Studies on Kinetics of Carbon Dioxide Conversion under Atmospheric Pressure

2014 ◽  
Vol 543-547 ◽  
pp. 3789-3792
Author(s):  
Yi Zhao ◽  
Zi Li Zhang ◽  
Peng Sun ◽  
Xin Feng Qian
Keyword(s):  
Carbon Dioxide ◽  
Activation Energy ◽  
Flue Gas ◽  
Atmospheric Pressure ◽  
Reaction Order ◽  
Carbon Dioxide Conversion ◽  
Product Analysis ◽  
Electrode Potentials ◽  
Dynamic Experiments ◽  
Kinetics Of

The dynamic experiments about the conversion of CO2from simulated flue gas were carried out in a bubbling reactor containing a kind of adsorption with M dissolving in ethanol and water at atmospheric pressure. Based on the results of product analysis and electrode potentials, the reaction mechanism of CO2reduced by M was deduced. The results of dynamic experiments showed that the reaction order was 1.0, the rate constant was 5.91×10-2s-1, and the apparent activation energy was 23.47 kJ·mol-1.

Study on the Kinetics of Wet Flue Gas Desulfurization by Carbide Slag

2011 ◽  
Vol 322 ◽  
pp. 252-255
Author(s):  
Sheng Yu Liu ◽  
Li Chao Nengzi ◽  
Cheng Wei Lu ◽  
Wei Qiu ◽  
Yun Ming Hu
Keyword(s):  
Activation Energy ◽  
Chemical Reaction ◽  
Flue Gas ◽  
Reaction Order ◽  
Frequency Factor ◽  
Reaction Model ◽  
Flue Gas Desulfurization ◽  
Economic Costs ◽  
Carbide Slag ◽  
Kinetics Of

Current industrial desulfurization processes involve in economic costs, if carbide slag can be used in those processes, the costs will be reduced and the goal treating waste with waste can be achieved. A mathematic reaction model was built based on the chemical reaction of desulfurization by carbide slag, the overall reaction order n=α+β=1.74, the activation energy Ea=21749.56173J/mol and the frequency factor k0=0.349533643 .

The role of Tween 80 and SDS in the kinetics of semi-clathrate hydrates formation for carbon dioxide capture from flue gas

2021 ◽  
pp. 1-15
Author(s):  
Anton Petukhov ◽  
Artem Atlaskin ◽  
Maria Sergeeva ◽  
Sergey Kryuchkov ◽  
Dmitry Shablykin ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Flue Gas ◽  
Carbon Dioxide Capture ◽  
Tween 80 ◽  
Clathrate Hydrates ◽  
Kinetics Of

scholarly journals Kinetic study of wood pyrolysis in presence of metal halides

2014 ◽  
Vol 12 (12) ◽  
pp. 1294-1303 ◽  
Author(s):  
Vladimir Beliy ◽  
Elena Udoratina
Keyword(s):  
Activation Energy ◽  
Lewis Acids ◽  
Alkaline Earth ◽  
Reaction Order ◽  
Earth Metal ◽  
Inorganic Salts ◽  
Alkaline Earth Metal ◽  
Metal Halides ◽  
Wood Pyrolysis ◽  
Kinetics Of

AbstractThe purpose of this work was to study the kinetics of wood pyrolysis in the presence of inorganic salts, representatives of classes of alkali and alkaline earth metal halides (NaCl, KCl, KBr, CaCl2, BaCl2·2H2O) and Lewis acids (AlCl3·6H2O, FeCl3·6H2O, CuCl2, CuBr2, ZnCl2·1.5H2O, NiCl2·6H2O, SnCl2·2H2O) using TG-DSC. The activity of these catalysts was estimated by the temperature of the beginning of pyrolysis, charcoal yield and kinetic parameters, such as energy of activation and reaction order. Using the Lewis acids as catalysts for pyrolysis leads to a decrease in the temperature of the process beginning and the activation energy. In the presence of other catalysts activation energy does not significantly change. The increase of a seeming reaction order in the presence of Lewis acids possibly is a consequence of complication of the thermodestruction mechanism, with the appearance of new parallel competing stages.

Chemical Vapor Deposition of SiO2 from Ozone-Organosilane Mixtures near Atmospheric Pressure

1992 ◽  
Vol 282 ◽  
Author(s):  
K. V. Guinn ◽  
J. A. Mucha
Keyword(s):  
Activation Energy ◽  
Chemical Vapor Deposition ◽  
Vapor Deposition ◽  
Atmospheric Pressure ◽  
Chemical Vapor ◽  
Zero Order ◽  
Kcal Mole ◽  
Consumption Ratio ◽  
Zero Order Kinetics ◽  
Kinetics Of

ABSTRACTThe kinetics of deposition of SiO2 by the reaction of tetramethylsilane (TMS) with ozone (O3) has been studied over the temperature range 180 – 380° C and compared with available data for the same process using tetraethoxysilane (TEOS). Both processes exhibit the same activation energy (17 kcal/mole) below 300 ° C which falls-off at higher temperatures due to transport limitations. Transition from first- to zero-order kinetics occurs with increasing concentrations of TMS and O3, which gives an overall O3/TMS consumption ratio of 10 at 258° C and5 at 325° C. TEOS is estimated to be 5 times more reactive than TMS above 300° C and over 10 times more reactive in the kinetically-limited regime below 300° C. Results suggest that O3-induced SiO2 deposition proceeds via surface reactions and is limited by heterogeneous decomposition of ozone.

Synthesis and Determination of the Kinetic Parameters for Non-Isothermal Decomposition of Complexes Ln(thd)3phen

2006 ◽  
Vol 530-531 ◽  
pp. 506-512 ◽  
Author(s):  
Wilton Silva Lopes ◽  
Crislene Rodrigues da Silva Morais ◽  
A.G. de Souza
Keyword(s):  
Activation Energy ◽  
Thermal Decomposition ◽  
Lanthanide Complexes ◽  
Reaction Order ◽  
Decomposition Reaction ◽  
Cylindrical Symmetry ◽  
Boundary Reaction ◽  
Phase Boundary Reaction ◽  
Kinetics Of

In this work the kinetics of the thermal decomposition of two ß-diketone lanthanide complexes of the general formula Ln(thd)3phen (where Ln = Nd+3 or Tm+3, thd = 2,2,6,6- tetramethyl-3,5-heptanodione and phen = 1,10-phenantroline) has been studied. The powders were characterized by several techniques. Thermal decomposition of the complexes was studied by non-isothermal thermogravimetry techniques. The kinetic model that best describes the process of the thermal decomposition of the complexes it was determined through the method proposed by Coats-Redfern. The average values the activation energy obtained were 136 and 114 kJ.mol-1 for the complexes Nd(thd)3phen and Tm(thd)3phen, respectively. The kinetic models that best described the thermal decomposition reaction the both complexes were R2. The model R2 indicating that the mechanism is controlled by phase-boundary reaction (cylindrical symmetry) and is defined by the function g(α) = 2[1-(1-a)1/2], indicating a mean reaction order. The values of activation energy suggests the following decreasing order of stability: Nd(thd)3phen > Tm(thd)3phen.

Reaction Kinetics of Fe2O3 and BaCO3 to Prepare Ba2Fe2O5

2014 ◽  
Vol 33 (4) ◽  
pp. 319-323 ◽  
Author(s):  
Jun-Hao Liu ◽  
Guo-Hua Zhang ◽  
Kuo-Chih Chou
Keyword(s):  
Climate Change ◽  
Carbon Dioxide ◽  
Activation Energy ◽  
Global Warming ◽  
Reaction Kinetics ◽  
Isothermal Condition ◽  
Product Layer ◽  
Thermo Gravimetric ◽  
Thermo Gravimetric Analyzer ◽  
Kinetics Of

AbstractCarbon dioxide is a greenhouse gas and substantially affects the global warming and climate change, so study on the adsorption of carbon dioxide is very urgent. As a new CO2 captor, Ba2Fe2O5 was prepared by the solid state reaction of Fe2O3 with BaCO3, following formula Fe2O3 + 2BaCO3 = Ba2Fe2O5 + 2CO2. The reaction kinetics in isothermal condition was investigated by using the method of thermo-gravimetric analyzer (TGA). It was found that the reaction of Fe2O3 with BaCO3 was controlled by the diffusion step in the product layer, and the kinetics process could be described by the RPP model (Real Physical Picture) with the apparent activation energy extracted to be 161.122 kJ/mol.

Kinetic Study of the Dehydrogenation of Isobutane over V-K-O /ZSM5 Catalyst

2013 ◽  
Vol 798-799 ◽  
pp. 174-177 ◽  
Author(s):  
Teng Teng Wu ◽  
Cheng Xue Wang
Keyword(s):  
Experimental Data ◽  
Activation Energy ◽  
Kinetic Model ◽  
Atmospheric Pressure ◽  
Contact Time ◽  
Model Parameters ◽  
Isobutane Dehydrogenation ◽  
Dehydrogenation Reaction ◽  
Reaction Pressure ◽  
Kinetics Of

The reaction kinetics of the dehydrogenation of isobutane over V-K-O /ZSM5 catalyst was investigated. The powerfunction model was established;The isobutane dehydrogenation reaction tests were carried out between 833-863K and reaction pressure to atmospheric pressure by changing the contact time(w/F=0.464-0.532gh/mol) ,through the experimental data the kinetics of model parameters were analyzed.The results show that the power-function kinetic model is reasonable,the apparent activation energy is 177.7492KJ/mol.

scholarly journals Kinetics of the Carbon Monoxide Oxidation Reaction Under Microwave Heating

1996 ◽  
Vol 430 ◽  
Author(s):  
W. Lee Perry ◽  
Joel D. Katz ◽  
Daniel Rees ◽  
Mark T. Paffett ◽  
Abhaya Datye
Keyword(s):  
Activation Energy ◽  
Carbon Monoxide ◽  
Co Oxidation ◽  
Microwave Heating ◽  
Oxidation Reaction ◽  
Reaction Order ◽  
Thermal Gradients ◽  
Exponential Factor ◽  
Co Oxidation Reaction ◽  
Kinetics Of

Abstract915 MHz microwave heating has been used to drive the CO oxidation reaction over Pd/Al2O3 without significantly affecting the reaction kinetics. As compared to an identical conventionally heated system, the activation energy, pre-exponential factor, and reaction order with respect to CO were unchanged. Temperature was measured using a thermocouple extrapolation technique. Microwave-induced thermal gradients were found to play a significant role in kinetic observations.

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