• Title/Summary/Keyword: 산화 분해

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Degradation of Phenol by "TiO2 Ceramic Membrane+UV+H2O2" AOP ("TiO2 촉매막+UV+H2O2" 고도산화법(AOP)을 이용한 페놀 분해)

  • Choung, Youn Kyoo;Kim, Jin Wook
    • KSCE Journal of Civil and Environmental Engineering Research
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    • v.14 no.3
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    • pp.645-654
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    • 1994
  • Photocatalytic oxidation conditions of reactant recirculation flow rate 275 mL/min, aeration rate 2 LPM and $UV+TiO_2+H_2O_2$(500 mg/L) proved to be appropriate for water including organic materials treatment. With increasing turbidity and suspended solids concentration, at turbidity 10 NTU-suspended solids concentration 29 mg/L the phenol degradation efficiency increased, which in turn decreased at turbidity 50 NTU-suspended solids concentration 170 mg/L, however no significant differences were observed, demonstrating similar results with those obtained at zero turbidity and suspended solids concentration. The degradation efficiency of phenol decreased with increasing influent phenol concentrations. The $UV+TiO_2+H_2O_2$ photocatalytic advanced oxidation process conducted is considered to be possibly applied to the drinking water treatment, and the post-treatment process of biological wastewater treatment.

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Inhibition of Over-oxidation of 11$\beta$-l7$\alpha$, 21-trihydroxy-pregna-1, 4-diene-3, 2-dione in Fermentative Process. (Prednisolone 발효중의 산화분해 저지법)

  • Bae, Moo
    • Microbiology and Biotechnology Letters
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    • v.2 no.3
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    • pp.127-131
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    • 1974
  • Inhibition of over-oxidation of prednisolone in the fermentation has been studied by using vegetative cells as enzyme source. firstly, A. simplex (ATCC 6946) was demonst.ated to degrade p.ednisolone in the vegetative culture of the microorganism. Over 72% of hydrocortisone was transformed into prednisoloneby 3 hours of the fermentation. However, the prednisolone produced was considerably oxidized forming over-oxidation product in 8hours of fermentation period with the intact cells. Secondly, in order to depress the over-oxidation and the breakdown of the steroid skeleton of prednisolone, chelating agents such as $\alpha$$\alpha$'-dipyridyl, o-phenanthroline and 8-hydroxyruinoline were added to the fermentation broth. Conseauently, the breakdown of prednisolone by the iutact cells was able to be remarkably retatded and an intermediate regarded as an oxidized product derived from prednisolone was accumulated, by the addition of $\alpha$$\alpha$'-dipytidyl in the fermentation.

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나노$TiO_2$계 화합물과 응용

  • Hwang, Yong-Gil;Gil, Sang-Cheol
    • Proceedings of the Materials Research Society of Korea Conference
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    • 2009.05a
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    • pp.57.1-57.1
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    • 2009
  • 나노이산화티타늄은 인체에는 화장품, 의약, 식품분야 등에 쓰이고 외부 환경 재료에는 광촉매로서 유독가스 정화제, 옥내 외 항균, 수소발생 가시광 응답형 촉매 및 멤브레인 필터 등과 전자소재용 유전재료, 발광 재료 등 용도가 다양하다. 나노 산화티타늄 화합물의 제조법은 수열합성법, 기상법 등 여러 방법이 있다. 이들에 대한 리뷰의 목적은 2009년도 정부의 투자 계획 중에서 본제목에 관련되는 핵심 산업 재원 원천기술 개발, 태양광, 풍력 등의 신재생 에너지 개발, 록색 기술 개발을 통한 에너지절약형 LED 개발, 차세대 핵심환경 기술 개발, 핵심나노기반기술개발 등의 개발을 위하여 4,363억 원의 예산을 편성하고 연구자와 기술자들이 참여하여 유익한 실적이 창출되기를 원하고 있으므로 본 발표자들은 이 분야에서 연구하는 연구자와 기술자들에게 이 분야에 관련되는 자료를 참고로 제시하는데 있다. 페로브스카이트형 산화물인 유전재료($BaTiO_3$), 발광재료(CaTiO3:Pr3+적색), 박막형 반응기재료($Ca0.8Sr0.2TiO_3$), 등의 여러 가지 산화물은 류통식 급속 승온 수열 합성법, 겔 졸 법, 수열 합성법 등 여러 방법에 의하여 페로브스카이트형 산화물 입자 직경이 약 20nm~100nm 범위까지 합성된다. 태양광을 조사하여 물을분해 해서 수소를 생산하는 산화티타늄계 가시광 응답형 Vis-$TiO_2$ 박막은 기상법으로 제조하는데 한 예로써 RF 스퍼터링법으로 박막을 제조하여 수소와 산소를 회수하였으며, 황도프산화티타늄, 질소 도프 산화티타늄은 유기물 분해에 의한 공해제거, $NO_x$ 제거 등 환경정화에 사용되고, 고온 고압수법/산화티타늄 복합기술에 의해서는 바이오매스 분해 하고, 일종의 수열법인 개량형 HyCOM 법은 가시광 응답성 산화티타늄을 합성하여 NO가스 제거에 사용한다. 이들 여러 방법에 관한 것을 소개하고저 한다.

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Production of Dry Oxidant through Catalytic H2O2 Decomposition over Mn-based Catalysts for NO Oxidation (NO 산화를 위한 Mn계 촉매상 과산화수소 분해를 이용한 건식산화제 생성)

  • Jang, Jung Hee;Choi, Hee Young;Han, Gi Bo
    • Clean Technology
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    • v.21 no.2
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    • pp.130-139
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    • 2015
  • The NO oxidation process has been applied to improve a removal efficiency of NO included in exhaust gas. In this study, to produce a dry oxidant for the NO oxidation process, the catalytic H2O2 decomposition method was proposed. A variety of the heterogeneous solid-acidic Mn-based catalysts were prepared for the catalytic H2O2 decomposition and the effect of their physico-chemical properties on the catalytic H2O2 decomposition were investigated. The results of this study showed that the acidic sites of the Mn-based catalysts has an influence on the catalytic H2O2 decomposition. The Mn-based catalyst having the abundant acidic sites within the wide temperature range in NH3-TPD shows the best performance for the catalytic H2O2 decomposition. Therefore, the NO oxidation efficiency, using the dry oxidant produced by the H2O2 decomposition over the Mn-based catalyst having the abundant acidic properties under the wide temperature range, was higher than the others. As a remarkable result, the best performances in the catalytic H2O2 decomposition and NO oxidation was shown when the Mn-based Fe2O3 support catalyst containing K component was used for the catalytic H2O2 decomposition.

Optimal Condition for Decomposition of Ethylenediaminetetraacetic Acid (EDTA) in Supercritical Water Oxidation (초임계수 산화공정에서 Ethylenediaminetetraacetic Acid (EDTA) 분해 최적화 연구)

  • Lee, Hyeon-Cheol;In, Jung-Hyun;Kim, Jong-Hwa;Lee, Chang-Ha
    • Korean Chemical Engineering Research
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    • v.43 no.2
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    • pp.318-323
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    • 2005
  • Supercritical water oxidation (SCWO, P>221 bar, T>$374^{\circ}C$) is a promising method for the decomposition of refractory organic compounds. In this study, the SCWO of Ethylenediaminetetraacetic acid (EDTA) was carried out in a tubular-type continusous reactor system with an $H_2O_2$ oxidant at $387-500^{\circ}C$, 250 bar and residence time (RT) of 15.9-88.9 s. The decomposition efficiencies increased with increasing temperature and oxidant amount, while it was inversely proportional to feed flow rate. The decomposition efficiency of 99.6% was obtained at $500^{\circ}C$, 250 bar, oxidant amount of 400% and residence time of 40.1 s. The effect of temperature on the decomposition efficiency was more significant than that of oxidant amount. In the case of the decomposition efficiency of 5,000 mg/L of EDTA (3,063 mg/L as $COD_{Cr}$), the decompostion of 99% or higher was obtained at the condition of over 40.1 s (RT) and 200 stoichiometric % of $H_2O_2$ in the supercritical water of $500^{\circ}C$ and 250 bar.

Degradation of Quercus serrata by Lentinus edodes (Berk) Singer (골목성분(?木成分)의 분해(分解))

  • Yoon, Byung-Ho
    • Journal of the Korean Wood Science and Technology
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    • v.6 no.1
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    • pp.3-7
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    • 1978
  • Quercus serrata degraded by Leminus edodes(berk) Singer was investigated. In order to evaluate on affect of the fungi on the sound logs, and the logs attacted for 2 years and five years were used as a sample tree. Large portions of carbohydrate mainly was decomposed by the fungy. It is supported by the increasing of alkaline extractives and the breaking up of crystallinity. Lignin is transformed considerably as shown the results of the determination of Klason lignin, gel filtration and nitrobezene oxidation. On the other hand, the decreasing of methoxyl group and the increasing of carboxyl group in parallel with demethlation and acidification are presented. Syringyl nuclei unit is decomposed easier than guaiacyl unit. It is also illustrated that the more decreasing of carboxyl group compared with aldehyde group was acidified biodegradation.

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산화아연-다층 그래핀 양자점을 이용한 전기화학셀

  • Sim, Jae-Ho;Lee, Gyu-Seung;Go, Yo-Han;Yang, Hui-Yeon;Son, Dong-Ik
    • Proceedings of the Korean Vacuum Society Conference
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    • 2016.02a
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    • pp.321-321
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    • 2016
  • 한경오염의 증가에 따라 광촉매 물질을 이용한 환경 정화의 필요성이 대두되고 있다 [1]. 광촉매와 전기화학셀은 빛을 이용하여 다른 에너지를 생산하는 능력을 가지고 있다. 이 전기화학셀의 성능향상을 위해서는 적절한 밴드갭을 이용한 광흡수의 증가, 전자재결합의 감소, 전기화학적 반응 표면의 증가가 필요하다. 산화 아연은 잘 알려진 n형 산화물 반도체로서 좋은 전기적 특성과 광촉매 성능으로 전기화학셀에 적합한 소재이다. 그러나 산화 아연은 액체 전해물질 상에서 안정성이 좋지 못하다 [2]. 이를 해결하기 위해 단층 그래핀 혹은 풀러렌(C60)을 이용하여 산화아연을 코팅하는 방법을 제안하였는데, 풀러렌을 사용 시 단층 그래핀에 비하여 전기화학셀의 전기화학적 반응은 높았으나 안정성은 더 떨어지는 모습을 보였다 [3]. 본 연구에서는 다층 그래핀을 이용하여 전기화학적 반응도 높고 안정성도 높은 산화아연-다층 그래핀 양자점의 합성 및 이를 이용한 전기화학셀 소자의 특성을 연구하였다. X선 회절법, 라만 분광법, 투과 전자 현미경, 광발광 분광기, 시간-분해성 광발광 분광기를 이용하여 산화아연-다층 그래핀 양자점의 특성을 분석하였고, 이를 이용하여 광양극을 제작하여 전기화학적 특성을 관측하였으며 로다민 B 염료를 이용한 분해 테스트를 통하여 광촉매 성능을 확인하였고 사이클 테스트를 통하여 안정성을 확인하였다.

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A study on production of dry oxidant by decomposition of H2O2 on K-Mn/Fe2O3 catalyst and NO oxidation process according to simulated flue gas flow (K-Mn/Fe2O3 촉매 상 H2O2 분해에 의한 건식산화제 생성 및 모사 배가스 유량에 따른 NO 산화공정)

  • Choi, Hee Young;Shin, Woo Jin;Jang, Jung Hee;Han, Gi Bo
    • Journal of the Korean Applied Science and Technology
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    • v.34 no.2
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    • pp.367-375
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    • 2017
  • In this study, NO oxidation process was studied to increase the NO treatment efficiency of pollutant present in exhaust gas. $H_2O_2$ catalytic cracking was introduced as a method of producing dry oxidizing agents with strong oxidizing power. The $K-Mn/Fe_2O_3$ heterogeneous catalysts applicable to the $H_2O_2$ decomposition process were prepared and their physico-chemical properties were investigated. The prepared dry oxidant was applied to the NO oxidation process to treat the simulated exhaust gas containing NO, NO conversion rates close to 100% were confirmed at various flow rates (5, 10, 20 L/min) of the simulated flue gas.

A Comparison between the Decomposition of Bisphenol A and the Concentration of Hydrogen Peroxide Formed during Ozone/Catalyst Oxidation Process (오존/촉매 산화공정에서 비스페놀 A의 분해와 생성된 과산화수소의 농도 비교)

  • Choi, Jae Won;Lee, Hak Sung
    • Applied Chemistry for Engineering
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    • v.28 no.6
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    • pp.619-625
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    • 2017
  • In this study, the formation of hydroxyl radical and decomposition characteristics of bisphenol A (BPA) was investigated by quantifying hydrogen peroxide formed as a reaction by-product during the formation stage of hydroperoxyl radical. The direct oxidation reaction by ozone only decomposed BPA just like the Criegee mechanism under the condition where radical chain reactions did not occur. Non-selective oxidation reactions occurred under the conditions of pH 6.5 and 9.5 where radical chain reactions do occur, confirming indirectly the formation of hydroxyl radical. The decomposition efficiency of BPA by the added catalysts appeared in the order of $O_3$/PAC ${\geq}$ $O_3/H_2O_2$ > $O_3$/high pH > $O_3$ alone. 0.03~0.08 mM of hydrogen peroxide were continuously measured during the oxidation reactions of ozone/catalyst processes. In the case of $O_3$/high pH process, BPA was completely decomposed in 50 min of the oxidation reaction, but reaction intermediates formed by oxidation reaction were not oxidized sufficiently with 29% of the removal ratio for total organic carbon (TOC, selective oxidation reaction). In the case of $O_3/H_2O_2$ and $O_3$/PAC processes, BPA was completely decomposed in 40 min of the oxidation reaction, and reaction intermediates formed by the oxidation reaction were oxidized with 57% and 66% of removal ratios for TOC, respectively (non-selective oxidation reactions).