• 공업화학
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• 제5권6호
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• pp.1068-1077
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• 1994

생분해성 고분자의 실용화 검토를 위하여 생분해성 Copolyesterethylene(CPEE)과 LDPE를 0~100%까지 10% 간격으로 전조성에 걸쳐 용융 블렌드하였다. 각 조성에서 블렌드한 시료의 녹는점 변화, 용융 엔탈피, 결정화 온도 및 결정화 엔탈피를 시차주사열량계고 측정하여 miscibility에 관하여 고찰하였으며 만능시험기를 이용하여 인장강도 및 신장률을 측정하였다. 열분석 결과로부터 CPEE의 조성이 30%일 때까지 약간의 miscibility를 보임을 알 수 있었으며, 인장 강도값으로부터는 CPEE조성이 30~80%를 제외한 조성에서 유용한 compatibility를 갖는 것을 알았다. SEM 관찰을 통한 각 조성에서의 형태학적 모습으로부터 이들 상용성의 결과를 확인하였으며, 또한 CPEE/LDPE 블렌드 각 조성에 대한 생분해성을 미생물 접종 4주 후의 중량감소율을 측정하여 확인하였다.

• Fibers and Polymers
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• 제2권2호
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• pp.98-107
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• 2001

The phase transition behavior isothermal micro-phase separation kinetics of polyester-based thermoplastic elastomer were studied using the synchrotron X-ray scattering(SAXS) method. The structural changes occurring during heating period were investigated by determining the changes of the one-dimensional correlation function, interfacial thickness and Porod constant. Based on the abrupt increases of the domain spacing and interfacial thickness, a major structural change occurring well below the melting transition temperature is suggested. Those changes are explained in terms of melting of the thermodynamically unstable hard domains or/and the interdiffusion of the hard and soft segments in the interfacial regions. SAXS profile changes during the micro-phase separation process were also clearly observed at various temperatures and the separation rate was found to be sensitively affected by the temperature. The peak position of maximum scattering intensity stayed constant during the entire course of the phase separation process. The scattering data during the isothermal phase separation process was interpreted with the Cahn-Hilliard diffusion equation. The experimental data obtained during the early stage of the phase separation seems to satisfy the Cahn-Hilliard spinodal mechanism. The transition temperature obtained from the extrapolation of the diffusion coefficient to zero value turned out to be about 147$\pm$$2^{\circ}$, which is close to the order-disorder transition temperature obtained from the Porod analysis. The transition temperature was also estimated from the inveriant growth rate. By extrapolating the inveriant growth rate to zero, a transition temperature of about 145$\pm$$\pm$$2^{\circ}$ was obtained.

• Progress in Superconductivity
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• 제6권2호
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• pp.129-132
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• 2005

The formation behavior of $YBa_2Cu_3O_{7-x}$(Y123) and CuO phases in the heat-treated Cu-sheathed YBCO thick films was studied. The thick films were prepared by screen-printing method using $BaCO_3$ and Y211 powders on Cu tapes. The screen-printed thick films were placed at the center of the tube furnace, heated to $930^{\circ}C$ in air atmosphere and then maintained at the temperature for 60 sec - 300 sec. The microstructure and phases formed in the thick films were investigated by using optical microscope, X-ray diffraction (XRD) and SEM image analysis. During the heat treatment, partial melting occurred rapidly in the printed layers by peritectic reaction between CuO and precursor powders, and then YBCO superconducting phases nucleated from the Cu tapes and grew in a form of thick films.

• Korea-Australia Rheology Journal
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• 제13권4호
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• pp.169-177
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• 2001

Morphological, thermal, rheological, and mechanical properties of reactive compatabilized blends of poly(butylene terephthalate) (PBT) and Polyamide-6 (PA) containing EGMA copolymer were investigated using scanning electron microscopy (SEM), differential scanning calorimetry (DSC), advanced rheometric expansion system (ARES), and universal testing machine (UTM). From the results of thermal analysis by DSC, the melting point of the 30/70 PBT-PA blend was broadened after EGMA was added in the blends, since the enthalpy of melting of the PBT-PA somewhat decreased with the increase of EGMA content. From this result, it is suggested that the EGMA affected to the crystallization behavior and crystallinity of the PBT-PA blends. From SEM micrographs of the 70/30, 50/50, and 30/70 PBT-PA blends, the droplet size of the 30/70 PBT-PA blend was about 0.8 ${\mu}{\textrm}{m}$ which was smaller than that of the 50/50 and 70/30 PBT-PA blends. The complex viscosity of the 30/70 PBT-PA blend observed to be higher than that of the 50/50 and 70/30 PBT-PA blends. From the results of the morphology and rheological properties for the PBT-PA blends, it is suggested that the compatibility is increased in the 30/70 PBT-PA blend than the 50/50 and 70/30 PBT-PA blends. From the results of mechanical properties, it was found that the tensile strength of the 30/70 PBT-PA blend increased with the increase of EGMA up to 2 phr, while tensile strength of the blend in which EGMA content was higher than 2 phr decreased with the increase of EGMA content. From the results of morphological, thermal, rheological, and mechanical properties for the PBT-PA-EGMA blends, it is suggested that the EGMA could be used as a compatibilization role in the blends.

• 반도체디스플레이기술학회지
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• 제15권4호
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• pp.10-15
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• 2016

In this paper, novel ball grid array (BGA) interconnection process using solderable anisotropic conductive adhesives (SACAs) with low-melting-point alloy (LMPA) fillers have been developed to enhance the processability in the conventional capillary underfill technique and to overcome the limitations in the no-flow underfill technique. To confirm the feasibility of the proposed technique, BGA interconnection test was performed using two types of SACA with different LMPA concentration (0 and 4 vol%). After the interconnection process, the interconnection characteristics such as morphology of conduction path and electrical properties of BGA assemblies were inspected and compared. The results indicated that BGA assemblies using SACA without LMPA fillers showed weak conduction path formation such as solder bump loss or short circuit formation because of the expansion of air bubbles within the interconnection area due to the relatively high reflow peak temperature. Meanwhile, assemblies using SACA with 4 vol% LMPAs showed stable metallurgical interconnection formation and electrical resistance due to the favorable selective wetting behavior of molten LMPAs for the solder bump and Cu metallization.

• Elastomers and Composites
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• 제36권3호
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• pp.169-176
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• 2001

2몰% 에틸가지를 포함하는 에틸 가지화 폴리에틸렌[(PE(2)]과 에틸렌-프로필렌 몰비가 50:50으로 같지만 입체규칙성이 서로 다른 랜덤-에틸렌-프로필렌 고무(r-EPR), 교호-에틸렌-프로필렌 고무(alt-EPR) 및 이소탁틱-교호-에틸렌-프로필렌 고무(iso-alt-EPR)를 에틸렌-프로필렌 고무의 입체규칙성에 대한 혼화성과 물성의 차이를 조사하기 위하여 혼합하였다. 이 세가지 블렌드들은 상온에서 상호간에 혼화성이 없었고, 밀도 측정에서 단순한 첨가 효과를 보여 주었다. 블렌드 조성에 따른 폴리에틸렌의 녹는점 감소는 PE(2)/r-EPR>PE(2)/alt-EPR>PE(2)/iso-alt-EPR의 순서로 증가하였다. 인장시험에서 이 블렌드계는 혼합 조성이 50:50 일때 가장 낯은 파난강도의 값을 보여 주어 이 블렌드 조성에서 두 고분자 상(phase)이 가장 분리된 형태학(morphology)을 가지고 있음을 알았다.

• 한국주조공학회지
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• 제26권6호
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• pp.272-276
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• 2006

[ $CaCO_3$ ]를 발포제로 사용하여 균일한 기공구조를 가지는 AZ91과 AM60 마그네슘 합금의 발포 금속을 주조법을 통하석 제조하였다. 발포 금속의 제조가 가능한 이유와 발포 마그네슘 합금의 기공구조가 연구를 통하여 논의되었다. 마그네슘 합금의 용탕은 $CaCO_3$의 분해 거동에 영향을 미친다. 제조된 AZ91 마그네슘 합금의 발포 금속은 높은 기공률과 큰 기공의 크기를 가졌으며, 발포 금속들 중에서 상대적으로 쉽게 발포되는 것으로 판단된다.

• 폴리머
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• 제24권3호
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• pp.333-341
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• 2000

선형 폴리락틱산/스타형 폴리락틱산 블렌드를 용융 및 용액 블렌딩에 의해 제조하여 이들의 열적 특성 및 결정화 거동을 살펴보고 블렌딩 방법이 이들에 미치는 영향을 살펴보았다. 분지형 구조를 갖는 스타형 폴리락틱산은 선형 폴리락틱산에 비하여 용융 및 용액 가공에서의 분자량 감소가 적음을 확인하였으며, 용융 가공에 비하여 용액 가공에서 분자량 분포가 넓어짐을 확인하였다. 스타형 폴리락틱산을 선형 폴리락틱산에 블렌딩하였을 경우 용융온도의 감소와 유리전이온도의 감소를 확인하였으며, 용액 블렌딩에 의하여 얻어진 블렌드는 용융 블렌딩에 의하여 얻어진 블렌드에 비하여 낮은 유리전이온도를 갖음을 알 수 있었다. 분지형 구조로 인하여 상대적으로 결정화가 어려운 스타형 폴리락틱산과 스타형 폴리락틱산 함량이 높은 블렌드의 경우, 용액 가공에 의하여 용융 가공에서 보다 높은 결정화도를 얻을 수 있었다.

• 폴리머
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• 제35권4호
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• pp.308-313
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• 2011

5원환의 2,3,5,6-tetrahydroimidazo[2,1-b] [1,3] oxazole(TIO)와 비교하여 6원환인 2,5,6,7-tetrahydro-3H-imidazo[2,1-b] [1,3] oxazine(TII)가 중합반응성이 낮은 결점을 개선하고자 각종의 조건하에서 중합을 실시한 결과, 최적의 중합조건으로 methyl trifluoromethanesulfonate(MeOTf)을 개시제로 사용한, 극성이 높은 니트로벤젠 용매의 $60^{\circ}C$에서 24시간 반응시킴에 의해 고수율의 중합체를 얻었다. 생성된 중합체를 $^1H$ NMR과$^{13}C$ NMR, IR 스펙트럼으로 분석하였으며, GPC로부터 구한 분자량과 이론분자량이 거의 일치함도 확인하였으며, 융점($T_m$)은 알킬 그룹의 길이에 따라 큰 차이를 나타내었다.

• 대한금속재료학회지
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• 제48권2호
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• pp.154-162
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• 2010

A fundamental study of the distillation behavior of ferromanganese alloy melts was carried out at 1773 K and 0.1333 kPa (=1 Torr). During the distillation of ferromanganese alloy melts under reduced pressure, manganese vaporizes preferentially to phosphorus and other solute elements. High purity manganese metal with a very low content of solute elements can be obtained by distillation of ferromanganese alloy melts. The evaporation of manganese is suppressed as the carbon content of ferromanganese alloy melt increases due to the decrease of activity and vapor pressure of the manganese. When the carbon content of ferromanganese alloy melt is high, melt droplets are ejected from the bath, especially in the early stages of the distillation, and the solute elements in the splashed droplets contaminate the condensed material. The ejection of melt droplets is presumed to be caused by the increase of melting temperature and viscosity of the surface layer of melt due to the enrichment of solute elements such as carbon and iron.