• Composites Research
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• 제35권2호
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• pp.115-119
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• 2022

탄소섬유의 성능은 탄소 섬유 강화 플라스틱(CFRP)과 같은 고품질 고분자 복합재료에 매우 중요하다. 이를 위해 탄소섬유 물성에 큰 영향을 주는 전구체 섬유의 기계적, 물리적, 구조적 특성을 개선할 수 있는 최적화된 방사공정과 이를 위한 적합한 전구체 공중합 고분자를 사용하는 것은 필수적이다. 본 연구에서는 메타크릴산(MAA)의 함량과 주입시간, 2,2'-아조비스(2-메틸프로피오니트릴) (AIBN)의 농도를 합성공정 변수로 설정하였으며, 용액 중합법(solution polymerization)에 의해 Poly(AN-co-MAA)가 합성되었다. 305,138 g/mol의 분자량과 4.2%의 MAA 비율을 가지는 Poly(AN-co-MAA)를 N,N-디메틸포름아미드(DMF)에 16.0 wt% 농도로 용해시킨 후 기격습식방사법(dry-jet-wet spinning)으로 전구체 섬유를 제조하였다. 섬유의 인장강도는 ~1.06 GPa, 인장탄성률은 ~22.01 GPa였으며, 섬유에서의 공극 및 구조적 결함은 관찰되지 않았다.

• 한국재료학회:학술대회논문집
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• 한국재료학회 2012년도 춘계학술발표대회
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• pp.88.1-88.1
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• 2012

Silicon nanowires (SiNWs), due to their unusual quantum-confinement effects that lead to superior electrical and optical properties compared to those of the bulk silicon, have been widely researched as a potential building block in a variety of novel electronic devices. The conventional means for the synthesis of SiNWs has been the vapor-liquid-solid method using chemical vapor deposition; however, this method is time consuming, environmentally unfriendly, and do not support vertical growth. As an alternate, the electroless etching method has been proposed, which uses metal catalysts contained in aqueous hydrofluoric acids (HF) for vertically etching the bulk silicon substrate. This new method can support large-area growth in a short time, and vertically aligned SiNWs with high aspect ratio can be readily synthesized with excellent reproducibility. Nonetheless, there still are rooms for improvement such as the poor surface characteristics that lead to degradation in electrical performance, and non-uniformity of the diameter and shapes of the synthesized SiNWs. Here, we report a facile method of SiNWs synthesis having uniform sizes, diameters, and shapes, which may be other than just cylindrical shapes using a modified nanosphere lithography technique. The diameters of the polystyrene nanospheres can be adjustable through varying the time of O2 plasma treatment, which serve as a mask template for metal deposition on a silicon substrate. After the removal of the nanospheres, SiNWs having the exact same shape as the mask are synthesized using wet etching technique in a solution of HF, hydrogen peroxide, and deionized water. Different electrical and optical characteristics were obtained according to the shapes and sizes of the SiNWs, which implies that they can serve specific purposes according to their types.

• Journal of Microbiology and Biotechnology
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• 제23권3호
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• pp.343-350
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• 2013

(R)-[3,5-Bis(trifluoromethyl)phenyl] ethanol is a key chiral intermediate for the synthesis of aprepitant. In this paper, an efficient synthetic process for (R)-[3,5- bis(trifluoromethyl)phenyl] ethanol was developed via the asymmetric reduction of 3,5-bis(trifluoromethyl) acetophenone, catalyzed by Leifsonia xyli CCTCC M 2010241 cells using isopropanol as the co-substrate for cofactor recycling. Firstly, the substrate and product solubility and cell membrane permeability of biocatalysts were evaluated with different co-substrate additions into the reaction system, in which isopropanol manifested as the best hydrogen donor of coupled NADH regeneration during the bioreduction of 3,5-bis(trifluoromethyl) acetophenone. Subsequently, the optimization of parameters for the bioreduction were undertaken to improve the effectiveness of the process. The determined efficient reaction system contained 200mM of 3,5-bis(trifluoromethyl) acetophenone, 20% (v/v) of isopropanol, and 300 g/l of wet cells. The bioreduction was executed at $30^{\circ}C$ and 200 rpm for 30 h, and 91.8% of product yield with 99.9% of enantiometric excess (e.e.) was obtained. The established bioreduction reaction system could tolerate higher substrate concentrations of 3,5- bis(trifluoromethyl) acetophenone, and afforded a satisfactory yield and excellent product e.e. for the desired (R)-chiral alcohol, thus providing an alternative to the chemical synthesis of (R)-[3,5-bis(trifluoromethyl)phenyl] ethanol.

• 대한화학회지
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• 제35권3호
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• pp.275-279
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• 1991

고순도 암모니움 명반 결정을 합성한 후 열분해 시켜 높은 순도의 초미세 산화알루미늄(${\alpha}-Al_2O_3$)분말을 합성하였다. 이 때 불순물인 Na$_2$O의 혼입과 Al(OH)$_3$의 침전을 최대한으로 방지하기 위해 pH = 1.5∼2.5의 영역에서 암모니움 명반을 합성하였으며, pH 조건은 수용액 중에서 Na와 Al 이온의 수산화물과 탄산염 형성을 고려, pH에 따른 각 이온종들의 농도가 이론적으로 계산되었다. 그 결과 ${\alpha}-Al_2O_3$의 순도는 99.7%이상이고, 입자는 ${\phi}$ = 0.1∼0.5 ${\mu}$m의 균일한 크기의 분말이 얻어졌다.

• 공업화학
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• 제19권1호
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• pp.37-44
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• 2008

저렴한 비용으로 도전성 투명 필름을 제조하기 위해 PET 필름 위에 습식 도포법으로 ITO/ATO 막을 적층시켰다. 압력 15 MPa, 온도 $50^{\circ}C$의 SAS 합성 조건으로 ITO를 합성하였으며 ITO의 최적 조성비(In/Sn)는 65, 합성된 ITO의 평균입경은 $15{\pm}2nm$, 표면저항 값은 $4{\times}10^4{\Omega}{\cdot}cm$였다. 도포액은 pH 10에서 제조하였으며 ATO 막의 표면조도(Ra), 표면저항 값, 빛투과율은 각각 9 nm, $5.5{\times}10^6{\Omega}{\cdot}cm$, 91%였다. 일차 도포된 ATO 막 위에 0.1, 0.5, 1.0, 2.0 ITO wt% 첨가한 도포액으로 ITO 막을 적층 제조하였으며, ITO/ATO 적층 필름의 표면조도는 4, 10, 12, 16 nm이였으며 표면저항 값은 각각 $3.7{\times}10^6$, $2.4{\times}10^6$, $8{\times}10^5$, $2{\times}10^5{\Omega}{\cdot}cm$로 측정되었다. 적층 필름의 빛투과율은 각각 89, 88, 86, 82%이였으며 ITO 농도가 높아질수록 빛투과율은 낮아졌다.

• 청정기술
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• 제13권3호
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• pp.180-187
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• 2007

도전성 PET투명 필름을 제조하기 위해 PET필름를 기재로 사용하여 그 위에 습식 도포법으로 인듐주석산화물(ITO) 필름을 제조하였다. 압력 15 MPa, 온도 $50^{\circ}C$의 SAS 합성조건으로 ITO를 합성하였으며 ITO의 최적 조성비(In/Sn)는 65이며 이 조건에서 합성된 ITO의 평균입경은 $15{\pm}2\;nm$, 표면저항 값은 $4{\times}10^4\;{\Omega}{\cdot}cm$였다. ITO 도포액은 pH 10에서 제조하였으며 PET 필름 위에 0.1, 0.5, 1, 2 ITO wt%를 첨가한 도포액을 붓고 바코터(bar-coater)로 ITO 필름을 제조하였다. ITO 필름의 표면조도는 4, 10, 12, 16 nm였으며 표면저항 값은 $3.7{\times}10^6,\;2.4{\times}10^6,\;8{\times}10^5,\;2{\times}10^5\;{\Omega}{\cdot}cm$였다. ITO 필름의 빛투과율은 각각 89, 88, 86, 82%였으며 ITO 농도가 높아질수록 표면조도와 도전성은 높아졌으나 빛투과율은 낮아졌다.

• 한국분말재료학회지
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• 제16권5호
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• pp.310-315
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• 2009

Ultra-fine TiC/Co composite powder was synthesized by the carbothermal reduction process without wet chemical processing. The starting powder was prepared by milling of titanium dioxide and cobalt oxalate powders followed by subsequent calcination to have a target composition of TiC-15 wt.%Co. The prepared oxide powder was mixed again with carbon black, and this mixture was then heat-treated under flowing argon atmosphere. The changes in the phase, mass and particle size of the mixture during heat treatment were investigated using XRD, TG-DTA and SEM. The synthesized oxide powder after heat treatment at 700$^{\circ}C$ has a mixed phase of TiO$_2$ and CoTiO$_3$ phases. This composite oxide powder was carbothermally reduced to TiC/Co composite powder by the solid carbon. The synthesized TiC/Co composite powder at 1300$^{\circ}C$ for 9 hours has particle size of under about 0.4 $\mu$m.

• 센서학회지
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• 제16권6호
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• pp.395-400
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• 2007

Ambient drying sol-gel processing was used for monolithic silica ambigels in the temperature range of $130-250^{\circ}C$. A new method of mesopore ambigels, which mean the aerogels prepared by ambient pressure drying process synthesis, is suggested at first. This method includes two important approaches. The first point is that $SiO_{2}$ surface modification of wet gel was performed by trimethylchlorosilane in n-butanol solution. This procedure is provided the silica gel mesopore structure formation. The second point is a creation of the ternary azeotropic mixture water/n-butanol/octane as porous liquid, which is effectively provided removing of water such a low temperature by 2 step drying condition under ambient pressure. The silica aerogels, which were prepared by ambient pressure drying from azeotropic mixture of water/n-butanol/octane, are transparent, crack-free and mesoporous (pore size ${\sim}$ 5.6 nm) with surface area of ${\sim}$ $923{\;}m^2/g$, bulk density of $0.4{\;}g/cm^3$ and porosity of 85 %.

• 한국결정성장학회지
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• 제10권4호
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• pp.302-308
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• 2000

탄산칼슘을 모재로 한 형광체 제조를 위하여 비정질 탄산칼슘 전구체를 합성할 때 용액의 농도, 반응온도, 유지시간 및 모액의 pH의 영향을 조사함으로써 안정한 비정질 탄산칼슘을 합성할 수 있었으며, 물 속에 침적하여 결정화 조건을 달리하여 줌으로써 calcite, aragonite, vaterite의 결정 상을 얻을 수 있었다. 또한 활성원소로서 Sn을 첨가하여 비정질 탄산칼슘을 합성하고, 이를 결정화시켜 각 결정형에 따른 형광특성을 조사하였다. 결정형에 따른 발광강도는 calcite가 가장 우수하였으며, 발광중 심파장은 순수한 청색을 나타내는 464 nm였다. calcite의 발광강도는 여기파장 255 nm에서 최대가 되었으며, 형광램프용의 형광체로 사용하기 적합한 것으로 기대된다.

• Advances in nano research
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• 제13권6호
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• pp.527-543
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• 2022

A novel, green, versatile and magnetically retrievable BiFeO₃/CDR (Bismuth ferrite/coriander) nanocomposites were fabricated via simple wet chemical method utilizing in situ functionalized, cheap coriander seed powder (CDR 5%, 10%, 15% and 20 wt%) as a fuel to enhance the efficiency of pristine BiFeO₃. A comparative study was performed between BiFeO₃/CDR and BiFeO₃/CNT (Bismuth ferrite/carbon nanotubes) nanocomposites for the removal of various hazardous pollutants from waste water. The successful synthesis of the fabricated nanomaterials was monitored via FT-IR, Powder XRD, FE-SEM, CV, VSM, CHNS/O and XPS studies. The synthesized nanomaterials were employed for the oxidative degradation of Carbol fuchsin, Reactive black 5, Ciprofloxacin and Doxorubicin; adsorption of a pesticide malathion; and reduction studies for Para-nitrophenol (PNP). The fabricated nanomaterials (BiFeO₃/CDR) showcased excellent efficiency and comparable results with (BiFeO₃/CNT) for the removal of model pollutants. Moreover, synthesized green heterojunction was also testified for mixture of textile and pharmaceutical waste. Hence CDR can be utilized as a better alternative of CNTs.