• Title/Summary/Keyword: 고체 촉매

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Humidification Characteristics & Modeling of The Membrane Humidifier for Operation of PEMFCs (고분자전해질 연료전직 운전용 막가습기의 가습특성 및 해석)

  • 박세규;신석재;하흥용;오인환;홍성안;이태희
    • Proceedings of the Korea Society for Energy Engineering kosee Conference
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    • 2002.05a
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    • pp.115-119
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    • 2002
  • 고분자 전해질 연료전지는 전해질로 고체고분자막을 사용하는 연료전지로 고분자막은 수소 이온의 활발한 전달을 위해 일정량의 수분이 존재해야 한다. 따라서 연료전지의 운전 중에 고분자막은 항상 수화되어 있어야 하며 수분이 부족하게 되면 수소이온 전도도가 떨어지고, 막의 수축으로 인해 전극과 막 계면의 저항이 증가한다. 반대로 수분이 많이 존재하면 촉매 표면에 반응기체의 확산이 어려워져 전지 성능이 감소하게 된다.(중략)

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Saccharification of Hardwood Hemicellulose by Solid Acid (고체산에 의한 활엽수 헤미셀룰로오스의 당화)

  • 김성배;이윤영
    • KSBB Journal
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    • v.4 no.2
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    • pp.99-103
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    • 1989
  • The kinetics of secondary hydrolysis of hemicellulose prehydrolyzate by a solid superacid, Nafion, was investigated. The maximum attainable xylose yields determined from continuous column reactor operation were about 90%. Nafion was found to be a stable hydrolytic catalyst provided that the feed solution was free of cationic substances.

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Polymerization of Norbornene with ${\eta}^3$-Allyl Pd(II) Complexes/MAO Catalysts (${\eta}^3$-알릴 Pd(II) 화합물/MAO 촉매를 이용한 노보넨 중합)

  • 윤근병;이동호
    • Polymer(Korea)
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    • v.28 no.3
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    • pp.281-284
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    • 2004
  • 비닐 형태의 부가중합에 의해 생성된 비결정 폴리노보넨은 주사슬이 고리화합물로 이루어져 있으며, 높은 고체밀도와 유리 전이 온도를 나타내며, 낮은 유전상수를 가지는 특징이 있다. 광학적으로 폴리노보넨은 낮은 투과손실을 가지고 있는데, 광통신 대역인 850 nm에서 삽입 손실이 0.1 dB/cm이고, 복굴절이 0.001을 나타내어 광결합 소자 및 광소자에 응용이 기대된다. 이는 주사슬의 고리화합물에 의해 결정화되지 않아, 유리 전이 온도가 28$0^{\circ}C$로 높으면서 비결정의 투명성을 가지기 때문이다.

Property and Catalytic Activity of Heteropoly Acid Supported on MCM-41, 48 Mesoporous Material and SiO2 (MCM-41, 48 메조포러스 물질 및 SiO2에 담지한 헤테로폴리산의 특성 및 촉매적 활성)

  • Park, Jung-Woo;Kim, Beom-Sik;Lee, Jung-Min;Lee, Kwan-Young
    • Applied Chemistry for Engineering
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    • v.10 no.7
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    • pp.1020-1027
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    • 1999
  • Heteropoly acid(HPW) catalysts supported on three different carriers, an amorphous silica, MCM-41 and MCM-48, with different loadings and calcination temperatures have been prepared and characterized by X-ray diffraction, nitrogen physorption, infrared spectroscopy, and $^{31}P$ magic angle spinning NMR. From the result of IR and NMR, it was shown that HPW retains the Keggin structure on the supported catalysts. No HPW crystal phase was developed even at HPW loadings as high as 35 wt % on the MCM-41 and 65 wt % MCM-48. Thus, HPW appeared to form finely dispersed species. In the hydrolysis reaction of di, bis, tri-pentaerythritol, HPW/MCM-41, 48 exhibited higher catalytic activity than $HPW/SiO_2$ or HPW.

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Low-rank Coal Char Gasification Research with Mixed Catalysts at Fixed Reactor (고정층 반응기에서의 저등급 석탄 혼합촉매가스화 반응특성)

  • An, Seung Ho;Park, Ji Yun;Jin, Gyoung Tae;Rhee, Young Woo
    • Korean Chemical Engineering Research
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    • v.55 no.1
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    • pp.99-106
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    • 2017
  • In this study, mixed catalytic char gasification of Indonesia low-rank coal Kideco was investigated under nitrogen atmosphere and isothermal conditions at a fixed reactor. The effects of the temperature were investigated at various temperature (700, 750, 800, $850^{\circ}C$). The effects of blend ratio of catalysts ($K_2CO_3$, Ni) were investigated with different blend ratios (1:9, 3:7, 5:5, 7:3 and 9:1). The sample was prepared by mixing with $K_2CO_3$ physically and by ionexchange method with Ni. The data from thermogravimetric analyzer and gas chromatography were applied to four gassolid reaction kinetic models including shrinking core model, volumetric reaction model, random pore model and modified volumetric reaction model.

Synthesis of TAME, ETBE, and MTBE Using Heteropolyacid Catalyst (헤테로폴리산 촉매를 이용한 TAME, ETBE 및 MTBE 합성반응의 연구)

  • Park, Jin-Hwa;Yi, Yong-Woo
    • Applied Chemistry for Engineering
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    • v.8 no.4
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    • pp.582-588
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    • 1997
  • Synthetic reaction of TAME, ETBE, and MTBE compounds used largely for gasoline octane number enhancer to prevent air pollution was investigated using heteropolyacid catalyst in a fixed bed flow reactor. In the synthetic reaction of TAME, ETBE and MTBE, after hetero atom being replaced with poly atom, the activity of the catalyst, $H_4SiW_{12}O_{40}$ with coordinated bond with W and an hetero atom of Si was the highest among the catalysts tested. Also the activity depended upon the metals replaced which are related to the catalyst acidity. $FeHPW_{12}O_{40}$ and $K_3PM_{o12}O_{40}$ catalysts showed high activity in TAME synthesis, while they were not effective in ETBE and MTBE synthesis. In this study catalysts showing high activity were selected and mixed with equal weight combination of $H_4SiW_{12}O_{40}$ and $Sr_2SiW_{12}O_{40}$ ;$H_4SiW_{12}O_{40}$ and $NaH_2PW_{12}O_{40}$ ; $Fe_{1.5}PW_{12}O_{40}$ and $Mg_2SiW_{12}O_{40}$ ; $Mg_2SiW_{12}O_{40}$ and $Ba_2SiW_{12}O_{40}$. The mixed heteropolyacid catalysts showed higher TBA conversion rate and better selectivity of ETBE and MTBE than the single catalysts.

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Pharmaceutical Characteristics of Korean Lumbricus rubellus Lumbrokinase (한국산 지렁이[Lumbricus rubellus]에서 분리한 Lumbrokinase의 약리학적 특성)

  • 조일환;이철규;임헌길;이형환
    • KSBB Journal
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    • v.19 no.4
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    • pp.274-283
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    • 2004
  • Six lumbrokinase (LK) fractions from Lumbricus rubellus lysates were purified by a series of column chromatographies. The molecular weights of the six LK fractions appeared to range from 24.6 to 33.1 kDa. In the experimental model of rat venous thrombosis, the thrombus weight and PAI activity decreased significantly when the LK was administered orally. However, the activities of APTT, PT and plasmin showed a significant increase. The aggregation of rat platelets pretreated with various LK doses was inhibited by thrombin, and the MDA generation decreased. The rat thoracic aorta and mesentric arteries contracted with phenylephrine relaxed due to the treatment of the LK fractions. These results suggest that the fibrinolytic effects of LK were mediated not only by proteolytic activity, but also by the inhibition of platelet agregation and the relaxation of blood vessels. It is concluded that the LK may be useful as a hemolytic agent for treatment of fibrin clot.

Esterification of Lactic Acid with Alcohols (젓산과 알코올간의 에스테르화 반응)

  • Kim, Jong-Hwa;Han, Jee-Yeun;Lee, Sang-Wha
    • Applied Chemistry for Engineering
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    • v.16 no.2
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    • pp.243-249
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    • 2005
  • Esterification of lactic acid with alcohols catalyzed by Amberlyst-type ion exchange resins and sulfuric acid was carried out in a batch reactor with total /or partial recycle of distilled condensates, respectively. The esterification of lactic acid in the total-recycling reactor (n-butanol/lactic acid = 4, $100^{\circ}C$) was promoted by decreasing the residual water and increasing the mole ratio of n-butanol/lactic acid. Also, it was confirmed that methanol with simple structure and tert-butanol with superior substitution reactivity were more effective in increasing the conversion of esterification reaction, compared to ethanol, n-butanol, and iso-butanol. In a partial-recycling reactor (n-butanol/ammonium lactate = 4, $115^{\circ}C$), the conversion of ammonium lactate into butyl lactate with 1.0 wt% Amberyst-type resins was higher in comparison to that with 0.2 mol $H_2SO_4$ (per 1.0 mol ammonium lactate). The esterification was gradually occurred during the initial stage of reaction in the presence of solid catalyst, whereas the initial addition of $H_2SO_4$ did not affect the initial rate of esterification reaction because of ammonium sulfate formation by the neutralizing reaction of ammonium lactate with sulfuric acid.

Kinetic Study on Char-CO2 Catalytic Gasification of an Indonesian lignite (인도네시아 갈탄의 촤-CO2 촉매가스화 반응특성연구)

  • Lee, Do Kyun;Kim, Sang Kyum;Hwang, Soon Choel;Lee, Si Hoon;Rhee, Young Woo
    • Korean Chemical Engineering Research
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    • v.52 no.4
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    • pp.544-552
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    • 2014
  • In this study, We have investigated the kinetics on the char-$CO_2$ gasification reaction. Thermogravimetric analysis (TGA) experiments were carried out for char-$CO_2$ catalytic gasification of an Indonesian Roto lignite. $Na_2CO_3$, $K_2CO_3$, $CaCO_3$ and dolomite were selected as catalyst which was physical mixed with coal. The char-$CO_2$ gasification reaction showed rapid an increase of carbon conversion rate at 60 vol% $CO_2$ and 7 wt% $Na_2CO_3$ mixed with coal. At the isothermal conditions range from $750^{\circ}C$ to $900^{\circ}C$, the carbon conversion rates increased as the temperature increased. Three kinetic models for gas-solid reaction including the shrinking core model (SCM), volumetric reaction model (VRM) and modified volumetric reaction model (MVRM) were applied to the experimental data against the measured kinetic data. The gasification kinetics were suitably described by the MVRM model for the Roto lignite. The activation energies for each char mixed with $Na_2CO_3$ and $K_2CO_3$ were found a 67.03~77.09 kJ/mol and 53.14~67.99 kJ/mol.

Esterification and Trans-esterification Reaction of Fish Oil for Bio-diesel Production (바이오디젤 생산을 위한 어유의 에스테르화 및 전이에스테르화 반응)

  • Lee, Young-Jae;Kim, Deog-Keun;Lee, Jin-Suk;Park, Soon-Chul;Lee, Jin-Won
    • Clean Technology
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    • v.19 no.3
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    • pp.313-319
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    • 2013
  • To produce biodiesel efficiently from fish oil containing 4% free fatty acid, esterification and trans-esterification were carried out with Vietnam catfish oil, which was kindly provided from GS-bio company. Heterogeneous solid acid catalysts such as Amberlyst-15 and Amberlyst BD-20 and sulfuric acid as homogeneous acid catalyst were used for the esterification of free fatty acids in the fish oil. Sulfuric acid showed the highest removal efficiency of free fatty acid and the shortest reaction time among three acid catalysts. The base catalysts for trans-esterification such as KOH, $NaOCH_3$ and NaOH were compared with each other and KOH was determined to be the best transesterification catalyst. Some solid material, which assumed to be saponified product from glycerol and biodiesel, were observed to form in the fish oil biodiesel when using $NaOCH_3$ and NaOH as the transesterification catalyst. The initial acid value of fish oil was proven to have a negative effect on biodiesel conversion. Of the three catalysts, KOH catalyst transesterification was shown to have high content of FAME and the optimal ratio of methanol/oil ratio was identified to be 9:1.