• 마이크로전자및패키징학회지
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• 제14권1호
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• pp.27-31
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• 2007

휨성 유기박막트랜지스터(organic thin film transistor, OTFT)를 제작하기 위하여 게이트 절연막으로 PVP(poly-4-vinylphenol) 유기막을 이용하여 MIM (metal-insulator-metal) 구조의 캐패시터 소자를 제작하였다. 유기 절연층의 형성은 Al/PES (polyethersulfone) 기판과 ITO/Glass 기판 위에 PVP를 용질로, PGMEA(propylene glycol monomethyl ether acetate)를 용매로 사용하였다 또한 열경화성 수지인 poly(melamine-co-(ormaldehyde)를 사용하여 cross-linked PVP 절연막을 합성하여 스핀코팅법으로 소자를 형성하였다. 제작된 소자에 대해 절연막 두께와 기판 종류에 따른 전기적 특성을 조사한 결과 Al/PES 기판을 사용하였을때 누설전류는 1.3 nA로 ITO/glass 기판을 사용했을때의 27.5 nA보다 크게 개선되었다. 또한 제작된 모든 캐패시터 소자의 정전용량은 $1.0{\sim}1.2nF/cm^2$ 범위로 나타났으며 계산값과 매우 유사한 결과를 얻을 수 있었다.

• Nuclear Engineering and Technology
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• 제47권6호
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• pp.738-745
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• 2015

The catalytic exchange of hydrogen isotopes between hydrogen and water has been known to be a very useful process for the separation of tritium from tritiated water. For the process, a highly active hydrophobic catalyst is needed. This study provides an effective fabrication method of size-controlled platinum/poly[styrene-divinylbenzene-tri(propylene glycol) diacrylate] [Pt/poly(SDB-TPGDA)] hydrophobic catalyst beads with a narrow size distribution. Platinum nanoparticles were prepared by ${\gamma}$-ray-induced reduction in the aqueous phase first, and then uniformly dispersed in SDB-TPGDA comonomer after the hydrophobization of platinum nanoparticles with alkylamine stabilizers. The porous Pt/poly(SDB-TPGDA) hydrophobic catalyst beads were synthesized by the UV-initiated polymerization of the mixture droplets prepared in a capillary-based microfluidic system. The size of as-prepared catalyst beads can be controlled in the range of $200-1,000{\mu}m$ by adjusting the flow rate of dispersed and continuous phases, as well as the viscosity of the continuous phase. Sorbitan monooleate and cyclohexanol were used as coporogens to control the porosities of the catalyst beads.

• Elastomers and Composites
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• 제39권3호
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• pp.234-243
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• 2004

본 연구에서는 poly(propylene glycol) (PPG), toluene 2,4-diisocyanate, 3-methylthiophene (3-MT)으로부터 반응시간, $FeCl_3$의 농도, 3-MT와 PU의 무게비, 반응온도 등의 다양한 조건에 따라 전도성 폴리우레탄 필름을 제조하였다. $FeCl_3$와 ethyl acetate로 구성된 유기용매에 제조한 필름을 함침 시킨 결과 3-MT와 $FeCl_3$의 확산-산화 반응을 통해 급속한 전도성 PMT 층이 형성되었다. 전도성 복합체의 전기 전도도는 제조조건에 따라 많은 영향을 받고 SEM 분석과 접촉각 측정으로부터 반응시간과 반응온도가 모폴로지와 표면 자유에너지에 미치는 영향을 조사하였으며 제조된 복합체의 전도도는 최대 42 S/cm 인 것으로 확인되었다.

• Elastomers and Composites
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• 제49권1호
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• pp.31-36
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• 2014

Sebacic acid, isophthalic acid, ethylene glycol, neopentyl glycol를 각각 1몰씩 사용하여 폴리에스터 폴리올을 합성하였다. 합성된 폴리올의 수산기가는 56.6 mg KOH/g이고 분자량은 1,980 g/mole 이었다. 합성한 폴리에스터 폴리올에 toluene diisocyanate와 쇄연장제로 ethylene glycol, 1,4-butandiol, 1,2-propylene glycol을 각각 넣고 폴리우레탄을 합성하였다. GPC로 측정한 3 가지 폴리우레탄의 분자량은 각각 5850, 6160, 6480 g/mole 이었다. FT-IR에 의한 구조분석에서 폴리에스터 폴리올은 3600 $cm^{-1}$ 부근에서 -OH 기가 관찰되었고, 2950 $cm^{-1}$ 에서 sebacic acid의 -CH shoulder가 나타났으며, ester의 carbonyl group은 1730 $cm^{-1}$ 부근에서 나타났고, isophthalic acid의 benzene ring은 1600 $cm^{-1}$, 740 $cm^{-1}$에 관찰되었다. 폴리우레탄의 -OH 피크가 3600 $cm^{-1}$ 에서 나타났고, 3300 $cm^{-1}$ 부근과 1530 $cm^{-1}$ 에서 우레탄기 중의 -NH 기를 확인할 수 있었다. $^1H$ NMR에 의한 구조분석에서 폴리에스터 폴리올은 sebacic acid는 1.3, 1.5, 2.1 ppm에서, isophthalic acid는 7.3, 8.1, 8.7 ppm에서, ethylene glycol은 4.2 ppm에서, neopentyl glycol은 0.8, 3.2, 3.9 ppm에서 관찰되었다. 폴리우레탄의 경우에는 폴리에스터 폴리올과 유사하나 toluene diisocyanate의 도입에 의한 벤젠고리의 피크가 7 ppm에서 미약하게 나타났다.

• 청정기술
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• 제19권3호
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• pp.219-225
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• 2013

본 연구에서는 계면활성제에 의한 수계 세정제의 문제점을 해결하고자 친환경적이고 계면활성제가 없는 수계세정제 개발연구를 진행하였다. 이를 위하여 전자 부품 세정대상의 주 오염물인 플럭스(flux)에 대해 용해력이 있고 수용성인 propylene glycol과 propylene glycol alkyl ether계 용제를 주성분으로 하고 여기에 여러 첨가제를 가하여 수계 surfactant-free 세정제 S-1, S-2를 배합하였고, 이들 개발세정제와 비교대상의 수계 surfactant-free 수입 세정제의 물성을 측정하여 세정성능을 예측하고 오염물인 플럭스와 솔더(flux and solder) 대하여 중량법을 이용한 초음파 세정성 평가를 진행하였다. 물성 측정 결과 비교대상 세정제인 수입세정제 V는 본 연구에서 개발한 배합세정제 S-1과 S-2의 세정제와 전반적으로 비슷한 결과 값을 가짐을 확인할 수 있었다. 비교대상 세정제 V와 배합세정제 모두 원액을 희석함에 따라 pH가 저하되다가 다시 상승하는 것이 관찰되었으며 습윤지수값은 세정능력에는 크게 영향을 주지 않는 것으로 판단되었다. 다양한 초음파 주파수(28, 45, 100 kHz)를 사용한 세정성 평가 실험 결과에서 솔더(solder)의 세정은 주파수 45 kHz에서 세정 성능이 가장 좋게 나타났고 플럭스(flux)의 세정 성능 결과는 실험 대상의 모든 세정제가 주파수 28 kHz에서 세정 성능이 가장 좋게 나타났다. 희석하지 않은 원액세정제의 플럭스 및 솔더(flux and solder) 세정의 경우 배합세정제 S-1, S-2 모두 수입세정제 V보다 빠른 세정력을 보여주었다. 그러나 수입세정제 V의 권장 사용농도인 25%에서는 수입 세정제 V가 배합세정제 보다 초기 세정효율이 좋음이 확인되었다. 따라서 본 실험결과를 가지고 판단할 때, 본 연구에서 개발한 배합세정제 S-1, S-2는 충분히 산업현장의 플럭스 및 솔더(flux and solder) 세정에 적용이 가능할 것으로 판단되어진다.

• 한국농업기계학회:학술대회논문집
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• 한국농업기계학회 2017년도 춘계공동학술대회
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• pp.107-107
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• 2017

3D bioprinting is a technology to produce complex tissue constructs through printing living cells with hydrogel in a layer-by-layer process. To produce more stable 3D cell-laden structures, various materials have been developed such as alginate, fibrin and gelatin. However, most of these hydrogels are chemically bound using crosslinkers which can cause some problems in cytotoxicity and cell viability. On the other hand, thermosensitive hydrogels are physically cross-linked by non-covalent interaction without crosslinker, facilitating stable cytotoxicity and cell viability. The examples of currently reported thermosensitive hydrogels are poly(ethylene glycol)/poly(propylene glycol)/poly(ethylene glycol) (PEG-PPG-PEG) and poly(ethylene glycol)/poly(lactic acid-co-glycolic acid) (PEG/PLGA). Chitosan, which have been widely used in tissue engineering due to its biocompatibility and osteoconductivity, can be used as thermosensitive hydrogels. However, despite the many advantages, chitosan hydrogel has not yet been used as a bioink. The purpose of this study was to develop a bioink by chitosan hydrogel for 3D bioprinting and to evaluate the suitability and potential ability of the developed chitosan hydrogel as a bioink. To prepare the chitosan hydrogel solution, ${\beta}-glycerolphosphate$ solution was added to the chitosan solution at the final pH ranged from 6.9 to 7.1. Gelation time decreased exponentially with increasing temperature. Scanning electron microscopy (SEM) image showed that chitosan hydrogel had irregular porous structure. From the water soluble tetrazolium salt (WST) and live and dead assay data, it was proven that there was no significant cytotoxicity and that cells were well dispersed. The chitosan hydrogel was well printed under temperature-controlled condition, and cells were well laden inside gel. The cytotoxicity of laden cells was evaluated by live and dead assay. In conclusion, chitosan bioink can be a candidate for 3D bioprinting.

• Archives of Pharmacal Research
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• 제29권10호
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• pp.928-933
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• 2006

Percutaneous delivery of NSAIDs has advantages of avoiding hepatic first pass effect and delivering the drug for extended period of time at a sustained, concentrated level at the inflammation site that mainly acts at the joint and the related regions. To develop the new topical formulations of pranoprofen that have suitable bioadhesion, the gel was formulated using hydroxypropyl methylcellulose (HPMC) and poloxamer 407. The effects of temperature on drug release was performed at $32^{\circ}C$, $37^{\circ}C$ and $42^{\circ}C$ according to drug concentration of 0.04%, 0.08%, 0.12%, 0.16%, and 0.2% (w/w) using synthetic cellulose membrane at $37{\pm}0.5^{\circ}C$. The increase of temperature showed the increased drug release. The activation energy (Ea), which were calculated from the slope of lop P versus 1000/T plots was 11.22 kcal/ mol for 0.04%, 10.79 kcal/mol for 0.08%, 10.41 kcal/mol for 0.12% and 8.88 kcal/mol for 0.16% loading dose from the pranoprofen gel. To increase the drug permeation, some kinds of penetration enhancers such as the ethylene glycols, the propylene glycols, the glycerides, the non-ionic surfactants and the fatty acids were incorporated in the gel formulation. Among the various enhancers used, propylene glycol mono laurate showed the highest enhancing effects with the enhancement factor of 2.74. The results of this study suggest that development of topical gel formulation of pranoprofen containing an enhancer is feasible.

• Restorative Dentistry and Endodontics
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• 제47권4호
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• pp.38.1-38.15
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• 2022

Objectives: This study investigated the cytotoxicity, radiopacity, pH, and dentinal tubule penetration of a paste of 1.0% calcium-doped zinc oxide nanocrystals (ZnO:1.0Ca) combined with propylene glycol (PRG) or polyethylene glycol and propylene glycol (PEG-PRG). Materials and Methods: The pastes were prepared by mixing calcium hydroxide [Ca(OH)₂] or ZnO:1.0Ca with PRG or a PEG-PRG mixture. The pH was evaluated after 24 and 96 hours of storage in deionized water. Digital radiographs were acquired for radiopacity analysis and bubble counting of each material. The materials were labeled with 0.1% fluorescein and applied to root canals, and images of their dentinal tubule penetration were obtained using confocal laser scanning microscopy. RAW264.7 macrophages were placed in different dilutions of culture media previously exposed to the materials for 24 and 96 hours and tested for cell viability using the MTT assay. Analysis of variance and the Tukey test (α = 0.05) were performed. Results: ZnO:1.0Ca materials showed lower viability at 1:1 and 1:2 dilutions than Ca(OH)₂ materials (p < 0.0001). Ca(OH)₂ had higher pH values than ZnO:1.0Ca at 24 and 96 hours, regardless of the vehicle (p < 0.05). ZnO:1.0Ca pastes showed higher radiopacity than Ca(OH)₂ pastes (p < 0.01). No between-material differences were found in bubble counting (p = 0.0902). The ZnO:1.0Ca pastes had a greater penetration depth than Ca(OH)₂ in the apical third (p < 0.0001). Conclusions: ZnO:1.0Ca medicaments presented higher penetrability, cell viability, and radiopacity than Ca(OH)₂. Higher values of cell viability and pH were present in Ca(OH)₂ than in ZnO:1.0Ca.

• 한국가축번식학회지
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• 제21권4호
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• pp.355-362
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• 1997

This study was undertaken in an effort to product embryos through in vitro maturation(IVM), in vitro fertilization(IVF) and in vitro culture(IVC) after cryopreservation of immature and mature porcine oocytes. The experiments were conducted to investigate IVM rate of oocytes frozen with 3 different cryoprotectants and to examine IVF and IVC of frozen-thawed oocytes. The CEI(cumulus cells expansion index) after IVM of frozen-thawed immature oocytes was higher in oocytes frozen with PG＋PEG(propylene glycol plus polyethylene glycol) than those frozen with single cryoprotectant and this index was almost 90% of unfrozen oocyte's index(2.39 vs. 2.66). The IVF rate of all frozen oocytes was very low(68% of unfrozen oocytes) and the IVF rate of frozen immature oocytes was slightly higher than that of frozen mature oocytes(39.0% vs. 34.4%), but polyspermic penetration was higher in frozen immature oocytes(21.9% vs. 19.1%). The cleavage rate after IVF of frozen-thawed oocytes was 9.3% for frozen mature oocytes and 11.3% for frozen immature oocytes and this rate was significantly lower(P<0.05) than that of control(60.7%). The development to 8-cell stage was greatly lower in frozen mature oocytes than in frozen immature oocytes. The results indicate that the use of PG plus PEG as cryoprotectant may be very effective for vitrification of porcine oocytes and the frozen-thawed immature porcine oocytes can be used fro in vitro embryo production based on IVM, IVF and IVC system.

• 한국응용과학기술학회지
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• 제31권4호
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• pp.711-718
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• 2014

본 논문에서는 피혁에 사용되는 수용성 폴리우레탄 사슬 연장제인 1,4-butanediol(1,4-BD)의 함유에 따른 물성변화를 조사하였다. 합성에 사용된 시약은 poly propylene glycol(PPG), isoporon diisocyanate((IPDI), dimethylolpropionic acid(DMPA), 1,4-BD를 사용하였다. 1,4-BD의 함유에 따른 내용제성과 내굴곡성 측정값은 시료 전부 우수한 물성을 보였다. 인장강도, 내마모성 측정결과 1,4-BD가 많이 함유된 시료들이 각각 $1.80kg_f/mm^2$, 49.54 mg.loss로 우수한 물성을 확인하였다. 연실율 측정결과 1,4-BD가 적게 함유된 시료가 364%로 가장 우수한 측정값을 나타냈다.