High temperature reactions of water with heavy oil and bitumen: Insights into aquathermolysis chemistry during steam-assisted recovery

被引:36
|
作者
Montgomery, Wren [1 ]
Court, Richard W. [1 ]
Rees, Andrew C. [2 ]
Sephton, Mark A. [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Earth Sci & Engn, London SW7 2AZ, England
[2] BP Amer Prod Co, Houston, TX 77079 USA
关键词
Aquathermolysis; SAGD; High pressure; HYDROUS PYROLYSIS; ORGANIC-COMPOUNDS; DORSET;
D O I
10.1016/j.fuel.2013.05.098
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
To better understand the hot water-mediated organic transformation process (aquathermolysis) that occurs during the steam-assisted recovery of heavy oils and bitumen we have performed a series of experiments that subject a heavy oil to progressively higher temperatures and pressures in the presence of liquid water. As temperature and pressure increases, from ambient conditions to 300 degrees C and 1250 psig (8.6 MPa), a floating oil (flotate) is generated and is composed of mostly aliphatic hydrocarbons that appear to be generated at the expense of polars and asphaltenes. Analyses of hopane maturity parameters for the flotate indicate lower temperatures than the starting material suggesting the liberation of hopanes and, therefore, other hydrocarbons, from asphaltenes. Infrared spectra confirm changes in overall organic constitution as the relative abundance of hydrocarbons to oxygen-containing functional groups increases in the flotate. At the highest temperatures and pressures (325 degrees C, 1750 psig (13.8 MPa)) the flotate is at a maximum relative amount, the untransformed heavy oil is at a minimum and significant amounts of methane are generated indicating the onset of cracking. Steam-assisted recovery of heavy oil, therefore, leads to changes in the chemical constitution of a number of chemical fractions generating a lighter oil and gases that must be taken into account when planning field operations for production. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:426 / 434
页数:9
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