• Title/Summary/Keyword: acidic gas

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Eletrochemical Characteristics of Ozone Generator using Boron-doped Diamond Electrode (붕소가 도핑된 다이아몬드전극을 이용한 오존발생기의 전기화학적 특성)

  • ;;Yasuaki Einaga;Akira Fujishima
    • Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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    • 2001.11a
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    • pp.585-588
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    • 2001
  • Thin, Boron-doped conducting diamond films are expected to be excellent electrodes for industrial electrolysis. Boron-doped conducting diamond films were used as anode for generating ozone gas by electrolysis of acidic solution. In this work, we have studied ozone generating system using Boron-doped Diamond electrode. Electrochemical cell and ozone generating system were designed for decreasing the temperature of the system, which was elevated during the reaction. by circulation of electrolyte in the system. In order to determine the ozone generation properties of diamond electrode, experimental conditions, electrolyte concentration, temperature, flow rate and reaction time were varied diversely. As a result, we could confirm that ozone gas was generated successfully and the performance of diamond electrode was stable while PbO$_2$ electrode was disintegrated. Actually we are found that ozone amount increased by lowering the temperature of electrolyte.

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Determination of Reactivity by MO Theory (Part 50). MO Studies on the Gas Phase Pyrolysis of Esters

  • Lee, Ik-Choon;Park, Young-Soo;Lee, Bon-Su
    • Bulletin of the Korean Chemical Society
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    • v.8 no.3
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    • pp.193-196
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    • 1987
  • The gas phase pyrolyses of eight esters have been studied by MNDO-MO method. In the ethylformate pyrolysis, ${\alpha}$-methylation had a steric releasing effect whereas ${\beta}$-methylation had a steric crowding in the transition state; the latter, however, is over-compensated by a greater electronic repulsion resulting in a net steric releasing effect. Considerations of formal charges and geometrical changes involved in the activation led us to propose a pyrolysis mechanism in which a preequilibrium of acidic proton transfer is followed by the rate-limiting bond polarization of $C_{\alpha}$-O bond in a cyclic transition state.

Hydrogen Embrittlement of TRIP Steel Charged with Hydrogen Under Two Type Electrolytes (2종 전해질 분위기하 수소주입된 TRIP 강의 수소취성)

  • Choi, Jong-Un;Lee, Sang-Wook;Lee, Kyung-Min;Kang, Kae-Myung
    • Journal of the Korean Institute of Gas
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    • v.19 no.1
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    • pp.57-63
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    • 2015
  • The hydrogen was charged TRIP steel by electrochemical method under 0.5M $H_2SO_4$ electrolyte and 0.5M NaOH electrolyte with hydrogen charging conditions respectively. The degree of hydrogen embrittlement of TRIP steel was evaluated by using micro Vickers hardness tests. These results showed that the degree of hydrogen embrittlement in acidic electrolyte with hydrogen penetration and hydrogen diffusion through the depth of specimen was more sensitive than its alkaine electrolyte between two type electrolytes. However, it was investigated that micro Vickers hardnesses of surface in acidic electrolyte under two electrolyte were higher than those of alkaine electrolyte. It was thought that in case of hydrogen embrittlement in acid-ice electrolyte, hydrogen charging time was more effective than current density, in case of alkaine electrolyte, hydrogen current density was more effective than charaging time.

The Characteristics of PM2.5 and Acidic Air Pollutants in the Vicinity of Industrial Complexes in Gwangyang (광양산업단지 인근지역 대기 중 미세먼지 (PM2.5)와 산성오염물질 특성)

  • Kang, Byung-Wook;Jeong, Man-Ho;Jeon, Jun-Min;Lee, Hak-Sung
    • Journal of Korean Society for Atmospheric Environment
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    • v.27 no.1
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    • pp.16-29
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    • 2011
  • The cyclone/annular denuder system/filter pack sampling system (ADS) was used to collect data set of the acidic air pollutants in the vicinity of industrial complexes in Gwangyang. The data set was collected during sixty different days with 24 hour sampling period from January 8, 2008 through November 12, 2008. The annual mean concentrations of $HNO_3$, $HNO_2$, $SO_2$ and $NH_3$ in the gas phase were 1.12, 1.40, 10.2 and 1.28 ${\mu}g/m^3$, respectively. The annual mean concentrations of $PM_{2.5}$ ($d_p$<2.5 ${\mu}m$), $SO_4^{2-}$, $NO_3^-$, and $NH_4^+$ in the particulate phase were 29.2, 8.25, 3.30 and 3.42${\mu}g/m^3$, respectively. $HNO_3$ and $NH_3$ exhibited higher concentrations during the summer, while $HNO_2$, $PM_{2.5}$, $NO_3^-$ and $NH_4^+$ were higher during the winter. The highest level of $SO_2$ was, unlikely, observed in the summer and $SO_4^{2-}$ was not showed seasonal variation. $SO_4^{2-}$, $NO_3^-$, and $NH_4^+$ accounted for 49~57% of the $PM_{2.5}$ mass. $SO_4^{2-}$ was the most abundant component, which constituted 23~40% of $PM_{2.5}$. High correlations were found among $PM_{2.5}$, $SO_4^{2-}$, $NO_3^-$, and $NH_4^+$.

A Seasonal Variation of Acidic Gases and Fine Particle Species in Chongju Area (청주지역 산성 가스상물질과 미세입자의 계절 변동 특성)

  • 강병욱;이학성;김희강
    • Journal of Korean Society for Atmospheric Environment
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    • v.13 no.5
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    • pp.333-343
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    • 1997
  • The cyclone/annular denuder system/filter pack sampling system (ADS) was used to collect the acidic air pollutants in Chongju city. The data set was collected on fifty -eight different days with 24 hour sampling period from October 27, 1995 through August 25, 1996. The chemical species measured were HN $O_3$, HN $O_2$, S $O_2$ and N $H_3$ in the gas phase, and PM2.5( $d_{p}$ <2.5 ${\mu}{\textrm}{m}$), S $O_4$$^{2-}$, N $O_3$$^{[-10]}$ and N $H_4$$^{+}$ in the Particulate Phase. Mean concentrations measured for this study were: 0.45 $\mu\textrm{g}$/㎥ for HN $O_3$, 3.39 $\mu\textrm{g}$/㎥ for HN $O_2$, 26.4 $\mu\textrm{g}$/㎥ for S $O_2$, 3.83$\mu\textrm{g}$/㎥ for N $H_3$, 44.2 $\mu\textrm{g}$/㎥ for P $M_{2.5}$, 8.22 $\mu\textrm{g}$/㎥ for S $O_4$$^{2-}$, 3.63 $\mu\textrm{g}$/㎥ for N $O_3$$^{[-10]}$ , and 2.84 $\mu\textrm{g}$/㎥ for N $H_4$$^{- }$. HN $O_3$ and N $H_3$ were higher during the summer. However, HN $O_2$ and S $O_2$ were higher during the fall and winter. P $M_{2.5}$ , S $O_4$/ sup 2-/ and N $H_4$$^{+}$ were not showed seasonal variations, but N $O_3$$^{[-10]}$ was higher in the winter.ter.r.

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Development of Marine Emission Control System on NOx and SOx through Seawater Electrolysis

  • Kim Houng-Soo
    • Journal of Advanced Marine Engineering and Technology
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    • v.30 no.1
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    • pp.81-87
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    • 2006
  • In marine air pollution control, SCR (Selective Catalytic Reduction) is reconized as the most effect method to control NOx, but on the other hand. seawater scrubber applying the basic characteristic that is naturally alkaline (pH typically around 8.1) is viewed as an economical SOx removal system at present. Especially, seawater scrubber would not be necessary to follow any of the various land based flue gas desulfurization methods. i.e. wet, dry or alkali scrubbing. However, these methods are not readily adaptable to marine conditions due to the quantifies of consumables required i.e. lime or limestone, the means of operation and the commercial availability. This research is undertaken to develop a new method as the main target of eliminating all exhaust emissions, particularly vessel, because of easy access to seawater and apt to apply a wet scrubber system. First, using the acidic seawater by seawater electrolysis, nitric monoxide(NO) is adequately oxidized to nitric dioxide $(NO_2)$by ClOx-in the acidic seawater, the electrolyzed alkaline seawater by electrolysis which contains mainly NaOH together with alkali metal ions $(i.e\;Na^{+}\;K^{+},\;Mg_{2}\;^{+},\;Ca_{2}\;^{+})$, is used as the absorption medium of NOx, the SOx are absorbed by relatively high solubility compared to other components of exhaust pollutants. The results found that the NOx and SOx removals could be achieved nearly Perfect.

A Study of Concentration Characteristics of Acidic Air Pollutants During the Summer and Winter Seasons in Seoul (서울지역 여름철과 겨울철 산성 오염물질의 농도 특성에 대한 연구)

  • 이학성;강충민;강병욱;김희강
    • Journal of Korean Society for Atmospheric Environment
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    • v.15 no.2
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    • pp.113-120
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    • 1999
  • Winter and summer samples were collected from January 3 to February 7, 1997 and July 26 to September 11, 1997, respectively, in Seoul. This study was to characterize the concentrations of the annular denuder system (ADS) were $HNO_3$, $HNO_2$, $SO_2$ and $NH_3$ in the gas phase, and $PM_{2.5}$ ($d_p$〈2.5$mu extrm{m}$), $SO_4^{2-}$, NO3-, and $NH_4^+$ in the particulate phase. All chemical species monitored from this study showed statistical seasonal variations except for $SO_4^{2-}$ . Nitric acid (HNO3) and ammonia ($NH_3$) exhibited substantially higher concentrations during the summer, while nitrous acid ($HNO_2$) and sulfur dioxide ($SO_2$) concentrations were higher during the winter. $PM_{2.5}$, $NO_3^-$, and $NH_4^+$ were higher leves in the winter. High correlations were found among $PM_{2.5}$, $NO_3^-$ $SO_4^{2-}$ and $NH_4^+$ during two seasons.

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Sulfate Reduction at pH 5 in a High-Rate Membrane Bioreactor: Reactor Performance and Microbial Community Analyses

  • Bijmans, Martijn F. M.;Dopson, Mark;Peeters, Tom W. T.;Lens, Piet N. L.;Buisman, Cees J. N.
    • Journal of Microbiology and Biotechnology
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    • v.19 no.7
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    • pp.698-708
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    • 2009
  • High rate sulfate reduction under acidic conditions opens possibilities for new process flow sheets that allow the selective recovery of metals from mining and metallurgical waste and process water. However, knowledge about high-rate sulfate reduction under acidic conditions is limited. This paper investigates sulfate reduction in a membrane bioreactor at a controlled pH of 5. Sulfate and formate were dosed using a pH-auxostat system while formate was converted into hydrogen, which was used for sulfate reduction. Sulfide was removed from the gas phase to prevent sulfide inhibition. This study shows a high-rate sulfate-reducing bioreactor system for the frrst time at pH 5, with a volumetric activity of 188 mmol $SO_4^{2-}$/I/d and a specific activity of 81 mmol $SO_4^{2-}$volatile suspended solids/d. The microbial community at the end of the reactor run consisted of a diverse mixed population including sulfate-reducing bacteria.

Sensitive Determination of Natural and Synthetic Steroidal Hormones of a Free and Conjugated Form in Surface Water by Gas Chromatography-Mass Spectrometry

  • Shin, Ho-Sang;Oh, Jin-Aa;Shin, Sun-Kyoung
    • Bulletin of the Korean Chemical Society
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    • v.32 no.3
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    • pp.809-814
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    • 2011
  • A method based on the TMS derivatives and acidic hydrolysis was developed for the simultaneous determination of free and conjugated steroidal hormones in surface water. A silylation of five natural and two synthetic steroidal hormones was achieved with N-methyl-N-(trimethylsilyl) trifluoroacetamide/$NH_4I$ (1000:3) under catalysis of dithioerythritol for 60 min at $80^{\circ}C$. TMS derivatives of the steroid hormones containing multifunctional groups offer a single derivative product under this condition. The accuracy of the analytes was in the range of 87 to 110% at a concentration of 20 and 50 ng/L with relative standard deviations of less than 10%. The method detection limit was in the range of 0.01 to 0.02 ng/L for surface water. Natural steroidal hormones were detected in a concentration range of 0 to 1.03 ng/L in free form and 0 to 14.6 ng/L in conjugated form, respectively. We found that most of the natural hormonal steroids exist in conjugate forms (43 to 100%) in river water.

Adsorption of p-Nitrophenol by Surface Modified Carbons from Aqueous Solution

  • Goyal, Meenakshi
    • Carbon letters
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    • v.5 no.2
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    • pp.55-61
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    • 2004
  • Adsorption isotherms of p-nitrophenol from its aqueous solutions on two samples of activated carbon fibres and two samples of granulated activated carbons have been determined in the concentration range 40~800 mg/L (ppm). The surface of these carbons was modified by oxidation with nitric acid and oxygen gas, and by degassing the carbon surface under vacuum at temperatures of $400^{\circ}C$, $650^{\circ}C$ and $950^{\circ}C$. The oxidation of carbon enhances the amount of carbon-oxygen surface groups, while degassing decreases the amount of these surface groups. The adsorption of p-nitrophenol does not depend upon the surface area alone but appears to be influenced by the presence of oxygen groups on the carbon surface. The adsorption decreases on oxidation while the degassing of the carbon surface enhances the adsorption. The decrease in adsorption depends upon the strength of the oxidative treatment being much larger in case of the oxidation with nitric acid, while the decrease in adsorption on degassing depends upon the temperature of degassing. The results show that while the presence of acidic surface groups which are evolved as $CO_2$ on degassing suppress the adsorption of p-nitrophenol, the presence of non acidic surface groups which are evolved as CO on degassing tend to enhance the adsorption. Suitable mechanisms compatible with the results have been presented.

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