• Applied Chemistry for Engineering
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• v.2 no.3
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• pp.262-269
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• 1991

Bleaching effect of ozone on unsaturated coloring material was compared quantitatively with the change of composition of reactants through the ozone oxidation of ${\beta}$-carotene. Beeswax colorized by carotenoids was reacted with ozone in water, 0.5 % and 1.0 % sodium hydroxide solution, and 20 % and 95 % acetic acid solution and bleaching effect of each reaction condition was compared with each other. And then the additive effect of hydrogen peroxide was investigated. Decrease of unsaturated double bond of ${\beta}$-carotene was proportioned quantitatively to the bleaching effect of ozone on ${\beta}$-carotene and was in accordance with the bleaching effect on beeswax. The bleaching effect of ozone on coloring material in 1.0 % sodium hydroxide solution was better than any other condition and the absorbance of beeswax at 390 nm was improved to 0.045 with the addition of hydrogen peroxide(2 % of wax). For the bleaching of beeswax, it was concluded that the ozone oxidation was more effective than physical adsorption.

• JOURNAL OF ELECTRICAL WORLD
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• s.271
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• pp.63-68
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• 1999

오존(Ozone) 이용의 역사는 19세기의 음료수 살균으로 거슬러 올라간다. 그후 선택적 화학반응을 이용한 화학합성, 1970년대의 공해대책시대의 배수(排水)탈색(脫色)$\cdot$탈취(脫臭), 수질 유지로 진전되어 왔다. 최근에는 특히 여러 가지 제품의 제조프로세스 등에서 환경부하가 적고 생산성이 좋은 프로세스가 요청되고 있어, 그러한 관점에서도 분해 후 무해한 산소로 되돌아가는 산화제인 오존의 활용이 기대를 모으고 있다. 기술면에서는 오존 단독처리에 더하여 과산화수소나 자외선과의 병용에 의한 촉진산화처리, 생물처리와의 병용처리 등 반응속도의 향상, 비처리물질의 확대를 겨냥한 새로운 반응기술, 대용량$\cdot$고농도 오조나이저(Ozonizer), 클린 오조나이저 등, 적용분야의 확대를 가능케 하는 오존발생기술, 하드웨어 기술의 진보가 현저하다. 최근에는 이 최신기술과 다른 기술과의 복합에 의한 새로운 제안도 많이 나오고 있으며, 수처리를 중심으로 신(新)프로세스에 더하여, 예를 들면 펄프 표백(漂白) 프로세스와 반도체 제조프로세스 등에의 적용이 급속하게 확대되는 경향이 있어, 바야흐로 새로운 분야를 개척하게 됨으로써 고객의 요구가 다시 신기술을 일으키는 쪽으로 돌아가고 있다고 할 수 있다.

• Proceedings of the Korean Radioactive Waste Society Conference
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• 2008.11a
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• pp.293-294
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• 2008

• Journal of Korean Society of Environmental Engineers
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• v.35 no.2
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• pp.144-150
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• 2013

Hybrid ceramic membrane (HCM) processes that combined ozonation with a ceramic membrane (CM) or a reactive ceramic membrane (RM), an iron oxide nanoparticles (IONs) incorporated-CM were investigated for membrane fouling control. Alumina disc type microfiltration and ultrafiltration membranes doped with IONs by sintering method were tested under varying mass fraction of IONs. Scanning electron microscope (SEM) images showed that IONs were well-doped on the CM surface and doped IONs were approximately 50 nm in size. Change in the pure water permeability of RM was negligible compared to that of CM. These results indicate that IONs incorporation onto CM had little effect on CM performance in terms of the flux. Natural organic matter (NOM) fouling and fouling recovery patterns during HCM processes confirmed that the RM-ozonation process enhanced the destruction of NOM and reduced the extent of fouling more than the CM-ozonation process by hydroxyl radical formation in the presence of IONs on RM. In addition, analyses of NOM in the feed water and the permeate showed that the efficiency of membrane fouling control results from the NOM degradation during HCM processes; leading to removal and transformation of relatively high contents of aromatic, high molecular weight and hydrophobic NOM fractions.

• Korean Chemical Engineering Research
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• v.56 no.5
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• pp.752-760
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• 2018

The lowering of temperature for combustion of diesel particulate matters (or diesel soot) is one of the important tasks in automotive industry that is searching for a way to meet up "high-fuel efficiency, low-emission" standard. In this study, it was discussed how the use of ozone over platinum-based catalyst promotes a low-temperature soot oxidation occurred at $150^{\circ}C$. The use of platinum catalyst did not increase oxidation rate largely but was very effective in improving the selectivity of carbon dioxide. The pre-oxidation of NO into $NO_2$ using ozone was rather crucial in improving the oxidation rate of soot at $150^{\circ}C$.

• Applied Chemistry for Engineering
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• v.5 no.4
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• pp.646-656
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• 1994

The ${\omega}$-formyl carboxylic acid was produced by ozone oxidation of cycloolefins in the presence of pyridine and its production yield was examined by varying temperature and solvent. As the reaction temperature increased, the yield of ${\alpha}$, ${\omega}$-dicarboxylic acid increased whereas that of ${\alpha}$, ${\omega}$-dialdehyde decreased. As the polarity of solvent increased, a higher yield of desired ${\omega}$-formyl carboxylic acid was obtained, whereas the yield of unwanted polymeric ozonide decreased. The yields of ${\omega}$-formyl carboxylic acid from ozone oxidation of cyclohexene, cyclooctene and cyclododecene at $0^{\circ}C$ and in methylene chloride solvent were 59.30%, 55.20%, and 36.72%, respectively.

• Proceedings of the Korea Air Pollution Research Association Conference
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• 2003.05b
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• pp.139-140
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• 2003

광화학 스모그를 야기하는 오존은 질소산화물과 VOC에 의한 다단계 광화학반응에 의하여 생성된다. 1990년대 초부터 자동차 보급률이 높아지면서, 수도권 지역을 중심으로 고농도 오존 현상이 관찰되었으며 최근에는 지방 주요 도시로 확산되고 있다. 오존은 광화학반응에 의해서 생성되는 제2차 대기오염물질이면서도 반응성이 높아서 다른 화학종의 산화에 지대한 영향을 미치며 일단 생성된 후에도 쉽게 파괴될 수 있다는 점에서 황산화물과 질소산화물과 같은 제2차 대기오염물질과 구별된다. (중략)

• Journal of Korean Society of Environmental Engineers
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• v.32 no.8
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• pp.767-773
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• 2010

In recent years, there has been considerable concern over the release of methyl tert-butyl ether (MTBE), a gasoline additive, into the aquifers used as potable water sources. MTBE readily dissolves in water and has entered the environment via gasoline spills and leaking storage tanks. In this study air stripping and ozonation of MTBE in aqueous solution were performed in a laboratory scale batch reacter. The mass transfer rate (N) was evaluated and a values about $1.24{\times}10^{-6}\;mol{\cdot}sec^{-1}$ was found. In the ozonation of MTBE a 8.3% decrease of the COD and a 6.5% decrease of the TOC lead to BOD/COD = 0.03. The peudo first-order rate constants of the ozonation of MTBE was $3.75{\times}10^{-5}\;sec^{-1}$. The resulting Ea of 4.80 kcal；mol-1 was observed for molecular ozone reactions.

• Proceedings of the Korea Air Pollution Research Association Conference
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• 2002.04a
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• pp.111-112
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• 2002

대기 중에 존재하는 hydrogen peroxide($H_2O$$_2$)는 특별한 source를 통해 배출되기보다는 오존이 광분해 되어 수증기와 반응하여 생성된 hydroperoxy radical (HO$_2$)의 self-reaction이나, 대기 중으로 배출된 VOCs의 산화 과정과 같은 광화학적 기원으로 생성된다. 이렇게 생성된 $H_2O$는 오존(O$_3$), hydroxy radical(OH)과 함께 대기 중으로 배출되는 물질과 반응하여 그 농도를 감소시키는 산화제를 역할을 한다. (중략)

• Proceedings of the Korea Air Pollution Research Association Conference
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• 2002.04a
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• pp.291-292
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• 2002

일반적으로 오존(O$_3$)은 친전자성 및 친핵성반응 때문에 탄소-탄소 이중결합을 가진 분자들을 떼어놓을 수 있는 매우 강한 산화능력을 갖고 있는 것으로서 살균, 맛과 냄새의 조절, 색도 제거 등에 이용되어왔다. 그러나, 오존은 대기 중에 미반응상태로 잔류하는 경우에는 광화학 스모그를 발생시키는 주된 요인이 되고 있으며, 강력한 산화력을 지니고 있기 때문에 0.1-l ppm의 범위에서 인체에 노출되면 두통, 목 건조증, 점막손상과 같은 호흡기 질환 등의 원인이 될 뿐만 아니라 악취를 유발하여 불쾌감을 야기한다. (중략)