Kinetics of combustion of petroleum coke and sub-bituminous coal char: Results of ignition and steady-state techniques

1988 ◽  
Vol 21 (1) ◽  
pp. 231-237 ◽  
Author(s):  
Wieslaw Rybak ◽  
Mieczyslaw Zembrzuski ◽  
Ian W. Smith
Energies ◽  
2019 ◽  
Vol 12 (3) ◽  
pp. 496 ◽  
Author(s):  
Junwei Chen ◽  
Weibin Chen ◽  
Yang Jiao ◽  
Xidong Wang

The gasification kinetics of bituminous coal char was investigated in a mixture of CO2, H2O, CO, H2, and N2 under isothermal conditions. In addition, the impacts of gasification temperature, gasification time, and gas composition on the gasification process were analyzed. As the experimental results suggest, there is a significant increase of the carbon conversion degree of bituminous coal char not just when gasification temperature and time increase, but also when H2 and CO concentration decreases. The kinetics of bituminous coal char in the gasification process was successfully modeled as a shrinking unreacted core. It is concluded that the gasification of bituminous coal char is controlled by an internal chemical reaction in the early stage and diffusion in the later stage. The activation energies of bituminous coal char gasification for different stages were studied. Moreover, it is proposed for the first time, to our knowledge, that the diffusion-control step is significantly shortened with the decrease of the CO2/H2O ratio. As scanning-electron-microscopy results suggest, bituminous coal char gasified in CO2/H2O = 1/3 atmosphere has numerous inner pores (0–5 m). Therefore, in the process of gasification, the inner pores provide a gas channel that reduces the gas diffusion resistance and thus shortens the diffusion-control step. These results can serve as a reference for industrialized application of the technology of coal gasification direct reduced iron.


Fuel ◽  
2001 ◽  
Vol 80 (11) ◽  
pp. 1651-1658 ◽  
Author(s):  
D.H. Ahn ◽  
B.M. Gibbs ◽  
K.H. Ko ◽  
J.J. Kim

1989 ◽  
Vol 28 (12) ◽  
pp. 1767-1778 ◽  
Author(s):  
Anil Goyal ◽  
Robert F. Zabransky ◽  
Amir Rehmat

1985 ◽  
Vol 248 (5) ◽  
pp. C498-C509 ◽  
Author(s):  
D. Restrepo ◽  
G. A. Kimmich

Zero-trans kinetics of Na+-sugar cotransport were investigated. Sugar influx was measured at various sodium and sugar concentrations in K+-loaded cells treated with rotenone and valinomycin. Sugar influx follows Michaelis-Menten kinetics as a function of sugar concentration but not as a function of Na+ concentration. Nine models with 1:1 or 2:1 sodium:sugar stoichiometry were considered. The flux equations for these models were solved assuming steady-state distribution of carrier forms and that translocation across the membrane is rate limiting. Classical enzyme kinetic methods and a least-squares fit of flux equations to the experimental data were used to assess the fit of the different models. Four models can be discarded on this basis. Of the remaining models, we discard two on the basis of the trans sodium dependence and the coupling stoichiometry [G. A. Kimmich and J. Randles, Am. J. Physiol. 247 (Cell Physiol. 16): C74-C82, 1984]. The remaining models are terter ordered mechanisms with sodium debinding first at the trans side. If transfer across the membrane is rate limiting, the binding order can be determined to be sodium:sugar:sodium.


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