Kinetic analysis of element evolution during low-temperature oxidation of coal

被引:0
|
作者
He K. [1 ,3 ]
Zhang Y.-L. [2 ]
Shi J.-W. [1 ]
Wang F.-Y. [1 ]
机构
[1] School of Mechanical Electronic and Information Engineering, China University of Mining and Technology(Beijing), Beijing
[2] State Key Laboratory Breeding Base of Coal Science and Technology Co-founded by Shanxi Province and the Ministry of Science and Technology, Taiyuan University of Technology, Taiyuan
[3] Technical and Testing Section, Mining Products Safety Approval and Certification Center, Beijing
来源
关键词
Coal; Element evolution; Kinetics; Low-temperature oxidation;
D O I
10.13225/j.cnki.jccs.2015.1745
中图分类号
学科分类号
摘要
The complex macromolecular matrix of coal was divided into the elements of C, O, H, S and N, which were involved in the oxidation reaction. Based on the changes of element contents during coal oxidation process at low temperature, the three kinetic models, including pseudo-first-order kinetics model, Coats and Redfern's model, and Freeman and Carroll's model, were introduced to investigate the kinetic characteristics of coal oxidation at low temperature. Kinetic study reveals that the evolutions of these elements during coal oxidation at low temperature follow pseudo-first order kinetics and Coats and Redfern's model. The activation energies for these elements evolution in the oxidation process by using the pseudo-first order kinetics have been found to be almost similar to those calculated by applying the Coats and Redfern's equation. The reaction rates computed by the pseudo-first order kinetics are very low and have been found to be 10-5-10-6, suggesting a very low rate of successful collisions for the formation of activated complex. A kinetic compensation effect between the activation energy and exponential facto was also observed for the evolutions of these elements. © 2016, Editorial Office of Journal of China Coal Society. All right reserved.
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页码:1460 / 1466
页数:6
相关论文
共 11 条
  • [1] Zhou F., Study on the coexistence of gas and coal spontaneous combustion(I): Disaster mechanism, Journal of China Coal Society, 37, 5, pp. 843-849, (2012)
  • [2] Cimadevilla J.L.G., Alvarez R., Pis J.J., Influence of coal forced oxidation on technological properties of cokes produced at laboratory scale, Fuel Process Technology, 87, pp. 1-10, (2005)
  • [3] Mastalerz M., Solano-Acosta W., Schimmelmann A., Et al., Effects of coal storage in air on physical and chemical properties of coal and on gas adsorption, International Journal of Coal Geology, 79, pp. 167-174, (2009)
  • [4] Wang H., Dlugogorski B.Z., Kennedy E.M., Coal oxidation at low temperatures: Oxygen consumption, oxidation products, reaction mechanism and kinetic modeling, Progress in Energy and Combustion Science, 29, pp. 487-513, (2003)
  • [5] Dai G., Relation between free radicals concentration and gas products in process of coal low temperature oxidation, Journal of China Coal Society, 37, 1, pp. 122-126, (2012)
  • [6] Lu W., Hu Q., Relation between the change rules of coal structures when being oxidized and spontaneous combustion process of coal, Journal of China Coal Society, 32, 9, pp. 939-944, (2007)
  • [7] Coats A.W., Redfern J.P., Kinetic parameters from thermogravimetric date, Nature, 201, pp. 68-69, (1964)
  • [8] Freeman E.S., Carroll B.J., The application of thermoanalytical techniques to reaction kinetics: The thermogravimetric evaluation of the kinetics of the decomposition of calcium oxalate monohydrate, Journal of Physical Chemistry, 62, pp. 394-397, (1958)
  • [9] Yurum Y., Altuntas N., Air oxidation of Beypazari lignite at 50℃, 100℃ and 150℃, Fuel, 77, pp. 1809-1814, (1998)
  • [10] Tahmasebi A., Yu J.L., Han Y.N., Et al., Study of chemical structure changes of Chinese lignite upon drying in superheated steam, microwave, and hot air, Energy & Fuels, 26, pp. 3651-3660, (2012)