Volume 33 Issue 04
Aug.  2005
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YU Xi-zhi, REN Xiao-qian, DONG Zhen-guo, WANG Jun, WANG Yan-ru. 工业NiW/Al2O3催化剂上二苯并噻吩的加氢脱硫动力学[J]. Journal of Fuel Chemistry and Technology, 2005, 33(04): 483-486.
Citation: YU Xi-zhi, REN Xiao-qian, DONG Zhen-guo, WANG Jun, WANG Yan-ru. 工业NiW/Al2O3催化剂上二苯并噻吩的加氢脱硫动力学[J]. Journal of Fuel Chemistry and Technology, 2005, 33(04): 483-486.

工业NiW/Al2O3催化剂上二苯并噻吩的加氢脱硫动力学

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  • Corresponding author: WANG Jun
  • Received Date: 2004-12-09
  • Rev Recd Date: 2005-05-07
  • Publish Date: 2005-08-30
  • The kinetics of the hydrodesulfurization (HDS) reaction of dibenzothiophene(DBT), as the model compound for S-bearing organics in middle distillates, were studied over the commercial NiW/Al2O3 catalyst RN-10 in a high-pressure trickle-bed reactor. The effect of reaction conditions on the catalytic behavior was studied at the hydrogen pressure of 1.5 MPa~4.5 MPa, volume ratio of hydrogen/oil of 150~700, weight hourly space velocity of 15 h-1~60 h-1 and reaction temperature of 280 ℃ to 380 ℃. The hydrogen pressure and volume ratio of hydrogen/oil exert little influence on the conversion of DBT at the high hydrogen pressures and volume ratios of hydrogen/oil. At low reaction temperatures, the conversion of DBT increases drastically with the increase of reaction temperature up to 330 ℃, while it increases slowly at high reaction temperatures. A kinetic model of HDS is established according to a second-order kinetics model at various reaction temperatures. The parameters of the model are calculated. The model correlation coefficient is above 0.989. The apparent activated energy at high reaction temperature region (≥330 ℃) is less than that at low temperature region, which are 13.4 kJ/mol and 121.4 kJ/mol respectively. Therefore, the HDS performance of the RN-10 catalyst could not be improved by just increasing the reaction temperature.
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