• Elastomers and Composites
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• 제31권2호
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• pp.111-121
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• 1996

The characteristic of silicone rubber can be seen from its resistance to both low and high temperature, whereas HNBR is resistant only in high temperature moderatly although it can be compounded to give good tensile properties, good oil resistance while silicone rubber severely lacks in these qualities. This study was initiated a balance of properties by blending HNBR and silicone rubber which is not considered for commercial blending; blends of HNBR with silicone rubber tend to show immiscible due to dissimilar nature of silicone and HNBR, the possibility of phase separation cannot be ruled out, in unfilled system after vulcanisation leading to premature failure. Attempt has been made to improve compatibility and minimise the layer seperation by the use of compatibilizer. Both filled and unfilled systems, in presence and absence of compatibilizer have been studied. Improvement in tensile properties of the blends or are observed as compared to the non-blended rubber. Different ratios of HNBR and silicone rubber are represented in this study. Blends of HNBR with silicone rubber were immiscible system. The tensile strength increased with filler loading.

• 자원환경지질
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• 제54권1호
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• pp.105-115
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• 2021

대규모로 포집된 이산화탄소를 고갈된 석유·가스 저류층, 대염수층과 같은 심부 지질구조에 주입하는 이산화탄소 지중저장은 대기중 CO2 배출을 저감하기 위한 가장 유망한 기술 중 하나로 연구되고 있다. 이산화탄소 지중저장은 공극수로 포화된 다공성 지질 구조 내부로 초임계상 이산화탄소를 주입함으로써 그 흐름이 공극수와 비혼성 대체를 일으키며 진행된다. 따라서, 공극 구조 내에서 초임계상 이산화탄소와 공극수의 거동과 분포, 그리고 그 결과로 나타나는 대체효율은 두 유체의 상호작용에 의해 좌우되는데, 특히, 점성력과 모세관력은 지질 구조 내부의 환경 조건과 주입 조건에 의해 결정된다. 본 연구에서는 상온상압조건에서 대체유체를 수적법에 적용하여 고온고압조건에서 계면활성제가 초임계상 이산화탄소와 공극수 간 계면장력에 미치는 영향을 산정하였다. 또한, 다공성 매체 내에서의 비혼성 유체의 거동과 분포 양상을 관찰함으로써 계면활성제 농도가 초임계상 이산화탄소의 대체율에 미치는 영향을 분석하였다. 이를 위하여 초임계상 이산화탄소와 공극수의 대체 유체로서 헥산과 탈이온수를 적용하는 마이크로모델 실험을 수행하였으며, 공극 구조 내로의 헥산 주입에 의한 탈이온수의 대체 과정을 정량적으로 분석하기 위하여 이미징 시스템을 통해 두 유체의 비혼성 대체 양상에 관한 이미지를 확득하여 분석하였다. 실험의 결과는 계면활성제의 첨가는 낮은 농도에서도 헥산과 탈이온수 간 계면장력을 급격하게 감소시키며 이후 농도가 증가함에 따라 일정한 값에 접근하는 양상을 보여주었으며, 이러한 변화는 다공성 매체 내부의 공극 규모에서 진입 유체의 흐름 경로에 직접적인 영향을 미침으로써 평형 상태에서 헥산의 대체율에도 동일한 효과를 나타내는 것으로 나타났다. 본 연구의 결과는 다공성 매체 내에서 일어나는 비혼성 유체의 대체에 관한 중요한 정보를 제공하며, 계면활성제의 적용이 이산화탄소 지중저장의 효율을 향상시킬 수 있는 가능성을 보여주었다.

• Journal of Ship and Ocean Technology
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• 제7권4호
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• pp.32-40
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• 2003

Numerical simulation code is developed to study the formation of liquid drops from a nozzle into another quiescent liquid. The Navier-Stokes equations for two immiscible, incompressible, Newtonian fluids are solved on a fixed, staggered grid of cylindrical axisymmetric coordinates. Interfacial motion is captured using a Front-Tracking Method. The time variation of interfacial shape simulated by the code is in excellent agreement with experiments. Simulation results show that the viscosity ratio affects the size of the satellite drops.

• 한국막학회:학술대회논문집
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• 한국막학회 1996년도 춘계 총회 및 학술발표회
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• pp.55-56
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• 1996

Heterophase polymer system has been attractive for a potential applicability to gas separation membrane material. It has been known that there is a trade-off between gas permeability and its selectivity in common polymers. Therefore, the heterophase polymer can be an alternative for a gas separation membrane material because its transport properties can be readily controlled by blending of two different polymers. The transport properties of immiscible polymer blends strongly depend upon the intrinsic transport properties of corresponding polymers. Another important factor to determine the transport properties is their morphology: volume fraction, size and shape of dispersed phase. Although the effect of the volume fraction of the dispersed phase on the transport properties has been widely investigated, the size and shape effects have been paid attention very much. In an immiscible polymer blend of two polymers, its morphology is primarily controlled by its volume fraction of dispersed phase. Therefore, the effect of the size of the dispersed phase can be hardly seen. Therefore, a block copolymer has been commonly employed to control their morphology when each block is miscible with one or the other phase. In this work, gas transport properties will be measured by varying the morphology of the heterophase polymer membrane. The transport properties will be interpreted in terms of their morphology. The effect of the volume fraction of the PI phase and, in particular, its size effect will be investigated experimentally and theoretically.

• KSBB Journal
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• 제27권4호
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• pp.207-214
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• 2012

Emulsions are mixture of immiscible liquids in which one is dispersed in all over the other. They have been applied to many applications including cosmetics, foods, drug delivery system (DDS), fine chemicals, and chemical separations. Especially, emulsion technology is one of the most useful technique to formulate cosmetics such as eye cream, foundation, and foam cleansing. In general, the emulsions can be generated by mechanical agitation of two immiscible fluids. However, the emulsions obtained by conventional method have limited in stability, monodispersity, and complicate process. We describe here preparation techniques of representative cosmetic emulsions such as liposome, liquid crystal emulsion, nanoemulsion, multiple emulsion, and pickering emulsion. Furthermore, various factors which can control the physical properties of each cosmetic emulsions are briefly discussed.

• Korea-Australia Rheology Journal
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• 제13권4호
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• pp.189-196
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• 2001

The phase morphology is an important factor in the rheology of immiscible polymer blends. Through its size and shape, the interface between the two phases determines how the components and the interface itself will contribute to the global stresses. Rheological measurements have been used successfully in the past to probe the morphological changes in model blends, particularly for dilute systems. For more concentrated blends only a limited amount of systematic rheological data is available. Here, viscosities and first normal stress differences are presented for a system with nearly Newtonian components, the whole concentration range is covered. The constituent polymers are PDMS and PIB, their viscosity ratio can be changed by varying the temperature. The data reported here have been obtained at 287 K where the viscosities of the two components are identical. By means of relaxation experiments the measured stresses are decomposed into component and interfacial contributions. The concentration dependence is quite different for the two types of contribution. Except for the component contributions to the shear stresses there is no clear indication of the phase inversion. Plotting either the interfacial shear or normal stresses as a function of composition produces in some cases two maxima. The relaxation times of these stresses display a similar concentration dependence. Although the components have the same viscosity, the stress-component curves are not symmetrical with respect to the 50/50 blend. A slight elasticity of one of the components seems to be the cause of this effect. The data for the more concentrated blends at higher shear rates are associated with a fibrillar morphology.

• 한국세라믹학회지
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• 제30권12호
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• pp.1071-1079
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• 1993

Interaction of alkali oxides and SO3 and C3S formation and microstructure was studied using K2CO3 and Na2CO3 as alkali sources and (NH4)2SO4 for SO3. When SO3/K2O=1.43 as mole ratio, K2O and SO3 react to form K2SO4, this phase is immiscible with other oxide melt and thus could not affect C3S formation as well as its microstructure. In a condition of SO3/K2O 1, C3S crystals were round and grown in a much larger size. With addition of Na2O and SO3 by only 1wt% each, C3S formation was strongly hindered. Since C2S was stabilized by Na+ and SO4-2, it could not react to give C3S formation. However in the condition of SO3/Na2O=1.43, a little amount of C3S was formed. It is considered that small amount of Na2SO4 was formed, this phase was immiscible with clinker liquid, and the C3S crystals were formed locally in the liquid part of relatively low Na2O and SO3 compositions. These crystals had irregular and rough surfaces and contained more inclusions than those grown from K2O.SO3 system.

• 한국결정성장학회지
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• 제16권5호
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• pp.210-215
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• 2006

본 연구에서는 순 Cu 및 Nb 혼합분말에 대하여 Ar 분위기 중 고에너지 볼밀처리를 실시하여 기계적 합금화(MA) 효과를 조사하였다. $Cu_xNb_{100-x}$(x=5-50) 조성의 혼합분말을 각각 120시간까지 MA 처리 한 결과, Cu의 bcc-Nb 과포화 고용체가 30 at% Cu까지 넓어짐을 X선 회절분석, DSC 열분석 및 저온비열 측정을 통한 초전도 천이온도 변화로부터 알수 있었다. 120시간 MA 처리한 $Cu_{30}Nb_{70}$ 조성합금의 열분석 결과 broad한 발열반응만이 관찰되었으며, 볼밀처리에 의하여 계에 축적되는 에너지는 볼밀시간에 따라 증가하여 7.5kJ/mol 에 포화됨을 알 수 있었다. Miedema et al.의 계산에 의하면 $Cu_{30}Nb_{70}$ 혼합분말과 과포화 고용체의 자유에너지 차가 7kJ/mol이며, 본 연구에서 MA에 의하여 계에 축적된 에너지 값과 거의 같은 사실로부터 이 계에서 열역학적으로 과포화 고용체가 충분히 얻어질 수 있음을 나타내는 것으로 판단된다.

• 한국지하수토양환경학회:학술대회논문집
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• 한국지하수토양환경학회 2003년도 추계학술발표회
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• pp.144-147
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• 2003

In this study, the mass transfer behaviors of phenanthrene, anthracene, and pyrene in soil slurry reactor (SSR) using two-liquid phase (TLP) system were investigated. The mass transfer ratio and rate of PAH in the TLP system using light paraffine oil, which has the highest solubility of PAH, were influenced by the amount of light paraffine oil and mixing speed. When the amount of light paraffine oil decreased from 15 % to 2.5 % (v/v), the mass transfer ratio of anthracene decreased significantly compared with that of phenanthrene and pyrene. As mixing speed increased, the initial mass transfer rate of PAH within 1 day was enhanced. However, each final mass transfer ratio of three PAHs after 5 day was similar irrespective of mixing speed.

• 한국진공학회:학술대회논문집
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• 한국진공학회 1999년도 제17회 학술발표회 논문개요집
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• pp.170-170
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• 1999

We studied Nb growth mode on Cu(100) surface by scanning tunneling microscopy (STM) at room temperature. Nb/Cu is immiscible at room temperature and thus is an ideal system for studying surface alloy formation. Initially deposited Nb atoms are incorporated subsurface on Cu(100). After annealing, they are preferentially found at step edges and appear as bright dots surrounded by dark rings. Ordering emerges from step edges as annealed. Ordered ({{{{ SQRT { 5} }$\times${{{{ SQRT { 5} }}}})R 26.6$^{\circ}$phase Nb structure is formed at $\theta$<0.2ML after annealing to 50$0^{\circ}C$. At higher coverage, $\theta$>0.25, annealing leads to p(2$\times$2) phase. due to large mismatch in lattice parameters, the domain is limited to a few tens of nm2. Growth kinetics of the system will be discussed.