• 공업화학
• /
• 제19권2호
• /
• pp.205-208
• /
• 2008

저가인 aromatic elastomer polymer인 polySEBS와 PS의 방향족 작용기에 술폰기를 도입시킴으로써 sulfonated polySEBS과 sulfonated PS를 얻었다. 이 술폰화된 고분자를 활용하여 고분자 전해질 연료전지의 이온 교환막으로 사용될 수 있는 새로운 sulfonated polySEBS/sulfonated PS blending films를 제조하였다. 이 필름들의 수소이온 전도도는 sulfonated polySEBS와 sulfonated PS의 혼합비에 따라 $10^{-2}{\sim}10^{-3}S/cm$로 다양하게 나타났다. 특히, sulfonated polySEBS 10.0 g에 sulfonated PS를 0.5 g 첨가하여 제조한 film이 0.75 meq/g의 이온교환용량 및 25%의 함수율과 함께 가장 우수한 0.07 S/cm의 이온전도도를 나타냈다.

• 폴리머
• /
• 제28권2호
• /
• pp.162-169
• /
• 2004

0-0.3phr의 디큐밀 퍼옥사이드를 개시제로 사용하여 0-3.0 phr 말레산 무수물에 의해 폴리[스티렌-블록-(에틸렌-1-부텐)-블록-스티렌] 삼블록 공중합체 (SEBS)는 관능화되었다. 개질 SEBS의 젤 함량은 자일렌 추출에 의해 결정되었고, 폴리(옥시메틸렌)이 개질 SEBS와 혼합되었다. 혼합물의 충격, 인장, 굴곡강도 그리고 형태학적 특성을 조사하였다. 폴리(옥시메틸렌)의 충격강도는 개질 SEBS와의 블렌드를 통하여 향상되었다. 그러나 개질 SEBS가 5% 보다 더 많아지면 블렌드의 충격강도가 감소하였다. 충격강도에 대한 디큐밀퍼옥사이드 농도의 영향을 살펴보면, 폴리(옥시메틸렌)이 디큐밀 퍼옥사이드 0.1phr을 사용하여 제조된 개질 SEBS와 블렌드시 최대 충격강도를 나타내었다. 또한 주사전자 현미경 사진에 의하면 폴리(옥시메틸렌)/개질 SEBS블렌드의 개질 SEBS 입자크기가 폴리(옥시메틸렌)/SEBS블렌드의 SEBS 입자 크기보다 작게 나타났다.

• 한국전기화학회:학술대회논문집
• /
• 한국전기화학회 2005년도 수소연료전지공동심포지움 2005논문집
• /
• pp.275-278
• /
• 2005

• Korea-Australia Rheology Journal
• /
• 제13권2호
• /
• pp.83-87
• /
• 2001

The morphology and mechanical properties of the blends of a syndiotactic polystyrene (SPS) and poly-styrene-block-poly(ethylene-co-butylene)-block-polystyrene copolymers (SEBS) with various polystyrene block contents are studied. Mechanical properties, especially elongation at break and impact strength (IS), of the blend depend upon the morphology and interfacial adhesion, which in rum are affected by the viscosity ratio of constituent components and the styrene block content in SEBS. The IS of a blend was affected by the combined effect of rubber content and the interfacial adhesion. A maximum IS was found for a blend with the weight fraction of the PS block in an SEBS of 0.18. The IS of blends with smaller weight fractions of the PS block exhibited lower due to poor interfacial adhesion between SPS/SEBS in spite of a larger amount of rubber block. On the other hand, the IS of blends with larger weight fraction of the PS block becomes smaller due to lower amounts of rubber block in spite of better interfacial adhesion.

• 대한전기학회논문지:전기물성ㆍ응용부문C
• /
• 제54권3호
• /
• pp.114-119
• /
• 2005

We investigated compatibilizing effects of electrical properties such as charge distributions and electrical breakdown in blends of low density polyethylene (LDPE) / polystyrene (PS) with poly [styrene-b-(ethylene-co-butylene)-b-styrene] (SEBS), the triblock copolymer. The blends with $70\;wt\%$ of LDPE and $30\;wt\%$ of PS were prepared through a melt blending in a batch type kneader at a temperature of $220^{\circ}C$ when the SEBS content increased up to $10\;wt\%$. Scanning electron microscopy (SEM) was investigated for observation of morphology of LDPE / PS blends increasing SEBS contents. The morphological observation showed that addition of SEBS results in the domain size reduction of the dispersed PS phase and a better interfacial adhesion between LDPE and PS phases. Measurements of space charge distributions for blends was carried out with pulsed electroacoustic (PEA) method. It was possible to observe that the amount of charge storage in the LDPE / PS blends decreased wiか increasing of SEBS content. The location of SEBS at a domain interface enables charges to move from one phase to the other via domain interface and results in a indicative decrease in the amount of space charge for the LDPE / PS blends with SEBS. Electrical breakdown strength of these blends was observed. It was found that the maximum breakdown strength of the blend was 51.55 kV/mm. These results were better than 38.38 kV/mm of LDPE used electrical insulator for cables and were caused by crystalinity of blends. Because the crystalinity of blends were lower than LDPE, electrical breakdown strength of LDPE / PS blends is higher than that of LDPE. We evaluated the possibility of these blends for insulating material substituted LDPE.

• Macromolecular Research
• /
• 제17권10호
• /
• pp.729-733
• /
• 2009

Solution casting films of sulfonated poly[styrene-b-(ethylene-r-butylene)-b-styrene] copolymer (sSEBS)-based composite membranes that contained different amounts of organic, nanorod-shaped polyrotaxane were annealed at various temperatures for 1 h. The films' properties were characterized with respect to their use as polymer electrolyte membranes in direct methanol fuel cells (DMFCs). Different aspect ratios of polyrotaxane were prepared using the inclusion-complex reaction between $\alpha$-cyclodextrin and poly(ethylene glycol). The presence of the organic polyrotaxane inside the membrane changed the morphology during the membrane preparation and reduced the transport of methanol. The conductivity and methanol permeability of the composite membranes decreased with increasing polyrotaxane content, while the annealing temperature increased. All of the sSEBS-based, polyrotaxane composite membranes annealed at $140^{\circ}C$ showed a higher selectivity parameter, suggesting their potential usage for DMFCs.

• 한국산학기술학회논문지
• /
• 제19권8호
• /
• pp.562-570
• /
• 2018

고분자 단독으로는 얻을 수 없는 다양한 물성을 얻기 위하여 두 가지 이상의 고분자를 블렌드하는 기법을 많이 사용하고 있다. 폴리올레핀계 TPE(Thermoplastic Elastomer)는 디스플레이, 자동차, 가전제품 등에 널리 사용되고 있다. 소비자는 고감성이고 고급화된 자동차 내장부품을 요구한다. 높은 폼형성도와 흐름성이 있는 고분자소재 개발이 필요하다. 내부에 폼층이 있는 TPE은 좋은 고분자소재이다. 두 종류의 TPE 소재를 개발하였다. 첫번째 소재는 Homo-PP(PolyPropylelne)에 SEBS/Oil을 혼합하였고, 두 번째 소재는 Co-PP와 SEBS/Oil을 혼합하였다. 혼합온도는 $180^{\circ}C$, $190^{\circ}C$. $260^{\circ}C$(두번째 소재), 혼합속도는 50rpm, 혼합시간은 5분이다. TPE의 MI(Melt Index)는 PP의 MI에 영향이 있고, 혼합온도의 영향은 미미하였다. 경도와 인장탄성률은 PP의 MI와 혼합온도의 영향은 적었으나, SEBS/Oil의 비율이 높아지면 낮아졌다. 소프트터치감은 SEBS/Oil의 비율이 증가하면 증대하였다. TPE릉 자일렌으로 SEBS/Oil 층을 녹여내어 IPN(Interpenentration polymer network) 구조를 확인할 수 있었으며, Strain-harding 현상도 확인하였다. 제조한 TPE가 고무현상을 보이고, 생성된 closed cell이 안정한 상태임을 알 수 있다.

• Tribology and Lubricants
• /
• 제17권5호
• /
• pp.386-390
• /
• 2001

Monolayers such as self-assembled monolayer (SAM) have received considerable attention to reduce stiction and friction in micro-devices and microelectromechanical systems (MEMS). Various organic molecular films were investigated to obtain better understanding of their tribological behaviors and adhesion property. The organic molecular films studied in this work are: epoxysilane SAMs, octadecyltricholosilane (OST), multi-layers composed of epoxysilane SAMs, poly[styrene-b-(ethylene-co-butylene)-b-styrene](SEBS) and compound of epoxy resin and poly (paraphenylene)(EP/PPP). The pull-off forces of these films were also obtained from force-distance curves measured in static mode of operation of atomic force microscope(AFM). Tribological tests were conducted with a ball-on-flat reciprocating friction tester. The OST showed the lowest pull-off force, indicating its low adhesion property. It was revealed that, the OST, EP/PPP and the multi-layer of epoxysilane SAMs, SEBS and EP/PPP exhibited good tribological properties at the lower load (0.3 N) whereas the OST showed best performance at the higher load (1.8 N).

• 한국윤활학회:학술대회논문집
• /
• 한국윤활학회 2001년도 제33회 춘계학술대회 개최
• /
• pp.49-54
• /
• 2001

Monolayers such as self-assembled monolayer (SAM) have received considerable attention to reduce stiction and friction in micro-devices and microelectromechanical systems (MEMS). Various organic molecular films were investigated to obtain better understanding of their tribological behaviors and adhesion property. The organic molecular films studied in this work are: epoxysilane SAMs, octadecyltricholosilane (OST), multi-layers composed of epoxysilane SAMs, poly〔styrene-b-(ethylene-co-butylene)-b-styrene〕(SEBS) and compound of epoxy resin and poly (paraphenylene) (EP/PPP). The pull-off forces of these films were also obtained from force-distance curves measured in static mode of operation of atomic force microscope (AFM). Tribological tests were conducted with a ball-on-flat reciprocating friction tester. The OST showed the lowest pull-off force, indicating its low adhesion property. It was revealed that, the OST, EP/PPP and the multi-layer of epoxysilane SAMs, SEBS and EP/PPP exhibited good tribological properties at the lower load (0.3 N) whereas the OST showed best performance at the higher load (1.8 N).

• 대한전기학회:학술대회논문집
• /
• 대한전기학회 2004년도 하계학술대회 논문집 C
• /
• pp.1661-1663
• /
• 2004

The effect of the triblock copolymer poly[styrene-b-(ethylene-co-butylene)-b-styrene](SEBS) on the formation of space charge of immiscible low density polyethylene/polystyrene(LDPE/PS) blends was investigated. The amount of charge accumulated in the 70/30(wt%) LDPE/PS blends decreased when the SEBS content increased up to 10 wt%. For compatibilzed and uncompatibilized blend, morphological observation showed that the addition of SEBS results in the domain size reduction of the dispersed PS phase and a better interfacial adhesion between LDPE and PS phases. The location of SEBS at a domain interface enables charges to migrate from one phase to the other via domain interface and therefore, results in a significant decrease in the amount of space charge for the LDPE/PS blends with SEBS.