• 한국재료학회지
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• 제8권12호
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• pp.1165-1169
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• 1998

제1세대 니켈계 단결정 초합금인 CMSX 6를 사용하여 셀렉타법으로 진공 정밀주조하여 단결정을 제작하였다. 주형온도 약 150$0^{\circ}C$, 주입온도 약 163$0^{\circ}C$와 용탕 주입 직후 주형을 2.5mm/분 속도로 하강시켜 단결정을 성장시켰다. 단결정 주조조직에서 기지와 공정조직은 ${\gamma}$' 석출물(Ni$_3$(Al, Ti)) 모양과 크기에 따라 각각 모두 두영역으로 구분되었으며, 공정조직의 Ti함랗은 기지보다 높았다. 즉, EPMA 및 CBED 분석 등으로 ${\gamma}$' 석출물을 분석한 결과, 기지내의 ${\gamma}$'은 크기가 0.5~0.7$\mu\textrm{m}$ 이하이며 화학조성상 Ni$_3$Al에 가까웠으며 격자구조도 Ll$_2$를 나타내었다. 반면에 공정조직에 가까울수록 ${\gamma}$' 크기는 1.0$\mu\textrm{m}$보다 컸으며, 모양도 판상형의 거대한 모양으로 바뀌었다. 화학조성 또한 Ni$_3$Ti에 가까웠으며 격자구조도 D $O_{24}$를 나타내었으므로 수지상과 공정조직의 ${\gamma}$' 석출물은 화학조성 및 격자구조가 상이함을 알 수 있었다.

• 공업화학
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• 제8권3호
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• pp.425-429
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• 1997

윤활유 첨가제 중간체인 polyisobutenylsuccinic anhydride(PIBSA)를 polyisobutylene(PIB)과 maleic anhydride(MA)을 이용하여 합성하였다. PIB-a와 MA의 결합반응은 각각의 이중결합사이의 반응을 통하여 이루어지는데 반응조건에 따른 결합도를 측정하였다. 용매를 사용하지 않고 $190^{\circ}C$로 12시간 반응한 경우는 결합도가 0.98을 보였으며 같은 온도에서 벤질알코올 용매를 사용한 경우는 0.21, 그리고 루이스 산촉매인 $AlCl_3$ 및 $SnCl_4$, $Et_2AlCl$, $TiCl_4$을 사용한 경우는 0.03~0.20을 보였다. 또한 PIB의 종류에 따라 결합도의 차이를 보였다. MA의 결합도는 PIB에 ${\alpha}$-올레핀(ego)형이 많이 포함될 수록 증가함을 확인하였다. PIB과 MA가 결합된 PIBSA의 구조는 FT IR과 $^1H$ NMR을 통하여 결정하였다. 결합된 MA의 anhyhide IR 흡수대가 1782 및 $1855cm^{-1}$에서 강하게 나타나며, 1639 및 $897cm^{-1}$에서 보인 PIB의 이중결합의 흡수대가 사라진 것으로부터 알 수 있다. $^1H$ NMR을 통하여 결합된 MA를 확인하는 것은 상대적으로 anhydride peak의 양이 적어 거의 불가능하지만, 확대된 5.5~2.5영역에서 PIB과 다른 peak를 확인할 수 있다. 제조한 PIBSA와 diaminoethane를 반응시키어 윤활유첨가제인 polyisobutenylsuccimide(PIBSI)을 제조하였다.

• 한국토양비료학회지
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• 제34권6호
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• pp.373-379
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• 2001

우리 나라 산지토양의 주요 모암에서 발달된 잔적층 암쇄를 대상으로 토양의 단면 특성, 이화학적 특성 X-선 형광분석 (XRF)을 통하여 모재에 따른 토양의 화학조성 변화와 주요한 구성원소의 풍화량을 토양층위 및 모암별로 비교하였다. 모암에 관계없이 토양의 C층에 비하여 A층에서 점토함량, 양이온 치환용량 (CEC), 유기물 함량은 높았으며, 용적밀도 ($kg\;m^{-3}$)와 pH는 낮은 경향을 보였다. 그러나 사암모재의 의성통에서는 점토함량이 감소하였는데 이는 토양과 함께 유실 되었거나 하부로 이동한 것으로 보였다. 토양 중 $SiO_2$함량은 화강암, 화강편마암, 석회암, 혈암 유래 토양에서, $Fe_2O_3$와 MgO는 현무암, 석회암, 혈암 유래 토양에서, CaO는 석회암 유래 토양에서 각각 높았다. 현무암 모재의 구좌통과 석회암 모재의 장성통 토양에서 작열감량(Igniton loss)이 크게 나타났다. 토양 화학성분별 풍화 정도는 공시 토양의 모암에 관계없이 염기이온(K, Ca, Mg, Na)들의 풍화량이 Si, Al, Fe 보다 크게 나타났다. C층과 비교하여 A층의 $TiO_2$의 함량비가 클수록 화학성분의 풍화정도가 큰 토양으로 나타났으며, 이는 $TiO_2$가 다른 원소보다 풍화에 상대적으로 안정된 광물이기 때문인 것으로 보인다. 각 원소의 절대적 함량비를 고려할 때 화강암, 화강편마암, 사암, 혈암, 현무암 유래 토양에서는 Si, Al의 유실이 심했으나 석회암 유래 토양에서는 탄산염의 빠른 풍화로 Ca, Mg이온의 풍화량이 많았다. 화학 성분의 풍회가 큰 토양은 사암 유래 의 성통과 화강암 유래 도산통 >> 혈암 유래 음성통과 석회암 유래 장성통 > 화강편마암 유래 덕산통 > 현무암 유래의 구좌통 순이었다.

• 전기학회논문지
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• 제57권11호
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• pp.2015-2022
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• 2008

The effect of content of $Al_2O_3+Y_2O_3$ sintering additives on the densification behavior, mechanical and electrical properties of the pressureless-sintered $SiC-ZrB_2$ electroconductive ceramic composites was investigated. The $SiC-ZrB_2$ electroconductive ceramic composites were pressurless-sintered for 2 hours at 1,700[$^{\circ}C$] temperatures with an addition of $Al_2O_3+Y_2O_3$(6 : 4 mixture of $Al_2O_3$ and $Y_2O_3$) as a sintering aid in the range of $8\;{\sim}\;20$[wt%]. Phase analysis of $SiC-ZrB_2$ composites by XRD revealed mostly of $\alpha$-SiC(6H), $ZrB_2$ and In Situ YAG($Al_5Y_3O_{12}$). The relative density, flexural strength, Young's modulus and vicker's hardness showed the highest value of 89.02[%], 81.58[MPa], 31.44[GPa] and 1.34[GPa] for $SiC-ZrB_2$ composites added with 16[wt%] $Al_2O_3+Y_2O_3$ additives at room temperature respectively. Abnormal grain growth takes place during phase transformation from $\beta$-SiC into $\alpha$-SiC was correlated with In Situ YAG phase by reaction between $Al_2O_3$ and $Y_2O_3$ additive during sintering. The electrical resistivity showed the lowest value of $3.l4{\times}10^{-2}{\Omega}{\cdot}cm$ for $SiC-ZrB_2$ composite added with 16[wt%] $Al_2O_3+Y_2O_3$ additives at 700[$^{\circ}C$]. The electrical resistivity of the $SiC-TiB_2$ and $SiC-ZrB_2$ composite was all negative temperature coefficient resistance (NTCR) in the temperature ranges from room temperature to 700[$^{\circ}C$]. Compositional design and optimization of processing parameters are key factors for controlling and improving the properties of SiC-based electroconductive ceramic composites.

• 한국정보디스플레이학회:학술대회논문집
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• 한국정보디스플레이학회 2004년도 Asia Display / IMID 04
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• pp.1091-1094
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• 2004

High-luminous efficiency full-color emissions in photoluminescence (PL) were obtained in $GdVO_4$ phosphor thin films co-doped with various amounts of Eu, Er and/or Tm and postannealed at approximately 1000$^{\circ}C$. The $GdVO_4$:Eu,Er,Tm phosphor thin films were deposited on thick $BaTiO_3$ ceramic sheets by r.f. magnetron sputtering using powder targets and postannealed in an air atmosphere. The rare earth (RE) content (RE/(Gd+V+RE) atomic ratio) in the oxide phosphor thin films was varied in the range from 0.1 to 2 at.%. It was found that the excitation of $GdVO_4$:Eu.Er,Tm thin films is attributed to band-to-band transition. A white PL emission was obtained in a $GdVO_4$:Eu,Er,Tm thin film with Eu, Er and Tm contents of 0.2, 0.7 and 1 at.%, respectively: CIE chromaticity color coordinates. (X=0.352 and Y=0.351). In addition, a white emission was obtained in a thin-film electroluminescent (TFEL) device made with this thin film.

• 한국윤활학회:학술대회논문집
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• 한국윤활학회 2002년도 제35회 춘계학술대회
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• pp.215-225
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• 2002

In order to enhance the thermal stability of binder materials of bonded type solid lubricants, several combinations of metal-alkoxide based sol-gel materials such as methyltrimethoxysilane(MTMOS), $titaniumisopropoxide(Ti(Opr^{j})_{4})$, $zirconiumisopropoxide(Zr(Opr^{j})_{4})$ and $aluminumbutoxide(Al(Obu^{t})_{4})$ were chemically modified by epoxy-, acrylic- and fluoro-silane compounds, respectively, in this work. Friction and wear characteristics of these hybrid ceramic materials were tested with a micro tribe-tester where a reciprocating steel ball slid on a test material, and the tribological property was also evaluated with respect to both heat-curing temperature and tile time. Test results generally showed that hybrid ceramic materials modified by epoxy-silane compounds had a low friction compared to others. And the higher heat-curing temperature and the longer heat treatment time resulted in the higher friction and the lower wear. IR spectroscopic analyses revealed that it was caused mainly by the increased metal oxide content in hybrid ceramics when the heat-curing temperature was over $320^{\circ}C$.

• Ocean and Polar Research
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• 제24권2호
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• pp.167-175
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• 2002

Sediment from six piston cores from the East Sea (Sea of Japan) was analyzed for evidence of paleoceanographic changes and paleoclimatic variation. A distinct geochemical boundary is evident in major element concentrations and organic carbon content of most cores near the 10-ka horizon. This distinctive basal Holocene change is interpreted to be largely the result of changing sediment sources, an interpretation supported by TiO_2/Al_2O_3$ ratios. Organic carbon and carbonate contents also differ significantly between the Holocene and glacial intervals. The C/N ratio of organic matter is greater than 10 during the glacial period, but is less than 10 for the Holocene, suggesting that the influx of terrigenous organic matter was more volumetrically important than marine organic matter during glacial times. The chemical index of weathering (CIW) is higher for the Holocene than the glacial interval, and changes markedly at the basal Holocene geochemical boundary. Silt fractions are higher in the glacial interval, suggesting a strong effect of climate on silt particle transportation: terrigenous aluminosilicates and continental organic carbon transport were higher during glacial times than during the Holocene. Differences in sediment composition between the Holocene and glacial period are interpreted to have been climatically induced.

• Tribology and Lubricants
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• 제18권5호
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• pp.324-332
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• 2002

In order to enhance the thermal stability of binder materials of bonded type solid lubricants, several metal-alkoxide based sol-gel materials such as methyltrimethoxysilane(MTMOS), titaniumisopropoxide$(Ti(Opr^i)_4),$ zirconiumisopropoxide $(Zr(Opr^i)_4)$ and aluminumbutoxide$(Al(Obu^t)_4)$ were chemically modified by epoxy-, acrylic- and fluoro-silane compounds, respectively. Friction and wear characteristics of these hybrid ceramic materials were tested with a micro tribo-tester, and evaluated with respect to both heat-curing temperature and the time. Test results generally showed that hybrid ceramic materials modified by epoxy-silane compounds had a low friction compared to others. And the higher het-curing temperature and the longer heat treatment time resulted in the higher friction and the lower wear. IR spectroscopic analyses revealed that these results were caused mainly by the increased metal oxide content in hybrid ceramics when the heat-curing temperature was over $320^{\circ}C.$

• 한국재료학회지
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• 제16권1호
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• pp.30-36
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• 2006

A novel method was proposed to grow an epitaxial $CoSi_2$ on (100)Si substrate. A $CoN_x$ interlayer was deposited by reactive sputtering of Co in an Ar+$N_2$ flow. From the Ti/Co/$CoN_x$/Si structure, a uniform and thin $CoSi_2$ layer was epitaxially grown on (100)Si by annealing above $700^{\circ}C$. Two amorphous layers were found at the $CoN_x$/Si interface, where the top layer has a silicon nitride (Si-N) bonding state with some Co content and the bottom layer has a Co-Si intermixing state. The SiNx amorphous layer seems to play a critical role of suppressing the diffusion of Co into Si substrate for the direct formation of epitaxial $CoSi_2$.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2003년도 제5회 영호남 학술대회 논문집
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• pp.31-34
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• 2003

($Ba_{0.6-x}Sr_{0.4}Ca_x)TiO_3$ (BSCT) (x=0.10, 0.15, 0.20) powder, prepared by the sol-gel method, were mixed with organic vehicle and the BSCT thick films were fabricated by the screen-printing techniques on alumina substrates using the BSCT paste. The structural and the electrical properties were investigated for various composition ratio and sintering temperature. BSCT thick film thickness, obtained by four printings, was approximately 110 ~ 120 ${\mu}m$. The Curie temperature and dielectric constant at room temperature were decreased with increasing Ca content. The relative dielectric constant, dielectric loss and tunability of the BSCT(50/40/10) specimen, which was sintered at $1420^{\circ}C$ and measured at 1MHz, were about 910, 0.46% and 9.28% at 5kV/cm, respectively.