Elsevier

Fuel

Volume 95, May 2012, Pages 159-168
Fuel

Effect of vapour–liquid phase behaviour of steam–light hydrocarbon systems on steam assisted gravity drainage process for bitumen recovery

https://doi.org/10.1016/j.fuel.2011.10.044Get rights and content

Abstract

The vapour–liquid phase behaviour of steam–solvent (light hydrocarbon) systems used in an oil sands recovery process called steam assisted gravity drainage (SAGD) is examined. Analysis shows that condensation occurs over a temperature range and that a concentration gradient exists between the liquid and vapour phases. In a large range of solvent concentrations, water condenses first from the vapour phase. Solvent only condenses first from the vapour phase at extremely high solvent volume fractions. Due to water condensing first at most concentrations, the ability of the solvent to directly contact the bitumen in the reservoir depends on the orientation of the vapour–liquid interface and the relative position in the vapour chamber. Addition of solvent into a mature SAGD operation can also cause a temporary suppression of the steam–oil ratio (SOR) due to the change in the temperature at the vapour–liquid interface. This effect must be taken into account in interpreting experimental or simulation results. The addition of solvent not only changes the temperature but also decreases the heat of condensation of the mixture. As the concentration of solvent changes, the SOR is also expected to change.

Highlights

► Steam–solvent phase behaviour during bitumen recovery is examined for the first time. ► Solvent only condenses first from a mixture at very high solvent concentrations. ► Water condensing first from the mixture reduces solvent contact with bitumen. ► Addition of solvent changes phase transition temperatures and enthalpies.

Introduction

Steam assisted gravity drainage (SAGD) is a thermal process currently being developed for widespread commercialization of bitumen recovery in Western Canada [1]. When it is applied to suitable reservoirs, SAGD is capable of high production rates and recovery factors exceeding 65% [2]. A major drawback of the process is its high energy intensity and associated CO2 emissions.

A process called expanding solvent SAGD (ES-SAGD) or solvent co-injection with SAGD is currently under intensive research to help address the high energy costs of SAGD. In general, the new technique continuously injects vaporized hydrocarbons, such as propane, butane, up to C12, or in various mixtures, along with the steam [3], [4], [5]. The injected solvent is intended to assist bitumen recovery through dissolution into the oil phase to reduce bitumen viscosity in conjunction with the viscosity reduction through heating. Many studies and trials project that the addition of solvent will increase recovery rates and simultaneously reduce the steam usage or steam oil ratio (SOR) [6], [7], [8].

One aspect of solvent co-injection with steam that has not been studied is the vapour–liquid phase behaviour involved in solvent–steam co-injection process. It is not well understood how the co-injection can impact the gravity drainage process. In a constant pressure process like SAGD where only one component (water) is used, the dew point and bubble point temperatures are the same. When hydrocarbon solvents are mixed with water, partial pressures come into play such that the dew point and bubble point of the system separate. In the steam chamber, the concentrations of water and solvent in the liquid and vapour phases are transient between the dew point and bubble point. The appearance of a temperature range for condensation and a concentration gradient between liquid and vapour phases introduces additional considerations when applying solvent co-injection. In this paper, both the phase behaviour and the potential impact on SAGD are examined.

Section snippets

Water–hydrocarbon vapour–liquid phase behaviour

To illustrate the vapour–liquid phase behaviour of water–hydrocarbon systems, a phase diagram of water–hexane (C6) mixture is generated for a system in a typical pressure–volume–temperature (PVT) test cell. Similar to a SAGD vapour chamber, the pressure in PVT cell is maintained constant. In this case, the phase change is achieved by the change in cell temperature through heat transfer between the mixture inside the cell and the heating system on the exterior of the cylinder. When the

Temperature and condensation profiles

Many studies [5], [6], [7], [11] point to hexane or heptane (C7) as the ideal solvent of the co-injection in SAGD since their saturation temperatures are the most similar to that of water. A common assumption is that a similar saturation temperature will promote co-condensation. Fig. 8 shows the comparison of saturation pressure and temperature for C6, C7, and water over the typical range of pressures seen in heavy oil reservoirs. As shown in Fig. 8, at the same pressure between 0.01 and 2.7 

Conclusions

Use of steam–solvent combinations to enhance recovery from horizontal well pairs presents a significantly number of additional variables to control from the operations perspective. The addition of solvents significantly changes the phase behaviour such that concentration gradients and temperature gradients will form in the vapour chamber where none previously exists for SAGD). This presents the problems of dealing with solvent contact with the bitumen and ensuring appropriate level of subcool

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