• 한국재료학회지
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• 제8권8호
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• pp.672-677
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• 1998

오원계 AI-합금의 용융산화에 의한 $AI_2O_3$ 복합재료의 형성속도와 미세구조에 대하여 연구하였다. AI-1Mg-3Si-3Zn 합금과 AI-1Mg-3Si-5Zn합금에 Cu, Ni 각각을 1% 무게비로 첨가하였다. 각 오원계 합금은 1373K, 1473K에서 최대 20시간 동안 산화시켰으며, 산화속도는 무게증가 측정을 통하여 조사하였다. 산화층의거시적 형상과 미세구조를 광학현미경으로 관찰하였다. AI-1Mg-3Si-5Zn-1Cu 합금이 가장 우수한 산화거동을 보였으나, 산화층이 불균일하였다. 합금위에 $SiO_2$를 도포하였더니 산화속도가 증진되었으며, 균일하고 조직이 친밀한 산화층이 얻어졌다.

• 한국지반환경공학회 논문집
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• 제11권6호
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• pp.31-37
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• 2010

본 연구에서는 multi-bed 플레이트로 폐열재생 부분과 촉매반응 부분으로 구성되어 있는 복합열산화 시스템(Hybrid Thermal Oxidation System)을 이용하여 저온에서 주입 밸브 교체 시간간격과 유입유량을 변화시켜 VOCs(MEK와 Toluene) 제거를 평가하고자 하였다. $350^{\circ}C$의 연소온도 조건에서 VOCs는 완전히 전환되었으며 당량비에 따른 전환율 또한 100%에 근접하였고, HTO 시스템의 연소실은 좌우측의 온도가 균형을 이루며 열효율이 매우 높아 폐열회수 및 재생이 효율적이었다. 주입 밸브 교체 시간간격과 유입 유량 변화에 따른 HTO시스템에서의 VOCs 제거 효율은, MEK와 Toluene 모두 안정적으로 높은 91.1~97.4%의 효율을 나타내었으며, 보조연료량 증가보다는 밸브교대시간을 길게 하였을때 제거 효율이 증가하는 경향을 보여 보조연료량 증가보다 밸브교대시간을 증가시키는 것이 제거 효율을 높이는데 효율적으로 판단된다. 이와 같은 연구결과를 고려할 때 HTO시스템은 저농에서도 VOCs 제거, 특히 MEK과 Toluene 제거에 매우 안정적이며 콤팩트한 시스템으로 판단되며, 적은 설치 부지로 중소기업이 요구하는 새로운 VOCs 제거 시스템으로 적용 가능하리라 판단된다.

• 한국해양학회지:바다
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• 제14권3호
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• pp.127-133
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• 2009

동해 울릉분지에서 망간산화물과 철산화물의 유기물 분해 기여율을 정량화하기 위하여 6개의 박스형 시추퇴적물을 채집하였다. 수심이 2,000 m 이상인 울릉분지 표층퇴적물에서 유기탄소 함량은 2.6% 가량으로 육상기원 유기물 유입이 많은 흑해와 용승 해역인 칠레 주변해역들과 비슷했다. 울릉분지에 위치한 정점들에서 망간산화물 함량은 퇴적물 최상부에서 2% 이상으로 매우 높았고, 철산화물 함량은 울릉분지 표층 $1{\sim}4cm$ 내외에서 2% 가량의 최고값을 나타냈다. 그러나 대륙사면 정점들에서 망간산화물과 철산화물 함량은 분지처럼 높은 값을 보이지 않았다. 동해 울릉분지에서 2% 이상으로 높은 망간산화물 함량은 높은 유기탄소 함량과 사면보다 비교적 느린 퇴적속도 때문이거나 망간 이온이 저탁류를 통해 사면에서 분지로 이동한 것으로 예상된다. 망간산화물 환원율은 $0.3{\sim}0.57\;mmol\;m^{-2}\;day^{-1}$의 범위를 보였고, 철산화물 환원율은 $0.10{\sim}0.24\;mmol\;m^{-2}\;day^{-1}$의 범위를 나타냈다. 울릉분지에서 금속산화물은 유기물 분해에 $13{\sim}26%$ 정도를 차지하였으며, 이는 칠레 용승 해역과 유사하고, 덴마크 연안보다 낮은 값이다.

• 한국연소학회지
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• 제13권1호
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• pp.31-43
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• 2008

Oxy-fuel flame has a significantly different structure from that of air-fuel flame because of its high temperature. This study is aimed to find out the difference of the oxy-fuel flame structure in order to understand reaction mechanism closely, which is crucial to design real-scale oxy-fuel combustion system. By examining pictures of counterflow flame and LIF images, we found that oxy-fuel flame had two-zone structure: fuel decomposition region and distributed CO oxidation region. In the oxy-fuel flame, OH radical was distributed intensely through the whole flame due to its higher flame temperature than crossover temperature. For showing those features of the oxy-fuel flame, 1 MW scale IFRF oxy-natural gas burner was simulated by conditional moment closure(CMC) model. Calculation results were compared with experimental data, and showed agreements in trend. In the simulated distributions of fuel decomposition/CO oxidation rates, CO oxidation region was also separated from fuel decomposition zone considerably, which showed the two-zone structure in the oxy-fuel flame.

• Carbon letters
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• 제5권4호
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• pp.170-179
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• 2004

The equilibrium and dynamic adsorption of methylene blue from aqueous solutions by activated carbons have been studied. The equilibrium studies have been carried out on two samples of activated carbon fibres and two samples of granulated activated carbons. These activated carbons have different BET surface areas and are associated with varying amounts of carbon oxygen surface groups. The amounts of these surface groups was enhanced by oxidation with $HNO_3$ and $O_2$ gas at $350^{\circ}C$ and decreased by degassing at increasing temperatures of $400^{\circ}$, $650^{\circ}$ and $950^{\circ}C$. The adsorption increases on oxidation of the carbon surface and decreases on degassing. The increase in adsorption has been attributed to the formation of acidic carbon-oxygen surface groups and the decrease in adsorption on degassing to their elimination. The dynamic adsorption studies have been carried out on the two granulated activated carbons using two 50 mm diameter glass columns at a feed concentration of 300 mg/L and at different hydraulic loading rates (HLR) and bed heights. The minimum achievable concentrations are comparatively lower while the adsorption capacities are higher for GAC-S under the same operating conditions. The adsorption capacity of a carbon increases with increase in HLR but the rate of increase decreases at higher HLR values.

• 한국물환경학회지
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• 제21권1호
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• pp.92-98
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• 2005

Nutrients removal performance of a contact oxidation reactor covered with soil was investigated when basalt rubble was used as a contact medium under various operating conditions. The objective of the experiment was to determine the effectiveness of the system by measuring the removal efficiencies of nutrients from a technical and economical viewpoint. Under the ranges of HRT(20 and 40 hrs) in the experiment, the removal rates of organic matter were as high as 97.5% by showing an effluent $BOD_5$ of less than 10 mg/L. The test of nitrogen removal when the turf was planted on the top soil showed that the average removal rate increased as much as 25% as compared to that without planting. It was suggested that the construction and maintenance cost could be reduced over 20% when the HRT of the system was decreased from 72 to 40 hrs.

• Preventive Nutrition and Food Science
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• 제6권2호
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• pp.83-86
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• 2001

The autoxidation reaction of L-ascorbic acid(AsA), and, particularly, the oxidation rates of AsA in the presence of Fe(III) or Cu(II) ions were determined in water and methanol. UV spectral measurement (at 265 nm) and HPLC were used to determine the remaining amounts of AsA in water and methanol, respectively. It was found that, in the presence of metal ions, the autoxidation rate of AsA was significantly affected by the kinds of solvents used, and also by the kinds of metal ions present. Moreover, the first-order rate constants for the oxidation of non-dissociated AsA compared with dissociated-AsA were investigated. It was confirmed that the oxidation of AsA was more accelerated in the dissociated form of AsA than in the non-dissociated form of AsA in either with Fe(III) or Cu(II). It was also found that the Cu(II) at a concentration of 0.1 $\mu$M had a more significant effect on the first-order rate constants for the autoxidation of AsA than Fe(III) at 5 $\mu$M.

• 한국신재생에너지학회:학술대회논문집
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• 한국신재생에너지학회 2009년도 추계학술대회 논문집
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• pp.203-206
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• 2009

Agglomeration of catalysts is known as one of the major degradation mechanisms. Reforming of liquid fuel, which requires high temperature over $800^{\circ}C$, accelerates agglomeration of catalysts. In this work, The effects of agglomeration on catalysts activity in partial oxidation reforming conditions were investigated. Metal supported catalysts(Pt-CGO, Ru-CGO) were compared to perovskite-structured catalysts(NECS-P1, NECS-P2). High thermal stability of perovskite-structured catalysts was reported. Micro-reactor installed in electric furnace was used. its Temperature was raised from $800^{\circ}C$ to $1000^{\circ}C$ to accelerate agglomeration effect. To measure rate of agglomeration, BET analysis and CO pulse chemisorption were conducted on catalysts exposed to $1100^{\circ}C$. Metal supported catalysts showed degradation at $1000^{\circ}C$ and The rates were different according to metal supported. On the other hand perovskite-structured catalysts showed no degradation at $1000^{\circ}C$.

• 한국산업융합학회 논문집
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• 제15권3호
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• pp.71-77
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• 2012

This study gives the optimal reaction conditions, reaction mechanisms, reaction rates leaded from the oxidation of phenol by electron beam accelerator and ozone used for recent water treatment. It gives the new possibility of water treatment process to effectively manage industrial sewage containing toxic organic compounds and biological refractory materials. The high decomposition of phenol was observed at the low dose rate, but at this low dose rate, the reaction time was lengthened. So we must find out the optimal dose rate to promote high oxidation of reactants. The reason why the TOC value of aqueous solution wasn't decreased at the low dose was that there were a lot of low molecular organic acids as an intermediates such as formic acid or glyoxalic acid. In order to use both electron beam accelerator and biological treatment for high concentration refractory organic compounds, biological treatment is needed when low molecular organic compounds exist abundantly in sewage. In this experiment, the condition of making a lot of organic acids is from 5 kGy into 20 kGy dose. Decomposition rate of phenol by electron beam accelerator was first order reaction up to 300ppm phenol solution on the basic of TOC value and also showed first order reaction by using both air and ozone as an oxidants.

• 한국전기전자재료학회논문지
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• 제19권8호
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• pp.724-731
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• 2006

We investigated the electrochemical properties for Langmuir-Blodgett (LB) films mixed with 4-octyl-4'-(5-carboxylpentamethyleneoxy)azobenzene (denoted as 8A5H) and phospholipid(L-a-dimyristoylphosphatidylcholine, denoted as DMPC and L-a-dilauroylphosphayidylcholine, denoted as DLPC). The LB films of 8A5H, 8A5H-DMPC and 8A5H-DLPC mixture monolayers were deposited by using the LB method on the indium tin oxide(ITO) glass. The electrochemical properties measured by using cyclic voltammetry with a three-electrode system, an Ag/AgCl reference electrode, a platinum wire counter electrode and LB film-coated ITO working electrode at various concentrations(0.1, 0.5, and 1.0 mol/L) of $NaClO_4$ solution. A measuring range was reduced from initial potential to -1350 mV, continuously oxidized to 1650 mV and measured to the initial point. The scan rates were 50, 100, 150 and 200 mV/s, respectively. As a result, LB films of 8A5H and 8A5H-DLPC mixture monolayers appeared irreversible process caused by only the oxidation current from the cyclic voltammogram and LB films of 8A5H-DMPC monolayer mixture was found to be caused by a reversible oxidation-reduction process.