• Title/Summary/Keyword: carbon conversion

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Characteristics of Coal Methanation in a Hydrogasifier (수소가스화기에서 석탄의 메탄화 반응 특성)

  • Lee, S.H.;Yoon, S.J.;Choi, Y.C.;Kim, J.H.;Lee, J.G .
    • Korean Chemical Engineering Research
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    • v.44 no.6
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    • pp.631-635
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    • 2006
  • To investigate the characteristics of substitute natural gas (SNG) production from direct coal methanation, the continuous lab-scale entrained flow hydrogasifier (I.D. : 0.025 m, Height : 1.0 m) was used in this experiment. The hydrogasification system consisted of high pressure gas handling system, high pressure coal feeder, entrained flow hydrogasifier, and unreacted char separator. The experiment was performed at the various conditions of reaction temperature ($600{\sim}800^{\circ}C$), $H_2$/coal ratio (0.2~0.4), and coal feed rate (0.8~2.5 g/min). Although it was shown that carbon conversion was different trends with coals from the methanation results for 6 sample coals, the carbon conversion increased with increasing reaction temperature. And it increased with increasing H2/coal ratio, whereas the concentration of CH4 decreased. Also. the carbon conversion increased with the carbon content of coal sample and had a maximum value at volatile matter content of 35 wt%.

Application of Pt/C (60 wt.%) on electrode catalyst layer of direct methanol fuel cell (백금담지 촉매의 직접메탄올 연료전지 환원전극 적용)

  • Cho, Yong-Hun;Cho, Yoon-Hwan;Park, Hyun-Seo;Jung, Nam-Gee;Sung, Yung-Eun
    • 한국신재생에너지학회:학술대회논문집
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    • 2007.06a
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    • pp.188-190
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    • 2007
  • The MEA with the catalyst layer containing PtRu black and 60 wt. %Pt/C as their anode and cathode catalysts. For find to effect of carbon support, the MEA with platinum black for cathode catalyst was fabricated. The performance of the MEA with the catalyst layer containing (PtRu black:60 wt.% Pt/C) as their anode and cathode catalyst has shown competitively higher value than the performance of the MEA with the catalyst layer containing (PtRu black:Pt black) as their anode and cathode catalyst.

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Conversion of CO2 and CH4 through Hybrid Reactor Composed of Plasma and Catalyst at Atmospheric Pressure (상압 플라즈마-촉매 하이브리드 반응기를 통한 CO2와 CH4의 전환처리)

  • Kim, Tae Kyung;Nguyen, Duc Ba;Lee, Won Gyu
    • Applied Chemistry for Engineering
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    • v.25 no.5
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    • pp.497-502
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    • 2014
  • The conversion reaction of methane and carbon dioxide at an atmospheric pressure plasma reactor filled with Ni-$Al_2O_3$ and Ni-$MgAl_2O_4$ catalyst was performed. Effects of various process parameters such as the applied electric power, reaction gas flow rate, reactor temperature, mixing ratio of reactants and the presence of the catalyst on the reaction between methane and carbon dioxide were analyzed. From the analysis of the contribution of the catalyst in the reaction step, even if the temperature raised to $400^{\circ}C$, there was no spontaneous catalytic conversion of methane and carbon dioxide without plasma discharges. When the catalysts for the conversion of methane and carbon dioxide would be adopted to the plasma reactor, the careful selection of suitable catalysts and process parameters should be essential.

Pyrolysis kinetics and microstructure of thermal conversion products on toluene soluble component from two kinds of modified pitch

  • Zhu, Yaming;Zhao, Xuefei;Gao, Lijuan;Cheng, Junxia
    • Carbon letters
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    • v.28
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    • pp.38-46
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    • 2018
  • Modified pitch A (MPA) and modified pitch B (MPB) were prepared by oxidative polymerization and thermal polycondensation reaction with refined pitch as the raw material, respectively. The toluene soluble components (TS-1 and TS-2) were obtained by solvent extraction from MPA and MPB, separately. The Flynn-Wall-Ozawa method and Kissinger-Akahira-Sunose method were used to calculate the pyrolysis activation energy of TS. The Satava-Sestak method was used to investigate the pyrolysis kinetic parameters of TS. Moreover, the optical microstructure of the thermal conversion products (TS-1-P and TS-2-P) by calcination shows that TS-1-P has more contents of mosaic structure and lower contents of fine fiber structure than TS-2-P. The research result obtained by a combination of X-ray diffraction and the curve-fitting method revealed that the ratios of ordered carbon crystallite (Ig) in TS-1-P and TS-2-P were 0.3793 and 0.4417, respectively. The distributions of carbon crystallite on TS-1-P and TS-2-P were calculated by Raman spectrum and curve-fitting analysis. They show that the thermal conversion product of TS-2 has a better graphite crystallite structure than TS-1.

Assessing Organic Matter and Organic Carbon Contents in Soils of Created Mitigation Wetlands in Virginia

  • Ahn, Changwoo;Jones, Stacy
    • Environmental Engineering Research
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    • v.18 no.3
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    • pp.151-156
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    • 2013
  • Several soil properties were studied from three young created mitigation wetlands (<10 years old), which were hydrologically comparable in the Piedmont region of Virginia. The properties included soil organic matter (SOM), soil organic carbon (SOC), pH, gravimetric soil moisture, and bulk density ($D_b$). No significant differences were found in the soil properties between the wetlands, except SOM and SOC. SOM and SOC indicated a slight increase with wetland age; the increase was more evident with SOC. Only about a half of SOC variability found in the wetlands was explained by SOM ($R^2$ = 0.499, p < 0.05). The majority of the ratios of SOM to SOC for these silt-loam soils ranged from 2.0 to 3.5, which was higher than the 1.724 Van Bemmelen factor, commonly applied for the conversion of SOM into SOC in estimating the carbon storage or accumulation capacity of wetlands. The results may caution the use of the conversion factor, which may lead to an overestimation of carbon sequestration potentials of newly created wetlands. SOC, but not SOM, was also correlated to $D_b$, which indicates soil compaction typical of most created wetlands that might limit vegetation growth and biomass production, eventually affecting carbon accumulation in the created wetlands.

Reduction Characteristics of Oxygen Carrier Particles for Chemical-looping Combustor with Different Fuels (매체순환식 가스연소기용 산소공여입자들의 연료별 연소특성)

  • Ryu, Ho-Jung;Kim, Kyung-Su;Park, Yeong-Seong;Park, Moon-Hee
    • Transactions of the Korean hydrogen and new energy society
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    • v.20 no.1
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    • pp.45-54
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    • 2009
  • Reduction reactivity and carbon deposition characteristics of three oxygen carrier particles(OCN01, OCN02, OCN03) have been investigated by using hydrogen, methane, syngas, and natural gas as fuels. For all particles, the maximum conversion, the oxygen transfer capacity, and the degree of carbon deposition increased as the reactive carbon contents increased. The reduction rate and the oxygen transfer rate increased as the moles of required oxygen per input gas increased. The change of maximum conversion, reduction rate, oxygen transfer capacity, oxygen transfer rate and degree of carbon deposition for different fuels can be explained consistently by using parameters such as the reactive carbon contents and the moles of require oxygen per input gas.

Nano-structured Carbon Support for Pt/C Anode Catalyst in Direct Methanol Fuel Cell

  • Choi Jae-Sik;Kwon Heock-Hoi;Chung Won Seob;Lee Ho-In
    • Journal of Powder Materials
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    • v.12 no.2 s.49
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    • pp.117-121
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    • 2005
  • Platinum catalysts for the DMFC (Direct Methanol Fuel Cell) were impregnated on several carbon supports and their catalytic activities were evaluated with cyclic voltammograms of methanol electro-oxidation. To increase the activities of the Pt/C catalyst, carbon supports with high electric conductivity such as mesoporous carbon, carbon nanofiber, and carbon nanotube were employed. The Pt/e-CNF (etched carbon nanofiber) catalyst showed higher maximum current density of $70 mA cm^{-2}$ and lower on-set voltage of 0.54 V vs. NHE than the Pt/Vulcan XC-72 in methanol oxidation. Although the carbon named by CNT (carbon nanotube) series turned out to have larger BET surface area than the carbon named by CNF (carbon nanofiber) series, the Pt catalysts supported on the CNT series were less active than those on the CNF series due to their lower electric conductivity and lower availability of pores for Pt loading. Considering that the BET surface area and electric conductivity of the e-CNF were similar to those of the Vulcan XC-72, smaller Pt particle size of the Pt/e-CNF catalyst and stronger metal-support interaction were believed to be the main reason for its higher catalytic activity.

Development of a Plasma-Dump Reformer for Syngas Production (합성가스 생산을 위한 플라즈마-덤프 개질기 개발)

  • Lim, Mun Sup;Kim, Eun Hyuk;Chun, Young Nam
    • Transactions of the Korean hydrogen and new energy society
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    • v.25 no.6
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    • pp.586-593
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    • 2014
  • Limited sources of fossil fuels and also global climate changes caused by $CO_2$ emissions are currently discussed around the world. As a renewable, carbon neutral and widely available energy source, biogas is regarded as a promising alternative to fossil fuels. In this study, a plasma dump reformer was proposed to produce $H_2$-rich synthesis gas by a model biogas. The three-phase gliding arc plasma and dump combustor were combined. Screening studies were carried out with the parameter of a dump injector flow rate, water feeding flow rate, air ratio, biogas component ratio and input power. As the results, methane conversion rate, carbon dioxide conversion rate, hydrogen selectivity, carbon monoxide yield at the optimum conditions were achieved to 98%, 69%, 42%, 24.7%, respectively.

Fast and Soft Functionalization of Carbon Nanotube with -SO3H, -COOH, -OH Groups for Catalytic Hydrolysis of Cellulose to Glucose

  • Lusha, Qin;Lee, Sungho;Li, Oi Lun
    • Journal of the Korean institute of surface engineering
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    • v.53 no.3
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    • pp.87-94
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    • 2020
  • Herein, sulfonated carbon nanotubes (CNT) have been prepared in dilute sulfuric acid (H2SO4) via a novel sulfonation approach based on gas-liquid interfacial plasma (GLIP) at room temperature. The sulfonic acid groups and total acid groups densities of CNT after GLIP treatment in 2 M H2SO4 for 45 min can reach to 0.53 mmol/g and 3.64 mmol/g, which is higher than that of sulfonated CNT prepared under 0.5 M / 1 M H2SO4. The plasma sulfonated CNT has been applied as catalysts for the conversion of microcrystalline cellulose to glucose. The effect of hydrolysis temperature and hydrolysis time on the conversion rate and product distribution have been discussed. It demonstrates that the total conversion rate of cellulose increasing with hydrolysis temperature and hydrolysis time. Furthermore, the GLIP sulfonated CNT prepared in 2 M H2SO4 for 45 min has shown high catalytic stability of 85.73 % after three cycle use.

Rate Capability of Electric Double-Layer Capacitor (EDLC) Electrodes According to Pore Length in Spherical Porous Carbons

  • Ka, Bok-H.;Yoon, Song-Hun;Oh, Seung-M.
    • Journal of the Korean Electrochemical Society
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    • v.10 no.4
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    • pp.252-256
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    • 2007
  • A series of spherical porous carbons were prepared via resorcinol-formaldehyde (RF) sol-gel polymerization in the presence of cationic surfactant (CTAB, cetyltrimethylammonium bromide), wherein the carbon sphere size was controlled by varying the CTAB introduction time after a pre-determined period of addition reaction (termed as "pre-curing"). The sphere size gradually decreases with an increase in the pre-curing time within the range of 30-150 nm. The carbons possess two types of pores; one inside carbon spheres (intra-particle pores) and the other at the interstitial sites made by carbon spheres (inter-particle pores). Of the two, the surface exposed on the former was dominant to determine the electric double-layer capacitor (EDLC) performance of porous carbons. As the intra-particle pores were generated inside RF gel spheres by gasification, the pore diameter was similar for all these carbons, thereby the pore length turned out to be a decisive factor controlling the EDLC performance. The charge-discharge voltage profiles and complex capacitance analysis consistently illustrate that the smaller-sized RF carbons deliver a better rate capability, which must be the direct result of facilitated ion penetration into shorter pores.