• Title/Summary/Keyword: CO2 Rate

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A Model on a Bubbling Fluidized Bed Process for CO2 Capture from Flue Gas (연소기체로부터 CO2를 포집하는 기포 유동층 공정에 관한 모델)

  • Choi, Jeong-Hoo;Youn, Pil-Sang;Kim, Ki-Chan;Yi, Chang-Keun;Jo, Sung-Ho;Ryu, Ho-Jung;Park, Young-Cheol
    • Korean Chemical Engineering Research
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    • v.50 no.3
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    • pp.516-521
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    • 2012
  • This study developed a simple model to investigate effects of important operating parameters on performance of a bubbling-bed adsorber and regenerator system collecting $CO_2$ from flue gas. The chemical reaction rate was used with mean particles residence time of a reactor to determine the extent of conversion in both adsorber and regenerator reactors. Effects of process parameters - temperature, gas velocity, solid circulation rate, moisture content of feed gas - on $CO_2$ capture efficiency were investigated in a laboratory scale process. The $CO_2$ capture efficiency decreased with increasing temperature or gas velocity of the adsorber. However, it increased with increasing the moisture content of the flue gas or the regenerator temperature. The calculated $CO_2$ capture efficiency agreed to the measured value reasonably well. However the present model did not agree well to the effect of the solid circulation rate on $CO_2$ capture efficiency. Better understanding on contact efficiency between gas and particles was needed to interpret the effect properly.

Study of reaction mechanism in pre-reforming for MCFC (MCFC의 예비 개질 반응 메커니즘 연구)

  • Lee, Woo-Hyung;Park, Yong-Ki
    • Industry Promotion Research
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    • v.3 no.2
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    • pp.1-8
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    • 2018
  • In this study, the reaction mechanism of ethane and the reaction rate equation suitable for hydrocarbon reforming were studied. Through the reaction mechanism analysis, it was confirmed that three reactions (CO2 + H2, C2H6 + H2, C2H6 + H2O) proceed during the reforming reaction of ethane, each reaction rate (CO2+H2($r=3.42{\times}10-5molgcat.-1\;s-1$), C2H6+H2($r=3.18{\times}10-5mol\;gcat.-1s-1$), C2H6+H2O($r=1.84{\times}10-5mol\;gcat.-1s-1$)) was determined. It was confirmed that the C2H6 + H2O reaction was a rate determining step (RDS). And the reaction equation of this reaction can be expressed as r = kS * (KAKBPC2H6PH2O) / (1 + KAPC2H6 + KBPH2O) (KA = 2.052, KB = 6.384, $kS=0.189{\times}10-2$) through the Langmuir-Hinshelwood model. The obtained equation was compared with the derived power rate law without regard to the reaction mechanism and the power rate law was relatively similar fitting in the narrow concentration change region (about 2.5-4% of ethane, about 60-75% of water) It was confirmed that the LH model reaction equation based on the reaction mechanism shows a similar value to the experimental value in the wide concentration change region.

Effect of Plating Condition and Surface on Electroless Co-Cu-P Alloy Plating Rate (무전해 Co-Cu-P 도금속도에 미치는 도금 조건과 표면상태의 영향)

  • Oh, L.S.
    • Journal of Power System Engineering
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    • v.4 no.2
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    • pp.31-39
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    • 2000
  • Relationships between the plating condition and the plating rate of the deposition film for the electroless plating of Co-Cu-P alloy were discussed in this report. The result obtained from this experiment were summarized as follow ; The optimum bath composition was consisted of 0.8 ppm thiourea as a stabilizing agent. Composition of the deposit was found to be uniform after two hours of electroless plating. Plating rates of nickel-catalytic surface and zincate-catalytic surface were found to be very closely equal, but the plating time of nickel-catalytic surface took longer than that of the zincated-catalytic surface.

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The Reaction Rate Constants of ${\alpha}-Methylstyrene-co-Methylmethacrylate\;{\alpha}Methylstyrene-co-Acrylonitrile$ (알파메틸스티렌-메틸메타이크릴레이트 및 알파메틸스티렌-아크릴로니트릴의 라디칼 공중합의 반응속도상수)

  • Kim, Nam-Seok;Seul, Soo-Duk
    • Elastomers and Composites
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    • v.28 no.3
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    • pp.183-190
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    • 1993
  • The radical copolymerization with propagation and depropagation is presented in order to estimate reactivity rate of monomers and $K_{11}$(the equilibrium constant for propagation and depropagation) in the copolymerization of ${\alpha}-methylstyrene-co-methylmethacrylate$ and ${\alpha}-methylstyrene-acrylonitrile$. The value of ${\alpha}-methylstyrene$ and methylmethacrylate and $K_{11}$ are found to be 0.48, 0.47 and 5.0 respectively. The value of ${\alpha}-methylstyrene$ and acrylonitrile and the $K_{11}$ are found to be 0.1251, 0.0577 and 23.8 respectively. The treatment rate constant of ${\alpha}-methylstyrene-co-methylmethacrylate$ and ${\alpha}-methylstyrene-co-acrylonitrile$ in the copolymerization is estimated to be 2.5, 80.72 regardless of monomer feed composition.

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Preparation and properties of $LiCoO_2$ cathode for Li rechargeable cell (리튬 2차전지용 $LiCoO_2$양극의 제조 및 특성)

  • 문성인;정의덕;도칠훈;윤문수
    • Electrical & Electronic Materials
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    • v.7 no.4
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    • pp.317-324
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    • 1994
  • In this study, new preparation method of LiCoO$_{2}$ was applied to develop cathode active material for Li rechargeable cell, and followed by X-ray diffraction analysis, electrochemical properties and initial charge/discharge characteristics as function of current density. HC8A72- and CC9A24-LiCoO$_{2}$ were prepared by heating treatment of the mixture of LiOH H$_{2}$O/CoCO$_{3}$(1:1 mole ratio) and the mixture of Li$_{2}$CO$_{3}$/CoCO$_{3}$(1:2 mole ratio) at 850 and 900.deg. C, respectively. Two prepared LiCoO$_{2}$s were identified as same structure by X-ray diffraction analysis. a and c lattice constant were 2.816.angs. and 14.046.angs., respectively. The electrochemical potential of CFM-LiCoO$_{2}$(Cyprus Foote Mineral Co.'s product), HC8A72-LiCoO$_{2}$ and CC9A24 LiCoO$_{2}$ electrode were approximately between 3.32V and 3.42V vs. Li/Li reference electrode. Stable cycling behavior was obtained during the cyclic voltammetry of LiCoO$_{2}$ electrode. According as scan rate increases, cathodic capacity decreases, but redox coulombic efficiency was about 100% at potential range between 3.6V and 4.2V vs. Li/Li reference electrode. Cathodic capacity of HC8A72-LiCoO$_{2}$ was 32% higher than that of CFM-LiCoO$_{2}$ and that of CC9A24-LiCoO$_{2}$ was 47% lower than that of CFM-LiCoO$_{2}$ at 130th cycle in the condition of lmV/sec scan rate. Constant cur-rent charge/discharge characteristics of LiCoO$_{2}$/Li cell showed increasing Ah efficiency with initial charge/discharge cycle. Specific discharge capacities of CFM and HC8A72-LiCoO$_{2}$ cathode active materials were about 93mAh/g correspondent to 34% of theretical value, 110mAh/g correspondent to 40% of theretical value, respectively. In the view of reversibility, HC8A72-LiCoO$_{2}$ was also more excellent than CFM- and CC9A24-LiCoO$_{2}$.

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An Efficient Method for Establishing Canopy Photosynthesis Curves of Lettuce (Lactuca sativa L.) with Light Intensity and CO2 Concentration Variables Using Controlled Growth Chamber (생육 챔버를 이용하여 광도 및 이산화탄소 농도 변수를 갖는 상추(Lactuca sativa L.)의 군락 광합성 곡선의 효율적 도출 방법)

  • Jung, Dae Ho;Kim, Tae Young;Son, Jung Eek
    • Journal of Bio-Environment Control
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    • v.29 no.1
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    • pp.43-51
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    • 2020
  • For developing a canopy photosynthesis model, an efficient method to measure the photosynthetic rate in a growth chamber is required. The objective of this study was to develop a method for establishing canopy photosynthetic rate curves of romaine lettuce (Lactuca sativa L.) with light intensity and CO2 concentration variables using controlled growth chamber. The plants were grown in plant factory modules, and the canopy photosynthesis rates were measured in sealed growth chambers made of acrylic (1.0 × 0.8 × 0.5 m). First, the canopy photosynthetic rates of the plants were measured, and then the time constants were compared between two application methods: 1) changing light intensity (340, 270, 200, and 130 μmol·m-2·s-1) at a fixed CO2 concentration (1,000 μmol·mol-1) and 2) changing CO2 concentration (600, 1,000, 1,400, and 1,800 μmol·mol-1) at a fixed light intensity (200 μmol·m-2·s-1). Second, the canopy photosynthetic rates were measured by changing the light intensity at a CO2 concentration of 1,000 μmol·mol-1 and compared with those measured by changing the CO2 concentration at a light intensity of 200 μmol·m-2·s-1. The time constant when changing the CO2 concentration at the fixed light intensity was 3.2 times longer, and the deviation in photosynthetic rate was larger than when changing the light intensity. The canopy photosynthetic rate was obtained stably with a time lag of one min when changing the light intensity, while a time lag of six min or longer was required when changing the CO2 concentration. Therefore, changing the light intensity at a fixed CO2 concentration is more appropriate for short-term measurement of canopy photosynthesis using a growth chamber.

Kinetics of Seed Growth of α-Ferric Oxyhydroxide (α-Ferric oxyhydroxide 입자의 핵성장 반응에 관한 연구)

  • Seul, Soo-Duk;Shin, Dong-Ock
    • Applied Chemistry for Engineering
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    • v.8 no.4
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    • pp.602-609
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    • 1997
  • The seed formation and growth of $\alpha$-ferric oxyhydroxide with aerial oxidative precipitation from aqueous solution of ferrous sulfate with KOH, NaOH, $Na_2CO_3$ and $K_2CO_3$ as precipitants have been studied by free pH drift experiment. It has been shown that all precipitants give same particle formation and growth path, and average particle length from KOH and NaOH as precipitants was about 1.5 times shorter than that of $K_2CO_3$ and $Na_2CO_3$. When initial mole ratio, $R_o=[Fe^{2+}]_o/[OH^-]_o$ of KOH was decreased the particle was grown oxyhydroxide seed growth from aqueous solution of ferrous sulfate with KOH has been studied. The influence of the air flow rate, reaction temperature and initial mole ratio, $R_o=[Fe^{2+}]_o/[OH^-]_o$, on the kinetics of seed growth are investigated by static pH experiment. The oxidation rate of seed growth increased with increase in the air low rate, reaction temperature and initial mole patio. The activation energy of seed growth is 16.16 KJ/mol and the rate equation of seed growth can be written as follows: $-\frac{d[Fe^{2+}]}{dt}=1.46{\times}10^4[P_{o2}]^{0.66}[OH^-]^{2.19}exp(-\frac{16.16}{dt})$.

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Early Hydration of Tricalcium Silicate(II) (Tricalcium Silicate의 초기수화반응(II))

  • 오희갑;최상흘
    • Journal of the Korean Ceramic Society
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    • v.24 no.2
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    • pp.133-138
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    • 1987
  • The behavior of CaO and SiO2 in the reaction produced which produced in the early hydration of C3S was studied by XRD and thermal analyzer. Polymerization of hydrated siltcates was also studied by TMS method. TMS derivatives were separated by gaschromatography. Cao/SiO2 molar ratios of the produced CSH gel under the air atmosphere were higher than that in the CO2. Dimerization rate of hydrated silicates was very fast in the early hydration stage. Trimer began to appear later than dimer and its increasing rate was very low. The amount of dimer and trimer formed under the CO2 atmosphere was less than that in the air.

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Effects of Picking Season, Size and Storage Conditions on Respiratory Characteristics of Korean Fresh Ginseng (Panax ginseng C. A. Meyer) (수삼의 수확시기, 크기 및 저장조건에 따른 호흡특성)

  • Kim Eun-Jeong;Seo Ja-Young;Hong Seok-In;Kim Dongman
    • Food Science and Preservation
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    • v.12 no.6
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    • pp.529-533
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    • 2005
  • The respiratory characteristics of Korean fresh ginseng were investigated from the aspect of picking season, size, and storage temperature and period to get basic data for extension of shelf-life. The respiration rate of fresh ginseng picked in March was 4.09 mL $CO_2/kg{\cdot}hr$ at $0^{\circ}C$. It was gradually increased to August, 7.88 mL $CO_2/kg{\cdot}hr$ at $0^{\circ}C$, and then decreased continuously until November. Although the rate of fresh ginseng was different by picking season, the respiration quotient showed the same level, $1.03\~1.07$. Respiration rate by size was ranged from 3.47 to 5.69 mL $CO_2/kg{\cdot}hr$ at $0^{\circ}C$, and smaller in the size was higher in the rate. $Q_{10}$ value of fresh ginseng was $2.68\~2.88$ when the temperature increased from $0^{\circ}C\;to\;10^{\circ}C$ and $1.77\~2.16$ from $10^{\circ}C\;to\;20^{\circ}C$, and it was slightly different by picking season. At the beginning of storage the respiration rate was 7.0 mL $CO_2/kg{\cdot}hr$ and it was .decreased to 3.38 mL $CO_2/kg{\cdot}hr$ after storage for 90 days at $0^{\circ}C$.

A Study on CO2 injectivity with Nodal Analysis in Depleted Oil Reservoirs (고갈 유전 저류층에서 노달분석을 이용한 CO2 주입성 분석 연구)

  • Yu-Bin An;Jea-Yun Kim;Sun-il Kwon
    • Journal of the Korean Institute of Gas
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    • v.28 no.2
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    • pp.66-75
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    • 2024
  • This paper presents development of a CO2 injectivity analysis model using nodal analysis for the depleted oil reservoirs in Malaysia. Based on the final well report of an appraisal well, a basic model was established, and sensitivity analysis was performed on injection pressure, tubing size, reservoir pressure, reservoir permeability, and thickness. Utilizing the well testing report of A appraisal well, permeability of 10md was determined through production nodal analysis. Using the basic input data from the A appraisal well, an injection well model was set. Nodal analysis of the basic model, at the bottomhole pressure of 3000.74psia, estimated the CO2 injection rate to be 13.29MMscfd. As the results of sensitivity analysis, the injection pressure, reservoir thickness, and permeability tend to exhibit a roughly linear increase in injection rate when they were higher, while a decrease in reservoir pressure at injection also resulted in an approximate linear increase in injection rate. Analyzing the injection rate per inch of tubing size, the optimal tubing size of 2.548inch was determined. It is recommended that if the formation parting pressure is known, performing nodal analysis can predict the maximum reservoir pressure and injection pressure by comparing with bottomhole pressure.