• 전기화학회지
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• 제19권4호
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• pp.141-147
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• 2016

본 실험에서는 2,2,6,6-tetramethyl-4-piperidyl methacrylate(TMA)와 합성된 스티렌 계열의 2,2,6,6-tetramethylpiperidine-4-vinylbenzyl ether(TVBE)으로 구성된 단독 및 공중합체를 합성하였으며 산화반응을 이용하여 고분자 라디칼로 변환시켰다. 제조된 고분자 라디칼은 카본블랙, 바인더와 함께 혼합되어 알루미늄 극판에 코팅되었으며 코인셀로 구성하여 전지특성을 평가하였다. 그 결과, 폴리스티렌 기반의 중합체는 폴리메타크릴레이트 기반의 재료에 비해 낮은 산화반응성과 낮은 방전용량을 보여주었다. 하지만 $60^{\circ}C$의 고온에서 실시된 방전실험에서는 폴리스티렌 기반에서 더욱 우수한 방전특성을 나타났다. 또한 예상대로 고분자 라디칼로 구성된 전지에서 우수한 율특성을 확인할 수 있었다.

• 한국대기환경학회지
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• 제23권1호
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• pp.64-73
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• 2007

The catalytic activity of transition metals (Cu, Co, Mn, Fe and Ni) supported on ${\gamma}-Al_2O_3$ for the oxidation of toluene was investigated in the microreactor of fixed-bed type. The catalytic activity of transition metals for the oxidation of toluene turned out to be increasing in the order of Ni$Cu/{\gamma}-Al_2O_3$ catalysts for the oxidation of toluene increased with the increasing loadings of copper, reached the maximum activity at 5% loadings of copper, and decreased with higher loadings of copper in the catalysts. The activity of $Cu/{\gamma}-Al_2O_3$ catalysts for the oxidation of toluene decreased with the increasing calcination temperatures. This might result from the decreasing surface area of catalysts due to the sintering of copper oxide as well as ${\gamma}-Al_2O_3$ supports. The 5wt% $Cu/{\gamma}-Al_2O_3$ catalysts calcined at $400^{\circ}C$ for 4 hrs in the air showed the highest activity for the oxidation of toluene. Mutual inhibition was observed for the binary mixture of toluene and xylene. The activity of the easy-to-oxidize toluene was greatly decreased while the difficult-to-oxidize xylene was slightly decreased in the binary mixture of toluene and xylene. It might suggest that the inhibition of toluene and xylene in the binary mixture resulted from the competitive adsorption for the adsorbed oxygen on the catalytic surface.

• 유기물자원화
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• 제18권1호
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• pp.73-80
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• 2010

음식물류폐기물 혐기소화액으로부터 아질산성 질소를 산화하는 세균 2종, NOB1 과 NOB2를 분리하여 이들의 아질산성 질소산화능 및 온도, pH, 용존산소의 농도에 따른 생장특성을 조사하였다. 분리된 두 균주 모두 최적의 생장조건은 pH 7.0과 배양온도 $35^{\circ}C$로 나타났으며 용존산소의 농도가 높을수록 생장율이 상승하는 것으로 나타났다. 두 균주의 생장을 억제하는 요인으로는 pH와 용존산소가 효과적인 것으로 나타났는데, pH 5.0 및 9.0에서, 용존산소 1.0 ppm 이하에서 생장율이 현저히 감소하는 결과를 보여주었다. 특히, 아질산성 질소의 산화능력은 1.0 ppm 이하의 농도에서 1.0 ppm 이상에서 보다 약 50% 감소하는 것으로 나타났다. 두 균주의 생성율 및 질소산화능은 NOB2가 NOB1에 비해 약 2배 이상 높은 것으로 조사되었다.

• KSBB Journal
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• 제23권6호
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• pp.484-488
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• 2008

본 연구에서는 peroxidase 활성의 신속한 스크리닝을 위해 peroxidase의 활성을 정량적으로 평가할 수 있는 분석으로 agar plate와 96-well plate에서 peroxdase의 활성에 비례하여 색상감도를 측정할 수 있는 colorimetric 분석법을 개발하였다. 이 방법은 RP-HPLC 결과와 매우 비례적으로 상관적인 결과를 보였다. 이 colorimetric 분석법을 사용하여, 폐수에서 한천 고체배지에서 7회에 걸친 스크리닝으로 높은 농도의 2,4-DCP(1000 ppm)에서 생존하는 균주를 스크리닝하였고 선별된 이들 균주들은 탄소원으로 2,4-DCP 만을 대사할 수 있으며 높은 peroxidase 생산량을 보였다. 분리된 균주들 중 높은 peroxidase 활성을 가지는 2,4-DCP 분해 균주를 분리하였고 최종 분리된 균주는 염색폐수의 COD를 4시간 동안 44%에서 61%까지 제거하였다. 상기의 결과에 의해 본 연구에서 개발된 발색법이 페놀화합물 분해 균주 스크리닝법이 빠르고 쉬운 난분해성 물질인 페놀 혼합물의 분해 균주 탐색에 대하여 성공적으로 적용될 수 있기를 기대한다.

• 한국지하수토양환경학회지:지하수토양환경
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• 제18권1호
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• pp.129-136
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• 2013

This research was conducted to investigate effects of acid buffering capacity and soil component in treatment of phenanthrene using electrokinetic-Fenton process. In Hadong clay of high acid buffering and low iron oxide content, it was difficult to oxidize phenanthrene due to shortage of iron catalyst and scavenger effect of carbonate minerals. The desorbed phenanthrene conductive to Fenton oxidation was transported toward cathode by electroosmotic flow. However, in Youngdong illitic clay, oxidation of phenanthrene near anode readily occurred compared to Hadong clay due to high iron content and low acid buffering capacity.

• Bulletin of the Korean Chemical Society
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• 제24권4호
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• pp.460-466
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• 2003

For the drug master file (DMF) of ketoconazole, four impurities (1-4) contained in ketoconazole were synthesized. During the synthesis of 2, a new synthetic method of 1,4-dihydropyrazine was established. To oxidize the aminoalcohol (2j) to the aminal (2j-1), the standard Swern oxidation condition was modified to mask the nucleophilicity of the amino group temporarily using one equivalent of acetic acid. Derivative 3 was synthesized via regioselective bromination at the 2 position of the 4-aminophenol derivative (3a) using $Br_2$ in the presence of p-TsOH. The etherification of aryl bromide with the phenol derivative (1f) was accomplished by a modification of the general Cu-mediated reaction condition using excess 1f itself as a solvent at elevated temperature (190 ℃).

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2003년도 제5회 학술대회 논문집 일렉트렛트 및 응용기술연구회
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• pp.45-48
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• 2003

BiSrCaCuO thin films were fabricated by atomic layer-by-layer deposition using an ion beam sputtering method. 10 wt% and 90 wt% ozone mixed with oxygen were used with ultraviolet light irradiation to assist oxidation. At early stages of the atomic layer by layer deposition, two dimensional epitaxial growth which covers the substrate surface would be suppressed by the stress and strain caused by the lattice misfit, then three dimensional growth takes place. Since Cu element is the most difficult to oxidize, only Sr and Bi react with each other predominantly, and forms a buffer layer on the substrate in an amorphous-like structure, which is changed to $SrBi_2O_4$ by in-situ anneal.

• 한국생물공학회:학술대회논문집
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• 한국생물공학회 2001년도 추계학술발표대회
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• pp.517-520
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• 2001

Fossil fuels such as coal and crude oil contain various organic sulfur compounds. Combustion of these fuels emit sulfur oxides which are considered as msjor air pollutants causing acid rain problem. Among various organic sulfur compounds, aromatic sulfur compounds of thiophenes which constitute major sulfur fractions of heavy oils are not easily removed by hydrodesulfurization. Many peroxidase and hemoproteins are known to oxidize dibenzothiophene (DBT) to dibenzothiophene-sulfoxide(DBT - sulfoxide) then dibenzothiophene- sulfone (DBT-sulfone). The oxidation of DBT by the immobilized hemoproteins in n-octane was increased significantly when the hemoproteins were deposited on celites of the particle size between 0.75 - 1.0 mm and a conventional substrates. such as t-butyl hydroperoxide and cumene hydroperoxide. In anhydrous organic solvents with log P values larger than 4.0 DBT was completely oxidized by cumene hydroperoxide catalyzed by cytochrome c deposited on celites.

• 한국미생물·생명공학회지
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• 제24권3호
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• pp.268-273
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• 1996

An extremely cadmium tolerant yeast, Hansenula anomala B-7 used to determine the modification of the intracellular enzyme activities by cadmium ion. The activities of alcohol dehydrogenase, phosphofructokinase, and cytidine deaminase were decreased up to 90%, 40%, and 86% compa- red with the control by 1 mM cadmium nitrate respectively, but the activities of malate dehydrogenase, 6- phosphogluconate dehydrogenase, cytochrome c oxidase, and alkaline phosphatase were increased up to 440%, 136%, 260% and 155% compared with the control by 1 mM cadmium nitrate respectively. These results show that the activities of the enzymes participating in Embden-Mayerhof pathway (e.g. anaerobic metabolism) were reduced by cadmium, but those involved in hexose monophosphate pathway and tricarboxylic acid cycle (e.g. aerobic metabolism) were stimulated in contrast. It has been suggested that the diminished activity of cytidine deaminase in pyrimidine nucleotide dissimilation occured due to the inhibited nucleotide dissimilation by cadmium ion; the enhanced activity of cytochrome c oxidase was specifically required in order to oxidize a raised amount of NADH and NADPH due to the increased aerobic metabolism.

• 한국세라믹학회지
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• 제32권3호
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• pp.331-340
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• 1995

Microwave (Hybrid) Heating (MHH) was used to oxidize and sinter Al-Al2O3 powder mixture. For 25 v/o Al specimen and 35 v/o Al specimen, the total processing to produce low-shrinkage reaction bonded alumina was carried out within 1 hour even though conventional furnace process took more than 10 hours. Compared with conventional fast firing process, MHH process increased more than 40% oxidation at the same temperature, and these high oxidation rates were thought to be caused by the surface ohmic current on Al particles.