• 공업화학
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• 제32권3호
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• pp.237-242
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• 2021

미세먼지와 함께 질소산화물, 황산화물, 휘발성 유기화합물, 암모니아 비롯한 유발물질에 대한 동시 저감기술은 엄격해지는 환경규제와 실질적인 저감효과 제고를 위해 꾸준히 주목받아 왔다. 오존산화에 의한 비수용성 질소산화물 고속산화 공정은 전통적으로 적용되고 있는 선택적 촉매환원 공정에 비해 공간절약형 시스템 적용을 가능하게 할 뿐만 아니라 운영비용 절감 측면에서 매우 효과적인 방법으로 평가되고 있으며 황산화물을 비롯한 산성가스와 동시 저감이 가능한 공정 구현이 가능하다는 장점까지 있다. 본 논문에서는 오존 고속산화 공정에 대한 기술 이슈 및 개발 동향을 소개하며 향후 산업적 이용 확대를 위한 개발 방향에 대해서 고찰하고자 한다.

• 한국물환경학회지
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• 제26권4호
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• pp.580-584
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• 2010

As water becomes more scarce around the world the reuse of treated wastewater is being recenlty considered as indispensible trend we need to follow. Especially, industrial area consuming large amount of water has been encouraged to reuse the treated wastewater to secure sufficient water for the production of merchandise. In this study, a study of advanced oxidation process for treatment of industrial wastewater. The treatment performance of UV and ozoznation and five types advanced oxidation processes such as UV/AC, UV/Catalyst, $O_3$/Catalyst, UV/$O_3$/Catalyst was experimentally investigated for reuse of industrial wastewater. The removal efficiency of $COD_{Cr}$, color were relatively evaluated in each treatment unit simulated outflow water of wastewater treatment area. UV/$O_3$/Catalyst process showed the highest $COD_{Cr}$ remaval and color remaval among proposed oxidation process.

• 한국환경보건학회지
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• 제31권5호
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• pp.404-410
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• 2005

The pH efforts on the removal of 1,4-dioxane and the biodegradobility enhancement of dioxane contaminated water were investigated using $O_3/H_2O_2$ baled advanced oxidation process. Experiments were conducted using a bubble column reactor under different initial pH. The $O_3/H_2O_2$ process effectively converted 1,4-dioxane to more biodegradable intermediates which had a maximum $BOD_5$ enhancement at pH 11 within the experimental range, precisely, when the initial pH increased, $BOD_5$ enhanced. However, in case of removal efficiencies of 1,4-dioxane during $O_3/H_2O_2$ oxidation the optimum condition was shown at pH 9 compared with pH 6 and 11. TOC and COD values were not largely changed for all reaction time. From the results of 1,4-dioxane removal efficiency, TOC, COD, and $BOD_5$ enhancement with reaction time, it was surely observed that 1,4-dioxane was just converted to biodegradable materials, not completely oxidized to carbon dioxide.

• 한국표면공학회지
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• 제45권4호
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• pp.155-161
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• 2012

Magnesium alloys of AZ31, AZ31 + (0.5, 1, 1.5)wt.% CaO were cast, hot rolled, and oxidized between 450 and $650^{\circ}C$ in atmospheric air. The added CaO enabled to cast the AZ31 alloy in air. It decomposed and precipitated along the grain boundaries of the AZ31 alloy as $Al_2Ca$. The more the amount of CaO was, the more $Al_2Ca$ formed. The oxidation limit was about $450^{\circ}C$ for the AZ31 alloy. But, It increased to $650^{\circ}C$ in the CaO-added alloys. Hot rolling destroyed the precipitates that formed along the grain boundaries of the AZ31 alloy. During oxidation, MgO oxide scales that incorporated CaO formed at the outer surface of the formed oxide layer.

• 상하수도학회지
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• 제34권6호
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• pp.445-462
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• 2020

Industrial wastewater often contains a number of recalcitrant organic contaminants. These contaminants are hardly degradable by biological wastewater treatment processes, which requires a more powerful treatment method based on chemical oxidation. Advanced oxidation technology (AOT) has been extensively studied for the treatment of nonbiodegradable organics in water and wastewater. Among different AOTs developed up to date, ozonation and the Fenton process are the representative technologies that widely used in the field. Based on the traditional ozonation and the Fenton process, several modified processes have been also developed to accelerate the production of reactive radicals. This article reviews the chemistry of ozonation and the Fenton process as well as the cases of application of these two AOTs to industrial wastewater treatment. In addition, research needs to improve the cost efficiency of ozonation and the Fenton process were discussed.

• Bulletin of the Korean Chemical Society
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• 제7권1호
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• pp.86-87
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• 1986

• Advances in environmental research
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• 제9권3호
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• pp.191-214
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• 2020

The rise in population and industrialization accounts for the generation of a huge amount of wastewaters. The treatment of this wastewater is obligatory to safeguard the environment and various life forms. Conventional methods for high strength wastewater treatment coming out to be ineffective. Advanced oxidation processes (AOPs) for such wastewater treatment proved to be very effective particularly for the removal of various refractory compounds present in the wastewater. Ozone based AOPs with its high oxidizing power and excellent disinfectant properties is considered to be an attractive choice for the elimination of a large spectrum of refractory compounds. Furthermore, it enhances the biodegradability of wastewaters after treatment which favors subsequent biological treatments. In this review, a detailed overview of the AOPs (like the Fenton process, photocatalysis, Electrochemical oxidation, wet air oxidation, and Supercritical water oxidation process) has been discussed explicitly focusing on ozone-based AOPs (like O₃, O₃/H₂O₂, O₃/UV, Ozone/Activated carbon process, Ozone/Ultrasound process, O₃/UV/H₂O₂ process). This review also comprises the involved mechanisms and applications of various ozone-based AOPs for effective municipal/industrial wastewaters and landfill leachate treatment. Process limitations and rough economical analysis were also introduced. The conclusive remarks with future research directions also underlined. It was found that ozonation in combination with other effective AOPs and biological methods enhances treatment efficacies. This review will serve as a reference document for the researchers working in the AOPs field particularly focusing on ozone-based AOPs for wastewater treatment and management systems.

• 대한환경공학회지
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• 제22권1호
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• pp.103-111
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• 2000

양어용수 재순환을 위한 생물여과상의 처리효율을 향상시키기 위하여 전처리로서 오존처리와 고급산화($H_2O_2/O_3$) 처리가 다양한 조건하에서 시도되었다. 오존처리시 암모니아는 일차속도반응식으로 제거되었으며, 중탄산염 알칼리도가 증가할수록 제거효율이 향상되어 200 mg/L as $CaCO_3$에서 약 46%가 제거되었다. 고급산화법($H_2O_2/O_3$)을 적용시 알칼리도를 포함한 폐수의 경우 중탄산염의 저해작용으로 암모니아 제거율이 저조하였으나 0.1 N KOH로 초기 pH를 약 8.2로 맞추어 실험한 결과 암모니아 제거율이 오존처리시보다 향상되었다. 특히, $H_2O_2/O_3=0.25$ 조건하에서 가장 높은 암모니아 제거율을 나타내었으며, pH가 9 이상일 때 반응시간 30분동안 약 90%의 암모니아가 제거되었다. 그러나 유기물과 암모니아가 공존시 오존처리와 고급산화처리 모두 유기물과 산화제와의 빠른 반응으로 인하여 암모니아 제거율이 크게 저하되었으며, 최적 $H_2O_2/O_3$ 비도 변하였다. 암모니아 제거와 마찬가지로 고급산화처리의 경우 입자성유기물의 빠른 분해로 인하여 초기 10분간 DOC(dissolved organic carbon)농도가 증가한 후 서서히 감소하였다. 초기 암모니아 농도를 2배 이상 증가시켜도 유기물 산화에 저해를 주지 못하였다.

• 한국표면공학회지
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• 제35권6호
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• pp.401-407
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• 2002

Most of organic compounds discharged from industrial wastewater are treated by chemical oxidation, adsorption and biodegradable process. This process has been demanded a new advanced environmental wastewater treatment process. From this point of view, an electrochemical oxidation process using electrocatalysts has been developed for the destruction of organic compounds. Through this study, a ruthenium oxide/iridium oxide supported on titanium expanded metal was fabricated by thermal decomposition method and its performance was excellent during this experiment.

• 한국표면공학회지
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• 제38권1호
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• pp.1-6
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• 2005

Ni-15at.% W coatings with film thicknesses of 20-40 ㎛ were electroplated on a steel substrate, and their oxidation behavior was investigated at 700 and 800℃ in air. For comparison, a pure Ni coating and a bulk Ni were also oxidized. The Ni-15at.%W coating displayed the worst oxidation resistance, due to the formation of less-protective NiO, Fe₂O₃, NiFe₂O₄ and NiWO₄. The corrosion behavior Ni-15at.%W coatings electroplated on a steel substrate was similarly investigated at 700 and 800℃ in the Ar-l%SO₂ atmosphere. For comparison, the uncoated steel substrate was also corrosion-tested in the Ar-l %SO₂ atmosphere. Severe scale spallation and the internal corrosion of the steel that occurred in the uncoated substrate were not observed in the coated specimen. However, it seemed that the Ni-15at.%W coating cannot be a potential candidate as a sulfidation-resistant coating, due to the formation of less-protective NiO, NiS, WO₃ and NiWO₄.