METHODS OF AND APPARATUS FOR DETERMINING THE VISCOSITY OF HEAVY OIL

Information

  • Patent Application
  • 20100043538
  • Publication Number
    20100043538
  • Date Filed
    August 05, 2009
    15 years ago
  • Date Published
    February 25, 2010
    14 years ago
Abstract
The viscosity of a heavy oil is estimated according to a power law equation which relates the heavy oil viscosity to a function of the assumed, measured, or estimated glass transition temperature of the heavy oil and the measured temperature of the heavy oil.
Description
BACKGROUND OF THE INVENTION

1. Field of the Invention


This invention relates broadly to the investigation of geological formations. More particularly, this invention relates to methods of determining the viscosity of a heavy oil at any temperature based on a glass transition temperature Tg of the heavy oil. Apparatus for implementing the methods are provided. For purposes herein, a “heavy oil” shall be defined and understood to be any oil having an API gravity of 22.3 degrees or less.


2. Description of Related Art


With conventional oil reserves rapidly depleting worldwide, deposits of heavy oils and tar sands, which contain significant energy reserves, are becoming increasingly important. High viscosity is a major concern in the recovery of these unconventional oils. Usually, thermal methods, particularly steam drive and steam soak, are used to recover heavy oils and bitumen. Thermal methods rely on several displacement mechanisms to recover oil, but the most important is the reduction of crude viscosity with increasing temperature. Therefore, it is pivotal to understand the heavy oil viscosity-temperature behavior.


Currently, heavy oil viscosity is usually predicted based on the principles of equations of state (EOS) in which the fluid composition is used in conjunction with tuned EOS parameters. However, when the heavy oil composition is dramatically different from the model system, the prediction results are effectively useless. There is no generally reliable method which can characterize heavy oil viscosity behavior over a wide range of heavy oil samples (worldwide) and temperatures (10-240° C.).


BRIEF SUMMARY OF THE INVENTION

In accordance with one aspect of the invention, the viscosity of a heavy oil can be estimated according to a power law equation which relates the heavy oil viscosity to a function of the assumed, measured, or estimated glass transition temperature of the heavy oil and the measured temperature of the heavy oil.


According to another aspect of the invention, the power law equation which relates the heavy oil viscosity η to the glass transition temperature Tg and the measured temperature T is ln(η)=a+b(T/Tg)c, where “a”, “b”, and “c” are constants, and “b” has a value between 18 and 22, and “c” has a value between −3.4 and −3.2.


In one embodiment of the invention, the glass transition temperature of a heavy oil sample is measured with a tool such as a differential scanning calorimeter or dielectric spectroscope, and an estimate of the viscosity of the heavy oil sample at any temperature is determined according to the power law equation.


In another embodiment of the invention, the viscosity of a heavy oil sample is measured at a given temperature with a tool such as a viscometer or a nuclear magnetic resonance (NMR) tool. The glass transition temperature is then calculated from the viscosity and temperature information according to the power law equation. Then, the viscosity of the heavy oil sample can be estimated at any other temperature according to the power law equation.


In a further embodiment, the temperature of a heavy oil sample is measured, and the glass transition temperature of the heavy oil is estimated. Then, using the power law equation, the viscosity of the heavy oil sample is estimated.


Objects and advantages of the invention will become apparent to those skilled in the art upon reference to the detailed description taken in conjunction with the provided figures.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 is a graph showing the relationship between the viscosity and temperature of fourteen different heavy oil samples.



FIG. 2 is a logarithmic plot showing the viscosities of the fourteen different heavy oil samples as a function of the reduced glass transition temperature (T/Tg).



FIG. 3 is a logarithmic plot showing the viscosities of the fourteen different heavy oil samples as a function of the adjusted reduced glass transition temperature (T/Tr), with a power law equation curve fit to the data.



FIGS. 4A-4C are flow diagrams of three methods of the invention.



FIG. 5 is schematic diagram of a borehole tool capable of implementing the methods of the invention.





DETAILED DESCRIPTION OF THE INVENTION

Fourteen heavy oil samples were collected from different regions of the world. Their viscosities at different temperatures were measured with a viscometer. FIG. 1 shows the relationship between the viscosity η and the temperature T for each heavy oil sample, where the “x” axis is the inverse of the temperature (Kelvin), and the “y” axis is the natural log of the heavy oil sample viscosity.


The temperature and viscosity of a polymer can be related to each other via the glass transition viscosity ηg (i.e., the viscosity at the glass transition temperature) and glass transition temperature Tg of the polymer according to the William-Landel-Ferry (WLF) equation (Williams, M. et al., Journal of the American Chemical Society 77, 3701 (1955):










ln






η

η
g



=



-
C






1
*

(

T
-

T
g


)




C





2

+

(

T
-

T
g


)







(
1
)







where C1 and C2 are constants. Using the WLF equation and the procedures set forth in the William, M. et al. article, it is possible to use the temperature and viscosity data and obtain a determination of the glass transition temperature Tg (as well as unknowns C1, C2, and ηg).


Having obtained the glass transition temperature for each sample, the heavy oil viscosity data for each sample was plotted against the reduced glass transition temperature (i.e., T/Tg) as seen in FIG. 2. The results show that the relationships between the viscosities of the heavy oils and their reduced glass transition temperatures are very similar, but deviate from a single curve. Considering that the glass transition temperature Tg is cooling rate dependent, even the best experimental determination of Tg can only be thought of as close to the calorimetric ideal glass transition temperature. Therefore, it is reasonable that by adjusting the glass transition temperatures Tg of the heavy oil samples within a range of ±10% to obtain adjusted glass transition temperatures Tr, the data relating the viscosity and the adjusted reduced glass transition temperature T/Tr can be forced to fit well along a single master curve as shown in FIG. 3. The master curve (solid line in FIG. 3) obeys the power law equation





ln η=a+b(T/Tr)c   (2)


where “a”, “b”, and “c” are constants. More particularly, the data can be empirically fitted according to the following power law equation:





ln η=−0.5734+20.4095(T/Tr)−3.3018.   (3)


With constant a=−0.5734, constant b=20.4095, and constant c=−3.3018, a good estimation of the viscosity is obtained for the fourteen samples at various temperatures; i.e., R2=0.97.


In order to fit the data along the master curve, the glass transition temperatures Tg of the samples found according to fitting results of the Equation (1) were adjusted as set forth in Table 1:














TABLE 1







Heavy Oil Sample
Tg (° K)
Tr (° K)
Tr/Tg





















HO #1
244
248
1.0176



HO #2
252
246
0.9750



HO #4
246
242
0.9829



HO #5
241
248
1.0270



HO #6
246
242
0.9837



HO #7
249
264
1.0602



HO #8
245
233
0.9510



HO #9
242
222
0.9174



HO #10
254
238
0.9362



HO #11
253
248
0.9802



HO #12
247
261
1.0567



HO #13
251
249
0.9920



HO #14
244
264
1.0820



HO #15
235
231
0.9830



Average
246.36
245.36
0.9961










From Table 1, several conclusions and suppositions can be drawn. First, on average, Tg and Tr are within one percent of one another. Therefore, in relating viscosity to temperature, Equation (3) can be modified to





ln η=−0.5734+20.4095(T/Tg)−3.3018.   (4)


Second, for each individual heavy oil sample, Tr was within ±10% of Tg. As seen in FIG. 3, these adjustments permitted the data for the samples to fall on or very close to a single curve. Thus, it is expected that Equation (4) will provide an excellent correlation between viscosity and the reduced glass transition temperature for most heavy oil samples. Third, even though an excellent correlation is expected using Equation (4), it will be appreciated that, because adjustments were required to obtain a close fit, different values for constants “a”, “b”, and “c” could be utilized and still provide good results. For example, it has been determined that good results can be obtained if constant “b” is between 18 and 22. Likewise, good results can be obtained if constant “c” has a value between −3.4 and −3.2. Constant “a” is an offset value which may result from the curve fitting, and therefore constant “a” may take a relatively wide range of values. Fourth, all of the glass transition temperatures were seen to be within ±5% of the average glass transition temperature. Thus, in the absence of glass transition temperature data with respect to a given heavy oil sample, it may be possible to assume that Tg=246° K.


Given the conclusions and suppositions set forth above, a first method is seen in FIG. 4A. At 110, the glass transition temperature Tg of a heavy oil sample is found in any manner or is measured with lab equipment (e.g., a differential scanning calorimeter or a dielectric spectroscope). Then, at 120, the viscosity η of that heavy oil sample or a similar heavy oil sample (e.g., an in situ sample from the same reservoir) at any temperature T is estimated according to the power law equation ln(η)=a+b(T/Tg)c, where “a”, “b”, and “c” are constants. Preferably, constant “b” has a value between 18 and 22, and constant “c” has a value between −3.4 and −3.2. More preferably, constant “a”=−0.5734, constant “b”=20.4095, and constant “c”=−3.3018.



FIG. 4B sets forth a second method. At 210, the viscosity of a heavy oil sample is measured with a viscometer or using nuclear magnetic resonance (NMR) techniques. Where NMR techniques are used, the viscosity may be found according to the correlations described in Canadian Patent Application ______, entitled “Methods for Determining In Situ the Viscosity of Heavy Oil”, filed Aug. 6, 2008. With the viscosity and temperature information, at 220, the glass transition temperature Tg is calculated (estimated) according to the power law equation ln(η)=a+b(T/Tg)c, where “a”, “b”, and “c” are constants. Preferably, constant “b” has a value between 18 and 22, and constant “c” has a value between −3.4 and −3.2. More preferably, constant “a”=−0.5734, constant “b”=20.4095, and constant “c”=−3.3018. Then, at 230, the viscosity η of that heavy oil sample or a similar heavy oil sample (e.g., an in situ sample from the same reservoir) at any temperature T is estimated according to the same power law equation with the calculated value of the glass transition temperature Tg from step 220 used in the equation.


Using the second method, five heavy oil samples (A-E) from different parts of the world were analyzed. A first viscosity was measured for each heavy oil sample using a viscometer at a first temperature (as seen in Tables 2-6 below). Then the glass transition temperature Tg was calculated for that heavy oil sample according Equation (4) above. The viscosities for different temperatures for that heavy oil sample were then predicted using Equation (4) using the calculated glass transition temperature. The predicted viscosities were then compared to the viscosities measured by the viscometer at those temperatures. The results are set forth in Tables 2-6 below:









TABLE 2







Viscosity Predictions for Live Heavy Oil Sample A (API - 9.7)











Temperature
Temperature
Capillary
Predicted
Relative Error,


° C.
° K
viscosity, cp
viscosity, cp
%














30
303.15
6253




20
293.15
19,123
18,615
−2.6


10
283.15
60,019
65,848
9.7
















TABLE 3







Viscosity Predictions for Live Heavy Oil Sample B (API - 16.0)











Temperature
Temperature
Capillary
Predicted
Relative Error,


° C.
° K
viscosity, cp
viscosity, cp
%














50
323.15
1241




90
363.15
139
106
−23.9


125
398.15
40
27
−33.5


160
433.15
18
11
−39.9


200
473.15
9
5
−41.7
















TABLE 4







Viscosity Predictions for Live Heavy Oil Sample C (API - 8.0)











Temperature
Temperature
Capillary
Predicted
Relative Error,


° C.
° K
viscosity, cp
viscosity, cp
%














80
353.15
195




150
423.15
16
14
−12.0


195
468.15
6
6
0
















TABLE 5







Viscosity Predictions for Live Heavy Oil Sample D (API - 11.7)











Temperature
Temperature
Capillary
Predicted
Relative Error,


° C.
° K
viscosity, cp
viscosity, cp
%














100
373.15
250




149
422.15
40
33
−18


190
463.15
15
11
−27


240
513.15
5
5
0
















TABLE 6







Viscosity Predictions for Live Heavy Oil Sample E (API - 13.7)











Temperature
Temperature
Capillary
Predicted
Relative Error,


° C.
° K
viscosity, cp
viscosity, cp
%














100
373.15
67




149
422.15
16
14
−12.5


189.5
462.65
7
6
−14.2


240
513.15
3
3
0









It will be appreciated from the above Tables, that in three of the five examples (Samples A, C, and E), the relative error between the predicted viscosity and the measured viscosity was very small; i.e., under (−)15%. In a fourth (Sample D) of the five examples, the relative error was up to (−)27%, which is quite small relative to prior art prediction techniques. In the fifth sample (Sample B), the relative error was still less (−42%) than typical prior art prediction techniques.


A third method is seen in FIG. 4C. The temperature of a heavy oil sample is measured at 310. Then, at 320, the viscosity η of that heavy oil sample at any temperature T is estimated according to the power law equation ln(η)=a+b(T/d246)c, where “a”, “b”, “c” and “d” are constants. Preferably, constant “b” has a value between 18 and 22, constant “c” has a value between −3.4 and −3.2, and constant “d” has a value between 0.95 and 1.05. More preferably, constant “a”=−0.5734, constant “b”=20.4095, constant “c”=−3.3018, and constant “d”=1.


Using the third method, the viscosities for the five heavy oil samples (Samples A-E) were predicted according to Equation (4) above and compared to the measured viscosities at those temperatures. The results are set forth in Tables 7-11 below:









TABLE 7







Viscosity Predictions for Live Heavy Oil Sample A (API - 9.7)











Temperature
Temperature
Capillary
Predicted
Relative Error,


° C.
° K
viscosity, cp
viscosity, cp
%














30
303.15
6253
15,776
152


20
293.15
19,123
52,339
174


10
283.15
60,019
209,911
250
















TABLE 8







Viscosity Predictions for Live Heavy Oil Sample B (API - 16.0)











Temperature
Temperature
Capillary
Predicted
Relative Error,


° C.
° K
viscosity, cp
viscosity, cp
%














50
323.15
1241
2250
81


90
363.15
139
159
14


125
398.15
40
36
−10


160
433.15
18
13
−28


200
473.15
9
6
−34
















TABLE 9







Viscosity Predictions for Live Heavy Oil Sample C (API - 8.0)











Temperature
Temperature
Capillary
Predicted
Relative Error,


° C.
° K
viscosity, cp
viscosity, cp
%














80
353.15
195
274
40.7


150
423.15
16
17
6.3


195
468.15
6
6
0
















TABLE 10







Viscosity Predictions for Live Heavy Oil Sample D (API - 11.7)











Temperature
Temperature
Capillary
Predicted
Relative Error,


° C.
° K
viscosity, cp
viscosity, cp
%














100
373.15
250
98
−60.8


149
422.15
40
17
−57.5


190
463.15
15
7
−53.4


240
513.15
5
3
−40
















TABLE 11







Viscosity Predictions for Live Heavy Oil Sample E (API - 13.7)











Temperature
Temperature
Capillary
Predicted
Relative Error,


° C.
° K
viscosity, cp
viscosity, cp
%














100
373.15
67
98
46.3


149
422.15
16
17
6.3


189.5
462.65
7
7
0


240
513.15
3
3
0









Various conclusions can be drawn from Tables 7-11. The range of relative error using the third method is considerably greater than the range of relative error using the second method. This suggests that it is beneficial to know or measure the glass transition temperature in finding the viscosity of a heavy oil. However, the relative error of the third method still matches or betters that of typical prior art results.


A tool for finding the in situ viscosity of a heavy oil sample is shown in FIG. 5. More particularly, tool 400 is a borehole tool which is located in a borehole 410 traversing earth formation 420. Borehole tool 400 includes a temperature sensor 430, electronics 440, and, optionally, a sample collection module 450. The electronics 440 are provided to transmit the temperature information uphole. Optionally, the electronics 440 can include processing means (e.g., a microprocessor or digital signal processor, or dedicated electronics) for calculating the viscosity of heavy oil detected at a particular depth in the formation using the temperature sensed by temperature sensor 430, and using Equation (4) or an equation of the same form having different constants. If the glass transition temperature of the oil at that depth in the formation is known, that information may be used by the processing means. If not, a value of 246° K. (±5%) may be used. If the processing means is provided downhole, the resulting calculated viscosity value may be transmitted uphole. Otherwise, a processing means may be provided on the surface of the formation (or remotely) for taking the temperature information and generating a viscosity value. The viscosity value may be displayed on a display screen or on paper. If the borehole tool 400 is moved to various locations in the borehole, viscosity values may be generated for those locations, and the values may be displayed in a log format or in any other desired format.


There have been described and illustrated herein several embodiments of a method of determining in situ the viscosity of heavy oils, and apparatus for implementing the method. While particular embodiments of the invention have been described, it is not intended that the invention be limited thereto, as it is intended that the invention be as broad in scope as the art will allow and that the specification be read likewise. Thus, while it was disclosed that a particular number (fourteen) of oil samples were used to generate values for certain constants of the power law equation curve, it will be appreciated that other numbers of samples could be utilized. Also, while particular methods of finding the glass transition temperature of an oil sample were described, it will be appreciated that other techniques could be utilized. It will therefore be appreciated by those skilled in the art that yet other modifications could be made to the provided invention without deviating from its scope as claimed.

Claims
  • 1. A method for determining the viscosity of a heavy oil, comprising: a) measuring a first temperature T of the heavy oil; andb) determining a first viscosity η of the heavy oil at said first temperature T according to a power law equation of the form ln(η)=a+b(T/Tg)c, where “a”, “b”, and “c” are constants, and Tg is the glass transition temperature of that heavy oil.
  • 2. A method according to claim 1, wherein constant “b” has a value between 18 and 22.
  • 3. A method according to claim 1, wherein constant “c” has a value between −3.4 and −3.2.
  • 4. A method according to claim 2, wherein constant “c” has a value between −3.4 and −3.2.
  • 5. A method according to claim 1, wherein constant “a”=−0.5734, constant “b”=20.4095, and constant “c”=−3.3018.
  • 6. A method according to claim 1, wherein said heavy oil is located in a formation traversed by a borehole, and said temperature T is measured in situ.
  • 7. A method according to claim 6, wherein said glass transition temperature Tg is set to d*246, where d is a constant having a value between 0.95 and 1.05.
  • 8. A method according to claim 1, wherein said glass transition temperature Tg is measured with an instrument.
  • 9. A method according to claim 4, wherein said glass transition temperature Tg is measured with an instrument.
  • 10. A method according to claim 1, wherein said glass transition temperature Tg is obtained by obtaining a second viscosity value of said heavy oil at a second temperature, and calculating said glass transition temperature Tg by solving said power law equation for said glass transition temperature using said second viscosity value and said second temperature.
  • 11. A method according to claim 4, wherein said glass transition temperature Tg is obtained by obtaining a second viscosity value of said heavy oil at a second temperature, and calculating said glass transition temperature Tg by solving said power law equation for said glass transition temperature using said second viscosity value and said second temperature.
  • 12. An apparatus for determining the viscosity of a heavy oil, comprising: a) means for measuring a first temperature T of the heavy oil; andb) processing means for determining a first viscosity η of the heavy oil at said first temperature T according to a power law equation of the form ln(η)=a+b(T/Tg)c, where “a”, “b”, and “c” are constants, and Tg is the glass transition temperature of that heavy oil.
  • 13. An apparatus according to claim 12, wherein constant “b” has a value between 18 and 22.
  • 14. An apparatus according to claim 12, wherein constant “c” has a value between −3.4 and −3.2.
  • 15. An apparatus according to claim 13, wherein constant “c” has a value between −3.4 and −3.2.
  • 16. An apparatus according to claim 12, wherein constant “a”=−0.5734, constant “b”=20.4095, and constant “c”=−3.3018.
  • 17. An apparatus according to claim 12, wherein said glass transition temperature Tg is set to d*246, where d is a constant having a value between 0.95 and 1.05.
  • 18. An apparatus according to claim 15, wherein said glass transition temperature Tg is set to d*246, where d is a constant having a value between 0.95 and 1.05.
Priority Claims (1)
Number Date Country Kind
2,638,949 Aug 2008 CA national