• Polymer(Korea)
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• v.26 no.5
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• pp.559-567
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• 2002

Poly (vinyl chloride) was blended with blended with vinyl chloride-acrylonitrile copolymers (MO-01 : M$\sub$w/=199049, AN=22.79%, MO-02 : M$\sub$w/=238523, AN=47.03%, MO-03 : M$\sub$w/=289496, AN=52.49%, MO-04 : M$\sub$w/=341837, AN=58.68% by mixing dimethylformamide (DMF) solution of each polymer and their morphology, viscosity, viscoelastic and mechanical properties were studied. Blends of PVC and MO-01 showed a homogeneous morphology. On the contrary, the other copolymer blends showed a large phase separation with spherical domains. Miscibility of blends of PVC and MO-01 was shown to be better than that of blends of other copolymers from morphological and viscoelastic studies. Even though blends of PVC and MO-01 were observed to be the considerable compatibility at a composition of PVC/MO-01=90/10, the mechanical properties of blend films were not improved too much in most blend cases.

• Proceedings of the Korea Electromagnetic Engineering Society Conference
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• 2002.11a
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• pp.406-410
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• 2002

최근 군사부문에서는 국방획득 비용 및 시간의 절감, 상용부문의 최신기술 활용등의 목적으로 상용품목을 적극 활용하고자 하는 노력이 있다. 그러나 상용과 군사부문의 특성 차이로 상용품목의 군사적 활용에는 많은 어려움이 있으며, EMC 관련 문제도 이를 어렵게 하는 이유중 하나이다. 상용과 군사부문의 EMC 표준은 주파수범위, 측정방법 등에 큰 차이가 있으며, 이로 인해 군사 EMC 표준을 충족하는 상용품목의 선정 및 상용표준에 의한 측정 결과의 군사적 해석이 어려운 실정이다. 상용품목의 군사적 활용에 따른 효율적인 EMC 문제의 해결을 위해서는 우선 상용품목의 사용이 의도되는 군사 전자파 환경에 대한 정확한 분석 및 이를 바탕으로 군사표준의 간소화, 상용표준과 군사표준의 연계성 연구, 상용품목의 개발단계에서의 설계반영 등이 필요하다.

• Journal of the Society of Cosmetic Scientists of Korea
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• v.47 no.4
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• pp.273-280
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• 2021

The water resistance is important factor for sunscreen formulations. Generally a sunscreen cream was formulated by a water-in-oil (W/O) emulsion. In the W/O emulsion system, silicone oils are added to improve the texture of formulations. Silicone oils have low compatibility with organic sunscreen agent, causing problems with the stability in emulsion. In this study, the compatibility between various oils in the W/O emulsion was derived numerically using Hansen solubility parameter (HSP) at first. HSP is represented a dispersion degree, a polarity, and a hydrgen bond in a composition. In this study, various emulsions were prepared according to the types of oils with different HSP values and then monitored by a viscosity and morphology according to the time and temperature. The HSP values of components and the experimental results have similar activities for the stability of emulsions. HSP made it easy to select oil with high compatibility. When the compatibility of the oil phase in the W/O emulsion was high, the viscosity change over time was small. The stability was improved under the freeze-thaw cycle (-15 ℃ ~ 45 ℃). In the future, if the composition of the ingredients is optimized through HSP, it is expected that it will be helpful in the development of W/O type sunscreen formulations that are excellent in use and stability.

• Proceedings of the Korean Fiber Society Conference
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• 1998.10a
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• pp.453-456
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• 1998

고분자들을 배합하여 기계적, 물리적, 화학적 성질이 우수한 새로운 고분자 재료를 제조할 때 이들 고분자의 상용성을 증가시켜 줄 수 있는 상용화제의 존재가 필수적인데, 주로 블록이나 그라프트 공중합체들이 많이 이용되고 있다. 이러한 공중합체들은 아주 최소량이 사용되고서도 소기의 목적을 달성할 수 있어야 하는데, 이를 위해서는 이러한 공중합체들은 분자구조상 몇 가지 조건을 만족해야 한다. 예를 들면 계면에 존재하면서 넓은 표면적을 감싸주어야 하고 블렌드되는 고분자들과 아주 잘 섞여야 한다는 것 등이 그것이다. (중략)

• Elastomers and Composites
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• v.46 no.2
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• pp.152-157
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• 2011

Effects of CR contents in NR/CR blends on the vulcanization kinetics and miscibility were studied by dynamic DSC and TGA, as well as the mechanical properties. While the vulcanization activation energy showed a constant value of $77.5{\pm}2.5$ kcal/mol regardless of CR contents, reaction rate, however, was observed to be somewhat lowered at increased CR contents. Partial miscibility was found between NR and CR phases at lower CR content of 3 wt%, but immiscibility was observed at higher CR content of 21 wt%. Mechanical properties were also affected by this miscibility, showing linear increase of compression set but decrease of tensile strength with CR contents in the blends.

• Polymer(Korea)
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• v.26 no.6
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• pp.737-744
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• 2002

Thermodynamic miscibility of the binary blends composed of semi-crystalline poly (butylene 2,6-naphthalate) (PBN) and amorphous poly (4-vinylphenol) (PVPh) was investigated using differential scanning calorimetry (DSC) and Fourier transform infrared (FTIR) spectroscopy. DSC scan results showed that there was a single glass transition temperature (T$\_$g/) for each blend. Crystalline melting temperature (T$\_$m/) depression of the PBN in the blends was also observed with the increase of PVPh content. Both results of the single T$\_$g/ and the depression of T$\_$m/ for the PBN/PVPh blends indicate that the blends are thermodynamically miscible at the molecular level. FTIR spectroscopic analysis confirmed that strong intermolecular hydrogen bonding interactions between the ester carbonyl groups of the PBN and the hydroxyl groups of the PVPh are occurred.

• Polymer(Korea)
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• v.24 no.4
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• pp.469-476
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• 2000

The miscibility between acrylic copolymers and tackifier resins influenced on adhesion properties of PSA. PSA with high molecular weight and narrow molecular weight distribution of acrylic copolymers showed systemical modification of adhesion properties of PSA by tackifier resins only in case of miscible system. It is concluded that the investigation of the miscibility between two Components is very important to adhesion properties of PSA.

• Polymer(Korea)
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• v.25 no.5
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• pp.649-656
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• 2001

Miscibility of poly(4-vinylpyridine) (P4VP) blends with poly(vinyl acetate-co-vinyl alcohol) (VAc-VAL copolymers) was investigated as a function of comonomer composition of VAc-VAL copolymers. Differential scanning calorimetry (DSC) and thermo-optical microscopic (TOM) analysis confirmed that P4VP is miscible with VAc-VAL copolymers containing more than 30 mole% VAL. Fourier transform inflated (FT-IR) spectroscopic analysis revealed that the strong intermolecular hydrongen bonding interaction between the vinylpyridine and VAL hydroxyl group was formed. Theoretical phase diagram was constructed by the calculation using the Association model, a thermodynamic model for hydrogen-bonded polymer blend systems developed by Coleman et al. The calculated theoretical binodal phase diagrams were in good agreement with the experimentally determined cloud point curves.

• Applied Chemistry for Engineering
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• v.21 no.3
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• pp.252-257
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• 2010

Nanocomposites of blends of polymethyl methacrylate (PMMA) and poly (styrene-co-maleic anhydride) (SMA) containing natural and organically modified montmorillonite clays ($Cloisite^{(R)}$25A and $Cloisite^{(R)}$15A) were prepared by solution mixing. Effect of clay on the miscibility, morphology and thermal properties of nanocomposites was investigated. DSC results showed that the addition of clay improved the miscibility of PMMA/SMA blends. Specifically, clay 15A was observed to be most effective than other clays in all nanocomposites regardless of MA contents of SMAs tested. Dispersion of clays was investigated using XRD and TEM and the nanocomposites containing clay 15A again showed the best clay dispersion than the ones with other clays.

• Applied Chemistry for Engineering
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• v.10 no.5
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• pp.743-747
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• 1999

The component polymer was modified to enable the formation of intermolecular hydrogen bonding in the immiscibile polystyrene(PS)/polymethacrylate(PMA) blends. The mole percentages of hydroxystyrene of the poly(styrene-co-4-hydroxystyrene) copolymer(modified polystyrene, MPS) were controlled to 7%, 10% and 18%, respectively. MPS was used with PMA to study the variation of the miscibility in blends. PMA which had such different length of side chain as methyl, butyl, hexyl and ethylhexyl, respectively, was selected to study the effect of side chain length on the formation of intermolecular hydrogen bonding. As the hydroxyl content of MPS increased, the formation of intermolecular hydrogen bonding increased. The length of side chain of PMA had enormous effect on the miscibility of blend as confirmed from the result of cloud point measurement. As the length of side chain increased, the formation and the strength of intermolecular hydrogen bonding decreased severely due to the steric effect and the increased chain mobility.