• 한국세라믹학회지
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• 제33권7호
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• pp.816-822
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• 1996

서로 다른 흑연화도를 갖는 furan 수지로 부터 얻어진 무기화합물(SiC, TiO2) 첨가 탄소재료의 산화반응의 흑연구조 의존성에 대하여 살펴보았다. 탄소재료의 산화는 시료의 표면적에 크게 의존하여, 흑연화가 상당히 진행된시료라 할지라도 표면적이 클 때는 살화속도도 빠른 것으로 밝혀졌으며, 단위 중량이 아닌 단위면적당의 산화속도로 바꿔 생각했을 때 흑연화가 진행될 수록 산화반응도 늦어지는 것을 알 수 있었다. 그리고 겉보기 활성화 에너지값으로 부터 생각할 때 흑연(TiO2 첨가시료)과 난층흑연(SiC 첨가시료)이 동일한 반응기구에 의해 산화가 진행되는 것으로 판단되었다. 또한 두종류 이상의 결정구조가 혼재하여 있는 시료의 경우 이들 성분들의 산화속도는 달라 반응의 초기에 흑연으로 결정화된 않은 비정질 탄소 성분이 흑연 성분보다 먼저 선택적으로 산화되는 것을 알 수 있었다.

• 한국물환경학회지
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• 제34권2호
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• pp.149-156
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• 2018

Oxidation of Ciprofloxacin, Trimethoprim, and Enrofloxacin by ozone was experimentally investigated to observe the effects of background water quality (such as ultrapure water, humic acid, and biologically treated wastewater) and water temperature on the removal rate of these antibiotics, and, thereby, to be able to provide design information when the ozone treatment process is adopted. Initial concentrations of the antibiotics spiked to $10{\mu}g/L$, and the ozone dose was 1, 2, 3, 5, and 8 mg/L. While the removal rate of Ciprofloxacin under ultrapure water background by ozone oxidation was over 99%, the removal rate under humic acid and biologically treated wastewater background was markedly lower, in the range of 49.3% ~ 99% and 19.8 % ~ 99 %, respectively. When water temperature is decreased from $20^{\circ}C$ to $4^{\circ}C$, the removal rate is reduced from the range of 19.8% ~ 99 % to the range of 7.5 % ~ 99 % under a biologically treated wastewater background. The effects of background and temperature on the removal rate of Trimethoprim and Enrofloxacin were similar to that of Ciprofloxacin, but the degree was different. Therefore, it is concluded that the background of water to be treated, as well as water temperature, should be taken into consideration when the design factor, such as ozone dose, is determined, so that the treatment objective of the ozone treatment process can be most effectively met.

• 한국대기환경학회지
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• 제29권6호
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• pp.811-817
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• 2013

A two-stage bioreactor system using sulfur-oxidizing bacteria was studied to abate high strength hydrogen sulfide ($H_2S$) from biogas. The two-stage bioreactor consisted of a $H_2S$ absorption column (0.5 L) and a microbial oxidation column (1 L) in series, and the liquid medium was continuously recirculated through the columns. The objectives of this study were to determine the feasibility of the bioreactor for biogas desulfurization and to investigate the effect of the medium circulation rate on the system performance. An averaged concentration of $H_2S$ introduced to the bioreactor was 530 ppm, corresponding to an overall loading rate of $44.4g/m^3/hr$. During the initial 20 days period at the medium recirculation rate of 8 reactor volumes per hour (12 L/hr), the dissolved oxygen (DO) concentration in the oxidation column was 6 mg/L, while the DO in the absorption column was 0.5 mg/L showing that the oxygen contents of the biogas stream was not altered. Because of the biological oxidation of $H_2S$ in the oxidation column, the sulfate concentration increased from 200 mg/L to 5,600 mg/L in the liquid medium. The removal efficiency of $H_2S$ was greater than 99% in the initial operation period. After the initial period, the medium recirculation rate between the two columns was stepwise changed eight times from 1.0 to 40 vol/hr (1.5~60 L/hr). At the recirculation rate of faster than 4 vol/hr, the $H_2S$ removal efficiencies were found to be high, but the efficiency declined at the lower recirculation rates than the threshold.

• 한국지하수토양환경학회지:지하수토양환경
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• 제17권6호
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• pp.43-51
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• 2012

Rreactivity of persulfate (PS) for oxidation of TCE under various conditions such as heat, $Fe^{2+}$, and UV was investigated. It was found that degradation rate of TCE increased with increasing temperature from 15 to $35^{\circ}C$. At pH 7.0, the rate constants (k) at 15, 25, 30, and $35^{\circ}C$ were 0.07, 0.30, 0.74, and $1.30h^{-1}$, respectively. For activation by $Fe^{2+}$, removal efficiency of TCE increased with increasing $Fe^{2+}$ concentration from 1.9 mM to 11 mM. The maximum removal efficiency of TCE was approximately 85% when pH of the solution dropped from 7.0 to 2.5. Degradation of TCE by UV-activated PS was the most effective, showing that the degradation rate of TCE increased with inreasing PS dosage; the rate constants (k) at 0.5, 2.5, and 10 mM were 34.2, 40.5, and $55.9h^{-1}$, respectively. Our results suggest that PS activation by UV/PS process could be the most effective in activation processes tested for TCE degradation. For oxidation process by PS, however, pH should be observed and adjusted to neutral conditions (i.e., 5.8-8.5) if necessary.

• 한국재료학회지
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• 제14권4호
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• pp.265-269
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• 2004

Plasma nitrocarburising and post oxidation were performed on SCM435 steel by a pulsed plasma ion nitriding system. Plasma oxidation resulted in the formation of a very thin ferritic oxide layer 1-2 $\mu\textrm{m}$ thick on top of a 15～25 $\mu\textrm{m}$ $\varepsilon$-F $e_{2-3}$(N,C) nitrocarburized compound layer. The growth rate of oxide layer increased with the treatment temperature and time. However, the oxide layer was easily spalled from the compound layer either for both oxidation temperatures above $450^{\circ}C$, or for oxidation time more than 2 hrs at oxidation temperature $400^{\circ}C$. It was confirmed that the relative amount of $Fe_2$$O_3$, compared with $e_3$$O_4$, increased rapidly with the oxidation temperature. The amounts of ${\gamma}$'-$Fe_4$(N,C) and $\theta$-$Fe_3$C, generated from dissociation from $\varepsilon$-$Fe_{2-3}$ /(N,C) phase during $O_2$ plasma sputtering, were also increased with the oxidation temperature.e.

• 한국재료학회지
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• 제4권6호
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• pp.669-680
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• 1994

합금원소(Cr, V, Si. Mo, Nb)가 첨가된 TiAi 금속간화합물의 고온 산화거동을 대기중의 900~$1100^{\circ}C$에서 관찰하였다. 산화반응물은 XRD, SEM, WDX을 이용하여 분석하였다. 등온 산화에 있어서 Cr과 V이 각각 첨가된 시편은 무게증가가 많았으나, Si, Mo, Vb가 각각 첨가된 시편은 상대적으로 무게증가각 적었아. 그리고, Cr과 V이 각각 첨가된 시편의 산화속도는 TiAi의 그것보다 항상 크게 나타났으며, Si, Mo, Vb가 각각 첨가된 시편의 산화속도는 TiAi의 그것보다 향상되지 않고, Si, Mo또는 Nb 첨가는 내산화성을 향상시킨다. Si, Mo, Nb이 각각 첨가된 TiAI합금표면에 형성된 산화물은 보호막 역할을 함으로 산소와 합금원소의 확산을 감소시키는 역할을 하였다. 특히, Nb는 산화의 초기단계에서는 $AI_{2}O_{3}$를 형성하려는 경향이 강하기 때문에 연속적인 $AI_{2}O_{3}$층과 조밀한 $Tio_{2}+AI_{2}O_{3}$ 혼합층이 형성되었다. Nb가 첨가된 합금의 백금 marker 실험결과에 따르면, 산소가 주로 합금내부로 확산하여 합금표면에서 산화물을 형성하였다. $900^{\circ}C$에서의 열반복주기(thermal cyclic)산화실험 결과, 다른 합금원소와 비교해 볼 때 Cr또는 Nb첨가가 금속기지와 산화층간의 접착력을 향상시키는 것으로 나타났다.

• Bulletin of the Korean Chemical Society
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• 제6권2호
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• pp.115-118
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• 1985

The oxidation of hydrazobenzene by oxygen in methanol solution is catalysed by Co(3MeOsalen) which is a synthetic oxygen carrier. The products are trans-azobenzene and water. The rate of the reaction has been studied spectrophotometrically and the rate law established. A mechanism involving a ternary complex of catalyst, hydrazobenzene and oxygen has been proposed.

• 상하수도학회지
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• 제10권4호
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• pp.64-72
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• 1996

The effect of $O_3$, $O_3/pH$, and $O_3/H_2O_2$, $O_3/UV$, and $H_2O_2/UV$ advanced oxidation process(AOP) were investigated for the treatment of tetrachloroethylen(PCE) at various condition. The removal efficiency of 10, 20, and 30ppm PCE by ozonation were almost same, only about 60%. And pseudo first-order rate constants, ko for overall oxidation was about 0.097($min^{-1}$). In the $O_3/pH$ AOP experiment for the 20ppm PCE, the removal rate of PCE increased with the increase of pH. However, mineralization rate of PCE at pH 7 was higher than at pH 10. In the $O_3/H_2O_2$ AOP, the removal rate of PCE was the highest at peroxide-to-ozone dosage ratio of about 0.9, which PCE was removed over 99.95%. Despite 42% of PCE was directly photolyzed by the UV irradiation, the removal efficiency of PCE by $O_3/UV$ AOP was only about 70%. In $H_2O_2/UV$ AOP, the removal efficiency of PCE increased to about 98% in proportion to the $H_2O_2$ injection concentration at constant UV intensity of 5W/l.

• Corrosion Science and Technology
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• 제10권6호
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• pp.189-193
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• 2011

In the current paper, we are reporting the results from an investigation of the surface and sub-surface oxidation of a TRIP steel containing 2 wt.% Mn and 0.5 wt.% Al with and without 0.03 wt.% Sb. The oxidizing conditions in the gas were successively varied in terms of the linear gas flow-rate and dew-point, from conditions were gas-phase mass transport limited conditions prevailed, to those were solid state processes became the rate determining conditions. It was found, that at sufficient low oxidizing conditions (defined as flow-rate/dew-point), the metal surfaces were clear of any external oxides, and as the oxidizing conditions were increased, Mn- and Si- oxide nodules formed along with magnetite. As the oxidizing conditions were increased further, a dense magnetite layer was present. The limits of the various regions were experimentally quantified and a proposed hypothesis for their occurrences is presented. No obvious effect of Sb was noted in this micro-structural research of the oxides that results from the various conditions investigated in this study.

• 한국식품과학회지
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• 제40권6호
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• pp.611-620
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• 2008

달걀 노른자에 함유된 인지질 중 PC와 PE를 추출, 분리하고 이를 토코페롤을 제거한 TSCO에 0, 200, 500, 2,000 ppm의 농도로 단독으로, 또는 1,000 ppm씩 혼합하여 첨가한 후 $180^{\circ}C$에서 12시간 동안 가열하여 함유된 인지질의 함량변화와 TSCO의 갈색화 정도를 살펴보고, TSCO의 가열산화에 미치는 영향을 지방산 조성, 공액이중산값, 아니시딘값으로 평가하였다. TSCO에 첨가된 인지질은 가열 시작 후 2-3시간 내에 매우 빠르게 소실되었고, 가열 중 PE의 분해속도가 PC에 비해 높았다. PC와 PE가함께 첨가된 TSCO를 가열할때 PE는 PC의 분해를 억제하였다. TSCO는 가열 시간이 증가함에 따라 갈색화가 증가하였고, PC와 PE는 갈색화를 촉진하였으며 PE가 PC보다 큰 영향을 주었다. 가열 중 TSCO의 P/L, P/Ln, 공액이중산값, 아니시딘값은 증가하였으며, PC의 첨가는 이들 값을 낮추어 가열 카놀라유의 산화방지제 역할을 하였으나 PE는 큰 영향을 나타내지 않았으며, PC와 PE는 TSCO의 가열산화 억제에 있어서 antagonism이 관찰되었다.