• 한국염색가공학회지
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• 제13권6호
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• pp.405-412
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• 2001

In order to impart dyeability on to Polypropylene fiber, PP/EVA blend in the form of fibers and film were preparared using melt blending process. Ethylene vinylacetate containing 28wt% of vinylacetate(EVA(28)) was used as a copolymer. In the study of mechanical properties, tenacity and initial modulus decreased with Increasing EVA concentrations, whilst extension at break increased with increasing EVA contents. Their results in the dyeing behavior show that dye adsorption increased with increased EVA contents iota both blend fibers and films. The extent of dye uptake of red dye to modified polypropylene fibers was greater than that of Blue and Yellow counterparts due to the difference behavior of dye particles in dyeing bath.

• 한국염색가공학회지
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• 제13권6호
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• pp.47-47
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• 2001

In order to impart dyeablility on to Polypropylene fiber, PP/EVA blend in the form of fibers and film were preparared using melt blending process. Ethylene vinylacetate containing 28wt% of vinylacetate(EVA(28)) was used as a copolymer. In the study of mechanical properties, tenacity and initial modulus decreased with increasing EVA concentrations, whilst extension at break increased with increasing EVA contents. Their results in the dyeing behavior show that dye adsorption increased with increased EVA contents for both blend fibers and films. The extent of dye uptake of red dye to modified polypropylene fibers was greater than that of Blue and Yellow counterparts due to the difference behavior of dye particles in dyeing bath.

• Macromolecular Research
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• 제13권2호
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• pp.88-95
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• 2005

Melt blending of Bisphenol A polycarbonate (PC) and poly(trimethylene terephthalate) (PTT) was carried out over the entire composition range. The mixing time was varied up to 90 min. The resulting samples were analyzed by FT-IR, DSC, XRD, DMTA, $^{1}H NMR$, and SEM. The process of transesterification between the two polymers and their resulting compatibilization were observed. The behaviors of the PTT-rich and PC-rich blends were different and an equilibrium was found to exist. Peculiar behavior, which was different from that of the PTT-rich and PC-rich blends, was exhibited by the 50/50 (PTT/PC) blend.

• 한국섬유공학회:학술대회논문집
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• 한국섬유공학회 1996년도 춘계학술발표회 논문집
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• pp.47-52
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• 1996

PP-PHE blends were prepared by mechanical blending using relatively high moecular weight polyhydrozyether(PHE) and popypropylene polymers. PP-PHE blends were prepared and characterized for the purpose of obtaining a dycable PP fibers with the composition of less than 10 wt.% of PHE. 1)yeable PP fibers were acquired through the melt spinning of the PP-PHE blend of comprising less than 10 wt.% of PHE. The resultant fibers had tensile strength of 2~3 g/d, elongation of 330~600%, initial modulus of 22~46 g/d and yield stress of 1.0 g/d, and exhibited markedly improved dyeing ability such as higher absorbance, higher dye adsorption and deeper shade than those of pure PP fiber.

• Macromolecular Research
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• 제9권3호
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• pp.150-156
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• 2001

Polystyrenes(PS) were grafted onto polypropylene(PP) in the PP solution by ultrasonic irradiation-initiated polymerization of styrene. The resulting products consisted of mixtures of homopolymers and PP-PS copolymer because of the homopolymerization of styrene itself and copolymerization with PP. The dependency of the designated polymerization on sonication times was investigated to monitor the evolution lion of the copolymerization. Formation of the PP-PS copolymer was confirmed by FTIR analysis of the reaction products after a proper separation procedure of free PS and PP-PS copolymer. It was found that the tendency for the formation of PP-PS copolymer was closely related with the phase behavior of the PP/styrene mixture which was also influenced by sonication time. In order to verify the effectiveness of the PP-PS copolymer as a compatibilizer for PP/PS blend, melt mixing of PP/PS/PP-PS was performed in a batch mixer. During the mixing, the average torque was higher for the blend containing PP-PS copolymer influencing compatibilization. In accordance with the results from FRIR analysis and torque measurement, the PS domain size remarkably decreased in the PP/PS/PP-PS blend.

• 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.

• Elastomers and Composites
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• 제35권2호
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• pp.149-156
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• 2000

trans-octylene rubber(TOR)를 비상용성 블렌드인 NBR/EPDM(70/30)에 첨가하고, 이에 따른 혼합 특성 모폴로지 및 물성의 변화에 관하여 조사하였다. TOR이 첨가됨으로써 블렌드 시 혼합에너지가 감소하였고, 혼합 시 수반되는 온도상승도 저하됨을 볼 수 있었다. 블렌드의 모폴로지를 SEM으로 관찰한 결과, EPDM이 NBR 매트릭스에 분산된 형태인 것을 알았으며, TOR의 첨가에 의해 분산상인 EPDM상이 균일하고 미세해지는 것이 관찰되었다. TOR이 첨가됨으로써 NBR/EPDM의 인장강도, 파단신율 및 모듈러스 둥의 인장물성이 향상되었다. 오존저항성은 임계 응력-변형관계로부터 정량적으로 평가하였으며, TOR이 첨가된 블렌드에서 오존크랙을 일으키는 임계에너지값이 증가됨을 알 수 있었다. TOR의 첨가로 인한 NBR/EPDM 블렌드의 물성 향상은 모폴로지의 미세화와 사슬얽힘으로 인한 가교밀도의 변화 때문인 것으로 판단된다.

• 한국안광학회지
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• 제17권1호
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• pp.1-10
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• 2012

목적: 본 연구는 cellulose acetate(CA)의 용융특성을 증가시키기 위해 polyethyleneglycol(PEG)를 도입함으로써 기존에 사용되는 환경유해성 가소제의 사용 없이 열가공성이 향상 된 CA/PEG 조성물을 제조하는데 목적이 있다. 방법: CA의 최적 가소화 조건을 확립하기 위해 PEG 분자량, 농도, 및 혼입온도를 제어하여 CA/PEG 조성물의 가소화 성능을 확인하였으며, CA와 PEG간의 혼화성을 확인하기 위해 제조된 조성물의 열분석 및 표면분석을 실시하였다. 또한 기존 상용 CA 레진과의 가소제 용출특성, 기계적 물성 및 광학적 특성들의 비교분석을 통해 가소제에 의한 물성차이를 검토하였다. 결과: PEG의 도입을 통해 기존 상용 CA 레진과 유사한 가소화 성능을 확인하였으며, 최적의 가소화 조건은 PEG분자량 400, PEG 함량 30~40 phr, 가소화온도 $175{\sim}180^{\circ}C$에서 우수한 용융특성을 나타냄을 확인 하였다. 또한 기존의 CA 안경테 소재와 비교 시 우수한 광택특성 및 안정성을 확인 하였으며, 동등수준 이상의 기계적 물성을 보임을 확인 하였다. 결론: CA/PEG 조성물은 환경 친화적 안경테 소재로써 기존 프탈레이트계 가소제를 사용한 CA 안경테 소재를 대체할 수 있을 것으로 판단된다.

• 한국염색가공학회지
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• 제22권2호
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• pp.155-162
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• 2010

Nylon 6 was blended with a brominated epoxy resin, tetrabromobisphenol A diglycidyl ether (DGEBBA), to enhance flame retardant property. Thermal properties of the blends were analyzed by DSC. Melting point and crystallization temperature decreased as the amount of epoxy resin increased. Melt index and relative viscosity decreased as the amount of the epoxy resin increased. When the blended amount of the epoxy resin was below 5%, the melt index decreased while the relative viscosity slightly increased. The blend resin was successfully spun into fiber without swelling or drawing the resonance phenomena. However, both the tenacity and elongation of the fiber decreased by increasing the amount of the DGEBBA.

• Fibers and Polymers
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• 제5권4호
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• pp.270-274
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• 2004

Blends of poly(l-lactide) (PLA) and low density polyethylene (LDPE) were prepared by melt mixing in order to improve the brittleness of PLA. A reactive compatibilizer with glycidyl methacrylate (GMA), PE-GMA, was required as a compatibilizer due to the immiscibility between PLA and LDPE. It contributes to reduce the domain size of dispersed phase and enhance the tensile properties of PLA/LDPE blends, especially for PLA matrix blends. A reaction product between PLA and PE-GMA, which was formed during melt-mixing and considered to act as a reactive compatibilizer, was characterized using $ ^1H-NMR$ spectroscopy.