[0001] This invention relates to the recovery and conversion by reforming of ultra heavy
tars and oils from both shallow and deep deposits.
[0002] With the traditional method of extraction and recovery of ultra heavy tar, only deposits
accessible to open-cast mining could be mined conventionally, the tar being heat-extracted
in retorts after having been excavated from the mine pit. None of the existing methods
can perform any conversion (reforming) of the oil at the mining site to allow the
pumping of an oil product into a transport pipeline. Furthermore, none of the existing
methods of thermal or chemical recovery can liquefy and extract any substantial amount
of ultra heavy hydrocarbons from the deposit, without violating the economic basis
of the mining operation.
[0003] A number of attempts have been made to achieve so called viscosity reduction in order
to increase the mobility of the hydrocarbons in the formation, thereby enabling them
to be withdrawn by conventional techniques, such as natural flow, pumping, etc. The
most popular method has been to reduce the viscosity of the hydrocarbons by elevating
the temperature, in consequence of introducing thermal energy by a wide variety of
means, such as hot water, in situ combustion, steam, heated natural and combustion
gases and chemicals convertible into high pressure hot gases. Some of those techniques
have received limited application in the recovery cf medium heavy oil, API gravity
in a range between 10° - 22°, with viscosity not much greater than 200 cp (both at
60°F) (16°C) and for a deposit with a medium thickness of 50 - 100 feet (15 - 30 metres).
[0004] The so-called medium-heavy oils just referred to are, by their nature, mobile to
a degree in the deposit, but their velocity of gravitational mobility is very low
and can be increased by decreasing their viscosity. Two basic thermal techniques of
recovery are known for these medium-heavy-oils.
[0005] One technique is usually referred to as "steam-drive", wherein steam is continuously
injected into a formation by means of an injection well. The injected steam heats
the formation and medium-viscous hydrocarbons and drives the heated hydrocarbons toward
one or more adjacent vertical production wells which are employed to withdraw them
to the surface. There are the strict conditions limiting this kind of steam driving
process, such as:
a) the formation must not be plugged by the gradually cooling products, which means
that the natural non-heated oil ought to be light and mobile enough by itself to avoid
its solidification when it cools.
b) the permeability of the formation should be high enough to allow penetration of
the steam, despite the fact that hydrocarbon material is consolidated in the pores.
c) the pressure of the steam and its temperature should be sufficiently high to allow
deep penetration into the formation.
[0006] Even when these conditions are fulfilled, only a small portion of the medium-heavy-crude,
and rather its light fraction only, can be mobilized and extracted by the steam-drive
system, and only from the very upper part of the formation, where the steam has a
natural tendency to sweep around the injection well. The lower part of the deposit
in general remains unheated and worse, becomes impregnated with the previously heated
heavier fractions of the oil from the upper part of the formation that have descended
and cooled in the lower part of the formation. As a result, the lower part of the
formation is converted into strata that are nonpermeable to any heat carriers, and
remains lost as regards further recovery processes.
[0007] An alternative to "steam-drive" is "hot water drive" which, in one of the most advanced
processes (U.S. Patent 4,305,463) employs a flushing medium injected in a series of
pressure pulses to force the heated fluids through the pores by hydraulic ramming.
However, despite dramatic improvements in the effect of "driving" the hydrocarbons
through the formation pores, the method still has application to light and medium
heavy oils only, and cannot be used for ultra heavy tars and asphalts.
[0008] In the second basic technique, commonly referred to as single well injection or "huff
and puff", steam, heated gases, combustion gases, or a combination of them is injected
into the formation through a single injection well in a batch quantity for a selected
period (huff phase). The formation is allowed to "soak", during which time the heat
permeates, heating a larger volume of the hydrocarbon reservoir, and the heated mobile
hydrocarbons are supposed then to be withdrawable from the formation through the same
well during an extraction period (puff phase).
[0009] The "huff and puff" technique has arisen due to the known inefficiency of the steam
and hot water driving methods, in an attempt to deal with heavier oils and thicker
deposits. However, this process basically contradicts the logic of the use of driving
forces in the formation, as commonly applied in the production of liquids from boreholes;
it delivers small quantities of melted, heated product, and only in the case of a
formation thick enough to allow some product to flow into the injection well from
the inverted cone region of the formation that is heated by the injection and soak.
The major portion of the heated, melted hydrocarbon is repelled in the "huff phase"
into peripheral parts of the well region where it impregnates, solidifies in and plugs
the pores of the formation.
[0010] There are, of course, many modified versions of these two basic techniques known
in the art. Many such processes involve the injection of chemicals along with, or
as an alternative to, steam into the formation; for example, see U.S. Patents Nos.
3,292,702; 3,409,083; 3,500,931; 3,782,470; 3,948,323; 4,305,463; which disclose modified
versions of the above techniques. From US-A-4008764 it is already known to recover
petroleum from formations containing viscous petroleum, including tar sand deposits,
by injecting into the formation a mixture of a liquid solvent, especially a hydrocarbon
solvent, and a carrier gas, the solvent and carrier gas being stripped from the recovered
petroleum and recycled for re-use. The solvent and carrier gas mixture may be heated
and, although not preferred, the carrier gas may be a flue gas or exhaust gas.
[0011] There are processes which include so-called "enhanced recovery" techniques employing
different chemicals and agents, all of them aiming to achieve better mobility of the
oil by gravitational and/or pressureforced flow of liquids. The majority of these
techniques are orientated towards decreasing surface tension between oil and water
phases, and/or decreasing the oil viscosity in the formation. Some of these known
techniques have limited use in the recovery of medium-heavy-crude under certain conditions.
However, despite all these efforts the majority of the oil-bearing formations all
around the world are known to contain enormous reserves of heavy and ultra-heavy hydrocarbons
from which the crude cannot technically and economically be recovered in large quantities
by the employment of any known process. None of the known processes is able to provide
any improvement in the mobility of ultra-heavy crude or any reforming and conversion
of ultra-heavy crude into a lighter product i.e. of pipeline quality - at the well
site.
[0012] Attention is directed to the European Application EP-A-0143626 filed on the same
date as the present application and claiming the same priority date, in which extraction
of heavy hydrocarbons by injection of gases and solvent into a production well and
reforming the recovered hydrocarbons on site adjacent the well head is also described
and other aspects of it claimed. Accordingly, it is an object of the present invention
to achieve a process for efficient recovery of ultra-heavy and heavy hydrocarbons
and tars, particularly crudes having SPI gravity below 15° (at 60°F) (16°C), from
consolidated or non-consolidated formations having low to very high relative permeability
to oil, gas and water.
[0013] In US-A-4008764 there is described a process for extracting viscous petroleum from
heavy hydrocarbon deposits in which a carrier gas saturated with a solvent liquid
is injected into the formation under pressure and, if desired, at a temperature elevated
above ambient. While the preferred carrier gas is nitrogen, other gases including
flue gas and exhaust gas may be used; and the solvent liquid which is preferably paraffinic
hydrocarbons, may include naphtha or carbon disulphide. At the well head the gas is
stripped from the recovered mixture for re-use and the solvent is also recovered for
re-use by a solvent distillation unit before the product is pumped away. During the
operation of the process, make-up of both carrier gas and solvent are, of course,
required.
[0014] According to the present invention, there is provided a process for the recovery
of heavy and ultra-heavy hydrocarbons from formations containing petroleum deposits,
comprising:
[0015] injecting into the formation either concurrently or cyclically:-
a) hot flue gases obtained from the combustion of fuel at high temperature and pressure;
and
b) a hydrogen donor solvent liquid; and raising the hydrocarbons thereby mobilised
and liquefied by gas lift,
[0016] and reforming the recovered hydrocarbons into a lighter product adjacent the well
head by the employment of a thermochemical reforming plant, the hot flue gases and
the solvent liquid for injection into the formation being obtained, respectively,
from the furnace of the thermochemical reforming plant and as a fraction from the
product output of the thermochemical reforming plant.
[0017] Preferably, the recovery is performed in a 'daisy' well having a main central bore
and a plurality of slant bores with their lower terminations lying in an array surrounding
the central bore. Preferably also, the flue gases are injected at high pressure down
the slant bores, the solvent is injected at a lower pressure down the main central
bore, and the gas lift is generated in a casing of the main central bore. The solvent
may be a highly hydrogenated naphthenic solvent obtained as a fraction from the product
output of the thermochemical reforming plant.
[0018] The invention further provides a well for the recovery of heavy and ultra-heavy hydrocarbons
from formations containing petroleum deposits, comprising a main central bore and
a plurality of slant bores terminating at their lower ends in an array around the
central bore, the main central bore containing at least a passage for delivering solvent
downward for injection into the formation and a passage in which extracted hycocarbons
are raised by gas lift, and the slant bores each containing at least a passage delivering
hot flue gases downward for injection into the formation.
[0019] In the preferred form, the main bore is formed at an intermediate level with a chamber
having a platform across it, the slant bores commence at and extend downward from
the platform, and above the intermediate chamber the main bore includes also a passage
delivering hot flue gases downward to the slant bores.
[0020] The well may be operated in conjunction with a thermochemical reforming plant adjacent
the well head which reforms the recovered hydrocarbons to produce a pipe-line quality
product, said plant including a furnace supplying the hot flue gases for the well,
and means for fractioning the plant output to obtain the solvent.
[0021] One example of a process, well system and plant for performing the invention will
now be described with reference to the accompanying drawing, which is a schematic
of the well and the plant.
[0022] In the example shown, the feed stock for the plant is obtained from a 'daisy' well
10 with a central solvent injection and production bore 12 surrounded by six slanting
gas injection bores 13. In the case of a thick deposit, one such 'daisy' well can
recover as much as 80% of the total accumulation of hydrocarbons over an area of approximately
1 to 1.2 acres (0.4 to 0.49 ha).
[0023] The feed stock from the annular casing 14 of the production bore 12, which will typically
be an emulsion of crude, solvent, water and gas, enters a main separator 11 at elevated
temperature and pressure, for example, 450°F (232°C) and 460 PSIG (3151 x 10³
N/m²).
[0024] The main separator 11, which has internal vertical apertured baffles 31, separates
the diluted crude from the water and sand. Vaporized hydrocarbons are condensed in
a condenser 15 which is an inlet stage of gas scrubber 16 from which carbon dioxide
and nitrogen are vented. The condenser has a coil which is cooled by raw water pumped
from a well or reservoir by a pump 17. The water, after passing through the condenser
15, is introduced into the cooling coil system 18 of the desander-desalter separator
19 from where it passes into a furnace water jacket 20 of a high pressure thermochemical
reformer 21 and thence as steam into the coil of a steam superheater 22 at about 450°F
(232°C). Between the water jacket 20 and the steam superheater 22, a by-pass stream
is withdrawn at a process control valve 24 and injected continuously, or cyclically,
into thermochemical reforming coils 23 through process control valves 25, 26. Superheated
steam from the steam superheater 22 is injected into a sand jet-washing system 27
in the main separator 11 where it condenses, and whence it carries entrained sand
into the desanding-desalting separator 19. The water is cooled somewhat in the separator
19, and the settling sand is discharged, at 28, by a screw feeder 32.
[0025] Separated, largely de-emulsified crude in solvent, under the internal pressure of
the main separator 11, is introduced at a temperature of about 420°F (216°C) into
a quencher-hydrogenator 29 in which it is reacted with superheated thermally cracked
hydrocarbon, and hydrogen generated principally in the coil system 23 of the thermochemical
reformer 21 from which it enters the quencher-hydrogenator usually at a temperature
not less than 1300°F (704°C). Quenched and hydrogenated crude under the internal pressure
of the quencher-hydrogenator 29 leaves at about 850°F (454°C) and is introduced into
a first stage fractionator 30 at an inlet temperature of, for example, 600°F (427°C).
The heavy liquid fraction separated in the fractionator 30 is recycled by a pump 33
to the process control valves 26, 25 and through the coils 23 of the thermochemical
reformer into the quencher-hydrogenator 29.
[0026] The light vapour fraction from the fractionator 30 is condensed in an air-cooled
condenser 34 and pumped by a pump 36 at about 550°F (288°C) into a second stage fractionator
35, from where the liquid fraction, which is a heavy distillate, is pumped off by
a pump 37 and recycled, via a process control valve 44 and the valves 25, 26, through
the coils 23 in the thermochemical reformer to the quencher-hydrogenator 29. The lighter
vapour fraction from the fractionator 35 is condensed in an air-cooled condenser 38
and pumped by a pump 39 at about 300°F (149°C) to a third stage fractionator 40. The
liquid fraction from the third stage fractionator is a final pipeline quality commercial
product, up to 40° API gravity, and is pumped away by a pump 41 via process control
valves 42, 43 to a final reformed product pipeline 45.
[0027] The vapour fraction from the fractionator 40 is condensed in an air-cooled condenser
46 and injected by a pump 47 via a process control valve 48, at a temperature of about
200°F (93°C), down the central pipe 49 of the production bore 12 to act as hydrogen
donor solvent to dissolve and partially reform the in situ crude by non-catalytic
hydrogenation in the presence of flue gas components and in reaction with them.
[0028] The hydrogen donor solvent is a highly hydrogenated naphthene fraction having a boiling
range usually between 150° and 250°F (66° - 121°C). The amount of solvent needed for
crude extraction is usually approximately 25% by weight of the recovered crude. Further
portions of it can be blended with the final product or employed to dilute the hydrocarbon
liquids returning to the thermochemical reformer from the first and second stage fractionators.
[0029] The high pressure, high temperature thermochemical reforming reactor 21 produces
high temperature combustion gases and performs the following functions:
i) thermal cracking,
ii) thermochemical reforming,
iii) hydrogen generation
iv) coke deposition and decoking.
[0030] The superheated flue gases leaving the thermochemical reformer at 800 - 1000°F (427
- 538°C) and 800 - 1000 PSI (5480 x 10³ - 6850 x 10³
N/m²) are fed to the outer casing 50 of the production well and thence into the gas
injection bores 13 to react with the hydrogen donor solvent and the in situ crude.
Hot water at about 200°F (93°C) is also supplied into the outer casing 50 from the
desander-desalter 19 by a pump 51.
[0031] The thermochemical reforming reactor 21 has a water-jacketed high pressure refractory
furnace 52 with a burner system fed by high pressure fuel pumps 53 and a compressor
54 into which the gaseous fraction from the condenser 46 is introduced for use as
fuel. The main fuel for the furnace may be gas or liquid hydrocarbon or pulverised
coal, but is preferably obtained from the crude being treated in the process. It is
injected at high pressure, together with compressed air which can, if desired, be
oxygen enriched. The furnace 52 opens into the section of the reactor containing the
reforming coils 23, which is followed by the section containing the steam super-heater
22. The system is designed to restrict the decompression and flow of the combustion
gases from the furnace so that a high intensity condensed flame is obtained and a
very high combustion gas temperature is reached, not less than 3000°F (1649°C).
[0032] The coil system 23 of the thermochemical reformer has dual interconnected passageways
55, 56 controlled by the process control valves 24, 25, 26. While one pass is charged
with heavy hydrocarbons from the fractionators 30, 35 for thermal cracking and coke
deposition, the other pass is fed with steam from the bypass valve 24 to provide a
water gas reaction with the deposited coke and generate hydrogen. The hydrogen mixes
with the crude and partially refined hydrocarbons and provides the hydrogenation reaction
in the quencher-hydrogenator 29. The process control valves 24, 25, 26 are operated
to switch the flows of hydrocarbons and steam cyclically between the coil passages
55 and 56 so as to maintain the water gas reaction, but the hydrogen flow into the
quencher hydrogenator, and hence the hydrogenation reaction, is substantially continuous.
Additional hydrogen is generated in the quencher hydrogenator by reaction of the flue
gases with residual steam from the coils 23.
[0033] The function of the water jacket 20 around the furnace 52 is to raise the water temperature
to generate steam for the water gas reaction with the deposited coke. Provision for
a large amount of coke deposition is made by enlargement of the diameter of the tubing
of each coil to form a coke deposition chamber in which the hydrocarbon flow velocity
is decreased, these chambers being situated toward the furnace end of the reforming
section where combustion is still continuing around the coils 23 so that the coke
deposition chambers are exposed to a very high heat intensity. With deposition of
a sufficient amount of coke, there is a lowering of the hydrocarbon viscosity, and
that means a better hydrocarbon quality is obtained after just the first stage of
reforming. The coke deposition chambers are constructed from high quality metal alloy
resistant to high temperature and high external pressure.
[0034] The process valves 24, 25, 26 have controllers designed to provide manual or automatic
control of the entire water gas reaction in the thermochemical reformer.
[0035] As regards the 'daisy' well itself, the slant bores 13 are fitted with internal tubes
60, of smaller diameter than the bore casings 62, to convey the hot flue gases from
the thermochemical reformer to discharge filters 61 at the bottom ends of the slant
wells. Seals 59 at the lower ends of the tubes 60 prevent passage of the gases up
the bores outside the tubes. The slant wells 13 can, if desired, be drilled from the
surface at points close around the main shaft 12, but in the example shown they are
drilled from inside the main shaft. To this end, the main shaft 12 has a larger diameter
upper section 12A and a smaller diameter lower section 12B, the bottom end portion
of the larger diameter upper section being constituted as a drilling gas-distributing
and product-collecting chamber 63, and the slant wells commence from a platform 64
across the chamber 63.
[0036] Above the chamber 63, the upper section 12A of the main shaft includes, concentrically
arranged and in increasing order of diameter, the central injection pipe 49 for hydrogen
donor solvent, the intermediate casing 14 for product upflow, the outer casing 50
for the hot flue gases, and finally the outer bore 65 of the shaft. The lower end
of the casing 50 terminates at the roof of the chamber 63 so that the hot flue gases
are discharged into the portion of the chamber above the platform 64 thereby to enter
the tubes 60. At the upper ends of the slant wells 13, the casings 62 are sealed to
the platform 64 and also the gaps between the casings 62 and the tubes 60 are sealed
by means of sealing cones 66, but the upper ends of the tubes 60 are open for entry
of the hot flue gases. Above the chamber 63, the annular space within the main shaft
bore 65 and the casing 50 is filled with thermally-insulating concrete 67. This concrete
can be placed by means of a tube lowered initially to the deepest part of the void
annular space to be filled and gradually retracted upwards as concrete is injected,
keeping the lower end of the tube always beneath the level of the liquid concrete.
One or more sliding thermal expansion joins may be provided in the metal casings of
the main shaft.
[0037] Below the platform 64 in the chamber 63, the lower section 12B of the main shaft
includes, concentrically arranged and in increasing order of diameter, the central
solvent injection pipe 49, the intermediate casing 14 for product upflow, and a outer
casing 68 with a multiplicity of openings 69 fitted with filters for admitting liquid
hydrocarbon product into the annular space between the casings 68 and 14. At the upper
end of the casing 68 there are openings 69 lying within and communicating with the
portion of the chamber 63 below the platform 64. The casings 62 of the slant wells
13 are likewise provided with openings 70 equipped with filters for the entry of hydrocarbon
product into the annular spaces between the casings 62 and the tubes 60, and at the
upper ends of the slant wells there are also openings 70 lying within and communicating
with the portion of the chamber 63 below the platform 64. Therefore, the hydrocarbon
product is able to pass from the casings 62 into the casing 68 by way of the lower
portion of the chamber 63.
[0038] The casings 50 and 68 of the upper and lower sections of the main shaft are sturdily
united by the chamber 63 to create an integral robust main shaft casing very resistant
to destruction by subsidence of the oil-bearing formation or the overburden. The central
injection pipe 49 opens into the lower end of the casing 68 which is formed as a filter
outlet 71 into the oil-bearing formation. Seals 72 and 73 prevent the injected solvent
from rising around the pipe 49 inside the casings 14 and 68. The lower section of
the main shaft can also be provided with small lateral tubes for discharging solvent
at different levels in the formation.
[0039] The upper end of the main shaft is equipped at the surface with a head-tree incorporating
control valves for all the downgoing and upcoming fluids and control mechanism for
a gas lift pump. To augment gas lift, the downflow of flue gases, or a portion of
it, can be switched from the casing 50 into the casing 14 which latter constitutes
the gas lift pump tube. Hydrocarbon product and gases from the formation enter the
pump tube 14 from the casing 68 through apertures 74, and the regulated entry of further
gases into the pump tube lowers the gravity of the product liquid and creates a lifting
effect according to the well known air/gas lift principle. The valve of the gas lift
pump may be simply a vertically sliding tube for selectively opening and closing gas
ports that admit into the pump tube 14 flue gas at comparatively low pressure from
the gas distribution chamber 63, or gas at higher pressure from the casing 50. If
desired, the flue gases entering the pump tube 14 may be passed in heat exchange with
the collected hydrocarbon product that is about to be extracted from the well by means
of the gas lift.
[0040] In operation, hot flue gases are injected under pressure into the formation at the
lower ends of the slant wells thereby creating a dynamic heated zone at elevated pressure
surrounding the central main shaft in very roughly hemispherical form as indicated
by the arrows 75. Hydrogen donor solvent is simultaneously injected at a controlled
pressure lower than the flue gas pressure at the bottom of the main shaft. As a consequence
of the injected flue gas pressure being higher than the pressure of the injected solvent,
a dynamic barrier is created against the outward flow and loss of solvent into the
surroundings. The heavy and ultra-heavy hydrocarbons in the formation are partially
upgraded and converted into lighter crude in situ by the action of the hydrogen donor
solvent at high temperature in the presence of components. of the flue gases. In general,
the hydrogen donor solvent will be a naphthenic material.
[0041] The hydrocarbons are thus rendered mobile by the combined actions of dissolution,
heat and partial reforming and are impelled toward the central main shaft. A continuous
inward flow of hydrocarbon liquids is produced by the displacement actions of the
solvent and flue gases and by the fact that the pressure in the vicinity of the main
shaft casing is reduced by the gas lift pumping effect in the main shaft, all fluids
therefore tending to migrate from the higher pressure injection zones to the region
around the main shaft casing. The gas lift pumping is generated by flue gases flowing
from the formation together with the liquids into the casings 68 and 14 of the main
shaft, augmented if desired by direct introduction of flue gases into the main shaft
gas lift from the chamber 63 and/or the casing 50.
[0042] The locally produced fuel burned in the thermochemical reformer will usually be highly
contaminated with sulphur, possibly as much as 5-7% by weight. The flue gases injected
into the formation will therefore contain, as major contaminants, S0₂, NO
x and CO, and the formation rock or sand will act as a decontaminating system to strip
these from the flue gases. The remaining components, primarily CO₂ and N₂ act as agents
in promoting the mobility of the hydrocarbons in the formation already liquefied by
the injected solvent. Any water in the formation will be converted in situ into steam
by the high temperature flue gases and will augment their action. If desired, further
steam can be produced by pumping or injecting waste water from the thermochemical
reforming plant into the main shaft casing where it will be gasified by the high temperature
flue gases on their way down the shaft.
[0043] If desired, a cyclical, instead of continuous, mode of operation can be employed.
Thus, in one phase the solvent can be injected not only at the bottom of the main
shaft but also at the bottoms of the slant wells and into the casings 14, 68 of the
main shaft, so that it emerges into the formation through the intake filters as well,
after which in a second phase flue gases, and steam generated in the main casing,
can be injected to sweep the liquefied hydrocarbons toward and into the lift pump
casing and generate the gas lift.
[0044] The whole process of extraction of the heavy hydrocarbons, with partial reforming,
followed by production of a pipe-line quality product adjacent the well head in the
thermochemical reforming plant, is entirely self-contained and has an advantageous
heat balance, losses of both heat and solvent being confined to a minimum. The energy
consumption for producing a valuable saleable product from previously irrecoverable
heavy hydrocarbons is therefore comparatively low, with no requirement for transport
of fuel or other consumable materials to the site. Futhermore, although the locally-produced
fuel used is heavily contaminated with sulphur, cleaning of the flue gases is largely
inherently achieved within the process itself before any residual, gases are discharged
to atmosphere, which is a major factor in pollution control.
[0045] The hydrogen donor solvent is largely recovered with the hydrocarbon product from
the well and is generated in the thermochemical reforming plant for reuse.
1. A process for the recovery of heavy and ultra-heavy hydrocarbons from formations containing
petroleum deposits, comprising:
Injecting into the formation either concurrently or cyclically:-
a) hot flue gases obtained from the combustion of fuel at high temperature and pressure;
and
b) a hydrogen donor solvent liquid;
and raising the hydrocarbons thereby mobilized and liquefied by gas lift,
and reforming the recovered hydrocarbons into a lighter product adjacent the well
head by the employment of a thermochemical reforming plant, the hot flue gases and
the solvent liquid for injection into the formation being obtained, respectively,
from the furnace of the thermochemical reforming plant and as a fraction from the
product output of the thermochemical reforming plant.
2. A process according to Claim 1, wherein the recovery is performed in a 'daisy' well
having a main central bore and a plurality of slant bores with their lower terminations
lying in an array surrounding the central bore.
3. A process according to Claim 2, wherein the flue gases are injected at high pressure
down the slant bores, the solvent is injected at a lower pressure down the main central
bore, and the gas lift is generated in a casing of the main central bore.
4. A process according to Claim 2, wherein in a first phase solvent is injected down
all bores, and in a second phase flue gases are injected down all bores and the gas
lift is generated in a casing of the main central bore.
5. A process according to any one of the preceding claims, wherein water is injected
together with the hot flue gases to generate steam.
6. A process according to any preceding claim, wherein the solvent is a highly hydrogenated
naphthenic solvent fraction from the product output.
7. A process according to any preceding claim, wherein the combustion conditions in the
furnace of the thermochemical reforming plant reach a temperature of 800-l000°F (427-538°C)
and a pressure of 800-1000 psi (5480 x 10³ - 6850 X 10³ N/m²).
8. A well for the recovery of heavy and ultra-heavy hydrocarbons from formations containing
petroleum deposits, comprising a main central bore and a plurality of slant bores
terminating at their lower ends in an array around the central bore, the main central
bore containing at least a passage for delivering solvent downward for injection into
the formation and a passage in which extracted hydrocarbons are raised by gas lift,
and the slant bores each containing at least a passage delivering hot flue gases downward
for injection into the formation.
9. A well according to Claim 8, wherein the main bore is formed at an intermediate level
with a chamber having a platform across it, the slant bores commence at and extend
downward from the platform, and above the intermediate chamber the main bore includes
also a passage delivering hot flue gases downward to the slant bores.
10. A well according to Claim 9, wherein below the platform the main bore has an outer
casing with openings for the entry of liquid hydrocarbons and gas to the gas lift
passage.
11. A well according to Claim 10, wherein the slant bores also have outer casings with
openings for the entry of liquid hydrocarbons and gas, said casings communicating
with the gas lift passage of the main bore.
12. A well according to Claim 9 or Claim 10 or Claim 11, wherein the main bore above the
intermediate chamber comprises, concentrically arranged, an inner pipe, an intermediate
casing and an outer casing surrounded by thermally-insulating concrete, the annular
passage between the intermediate and outer casings communicating with the upper part
of said chamber.
13. A well according to Claim 12, wherein each slant bore comprises an inner tube and
a concentric apertured outer casing, the inner tube communicating with the upper part
of said chamber.
14. A well according to any one of Claims 9 to 13, wherein the main bore below the platform
in the intermediate chamber comprises, concentrically arranged, an inner pipe, an
apertured intermediate casing and an apertured outer casing.
15. A well according to any one of Claims 8 to 14, further comprising valve means for
selectively admitting hot flue gases to the gas lift passage of the main bore.
16. A well according to any one of Claims 8 to 15, in combination with a thermochemical
reforming plant adjacent the well head which reforms the recovered hydrocarbons to
produce a pipe-line quality product, said plant including a furnace supplying the
hot flue gases for the well, and means for fractionating the plant output to obtain
the solvent.
1. Un procédé de récupération des hydrocarbures lourds et ultra-lourds dans des formations
contenant des gisements pétroliers, comprenant :
l'injection dans la formation, soit concomitamment soit cycliquement :
a) des gaz d'échappement provenant de la combustion, à température et sous pression
élevées, du fioul; et
b) d'un liquide solvant donneur d'hydrogène;
et la remontée des hydrocarbures ainsi mobilisés et liquéfiés grâce à une extraction
au gaz,
et le reformage des hydrocarbures récupérés pour donner un produit plus léger, proche
de la tête de puits, grâce à l'emploi d'une installation de reformage thermochimique,
les gaz d'échappement chauds et le liquide solvant servant à l'injection dans la formation
étant obtenue, respectivement, à partir du four de l'installation de reformage thermochimique
et à titre de fraction des produits sortant de l'installation de reformage thermochimique.
2. Un procédé selon la revendication 1, dans lequel la récupération est effectuée dans
un puits en "marguerite" présentant un forage central principal et une pluralité de
forages obliques ayant leur extrémités situés dans une aire entourant le forage central.
3. Un procédé selon la revendication 2, dans lequel les gaz d'échappement sont injectés
sous haute pression au fond des forages obliques, le solvant étant injecté à une pression
inférieure au fond du puits central , et l'extraction au gaz étant produite dans un
chemisage du forage central principal.
4. Un procédé selon la revendication 2, dans lequel le solvant est injecté dans une première
phase au fond de tous les forages et où les gaz d'échappement sont injectés au fond
de tous les forages dans une seconde phase et l'extraction au gaz étant produite dans
un chemisage du forage central principal.
5. Un procédé selon l'une quelconque des revendications précédentes, dans lequel de l'eau
est injectée conjointement avec les gaz d'échappement chauds pour produire de la vapeur.
6. Un procédé selon l'une quelconque des revendications précédentes, dans lequel le solvant
est une fraction de solvant naphténique fortement hydrogénée du produit de sortie.
7. Un procédé selon l'une quelconque des revendications précédentes, dans lequel les
conditions de combustion dans le four de l'installation de reformage thermochimique
atteignent une température de 427 à 538°G et une pression de 5480 x 10³ à 6850 x 10³
N/m².
8. Un puits pour la récupération des hydrocarbures lourds et ultra-lourds dans les formations
contenant des gisements de pétrole, comprenant un forage central principal et une
pluralité de forages obliques finissant à leurs extrémités inférieures dans une aire
située autour du forage central , le forage central principal contenant au moins un
passage pour faire descendre un solvant devant etre injecté dans la formation et un
passage dans lequel les hydrocarbures extraits montent par extraction au gaz, et les
forages obliques contenant chacun au moins un passage pour faire descendre les gaz
d'échappement chauds devant etre injectés dans la formation.
9. Un puits selon la revendication 8, dans lequel le forage principal est formé à un
niveau intermédiaire avec une chambre comportant une plate-forme transversale, les
forages obliques commençant et descendant à partir de la plate-forme, et le forage
principal comportant également, au-dessus de la chambre intermédiaire, un passage
pour les gaz d'échappement chauds descendant vers les forages obliques.
10. Un puits selon la revendication 9, dans lequel au-dessous de la plate-forme, le forage
principal présente un chemisage extérieur avec des ouvertures pour l'entrée des hydrocarbures
liquides et du gaz allant au passage d'extraction au gaz.
11. Un puits selon la revendication 10, dans lequel les forages obliques présentent également
des chemisages extérieurs avec des ouvertures pour l'entrée des hydrocarbures liquide
et des gaz, lesdits chemisages communiquant avec le passage d'extraction au gaz du
forage principal.
12. Un puits selon la revendication 9, ou 10 ou 11, dans lequel le forage principal situé
au-dessus de la chambre intermédiaire comprend disposés concentriquement, un tube
intérieur, un chemisage intermédiaire et un chemisage extérieure entouré par du béton
d' isolation thermique, le passage annulaire entre les chemisages intermédiaire et
extérieure communiquant avec la partie supérieure de ladite chambre.
13. Un puits selon la revendication 12, dans lequel chaque forage oblique comprend un
tube intérieur et un chemisage extérieur doté d'ouvertures concentriques, le tube
intérieure communiquant avec la partie supérieure de ladite chambre.
14. Un puits selon l'une quelconque des revendications 9 à 13, dans lequel, en dessous
de la plate-forme située dans la chambre intermédiaire, le forage principal comprend,
disposés concentriquement, un tube intérieur, un chemisage intermédiaire doté d'ouvertures
et un chemisage extérieur doté d'ouvertures.
15. Un puits selon l'une quelconque des revendications 8 à 14, comprenant en outre des
moyens de soupape pour admettre sélectivement les gaz chauds au passage, servant à
l'extraction au gaz du forage principal.
16. Un puits selon l'une quelconque des revendications 8 à 15, en combinaison avec une
installation de reformage thermochimique adjacente à la tête de puits qui réforme
les hydrocarbures récupérés pour produire un produit de qualité pipe-line, ladite
installation comprenant un four produisant les gaz chauds pour le puits, et des moyens
pour fractionner le produit de sortie de l'installation pour obtenir le solvant.
1. Verfahren zur Gewinnung von schweren ultraschweren Kohlenwasserstoffen aus Erdöl-Lagerstätte
aufweisenden Formationen,
gekennzeichnet durch
gleichlaufendes oder zyklisches Einspritzen in die Formation
a) eines heißen Abgases, das aus der Brennstoffverbrennung bei hoher Temperatur und
hohem Druck gewonnen wird, und
b) einer Wasserstoffdonatorlösemittelflüssigkeit, und durch
An- oder Emporheben der hierdurch mobilisierten und durch Gasliften verflüssigten
Kohlenwasserstoffe sowie
Reformieren der gewonnenen Kohlenwasserstoffe in ein leichteres Produkt neben dem
Bohrlochkopf durch die Anwendung einer thermochemischen Reformierungsanlage, wobei
die heißen Abgase und die Lösemittelflüssigkeit zum Einspritzen in die Formation von
dem Ofen der thermochemischen Reformierungsanlage bzw. als eine Fraktion aus dem Produktausstoß
der thermochemischen Reformierungsanlage gewonnen werden.
2. Verfahren nach Anspruch 1, dadurch gekennzeichnet, daß die Gewinnung durchgeführt wird in einem Bohrloch ('daisy' well), das eine zentrale
Bohrung sowie mehrere schräg verlaufende Bohrungen aufweist, deren untere auslaufenden
Enden in einem die zentrale Bohrung umgebenden Feld liegen.
3. Verfahren nach Anspruch 2, dadurch gekennzeichnet, daß die Abgase unter hohem Druck in die schräg verlaufenden Bohrungen und die Lösemittelflüssigkeit
unter einem geringeren Druck in die Hauptzentralbohrung eingespritzt und der Gaslift
in einem Gehäuse der Hauptzentralbohrung erzeugt wird.
4. Verfahren nach Anspruch 2, dadurch gekennzeichnet, daß in einer ersten Phase Lösemittel in sämtliche Bohrungen und in einer zweiten
Phase Abgase in sämtliche Bohrungen eingespritzt werden und der Gaslift im Gehäuse
der Hauptzentralbohrung erzeugt wird.
5. Verfahren nach einem der vorhergehenden Ansprüche 1 bis 4, dadurch gekennzeichnet, daß Wassser zusammen mit den heißen Abgasen zur Erzeugung von Dampf eingespritzt
wird.
6. Verfahren nach einem der vorhergehenden Ansprüche 1 bis 5, dadurch gekennzeichnet, daß als Lösemittel eine hochhydrierte Naphthensolventfraktion zur Dampferzeugung
verwendet wird.
7. Verfahren nach einem der vorhergehenden Ansprüche 1 bis 6, dadurch gekennzeichnet, daß die Verbrennungsbedingungen im Ofen der thermochemischen Reformierungsanlage
eine Temperatur von 427 - 538°C (800-1000°F) sowie einen Druck von 5480 x 10³ - 6850
x 10³ N/m² (800 - 1000 Pfund je Quadratzoll) erreichen.
8. Bohrloch zur Gewinnung von schweren und ultraschweren Kohlenwasserstoffen aus Erdöl-Lagerstätte
aufweisenden Formationen, gekennzeichnet durch eine Hauptzentralbohrung und mehrere schräg verlaufende Bohrungen, die an ihren
unteren Enden in ein die Zentralbohrung umgebendes Feld auslaufen, wobei die Hauptzentralbohrung
zumindest einen Durchgang für die Abgabe von Lösemittel nach unten zum Einspritzen
in die Formation und einen Durchgang aufweist, in dem extrahierte Kohlenwasserstoffe
durch Gaslift an- oder emporgehoben werden, und die schräg verlaufenden Bohrungen
jeweils zumindest einen Durchgang aufweisen, durch den heiße Abgase nach unten zum
Einspritzen in die Formation abgegeben werden.
9. Bohrloch nach Anspruch , dadurch gekennzeichnet, daß die Hauptbohrung bei einer Zwischenhöhe mit einer Kammer gebildet ist, die eine
über sie laufende Plattform besitzt, wobei die schräg verlaufenden Bohrungen an der
Plattform ansetzen und sich von dieser nach unten erstrecken und die Hauptbohrung
über der Zwischenkammer auch einen Durchgang aufweist, durch den heiße Abgase nach
unten zu den schräg verlaufenden Bohrungen abgegeben werden.
10. Bohrloch nach Anspruch 9, dadurch gekennzeichnet, daß unter der Plattform die Hauptbohrung ein Aussengehäuse mit Öffnungen für den
Eintritt der flüssigen Kohlenwasserstoffe und des Gases zum Gasliftdurchgang aufweist.
11. Bohrloch nach Anspruch 10, dadurch gekennzeichnet, daß die schrägverlaufenden Bohrungen auch Aussengehäuse mit Öffnungen für den Eintritt
der flüssigen Kohlenwasserstoffe und des Gases aufweisen, wobei die Gehäuse mit dem
Gasliftdurchgang der Hauptbohrung in Verbindung stehen.
12. Bohrloch nach einem der vorhergehenden Ansprüche 9 oder 10 oder 11, dadurch gekennzeichnet, daß die Nauptbohrung über der Zwischenkammer konzentrisch angeordnet ein Innenrohr,
ein Zwischengehäuse und ein Aussengehäuse aufweist, das von thermisch isolierendem
Beton umgeben ist, wobei der ringförmige Durchgang zwischen dem Zwischen- und dem
Aussengehäuse mit dem oberen Teil der Kammer in Verbindung steht.
13. Bohrloch nach Anspruch 12, dadurch gekennzeichnet, daß jede schräg verlaufende Bohrung ein Innenrohr und ein konzentrisch mit einer
Öffnung versehenes Aussengehäuse aufweist, wobei das Innenrohr mit dem oberen Teil
der Kammer in Verbindung steht.
14. Bohrloch nach einem f der vorhergehenden Ansprüche 9 bis 13, dadurch gekennzeichnet, daß die Hauptbohrung unter der Plattform in der Zwischenkammer konzentrisch angeordnet
ein Innenrohr, ein mit einer Öffnung versehenes Zwischengehäuse sowie ein mit einer
Öffnung versehenes Aussengehäuse aufweist.
15. Bohrloch nach einem der vorhergehenden Ansprüche 8 bis 14, gekennzeichnet durch eine Ventil- oder Schiebereinrichtung zum selektiven Einlassen von heißen Abgasen
in den Gasliftdurchtgang der Hauptbohrung.
16. Bohrloch nach einem der vorhergehenden Ansprüche 8 bis 15, gekennzeichnet durch die Kombination mit einer nahe dem Bohrkopf liegenden thermochemischen Reformierungsanlage,
durch die die gewonnenen Kohlenwasserstoffe zur Erzeugung eines zur Förderung in einer
Pipeline geeigneten Produkts reformiert werden und die einen Ofen, von dem die heißen
Abgase für das Bohrloch geliefert werden, sowie eine Einrichtung zum Fraktionieren
des Anlageausstoßes für die Gewinnung des Lösemittels aufweist.