Hydrodesulfurization and hydrodemetallization of different origin vacuum residues: Characterization and reactivity

被引:28
|
作者
Ferreira, C. [2 ,3 ]
Tayakout-Fayolle, M. [1 ]
Guibard, I. [2 ]
Lemos, F. [3 ]
Toulhoat, H. [4 ]
Ramoa Ribeiro, F. [3 ]
机构
[1] Univ Lyon 1, IRCELYON, Inst Rech Catalyse & Environm Lyon, CNRS,UMR 5256, F-69626 Villeurbanne, France
[2] IFP Energies Nouvelles, Rond Point Echangeur Solaize, F-69360 Solaize, France
[3] Inst Super Tecn, Ctr Engn Biol & Quim, P-1049001 Lisbon, Portugal
[4] IFP Energies Nouvelles, F-92852 Rueil Malmaison, France
关键词
Hydrodesulfurization; Hydrodemetallization; Kinetics; Vacuum residue; ASPHALTENES; KINETICS; SULFUR;
D O I
10.1016/j.fuel.2012.03.054
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
This work presents an insight on the reactivities of different geographical origin residues in hydrotreatment processes. Hydrodemetallization (HDM) and hydrodesulfurization (HDS) experiments have been performed on different vacuum residue (Arabian Light, Buzurgan, Djeno and Ural) with commercial catalysts under industrial conditions. Depending on its origin each residue appears to have a specific behavior; however, some general trends can also be highlighted. One key reactivity parameter (both for HDM and HDS reactions) seems to be the size of residue molecules that depends strongly on its origin. In fact, diffusion limitations may occur, even in the HDM section. Hydrodesulfurization (HDS) reactions are not completely controlled by diffusion; the nature of chemical structures also appears to be an important parameter for reactivity. A better knowledge of the chemical structures is therefore still necessary to understand these different reactivities. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:218 / 228
页数:11
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