• KSBB Journal
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• 제16권6호
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• pp.573-578
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• 2001

직경 0.613mm 활성탄 입자를 생물입자 담체로 사용한 공기리프트 생물막 반응기를 폐수 질화에 적용하여 생물막을 형성시켰다. 공기유속과 암모니움 부하속도(유입수 유량)를 순차적으로 증가시키어 반응기 운전 약 130일 만에 140um 두께의 생물막을 형성시켰다. 온도 3$0^{\circ}C$ 및 상승관 공기유속 6.3cm/s에서 5.0 kg N/㎥.d의 암모니움 산화속도를 얻었다. 생물막 형성 초기에는 암모니움 산화 균주가 주로 형성되어 아질산 축적이 발생하였으며 아질산 완전 산화되었다. 유기물 부하율을 증가시킴에 따라 COD 제거속도는 증가하여 26.6 kg COD/㎥.d의 부하율에서 25.0 kg COD/㎥.d의 제거속도를 보여 94%의 제거효율을 보였다. 반면에 COD 제거속도가 증가함에 따라 암모니움 및 아질산 산화속도는 감소하였다. 특히 약 11 kg/㎥.d 이상의 COD 제거속도에서 많은 종속영양균주 과잉 슬러지가 반응기 액상에서 관찰되었으며 암모니움 및 아질산 산화속도는 COD 제거속도가 증가함에 따라 급격히 감소하였다. 용존산소가 물질확산 저항을 적게 받는 반응기 액상 부유 유기물 산화 균체에 의해 우선적으로 이용되어 반응기 액상 농도가 낮은 값을 보여서 물질확산 저항이 크게 작용하는 생물막에 주로 존재하는 질화균체에 의해 적게 사용된 것으로 생각된다. 이러한 결과는 종속영양균주의 반응기 액상 부유 생장이 생물입자 생물막에서의 독립영양균주 생장에 의한 질화에 유리하다는 제안과 일치하지 않는다. 용존산소 농도를 증가시킴에 따라 순수질화에서 암모니움 및 아질산 산화속도는 증가하였으며, 순산소를 사용할 경우 공기를 사용한 경우에 비하여 약 5배의 높은 암모니움 산화속도를 보였다.

• 한국대기환경학회지
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• 제24권5호
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• pp.512-522
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• 2008

Ammonia is a major compound of odor in livestock house. To enhance the performance of ammonia oxidation (decomposition). the gas-liquid, two phase photocatalytic oxidation system was designed and prepared in this study. Commercial P-25 as $TiO_2$ catalyst was used for ammonia decomposition. V/P-25 catalyst prepared by sol gel method was also used for the removal of by-producted $NO_x$ in $NH_3$ oxidation reaction. When $TiO_2$ was used as a photocatalyst, the conversion to $N_2$ in ammonia decomposition reached above 90% until 200hr (The air flow rate of 4L/min with the ammonia concentration up to 25ppm.). However, considerable amounts of NO and $NO_2$ were formed as a result of $NH_3$ oxidation (as a by-product). Therefore, we added Vanadia impregnated $TiO_2$(P-25) catalyst for the removal of $NO_x$ at the end of reaction trail. The results of a pilot-scale operation were successful to achieve the simultaneous removal of $NH_3\;and\;NO_x$ about 81 and 87%, respectively.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2011년도 제41회 하계 정기 학술대회 초록집
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• pp.212-212
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• 2011

In addition to the catalysts' activity and selectivity, the deactivation of catalysts during use is of practical importance. It is crucial to understand the phenomena of the deactivation to predict the loss of activity during catalyst usage so that the high operational costs associated with catalyst replacement can be reduced. In this study, the activity of Ru catalysts, such as nanoparticles (3~6 nm) and polycrystalline thin film (50 nm), have been investigated under CO oxidation and oxidative/reductive reaction conditions at various temperatures with the ambient pressure X-Ray photoelectron spectroscopy (APXPS). With APXPS, the surface oxides on the catalyst are measured and monitored in-situ. It was found that the Ru film exhibited faster oxidation-and-reduction compared to that of nanoparticles showing mild oxidative-and-reductive characteristics. Additionally, the larger Ru nanoparticles showed a higher degree of oxide formation at all temperatures, suggesting a higher stability of the oxide. These observations are in agreement with the catalytic activity of Ru catalysts. The loss of activity of Ru films is correlated with bulk oxide formation, which is inactive in CO oxidation. The Ru nanoparticle, however, does not exhibit deactivation under similar conditions, suggesting that its surface is covered with a highly active ultrathin surface oxide. Since the active oxide is more stable as nanoparticles than as a film, the nanoparticles showed mild oxidative/reductive behavior, as confirmed by APXPS results. We believe these simultaneous observations of both the surface oxide of Ru catalysts and the reactivity in real time enable us to pinpoint the deactivation phenomena more precisely and help in designing more efficient and stable catalytic systems.

• 한국환경보건학회지
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• 제30권5호
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• pp.358-365
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• 2004

The photocatalytic oxidation of Rhodamine B(RhB) was studied using photocatalytic reactor filled with module of quartz tube. Module of quartz tube consisted of small quartz tube (inner diameter, 1.5 mm; outer diameter, 3 mm) bundle coated with powder $TiO_2$ and uncoated large quartz tube (inner diameter, 20 mm; outer diameter, 22 mm). Two 30 W germicidal lamp was used as the light source and the reactor volume was 0.5 l. The effects of parameters such as the coating materials and numbers, initial concentration, $H_{2}O_2$ dose and metal deposition (Ag, Pt and Fe) and simultaneous application of $H_{2}O_2$ and metal deposition. The results showed that the initial reaction constant of quartz module coated with powder $TiO_2$ was higher 1.4 time than that of the $TiO_2$ sol and optimum coating number is twice. In order to increase reaction rate, simultaneous application of photocatalytic and photo-fenton reaction using Fe coating and dose $H_{2}O_2$ dose increased reaction rate largely.

• 환경위생공학
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• 제14권4호
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• pp.21-28
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• 1999

This study was carried out the simultaneous removal or organics and Cr(VI) in aqueous suspensions of phtocatalyst under circular type reactor and UV light illumination. In this experiment, comparison on the removal of Cr(VI) by photoreduction using UV light, photocatalyst adsorption using TiO2, ZnO, and FeCl3 as photocatalyst, and phtocatalysis using UV light with photocatalysts as well as the effect of experimental parameters such as phtocatalyst dosage, a kinds of organics and their concentration was examined. The major results of this study were as follows; 1. It was found that photocatalyst adsorption and phtocatalysis were applicable to the removal of Cr(VI), and Cr(VI) was more effectively eliminated by TiO2 than ZnO, and FeCl3. 2. phtocatalytic removal efficiency of Cr (VI) increased with increasing phtocatalyst dosage. However, over 1.0g/l of phtocatalyst dosage, the efficiency reached a plateau. 3. phtocatalytic removal of Cr(VI) was enhanced by addition of organics such as salicylic acid, mandelic acid, EDTA, and citric acid, and phtocatalytic oxidation of organics were also observed. 4. It was found that the simultaneous removal of organics and Cr(VI) using phtocatalysis was possible.

• 한국응용과학기술학회지
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• 제31권1호
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• pp.159-166
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• 2014

In recent years, researchers have put a considerable effort to decrease the emission of harmful gaseous pollutants to the atmosphere. In order to remove simultaneously $SO_2$ and $NO_X$ from the flue gas of small and medium-sized ship, we designed minimal wet scrubber inside a compact multistage modular system. In this study we proceed experiment of elemental technology at each stage of the scrubber. The each stage is oxidation of NO which is the main component of $NO_X$, and removal of $SO_2$, respectively. $NaClO_2$ was used to oxidize NO gas, and NaOH was used to remove $SO_2$ gas. The maximum NO conversion efficiency and the $SO_2$ removal efficiency are both indicate 100%.

• 자원리싸이클링
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• 제21권4호
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• pp.53-59
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• 2012

본 연구에서는 비철제련의 공정 부산물에서 얻어진 Bi-Pb-Sb 3원계 합금 용탕의 산화반응에 따른 Sb과 Pb의 제거거동에 대하여 조사하였다. $N_2+O_2$ 가스를 침지 노즐을 통해 1173 K의 합금 용탕 중에 취입하여 Sb을 산화물과 금속상의 혼합물로 분리 회수할 수 있었다. 그리고 923 K의 Bi-Pb 2원계 용탕에 $N_2+O_2$ 가스를 취입하면 Pb가 산화되어 슬래그상으로 제거될 수 있으나, Bi도 동시에 산화되어 Bi를 정제할 수 없었다.

• Journal of Electrochemical Science and Technology
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• 제9권2호
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• pp.109-117
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• 2018

A novel carbon paste electrode modified with $Cu-TiO_2$ nanocomposite, 2-(ferrocenylethynyl)fluoren-9-one (2FF) and ionic liquid (IL) (2FF/$Cu-TiO_2$/IL/CPE) was fabricated and employed to study the electrocatalytic oxidation of droxidopa, using cyclic voltammetry (CV), chronoamperometry (CHA) and differential pulse voltammetry (DPV) as diagnostic techniques. It has been found that the oxidation of droxidopa at the surface of modified electrode occurs at a potential of about 295 mV less positive than that of an unmodified CPE. DPV exhibits a linear dynamic range from $5.0{\times}10^{-8}$ to $4.0{\times}10^{-4}M$ and a detection limit of 30.0 nM for droxidopa. Finally this modified electrode was used for simultaneous determination of droxidopa and tryptophan. Also the 2FF/$Cu-TiO_2$/IL/CPE shows excellent ability to determination of droxidopa and tryptophan in real samples.

• Corrosion Science and Technology
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• 제7권3호
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• pp.182-186
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• 2008

The microstructures of the oxide scale developed at high temperature on steels are very complex and their development depends on many factors including time, temperature, oxidation conditions and alloying elements. The classical model of an oxide scale on steel consisting of wüstite, magnetite and haematite layers, is more complicated in reality and its properties change with the factors that affect their development. An understanding of the oxide scale formation and its properties can only be achieved by careful examination of the scale microstructure. The oxide scale microstructure may be difficult to characterise by conventional techniques such as optical or standard scanning electron microscopy. An unambiguous characterisation of the scale and the correct identification of the phases within the scale are difficult unless the crystallographic structure for each phase in the scale is considered and a simultaneous microstructure-microtexture analysis is carried out. In the current study Electron Backscatter Diffraction (EBSD) has been used to investigate the microstructure of iron oxide layers grown on low carbon steels at different times and temperatures. EBSD has proved to be a powerful technique for identifying the individual phases in the oxide scale accurately. The results show that different grain shapes and sizes develop for each phase in the scale depending on time and temperature.

• Elastomers and Composites
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• 제22권2호
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• pp.109-120
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• 1987

In this study, as one of the developing ways of the functional elastomer, improvement of the functionality of CB-BR was attemped through stabilization. At first the stabilization effect of CB-BR and the concentration dependancy in CB-BR were determined. Then, triazine thiol derivative(BPTT) was synthesized by reacting p-aminodiphenylamine with cyanuric chloride. Further the functional mechanism and the effects of the antioxidants were investigated using BPTT together with other various antioxidants in liquid and solid states. The results obtained are as follows: 1) The aging of CB-BR depended on the concentration and temperature. Thus, at a low temperature of $50^{\circ}C$, the aging proceeded with gel formation; at high temperature above $100^{\circ}C$ and in above 4wt% concentration, the aging occured by the formation of gel. And in concentrations below that, the aging proceeds with a decomposition caused by oxygen attacked to elastomer molecules. 2) The effect of antioxidation of CB-BR in the liquid state was at it's best when the MBIZ and BPTT were used at $110^{\circ}C$, 4hrs after the oxidation. 3) The effect of antioxidation of CB-BR in the solid state was the best choice the simultaneous use of NDBC and BPTT at $50^{\circ}C$, 30days after the oxidation.