Structural change of supported NiMo sulfide catalysts during the hydrogenation of coal-derived liquids

1995 ◽  
Vol 41 (3) ◽  
pp. 261-271 ◽  
Author(s):  
Nobuyuki Matsubayashi ◽  
Hiromichi Shimada ◽  
Toshio Sato ◽  
Yuji Yoshimura ◽  
Motoyasu Imamura ◽  
...  
1992 ◽  
Vol 57 (12) ◽  
pp. 2515-2523 ◽  
Author(s):  
Alexandra Drahorádová ◽  
Miroslav Zdražil

Selectivity of hydrodenitrogenation/hydrodesulfurization (HDN/HDS) using carbon supported Ni, Mo, and Ni-Mo sulfide catalysts was studied at a pressure of 2 MPa and over a temperature range of 280-350 °C. A commercial alumina supported Ni-Mo sample was also included as reference catalyst. Model compounds used were pyridine and thiophene. Selectivity (HDN/HDS) increased with decreasing temperature and decreased in the order Ni, Mo, Ni-Mo. Ni/C catalyst exhibited unusually high HDN/HDS selectivity at low temperature, where HDN of pyridine was faster than HDS of thiophene. Selectivity was interpreted as an intensive property of a catalyst characterizing quality of active surface. The combination of Ni and Mo sulfides in Ni-Mo catalyst resulted in a strong shift in HDN/HDS selectivity to the HDS side; the selectivity of Ni-Mo sample was very low and was not an average of the selectivities of Ni and Mo catalyst. This was interpreted as the evidence of the chemical synergism in the Ni-Mo sulfide system, because structure synergism cannot cause such selectivity changes accompanying combination of Ni and Mo sulfide into the mixed catalyst.


2019 ◽  
Vol 329 ◽  
pp. 156-166 ◽  
Author(s):  
A.V. Vutolkina ◽  
A.P. Glotov ◽  
A.V. Zanina ◽  
D.F. Makhmutov ◽  
A.L. Maximov ◽  
...  

2021 ◽  
Vol 163 ◽  
pp. 1648-1659
Author(s):  
Thikhamporn Burimsitthigul ◽  
Boonyawan Yoosuk ◽  
Chawalit Ngamcharussrivichai ◽  
Pattarapan Prasassarakich

2016 ◽  
Vol 512 ◽  
pp. 85-92 ◽  
Author(s):  
Li Yue ◽  
Guangci Li ◽  
Feng Zhang ◽  
Lei Chen ◽  
Xuebing Li ◽  
...  

2004 ◽  
Vol 83 (2) ◽  
pp. 237-244 ◽  
Author(s):  
Zdenìk Vít ◽  
Daniela Gulková ◽  
Ludìk Kaluža ◽  
Miroslav Zdražil

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