• 제목/요약/키워드: heterogeneous phase chemical reactions

검색결과 8건 처리시간 0.02초

연소가스내 탈황탈질처리를 위한 저온 플라즈마 기술 (Non-Thermal Plasma Technique for Removing $SO_2$ and $NO_x$ from Combustion Flue Gas)

  • 송영훈;신완호;김석준;장길홍
    • 한국연소학회:학술대회논문집
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    • 한국연소학회 1997년도 제15회 KOSCO SYMPOSIUM 논문집
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    • pp.69-76
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    • 1997
  • Industrial-scale pulse corona process to remove $SO_2$ and $NO_x$ simultaneously from combustion flue gas has been studied. The pilot plant built in the present study treats 2,000 $Nm^3$/hr of flue gas from a boiler. The geometry of the pulse corona reactor is similar to that of an electrostatic precipitator commonly used in industry, A thyratron switch and magnetic pulse compressors, which can generate up to 130 kV of peak pulse voltage and up to 30 kW of average pulse power, have been used to produce pulsed corona. The removal efficiencies of $S0_2$ and $NO_x$ with the present process are maximum of 95 % and 85 %, respectively. Electrical power consumption to produce the pulsed corona, which has been one of the major difficulties to apply this process to industry, has been evaluated in the present study. The results showed that the power consumption can be reduced significantly by simultaneous addition of hydrocarbon injection and heterogeneous phase reactions to the process.

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Polymer-Supported Crown Ethers(Ⅳ) Synthesis and Phase-transfer Catalytic Activity

  • Shim Jae Hu;Chung Kwang Bo;Masao Tomoi
    • Bulletin of the Korean Chemical Society
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    • 제13권3호
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    • pp.274-279
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    • 1992
  • Immobilization method of lariat azacrown ethers, containing hydroxyl group in the side arm of crown ring, on the polymer matrix and the phase-transfer catalytic activity of thus obtained immobilized lariat azacrown ethers were studied. Polystyrene resins with crown ether structures and hydroxyl groups adjacent to the macrorings were prepared by the reaction of crosslinked polystyrene resins containing epoxy groups with monoaza-15-crown-5 or monoaza-18-crown-6. Microporous crosslinked polystyrene resins containing epoxy group for the syntheses of these immobilized lariat crown catalysts were prepared by suspension polymerization of styrene, divinylbenzene (DVB 2%) and vinylbenzylglycidyl ether. The immobilized lariat catalysts with 10-20% ring substitution exhibited maximal activity for the halogen exchange reactions of 1-bromooctane with aqueous KI or NaI under triphase heterogeneous conditions. Immobilized catalyst exhibited higher activity than corresponding catalyst without the hydroxyl group and this result was suggested that the active site have a structure in which the $K^+$ ion was bound by the cooperative coordination of the crown ring donors and the hydroxyl group in the side arm.

불균일 촉매를 이용한 CFC-113a$(CF_3CCl_3)$의 액상 가수소 분해 반응 (Hydrogenolysis of CFC-113a$(CF_3CCl_3)$ Catalyzed by Heterogeneous Catalysts in the Liquid Phase)

  • 조욱재;이익모;김홍곤;김훈식
    • 대한화학회지
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    • 제38권9호
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    • pp.695-700
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    • 1994
  • 여러가지 불균일 촉매$(Rh/Al_2O_3,\;Pd/C,\;Ni,\;Al_2O_3,\;Active\;carbon)$를 이용하여 CFC-113a의 가수소 분해반응을 액상과 기상에서 각각 조사하였다. 액상반응에서는 각 촉매에 따라 반응성은 차이가 났지만, 95% 이상의 높은 선택성으로 $HCFC-123(CF_3CHCl_2)$을 주었다. 특히 $Al_2O-3$가 액상반응에서 상당히 높은 반응성과 선택성을 보인 것은 주목할 만하다. 기상반응의 경우, 전이금속이 포함된 촉매(Pd/C, Pt/C)를 사용하였을 때에는 과수소화물인 $HCFC-133a(CF_3CH_2Cl)$HFC-143a(CF_3CH_3)$가 생성되었다. 한편, 액상반응에서 활성을 보이던 $Al_2O_3$는 기상반응에서는 거의 반응성을 보이지 않았다. $Al_2O_3$의 경우 용매로 THF를 사용하였을 경우에는 비교적 부반응 없이 깨끗하게 반응이 진행되었지만, MeOH를 사용하였을 때는 용매로 부터 $CH_3OCH_3$$CH_3CH_2OCH_3$ 등이 생성되면서 가수소 분해반응이 진행되었다. 따라서 액상반응에서는 용매의 역할이 중요한 것으로 해석하였다.

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Membrane reactors in gas phase oxidations

  • Bottino, A.;Capannelli, G.;Comite, A.;Felice, R.Di
    • 한국막학회:학술대회논문집
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    • 한국막학회 2003년도 The 4th Korea-Italy Workshop
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    • pp.33-36
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    • 2003
  • This research was aimed at developing new catalytic membrane reactors to be used for : i) partial oxidation of toluene (to benzaldehyde and benzoic acid) ii) oxidative dehydrogenation of propane iii) complete oxidation of propane and toluene. The reactor is particularly useful for the optimisation and the industrial development of heterogeneous catalytic processes, particularly for those processes where it is necessary to control the reactants stoichiometry in the reaction zone. This control limits consecutive reactions, thus obtaining high selectivity with industrially interesting conversions. This presentation will concentrate on the partial oxidation of toluene.

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티오시안산 염에 의한 염화벤질의 치환반응에 미치는 상이동 촉매효과 (Phase Transfer Catalytic Effects for Thiocyanate Displacement on Benzyl Chloride)

  • 장승현;윤무홍;김창수;정광보;심재후
    • 대한화학회지
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    • 제33권6호
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    • pp.651-656
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    • 1989
  • 액-액 불균일계에서 염화벤질의 KSCN에 의한 친핵치환반응에 미치는 상이동 촉매 효능을 검토하였다. 반응은 염화벤질의 농도에 의존하는 유사일차 반응이었고, 반응속도 상수$(k_{obsd})$는 촉매농도에 비례하였으며, 반응온도 및 용매 등에 영향을 받았다. 본 치환반응에 대한 상이동 촉매능의 순위는 $NH_4Cl$ < BTMAC < 18-crown-6 < BTEAC < PEG < TBAC < CTMAB 이었다. 반응의 활성화 엔탈피 및 엔트로피는 각각 15∼20 Kcal${\cdot}mo^{l-1}$, -12∼-29 eu.이었으며, 반응은 미세한 유탁액으로 이루어지는 중간상인 interphase에서 일어남을 알 수 있었다.

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Synthesis, Characterization and Catalytic Evaluation of Zinc Fluorides for Biodiesel Production

  • Indrayanah, Sus;Marsih, I Nyoman;Murwani, Irmina Kris
    • 대한화학회지
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    • 제62권1호
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    • pp.7-13
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    • 2018
  • The potential of zinc fluorides with different molar ratios of Zn/F was applied as a solid catalyst in the simultaneous reaction of transesterification and esterification of crude palm oil (CPO) for biodiesel production. These materials were prepared by the fluorolytic sol-gel technique with different fluorine contents. The resulting samples were investigated using elemental analysis, XRD, FT-IR, TG/DTG, $N_2$ physisorption measurements and SEM. The results exhibited that the presence of fluorine strongly affected the catalytic activity in the biodiesel production. The catalysts with smaller fluorine contents (${\leq}1$) showed the best performance in all of the observed samples, yields from 92.94 to 89.95, 87.38 and 85.21% with increasing fluorine contents, respectively. The yield toward the formation of biodiesel depended on the phase and particle sizes of catalysts, but it was not influenced by surface area, pore size, and volume of the samples. The recovered catalyst showed a gradual decrease in activity over three cycles of same reactions.

유기용매 내에서의 유지의 리파제 촉매반응 (Lipase-Catalyzed Reactions for Fats and Oils in Non-Polar Solvent)

  • Daeseok Han;Kwon, Dae-Young;Rhee, Joon-Shick
    • 한국미생물·생명공학회지
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    • 제16권3호
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    • pp.250-258
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    • 1988
  • 리파제는 모노, 디, 트리글리세리드 분자 내의 에스테르 결합을 가수분해 시키는 효소로 잘 알려져 있다. 그런데, 이 효소의 기질인 유지는 물에 용해되지 않아 그 반응이 불균일계에서 일어남으로 리파제 반응의 반응속도론적 해석이 곤란하였다. 이러한 성질은 유지공업에서 리파제를 산업적 촉매로 사용하는데 커다란 장해 요인이 되었었다. 그러나, 최근에 이상계, 역미셀계, 미수계와 같이 반응매질로 유기용매를 도입한 효소반응계가 개발됨에 따라 리파제를 이용한 유지의 전환에 대한 관심이 집중하는 추세에 있다. 리파제를 사용하여 유지를 가수분해시킴으로써 지방간을 생산하고자 할 때 효소반응계로 재래식의 에멀젼보다 이상계 또는 역미셀계를 사용하면 생산성, 굳기름의 가수분해 속도, 생성물 분리등의 측면에서 전체 공정의 효율이 향상될 수 있었다. 한편, 미수계에서 리파제는 에멀젼에서는 불가능한 에스테르 교환반응, 글리세리드 합성, aminolysis, thiotransesterification 및 oximolysis 같은 반응을 촉매 할 수 있는 획기적인 특성을 나타냈다. 공업적 측면에서 이 반응계는 물리적 또는 화학적 특성 (특히 융점)이 변형된 유지를 생산하고자 하는 에스테르 교환반응의 효소반응계로 널리 이용되고 있다. 앞으로 유기용매 내에서 효소의 안정성을 확보할 수 있는 수단 및 연속조작이 가능한 효소반응기의 개발에 관한 연구가 계속된다면 이러한 효소공정이 공업적 제조기술로 발전될 수 있을 것이다.

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광주 지역에서 2015년 10월에 발생한 PM2.5 고농도 사례 특성 분석 (Investigation on Characteristics of High PM2.5 Pollution Occurred during October 2015 in Gwangju)

  • 유근혜;박승식;정선아;조미라;임용재;신혜정;이상보;김영성
    • 한국대기환경학회지
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    • 제34권4호
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    • pp.567-587
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    • 2018
  • A severe haze event occurred in October 2015 in Gwangju, Korea. In this study, the driving chemical species and the formation mechanisms of $PM_{2.5}$ pollution were investigated to better understand the haze event. Hourly concentrations of $PM_{2.5}$, organic and elemental carbon, water-soluble ions, and elemental constituents were measured at the air quality intensive monitoring station in Gwangju. The haze event occurred was attributed to a significant contribution (72.3%) of secondary inorganic species concentration to the $PM_{2.5}$, along with the contribution of organic aerosols that were strongly attributed to traffic emissions over the study site. MODIS images, weather charts, and air mass backward trajectories supported the significant impact of long-range transportation (LTP) of aerosol particles from northeastern China on haze formation over Gwangju in October 2015. The driving factor for the haze formation was stagnant atmospheric flows around the Korean peninsula, and high relative humidity (RH) promoted the haze formation at the site. Under the high RH conditions, $SO{_4}^{2-}$ and $NO_3{^-}$ were mainly produced through the heterogenous aqueous-phase reactions of $SO_2$ and $NO_2$, respectively. Moreover, hourly $O_3$ concentration during the study period was highly elevated, with hourly peaks ranging from 79 to 95ppb, suggesting that photochemical reaction was a possible formation process of secondary aerosols. Over the $PM_{2.5}$ pollution, behavior and formation of secondary ionic species varied with the difference in the impact of LTP. Prior to October 19 when the influence of LTP was low, increasing rate in $NO_3{^-}$ was greater than that in $NO_2$, but both $SO_2$ and $SO{_4}^{2-}$ had similar increasing rates. While, after October 20 when the impact of haze by LTP was significant, $SO{_4}^{2-}$ and $NO_3{^-}$ concentrations increased significantly more than their gaseous precursors, but with greater increasing rate of $NO_3{^-}$. These results suggest the enhanced secondary transformation of $SO_2$ and $NO_2$ during the haze event. Overall, the result from the study suggests that control of anthropogenic combustion sources including vehicle emissions is needed to reduce the high levels of nitrogen oxide and $NO_3{^-}$ and the high $PM_{2.5}$ pollution occurred over fall season in Gwangju.