69-1.68mA/cm^2$, respectively. The friction coefficient and wear loss of the 0.087 w/o Gd-lean duplex stainless steels in artificial seawater were about 67% and 65% lower than in air, whereas the wear efficiency was 22% higher. The corrosion and wear behaviors of the 0.087 w/o Gd-lean duplex stainless steels significantly depended on the Gd phases.

비활성 세라믹 분말이 고분자 전해질의 전기적, 기계적 특성에 미치는 영향 (Effect of the Inert Ceramic Powder on the Electrical and Mechanical Properties of the Polymer Electrolytes)

  • 김동원;박정기;김창정;노광수
    • 한국재료학회지
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    • 제3권3호
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    • pp.237-244
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    • 1993
  • 폴리에틸렌 옥사이드(PEO)/리튬 삼불화메탄 술포네이트(${LiCF}_{3}{SO}_{3}$)착제에 평균 직경 $1{\mu}$m인 미세 세라믹 분말 ($\gamma -{LiALO}_{2}$)을 혼합하여 얻은 복합체 고분자 전해질의 특성을 형태학 및 기계적 성질의 관점에서 고찰하였다. 균일하게 분산된 세라믹 분말을 상온에서 고체 고분자 전해질의 전기적, 기계적 성질을 크게 향상시키는 것으로 관찰되었으며, 그 조성에 따라 그 특성이 변하였다. 본 연구에서 조사된 복합체 고분자 전해질의 경우, 상온에서 최대 이온 전도도를 나타내는 ${LiAlO}_{2}$의 최적 함량은 약 20%인 것으로 나타났다.

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플라즈마 처리 방법을 이용한 PAN 전구체 특성 변화 연구 (Study of Stabilization Process of PAN Precursor and its Characteristics Change by Plasma Treatment)

  • 강효경;김정연;김학용;최영옥
    • Composites Research
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    • 제34권1호
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    • pp.23-29
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    • 2021
  • 탄소섬유는 단위 중량 당 높은 강도 및 모듈러스를 갖기 때문에 고성능 복합 재료 제조 시 탄소보강재로 많이 사용된다. 그러나 탄소 섬유를 제조하는 공정에서 많은 시간과 높은 에너지를 소모하여 제조비용이 크게 증가하기 때문에 상용화에 어려움을 겪고 있다. 따라서 생산 비용 절감을 위하여 제조 공정에 사용되는 에너지를 대체할 수 있는 고속의 저 에너지원을 적극적으로 찾아 연구할 필요가 높아졌다. 폴리아크릴로니트릴(PAN) 전구체(Precursor)로 상용화 된 탄소 섬유는 180~300℃의 대기 분위기에서 안정화 과정이 이루어지고, 1600℃ 이하의 불활성 가스 분위기에서 탄화하여 탄소 섬유를 생산할 수 있다. 이 두 공정은 많은 시간과 높은 에너지를 사용하지만, 고성능 탄소 섬유를 생산하는 데 필수적이며 중요하다. 따라서 최근에는 공정 시간을 단축하고 에너지 소비를 줄일 수 있는 플라즈마, 전자 빔 및 마이크로파와 같은 다양한 다른 에너지원을 보조적으로 사용 함으로써 저 에너지·고속 안정화 공정 기술이 시도되고 있다. 본 연구에서는 플라즈마 공정과 열처리를 연속적으로 수행하여 PAN 전구체 안정화 공정을 연구하였으며, 모폴로지, 구조적 변화, 열적 및 물리적 특성 변화를 연구하였다.

저가의 cryogenic milling 비진공법을 이용한 나노입자 CuInSe2 광흡수층 제조 (Preparation of nanoparticles CuInSe2 absorber layer by a non-vacuum process of low cost cryogenic milling)

  • 김기현;박병옥
    • 한국결정성장학회지
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    • 제23권2호
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    • pp.108-113
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    • 2013
  • $CuInSe_2$(CIS) chalcopyrite 물질은 고효율 박막 태양전지를 위한 광흡수층의 물질로 매우 잘 알려져 있다. 최근 태양광 산업의 흐름은 안정적인 재료 개발과 가격 경쟁력 있는 태양전지를 위한 효율적인 제조 공정을 일치시키는 것이다. 저가의 CIS 광흡수층 위해 다양한 방법으로 제조를 시도하였고, 본 논문에서는 CIS 광흡수층을 저가형으로 제조를 위해 상용화되는 6 mm pieces를 사용하여 high frequency ball milling과 cryogenic milling을 이용해 CIS 나노입자를 얻었다. 그리고, CIS 광흡수층은 불활성 분위기의 glove box 안에서 milling된 나노입자를 사용하여 paste coating법으로 제조하였다. Chalcopyrite CIS 박막은 기판온도 550도에서 30분간 셀렌화 한 후 성공적으로 제조되었으며, Al/ZnO/CdS/CIS/Mo 구조의 CIS 태양전지는 evaporation, sputtering 및 chemical bath deposition(CBD) 등 다양한 증착 방법으로 각각 제조하였다. 결론적으로, 나노입자를 이용한 CIS 태양전지 전기적 변환효율은 1.74 %를 얻었으며, 개방전압(Voc)는 29 mV, 합선전류밀도(Jsc)는 35 $mA/cm^2$, 그리고 충진율(FF)은 17.2 %였다. 나노입자 CIS 광흡수층은 energy dispersive spectroscopy(EDS), x-ray diffraction(XRD) 그리고 high-resolution scanning electron microscopy(HRSEM) 등으로 특성 분석을 하였다.

Evaluations of Si based ternary anode materials by using RF/DC magnetron sputtering for lithium ion batteries

  • 황창묵;박종완
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2010년도 제39회 하계학술대회 초록집
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    • pp.302-303
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    • 2010
  • Generally, the high energy lithium ion batteries depend intimately on the high capacity of electrode materials. For anode materials, the capacity of commercial graphite is unlike to increase much further due to its lower theoretical capacity of 372 mAhg-1. To improve upon graphite-based negative electrode materials for Li-ion rechargeable batteries, alternative anode materials with higher capacity are needed. Therefore, some metal anodes with high theoretic capacity, such as Si, Sn, Ge, Al, and Sb have been studied extensively. This work focuses on ternary Si-M1-M2 composite system, where M1 is Ge that alloys with Li, which has good cyclability and high specific capacity and M2 is Mo that does not alloy with Li. The Si shows the highest gravimetric capacity (up to 4000mAhg-1 for Li21Si5). Although Si is the most promising of the next generation anodes, it undergoes a large volume change during lithium insertion and extraction. It results in pulverization of the Si and loss of electrical contact between the Si and the current collector during the lithiation and delithiation. Thus, its capacity fades rapidly during cycling. Si thin film is more resistant to fracture than bulk Si because the film is firmly attached to the substrate. Thus, Si film could achieve good cycleability as well as high capacity. To improve the cycle performance of Si, Suzuki et al. prepared two components active (Si)-active(Sn, like Ge) elements film by vacuum deposition, where Sn particles dispersed homogeneously in the Si matrix. This film showed excellent rate capability than pure Si thin film. In this work, second element, Ge shows also high capacity (about 2500mAhg-1 for Li21Ge5) and has good cyclability although it undergoes a large volume change likewise Si. But only Ge does not use the anode due to its costs. Therefore, the electrode should be consisted of moderately Ge contents. Third element, Mo is an element that does not alloys with Li such as Co, Cr, Fe, Mn, Ni, V, Zr. In our previous research work, we have fabricated Si-Mo (active-inactive elements) composite negative electrodes by using RF/DC magnetron sputtering method. The electrodes showed excellent cycle characteristics. The Mo-silicide (inert matrix) dispersed homogeneously in the Si matrix and prevents the active material from aggregating. However, the thicker film than $3\;{\mu}m$ with high Mo contents showed poor cycling performance, which was attributed to the internal stress related to thickness. In order to deal with the large volume expansion of Si anode, great efforts were paid on material design. One of the effective ways is to find suitably three-elements (Si-Ge-Mo) contents. In this study, the Si based composites of 45~65 Si at.% and 23~43 Ge at.%, and 12~32 Mo at.% are evaluated the electrochemical characteristics and cycle performances as an anode. Results from six different compositions of Si-Ge-Mo are presented compared to only the Si and Ge negative electrodes.

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Effects of Sulfur Substitution on Chemical Bonding Nature and Electrochemical Performance of Layered LiMn0.9Cr0.1O2-xSx

  • Lim, Seung-Tae;Park, Dae-Hoon;Lee, Sun-Hee;Hwang, Seong-Ju;Yoon, Young-Soo;Kang, Seong-Gu
    • Bulletin of the Korean Chemical Society
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    • 제27권9호
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    • pp.1310-1314
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    • 2006
  • Sulfur-substituted $LiMn_{0.9}Cr_{0.1}O_{2-x}S_x$ $(0\;\leq\;x\;\leq\;0.1)$ layered oxides have been prepared by solid state reaction under inert atmosphere. From powder X-ray diffraction analyses, all the present lithium manganates were found to be crystallized with monoclinic-layered structure. Electrochemical measurements clearly demonstrated that, in comparison with the pristine $LiMn_{0.9}Cr_{0.1}O_2$, the sulfur-substituted derivatives exhibit smaller discharge capacities for the entire cycle range but the recovery of discharge capacity after the initial several cycles becomes faster upon sulfur substitution. The effect of the sulfur substitution on the chemical bonding nature of $LiMn_{0.9}Cr_{0.1}O_{2-x}S_x$has been investigated using X-ray absorption spectroscopic (XAS) analyses at Mn and Cr K-edges. According to Mn K-edge XAS results, the trivalent oxidation state of manganese ion remains unchanged before and after the substitution whereas the local structure around manganese ions becomes more distorted with increasing the substitution rate of sulfur. On the other hand, the replacement of oxygen with sulfur has negligible influence on the local atomic arrangement around chromium ions, which is surely due to the high octahedral stabilization energy of $Cr^{+III} $ ions. Based on the present experimental findings, we have suggested that the decrease of discharge capacity upon sulfur substitution is ascribable to the enhanced structural distortion of $MnO_6$ octahedra and/or to the formation of covalent Li-S bonds, and the accompanying improvement of cyclability would be related to the depression of Mn migration and/or to the pillaring effect of larger sulfur anion.

퍼멀로이 합금도금을 위한 나노실리카 분산방법에 관한 연구 (Dispersion Method of Silica Nanopowders for Permalloy Composite Coating)

  • 박소연;정명원;이재호
    • 마이크로전자및패키징학회지
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    • 제18권4호
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    • pp.39-42
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    • 2011
  • 복합전기도금은 도금 중 반응성이 없는 물질을 첨가하여 도금층 내부에 함께 존재하도록 함으로써 이루어진다. 퍼멀로이는 철과 니켈의 합금을 말하는 것으로써 마모 특성과 내부식성이 우수하고 복합도금을 함으로써 도금층의 잔류응력 완화와 경도증가, 높은 투자율를 나타내기 때문에 산업 여러 분야에 응용된다. 복합도금을 통해 제품의 미세경도를 향상시킬 수 있으며 이는 제품의 수명과 연관된다. 하지만 실리카 나노분말 표면의 수산화기는 표면을 수분에 취약하게 만들고 이는 나노분말의 응집을 발생시켜 균일한 도금층의 형성을 어렵게 하는 요인이 된다. 본 연구에서는 실리카 나노분말의 zeta potential의 측정과 실리카 나노분말의 응집을 줄이기 위하여 전류밀도의 변화, 첨가제의 변화를 살펴보았다. 표면은 전류밀도 20 $mA/cm^2$에서 가장 효과적이었으며 이 때 실리카의 함량은 $50^{\circ}C$에서 9%로 확인되었다. 첨가제에 따라 표면 형상과 공석되는 실리카 나노입자의 함량 차이가 나타났다. 염기성 도금용액에서 sodium lauryl sulfate를 사용하였을 경우 표면이 매끄럽고 공석되는 실리카 나노분말의 양도 높았다.

프로필렌의 공정안전 운전을 위한 CO2 첨가량에 따른 폭발범위 측정에 관한 연구 (A Study on the Measurement of Explosion Range by CO2 Addition for the Process Safety Operation of Propylene)

  • 최유정;허종만;김정훈;최재욱
    • 한국산학기술학회논문지
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    • 제20권7호
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    • pp.599-606
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    • 2019
  • 위험물질에 의한 제조물을 취급하는 설비와 시설은 대부분 고온, 고압으로 공정을 운전을 한다. 이로 인해 화재폭발로 인한 위험성이 증대되고 있다. 특히, 폭발 사고는 석유 화학 가스설비 등 위험물 시설의 가장 주된 위험요인으로 작용하고 있으며, 그 중, 프로필렌은 석유화학 플랜트의 기초 원료 및 첨가 중합반응에 의한 합성물질을 제조하는 현장에서 많이 사용되고 있다. 산소농도의 변화에 대한 폭발범위를 구함으로써 프로필렌을 사용하는 사업장에서 발생 될 수 있는 폭발을 예방하기 위하여 불활성 가스인 $CO_2$를 이용하여 온도와 압력의 변화에 따라 산소농도의 변화에 대한 폭발범위를 구하였다. 온도는 $25^{\circ}C$, $100^{\circ}C$, $200^{\circ}C$로 변화시켜 측정하였으며, 용기 내 압력을 $1.0kgf/cm^2.G$, $1.5kgf/cm^2.G$, $2.0kgf/cm^2.G$, $2.5kgf/cm^2.G$$CO_2$를 가압시켜 측정하였다. 폭발한계는 온도, 압력 및 산소농도와 관계가 있으며, 온도와 압력이 높아질수록 최소산소농도는 낮아지고, 산소농도가 낮아질수록 폭발범위는 좁아졌다. 또한, 최소산소농도 이하의 농도에서는 프로필렌의 증기와 점화원이 존재하여도 폭발이 발생하지 않는 것을 알 수 있다.

Luminescent Lanthanide Complexes for Advanced Photonics Applications

  • Eom, Yu Kyung;Ryu, Jung Ho;Kim, Hwan Kyu
    • Rapid Communication in Photoscience
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    • 제1권1호
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    • pp.1-9
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    • 2012
  • Luminescent lanthanide complexes have been overviewed for advanced photonics applications. Lanthanide(III) ions ($Ln^{3+}$) were encapsulated by the luminescent ligands such as metalloporphyrins, naphthalenes, anthracene, push-pull diketone derivatives and boron dipyrromethene(bodipy). The energy levels of the luminescent ligands were tailored to maintain the effective energy transfer process from luminescent ligands to $Ln^{3+}$ ions for getting a higher optical amplification gain. Also, key parameters for emission enhancement and efficient energy transfer pathways for the sensitization of $Ln^{3+}$ ions by luminescent ligands were investigated. Furthermore, to enhance the optophysical properties of novel luminescent $Ln^{3+}$ complexes, aryl ether-functionalized dendrons as photon antennas have been incorporated into luminescent $Ln^{3+}$ complexes, yielding novel $Ln^{3+}$-cored dendrimer complex such as metalloporphyrins, naphthalenes, and anthracenes bearing the Fr$\acute{e}$chet aryl-ether dendrons, namely, ($Er^{3+}-[Gn-Pt-Por]_3$ (terpy), $Er^{3+}-[Gn-Naph]_3$(terpy) and $Er^{3+}-[Gn-An]_3$(terpy)). These complexs showed much stronger near-IR emission bands at 1530 nm, originated from the 4f-4f electronic transition of the first excited state ($^4I_{13/2}$) to the ground state ($^4I_{15/2}$) of the partially filled 4f shell. A significant decrease in the fluorescence of metalloporphyrins, naphthalenes and anthracene ligand were accompanied by a strong increase in the near IR emission of the $Ln^{3+}$ ions. The near IR emission intensities of $Ln^{3+}$ ions in the lanthanide(III)-encapsulated dendrimer complexes were dramatically enhanced with increasing the generation number (n) of dendrons, due to the site-isolation and the light-harvesting(LH) effects. Furthermore, it was first attempted to distinguish between the site-isolation and the light-harvesting effects in the present complexes. In this review, synthesis and photophysical studies of inert and stable luminescent $Ln^{3+}$ complexes will be dealt for the advanced photonics applications. Also, the review will include the exploratory investigation of the key parameters for emission enhancement and the effective energy transfer pathways from luminescent ligands to $Ln^{3+}$ ions with $Ln^{3+}$-chelated prototype complexes.