• 한국수소및신에너지학회논문집
• /
• 제29권6호
• /
• pp.578-586
• /
• 2018

In this study, we prepared the modified PBI random copolymer to reduce the problems of the pristine PBI about low solubility and proton conductivity. The random copolymer was synthesized from suberic acid, 5-aminoisophthalic acid, and 3,3'-diaminobenzidine to obtain $X_1Y_9$, $X_1Y_1$, $X_9Y_1$. Then, the membrane was fabricated by using solvent casting method with methanesulfonic acid at $140^{\circ}C$. Subsequently, the membrane was doped with phosphoric acid at $40^{\circ}C$. The chemical structure of the polymers was characterized by FT-IR. In addition, the physiochemical properties of the PBI were investigated by TGA, oxidative stability, acid uptake. Finally, the proton conductivity was measured at $100-180^{\circ}C$ without humidification. As the result, $X_1Y_9$ PBI random copolymer membrane showed higher conductivity.

• 산업기술연구
• /
• 제18권
• /
• pp.277-287
• /
• 1998

In this work continuous thermodynamics was adopted for describing the influence of copolymer polydispersity on phase separations in random copolymer solutions. Continuous themodynamic frameworks were formulated using the Flory-Huggin's excess Gibbs free energy model in which the concentration- and temperature-depentent terms of interaction parameter x were modified. Cloud-point curves and coexistence curves of poly(ethylene-vinylactate)/methylacetate solutions and poly(ehtylene-vinylacetate)/ethylacetate solutions were measured, and experimental data were fitted with theoretical relations formulated in this work. Calculated could-point curves were more good ageeable with experimental data than the modified Flory-Huggins's relations. Coexistence curves which were evaluated by using parameters of x estimated from experimental cloud-point curves, were found to coincide with experimental data.

• 공업화학
• /
• 제4권4호
• /
• pp.770-775
• /
• 1993

에틸렌글리콜과 1, 4-시클로헥산디메탄올의 테레프탈산 공중합체인, poly(ethylene terephthalate-co-1, 4-cyelohexylene dimethylene terephthalate), P(ET-CT)의 화학 구조를 고분해능 NMR 분석을 통하여 조사하였다. $^1H$ NMR 분석에서 메칠렌기에 의한 chemical shift가 ET, 트란스 CT, 및 시스 CT로 분리됨에 따라 공중합조성 및 이성질체의 비율을 구할 수 있었다. $^{13}C$ NMR 분석에서 카르보닐기에 연결된 벤젠기의 탄소가 diad로 분리됨에 따라 공중합 연쇄 분포(copolymer sequence distribution)를 구한 결과, P(ET-CT) 공중합체는 랜덤공중합체임이 판명되었다. 아울러 랜덤 통계식을 이용하여 공중합 연쇄의 분포 및 평균길이를 구할 수 있었다.

• 멤브레인
• /
• 제16권3호
• /
• pp.221-229
• /
• 2006

본 연구는 불소관능기인 perfluorocyclobutane (PFCB), fluorenyl, sulfonyl계 방향족 화합물을 동시에 포함하는 술폰화된 랜덤 고분자 전해질 막의 제조 및 그 특성에 관한 것이다. 이러한 고분자 전해질 막은 세단계의 합성, 즉 trifluorovinyloxy그룹을 양말단에 포함하는 단량체의 합성, 중부가반응 형태의 열중합, 그리고 chlorosulfonic acid를 이용한 후술폰화를 통하여 얻어졌다. 후술폰화 반응은 고분자 내에 포함된 fluorenyl기의 함량에 따라 일정한 몰비의 술폰화제 비율로 고정하여 진행되었으며, 이에 따라 다양한 이온교환 능력(IEC)을 가지는 고분자를 쉽게 합성할 수 있었다. 제조된 단량체 및 고분자들의 구조와 순도는 각각 FT-IR과 NMR 그리고 질량분석기를 통하여 확인되었다. 술폰화된 fluorenyl기가 많아질수록 술폰화도와 이온교환 능력이 증가하는 것을 확인할 수 있었고 그에 따른 함수율도 역시 증가하는 거동을 보였다. 술폰화된 고분자들의 이온전도도를 측정한 결과 술폰화도가 증가할수록 이온 전도도가 증가하는 것을 관찰할 수 있었다, 이렇게 제조된 전해질막 중 S-1과 S-2의 경우 다양한 온도범위($25{\sim}80^{\circ}C$)에서 상용 전해질막인 Nafion-115를 능가하는 우수한 이온전도도를 나타냈다.

• 한국신재생에너지학회:학술대회논문집
• /
• 한국신재생에너지학회 2010년도 춘계학술대회 초록집
• /
• pp.64.1-64.1
• /
• 2010

The morphology of mesoporous $TiO_2$ films plays an important role in the operation of a DSSC. For example, the energy conversion efficiency of DSSCs with well-organized mesoporous $TiO_2$ films is much higher than those with traditional films possessing a random morphology. In previous research, well-organized mesoporous $TiO_2$ films have mainly been synthesized using an amphiphilic block copolymer, e.g., a poly(ethylene oxide) (PEO)-based template. A graft copolymer is more attractive than a block copolymer due to its low cost and the ease with which it can be synthesized. In this work, we provide the first report on the successful synthesis of well-organized mesoporous $TiO_2$ films templated by an organized graft copolymer as a structure directing agent. Well-organized mesoporous $TiO_2$ films with excellent channel connectivities were developed via the sol gel processusing an organized PVC-g-POEM graft copolymer synthesized by one-pot ATRP. The careful adjustment of copolymer composition and solvent affinity using a THF/$H_2O$/HCl mixture was used to systematically vary the material structure. The influence of the material structure on solar cell performance was then investigated. A solid-state DSSC employing both the graft copolymer templated organized 700 nm-thick $TiO_2$ films and graft copolymer electrolytes exhibited a solar conversion efficiency of 2.2% at 100 $mW/cm^2$. This value was approximately two-fold higher than that attained from a DSSC employing a random mesoporous $TiO_2$ film. The solar cell performance was maximized at 4.6% when the film thickness was increased to $2.5{\mu}m$. We believe that this graft copolymer-directed approach introduces a new and simple route toward the synthesis of well-organized metal oxide films as an alternative to a conventional block copolymer-based template.

• 한국재료학회:학술대회논문집
• /
• 한국재료학회 2009년도 추계학술발표대회
• /
• pp.33.2-33.2
• /
• 2009

Block copolymer lithography has attracted great attention for emerging nanolithography since nanoscaleperiodic patterns can be easily obtained through self-assembly process without conventional top-down patterning process. Since the morphologies of self-assembled block copolymer patterns are strongly dependent on surface energy of a substrate, suitable surface modification is required. Until now, the surface modification has been studied by using random copolymer or self-assembled mono layers (SAMs). However, the research on surface modifications has been limited within several substrates such as Si-based materials. In present study, we investigated the formation of block copolymer on Au substrate by $O_2$ plasma treatment with the SAM of 3-(p-methoxy-phenyl)propyltrichloro-silane [MPTS, $CH_3OPh(CH_2)_3SiCl_3$]. After $O_2$ plasma treatment, the chemical bonding states of the surface were analyzed by X-ray photoelectron spectroscopy (XPS). The static contact angle measurement was performed to study the effects of $O_2$ plasma treatment on the formation of MPTS monolayer. The block copolymer nanotemplates formed on Au surface were analyzed by scanning electron microscopy. The results showed that the ordering of self-assembled block copolymer pattern and the formation of cylindrical nano hole arrays were enhanced dramatically by oxygen plasma treatment. Thus, the oxidation of gold surface by $O_2$ plasma treatment enables the MPTS to form the monolayer assembly leading to surface neutralization of gold substrates.

• 한국섬유공학회:학술대회논문집
• /
• 한국섬유공학회 1999년도 봄 학술발표회 논문집
• /
• pp.86-89
• /
• 1999

• 한국섬유공학회:학술대회논문집
• /
• 한국섬유공학회 1993년도 ACT 93
• /
• pp.644-649
• /
• 1993

• 한국재료학회:학술대회논문집
• /
• 한국재료학회 2011년도 춘계학술발표대회
• /
• pp.6.2-6.2
• /
• 2011

Block copolymer (BCP) self-assembly in a film geometry has recently been the focus of increased research interest due to their potential use as templates and scaffolds for the fabrication of nanostructured materials. The phase behavior in a thin film geometry that confines polymer chains to the interfaces will be influenced by the interfacial interactions at substrate/polymer and polymer/air and the commensurability between the equilibrium period (L0) of the BCP and the total film thickness. We investigated the phase transitions for the films of block copolymers (BCPs) on the modified surface, like the order-to-disorder transition (ODT) by in-situ grazing incidence small angle x-ray scattering (GISAXS) and transmission electron microscopy (TEM). The selective interactions on the surface by a PS-grafted substrate provide the preferential interactions with the PS component of the block, while a random copolymer (PS-r-PMMA) grafted substrate do the balanced interfacial interactions on the surface. The thickness dependence of order-to-disorder behavior for BCP films will be discussed in terms of the surface interactions.

• Macromolecular Research
• /
• 제15권7호
• /
• pp.656-661
• /
• 2007

The effects of a neutral solvent of dioctyl phthalate (DOP) on the phase behavior of symmetric polystyrene-block-poly(n-butyl methacrylate) copolymers (PS-b-PnBMA) were assessed herein. Closed-loop phase behavior with a lower disorder-to-order transition (LDOT) and an upper order-to-disorder transition (UODT) was observed for PS-b-PnBMA/DOP solution when the quantity of DOP was carefully controlled. When the molecular weight of PS-b-PnBMA became larger, the LDOT did not appreciably change at smaller quantities of DOP. With larger quantities of DOP, the reduction in the UODT is greater than the increase in the LDOT. This behavior is discussed in accordance with a molecular theory predicated on a compressible random-phase approximation.