• Macromolecular Research
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• v.9 no.4
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• pp.238-246
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• 2001

Properties of ternary blends of nylon 6 (Ny6), a thermotropic liquid crystalline polymer (TLCP, poly(ester amide), 20 wt%) and a maleic anhydride grafted polypropylene (2 wt%) (MAPP) were studied under various processing conditions. TLCP was pre-blended with MAPP first and then the binary one blended again with Ny6. The processing temperature of the second mixing was varied. Thermal properties show the partial miscibility of the ternary blend. The morphology of the TLCP phase in the first blending shows mostly in the fibril bundle shape, but varies between droplets and oriented fibrils after the second processing. Some of TLCP phase lost the fibril morphology during the second processing stage. The morphology variation invokes the change in tensile properties. Low extrusion temperature (270$\^{C}$) provides more fibril shapes, which are associated with less deformation in the second stage. The processing temperature effect was more evident when the draw ratio was high. High drawing was applicable due to the stabilizing action of tile compatibilizer.

• Macromolecular Research
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• v.9 no.1
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• pp.66-70
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• 2001

In this work, we present the development of phase structure of the poly(methyl methacrylate)(PMMA)/ poly(vinylacetate)(PVAc) mixtures in ethyl acetate solution by light scattering. The PMMA/PVAc blends cast from ethyl acetate solutions exhibited fine "modulated structures" over broad blend composition ranges, which originated from the spinodal decomposition of the ternary polymer solutions at low polymer concentrations during the casting. The periodic distance was depended on the blend compositions and evaporation times.

• Computers and Concrete
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• v.6 no.5
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• pp.391-401
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• 2009

This paper presents a study of the strength and chloride penetration of blended Portland cement mortar containing ground palm oil fuel ash (POA) and ground river sand (GS). Ordinary Portland cement (OPC) was partially replaced with POA and GS. Compressive strength, rapid chloride penetration test (RCPT) and chloride penetration depth of mortars were determined. The GS only asserted the packing effect and its incorporation reduced the strength and the resistance to chloride penetration of mortar. The POA asserted both packing and pozzolanic effects. The use of the blend of equal portion of POA and GS also produced high strength mortars, save cost and excellent resistance to chloride penetration owing to the synergic effect of the blend of POA and GS. For chloride depth, the mathematical model correlates well with the experimental results. The computer graphics of chloride depth of the ternary blended mortars are also constructed and can be used to aid the understanding and the proportioning of the blended system.

• Macromolecular Research
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• v.15 no.7
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• pp.605-609
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• 2007

The molecular interactions of polyacrylonitrile (PAN) and cellulose acetate (CA) were investigated thoroughly via dilute solution viscometry in dimethylformamide (DMF) as a common solvent at $30^{\circ}C$. The intrinsic viscosities and viscometric interaction parameters were experimentally determined for both binary (polymer/dimethylformamide) and ternary (PAN/CA/dimethylformamide) systems. As all investigated PAN/CA ternaries evidenced negative viscometric interaction parameter values $({\Delta}b\;&{\Delta}k<0)$, the existence of repulsive intermolecular interactions was deduced, and PAN/CA blends were assigned as immiscible. Moreover, the results of microscopy photograph analysis indicated that pure PAN film evidences a homophasic structure, and the size of the phase domain increases gradually with increases in CA. In DSC analysis, it was determined that the glass transition temperature of the blend film increased slightly with increases in the CA content of the blend film.

• Elastomers and Composites
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• v.35 no.2
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• pp.149-156
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• 2000

trans-octylene rubber(TOR) was melt-blended with an incompatible NBR/EPDM (70/30) blend. Mixing torque and temperature were reduced as TOR was added to the NBR/EPDM blend. Rheometer results indicated that TOR participated in vulcanization and became a part of network. A scanning electron micrograph demonstrated that EPDM was dispersed in NBR matrix in the blend and the addition of TOR led to a finer dispersion of EPDM particles. On the addition of TOR, the tensile strength, the tensile strain as well as the modulus of the blend vulcanizates increased. The ozone resistance of the blends determined in terms of critical stress-strain parameter was significantly enhanced in the blend as TOR was added. Improvements in the properties were believed to be associated with fine morphology and the increase in crosslink density due to the chain entanglement of the ternary blends.

• Proceedings of the Korean Fiber Society Conference
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• 2003.04a
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• pp.227-230
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• 2003

열방성 액정고분자 (Thermotropic liquid crystal polymer, TLCP)는 초고강도 섬유로의 응용가능성을 갖고 있어 많은 관심이 집중되고 있으며, 액정고분자의 고강도와 고탄성, 우수한 내열성과 내화학성, 가공시 성형수축률 및 선팽창계수가 작기 때문에 고성능 섬유 및 엔지니어링 플라스틱, 그리고 고분자 복합재료 등 다양한 분야에 응용되고 있다 [1]. 또한 범용성 열가소성 수지와 TLCP와의 용융블렌드는 고분자 복합재료의 강도 및 탄성의 향상뿐만 아니라 우수한 가공성 및 고성능 발현이 가능하기 때문에 현재 많은 연구가 진행되고 있다 [2]. (중략)

• Proceedings of the Korean Fiber Society Conference
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• 1998.04a
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• pp.20-24
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• 1998

Poly(ethylene 2,6-naphthalate) (PEN) has been known since 1948, when its synthesis was first reported by ICI. Co. In spite of its long history. application of PEN is limited as compared with poly(ethylene terephthalate) (PET). because PEN monomer is very expensive, and PEN exhibits relatively high melt viscosity that is not easy for fiber spinning and injection molding.(omitted)

• Macromolecular Research
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• v.14 no.2
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• pp.179-186
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• 2006

In the present work, low density polyethylene (LDPE)/aliphatic polyester (APES)/organoclay ternary nanocomposites were prepared. In particular, the effect of a compatibilizer, polyethylene-graft-maleic anhydride (PE-g-MAH), on the morphology and properties of the ternary nanocomposites was investigated. LDPE/APES/organoclay nanocomposites were prepared through melt intercalation method using two different kinds of organoclay. The dispersibility of silicate clays in the nanocomposites was investigated by X-ray diffraction and atomic force microscopy. The ternary nanocomposites showed higher tensile properties than the LDPE/APES blend did. The dispersibility and properties of nanocomposites containing Cloisite 30B were better than those of the nanocomposites containing Cloisite 20A. Unlike Cloisite 20A, hydroxyl groups in the intercalants in Cloisite 30B interlayer underwent a certain polar interaction with the carboxyl group of APES, favoring the intercalation of APES chains and the formation of LDPE/APES/Closite 30B nanocomposites. However, the introduction of the polar hydroxyl groups also enhanced the interaction with the silicate surface at the same time, thereby rendering somewhat difficult the replacement of the surface contacts by LDPE chains, and impeding the extensive intercalation and further exfoliation of Cloisite 30B in the LDPE/APES matrix. The compatibilizer enhanced the intercalation of the polymer chain inside the clay gallery and thus improved the mechanical properties of the ternary nanocomposites. Rheological measurements of the nanocomposites via frequency sweep experiment indicated a certain interaction between the clay platelet and the polymer molecules in the melted state.

• The Korean Journal of Rheology
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• v.10 no.4
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• pp.247-255
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• 1998

The morphological changes during melt compounding of ternary blends containing various combinations of acrylonitrile-butadiene-styrene(ABS), methyl methacrylate-butadiene-ethyl acrylate(MBE), styrene-acrylonitrile(SAM) copolymers, and poly(methyl methacrylate)(PMMA) as dispersed components in a fixed matrix of polycarbonate(PC) have been investigated. Depending on the composition of the blend, MBE particles and PMMA phase appear to locate at the PC-SAN interface under the influence of interfacial tensions and motion induced coalescence. The interfacial viscosity is found to be a critical factor that affects the amount of coalescence.

• Elastomers and Composites
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• v.40 no.3
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• pp.204-211
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• 2005

Effect of chlorinated polyethylene(cPE) on the morphology and mechanical properties of isotactic polypropylene(iPP) and nitrile rubber(NBR) blends was investigated. It was found that incorporation of a small amounts of cPE leads to a decrease in domain size of the dispersed phase, and uniform distribution of the dispersed phase in the blends. The PP/NBR/cPE ternary blends showed an improved tensile and tear strength as well as elongation-at-break as compared to binary PP/NBR blends. From the results on morphology and mechanical properties, optimum amount of the cPE is 5-10 wt% with repect to NBR in the blend.