• Bulletin of the Korean Chemical Society
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• 제35권4호
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• pp.1191-1194
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• 2014

Imaging Differential Optical Absorption Spectroscopy (Imaging-DOAS) has been utilized in recent years to provide slant column density (SCD) distributions of several trace gas species in the plume. The present study introduces a new method using Imaging-DOAS data to determine two-dimensional plume structure from the plume emissions of power plant in conditions of negligible aerosol effects on radiative transfer within the plume. We demonstrates for the first time that two-dimensional distributions of sulfur dioxide ($SO_2$) and nitrogen dioxide ($NO_2$) in power plant emissions can be determined simultaneously in terms of SCD distribution. The $SO_2$ SCD values generally decreased with increasing distance from the stack and with distance from the center of the plume. Meanwhile, high $NO_2$ SCD was observed at locations several hundred meters away from the first stack due to the ratio change of NO to $NO_2$ in NOx concentration, attributed to the NO oxidation by $O_3$. The results of this study show the capability of the Imaging-DOAS technique as a tool to estimate plume dimensions in power plant emissions.

• 대한금속재료학회지
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• 제47권2호
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• pp.99-106
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• 2009

The high temperature corrosion properties of heat resistant steels were investigated in oxidation atmosphere including sulfur dioxide. The heat resistant steels of T22, T92, T122, T347HFG and T304H were evaluated at 620, $670^{\circ}C$ for 400 hours. The corrosion rates showed a decreasing tendency while chrome contents of those steels increased from 2 mass.% to 19 mass.%. The in crease in temperature increasement has an more effect on the corrosion rates of low chrome steels than high chrome steels. The weight gains of T22, T92, T304H at $670^{\circ}C$ were 3.7, 1.65, 1.23 times compared with those at $620^{\circ}C$. The external scale formed on T22 was composed of hematite, magnetite and Fe-Cr spinel and internal layer including iron oxide mixed with sulfide. The scales formed on T92, T122, T304H consisted of an outer layer of hematite and inner layer of chrome oxide and hematite. The proportion of chrome oxide at inner layer was increased when the chrome contents in heat resistant steels were increased.

• 한국축산식품학회지
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• 제34권2호
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• pp.166-171
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• 2014

The aim of this study is to examine the influences of spices on the amounts and compositions of volatile compounds released from cooked beef patty. Beef patty with 0.5% of spice (nutmeg, onion, garlic, or ginger powder, w/w) was cooked by electronic pan until they reached an internal temperature of $75^{\circ}C$. A total of 46 volatile compounds (6 alcohols, 6 aldehydes, 5 hydrocarbons, 6 ketones, 9 sulfur compounds, and 14 terpenes) from cooked beef patties were detected by using purge-and-trap GC/MS. The addition of nutmeg, onion, or ginger powder significantly reduced the production of the volatile compounds via lipid oxidation in cooked beef patty when compared to those from the control. Also, the addition of nutmeg and garlic powder to beef patty generated a lot of trepans or sulfur volatile compounds, respectively. From these results, the major proportion by chemical classes such as alcohols, aldehydes, hydrocarbons, ketones, sulfur compounds, and terpenes was different depending on the spice variations. The results indicate that addition of spices to the beef patty meaningfully changes the volatile compounds released from within. Therefore, it can be concluded that spices can interact with meat aroma significantly, and thus, the character of each spice should be considered before adding to the beef patty.

• Asian-Australasian Journal of Animal Sciences
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• 제16권3호
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• pp.435-444
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• 2003

In 1957, Schwarz and Foltz discovered that selenium (Se) was an essential trace mineral and nutritionists then started extensive studies to figure out the metabolic function of this element which has been called as toxic mineral. The discovery that glutathione peroxidase (GSH-Px) contained Se demonstrated a biochemical role for Se as an essential trace element. The major physiological function of Se containing GSH-Px is thought to maintain low levels of $H_2O_2$ and other hydroperoxides in the cell to prevent tissues from peroxidation damages. It is known that the GSH-Px activity is increased when animals were fed high dietary levels of Se. Chemical properties of Se have much in common with sulfur (S) therefore Se would follow the sulfur pathways in its metabolism in animal body. Two sources of Se are available for supplementation of Se in animal feed. Inorganic Se can also exist in selenide (-2), elemental (0), selenite (+4) and selenate (+6) oxidation state with other minerals. When sulfur in S containing amino acids is replaced by Se, organic Se can be made and named "eleno"prior to the name of S containing amino acid, i.e. selenomethionine. Selenium deficiency affects humans as well as animals and dysfunctions such as exudative diathesis, retained placenta, mastitis, liver necrosis, Keshan disease, numerous diseases and cancer. From several centuries ago, Se toxicity was recognized in various animal species and much of the current toxic Se levels has been established largely based upon the controlled toxicity studies used inorganic Se. Toxic effects of Se in animal result in reduced feed intake, growth retardation, ataxia, diarrhea, alopecia and sloughing of hooves. However, several experiments demonstrated that Se deficiencies or toxicities were varied by dietary Se levels and sources. Recent studies demonstrated that the incidence of colorectal and prostate cancer was reduced by approximately 50% when humans consumed 200 ${\mu}g$ of Se daily.

• 플랜트 저널
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• 제15권1호
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• pp.38-44
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• 2019

본 연구에서는 1,000 MW급 석탄화력발전소용 탈황흡수탑을 대상으로 대기환경보전법 및 발전소 자체 배출규제치를 준수하면서 운전할 때, 석회석 슬러리 투입량을 조절하여 흡수탑 내부 슬러리 pH의 적정 범위를 찾고자 하였다. 배기가스 유량, 발전기 출력, 흡수탑 압력강하, 산화용 공기량을 고정한 상태에서 흡수탑 유입가스에 포함된 이산화황의 평균 농도, ${\bar{C\;in}}$ [ppm]을 500 ppm, 550 ppm, 600 ppm 그리고 635 ppm으로 변동시키며 운전하였을 때, 흡수탑 내부 적정슬러리 pH, 는 5.0, 5.2, 5.3 그리고 5.4였다. 이러한 결과로부터 흡수탑 유입가스에 포함된 이산화황의 평균 농도가 500~635 ppm의 범위일 때 상관관계식 을 이용하여 적정슬러리 pH를 산출하여 운전하는 것이 추천된다.

• 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.

• 유기물자원화
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• 제20권4호
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• pp.118-126
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• 2012

본 연구를 위한 실험 장치는 하루에 100톤 규모의 돼지분뇨를 퇴비화와 액비화 하는 방식으로 처리하는 시설에 설치되었다. 액비조의 경우 폭기되는 분뇨의 상층부에 흡입부를 설치하고 기체를 빨아들이는 방식으로 실험용 기체시료를 포집하였다. 포집된 시료는 오존이 존재하는 2 종류의 반응조에 유입된 후 오존과 접촉하는 방식으로 처리되었다. 처리효율 분석은 처리시설 유입부 배관에서 채취한 시료와 오존과 반응한 후 배출되는 배관에서 채취한 시료의 성분함량을 비교하여 결정하였다. 퇴비사의 시료는 교반 후 발생하는 기체를 흡입한 후 액비조에서와 같은 방식으로 처리하고 그 효율을 분석하였다. 오존접촉에 의한 반응효과는 암모니아보다는 황 화합물에서 더 크게 나타났다. 암모니아의 경우 오존접촉 방법에 관계없이 10% 내외의 감소효과를 보였다. 반면에 황 화합물은 오존 처리에 의해 상당량 감소하는 결과를 나타냈다. 액비화 시설로부터 발생된 시료의 경우, 유입부에서 50.091, 4.9089, 27.8109, 0.4683 ppvs 의 농도를 보였던 $H_2S$, MM, DMS, DMDS가 반응 후 유출부에서는 각각 1.2317, 0.3839, 14.7279 0.3145 ppvs 수준으로 감소하였다. 같은 조건으로 호기적 퇴비화 과정에서 발생한 시료를 처리한 결과 $H_2S$, MM, DMS, DMDS 농도는 40.6682, 1.3675, 24.2458, 0.8289 ppvs에서 3.013, 불검출, 8.8998, 0.3651 ppvs 수준으로 감소하였다. 액비화 시설에서 발생하는 시료에 또 다른 형태의 오존을 적용한 결과 $H_2S$, MM, DMS, DMDS가 43.397, 1.4559, 3.6021, 0.4061 ppvs 농도 수준에서 각각 불검출, 불검출, 불검출, 0.2185 ppvs 수준으로 감소하였다.

• 한국환경농학회지
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• 제29권3호
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• pp.221-226
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• 2010

축산폐수는 고농도의 유기물 및 질소를 함유하고 있으므로 적절한 처리 방법이 요구된다. 본 연구는 황을 이용한 독립영양 탈질 방법으로 질산성 질소에서 질소가스로의 탈질이 아닌 아질산성질소에서의 황산화 탈질을 연구하였으며 탈질 미생물의 최적 성장 조건을 찾고자 하였다. 초기 알칼리도가 충분한 조건에서는 아질산성질소 탈질 저해가 관찰되지 않았으며 실험온도가 $20^{\circ}C$인 경우에도 $30^{\circ}C$와 비교할 때 큰 저해 없이 탈질이 진행되었다. 하지만 초기 아질산성질소의 농도 300 mg/L 이상에서 lag phase가 늘어나 기질저해가 나타났다. 알칼리도가 충분하지 않은 조건에서 질산성질소의 탈질효율은 10%인 반면 아질산성질소의 탈질의 95% 이상이었다. 산소가 존재할 경우 산소를 이용하여 탈질이 이루어지지 않았음에도 불구하고 황산화 미생물이 산소를 이용하여 황산염의 농도가 증가하였다. 아질산성질소 탈질 시 알칼리도의 소모가 관찰되었으나 질산염 탈질시 보다 알칼리도의 소모가 적었으며 황산염 생성 또한 적었다. 황이용 아질산성 질소 탈질은 외부탄소원의 추가적인 주입 없이 저렴한 황입자를 이용하며 질산성질소 황산화 탈질의 단점인 알칼리도 파괴, 황산염이온 생성의 단점을 보완할 수 있는 효과적인 탈질 방법이 될 것으로 기대된다.

• 한국대기환경학회지
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• 제14권5호
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• pp.443-454
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• 1998

Pt-V catalytic converter was installed on a heavy duty diesel engine and the characteristics of the emission reduction were tested using a engine dynamometer at various operating conditions. The emission reduction performance of Pt-V catalyst was also compared with that of a commercialized Pt catalyst currently being used in some of the heavy duty diesel engines in advanced countries. The effects of Pt-V and Pt catalysts on regulated and unregulated emissions were investigated using a 0.05 weight percent sulfur content fuel with an engine dynamometer Experiments for gaseous emissions (CO, HC and aldehyde) as well as particulate emissions (TPM, SOF and sulfate) have been conducted at several operating conditions such as T-7 mode, D-13 mode and S-13 mode before and after installing the Pt-V and Pt catalysts in the exhaust system. The emission reduction performance of Pt catalyst with respect to CO, HC, SOF, PAHs and aldehyde was found to be a little higher than that of Pt-V catalyst, but the Pt catalyst showed innate disadvantage of causing an increase of PM due to the sulfate formation via high SO2 conversion at high exhaust temperature, especially above 45$0^{\circ}C$.

• 한국환경과학회:학술대회논문집
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• 한국환경과학회 1998년도 가을 학술발표회 프로그램
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• pp.1-1
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• 1998

Advanced (Chemical) oxidation processes (AOP) differ from most conventional ones in that hydroxyl radical(OH.) is considered to be the primary oxidant. Hydroxyl radicalcan react non-selectively with a great number of organic and inorganic chemicals. The typical rate constants of true hydroxyl radical reactions are in the range of between 109 to 1012 sec-1. Many processes are possible to generate hydroxyl radical. These include physical and chemical methods and their combinations. Physical means involves the use of high energy radiation such as gamma ray, electron beam, and acoustic wave. Under an applied high energy radiation, water molecules can be decomposed to yield hydroxyl radicals or aqueous electrons. Chemical means include the use of conventional oxidants such as hydrogen peroxide and ozone, two of the most efficient oxidants in the presence of promoter or catalyst. Hydrogen peroxide in the presence of a catalyst such as divalent iron ions can readily produce hydroxyl radicals. Ozone in the presence of specific chemical species such as OH- or hydrogen peroxide, can also generate hydroxyl radicals. Finally the combination of chemical and physical means can also yield hydroxyl radicals. Hydrogen peroxide in the presence of acoustic wave or ultra violet beam can generate hydroxyl radicals. The principles for hydroxyl radical generation will be discussed. Recent case studied of AOP for water treatment and other environmental of applications will be presented. These include the treatment of contaminated soils using electro-Fenton, lechate treatment with conventional Ponton, treatment of coal for sulfur removal using sonochemical and the treatment of groundwater with enhanced sonochemical processes.