• Title/Summary/Keyword: KOH catalyst

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Investigation of Liquid Phase Formaldehyde Removal Efficiency by Enzymatic Formaldehyde Dehydrogenase and Catalytic Chemisorption Reactions (탈수소화효소 반응 및 촉매적 흡착 반응에 의한 액상 포름알데하이드의 제거 효율 연구)

  • Ham, Kyu Jin;Park, Min Seob;Choi, Kwon-Young
    • Applied Chemistry for Engineering
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    • v.28 no.1
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    • pp.50-56
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    • 2017
  • Formaldehyde is one of the toxic substances without any color and smell. Several methods to remove formaldehyde has been investigated up to now. Here, both the enzymatic and chemisorptive/catalytic liquid phase formaldehyde removal were investigated, and their catalytic activities in terms of specific activities were compared. Firstly, formaldehyde dehydrogenase (FDH) enzyme from Escherichia coli K12 was cloned, and expressed in Escherichia coli BL21(DE3). And the catalytic activity was characterized as $2.49{\times}10^3sec^{-1}mM^{-1}$ of $k_{cat}/K_m$ with 8.69 U/mg of the specific activity. Secondly, the chemisorptive and oxidative catalytic removals were investigated simultaneously. Activated carbons and zeolites treated with heat, KI, and KOH were used as chemisorption medium. And $Pd/TiO_2$ was used as an oxidative catalyst for the formaldehyde removal. All of the tested chemicals showed similar formaldehyde removal efficiencies of around 50%. However, the specific activity of FDH dependent formaldehyde removal was absolutely higher than that of using chemisorptive and catalytic removal processes with the ranges of 0.01 to 0.26 U/g.

Coffee Grounds Oil Extraction and Bio-diesel Production Study (커피찌꺼기로부터 오일 추출 및 바이오디젤 생산 연구)

  • Kim, Deogkeun;Kim, Sungmin;Choi, Byoungyun;Park, Soonchul
    • 한국신재생에너지학회:학술대회논문집
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    • 2010.06a
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    • pp.250.1-250.1
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    • 2010
  • 최근 석유공급 불안정성과 이산화탄소 배출 규제 움직임에 대응하기 위한 수단으로 바이오연료의 공급이 전세계적으로 증가하고 있다. 이와 같은 바이오디젤의 보급 활성화는 식물성 기름의 가격 상승과 수급 불안정 문제, 그리고 식량자원과의 충돌 문제를 야기하고 있다. 국내 바이오디젤 생산 원료로 사용되는 대두, 유채, 해바라기, 팜 등은 모두 식용시장과 수급 균형을 형성하고 있어 바이오디젤의 생산이 증가하게 되면 식용 오일 시장의 수급균형이 깨져 오일곡물 가격의 변동을 초래하게 될 것이다. 과거에는 수거비용을 들여 폐기하던 폐식용유 마저 이제는 돈을 주고 구입해야하는 실정에 다다랐다. 바이오디젤 생산비의 70~80%를 차지하는 원료유의 부족 현상에 따라 바이오디젤 업계에서는 soapstock, trapped grease, 폐식용유 등의 저급유지 활용 방안을 강구하고 있으며 자트로파와 같은 비식용 작물의 해외플랜테이션도 진행하고 있다. 본 연구에서는 커피찌거기에 남아 있는 오일을 속슬렛추출장치를 이용해 추출하고 전이에스테르화 반응을 수행하여 반응 특성과 커피오일 바이오디젤의 지방산 조성을 알아보고 바이오디젤 원료유로서의 사용가능성에 대해 알아보았다. 석유에테르를 용매로 속슬렛 추출장치를 이용해 추출시 원료대비 약 17%(w/w)의 오일을 추출할 수 있었다. 추출된 오일의 산가는 18.79mgKOH/g으로 매우 높아 직접 전이에스테르화 반응이 불가능하다. 고체 산 촉매 하에서 전처리 반응을 실시하여 유리지방산을 전환 제거한 후 염기촉매를 이용해 전이에스테르화 반응을 진행한 결과 약 80%의 바이오디젤(FAME) 함량을 얻을 수 있었다. 지방산 조성 분석 결과 리놀레익산(Linoleic acid, C18:2), 올레익산(Oleic acid, C18:1), 팔미틱산(Palmitic acid, C16:0)이 대부분을 차지하며 이 중에서도 리놀레익산이 44.17%로 가장 많은 함량을 보였다. 이는 커피찌꺼기 추출 오일이 바이오디젤 원료유로 활용 가능성을 나타내는 결과로, 색소성분 등의 불순물을 효율적으로 제거하여 증류정제 전단계에서의 바이오디젤 순도와 생산 수율을 증대시키기 위한 추가 연구가 필요한 것으로 판단된다.

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Studies on Activity and Characteristics of CuO/ZnO/TiO2 Catalysts for Methanol Steam Reforming (메탄올 수증기 개질반응을 위한 CuO/ZnO/TiO2계 촉매의 활성 및 특성에 관한 연구)

  • Koh, Hyoung-Lim;Kim, Tae-Won;Lee, Jihn-Koo;Kim, Kyung-Lim
    • Applied Chemistry for Engineering
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    • v.9 no.7
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    • pp.956-960
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    • 1998
  • Cu-Zn and Cu-Zn-Ti catalysts for the steam reforming of methanol were prepared. This reaction was carried out at atmospheric pressure, $250^{\circ}C$, steam/methanol molar ratio 1.5, and contact time 0.1 g-cat.hr/mL-feed. In case of the catalyst with 3 mol% of $TiO_2$, the activity was superior to that of catalysts without $TiO_2$. The reaction products were mainly hydrogen and carbon dioxide. It was found that catalytic activity was not related to specific surface area but affected by metallic copper area which was measured by $N_2O$ decomposition and increased with the addition of $TiO_2$ content. XPS and XRD showed that the oxidation state of zinc was not changed during reaction, but oxidation states of copper existed in Cu(0) or Cu(I).

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Catalystic effect of Sludge on $NO_x$ removal in Packed bed reactor (Packed bed형 반응기에서 $NO_x$ 제거에 미치는 슬러지의 촉매효과)

  • Park, Jae-Yoon;Lee, Dong-Hoon;Koh, Hee-Suk;Jung, Jang-Gun;Bae, Myung-Whan;Kim, Jong-Dal
    • Proceedings of the KIEE Conference
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    • 2001.07c
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    • pp.1780-1782
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    • 2001
  • In this experiment, an attempt to use the sludge pellets as catalyst for NO removal from simulated gas is experimentally investigated by using $BaTiO_3$-sludge packed-bed reactor of plate-plate geometry. An experimental investigation has been conducted for NO concentration of 50[ppm] balanced with air, a gas flow rate of 5[1/min]. $BaTiO_3$ pellets are filled at upstream of reactor for corona discharge and sludge pellets are put at downstream of reactor for catalystic effect. The volume rate of sludge pellets to $BaTiO_3$ pellets is 50[%] and AC voltage to dischare the gases was supplied. In the result, when sludge pellets is seperated to $BaTiO_3$ by other reactor and AC voltage is supplied to $BaTiO_3$ and sludge pellets NO, $NO_2$ removal rate is higher. When gas temperature increase from room temperature to 100[$^{\circ}C$], NO removal is decreased while $NO_2$ concentration is independent on gas temperature. This result suggest that the removal mechanism of active oxyzen species and $NO_2$ in sludge is not absorption, but chemical reaction. Temperature of heating treatment is on sludge pellets increased, $NO_x$ removal rate is decrease. It is thought that organic compound is removed by heating treatment.

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Synthesis of Renewable Jet Fuel Precursors from C-C Bond Condensation of Furfural and Ethyl Levulinate in Water

  • Cai, Chiliu;Liu, Qiying;Tan, Jin;Wang, Tiejun;Zhang, Qi;Ma, Longlong
    • Korean Chemical Engineering Research
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    • v.54 no.4
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    • pp.519-526
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    • 2016
  • Biomass derived jet fuel is proven as a potential alternative for the currently used fossil oriented energy. The efficient production of jet fuel precursor with special molecular structure is prerequisite in producing biomass derived jet fuel. We synthesized a new jet fuel precursor containing branched $C_{15}$ framework by aldol condensation of furfural (FA) and ethyl levulinate (EL), where the latter of two could be easily produced from lignocellulose by acid catalyzed processes. The highest yield of 56% for target jet fuel precursor could be obtained at the optimal reaction condition (molar ratio of FA/EL of 2, 323 K, 50 min) by using KOH as catalyst. The chemical structure of $C_{15}$ precursor was specified as (3E, 5E)-6-(furan-2-yl)-3-(furan-2-ylmethylene)-4-oxohex-5-enoic acid ($F_2E$). For stabilization, this yellowish solid precursor was hydrogenated at low temperature to obtain C=C bonds saturated product, and the chemical structure was proposed as 4-oxo-6-(tetrahydrofuran-2-yl)-3-(tetrahydrofuran-2-yl)-methyl hexanoic acid ($H-F_2E$). The successful synthesis of the new jet fuel precursors showed the significance that branched jet fuel could be potentially produced from biomass derived FA and EL via fewer steps.

Effect of Different Zeolite Supported Bifunctional Catalysts for Hydrodeoxygenation of Waste Wood Bio-oil

  • Oh, Shinyoung;Ahn, Sye-Hee;Choi, Joon Weon
    • Journal of the Korean Wood Science and Technology
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    • v.47 no.3
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    • pp.344-359
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    • 2019
  • Effects of various types of zeolite on the catalytic performance of hydrodeoxygenation (HDO) of bio-oil obtained from waste larch wood pyrolysis were investigated herein. Bifunctional catalysts were prepared via wet impregnation. The catalysts were characterized through XRD, BET, and SEM. Experimental results demonstrated that HDO enhanced the fuel properties of waste wood bio-oil, such as higher heating values (HHV) (20.4-28.3 MJ/kg) than bio-oil (13.7 MJ/kg). Water content (from 19.3 in bio-oil to 3.1-16.6 wt% in heavy oils), the total acid number (from 150 in bio-oil to 28-77 mg KOH/g oil in heavy oils), and viscosity (from 103 in bio-oil to $40-69mm^2/s$ in heavy oils) also improved post HDO. In our experiments, depending on the zeolite support, NiFe/HBeta exhibited a high Si/Al ratio of 38 with a high specific surface area ($545.1m^2/g$), and, based on the yield of heavy oil (18.3-18.9 wt%) and HHV (22.4-25.2 MJ/kg), its performance was not significantly affected by temperature and solvent concentration variations. In contrast, NiFe/zeolite Y, which had a low Si/Al ratio of 5.2, exhibited the highest improved quality for heavy oil at high temperature, with an HHV of 28.3 MJ/kg at $350^{\circ}C$ with 25 wt% of solvent.

The Si Microwire Solar Cell Fabricated by Noble Metal Catalytic Etching (Noble metal catalytic etching법으로 제조한 실리콘 마이크로와이어 태양전지)

  • Kim, Jae-Hyun;Baek, Sung-Ho;Choi, Ho-Jin
    • Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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    • 2009.11a
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    • pp.278-278
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    • 2009
  • A photovoltaic device consisting of arrays of radial p-n junction wires enables a decoupling of the requirements for light absorption and carrier extraction into orthogonal spatial directions. Each individual p-n junction wire in the cell is long in the direction of incident light, allowing for effective light absorption, but thin in orthogonal direction, allowing for effective carrier collection. To fabricate radial p-n junction solar cells, p or n-type vertical Si wire cores need to be produced. The majority of Si wires are produced by the vapor-liquid-solid (VLS) method. But contamination of the Si wires by metallic impurities such as Au, which is used for metal catalyst in the VLS technique, results in reduction of conversion efficiency of solar cells. To overcome impurity issue, top-down methods like noble metal catalytic etching is an excellent candidate. We used noble metal catalytic etching methods to make Si wire arrays. The used noble metal is two; Au and Pt. The method is noble metal deposition on photolithographycally defined Si surface by sputtering and then etching in various BOE and $H_2O_2$ solutions. The Si substrates were p-type ($10{\sim}20ohm{\cdot}cm$). The areas that noble metal was not deposited due to photo resist covering were not etched in noble metal catalytic etching. The Si wires of several tens of ${\mu}m$ in height were formed in uncovered areas by photo resist. The side surface of Si wires was very rough. When the distance of Si wires is longer than diameter of that Si nanowires are formed between Si wires. Theses Si nanowires can be removed by immersing the specimen in KOH solution. The optimum noble metal thickness exists for Si wires fabrication. The thicker or the thinner noble metal than the optimum thickness could not show well defined Si wire arrays. The solution composition observed in the highest etching rate was BOE(16.3ml)/$H_2O_2$(0.44M) in Au assisted chemical etching method. The morphology difference was compared between Au and Pt metal assisted chemical etching. The efficiencies of radial p-n junction solar Cells made of the Si wire arrays were also measured.

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Effect of Ozone Injection into Exhaust Gas on Catalytic Reduction of Nitrogen Oxides (촉매 공정의 배기가스 질소산화물 저감 성능에 미치는 오존주입의 영향)

  • Yun, Eun-Young;Mok, Young-Sun;Shin, Dong-Nam;Koh, Dong-Jun;Kim, Kyong-Tae
    • Journal of Korean Society of Environmental Engineers
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    • v.27 no.3
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    • pp.330-336
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    • 2005
  • The ozone injection method was proposed to improve the catalytic process for the removal of nitrogen oxides ($NO_x$). Nitric oxide (NO) in the exhaust gas was first oxidized to nitrogen dioxide ($NO_2$) by ozone produced by dielectric barrier discharge, and then the exhaust gas containing the mixture of NO and $NO_2$ was directed to the catalytic reactor where both NO and $NO_2$ were reduced to $N_2$ in the presence of ammonia as the reducing agent. A commercially available $V_2O_5-WO_3/TiO_2$ catalyst was used as the catalytic reactor. The $NO_2$ content in the mixture of NO and $NO_2$ was changed by the amount of ozone added the exhaust gas. The effect of reaction temperature, initial $NO_x$ concentration, feed gas flow rate, and ammonia concentration on the removal of $NO_x$ at various $NO_2$ contents was examined and discussed. The increase in the content of $NO_2$ by the ozone injection remarkably improved the performance of the catalytic reactor, especially at low temperatures. The present ozone injection method appears to be promising for the improvement of the catalytic reduction of $NO_x$.

Comparative Study on Phenolic Compounds of Cheorwon Onion by Phosphite Treatment (아인산염 처리에 따른 철원양파의 페놀화합물 비교 연구)

  • Kim, Y.B.;Lee, H.J.;Park, C.H.;Kim, D.H.;Koo, H.J.;Chang, K.J.
    • Journal of Practical Agriculture & Fisheries Research
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    • v.20 no.2
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    • pp.105-114
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    • 2018
  • The aim of this study was to evaluate the change of phenolic compounds after phosphite treatment on Cheorwon onion. Onion is a perennial plant belonging to the lily family. It is native to Persia of Southwest Asia. It is widely cultivated in the temperate regions of the world. Onion is a good name for the 'Okchong' to drop blood cholesterol and cardiovascular blood flow to increase the prevention of adult diseases. Cheorwon area is inland, but it has high continental climate due to its high altitude. Therefore it is said that the onion cultivated in this region has higher sugar content and higher taste than onion grown in the southern region. Phosphorus components are particularly important ingredients for promoting muscle development. However, if the phosphoric acid content of the soil part is maintained to a large extent until the harvest, the competition of the nutrients tends to cause decay of the root part. Therefore, it is important to improve the quality and shelf life of onion by inducing nutrient balance by applying foliar fertilization method on the reducing phosphorus at harvest time. In this study, acidity was controlled by diluting phosphorous acid(H3PO3) and potassium hydroxide(KOH), followed by leaf surface treatment with phosphite on onion. In this study, the concentration of phosphite was diluted to 500, 1,000, 1,500ppm and sprayed three times over the onion leaves in May 2018 using an atomizer and harvested at the end of June, and the phenolic compounds were analyzed by HPLC. As a result, the content of quercetin, one of the important substances in onion, was phosphite 500ppm(179.70㎍/g), 1,000(150.27), 1,500(105.95). The contents of caffeic acid, p-coumaric acid, ferulic acid, rutin, kaempferol, and sugar content were higher in the treatments than in the control. Therefore, the phosphite does not have a great influence on the growth, but it may play a role as a method of achieving balance with nitrogen in the rainy season by supplying the role of the material catalyst and the water soluble phosphoric acid and the potassium in the influence of the material change.