• 한국고분자학회:학술대회논문집
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• 한국고분자학회 2006년도 IUPAC International Symposium on Advanced Polymers for Emerging Technologies
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• pp.340-340
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• 2006

Applying force-distance curve measurement by atomic force microscopy to a theoretical mechanical model gives us elastic properties of polymer surfaces. Our group focuses on force-mapping method, in which force-distance curve is performed at each lattice point on a sample surface and subsequently a variety of properties derived from analytical results are combined to construct a 2-dimensional image. With this method we succeeded in deriving Young' s modulus distribution map method of rubbery/rubbery polymer blend surfaces with ${\sim}100\;nm$ lateral resolution. We also applied force-mapping method to another theory to divide distribution of hardness from that of adhesion. We will demonstrate recent progress.

• 한국고분자학회지:고분자과학과기술
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• 제8권6호
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• pp.738-747
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• 1997

• Journal of Pharmaceutical Investigation
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• 제21권2호
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• pp.91-95
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• 1991

Polyethylene glycol, polypropylene glycol and block copolymer of ethylene glycol and propylene glycol were crosslinked by triisocyanate to form water swellable, rubbery polymer. The equilibrium swelling of the hydrogels ranged from 3% to 60% according to the hydrophobic-hydrophilic properties of the prepolymers. Model drugs, sodium salicylate and prednisolone were incorporated in the polymer matrices by swelling loading. Physical properties of the drugs affected the drug release mechanisms due to the change in the swelling behaviors of the polymeric devices. Zero order release was observed in the case of relatively hydrophobic polymer matrices.

• 한국정보디스플레이학회:학술대회논문집
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• 한국정보디스플레이학회 2003년도 International Meeting on Information Display
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• pp.520-523
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• 2003

We used three types of reactive diluents with different chemical structures, N-vinyl-pyrrollidone(NVP), ethyl hexyl acrylate(EHA) and hydroxyehtyl methacrylate(HEMA). It was founded that N-vinylpyrrollidone(NVP) and ethyl hexyl acrylate(EHA) based PUA with low molecular weight polypropylene glycol(PPG) at low oligomer content give high diffraction efficiency. The morphology of the resultant gratings was analyzed by using scanning electron microscopy(SEM) and Tg of the polymer matrix by dynamic mechanical thermal analysis(DMTA).

• 한국막학회:학술대회논문집
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• 한국막학회 2005년도 추계 총회 및 학술발표회
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• pp.178-180
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• 2005

• 멤브레인
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• 제29권1호
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• pp.1-10
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• 2019

Poly(ether block amide) (PEBA)는 이산화탄소 분리에 매우 적합한 상용 블록 공중합체 중 하나이다. 기체분리막의 경우 높은 투과도 뿐 아니라 강한 기계적 강도 또한 필요로 한다. PEBA공중합체의 결정성 폴리아마이드(polyamide) 블록은 기계적 강도를 제공하며 동시에 rubbery한 폴리에테르(polyether) 부분은 이산화탄소와의 친화도를 부여하여 이산화탄소 촉진 수송에 기여한다. PEBA공중합체에서 결정성 상과 rubber한 상의 조성은 기체분리막에 적합하게 조절될 수 있다. PEBA 공중합체를 기반으로 한 분리막은 좋은 투과도를 갖지만 추가적으로 분자체 효과를 이용하여 큰 기체 투과도 손실 없이 분리막의 선택도를 향상시킬 수 있다. 혼합 매질 분리막은 혼합막의 한 종류로서 고분자 매트릭스와 유기 첨가제로 이루어져 있다. 하지만 고분자 매트릭스와 유기 첨가제간의 양립성(compatibility)에 따른 문제점 또한 존재한다. 따라서 본 총설에서는 PEBA 공중합체를 기반으로 한 혼합막의 장점과 한계에 대해 다루고자 한다.

• Korean Membrane Journal
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• 제5권1호
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• pp.36-42
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• 2003

A Prediction of pervaporation performance was studied by solubility parameter calculation approach for the benzene/cyclohexane mixture system using rubbery blend membrane with various solubility parameters. The solubility parameter of the rubbery blend membranes were controlled with different blend ratio of the poly(acrylonitrile-co-butadiene), poly(styrene-co-butadiene) and poly(vinyl chloride). Screening of blend formulations was accomplished by simple swelling tests. When the content of NBR is increased, the swelling of both benzene and cyclohexane are decreased. However, the ratio of benzene swelling to swelling by cyclohexane (the swelling selectivity) increases. The same is true for blends in which the PVC content is increased. Adoption of a solubility parameter calculation provides an a priori methodology for seeking the best blend formulation.

• Korean Chemical Engineering Research
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• 제46권1호
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• pp.15-22
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• 2008

최근 메탈로센 촉매를 통한 올레핀 합성 기술의 발달로 폴리올레핀 블록공중합체를 제조할 수 있는 기술이 개발되었으며 향후 고분자 산업에 크게 기여할 것으로 기대되고 있다. 하지만 현재까지 폴리올레핀 블록공중합체의 특성에 대한 체계적인 연구가 보고되고 있지 못한 실정이다. 본 리뷰 논문에서는 결정질의 poly(ethylene) (E) 블록과 고무질(rubbery)의 블록을 가지는 선형 폴리올레핀 블록공중합체를 통하여 폴리올레핀 블록공중합체의 열가소성 탄성체로서의 열역학적, 기계적 특성 및 분자 구조의 효과 특성 등에 관하여 살펴보고자 한다.

• Bulletin of the Korean Chemical Society
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• 제16권2호
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• pp.169-180
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• 1995

A topological theory is introduced to extend Tsenoglou's theory to polymer blends having temporary and permanent networks composed of multicomponent polymers which have miscible and flexible chains. The topological theory may estimate the values of free elastic energy, the molecular weight between entanglements, and the equilibrium shear moduli, and it may establish more correctly the topological relations among these physical quantities. Through such introduction of the topological theory, there can be topologically analyzed the mixing law for the rubbery plateau modulus of a fluid polymer blend, and there can be considered the topological relationship to the equilibrium modulus of an interpenetrating polymer network containing trapped entanglements and dangling segments. The theoretically predictive values are compared and show good agreement with the experimental data for several miscible polymer blends.

• Macromolecular Research
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• 제15권2호
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• pp.109-113
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• 2007

The surface molecular motion of monodisperse polystyrene (PS) films was examined using scanning vis-coelasticity microscopy (SVM) in conjunction with lateral force microscopy (LFM). The dynamic storage modulus, E', and loss tangent, $tan\delta$, at a PS film surface with number-average molecular weights, $M_n$, smaller than 30 k were found to be smaller and larger than those for the bulk sample, even at room temperature, meaning that the PS surface is in a glass-rubber transition or fully rubbery sate at this temperature when the $M_n$ is small. In order to quantitatively elucidate the dynamics of the molecular motion at the PS surface, SVM and LFM measurements were performed at various temperatures. The glass transition temperature, $T_g$, at the surface was found to be markedly lower than the bulk $T_g$, and this discrepancy between the surface and bulk became larger with decreasing $M_n$. Such an intensive activation of the thermal molecular motion at the PS surfaces can be explained in terms of an excess free volume in the vicinity of the film surface induced by the preferential segregation of the chain end groups.