Chuikina D.I., Sherstyuk S.N., * Stakhina L.D., Serebrennikova O.V.
Institute of Petroleum Chemistry SB RAS, Tomsk, Russia
The
composition of high-viscosity crude oils extracted using EOR technologies
The production of heavy-viscosity crude oils
in most oil fields of Russia and other countries is carried on using water
shutoff technology. It is known that the application of EOR methods, e.g. oil-water
two-phase flows or oil displacement agents, is liable to cause a change in the
composition and physical and chemical properties of recovered crude oil. Crude oil production results in local underbalance
condition of the well; therefore, the volume of injected water would make up
for that of produced crude [1].
New
EOR technologies developed at the Institute of Petroleum Chemistry (Tomsk,
Russia) are intended for the recovery of high-viscosity crude oils, which make
up a large proportion of the total oil production. The use of technologies developed
in combination with thermal-steam treatment methods permits reduction in crude
oil viscosity and increase in oil displacement factor. Some of these methods
employ thermotropic inorganic and polymer gels intended for the regulation of
filtration flows as well as for increasing formation steam sweeping factor and
decreasing water cut of wells. Other methods employ surfactant-based systems,
which cause generation of carbon dioxide and ammonia, thereby creating an
alkaline buffer system. The systems developed are widely used commercially not
only in Russia but also in other countries, e.g. China [2].
The goal of the present work
is to study the effect of physico-chemical EOR technologies on the dynamics of
variation in the composition of high-viscosity crude oils produced from oil fields of Russia and Germany.
Two crude oil samples were collected from No. 1- G well (Germany) before and after treatment NINKA
system. Three crude oil samples were collected from No. 3063-R (Russia) well
at different time intervals after the Netrol system injection and three samples - from No. 611-R well, which
had been subjected to the sequential treatment first with the Netrol system and then with the NINKA system. Two samples were obtained from
No. 1073-R well, which had been subjected to thermal-steam treatment followed
by the NINKA system injection. Two test samples of native oil were
collected from Nos. 3000-R and 2983-R wells located in the vicinity of Nos.
3000-R and 2983-R wells, respectively, which had not been treated by any
physico-chemical methods [3].
The group
composition of the oil samples were determined by the method of
liquid-adsorption chromatography of the deasphalted oil [4]. The data obtained is listed in the Table (here alkanes and naphthenes are designated as Sat
and aromatic hydrocarbons, resins and asphaltenes as Ar, R and A, respectively).
Table.
The composition of the crude oils produced from the oil fields of Russia
(R) and
Germany (G)
Well No. (date of sampling) |
EOR methods |
Content, wt % |
||||
Fraction Tb.p-200îC |
Sat |
Ar |
R |
À |
||
3000-R (02.2007) |
- |
22.8 |
24.1 |
38.7 |
7.0 |
7.4 |
3063-R (02.2007) |
Netrol
system |
16.3 |
23.5 |
40.3 |
12.5 |
7.4 |
3063-R (11.2008) |
Netrol
system |
13.3 |
36.4 |
31.4 |
10.0 |
8.9 |
2983-R (02.2007) |
- |
25.0 |
34.3 |
25.4 |
8.3 |
7.0 |
6111-R (02.2007) |
NINKA
system |
22.5 |
33.5 |
28.6 |
7.2 |
8.2 |
6111-R (11.2008) |
NINKA
system |
26.1 |
35.2 |
21.6 |
9.2 |
7.9 |
1073-R (12.2007) |
Thermal-steam
treatment |
4.8 |
48.9 |
21.6 |
14.9 |
9.8 |
1073-R (11.2008) |
NINKA
system + thermal-steam treatment |
24.2 |
33.7 |
24.3 |
8.4 |
9.4 |
1-G |
- |
25.2 |
36.2 |
21.9 |
12.2 |
0.3 |
1-G |
NINKA
system |
11.8 |
43.9 |
22.5 |
17.8 |
1.6 |
We examined the effect of the Netrol and NINKA systems on the group
composition of the studied crude oils. The data listed in the Table suggests
that the studied samples of the crude oil collected from the oil fields of Komi Republic are
characterized by high contents of resins+asphaltenes and those collected from the
oil fields of Germany have also high
paraffine contents. The resin+asphaltene contents of the native and treated oil
samples are in the range of 12.0 -
16.3 % and 15.0 - 20.4 % (by mass),
respectively.
The individual composition of
n-alkanes of the original and treated crude
oil samples was analyzed using gas
chromatography technique on a unit «Chromos
GC-1000» (Russia), equipped with flame-ionization detector, using helium as gas carrier; the capillary column having length of 25 m was
coated with SE-54 phase. Chromatogram recording was performed using linear
temperature programming from +80 °C
to +280 °C at a rate of 4 °C per min (see the figure).
Figure.
Molecular mass distribution of
n-alkanes of the original and treated
crude oil samples
The
data presented in Table 1 and Fig. 1suggests that no significant change has
occurred in the molecular mass distribution and in the contents of light and
heavy n-alkanes of the oils treated with the NINKA composition.
The
above changes in the group composition and properties of the crude oil must be
due to the application of the EOR technologies (for enhanced oil recovery). It
can thus be concluded that the analyzed parameters can serve as criteria of the
treatment effectiveness; besides, these might help determine the time of
operation of oil displacement systems.
Conclusions
1. It is found that
the NINKA and thermal-steam
system injections cause an increase in the hydrocarbon content of the
treated crude oil, in particular, low-boiling hydrocarbon content (oils included).
2. The resin+asphaltene
contents of the crude oils treated by the NINKA system injection are found to
decrease. A two-fold increase in the resin+asphaltene and saturated hydrocarbon
contents as well as a decrease in the aromatic hydrocarbon content is observed
for the crude oils treated by the Netrol system injection relative to the
untreated native oils.
References
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