• 공업화학
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• 제10권5호
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• pp.748-753
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• 1999

아크릴아마이드계 단량체와 실리콘분말의 혼합 슬러리를 이용한 겔캐스팅법에 있어서 단량체의 혼합비, 각종 첨가제(고분자 중합 개시제, 촉매, 분산제)의 양, 실리콘 분말 함량, 건조시 습도 등과 같은 화학적 변수가 점도, 겔화시간 등 성형변수와 성형체의 수축율과 강도에 미치는 영향을 조사하였다. 겔화시간은 개시제와 촉매의 양이 증가할수록 단축되지만 개시제의 양에 대한 의존성이 더 크게 나타났고, 슬러리의 겔화시간은 단량체용액에 비해 약 1/2 이하로 대폭 감소되었으며, 가교제 MBAM 비율이 높을수록 겔화는 지연되었다. 또한 분산제의 함량이 0.6 wt % 이상일 때는 슬러리의 유동성이 낮아졌다. 성형체는 98%의 높은 습도 하에서 300시간 이상 건조 처리할 때 7% 이하의 균일한 수축에 의해 균열과 뒤틀림 현상이 발생하지 않았으며 40, 50 vol % 실리콘 분말을 함유한 건조 겔체는 각각 평균 64 MPa, 36 MPa의 강도를 보였다.

• 폴리머
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• 제34권6호
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• pp.588-593
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• 2010

실리콘, 게르마늄, 주석이 결합된 7개의 아크릴 단량체가 개발되었고 이를 광경화시킨 필름의 굴절률을 측정하였다. 공단량체로 가교도가 높은 triacrylate(Trimer)를 사용하여 형성된 공중합체의 굴절률로부터 단일중합체의 굴절률을 계산하였다. 공유 결합된 $Ph_3Si$, $Ph_3Ge$, $Ph_3Sn$은 각각 아크릴 고분자 필름의 굴절률을 향상시키는데 기여하였고 주석이 게르마늄에 비해 약간 높은 기여도로 나타났다. 주석에 의한 굴절률 향상 효과는 $Bu_3Sn$을 도입한 결과와 aliphatic acrylate의 비교로 보다 명확하게 입증되었다. 주석과 황의 안정된 결합을 이용하여 $Ph_3SnS$가 도입된 아크릴 고분자의 굴절률은 589 nm에서 1.671로 높게 측정되었다. 측정 파장으로 656, 830, 1310, 1550 nm에서도 비슷한 굴절률이 관찰되었다.

• 한국치위생학회지
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• 제14권5호
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• pp.775-781
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• 2014

Objectives : The purpose of the study is to investigate the protective effect of coenzyme $Q_{10}$ on cytotoxicity effect of dental monomers in odontoblast(MDPC-23). Methods : MDPC-23 was incubated with the(co)monomers triethylene glycol dimethacrylate (TEGDMA) with and without addition of coenzyme $Q_{10}$. The cell proliferation and survival was determined using WST-1 assay. The level of reactive oxygen species(ROS) was measured by immunofluorescent staining for DCF-DA. Results : TEGDMA treatment decreased the cell proliferation by dose dependently(0.1, 1, 2.5, 5, 10 mM) on the growth of MDPC-23 cells. Coenzyme $Q_{10}$ showed cell proliferation from 5 to $500{\mu}M$ by WST-1 assay. Pre-treatment coenzyme $Q_{10}$ showed the antioxidant effect on proliferation and viability of MDPC-23 after 48h(p<0.05). The positive cells were observed in non-coenyme $Q_{10}$ treatment group(group 2) in comparison with coenyme $Q_{10}$ pre-treatment group(group 1) by DCF-DA. The fluorescence positive cells showed 14.715(group 1) and 19.788(group 2) using image J system. Conclusions : TEGDMA induced cytotoxicity. The MDPC-23 cell death was associated with the increasing ROS. Coenyme $Q_{10}$ showed the antioxidant effects by decreasing ROS. This effects may contribute to the treatment of periodontal disease induced by TEGDMA after operation.

• Journal of Microbiology and Biotechnology
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• 제13권1호
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• pp.64-69
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• 2003

Pseudomonas chlororaphis HS21 was isolated from a soil sample and found to produce medium-chain-length polyhydroxyalkanoates (MCL-PHAs) using palm kernel oil (PKO) as the sole carbon source. Up to 3.3 g/1 dry cell weight containing $45\%$ MCL-PHA was produced, when the strain was grown for 21 h in a jar fermentor culture containing 5 g/1 PKO. The polymer produced from PKO consisted of unsaturated monomers of $7.3\%$ 3-hydroxy-5-cis-tetradecenoate and $2.3\%$ 3-hydroxy-5,8,-cis, cis-tetradecadienoate as well as saturated even-carbon number monomers ranging from $C_6\;to\;C_14$, as determined by GC and El GC/MS The PHA was a transparent, sticky material at room temperature. A differential scanning calorimetric analysis revealed that the polymer was amorphous with a $-44^{\circ}C$ glass transition temperature. The number average molecular weight and polydispersity index of the PHA were 83,000 and 1.53, respectively. Although the PHA was practically biodegradable, its degradability was lower than that of poly(3-hydroxyoctanoate) based on a comp:trison of the clear zones formed by growing PHA depolymerase-producing bacteria on an agar plate containing the respective polymers.

• Journal of Microbiology and Biotechnology
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• 제18권8호
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• pp.1475-1481
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• 2008

B3 antibody specifically binds the $Lewis^Y$-related carbohydrate antigen of many carcinomas, and it is used as a model antibody in this study. In a previous study, the Fab fragment of the antibody was fused to a 38 kDa truncated form of Pseudomonas exotoxin A, PE38, to make Fab-PE38, where PE38 is fused to the Fd fragment of the Fab domain. This parent monomer molecule, Fab-PE38, had no cysteine in the hinge region, and it could not make a disulfide bond to form a disulfide bond bridged homodimer. In this study, we constructed three different kinds of divalent Fab-toxin fusion homodimers where the toxin is fused to the light chain of Fab, $(Fab-PE38fl)_2$. In addition to the PE38 toxin fused to the light chain, these three molecules have different hinge sequences hi, h2, and h3 making Fabh1-, Fabh2-, and Fabh3-PE38fl monomers, respectively. These hinges contain only one cysteine on different positions of the hinge sequence. The disulfide bond between the hinge region of two monomers forms homodimers $(Fabh1-PE38fl)_2$, $(Fabh2-PE38fl)_2$, and $(Fabh3-PE38fl)_2$. The refolding yields of these dimers were 5-16-fold higher than a previously constructed dimer where the PE38 was fused to the Fd fragment $(Fabh2-PE38)_2$ [8]. Our data suggest that the steric repulsion between the two PE38s in $(Fabh1-PE38)_2$ during disulfide bridge formation is relieved by fusing it at the end of the light chain. The best cytotoxicity value of these dimers showed about 2.5-fold higher on an MCF7 cell line than that of the monovalent reference molecule in ng/ml scale, which is 15-fold higher in pM scale.

• 한국응용과학기술학회지
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• 제26권4호
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• pp.467-472
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• 2009

Ultraviolet curable coating solution was prepared with poly(ethylene glycol) acrylate oligomer and various mono and multi-functional acrylate monomers. The optical properties of UV cured coating layer on PET film with acrylate coating solution containing metal oxides, such as fumed silica and alumina, were also investigated to reduce light reflection on films. Poly(ethylene glycol) diacrylate which has 575 of average molecular weight was used as oligomer acrylate, and pentaerythritol triacrylate and dipentaerythritolpenta-/hexa acrylate were used as multi-functional acrylate monomers. Also, butyl acrylate was used to improve the adhesion as well as to reduce glass transition temperature to give a better flexability. 1-hydroxy cyclohexyl phenyl ketone was used as photoinitiator. We found out the metal oxides in acrylate coating solution showed a homogeneous dispersion from energy dispersive spectroscopy data. Transmittance and light reflection of coated PET film was measured with UV/vis spectrometer and gloss meter, respectively. When 1.00 g of both metal oxides was added into coating solution, the transmittance and the glossiness were reduced from 90% to 30% and from 190 GU to 35 GU, respectively. However, adding up to 1.00 g of the metal oxide into coating solution did not affect on the hardness of coating layer and adhesion between coated layer and PET film. Conclusively, we can control transmittance and light reflection of coated film by adjusting the amounts of metal oxide in coating solution.

• 한국재료학회:학술대회논문집
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• 한국재료학회 2011년도 춘계학술발표대회
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• pp.11.2-11.2
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• 2011

Polymer based organic photovoltaics have attracted a great deal of attention due to the potential cost-effectiveness of light-weight and flexible solar cells. However, most BHJ polymer solar cells are not thermally stable as subsequent exposure to heat drives further development of the morphology towards a state of macrophase separation in the micrometer scale. Here we would like to show three different approaches for developing new electroactive polymers to improve the thermal stability of the BHJ solar cells, which is a critical problem for the commercialization of these solar cells. For one of the examples, we report a new series of functionalized polythiophene (PT-x) copolymers for use in solution processed organic photovoltaics (OPVs). PT-x copolymers were synthesized from two different monomers, where the ratio of the monomers was carefully controlled to achieve a UV photo-crosslinkable layer while leaving the ${\pi}-{\pi}$ stacking feature of conjugated polymers unchanged. The crosslinking stabilizes PT-x/PCBM blend morphology preventing the macro phase separation between two components, which lead to OPVs with remarkably enhanced thermal stability. The drastic improvement in thermal stabilities is further characterized by microscopy as well as grazing incidence X-ray scattering (GIXS). In the second part of talk, we will discuss the use of block copolymers as active materials for WOLEDs in which phosphorescent emitter isolation can be achieved. We have exploited the use of triarylamine (TPA) oxadiazole (OXA) diblock copolymers (TPA-b-OXA), which have been used as host materials due to their high triplet energy and charge-transport properties enabling a balance of holes and electrons. Organization of phosphorescent domains in TPA-b-OXA block copolymers is demonstrated to yield dual emission for white electroluminescence. Our approach minimizes energy transfer between two colored species by site isolation through morphology control, allowing higher loading concentration of red emitters with improved device performance. Furthermore, by varying the molecular weight of TPA-b-OXA and the ratio of blue to red emitters, we have investigated the effect of domain spacing on the electroluminescence spectrum and device performance.

• Korean Chemical Engineering Research
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• 제47권4호
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• pp.470-475
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• 2009

본 연구에서는 유화중합을 이용한 수분산성 아크릴계접착제의 최적의 합성조건을 구하기 위하여 주단량체로 2-EHA(2-ethylhexyl acrylate), n-BA(n-butyl acrylate), MMA(methyl metacrylate), 기능성단량체로 2-HEMA(2-hydroxylethylmethacrylate), AAc(acrylic acid), 유화제로는 음이온성 유화제인 SLS(Sodium Lauryl Sulfate), 그리고 개시제로 APS(Ammonium persulfate)를 사용하여 전환율, 입자 크기, 박리강도, 유리전이온도에 대한 유화제, 개시제, 단량체 함량의 영향을 고찰하였다. 반응온도 $82^{\circ}C$, 유화제(SLS/monomer) 3.75%, 개시제(APS/monomer) 0.612%에서 95% 이상의 전환율을 얻을 수 있었고, 유화제나 개시제의 양이 너무 많을 때는 박리접착강도가 감소하는 경향을 보였으며, 65% 2-EHA/monomer, 20% BA/monomer, 10% MMA/monomer에서 최대 전환율과 최대 박리접착강도를 얻을 수 있었다.

• 폴리머
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• 제25권1호
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• pp.49-55
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• 2001

비닐계 단량체인 아크릴로니트릴과 스티렌을 E-beam 전조사법에 의해 폴리프로필렌 섬유에 그라프트 반응시켜 PP-g-(AN/St) 공중합체를 제조한 후 아미드옥심기와 슬폰기를 도입하여 이관능성 이온교환섬유를 제조하였다. 그라프트율은 단량체 내에 아크릴로니트릴의 조성이 감소할수록 증가하였으며 최대 101.1%이었고 최대 아미드옥심화율은 7.2 mmol/g이었다. 또한 섬유상 이온교환체의 초기 열분해 온도는 120 ${\circ}C$ 이었고 함수율은 공중합체 내에 아미드옥심화율이 증가할수록 감소하였고 슬폰화율이 증가할수록 증가하는 경향을 나타냈다. APP-g-AN, SPP-g-St, ASPP-g-(AN/St) 이온교환체의 우라늄 흡착량은 각각 12.4, 34, 38mg/g이었으며 최적 흡착시간은 약 50시간이었다. 우라늄 흡착 실험결과, 본 실험에서 합성한 이온교환체 ASPP-g-(AN/St)는 $UO_2^{2+}$에 대하여 우수한 성능을 보였다.

• 공업화학
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• 제3권4호
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• pp.678-685
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• 1992

기능성 단량체가 점착물성에 미치는 영향을 알아보기 위하여 아크릴산과 기타 단량체로 아크릴 수지를 라디칼 용액중합을 이용하여 4원공중합시킨 후 물성을 측정하였으며, 또한 최적 점착 물성을 얻기 위하여 통계적 분석 방법을 이용하여 검토하였다. 점착물성에 있어서 아크릴산이 아크릴아미드보다 점착력의 증가에 미치는 영향이 컸다. 반면에 tackiness의 감소에 있어서는 아크릴아미드의 영향이 아크릴산 보다 컸다. 통계적 방법을 인용하여 점착물성 중 점착력, tackiness 그리고 응집력을 최적화 시킨 결과 단량체의 성분 비율은 부틸 아크릴레이트 81.7 mole%, 아크릴산 8.0 mole%, 아크릴아미드 2.1 mole%, 비닐아세테이트 8.2 mole% 일 때로 나타났고 이 때의 추정 회귀식은 다음과 같았다. $D=.857+.072X_1-.114X_2-.027X_3-.126X_1{^2}-.046X_1{\cdot}X_2-.063X_1{\cdot}X_3-.152X_2{^2}+.027X2{\cdot}X_3-.120X_3{^2}$ $X_1$:coded acylic acid, $X_2$:coded acylamide, $X_3$:coded vinylacetate