• 폴리머
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• 제29권1호
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• pp.54-58
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• 2005

미생물 합성 poly[(R)3-hydroxybutyrate]](P(3HB))의 알칼리 및 효소 분해거동을 단결정과 Langmuir 단분자막을 모델시스템으로 하여 연구하였다. 단결정의 초기효소 및 알칼리 분해거동은 단결정의 장축에 대해 수직방향(b축)으로 분해가 일어났고 용융점 이하의 온도에서 열처리 또한 단결정의 b축을 따라 봉우리 형태의 형태학적 변화를 관찰하였다. 이러한 결과는 라멜라 단결정은 b축을 따라 불규칙한 영역을 가지고 있음을 의미하고 효소분해가 불규칙한 영역에서 선호적으로 일어난다고 설명할 수 있다. 한편, P(3HB), 단분자막의 효소 및 알칼리 분해경향은 분해매체와 표면압력에 크게 의존하였다. 알칼리 분해의 경우 낮은 표면압력에서도 분해를 나타내는 반면 효소 분해는 높은 표면 압력 하에서 분해거동을 나타내었다. 이러한 현상은 분자수준의 크기인 알칼리 분해매체는 P(3HB) 단분자막과 좁은 접촉면적(낮은 표면압력)에서도 활성을 보이는 반면 크기가 큰 분해효소는 보다 큰 활성 접촉면적(높은 표면압력)을 필요로 하는 것으로 판단된다.

• 한국분말재료학회지
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• 제25권3호
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• pp.208-212
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• 2018

In this paper, a new $Co_{10}Fe_{10}Mn_{35}Ni_{35}Zn_{10}$ high entropy alloy (HEA) is identified as a strong candidate for the single face-centered cubic (FCC) structure screened using the upgraded TCFE2000 thermodynamic CALPHAD database. The $Co_{10}Fe_{10}Mn_{35}Ni_{35}Zn_{10}$ HEA is fabricated using the mechanical (MA) procedure and pressure-less sintering method. The $Co_{10}Fe_{10}Mn_{35}Ni_{35}Zn_{10}$ HEA, which consists of elements with a large difference in melting point and atomic size, is successfully fabricated using powder metallurgy techniques. The MA behavior, microstructure, and mechanical properties of the $Co_{10}Fe_{10}Mn_{35}Ni_{35}Zn_{10}$ HEA are systematically studied to understand the MA behavior and develop advanced techniques for fabricating HEA products. After MA, a single FCC phase is found. After sintering at $900^{\circ}C$, the microstructure has an FCC single phase with an average grain size of $18{\mu}m$. Finally, the $Co_{10}Fe_{10}Mn_{35}Ni_{35}Zn_{10}$ HEA has a compressive yield strength of 302 MPa.

• 폴리머
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• 제27권4호
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• pp.293-298
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• 2003

제한공간에서 형성되는 폴리(트리메틸렌 테레프탈레이트) (PTT)의 결정구조를 광학현미경, 소각 광산란 및 X-선 회절로 조사하였다. 인자 $\delta$로 대표할 수 있는 배제 성분의 이동거리는 폴리(에틸렌 테레프탈레이트) (PET/PTT) 블렌드의 형태구조 패턴을 결정하는데 중요한 역할을 하였다. 단계 결정화할 경우, PTT 결정화는 앞서 성장한 PET 결정의 구정 사이 영역에서 시작되었으며, 구정 사이 영역이 채워질 때까지 진행하였다. PET 구정 표면은 PTT 결정화에 매우 효과적인 핵 생성 작용을 유도함으로써 transcrystalline 구조의 PTT 결정을 유도하였다. 그 결과 PTT가 많은 상에서 전형적인 구정 구조와 함께 transcrystalline구조가 혼재하는 독특한 형태구조가 관찰되었다. PET 구정의 라멜라 사이나 피브릴 사이의 영역에서는 공간적 제한으로 인하여 PTT분자들의 형태 자유도가 감소하였으며, 이러한 감소 요인은 PET구정 내ㆍ외부에서의 PTT 결정화와 용융 거동에 차이를 유발하였다.

• 한국재료학회지
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• 제5권2호
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• pp.223-231
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• 1995

열전발전용 재료인 PbTe의 밀링 시간, 볼과 분말의 무게비에 따른 기계적 합금화 거동을 연구하였다. Pb와 Te 분말을 볼과 분말의 무게비 2 : 1에서 2분간 기계적 합금화 함으로써 PbTe 금속간 화합물의 형성이 완료되었다. 밀링 공정중 vial 표면 온도의 in situ 측정에서 기계적 합금화에 의한 PbTe 금속간 화합물의 형성이 분말 계면에서의 확산 공정보다는 합금화 반응이 자발적으로 전파하는 자전 반응에 의하여 이루어지는 것을 알 수 있었다. 기계적 합금화로 제조한 PbTe 합금분말의 격자상수는 0.6462nm로 용해 및 분쇄법으로 제조한 PbTe 분말에서 보고된 값인 0.6459nm와 잘 일치하였으며, 밀링 시간의 증가 및 볼과 분말의 무게비의 변화에 의하여 변하지않았다.

• 한국세라믹학회지
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• 제40권12호
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• pp.1224-1228
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• 2003

장석, 규석, 석회석 등의 천연원료와 CeO$_2$를 출발원료로 하여 프릿 형태의 러스터 유약을 제조하고 결정화 특성과 러스터 효과의 발현기구를 분석하였다. 시유한 시편이 110$0^{\circ}C$에서 소성되었을 때, 유면과 수평한 방향으로 (100)면이 배향된 200nm 크기의 CeO$_2$ 결정이 시편의 표면에 생성되었다. 표면에서 결정화된 입자의 빈도는 유약의 내부보다 훨씬 높았으며, 전체 표면적의 60% 이상을 배향된 CeO$_2$ 결정이 점유하였다. 배향된 CeO$_2$ 결정립은 유약내의 프릿 입자가 완전히 용융되어 내부 계면이 사라진 이후부터 발달하기 시작하였다. 본 연구에서 개발된 유약의 러스터 효과는 유약표면에 석출된 CeO$_2$가 고굴절을 갖는 물직일 뿐만 아니라 최대 산란을 일으키는 결정크기(200nm)이고 판상형태로 배열되어 있기 때문인 것으로 판단된다.

• 한국세라믹학회지
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• 제46권6호
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• pp.587-591
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• 2009

Lithium salt have been used mainly as electrolyte of thermal battery for electricity storage. Recently, The 3phase lithium salt(LiCl-LiF-LiBr) is tried to use as electrolyte of thermal battery for high electric power. It is reported that LiCl-LiF-LiBr salt have high ion mobility due to its high lithium ion concentration. Solid lithium salt is melt to liquid state at above $500{^{\circ}C}$. The lithium ion is easily reacted with support materials. Because the melted lithium ion has small ion size and high ion mobility. For the increasing mechanical strength of electrolyte pellet, the research was started to apply ceramic filter to support of electrolyte. In this study, authors used SiOC web and glass fiber filter as ceramic mat for support of electrolyte and impregnated LiCl-LiF-LiBr salt into ceramic mat at above $500{^{\circ}C}$. The fabricated electrolyte using ceramic mat was washed with distilled water for removing lithium salt on ceramic mat. The washed ceramic mat was observed for lithium ion reaction behavior with XRD, SEM-EDS and so on.

• 한국재료학회지
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• 제30권10호
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• pp.502-508
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• 2020

This paper focuses on the electrical properties and stability against DC accelerated aging stress of ZnO-V₂O₅-MnO₂-Nb₂O₅-Bi₂O₃-Co₃O₄-Dy₂O₃ (ZVMNBCD) varistor ceramics sintered at 850 - 925 ℃. With the increase of sintering temperature, the average grain size increases from 4.4 to 11.8 mm, and the density of the sintered pellets decreases from 5.53 to 5.40 g/㎤ due to the volatility of V₂O₅, which has a low melting point. The breakdown field abruptly decreases from 8016 to 1,715 V/cm with the increase of the sintering temperature. The maximum non-ohmic coefficient (59) is obtained when the sample is sintered at 875 ℃. The samples sintered at below 900 ℃ exhibit a relatively low leakage current, less than 60 mA/㎠. The apparent dielectric constant increases due to the increase of the average grain size with the increase of the sintering temperature. The change tendency of dissipation factor at 1 kHz according to the sintering temperature coincides with the tendency of the leakage current. In terms of stability, the samples sintered at 900 ℃ exhibit both high non-ohmic coefficient (45) and excellent stability, 0.8% in 𝚫E_B/E_B and -0.7 % in 𝚫α/α after application of DC accelerated aging stress (0.85 E_B/85 ℃/24 h).

• 열처리공학회지
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• 제9권1호
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• pp.1-11
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• 1996

Mechanical alloying is an effective process to finely distribute inert dispersoids in an Al-TM(TM is a transition metal) system. It has been considered that high melting point aluminides are formed by precipitation from supersaturated Al(Ti) powder. This analysis is based on the fact that much higher content of TM than the solubioity can be dissolved in alpha aluminum during the high energy ball milling. Thus, decomposition behavior of Ti in the Al(Ti) was considered very important. But it is confirmed that the higher portion of Ti than Al(Ti) solid solution is existed as nano-sized Ti particles in the MA powders by high energy ball nilling from the XRD spectrum and TEM analysis in this study. Therefore, the role of undissolved TM particles affect the formation of aluminides should be suitably considered. In this study, we present experimental observation on the formation of $Al_3Ti$ fron mechanical alloyed Al-Ti alloys in the hyperperitectic region. This study showed that, in the mechanically alloyed Al-20wt%Ti specimen, intermediate phase of cubic $Al_3Ti$ and tetragonal $Al_{24}Ti_8$ formed at $300{\sim}400^{\circ}C$ and $400{\sim}500^{\circ}C$, respectively, before the MA state reaches to equilibrium at higher temperatures. The formation behavior of $Ll_2-Al_3Ti$ is interpreted by interdiffusion of Al and Ti in solid state based on the fact that large amount of nano-sized Ti particles exist in the milled powder. Present analysis indicated undissolved Ti particles of nanosize should have played an important role initiation the formation of $Al_3Ti$ phase during annealing.

• 한국표면공학회지
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• 제44권1호
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• pp.13-20
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• 2011

This study investigated the high temperature oxidation behavior of Fe-22%Cr-5.8%Al alloy and the oxidation kinetics of the alloy were discussed. Bulk samples were prepared by VAM (vacuum arc melting) and hot forging. High temperature oxidation testes were isothermally conducted up to 100 hours in 79%$N_2$+21%$O_2$ environment at three different temperatures ($900^{\circ}C$, $1000^{\circ}C$, $1100^{\circ}C$). The weight gain was measured after oxidation according to oxidation time (2, 4, 6, 8, 10, 15, 20, 25, 30, 60, 80, 100 hours). The weight gain significantly increased with increasing oxidation temperature. As the temperature increased, the oxidized samples showed sequential formation of $Al_2O_3$, Cr-rich oxide, Fe-rich oxide. The activation energy of high temperature oxidation was obtained as 306.63 KJ/mol. $Al_2O_3$ were developed on the surface in the early stage of oxidation, representing protective role of oxidation. However, Fe-based and Cr-based oxides leaded to breakaway of oxide layer, thus resulted in the significant increase of additional oxidation.

• 한국분말재료학회지
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• 제11권5호
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• pp.383-390
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• 2004

In order to investigate behavior of abnormal expansion of the iron-copper compacts, we compared the dilatometric curves of the compacts which mixed the copper powder to the iron powder with those of compacts which mixed the copper powder to the iron-copper alloy powder. The dilatometric curves were obtained below the sintering conditions, which heated up to 115$0^{\circ}C$ by a heating rate of 1$0^{\circ}C$/min, held for 60min at 115$0^{\circ}C$ and cooled down at a rate of 2$0^{\circ}C$/min to room temperature. The dilatometric curves of the compacts showed the different expansion behavior at temperatures above the copper melting point in spite of same chemical composition. All of the compacts of former case showed large expansion, but all of the compacts in latter case showed large contraction. The microstructures of sintered compacts also showed the different progress in alloying of the copper into the iron powder. Namely we could observe the segregation at alloy part of copper into iron powder in case of the sintered compacts, which mixed the copper powder to the iron powder, but could not observe the segregation in compacts which mixed the copper powder to the iron-copper alloy powder. But the penetration of liquid copper into the interstices between solid particles was occurred at both cases. Therefore, the showing of the different dimensional changes in the compacts in spite of same chemical composition is due to more the alloying of copper into iron powder than the penetration of liquid copper into the interstices between solid particles.