• 제목/요약/키워드: peak carbon monoxide

검색결과 33건 처리시간 0.029초

오존농도의 動態 및 影響因子에 關한 硏究 (Studies on the Behaviour of Ozone Concentration and the Influencing Factors)

  • 金旻永;姜熙坤;李完宗;李相七;張鳳勳;朴聖培
    • 한국대기환경학회지
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    • 제5권2호
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    • pp.55-71
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    • 1989
  • This study was carried out to determine the ozone concentration to behaviour and the factors to be influenced the variation of its concentration in the ambient air in Seoul. Measurements of ozone concentrations were made at 10 monitoring station to take care of SIHE (Seoul Institute of Health & Environment) during December 1987 to November 1988, also measured the hourly average concentration of sulfur dioxide, total suspended particulate, nitrogen oxide $(NO & NO_2)$, carbon monoxide, hydro carbon $(n-CH_4 & THC)$ and meteorological factors, that is, temperature, humidity, wind velocity wind direction and ultraviolet intensity etc, for the same period at same place. The basis of the data obtained were analyzed statistically along with the various data. The results were as follows; 1. The annually arithmetic mean concentration of ozone for the 10 sites during one years was 10.0 ppb and ranged from 3.1 $\pm$ 4.5ppb at the Kuro industrial complex to 17.2 $\pm$ 18.7 ppb at the Ssangmun site. 2. The frequency of hours on which oxidant concentrations exceeded the present short term standard of ozone (100 ppb) were 78 times. 3. The diurnal patterns of hourly ozone concentrations in Seoul area was a typical bi-modal variation which have 4 to 5 a.m. peak and 3. to 4 p.m peak. 4. The time ozone of highest ozone concentration in a whole day and hight was 1 to 5 p.m and 90.9 percent of appearence rate. 5. The diurnal patterns of hourly ozone concentrations in Seoul were on the whole the order of daytime from 5.8ppb to 28.7 ppb evening from 1.7 to 18.7 ppb night time from 1.9 to 9.3 ppb daybreak from 1.4ppb according to measuring sites, and the highest that observed at the Ssangmun area while the lowest was the Kuro industrial complex monitor sites. 6. The weekly variation of ozone concentration was the higher level ozone concentration in the day of the week occured sunday-monday and weekend but the decrease were observed from wednesday to thursday.

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Methylobacillus sp. Strain SK1에 존재하는 Soluble cytochrome c의 정제 및 특성 (Purification and Some Properties of Soluble Cytochrome c from Methylobacillus sp. Strain SK1)

  • 김시욱;노영태;김영민
    • 미생물학회지
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    • 제29권6호
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    • pp.380-386
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    • 1991
  • Three types of soluble cytochrome c were purified to homogeneity from Methylobacillus sp. strain SK1 which grows only on methanol. Cytochrome c-I was purified 58.5-fold in seven steps. Cytochrome c-II and c-III were purified 57.3- and 122.1-fold in eight steps, respectively. The molecular weights of the cytochrome c-I was determined to be 12,500, while those of the cytochrome c-II and c-III were 16,000. The isoelectric points of the c-I, c-II and c-III were found to be 8.8, 6.6, and 6.6 respectively. The spectrum of reduced cytochrome c-I showed .alpha.-, .betha.-, .gamma.-peaks at 551.4, 522.2, and 416.6nm. The peaks for c-II were found at 551.0, 521.6, and 416.5nm, while those for c-III were shown at 551.2, 521.8, and 416.0 nm. The spectra of oxidized cytochrome c-I, c-II, and c-III showed .gamma.-peak at 411.8, 409.0, and 410.2 nm, respectively. The absorption coefficients of .alpha.- and .gamma.-peak for c-I in the reduced state were determined as 47 and 197 $mM^{-1}$ $cm^{-1}$ , respectively. The coefficients of .alpha.- and .gamma.-peak for c-II were determined to be 43 and 137 $mM^{-1}$ $cm^{-1}$ , while those for c-III were 41 and 172 $mM^{-1}$ $cm^{-1}$ , respectively. The c-I and c-III were found to bind carbon monoxide.

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SI엔진에서 바이오에탄올-가솔린 혼합율 및 공연비 변화에 따른 연소 및 배기배출물 특성에 관한 연구 (A Study on the Combustion and Exhaust Emission Characteristics with the Variations of Mixing and Air-fuel Ratio of Bio-ethanol - Gasoline in a SI Engine)

  • 윤승현;하성용
    • 한국자동차공학회논문집
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    • 제24권3호
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    • pp.358-364
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    • 2016
  • The combustion and exhaust emission characteristics in a spark ignition (SI) engine with various test fuels (bioethanol - gasoline blends) and air-fuel ratio were investigated in this research. To investigate the influence of the excess air ratio and ethanol blends on the combustion characteristics such as the cylinder pressure, rate of heat release (ROHR), and fuel consumption rate were analyzed. In addition, the reduction effects of exhaust emissions such as carbon monoxide (CO), unburned hydrocarbon (HC), and oxides of nitrogen (NOx) were compared with those of neat gasoline fuel under the various excess-air ratios. The results showed that the peak combustion pressures and the ROHR of bioethanol fuel cases were slightly higher than those of gasoline fuel at all test ranges and fuel ratio. As compared with gasoline fuel (G100) at each given excess air ratio, BSFC of bio-ethanol was increased. The CO, HC, NOx emissions of bio-ethanol blends were lower than those of gasoline fuel under overall experimental conditions.

A STUDY ON THE FLAMMABILITY OF NON-FLAME-RETARDANT AND FLAME-RETARDANT MATERIALS BY USING CONE CALORIMETER

  • Yanai, Eiji;Suzuki, Takeshi;Yamada, Tokiyoshi
    • 한국화재소방학회:학술대회논문집
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    • 한국화재소방학회 1997년도 International Symposium on Fire Science and Technology
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    • pp.85-92
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    • 1997
  • Flammability of non-flame-retardant and flame-retardant materials was studied by using cone calorimeter Also, relations between the results obtained by using cone calorimeter and those obtained by the flammability test of japanese fire Service Law were examined. The results are as follows: 1) The ignition time of the molten specimens is relatively long, whereas the ignition time of the non-molten specimens is short. None of remarkable difference of the ignition time has been found between non-flame-retardant and flame-retardant materials specimens. 2) The peak heat release rates of flame-retardant materials are smaller than those of non-flame- retardant materials. 3) The carbon monoxide and smoke evolved from flame-retardant materials generate much more than those evolved from non-flame-retardant materials. 4) Even if flame-retardant materials are passed by the flammability test of Japanese Fire Service Law, they burn easily under external radiative heating condition.

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탄화왕겨, 제지슬러지, 커피찌거기 및 실리카 혼합물로부터 탄화규소 결정체 합성 (SiC aggregates synthesized from carbonized rice husks, paper sludge, coffee grounds, and silica powder)

  • 박경욱;윤영훈
    • 한국결정성장학회지
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    • 제29권2호
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    • pp.45-49
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    • 2019
  • 본 연구에서는, 탄소성분으로서 탄화왕겨, 제지슬러지, 커피찌꺼기와 실리카 분말로부터, 비교적 미세한 탄화규소 결정질 응집체를 합성하였다. 탄소성분들과 실리카의 혼합물로부터 탄화규소 응집체를 얻기 위한 주요 반응물질은 열탄화환원 반응에 의해 생성된 일산화규소 기체로 추정되었다. 탄화왕겨, 제지슬러지, 커피찌꺼기와 실리카 분말의 혼합물로부터 열탄화환원반응법을 거쳐 생성된 탄화규소 결정질 응집체들에 대한 XRD 회절패턴으로부터 결정상을 분석하였고, FE-SEM과 FE-TEM을 통한 미세구조, 결정구조 분석이 이루어졌다. 탄화왕겨, 제지슬러지, 그리고 실리카 분말의 시료의 경우, XRD 분석에서는 $35^{\circ}$ 부근의 (111) peak은 비교적 높은 강도를 나타내었다. 탄화왕겨, 제지슬러지, 커피찌꺼기와 실리카 분말의 혼합물로부터 합성된 시료들에 대해 FE-SEM 관찰을 통하여 $1{\mu}m$ 이하의 미세입자들을 관찰하였으며, TEM 측정 결과에서는 탄화규소 결정질상의 (110) 회절패턴들을 확인하였다.

인-질소 화합물 조합에 의해 처리된 목재의 연소성 (Combustion Properties of Wood Treated by Combining Phosphorus-Nitrogen Compounds)

  • 진의;정영진;김시국
    • 공업화학
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    • 제27권1호
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    • pp.39-44
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    • 2016
  • 이 연구에서는 피로인산/암모늄이온, 메틸렌피페라지노메틸-비스-포스폰산, 메틸렌피페라지노메틸-비스-포스폰산/암모늄이온의 화학 첨가제로 처리된 리기다 소나무의 연소 특성을 고찰하였다. 15 wt%의 화학 첨가제 수용액으로 각각 리기다 소나무에 3회 붓칠하여 실온에서 건조시킨 후, 콘칼로리미터(ISO 5660-1)를 이용하여 연소성을 시험하였다. 그 결과, 화학 첨가제로 처리한 시험편의 최대질량감소율도달시간(PMLR time)은 무처리 시험편에 비교하여 10.5~47.4% 지연되었다. 그리고 최대일산화탄소발생률($CO\;_{peak}$)은 무처리 시험편에 비교하여 32.1~71.4% 증가하였다. 또한 총연기방출률(TSRR)은 화학 첨가제로 처리한 시험편이 무처리한 시험편보다 15.6~43.6% 증가하였다. 특히, 단위면적당 연기방출속도(RSR)에 대하여 $PP/4NH_4{^+}$로 처리한 시험편을 제외하고, 무처리 시험편보다 29.4~41.5% 높게 나타났다. 이와 같이 유기성 화학 첨가제로 처리한 시험편은 연소억제 작용에 의하여 연소시간이 길어짐에 따라 연기방출률이 높았다. 그러나 $PP/4NH_4{^+}$은 무기물 첨가제로서 일부 감연 작용을 하는 것으로 보인다. 따라서 화학 첨가제로 처리한 시험편은 무처리 시험편과 비교하여 연소가스 및 연기발생을 부분적으로 증가시켰다.

직접분사식 가솔린엔진에서 운전조건에 따른 바이오에탄올의 연소 및 배기배출물 특성 (Effect of Engine Operating Conditions on Combustion and Exhaust Emission Characteristics of a Gasoline Direct Injection(GDI) Engine Fueled with Bio-ethanol)

  • 윤승현;박수한
    • 대한기계학회논문집B
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    • 제39권7호
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    • pp.609-615
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    • 2015
  • 본 연구는 직접분사식 가솔린엔진에서 공기 과잉률 및 바이오에탄올-가솔린 혼합연료의 혼합비에 따른 연소특성과 배기배출물 특성을 실험적으로 규명한 것이다. 다양한 공기 과잉률 및 혼합비 조건에서 실험을 수행하였으며, 연소실 압력, 열발생률, 연료소비율 등을 통해 연소특성을 분석하였으며, 배기배출물 특성은 미연탄화수소(HC), 일산화탄소(CO), 질소산화물($NO_x$) 분석을 통해 확인하였다. 혼합연료의 실험결과는 100% 가솔린 및 바이오에탄올 실험결과와 비교하였다. 실험결과 최고연소압력과 열발생률, 제동연료소비율은 혼합비의 증가에 따라 증가하였으며, CO, HC, $NO_x$와 같은 배기배출물은 바이오 에탄올 혼합비율이 증가함에 따라 감소하였다. 혼합연료의 배기배출물 수준은 가솔린 보다 낮게 나타났다.

Biochemical and Cellular Investigation of Vitreoscilla Hemoglobin (VHb) Variants Possessing Efficient Peroxidase Activity

  • Isarankura-Na-Ayudhya, Chartchalerm;Tansila, Natta;Worachartcheewan, Apilak;Bulow, Leif;Prachayasittikul, Virapong
    • Journal of Microbiology and Biotechnology
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    • 제20권3호
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    • pp.532-541
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    • 2010
  • Peroxidase-like activity of Vitreoscilla hemoglobin (VHb) has been recently disclosed. To maximize such activity, two catalytically conserved residues (histidine and arginine) found in the distal pocket of peroxidases have successfully been introduced into that of the VHb. A 15-fold increase in catalytic constant ($k_{cat}$) was obtained in P54R variant,which was presumably attributable to the lower rigidity and higher hydrophilicity of the distal cavity arising from substitution of proline to arginine. None of the modifications altered the affinity towards either $H_2O_2$ or ABTS substrate. Spectroscopic studies revealed that VHb variants harboring the T29H mutation apparently demonstrated a spectral shift in both ferric and ferrous forms (406-408 to 411 nm, and 432 to 424-425 nm, respectively). All VHb proteins in the ferrous state had a $\lambda_{soret}$ peak at ~419 nm following the carbon monoxide (CO) binding. Expression of the P54R mutant mediated the downregulation of iron superoxide dismutase (FeSOD) as identified by two-dimensional gel electrophoresis (2-DE) and peptide mass fingerprinting (PMF). According to the high peroxidase activity of P54R, it could effectively eliminate autoxidation-derived $H_2O_2$, which is a cause of heme degradation and iron release. This decreased the iron availability and consequently reduced the formation of the $Fe^{2+}$-ferric uptake regulator protein ($Fe^{2+}$-Fur), an inducer of FeSOD expression.

Lung Function Profiles among Individuals with Nonmalignant Asbestos-related Disorders

  • Park, Eun-Kee;Yates, Deborah H.;Wilson, Donald
    • Safety and Health at Work
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    • 제5권4호
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    • pp.234-237
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    • 2014
  • Background: Inhalation of asbestos fibers can lead to adverse health effects on the lungs. This study describes lung function profiles among individuals with nonmalignant asbestos-related disorders (ARDs). Methods: The study population was from the Workers' Compensation (Dust Diseases) Board of New South Wales, Sydney, Australia. Lung function measurements were conducted in males with asbestosis (n = 26), diffuse pleural thickening (DPT; n = 129), asbestosis and DPT (n = 14), pleural plaques only (n = 160) and also apparently healthy individuals with a history of asbestos exposure (n = 248). Standardized spirometric and single-breath diffusing capacity for carbon monoxide ($DL_{CO}$) measurements were used. Results: Mean age [standard deviation (SD)] was 66.7 (10.3) years for all participants. Current and ex-smokers among all participants comprised about 9.0% and 54.8%, respectively. Median pack-years (SD) of smoking for ex- and current-smokers were 22.7 (19.9). Overall 222 participants (38.6%) and 139 participants (24.2%) had forced expiratory volume in 1 second ($FEV_1$) and forced vital capacity (FVC) measurements < 80% predicted, and 217 participants (37.7%) had $FEV_1/FVC$ results < 70%. A total of 249 individuals (43.8%) had DLCO values < 80% predicted and only 75 (13.2%) had DLCO/VA results < 80% predicted. A total of 147 participants (25.6%) had peak expiratory flow (PEF) measurements < 80% predicted. The presence of ARDs lowered the lung function measurements compared to those of healthy individuals exposed to asbestos. Conclusion: Lung function measurement differs in individuals with different ARDs. Monitoring of lung function among asbestos-exposed populations is a simple means of facilitating earlier interventions.

알칼리 처리에 의한 Zeolite 광물의 물리화학적 특성 (Physicochemical Characteristics of Zeolite Mineral by Alkali Solution Treatment)

  • 임굉
    • 자연과학논문집
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    • 제8권2호
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    • pp.119-127
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    • 1996
  • Zeolite인 mordenite 광물을 수산화나트륨용액으로 화학처리한 효과에 대해서 화학분석, X-선 분말회절, 열분석, 이산화탄소의 흡착측정 및 GC를 통하여 조사하였다. 출발원료로 mordenite 광물을 3시간동안 water bath 중 약 $95^{\circ}C$에서 NaOH 0.1-5N의 농도범위로 화학 처리한 결과, 시료중 함유된 모든 화학성분은 NaOH 0.5N 이하의 농도에서는 불용이고 mordenite 구조는 변화하지 않았으며 1N 이상의 농도에서는 실리카, 알루미나 등과 같이 성분들이 용해되었고 시료중 실리카의 용해비율이 알루미나의 용해보다 높으며 실리카와 알루미나의 비가 2-3N 농도 범위에서는 급격히 감소하였다.Mordenite 의 (202)면의 X-선 회절피크 강도와 $CO_2$ 흡착량은 1N 이상의 NaOH 농도가 증가함에 따라 감소하며 이로 인하여 mordenite 구조의 붕괴가 나타났다.산소, 질소 및 일산화탄소의 GC분리공정에서는 NaOH 용액 처리에 의한 영향을 받지 않으나 메탄과 크립톤의 용출피크가 넓어지는 경향이 나타나며 retention time 은 단축되었고 이 두 기체모두 용리피크는 산소 또는 질소와 중복되기 쉬운 경향을 보여주었다.

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