• 한국대기환경학회지
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• 제16권5호
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• pp.529-537
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• 2000

Several Pt-based oxidation catalysts with different loading were prepared with various metal precursor solutions and characterized with H$_2$ chemisorption and TEM for Pt particle size. V was added to Pt-based catalyst for inhibiting SO$_2$oxidation reaction, as result, Pt-V/Ti-Si catalyst prepared by ERMS(Free Reduced Metal in Solution) method showed high enough activity and better inhibition on SO$_2$oxidation than Pt only catalyst. Optimum Pt particle size for diesel oxidation reaction turned out to be the size of around 20 nm. A prototype catalyst was prepared for light=duty diesel passenger car, and teated for the emission reduction performance with Korean regulation test mode(CVS-75 mode) on chassis dynamometer. The catalyst shows the performance reduction of 75~94% for CO, 53~67% for HC and 10~31% for PM. In the case of heavy-duty diesel catalyst, the domestic formal regulation teat mode D-13 was adopted for both Na engine and Turbo engine. The conversions of CO and THC are high enough(86% and 41%) while the reductions of NOx and PM are relatively low(3~11%).

• 공업화학
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• 제28권3호
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• pp.326-331
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• 2017

캐스터오일은 수소화반응을 통해 계면활성제의 중간체 등 유용한 화학산업의 원료로 활용 가능하다. 본 연구에서는 캐스터오일의 수소화용 니켈촉매의 제조조건과 전처리 조건에 대한 영향을 연구하였다. 니켈촉매는 침전제와 pH를 다르게 하여 실리카 담체상에 침전법으로 담지되었고, 다시 산화와 환원의 반복된 전처리를 행하였다. 니켈촉매의 활성은 캐스터오일의 요오드 가를 측정하여 비교하였고, 니켈촉매의 분산도는 XRD, BET, TEM을 통하여 분석하였다. 니켈촉매의 활성을 CO산화반응실험을 통하여도 비교하였다. 산화와 환원 사이클의 반복에 의해 니켈의 재분산이 실리카 상에서 발생하였고, 이것이 캐스터오일 수소화반응 활성을 증진시키는데 기여하였다.

• Environmental Engineering Research
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• 제13권4호
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• pp.210-215
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• 2008

The present study investigates the effect of oxidation-reduction potential (ORP) and organic compounds on specific anaerobic ammonium oxidation activity (SAA) using batch experiments. The batch tests were based on the measurement of nitrogen gas production. The relationship between ORP and dissolved oxygen (DO) concentration was found to be ORP (mV) = 160.38 + 68 log [$O_2$], where [$O_2$] is the DO concentration in mg/L. The linear relationship obtained between ORP and SAA ($R^2$ = 0.99) clearly demonstrated that ORP can be employed as an operational parameter in the Anammox process. At ORP value of -110 mV, the SAA was $0.272{\pm}0.03\;g\;N_2-N\;(g\;VSS)^{-1}\;d^{-1}$. The investigation also revealed inhibitory effect of glucose on the SAA while acetate concentration up to 640 mg COD/L (corresponding to 10 mM) had stimulating effect on the SAA. However, acetate concentration beyond 640 mg COD/L had inhibitory effect on the Anammox activity. The results indicated that nitrogen rich wastewaters containing low level organic matter could be better treated by Anammox microorganisms in real-world conditions after some acidification process.

• 한국재료학회지
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• 제14권3호
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• pp.163-167
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• 2004

TiAl(La)N thin films were oxidized in vacuum of about 7 Pa to reduce the oxidation of WC-Co as a substrate. The oxidation rate constants of the thin films were quantified by an assumption of parabolic oxidation. Increasing AI content significantly decreased the parabolic oxidation rate constant. A simultaneous addition of AI and La was more effective to reduce the oxidation rate. The parabolic oxidation rate constant of $Ti_{0.66}$ $Al_{0.32}$ $La_{ 0.02}$N thin film at 1273 K showed about ten times lower than that of TiN. The addition of a small amount of La with Al induced the preferential formation of dense $\alpha$ $-Al_2$$O_3$ film in oxide film, leading to the abrupt reduction of oxidation rate.

• 한국토양비료학회지
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• 제26권3호
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• pp.204-214
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• 1993

김해평야(金海平野)에 분포(分布)하는 특이산성토(特異酸性土)인 김해통(金海統)에 대하여 산화(酸化)와 환원조건(還元條件)에서 토양(土壤)의 pH 및 Eh와 수용성(水溶性)의 $SO_4$, Fe, K, Na 및 Ca 함량(含量) 변화(變化)에 따른 토양(土壤)중 pyrite-S와 jarosite-S 형태(形態)의 변화(變化)와 이들 광물(鑛物)의 생성과정(生成過程)을 항온시험(恒溫試驗)으로 연구(硏究)하였다. 항온시험(恒溫試驗)의 결과(結果) 환원조건(還元條件)에서 pH는 상승(上昇)되고 Eh는 하강(下降)하였다. 산화조건(酸化條件)으로 전환(轉換)시킬 때 심토(心土) 시료(試料)의 pH가 4 이하(以下)로 유지(唯持)되고 Eh는 400mV 이상(以上)으로 상승(上昇)되어 jarosite가 생성(生成)될 수 있는 조건(條件)을 충족(充足)시켰다. 수용성(水溶性) K함량(含量)은 환원(還元)에 의하여 증가(增加)하였고 산화(酸化)에 의하여 감소(減少)하였으며 산화조건(酸化條件)에서 Ca 함량(含量)을 높인 경우 jarosite의 분해(分解)로 인하여 급증(急增)하였다. 수용성(水溶性) Ca는 Ca 함량(含量)을 높인 경우 산화진전(酸化進展)에 따라 석고(石膏) 생성(生成)으로 인하여 격감(激減)한 것으로 생각된다. Jarosite는 환원진전(還元進展)에 따라 생성(生成)되었으나, Ca 함량(含量)을 높인 경우는 환원(還元) 및 산화상태(酸化狀態)에서 계속 분해(分解)되었다. 그러나 pyrite는 환원진전(還元進展)에 따라 생성(生成)되고 산화진전(酸化進展)에 따라 분해(分解)되었다.

• 자원리싸이클링
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• 제16권2호
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• pp.12-16
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• 2007

Chalcopyrite 를 대상으로 광미 중에 함유된 Sulfide 물질의 부유선별에 의한 분리회수 과정에서 산화가 부유성에 미치는 영향을 고찰하였다. Zisman Plot에 의해 도출된 Chalcopyrite 의 임계계면장력은 약 15.5 dyne/cm인 것으로 파악되었으며 포수제의 농도가 증가함에 따라 그 값은 감소하여 Chalcopyrite의 부유성이 상승하는 것으로 관찰되었다. 초기 산화에 의한 Chalcopyrite의 부유성 상승은 $S_2^{2-}$의 $S^o$로의 전환에 기인하는 것으로 판단되었으며 형성된 $S^o$가 $S_4^{2-}$ 및 $S_2O_3^{2-}$로 재전환됨에 따라 Chalcopyrite의 부유성은 다시 감소하는 것으로 사료되었다. 산화된 Chalcopyrite의 환원 시 부유성은 상승하는 것으로 나타났으며 산화/환원 과정에서의 임계계면장력의 변화 양상은 원자간 Bond Energy의 변화에 의거한 Energy Diagram으로 해석되었다.

• 한국수소및신에너지학회논문집
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• 제27권4호
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• pp.412-420
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• 2016

Effect of $H_2S$ on reactivity of oxygen carrier was measured and discussed using fluidized bed reactor and SDN70 oxygen carrier. We could get 100% of fuel conversion and $CO_2$ selectivity even though $H_2S$ containing simulated syngas was used as fuel for reduction. Absorbed sulfur was released during oxidation and $N_2$ purge step after oxidation as $SO_2$ form. We could get 100% of fuel conversion and $CO_2$ selectivity during cyclic reduction-oxidation tests up to 10th cycle. However, only 6~7% of sulfur can be removed during oxidation and $N_2$ purge step and 93~94% of sulfur was accumulated in the oxygen carrier. Therefore we could conclude that total removal of sulfur was not possible. $SO_2$ emission during oxidation decreased as the number of cycle increased. Therefore we could expect that the reactivity of oxygen carrier will be decreased with time.

• Corrosion Science and Technology
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• 제16권1호
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• pp.15-22
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• 2017

An oxidation-reduction scheme is an alternative approach for improving the galvanizability of advanced high-strength steel in the continuous hot-dip galvanizing process. Here, we investigated the effect of oxygen partial pressure ($P_{O_2}$) on the oxidation behavior of a transformation-induced plasticity steel containing 1.5 wt% Si and 1.6 wt% Mn during heating to and holding for 60 s at $700^{\circ}C$ under atmospheres with various $P_{O_2}$ values. Irrespective of $P_{O_2}$, a thin amorphous Si-rich layer of Si-Mn-O was formed underneath the Fe oxide scale (a $Fe_2O_3/Fe_3O_4$ bilayer) in the heating stage. In contrast to Si, Mn tended to segregate at the scale surface as $(Fe,Mn)_2O_3$. The multilayered structure of $(Fe,Mn)_2O_3/Fe_2O_3/Fe_3O_4$/amorphous Si-Mn-O remained even after extended oxidizing at $700^{\circ}C$ for 60 s. $Fe_2O_3$ was the dominantly growing oxide phase in the scale. The enhanced growth rate of $Fe_2O_3$ with increasing $P_{O_2}$ resulted in the formation of more Kirkendall voids in the amorphous Si-rich layer and a less Mn segregation at the scale surface. The mechanisms underlying the absence of FeO and the formation of Kirkendall voids are discussed.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2015년도 제49회 하계 정기학술대회 초록집
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• pp.222.1-222.1
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• 2015

Recently, graphene quantum dots (GQDs) have attracted great attention due to various properties including cost-effectiveness of synthesis, low toxicity, and high photostability. Nevertheless, the origins of photoluminescence (PL) from GQDs are unclear because of extrinsic states of the impurities, disorder structures, and oxygen-functional groups. Therefore, to utilize GQDs in various applications, their optical properties generated from the extrinsic states should be understood. In this work, we have focused on the effect of oxygen-functional groups in PL of the GQDs. The GQDs with nanoscale and single layer are synthesized by employing graphite nanoparticles (GNPs) with 4 nm. The series of GQDs with different amount of oxygen-functional groups were prepared by the chain of chemical oxidation and reduction process. The fabrication of a series of graphene oxide QDs (GOQDs) with different amounts of oxygen-contents is first reported by a direct oxidation route of GNPs. In addition, for preparing a series of reduced GOQDs (rGOQDs), we employed the conventional chemical reduction to GOQDs solution and controlled the amount of reduction agents. The GOQDs and rGOQDs showed irreversible PL properties even though both routes have similar amount of oxyen-functional groups. In the case of a series of GOQDs, the PL spectrum was clearly redshifted into blue and green-yellowish color. On the other hand, the PL spectrum of rGOQDs did not change significantly. By various optical measurement such as the PL excitation, UV-vis absorbance, and time-resolved PL, we could verify that their PL mechanisms of GOQDs and rGOQDs are closely associated with different atomic structures formed by chemical oxidation and reduction. Our study provides an important insights for understanding the optical properties of GQDs affected by oxygen-functional groups. [1]

• 한국재료학회:학술대회논문집
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• 한국재료학회 1992년도 춘계학술발표회
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• pp.57-58
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• 1992

The NH$_3$oxidation, which forms thermal oxide layer on silicon substrate with pure $O_2$gas added with small amounts of NH$_3$gas, has good interface sates due to activated gettering effect during oxidation. The superiority of interfae state in NH$_3$ oxidation method is not affected by preprocess but by gettering during oxidation. The dramatec reduction fo interface state is conformed with observing OSF when NH$_3$ oxide is annealed in NH$_3$ atmosphere.