• 한국산학기술학회논문지
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• 제12권4호
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• pp.1988-1992
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• 2011

폴리프로필렌(polypropylene, PP)-SEBS(styrene-ethylene/butylene-styrene triblock copolymer)/실리케이트 복합체를 PP의 조성을 35, 40 그리고 45wt%로 변화시키며 실험실 규모의 Brabender Mixer를 이용하여 $200^{\circ}C$에서 용융상태에서 제조하였다. 실리케이트 조성은 5wt%로 고정하였다. PP-SEBS/실리케이트 복합체의 열적특성을 DSC와 TGA를 이용하여 분석하였다. PP-SEBS 콤파운드의 용융온도는 SEBS 함량에 따라 $141^{\circ}C$까지 감소하였다. 실리케이트가 PP-SEBS에 첨가되었을 때 분해온도가 증가하는 것을 TGA 결과로부터 확인할 수 있었다. 콤파운드의 유변학적 특성을 동적유변측정기를 이용하여 측정하였다. PP-SEBS/실리케이트 복합체는 PP-SEBS 콤파운드보다 shear thinning과 탄성특성이 증가하였다. 탄성특성 증가를 확인하기 위해 Van Gurp-Palmen 분석을 이용하였다.

• Bulletin of the Korean Chemical Society
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• 제35권8호
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• pp.2342-2348
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• 2014

Poly(lactic-co-glycolic acid) (PLGA) were grafted to both ends of Pluronic$^{(R)}$ F68 ($(EO)_{75}(PO)_{30}(EO)_{75}$) triblock copolymer to produce poly{(lactic acid)$_m$-co-(glycolic acid)$_n$}-b-poly(ethylene oxide)$_{75}$-b-poly(propylene oxide)$_{30}$-b-poly(ethylene oxide)$_{75}$-b-poly{(lactic acid)$_m$-co-(glycolic acid)$_n$} (PLGA-F68-PLGA) pentablock copolymers. Molecular weights of PLGA blocks were controlled and five kinds of pentablock copolymers with different PLGA block lengths were synthesized using in-situ ring-opening polymerization of D,L-lactide and glycolide with tin(II) 2-ethylhexanoate ($Sn(Oct)_2$) catalyst. PLGA-F68-PLGA pentablock copolymers were characterized by $^1H$- and $^{13}C$-NMR, GPC, and TGA. The numbers (2m, 2n) of repeating units for lactic acid and glycolic acid inside PLGA segments were obtained as (48, 17), (90, 23), (125, 40), (180, 59), and (246, 64), with $^1H$-NMR measurement. From NMR data, the resultant molecular weights were determined in the range of 12,700-29,700, which were similar to those obtained from GPC. Polydispersity index was increased in the range of 1.32-1.91 as the content of PLGA blocks increased. TG and DTG thermograms showed discrete degradation traces for PLGA and F68 blocks, which indicate the weight fractions of PLGA blocks in pentablock copolymers can be calculated by TG profile and it is possible to remove PLGA block selectively. Hydrodynamic radius and radius of gyration of pentablock copolymer micelle were obtained in the range of 46-68 nm and 31-49 nm, respectively, in very dilute (i.e. 0.005 wt %) aqueous solution of THF:$H_2O$ = 10:90 by volume at $25^{\circ}C$.

• 대한화장품학회지
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• 제45권2호
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• pp.199-208
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• 2019

본 연구는 poly(ethylene glycol)-poly(${\varepsilon}$-caprolactone)-poly(ethylene glycol) (PEG-PCL-PEG) 삼중블록 고분자 계면활성제를 이용하여 제조된 우수한 사용감과 선택적인 클렌징 효과를 갖는 수중유(O/W) 에멀젼 타입의 내수성 자외선 차단 제형에 관한 것이다. 수영, 등산 등 다양한 야외 레저 활동이 많아짐에 따라 내수성 자외선 차단제의 수요가 증가하고 있다. 내수성 자외선 차단제는 물이나 땀에 지워지지 않아야하기 때문에 대부분 유중수(W/O) 에멀젼 제형으로 만들어진다. 하지만, W/O 에멀젼 제형은 오일리한 사용감과 클렌징이 어렵다는 단점이 있다. 이에 비해 O/W 에멀젼 제형은 사용감이 우수하고, 클렌징도 용이하지만, 물과의 재유화가 쉽기 때문에 내수성 특성을 갖는 것이 매우 어렵다. 본 연구에서는 이러한 문제를 해결하기 위해 O/W 에멀젼 제형의 HLB 값(~ 10)을 가지면서도 상대적으로 높은 계면장력을 가짐으로써 재유화에 강한 삼중블록 고분자 계면활성제를 도입하였고, 이를 통해 O/W 에멀젼형 지속내수성 자외선 차단제를 개발하였다. 본 연구를 통해 개발된 자외선 차단제는 우수한 사용감과 지속내수성, 그리고 폼 클렌저와의 선택적인 클렌징 효과를 보여준다. 향후 사용감이 다양화된 새로운 O/W 에멀젼형 자외선 차단제 제품 개발에 도움이 될 것으로 기대된다.

• 폴리머
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• 제39권3호
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• pp.461-467
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• 2015

본 논문은 ferric p-toluenesulfonate를 산화제에 약 염기인 이미다졸과 poly(ethylene glycol)-poly(propylene glycol)-poly(ethylene glycol) (PEG-PPG-PEG) 계면활성제를 동시 첨가하여 기상중합법으로 제조된 poly(3,4-ethylenedioxythiophene) (PEDOT) 박막의 광-전기적 특성 향상에 대한 것이다. 여러 가지 조건에서 제조된 PEDOT 박막 특성과 산화제의 첨가제로 사용된 약 염기와 계면활성제의 조합 효과의 상관관계를 규명하고자 하였다. 이미다졸과 PEG-PPG-PEG로 구성된 첨가제를 사용하여 제조된 PEDOT 박막은 $1300S{\cdot}cm^{-1}$ 이상의 전도성을 가졌다. PEG-PPG-PEG계 계면활성제의 분자량이 기상 중합을 이용한 PEDOT 박막의 특성에 미치는 영향도 조사하였다.

• Elastomers and Composites
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• 제49권1호
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• pp.13-23
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• 2014

본 연구에서는 생체분해성 폴리에스터 계열의 glycolide, L-lactide 및 ${\varepsilon}$-caprolactone 단량체를 이용하여 2단계 중합법에 의한 삼원 공중합체를 제조하여, DSC를 이용한 비등온 결정화 거동을 고찰하였다. 보다 더 정확한 거동을 검토하기 위하여 Avrami 식과 Ozawa 식을 조합하여 비등온 결정화 거동을 고찰하였다. 과냉각도를 분석한 결과 PGCLA21의 값이 가장 큰 값을 보이고 있으며 L-lactide 함량이 증가함에 따라 과냉각도는 증가하는 경향을 보이고 있다. 수정된 Avrami 식을 이용하여 다양한 냉각속도에서 비등온 결정화 거동 결정화 속도 상수는 큰 경향을 보이고 있지 않는 것을 알 수 있었다. Avrami 및 Ozawa 식을 조합하여 특정한 상대적 결정화도에서의 냉각함수를 구한결과 L-lactide 함량이 증가하면서 PGCL과 비교시 결정화 속도를 향상시키는 역할을 하고 있는 것으로 여겨지는 반면 PGCLA41과 PGCLA21을 비교시 L-lactide 함량이 일정 이상 증가시 logF(T) 값이 큰 것을 확인 할 수 있는데 이는 동일한 결정을 얻는데 더 많은 냉각 속도를 필요로 한다는 것을 의미하며 결정화 속도 향상에 부정적인 영향을 미치는 것으로 판단된다.

• International Journal of Internet, Broadcasting and Communication
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• 제7권2호
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• pp.96-104
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• 2015

Fischer Tropsch reaction is one of the interesting topic for renewable and clean energy. Polymerization of carbon monoxide or carbon dioxide with hydrogen over metal supported catalyst can produce long chain hydrocarbons. Synthetic liquid hydrocarbons are promising alternative to fossil fuels. This research work has been focused on the synthesis of Fe based catalyst for Fischer Tropsch reaction. Mesoporous silica (MS) support prepared by a precipitation method using two different washing solution, distilled water (DW) and acid in ethanol solution (ET), and different calcination temperature. Then, Fe/MS was prepared by an incipient wetness impregnation method. All of samples were systematically characterized using various physical and chemical techniques. TEM and XRD analysis were used to ensure that the cubic Ia3d mesostructure is stable after calcination. FTIR spectra are useful to ascertain the existence of template in the support. TPR studies were also used to understand the nature of Fe species and their reducibility. The results reveal that washing the support with distilled water and calcination at $550^{\circ}C$ can efficiently remove the triblock copolymer templates. The existence of template in the support affects the textural properties of all catalyst investigated.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2011년도 제41회 하계 정기 학술대회 초록집
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• pp.199-199
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• 2011

The addition of a carbanion to ${\yen}{\acute{a}}{\yen}{\hat{a}}$-unsaturated carbonyl compounds is of importance in the C-C bond formation reactions for modern pharmaceuticals and organic synthesis. Recently, heterogeneous asymmetric catalysis became more attractive area of research because of the easy recovery and separation of the catalyst from the reaction system. Most of synthetic methods for heterogeneous catalysts were grafting or immobilization of homogeneous catalyst onto the solid supports. Trans-1,2-Diaminocyclohexane(DACH) and L-proline ligands have been enormously used as chiral ligands in several catalytic transformation under homogenous conditions. Our group prepared l-proline functionalized mesoporous silica was synthesized under acidic condition using a poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) triblock copolymer template (EO20PO70EO20, Pluronic P-123, BASF). Furthermore, we successfully directly synthesized trans-1,2 diaminocyclohexane functionalized mesoporous silica by using microwave method. The direct functionalization of chiral ligand into the framework of mesoporous materials is expected to be useful for the heterogeneous asymmetric catalysis. So, we adopt the direct synthesis of chiral ligand functionalized mesoporous silica by using thermal and microwave irradiation. Then, chiral ligand functionalized mesoporous silicas were applied to enantioselective asymmetric catalytic reactions.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2011년도 제41회 하계 정기 학술대회 초록집
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• pp.75-75
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• 2011

Recently, dye-sensitized solar cell (DSSC) attracts great attention as a promising alternative to conventional silicon solar cells. One of the key components for the DSSC would be the nanocrystalline TiO2 electrode, and the control of interface between TiO2 and TCO is a highly important issue in improving the photovoltaic conversion efficiency. In this work, we applied various interfacial layers, and analyzed their effect in enhancing photovoltaic properties. In overall, introduction of interfacial layers increased both the Voc and Jsc, since the back-reaction of electrons from TCO to electrolyte could be blocked. First, several metal oxides with different band gaps and positions were employed as interfacial layer. SnO2, TiO2, and ZrO2 nanoparticles in the size of 3-5 nm have been synthesized. Among them, the interfacial layer of SnO2, which has lower flat-band potential than that of TiO2, exhibited the best performance in increasing the photovoltaic efficiency of DSSC. Second, long-range ordered cubic mesoporous TiO2 films, prepared by using triblock copolymer-templated sol-gel method via evaporation-induced self-assembly (EISA) process, were utilized as an interfacial layer. Mesoporous TiO2 films seem to be one of the best interfacial layers, due to their additional effect, improving the adhesion to TCO and showing an anti-reflective effect. Third, we handled the issues related to the optimum thickness of interfacial layers. It was also found that in fabricating DSSC at low temperature, the role of interfacial layer turned out to be a lot more important. The self-assembled interfacial layer fabricated at room temperature leads to the efficient transport of photo-injected electrons from TiO2 to TCO, as well as blocking the back-reaction from TCO to I3-. As a result, fill factor (FF) was remarkably increased, as well as increase in Voc and Jsc.

• 접착 및 계면
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• 제14권2호
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• pp.82-87
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• 2013

본 연구에서는 레졸, 질산철 그리고 트리블럭 공중합체를 이용하여 직접 탄화과정에 의해 자성체 나노입자가 분산된 탄소나노세공체를 합성하였다. 나노세공 마그네타이트/카본($Fe_3O_4$/carbon) 나노복합체는 낮은 마그네타이트 함량(1 wt%)을 가지고 잘 배열된 이차원적 육방체 구조(p6mm)를 보이며, 균일한 세공크기(3.6 nm), 높은 표면적(635 $m^2/g$)과 세공부피(0.48 $cm^3/g$)를 가진다. 작은 입자크기(10.2 nm)를 가지는 마그네타이트 나노입자는 초상자기성(7.7 emu/g)을 보이고 탄소 세공벽 내에 잘 분산되었다. 나노세공 마그네타이트/카본 물질은 최대 995 mg/g의 아이부프로펜 흡착량을 보였다. 또한, 자석을 이용하여 용액과 나노세공 마그네타이트/카본 물질의 분리가 용이하였다. 본 연구에서 제조된 나노복합체는 우수한 아이부프로펜 흡착제로 작용하였다.

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