• 한국추진공학회지
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• 제19권4호
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• pp.61-68
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• 2015

초임계 연소에 대한 기초연구로써 축소형 액체 로켓 엔진에서 기체산소/케로신, 기체아산화질소/에탄올 추진제 조합의 정상상태 연소의 분무를 관찰하고 비교하였다. 분무의 가시화에는 shadowgraph 기법을 사용하였으며 실험결과를 분석하기 위해 shadowgraph를 후처리하여 밀도구배강도 이미지를 사용하였다. 정상상태 연소압력이 동일한 조건에서 기체산소/케로신 추진제의 액체 제트 표면의 굴곡이 심하고 분사기 팁 근처에서 급격한 밀도구배를 보이는 것이 관찰되었다. 밀도구배강도의 평균 이미지에서 분무 중심 길이를 도출하였으며 더 낮은 운동량 플럭스 비 조건에서도 기체산소/케로신의 분무중심 길이가 더 짧은 것으로 나타났다.

• 한국추진공학회:학술대회논문집
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• 한국추진공학회 2006년도 제27회 추계학술대회논문집
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• pp.223-227
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• 2006

하이브리드 추진 시스템에서의 산화제 종류에 따른 연소특성을 알아보기 위한 연구를 수행하였다. 산화제는 $GN_2O$와 GOX를 사용하고, 고체연료는 폴리에틸렌(PE)을 사용해 연소시험을 하였다. 산화제 종류에 따른 연소특성은 O/F 비에 따른 화염온도로 해석이 가능하였으며, $GN_2O$가 GOX보다 하이브리드 추진 시스템의 산화제로 효율이 좋음을 확인하였다 산화제의 유량은 직경이 다른 여러 개의 쵸킹 오리피스로 제어했고, 산화제 공급 유량범위는 $0.0138{\sim}0.0427kg/sec$ 이었다. 산화제 종류에 따른 연소특성을 표현하는 실험식은 고체연료의 질량유속으로 나타냈고, 이는 물질전달 수와 산화제의 질량유속으로 얻어진다.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2000년도 영호남학술대회 논문집
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• pp.316-319
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• 2000

In the case of immobilizing of glucose oxidase into polypyrrole (PPy) using electrosynthesis, the glucose oxidase (GOx) forms a coordinate bond with the polymer's backbone. However, because of intrinsic insulation and net-chain of the enzyme, the charge transfer and mass transport are obstructed during the film growth. Therefore, the film growth is dull. We synthesized the enzyme electrode by electropolymerization added some organic solvent, A formative seeds of film growth is delayed by adding the solvent. The delay is induced by radical transfer between the solvent and pyrrole monomer. In the case of adding ethanol, the radical transfer shares the contribution of dopant between electrolyte anion and GOx polyanion. This may lead to increase amount of immobilized the enzyme in ppy. However, adding tetrahydrofuran (THF), the radical transfer is more brisk, resulting in short chained polymer. Therefore, the doping level is lowered and then amount of immobilized of enzyme is decreased. For the UV absorption spectra of synthetic solution before synthesis and after, in the case of ethanol added, the optical density was slightly decreased for the GOx peaks. It suggests amount of GOx in the solution was decreased and amount of GOx in the film was increased. We established qualitatively that amount of immobilization can be improved by adding a little ethanol in the synthetic solution. It is due to radical transfer reaction. The radical transfer shares the contribution of dopant between small and fast electrolyte anion and big and slow GOx polyanion.

• Journal of Ginseng Research
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• 제33권4호
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• pp.249-255
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• 2009

The oxidation of glycolate to glyoxylate, a key step in plant photorespiration, is carried out by the peroxisomal flavoprotein glycolate oxidase (EC 1.1.3.15). To investigate the altered gene expression and the role of GOX in ginseng plant defense system, a cDNA clone containing a GOX gene designated as PgGOX was isolated and sequenced from Panax ginseng. The cDNA was 692 nucleotides long and have an open reading frame of 552 bp with a deduced amino acid sequence of 183 residues. A GenBank BlastX search revealed that the deduced amino acid of PgGOX shares a high degree homology with the Glycine max (95% identity). In the present study we analyzed the expression of PgGOX under various environmental stresses at different times using real time-PCR. The results showed that the expressions of PgGOX increased after various treatments involving salt, light, cold, ABA, SA, and copper treatment.

• Korean Chemical Engineering Research
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• 제55권2호
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• pp.258-263
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• 2017

본 연구에서는 글루코스 산화효소(glucose oxidase, GOx), 고분자인 폴리에틸렌이민(polyethyleneimine, PEI), 카본나노튜브(carbon nanotube, CNT)와 벤조퀴논(benzoquinone, BQ)을 이용하여 글루코스 바이오연료전지를 위한 바이오 촉매를 합성하였다. 이를 위해, 지지체인 PEI/CNT 복합체에 BQ를 정전기적 인력을 통해 물리적으로 포집한 뒤, GOx를 담지시켜 합성하였다. 이는 기존에 전자 매개체로서 전해질에 풀어서 사용했던 BQ를 전해질이 아닌 촉매 내에 포집하여 촉매를 구성하였다는 개선점이 크며, 그 결과, BQ가 포집되지 않은 촉매 대비, 1.9배 상승한 $34.16{\mu}A/cm^2$의 최대전류밀도를 얻음을 통해 촉매활성이 개선되었음을 증명하였고, 바이오연료전지의 산화극 촉매로 이용 시, BQ가 포집되지 않은 촉매를 이용한 바이오연료전지에 비해 1.2배 상승한 $0.91mW/cm^2$의 최대출력밀도를 얻었다. 이를 통해 바이오연료전지의 산화극을 위한 촉매로서 GOx와 함께 담지된 매개체 BQ를 포함한 촉매 제조 가능성을 확인하였다.

• 한국수소및신에너지학회논문집
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• 제26권2호
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• pp.179-183
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• 2015

In this study, we propose a catalyst structure including enzyme and metal nano rod for glucose sensing. In the catalyst structure, glucose oxidase (GOx) and gold nano rod (GNR) are alternatingly immobilized on the surface of carbon nanotube (CNT), while poly(ethyleneimine) (PEI) is inserted in between the GOx and GNR to fortify their bonding and give them opposite polarization ($[GOx/GNR]_nPEI/CNT$). To investigate the impact of $[GOx/GNR]_nPEI/CNT$ on glucose sensing, some electrochemical measurements are carried out. Initially, their optimal layer is determined by using cyclic voltammogram and as a result of that, it is proved that $[GOx/GNR/PEI]_2/CNT$ is the best layer. Its glucose sensitivity is $13.315{\mu}AmM^{-1}cm^{-2}$. When it comes to the redox reaction mechanism of flavin adenine dinucleotide (FAD) within $[GOx/GNR/PEI]_2/CNT$, (i) oxygen plays a mediator role in moving electrons and protons generated by glucose oxidation reaction to those for the reduction reaction of FAD and (ii) glucose does not affect the redox reaction of FAD. It is also recognized that the $[GOx/GNR/PEI]_3/CNT$ is limited to the surface reaction and the reaction is quasi-reversible.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2003년도 하계학술대회 논문집 Vol.4 No.1
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• pp.223-226
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• 2003

We propose an improvement method for a $\underline{G}ate$ $\underline{OX}ide(GOX)$ thinning at the edge of $\underline{S}hallow$ $\underline{T}rench$ $\underline{I}solation(STI)$, when STI is adopted to Dual Gate Oxide(DGOX) Process. In the case of SOC(System On-a-Chip), the DGOX process is usually used for realizing both a low and a high voltage parts in one chip. However, it is found that the severe GOX thinning occurs from at STI top edge region and a dent profile exists at the top edge of STI, when conventional DGOX and STI process carried out in high density device chip. In order to overcome this problem, a new DGOX process is tried in this study. And we are able to prevent the GOX thinning by H2 anneal, partially SiN liner skip, and a method which is merged a thick sidewall oxide(S/O) with a SiN pull-back process. Therefore, a good subthreshold characteristics without a double hump is obtained by the prevention of a GOX thinning and a deep dent profile.

• 한국재료학회지
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• 제19권1호
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• pp.44-49
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• 2009

Conjugated nanocrystals using CdSe/ZnS core/shell nanocrystal quantum dots modified by organic linkers and glucose oxidase (GOx) were prepared for use as biosensors. The trioctylphophine oxide (TOPO)-capped QDs were first modified to give them water-solubility by terminal carboxyl groups that were bonded to the amino groups of GOx through an EDC/NHS coupling reaction. As the glucose concentration increased, the photoluminescence intensity was enhanced linearly due to the electron transfer during the enzymatic reaction. The UV-visible spectra of the as-prepared QDs are identical to that of QDs-MAA. This shows that these QDs do not become agglomerated during ligand exchanges. A photoluminescence (PL) spectroscopic study showed that the PL intensity of the QDs-GOx bioconjugates was increased in the presence of glucose. These glucose sensors showed linearity up to approximately 15 mM and became gradually saturated above 15 mM because the excess glucose did not affect the enzymatic oxidation reaction past that amount. These biosensors show highly sensitive variation in terms of their photoluminescence depending on the glucose concentration.

• Korean Journal of Chemical Engineering
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• 제35권12호
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• pp.2421-2429
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• 2018

Thiol-based self-assembled anchor linked to glucose oxidase (GOx) and gold nanoparticle (GNP) cluster is suggested to enhance the performance of glucose biosensor. By the adoption of thiol-based anchors, the activity of biocatalyst consisting of GOx, GNP, polyethyleneimine (PEI) and carbon nanotube (CNT) is improved because they play a crucial role in preventing the leaching out of GOx. They also promote electron collection and transfer, and this is due to a strong hydrophobic interaction between the active site of GOx and the aromatic ring of anchor, while the effect is optimized with the use of thiophenol anchor due to its simple configuration. Based on that, it is quantified that by the adoption of thiophenol as anchor, the current density of flavin adenine dinucleotide (FAD) redox reaction increases about 42%, electron transfer rate constant ($k_s$) is $9.1{\pm}0.1s^{-1}$ and the value is 26% higher than that of catalyst that does not use the anchor structure.

• 한국추진공학회:학술대회논문집
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• 한국추진공학회 2008년도 제31회 추계학술대회논문집
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• pp.239-242
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• 2008

원통형 형상의 연료 그레인을 적용한 하이브리드 추진 시스템에서 연료포트 초기 직경에 따른 연소특성을 고찰하였다. 산화제에 따라 달라지는 연료포트 직경에 따른 연소특성 변화를 알아보고자 산화제로는 GOX와 $GN_2O$를 적용하였고, 고체연료로는 PE를 적용해 실험을 수행하였다. 동일 산화제 유량에서 산화제와 상관없이 고체연료의 초기 포트직경이 커짐에 따라 연소량이 감소함을 확인했고, 산화제로 $GN_2O$를 적용한 경우가 산화제로 GOX를 적용한 경우보다 연료포트 초기 직경에 따른 연소량 차이가 줄어듦을 확인하였다.