Upgrading of bitumen in supercritical fluids

被引:46
|
作者
Scott, DS [1 ]
Radlein, D
Piskorz, J
Majerski, P
deBruijn, TJW
机构
[1] Univ Waterloo, Dept Chem Engn, Waterloo, ON N2L 3G1, Canada
[2] Resource Transforms Int Ltd, Waterloo, ON N2V 1Z7, Canada
[3] Nat Resources Canada, NCUT, Devon, AB, Canada
关键词
bitumen; upgrading; supercritical fluids; activated carbon catalysts;
D O I
10.1016/S0016-2361(00)00174-5
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
An upgrading process for heavy oils and bitumens, based on the use of activated carbon catalysts, was investigated in a bench-scale plug flow reactor. Good results were obtained at pressures as low as 7.0 MPa at temperatures of 400-450 degreesC. The process required the presence of hydrogen gas and a hydrogen-rich solvent in a supercritical state. If the solvent was a highly saturated alkane, very little solvent decomposition occurred. A number of n-alkanes were tested as solvents, as well as paraffinic petroleum cuts and donor solvents such as tetralin and decalin. A range of values of other operating parameters was also investigated. With an Athabasca bitumen coker feed, bitumen conversions to distillable liquids of 82-88% by weight (95-105% vol%) were achieved, with 6-8 wt% (coke + pitch) yields. Demetallization was almost 100%, and hydrodesulfurization and hydrodenitrification levels of over 80% also resulted. Under similar conditions, a conventional Co/Mo hydrotreating catalyst gave higher hydrogen uptake but lower pitch conversion, supporting the concept that carbon-based catalysts may give a unique product distribution and utilize hydrogen more effectively. It is postulated that four conditions must be met to obtain the favorable results found in this work: there must be a significant level of supercritical fluid; there must be a highly saturated or paraffinic supercritical solvent present; hydrogen gas must be present; and there must be an activated carbon catalyst used which may also have incorporated in it a catalytically active metal. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1087 / 1099
页数:13
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