• 폴리머
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• 제31권1호
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• pp.8-13
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• 2007

나일론 6/poly(acrylonitrile-co-butadiene-co--styrene) (ABS) 블렌드의 단점을 해결하기 위해 ABS의 고무상인 폴리부타디엔 대신 폴리(부틸 아크릴레이트)를 고무상으로 포함하고 있는 poly(acrylonitrile-co-styrene-co-acrylic rubber) (ASA)를 사용하여 새로운 나일론/ASA 블렌드를 실험하였다. 고충격성을 갖는 블렌드 제조를 위하여 상용화제로 무수 말레산을 25 wt% 포함한 poly(styrene-co-maleic anhydride) (SMA)와 이를 3 wt% 이하 포함한 poly(styrene-co-acrylonitrile-co-maleic anhydride) (SANMA)를 사용하여 블렌드를 제조하였다. 나일론/ASA 블렌드에서 상용화제의 함량에 따른 물성 변화는 나일론/ABS 블렌드와 유사한 경향을 나타내었다. 블렌드 내의 고무 함량이 20 wt% 이상일 때 안정된 물성의 고충격 블렌드가 제조되었다. 블렌드를 사출 성형 온도에서 사출 성형기 내에 체류시킨 후 제조한 시편의 충격 강도를 시험한 결과 SMA를 상용화제로 사용한 경우 충격 강도의 감소가 관찰된 반면 SANMA를 상용화제로 사용한 블렌드에서는 충격 강도의 변화가 거의 없었다.

• 폴리머
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• 제26권2호
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• pp.245-252
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• 2002

상용화제로 poly(styrene-b-methylmethacrylate) [U(S-b-MMA)] 블록 공중합체를 포함한 polymethylmethacrylate (PMMA)와 polyvinylmethylether (PVME) 블렌드의 열역학적 특성과 이들의 기체 투과특성을 조사하였다. 블렌드에 포함된 여러 고분자들 간의 상호작용 에너지를 상분리 온도와 상태방정식 이론으로부터 구하기 위해 다양한 조성의 poly(styrene-co-methylmetha-crylate) (SMMA) 랜덤 공중합체를 제조하고 이를 PVME와 블렌드하여 단상의 블렌드를 제조하였다. 공중합체 내의 스티렌 함량이 70 wt% 이상에서는 SMMA/PVME 블렌드는 단상을 형성할 뿐아니라 LCST 거동을 나타내었다. 여기서 구한 상호작용 에너지를 기초로 PMMA/PVME 블렌드의 상용성을 향상시키기 위해 P(S-b-MMA) 블록 공중합체를 상용화제로 첨가하였다. 분산상으로 존재하는 PVME 고무 입자들의 평균 크기는 상용화제 첨가량이 5 phr 이하에서는 점차 감소하지만 더 이상의 상용화제를 첨가해도 분산상의 크기 변화는 관찰되지 않았다. 일정 블렌드 조성에서 기체 투과도도 상용화제의 양이 5 phr 일때까지는 증가하지만 그 이상의 상용화제 함량에서는 기체 투과도 변화가 관찰되지 않았다.

• 한국섬유공학회:학술대회논문집
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• 한국섬유공학회 2003년도 봄 학술발표회 논문집
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• pp.289-290
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• 2003

Polymer blending constitutes a most useful method for the improvement or modification of the physicochemical properties of polymeric materials. So polymer blends have gained an increasing interest in both industrial and scientific fields. Some of the polymer blends exhibit unusual properties, unexpected from homopolymers. An important property of a polymer blend is the miscibility of its component, because it affects the mechanical properties, the morphology, its permeability and dogradation [1,2]. (omitted)

• 한국정보디스플레이학회:학술대회논문집
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• 한국정보디스플레이학회 2004년도 Asia Display / IMID 04
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• pp.585-587
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• 2004

We report the characterization of white light emitting devices fabricated using conjugated polymer blends. Blue emissive poly[9,9-bis(4'-n-octyloxyphenyl) fluorene-2,7-diyl-co-10-(2'-ethylhexyl)phenothiazine-3,7-diyl] [poly(BOPF-co-PTZ)] and red emissive poly(2-(2'-ethylhexyloxy)-5-methoxy-1,4-phenylenevinylene) (MEH-PPV) were employed in the blends. The inefficient energy transfer between these blue and red light emitting polymers (previously deduced from the PL spectra of the blend films) enables the production of white light emission through control of the blend ratio. The PL and EL emission spectra of the blend systems were found to vary with the blend ratio. The EL devices were fabricated in the ITO/PEDOT/blend/LiF/Al configuration and white light emission was obtained for one of the tested blend ratios.

• Fibers and Polymers
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• 제4권4호
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• pp.195-198
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• 2003

Epoxidized polybutadiene (EPB) was prepared by polybutadiene (PB) with m-chloroperbenzoic acid (MCPBA) in homogeneous solution. EPB was blended with poly(3-hydroxybutyrate) (PHB) up to 30 wt% by solution-precipitation procedure. The thermal decomposition of PHB/EPB blends was studied by thermogravimetric analysis (TGA), differential scanning calorimetry (DSC) and differential thermal analysis (DTA). The thermograms of PHB/EPB blends contained a two-step degradation process, while that of pure PHB sample exhibited only one-step degradation process. This degradation behavior of PHB/EPB blends, which have a higher thermal stability as measured by maximum decomposition temperature and residual weight, is probably due to crosslinking reactions of the epoxide groups in the EPB component with the carboxyl chain ends of PHB fragments during the degradation process, and the occurrence of such reactions can be assigned to the exothermic peaks in their DTA thermograms.

• 한국섬유공학회:학술대회논문집
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• 한국섬유공학회 2001년도 가을 학술발표회 논문집
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• pp.9-12
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• 2001

Blending is an easy and popular means to achieve a desired set of characteristic properties. The blends, by melt mixing of thermoplastic materials and elastomer, have received considerable attention in recent years. It is well known that nearly all blends comprise one polymer domain dispersed in the matrices of the other polymer [1]. (omitted)

• 폴리머
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• 제32권6호
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• pp.523-528
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• 2008

Diglycidyl ether of bisphenol-A (DGEBA) was selected as a compatibilizer in Nylon 6 and bisphenol-A polycarbonate (PC) blends. SEM revealed a much finer morphology in the presence of DGEBA. The thermal properties, such as glass transition, melting point, crystallization temperature and rate, of the blends were examined using DSC. Overall, the introduction of DGEBA caused a strong dependence of these thermal properties on the composition due to compatibilization.

• Elastomers and Composites
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• 제26권1호
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• pp.15-22
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• 1991

Blends of ethylene-propylene-diene terpolymer(EPDM) and high density polyethylene(HDPE) have been prepared in a roll mill by the process "dynamic curing" where both blending and a crosslinking reaction was carried out simultaneously. As a crosslinking agent, dicumyl peroxide(DCP) was used. Throughout the experimental ranges, the dynamically cured polyblends were shown to be thermoplastic elastomers except highly crosslinked blends of high compositions of EPDM. The increase of melt viscosity was observed as EPDM composition and DCP contents increased. From DSC determinations, the crystallinity decreased with increasing contents of DCP. The tensile strength and elongation at break generally increased with increasing DCP content and increasing HDPE compositions, but highly depended on the combined effects of decreasing crystallinity and increasing crosslinking density.

• 한국고분자학회지:고분자과학과기술
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• 제8권1호
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• pp.24-31
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• 1997

• Macromolecular Research
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• 제15권2호
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• pp.142-146
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• 2007

Poly[(1-(9-carbazoly1)ethylene)-co-(3-cinnamoyloxyoctyl-9-carbazolyl)] ethylene (PVK-Cin) was prepared by tethering cinnamate pendants to a carbazole group via an octylene spacer. The photopatternability of the new PVK based-polymer was investigated using a photocrosslinking reaction under UV light illumination $(\lambda=254nm)$. Blends of the PVK-Cin and a soluble poly(phenylene vinylene) (CzEh-PPV) were employed to study the photocrosslinking behavior. Well resolved lithographic patterns were observed in these polymer systems. PVK-Cin produced a blue light emitting pattern both before and after the photocrosslinking reaction. The blends of PVK-Cin and CzEh-PPV also showed corresponding emissions at 398 and 525 (560) nm in the film state.