On the Effects of High Pressure and Heating Rate during Coal Pyrolysis on Char Gasification Reactivity

2003 ◽  
Vol 17 (4) ◽  
pp. 887-895 ◽  
Author(s):  
D. G. Roberts ◽  
D. J. Harris ◽  
T. F. Wall
Author(s):  
Chi Huanying ◽  
Li Hanjian ◽  
Su Sheng ◽  
Abdulmajid Abdullahi Shagali ◽  
An Xiaoxue ◽  
...  
Keyword(s):  

2012 ◽  
Vol 550-553 ◽  
pp. 2758-2762 ◽  
Author(s):  
Xi Jie Chu ◽  
Yong Gang Wang ◽  
Li Hong Zhao

The pyrolysis tests of Shenhua coal and Shenhua direct liquefaction residue have been carried out using thermogravimetric at the differential heating rate. The kinetic parameters k and E were calculated using DAEM method. Results show DAME model can describe the pyrolysis behavior of Shenhua coal within the range of 20% to 95%, the activation energy of coal pyrolysis ranges from 53.98 to 279.38 kJ/mol, and DAME model can describe the behavior of Shenhua direct liquefaction residue within the range of 10% to 80%, the activation energy of residue pyrolysis is about 170 kJ/mol. The results of which are basically consistent with the experimental data.


2018 ◽  
Vol 215 ◽  
pp. 348-355 ◽  
Author(s):  
Zhaohui Chen ◽  
Yunjia Li ◽  
Dengguo Lai ◽  
Sulong Geng ◽  
Qi Zhou ◽  
...  

Fuel ◽  
2020 ◽  
Vol 267 ◽  
pp. 117237 ◽  
Author(s):  
Rathziel Roncancio ◽  
Mehmed S. Ulcay ◽  
Jorge E. Arango ◽  
Jay P. Gore

2020 ◽  
Vol 7 (3) ◽  
pp. 464-475 ◽  
Author(s):  
Xiaoming Li ◽  
Caifeng Yang ◽  
Mengjie Liu ◽  
Jin Bai ◽  
Wen Li

Abstract Catalytic coal gasification technology shows prominent advantages in enhancing coal gasification reactivity and is restrained by the cost of catalyst. Two typical biomass ash additions, corn stalk ash (CSA, high K–Na and low Si) and poplar sawdust ash (PSA, high K–Ca and high Si), were employed to study the influence of biomass ash on pyrolysis process and char gasification reactivity of the typical anthracite. Microstructure characteristics of the char samples were examined by X-ray diffraction (XRD). Based on isothermal char-CO2 gasification experiments, the influence of biomass ash on reactivity of anthracite char was determined using thermogravimetric analyzer. Furthermore, structural parameters were correlated with different reactivity parameters to illustrate the crucial factor on the gasification reactivity varied with char reaction stages. The results indicate that both CSA and PSA additives hinder the growth of adjacent basic structural units in a vertical direction of the carbon structure, and then slow down the graphitization process of the anthracite during pyrolysis. The inhibition effect is more prominent with the increasing of biomass ash. In addition, the gasification reactivity of anthracite char is significantly promoted, which could be mainly attributed to the abundant active AAEM (especially K and Na) contents of biomass ash and a lower graphitization degree of mixed chars. Higher K and Na contents illustrate that the CSA has more remarkable promotion effect on char gasification reactivity than PSA, in accordance with the inhibition effect on the order degree of anthracite char. The stacking layer number could reasonably act as a rough indicator for evaluating the gasification reactivity of the char samples.


2011 ◽  
Vol 695 ◽  
pp. 493-496 ◽  
Author(s):  
Yong Hui Song ◽  
Jian Mei She ◽  
Xin Zhe Lan ◽  
Jun Zhou

The pyrolysis characteristics of Jianfanggou(JFG) coal was studied using a thermo-gravimetric analyzer and the pyrolysis kinetic parameters were calculated at the different heating rate. The results showed the DTG curves under different heating rate had three peaks and the corresponding temperature were 100°C, 470°C and 750°C, the pyrolysis process can be divided into three stages conclusively. The maximum weight loss rate at 470°C indicated the major weight loss occurred in the second stage. The Tb, Tf and T∞ obtained under experiment situation. The results of the JFG coal pyrolysis kinetic showed the Tb, Tf and T∞ increased gradually with the accretion of the heating rate. In the meantime, the variation of frequency factor was consistent with the trend of activation energy.


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