• Title/Summary/Keyword: 수소수율

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Reaction characteristics of hydrocarbon fuels under various operation conditions of hydro-upgrading process for vegetable oil-based bio-jet fuel production (식물성 오일 기반 바이오항공유 제조공정에서 수소첨가 업그레이딩을 위한 운전조건에 따른 탄화수소화합물의 특성)

  • Kwak, Yeonsu;Jang, Jung Hee;Kim, Sungtak;Ahn, Minhwei;Lee, Eun-Sil;Han, Gi Bo;Jeong, Byung Hun;Han, Jeong Sik;Jeon, Cheol-Hwan
    • Journal of the Korean Applied Science and Technology
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    • v.35 no.3
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    • pp.731-743
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    • 2018
  • In bio-jet fuel production, selecting operating conditions of hydro-upgrading is of great importance to make iso-Paraffin rich hydrocarbons with carbon distribution including jet fuel range. Herein, iso-Paraffin rich biofuel including jet fuel range hydrocarbons ($C_8-C_{16}$) is produced from simultaneous cracking and isomerization using n-Paraffin rich hydrocarbon derived from hydrotreated vegetable oil over 0.5 wt..% Pt/Zeolite catalyst. We report and analyze the yields and compositions in the produced hydrocarbons affected by various operating conditions, such as reaction temperature, reaction pressure, molar ratio of reactants, and weight hourly space velocity. Aforementioned operating conditions not only can help interpret the reaction dynamics of hydro-upgrading, but also further produce bio jet-fuel after distillation.

The Study of Model Biogas Catalyst Reforming Using 3D IR Matrix Burner (3D IR 매트릭스 버너에 의한 모사 바이오가스 촉매 개질 연구)

  • Lim, Mun Sup;Chun, Young Nam
    • Journal of Korean Society of Environmental Engineers
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    • v.34 no.12
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    • pp.840-846
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    • 2012
  • Global climate changes caused by $CO_2$ emissions are currently debated around the world; green sources of energy are being sought as alternatives to replace fossil fuels. The sustainable use of biogas for energy production does not contribute to $CO_2$ emission and has therefore a high potential to reduce them. Catalytic steam reforming of a model biogas ($CH_4:CO_2$ = 60%:40%) is investigated to produce $H_2$-rich synthesis gas. The biogas utilized 3D-IR matrix burner in which the surface combustion is applied. The ruthenium catalyst was used inside a reformer. Parametric screening studies were achieved as Steam/Carbon ratio, biogas component ratio, Space velocity and Reformer temperature. When the condition of Steam/Carbon ratio, $CH_4/CO_2$ ratio, Space velocity and Refomer temperature were 3.25, 60% : 40%, $14.7L/g{\cdot}hr$ and $550^{\circ}C$ respectively, the hydrogen concentration and methane conversion rate were showed maximum values. Under the condition mentioned above, $H_2$ yield, $H_2$/CO ratio, CO selectivity and energy efficiency were 0.65, 2.14, 0.59, 51.29%.

Hydrogen Production for PEMFC Application in Plasma Reforming System (PEMFC용 플라즈마 개질 시스템의 수소 생산)

  • Yang, Yoon Cheol;Chun, Young Nam
    • Korean Chemical Engineering Research
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    • v.46 no.5
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    • pp.1002-1007
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    • 2008
  • The purpose of this paper studied the optimal hydrogen production condition of plasma reforming system to operate the PEMFC. Plasma reforming reactor used with Ni catalyst reactor at the same time, So $H_2$ concentration increased. Also the WGS and PrOx reactor were designed to remove CO concentration under 10 ppm, because CO has effect on catalyst poisoning of PEMFC. The maximum $H_2$ production condition in plasma reforming system was S/C ratio 3.2, $CH_4$ flow rate 2.0 L/min, catalytic reactor temperature $700{\pm}5^{\circ}C$ and input power 900 W. At this time, the concentration of produced syngas was $H_2$ 70.2%, CO 7.5%, $CO_2$ 16.2%,$CH_4$ 1.8%. The hydrogen yield, hydrogen selectivity and $CH_4$ conversion rate were 56.8%, 38.1% and 92.2% respectively. The energy efficiency and specific energy requirement were 37.0%, 183.6 kJ/mol. In additional, The experiment of $CO_2/CH_4$ ratio proceeded. Also WGS reactor experiment was proceeding on optimum condition of plasma reactor and the exit concentration were $H_2$ 68%, CO 337 ppm, $CO_2$ 24.0%, $CH_4$ 2.2%, $C_2H_4$ 0.4%, $C_2H_6$ 4.1%. At this time, experiment result of PrOx reactor were $H_2$ 51.9%, CO 0%, $CO_2$ 17.3%.

Generation of Hydrogen from Hydrolysis Reaction of NaBH4 Using Fresh Water (담수 사용 NaBH4 가수 분해반응에 의한 수소발생)

  • Oh, Sohyeong;Yoo, Donggeun;Kim, Taeho;Kim, Ikgyun;Park, Kwon-Pil
    • Korean Chemical Engineering Research
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    • v.59 no.4
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    • pp.503-507
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    • 2021
  • Sodium borohydride, NaBH4, has many advantages as hydrogen source for portable proton exchange membrane fuel cells (PEMFC). When PEMFC is used outdoors as a transport type, it is economical to hydrolyze NaBH4 using fresh water instead of distilled water. Therefore, in this study, hydrogen was generated using fresh water instead of distilled water during the NaBH4 hydrolysis process. The properties of NaBH4 hydrolysis were studied using an activated carbon-supported Co-P-B/C catalyst. Fresh water did not generate tetrahydrate during the NaBH4 hydrolysis process, and distilled water produced tetrahydrate by-products, which consumed a lot of water during the hydrolysis process, indicating that at the end of the reaction at a high concentration of 25% or more of NaBH4, dry by-products and unreacted NaBH4 remained. As a result, when fresh water was used, the hydrogen yield and hydrogen generation rate were higher than that of distilled water at a high concentration of 25% or more of NaBH4, indicating that it is suitable for use in transport-type fuel cells such as unmanned aerial vehicles.

Study of Catalytic Performance of $La_{0.7}Sr_{0.3}Cr_{1-x}Ni_{x}O_{3}$ Perovskite for Steam Reforming of Propane ($La_{0.7}Sr_{0.3}Cr_{1-x}Ni_{x}O_{3-{\delta}$ Perovskite 촉매의 프로판 수증기 개질 반응에서의 특성 연구)

  • Kim, Jae-Ro;Kim, Nak-Hyeon;Sohn, Jung-Min
    • Korean Chemical Engineering Research
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    • v.49 no.6
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    • pp.715-719
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    • 2011
  • The $La_{0.7}Sr_{0.3}Cr_{1-x}Ni_{x}O_{3}$(LSCN-x) perovskites were prepared by citric acid and EDTA using a sol-gel method. The LSCN-x was characterized by BET, XRD, SEM, $H_2$-TPR, EA and TEM. The catalytic performance of LSCN-x catalysts in steam reforming of propane in the temperature range 600~$800^{\circ}C$ was investigated. Propane conversion and hydrogen yield increased with an increase in the amount of added Ni up to x=0.5 in the B-site, denoted as LSCN-0.5, under S/C=1 and S/C=1.7 reaction conditions. The LSCN-0.5 catalyst exhibited the best performance under Ni-substitution of which propane conversion and hydrogen yield was 100%, 95.9% at $800^{\circ}C$ in the S/C=1.7 condition, respectively. The morphology of carbon deposited on the catalysts after reaction exhibited filamentous carbon and amount of carbon deposited on the catalysts after reaction increased with an increase in the amount of added Ni.

Toxicity Reduction and Improvement of Anticancer Activities from Rhodiola sachalinensis A. Bor by Ultra High Pressure Extracts Process (초고압 공정에 의한 홍경천의 독성 감소 및 항암활성 증진)

  • Kim, Cheol-Hee;Kwon, Min-Chul;Qadir, Syed Abdul;Hwang, Baik;Nam, Jong-Hyeon;Lee, Hyeon-Yong
    • Korean Journal of Medicinal Crop Science
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    • v.15 no.6
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    • pp.411-416
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    • 2007
  • This study was performed to investigate the reduction of toxicity and improvement of anticancer activities from R. sachalinensis by ultra high pressure extracts process. The cytotoxicity on human kidney cell (HEK293) and human lung cell (HEL299) was showed below 20.4% and 21.6% as compare to normal extracts in adding 1.0 $mg/m{\ell}$ concentration. This showed that toxic materials through ultra high pressure processing is broken or degraded. Because bond such as hydrogen bond, electrostatic bond, Van der waals bond, the hydrophobic bond, can be broken by high pressure. The anticancer activity was also increased in over 7% by high pressure processing in A549, AGS, MCF-7 and Hep3B cells. The result showed that extraction by high pressure have low cytotoxicity and high anticancer activity. So, the high pressure extraction technology can play an important role in eruption of new material with high biological activity.

Study on Torrefaction Characteristics of Baggase (사탕수수 부산물의 반탄화 특성에 관한 연구)

  • Jeeban, Poudel;Kim, Won-Tae;Ohm, Tae-In;Oh, Sea Cheon
    • Korean Chemical Engineering Research
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    • v.52 no.5
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    • pp.672-677
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    • 2014
  • Torrefaction is a thermal treatment process to pre-treat biomass at temperature of $200{\sim}300^{\circ}C$ under an inert atmosphere. It was known that torrefaction process strongly depended on the decomposition temperature of the lignocellulosic constituents in biomass. In this work, the torrefaction characteristics of baggase has been studied. This study focuses on the relation between the energy yields, heating values, gas emission, volatile and ash constituents with torrefaction temperatures and times. The activation energies of baggase torrefaction has been studied by using TGA (Thermogravimetric Analyzer). From this work, it was seen that ash constituents and heating values were increased with torrefaction temperature, while volatile constituents and energy yields decreased. It was also found that carbon monoxide containing oxygen were decomposed at a lower temperature than those of hydrocarbon compounds, $C_xH_y$.

A Study on Torrefaction Characteristics of Sewage Sludge (하수슬러지의 반탄화 특성에 관한 연구)

  • Lim, Dae-Won;Poudel, Jeeban;Oh, Sea Cheon
    • Applied Chemistry for Engineering
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    • v.25 no.5
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    • pp.510-514
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    • 2014
  • In this work, the effect of torrefaction on the basic characteristic of sewage sludge was studied to evaluate the energy potential as a solid fuel. Torrefaction experiments were performed at temperatures of $150{\sim}600^{\circ}C$. The torrefied sewage sludge was characterized by the energy yield, ash content, volatile fraction and high heating value (HHV). The gaseous products from torrefaction of the sewage sludge were also analyzed. Thermogravimetric analysis was carried out for the kinetic analysis of sewage sludge torrefaction. From this work, it was found that the ash content increased with an increase of the torrefaction temperature while the energy yield, HHV and volatile fraction decreased. It was also found that the emission of carbon monoxide and hydrocarbon gases started at $300^{\circ}C$ by the thermal degradation of volatile components in the sewage sludge.

A Study on the Catalytic Reduction of Carbon Dioxide by Methane (메탄에 의한 이산화탄소의 환원반응에 관한 연구)

  • Hong, Seong-Soo;Yang, Jin-Seop;Kim, Byung-Kee;Ju, Chang-Sik;Lee, Gun-Dae
    • Applied Chemistry for Engineering
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    • v.8 no.4
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    • pp.685-693
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    • 1997
  • We have studied the reforming of carbon dioxide with methane over various supported nickel catalysts. The nickel supported on natural zeolite showed the highest activity and the nickel on acidic support showed higher activity and slow deactivation compared to nickel on basic support. The activity of nickel on natural zeolite increased with increasing loading ratio and showed almost constant activity above 10wt.% loading of nickel. The conversion and yield of products were affected by the mole ratio of reactants and the highest yields of CO and $H_2$ were obtained at $CH_4/CO_2=1$. The deactivation of catalyst was caused by deposition of coke which was formed by the decomposition of methane. The shape of coke was shown to be whisker tripe carbon, and it brought out the slow deactivation of catalyst.

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Preparation of Synthesis Gas from Methane in a Capacitive rf Discharge (용량성 rf 플라즈마를 이용한 메탄으로부터의 합성가스 제조)

  • Song, Hyung Keun;Choi, Jae-Wook;Lee, Hwaung;Kim, Seung-Soo;Na, Byung-Ki
    • Clean Technology
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    • v.12 no.3
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    • pp.138-144
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    • 2006
  • Conversion of methane to synthesis gas in a capacitive rf plasma at low pressure was experimentally studied. In this plasma, electrons which had sufficient energy-level collided with the molecules of methane or oxygen-containing gas, which were than activated and converted to synthesis gas. The effect of input power, various oxygen-containing gas and composition of the gas mixture were investigated. The conversion of methane reached up to 100%. In all cases, hydrogen and carbon oxide were produced as primary products, and other compounds was generated. The conversion of methane and the yield of hydrogen and carbon oxides were increased with increasing the input power. Depending on the oxygen-containing gases, the composition of synthesis gas was varied.

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