• Tribology and Lubricants
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• 제32권5호
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• pp.141-146
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• 2016

The diketopyrrolopyrrole (DPP) pigment is a bicyclic 8-π-electron system containing two lactam units. Typical DPP derivative pigments have melting points of over 350°C and very low solubility in most solvents, and show absorption in the visible region with a molar extinction coefficient of 33,000 dm²mol⁻¹ and strong photoluminescence with maxima in the range 500–600 nm. X-ray structure analyses of DPP show that the whole molecule is almost in one plane. The phenyl rings are twisted out of the heterocyclic plane and the intermolecular hydrogen bonding between neighboring lactam NH and carbonyl units influences the structure of the DPP pigment in the solid state. In this study, mono-N-alkylation and mono-N-arylation were undertaken for Pigment Red 264 or Pigment Orange 73 with alkyl halide and aryl halide, respectively, in the presence of sodium tert-butoxide as a base catalyst to improve the solubility of DPP pigments and their application as CO₂ indicators. The synthetic yield was in the range 11–88%. The indicator dyes are highly soluble in organic solvents and shows pH-dependent absorption (λ_max 501 and 572 nm for the protonated and deprotonated forms, respectively) and emission (λ_max 524 and 605 nm for the protonated and deprotonated forms, respectively) spectra. The mono-N-alkylated and mono-N-arylated DPP pigment was identified by ¹H-NMR (¹H-Nuclear Magnetic Resonance Spectrometer), FT-IR (Fourier Transform Infrared Spectroscopy), and MS (Mass Spectrometry). According to the results of color and hue properties obtained by a color matching analyzer, the synthesized DPP pigment material can be used as a CO₂ indicator.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2013년도 제44회 동계 정기학술대회 초록집
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• pp.636-636
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• 2013

Since first discovery of strong Raman spectrum of molecules adsorbed on rough noble metal, surface enhanced Raman scattering (SERS) has been widely used for detection of molecules with low concentration. Surface plasmons at noble metal can enhance Raman spectrum and using Au nanostructures as substrates of SERS has advantages due to it has chemical stability and biocompatibility. However, the photoluminescence (PL) background from Au remains a problem because of obtaining molecular vibration information. Recently, graphene, two-dimensional atomic layer of carbon atoms, is also well known as PL quenchers for electronic and vibrational excitation. In this study, we observed SERS of single layer graphene on or under monolayer of Au nanoparticles (NPs). Single layer graphene is grown by chemical vapor deposition and transferred onto or under the monolayer of Au NPs by using PMMA transfer method. Monolayer of Au NPs prepared using Langmuir-Blodgett method on or under graphene surface provides closed and well-packed monolayer of Au NPs. Scanning electron microscopy (SEM) and Raman spectroscopy (WItec, 532 nm) were performed in order to confirm effects of Au NPs on enhanced Raman spectrum. Highly enhanced Raman signal of graphene by Au NPs were observed due to many hot-spots at gap of closed well-packed Au NPs. The results showed that single layer graphene provides larger SERS effects compared to multilayer graphene and the enhancement of the G band was larger than that of 2D band. Moreover, we confirm the appearance of D band in this study that is not clear in normal Raman spectrum. In our study, D band appearance is ascribed to the SERS effect resulted from defects induced graphene on Au NPs. Monolayer film of Au NPs under the graphene provided more highly enhanced graphene Raman signal compared to that on the graphene. The Au NPs-graphene SERS substrate can be possibly applied to biochemical sensing applications requiring highly sensitive and selective assays.

• 마이크로전자및패키징학회지
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• 제27권2호
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• pp.11-17
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• 2020

본 연구에서는 Ag 금속입자가 기능화된 SnO₂ 나노선을 제작 및 저온 NO₂ 가스 센싱 특성을 평가하였다. Vapor-liquid-solid 공법을 이용하여 SnO₂ 나노선을 합성하였고, flame chemical vapour deposition 공법을 이용하여 Ag 금속입자를 SnO₂ 나노선 표면에 기능화하였다. 합성된 Ag 금속입자가 기능화된 SnO₂ 나노선을 이용하여 50℃에서 NO₂ 10 ppm에 대한 가스 센싱 테스트를 진행한 결과, 감응도(R_g/R_a) 1.252를 얻었다. 본 연구를 통하여, 금속입자가 기능화된 나노선을 이용한 저온동작 반도체식 가스센서의 산업 적용을 현실화 할 수 있을 것으로 기대된다.

• Bulletin of the Korean Chemical Society
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• 제25권8호
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• pp.1195-1201
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• 2004

Tyrosinase was covalently immobilized on platinum electrode according to the method we developed for laccase (Bull. Korean Chem. Soc. 2002, 23(7), 385) and p-chlorophenol, p-cresol, and phenol could be detected with sensitivities of 334, 139 and 122 nA/ ${\mu}M$ and the detection limits of 1.0, 2.0, and 2.5 ${\mu}M$, respectively. The response time ($t_{90\%}$) is 3 seconds for p-chlorophenol, and 5 seconds for p-cresol and phenol. The optimal pHs of the sensor are in the range of 5.0- 6.0. This sensor can tolerate at least 500 times repeated injections of p-chlorophenol with retaining 80% of initial activity. In case of tyrosinase and laccase co immobilized platinum electrode, the sensitivities are 560 nA/ ${\mu}M$ for p-phenylenediamine (PPD) and 195 nA/ ${\mu}M$ for p-chlorophenol, respectively. The sensitivity of the bi-enzyme sensor for PPD increases 70% compared to that of only laccase immobilized one, but the sensitivity for p-chlorophenol decreases 40% compared to that of only tyrosinase immobilized one. The sensitivity increase for the bi-enzyme sensor for PPD can be ascribed to the additional catalytic function of the co-immobilized tyrosinase. The sensitivity decrease for p-chlorophenol can be explained by the “blocking effect” of the co-immobilized laccase, which hinders the mass transport through the immobilized layer. If PPD was detected with the electrode that had been used for p-chlorophenol, the sensitivity decreased 20% compared to that of the electrode that had been used only for PPD. Similarly, if p-chlorophenol was detected with PPD detected electrode, the sensitivity also decreased 20%. The substrate-induced conformation changes of the enzymes in a confined layer may be responsible for the phenomena.

• 한국수소및신에너지학회논문집
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• 제22권6호
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• pp.842-851
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• 2011

A multi-cell test system with 25 independent cells is used to test different electrode materials simultaneously for polymer electrolyte membrane fuel cells (PEMFCs). Twenty-five segmented membrane electrode assemblies (MEAs) having the same or different Pt-loading are prepared to analyze the performance deviation of cells in the multi-cell test system. Improvements in the multi-cell test system are made by ensuring that the system performs voltage sensing for the cells individually and inserting optimum gaskets between the MEAs and the graphite plates. The cell performances are improved and their deviations are significantly decreased by these modifications. The performance deviations changed according to various cell configurations because the operating conditions of the cells, such as the gas flow and concentration, differed. This cell system can be used to test multiple electrodes simultaneously because it shows relatively uniform performance under the same conditions as well as linear correlation with various catalyst loadings.

• Korean Chemical Engineering Research
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• 제44권2호
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• pp.166-171
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• 2006

본 연구에서는 전기적 결합 계수가 큰 PMN-PT 압전 재료를 사용하여 탄성표면파를 발진시켜 단백질을 검출할 수 있는 새로운 바이오센서로써 이용 가능성을 확인하고자 시도하였다. 실험결과 PMN-PT 압전 재료의 중심 주파수 필터링은 LT 압전 재료보다 우수하였지만, 만족할만한 결과를 얻을 수는 없었다. 또한, 본 연구에서는 위암을 일으키는 mismatched DNA를 검출하기 위한 방법을 개발하고자 하였다. 그 결과 EDC 용액을 사용하여 NTA에 MutS를 고정화 하였다. 그러나 Ni(니켈)을 사용하여 MutS를 고정화하여 mismatched DNA를 측정하는 것이 더 효과적인 방법이라 판단된다.

• 대한화학회지
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• 제35권1호
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• pp.51-58
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• 1991

새로운 管形 PVC膜 질산이온 選擇性 電極을 제작하여 그 性能을 조사하였다. 電極膜의 組成을 5${\%}$ aliquat-NO$_3$ 용액+ 32${\%}$ poly(vinyl chloride) + 63${\%}$ dibutyl sebecate로 하였을 때 전극의 感應特性이 최적이었으며, 이 때의 감응기울기는 58.5 ${\pm}$ 0.1 mV/decade, 檢出限界는 0.02mM, 感應時間 (t$_{99}$)은 25초이었다. 이 전극을 써서 아질산이온을 連續${\cdot}$自動化法으로 정량하였다. Recipient 용액은 pH 7.6의 10$^{-2}$ M 燐酸鹽 緩衝溶液을 쓰고, 여기에 酸化劑로서 過酸化水素를 0.3${\%}$가 되도록 포함시켰다. 전극계의 最適條件에서 아질산이온 標集溶液 8.0 ${\times}$ 10$^{-5}$ M ∼ 5.0 ${\times}$ 10$^{-2}$ M의 범위에서 직선적인 감응을 나타내었으며, 이 때의 감응기울기는 56.8 ${\pm}$ 0.2 mV/decade이었다.

• 대한화학회지
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• 제47권1호
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• pp.59-66
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• 2003

생물학적 의약품, 식품 등과 같이 저온 유통 체계(cold chain)를 관리하는데 있어서 제품 용기에 부착하여 보관 온도 이상에 노출될 경우 비가역적인 변화를 일으켜 고온 노출여부를 검지 할 수 있는 라벨의 소재로소 poly(N-isopropylacrylamide-co-t-butylacrylamide) [p(NIPAAm-co-t-BAM)]수화겔의 적용 가능성을 평가하였다. p(NIPAAm-co-t-BAM)수화겔은 cold chain 온도인 8$^{\circ}$C 이하에서 온도 민감성을 갖도록 t-BAM양을 조절하여 레독스 중합반응을 통하여 저온 (4$^{\circ}$C)합성하였고, 또한 oli해(NIPAAm-co-t-BAM) 공중합체를 그라프트하여 빗살 구조를 가지는 가교수화겔을 제조함으로써 수화겔의 수축 팽윤 속도를 향상시키고자 하였다. 합성 된 수화겔의 lower critical solution temperatures(LCSTs)는 흐림 점 측정법과 시차주사열량계(DSC)를 이용하여 측정하였으며, NIPAAm 단량체와 빗살형태의 t-BAM 공중합체의 조성비가 가교제의 양에 따라 수화겔의 수축과 팽윤 거동을 관찰하였다. 소수성기를 포함하는 t-BAM의 조성비율에 따라 8$^{\circ}$C 이하 저온에서 수화겔의 LCST조절이 가능하며, 빗살 형태로 그라프트된 공중합체의 조성비에 따라 수축-팽윤율 및 속도의 조절이 가능한 것으로 확인되었다.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2013년도 제45회 하계 정기학술대회 초록집
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• pp.252.2-252.2
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• 2013

ZnO nanostructures have a lot of interest for decades due to its varied applications such as light-emitting devices, power generators, solar cells, and sensing devices etc. To get the high performance of these devices, the factors of nanostructure geometry, spacing, and alignment are important. So, Patterning of vertically- aligned ZnO nanowires are currently attractive. However, many of ZnO nanowire or nanorod fabrication methods are needs high temperature, such vapor phase transport process, metal-organic chemical vapor deposition (MOCVD), metal-organic vapor phase epitaxy, thermal evaporation, pulse laser deposition and thermal chemical vapor deposition. While hydrothermal process has great advantages-low temperature (less than $100^{\circ}C$), simple steps, short time consuming, without catalyst, and relatively ease to control than as mentioned various methods. In this work, we investigate the dependence of ZnO nanowire alignment and morphology on si substrate using of nanosphere template with various precursor concentration and components via hydrothermal process. The brief experimental scheme is as follow. First synthesized ZnO seed solution was spun coated on to cleaned Si substrate, and then annealed $350^{\circ}C$ for 1h in the furnace. Second, 200nm sized close-packed nanospheres were formed on the seed layer-coated substrate by using of gas-liquid-solid interfacial self-assembly method and drying in vaccum desicator for about a day to enhance the adhesion between seed layer and nanospheres. After that, zinc oxide nanowires were synthesized using a low temperature hydrothermal method based on alkali solution. The specimens were immersed upside down in the autoclave bath to prevent some precipitates which formed and covered on the surface. The hydrothermal conditions such as growth temperature, growth time, solution concentration, and additives are variously performed to optimize the morphologies of nanowire. To characterize the crystal structure of seed layer and nanowires, morphology, and optical properties, X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), Raman spectroscopy, and photoluminescence (PL) studies were investigated.

• 대한화학회지
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• 제38권3호
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• pp.200-207
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• 1994

Wistar계 쥐의 신장 조직을 암모니아 기체 감응전극에 고정화하여 조직센서를 제작하고, L-glutamine을 정량하기 위한 최적 조건을 조사하였다. 그 결과, $30^{\circ}C$, pH 7.8의 0.05M 인산완충용액과 30 ${\mu}m$ 두께의 신장을 사용하였을 경우, 정량 가능한 직선범위는$ 8.0{\times}10^{-5}{\sim}1.0{\times}10^{-2} M$이었으며, 감응도는 53.8 mV/decade로 나타났고, 감응시간은 3~5분 소요되었다. 또한 같은 최적 조건하에서 조직을 파쇄하여 얻은 세포소기관을 전극에 고정화시킨 센서의 경우, 정량 가능한 직선범위는 $1.2{\times}10^{-4}{\sim}5.0{\times}10^{-3} M$이었으며, 감응도는 54.0 mV/decade, 감응시간은 6~7분이 소요되었다. 이와 같이 본 연구에서는 쥐의 신장 조직 및 세포 소기관을 이용하여 L-glutamine을 정량 분석할 수 있는 조직센서 개발에 관하여 연구하였다.