AU2011279476A1 - Water sensitive porous medium to control downhole water production and method therefor - Google Patents
Water sensitive porous medium to control downhole water production and method therefor Download PDFInfo
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims abstract description 101
- 238000000034 method Methods 0.000 title claims description 39
- 238000004519 manufacturing process Methods 0.000 title abstract description 23
- 229920000642 polymer Polymers 0.000 claims abstract description 82
- 239000002245 particle Substances 0.000 claims abstract description 62
- 239000007787 solid Substances 0.000 claims abstract description 38
- 239000012530 fluid Substances 0.000 claims abstract description 30
- 230000007423 decrease Effects 0.000 claims abstract description 6
- 229920001577 copolymer Polymers 0.000 claims description 35
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 28
- 239000000178 monomer Substances 0.000 claims description 28
- 239000011324 bead Substances 0.000 claims description 16
- 229920001519 homopolymer Polymers 0.000 claims description 16
- -1 polysiloxanes Polymers 0.000 claims description 13
- 239000000919 ceramic Substances 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 12
- 239000008188 pellet Substances 0.000 claims description 10
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 8
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 8
- 239000012267 brine Substances 0.000 claims description 8
- 239000000945 filler Substances 0.000 claims description 8
- 229920001206 natural gum Polymers 0.000 claims description 8
- 229920001296 polysiloxane Polymers 0.000 claims description 8
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 8
- 235000019422 polyvinyl alcohol Nutrition 0.000 claims description 8
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 claims description 8
- 239000004576 sand Substances 0.000 claims description 7
- 229910052782 aluminium Inorganic materials 0.000 claims description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 6
- 239000011521 glass Substances 0.000 claims description 6
- XHZPRMZZQOIPDS-UHFFFAOYSA-N 2-Methyl-2-[(1-oxo-2-propenyl)amino]-1-propanesulfonic acid Chemical compound OS(=O)(=O)CC(C)(C)NC(=O)C=C XHZPRMZZQOIPDS-UHFFFAOYSA-N 0.000 claims description 5
- 241000758789 Juglans Species 0.000 claims description 5
- 235000009496 Juglans regia Nutrition 0.000 claims description 5
- 239000004677 Nylon Substances 0.000 claims description 5
- 229910001570 bauxite Inorganic materials 0.000 claims description 5
- 238000004132 cross linking Methods 0.000 claims description 5
- 239000003431 cross linking reagent Substances 0.000 claims description 5
- 239000012634 fragment Substances 0.000 claims description 5
- 229910052751 metal Inorganic materials 0.000 claims description 5
- 239000002184 metal Substances 0.000 claims description 5
- 229920001778 nylon Polymers 0.000 claims description 5
- 238000012856 packing Methods 0.000 claims description 5
- 235000020234 walnut Nutrition 0.000 claims description 5
- 229910052783 alkali metal Inorganic materials 0.000 claims description 4
- 238000004873 anchoring Methods 0.000 claims description 4
- QRHCILLLMDEFSD-UHFFFAOYSA-N bis(ethenyl)-dimethylsilane Chemical compound C=C[Si](C)(C)C=C QRHCILLLMDEFSD-UHFFFAOYSA-N 0.000 claims description 4
- KUQWZSZYIQGTHT-UHFFFAOYSA-N hexa-1,5-diene-3,4-diol Chemical compound C=CC(O)C(O)C=C KUQWZSZYIQGTHT-UHFFFAOYSA-N 0.000 claims description 4
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- ZIUHHBKFKCYYJD-UHFFFAOYSA-N n,n'-methylenebisacrylamide Chemical compound C=CC(=O)NCNC(=O)C=C ZIUHHBKFKCYYJD-UHFFFAOYSA-N 0.000 claims description 4
- BLYOHBPLFYXHQA-UHFFFAOYSA-N n,n-bis(prop-2-enyl)prop-2-enamide Chemical compound C=CCN(CC=C)C(=O)C=C BLYOHBPLFYXHQA-UHFFFAOYSA-N 0.000 claims description 4
- ZQXSMRAEXCEDJD-UHFFFAOYSA-N n-ethenylformamide Chemical compound C=CNC=O ZQXSMRAEXCEDJD-UHFFFAOYSA-N 0.000 claims description 4
- 125000001453 quaternary ammonium group Chemical group 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 claims description 4
- 238000001035 drying Methods 0.000 claims description 3
- DYUWTXWIYMHBQS-UHFFFAOYSA-N n-prop-2-enylprop-2-en-1-amine Chemical compound C=CCNCC=C DYUWTXWIYMHBQS-UHFFFAOYSA-N 0.000 claims description 3
- 239000011363 dried mixture Substances 0.000 claims description 2
- 230000015572 biosynthetic process Effects 0.000 abstract description 13
- 238000000576 coating method Methods 0.000 abstract description 9
- 239000011248 coating agent Substances 0.000 abstract description 7
- 239000003921 oil Substances 0.000 description 23
- 238000005755 formation reaction Methods 0.000 description 12
- 239000007789 gas Substances 0.000 description 12
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
- 229910001220 stainless steel Inorganic materials 0.000 description 6
- 239000010935 stainless steel Substances 0.000 description 6
- 229930195733 hydrocarbon Natural products 0.000 description 5
- 150000002430 hydrocarbons Chemical class 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 239000008398 formation water Substances 0.000 description 4
- 230000000670 limiting effect Effects 0.000 description 4
- 238000001000 micrograph Methods 0.000 description 4
- 230000004044 response Effects 0.000 description 4
- 230000002401 inhibitory effect Effects 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000011068 loading method Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 230000004913 activation Effects 0.000 description 2
- 239000003570 air Substances 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 229920006158 high molecular weight polymer Polymers 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 230000035699 permeability Effects 0.000 description 2
- 238000005086 pumping Methods 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 208000002565 Open Fractures Diseases 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 230000002730 additional effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000012080 ambient air Substances 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000004941 influx Effects 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 230000003715 interstitial flow Effects 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 239000003129 oil well Substances 0.000 description 1
- 239000011236 particulate material Substances 0.000 description 1
- 239000013618 particulate matter Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 125000006850 spacer group Chemical group 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- E—FIXED CONSTRUCTIONS
- E21—EARTH OR ROCK DRILLING; MINING
- E21B—EARTH OR ROCK DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
- E21B34/00—Valve arrangements for boreholes or wells
- E21B34/06—Valve arrangements for boreholes or wells in wells
- E21B34/08—Valve arrangements for boreholes or wells in wells responsive to flow or pressure of the fluid obtained
-
- E—FIXED CONSTRUCTIONS
- E21—EARTH OR ROCK DRILLING; MINING
- E21B—EARTH OR ROCK DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
- E21B43/00—Methods or apparatus for obtaining oil, gas, water, soluble or meltable materials or a slurry of minerals from wells
- E21B43/32—Preventing gas- or water-coning phenomena, i.e. the formation of a conical column of gas or water around wells
-
- E—FIXED CONSTRUCTIONS
- E21—EARTH OR ROCK DRILLING; MINING
- E21B—EARTH OR ROCK DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
- E21B43/00—Methods or apparatus for obtaining oil, gas, water, soluble or meltable materials or a slurry of minerals from wells
- E21B43/34—Arrangements for separating materials produced by the well
Landscapes
- Geology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Mining & Mineral Resources (AREA)
- Environmental & Geological Engineering (AREA)
- Fluid Mechanics (AREA)
- Physics & Mathematics (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Silicates, Zeolites, And Molecular Sieves (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Manufacturing Of Micro-Capsules (AREA)
Abstract
Water production produced from a subterranean formation is inhibited or controlled by consolidated water sensitive porous medium (WSPM) packed within the flow path of the wellbore device container. The WSPM includes solid particles having a water hydrolyzable polymer at least partially coating the particles. The WSPM is packed under pressure within the flow path of the wellbore device container to consolidate it. The WSPM increases resistance to flow as water content increases in the fluid flowing through the flow path and decreases resistance to flow as water content decreases in the fluid flowing through the flow path.
Description
WO 2012/009184 PCT/US20111/042993 WATER SENSITIVE POROUS MEDIUM TO CONTROL DOWNHOLE WATER PRODUCTION AND METHOD THEREFOR TECHNICAL FIELD [0001] The present invention relates to apparatus and methods for controlling the production of fluid through a device in a wellbore and methods for constructing said apparatus, and more particularly relates, in one non limiting embodiment, to apparatus for and methods of inhibiting and controlling the flow of water through a wellbore from subterranean formations during hydrocarbon recovery operations and methods for constructing said apparatus. TECHNICAL BACKGROUND [0002] Hydrocarbons such as oil and gas are recovered from a subterra nean formation using a wellbore drilled into the formation. Unwanted water production is a major problem in maximizing the hydrocarbon production potential of a subterranean well. Tremendous costs may be incurred from separating and disposing of large amounts of produced water, inhibiting the corrosion of tubulars contacted by the water, replacing corroded tubular equipment downhole, and surface equipment maintenance. Shutting off, preventing and controlling unwanted water production is a necessary condition to maintaining a productive field. [0003] Oil and gas wells are typically completed by placing a casing along the wellbore length and perforating the casing adjacent each such production zone to extract the formation fluids (such as hydrocarbons) into the wellbore. These production zones are sometimes separated or isolated from each other by installing a packer between the production zones. Fluid from each production zone entering the wellbore is drawn into a tubing that runs to the surface. It is desirable to have substantially even drainage along the pro duction zone. Uneven drainage may result in undesirable conditions such as an invasive gas cone or water cone. In the instance of an oil-producing well, for example, a gas cone may cause an in-flow of gas into the wellbore that could WO 2012/009184 PCT/US2011/042993 2 significantly reduce oil production. Similarly, a water cone may cause an in-flow of water into the oil production flow that reduces the amount and quality of the produced oil. [0004] Accordingly, it is desired to provide even drainage across a pro duction zone and/or the ability to selectively close off or reduce in-flow within production zones experiencing an undesirable influx of water and/or gas. In other words, it would additionally be desirable to discover an apparatus and method which could improve the control of unwanted water production from subsurface formations. SUMMARY [0005] There is provided in one non-limiting embodiment a wellbore device for controlling a flow of a fluid through a flow path therein. The wellbore device includes a container comprising a flow path and a consolidated water sensitive porous medium (WSPM) packed within the flow path of the wellbore device container. In turn, the WSPM includes solid particles and at least one water hydrolyzable polymer at least partially coated on the solid particles. [0006] There is additionally provided in one non-restrictive version, a method of constructing a wellbore device for controlling a flow of a fluid through a flow path in the wellbore device, where the method involves mixing solid particles with at least one water hydrolyzable polymer in the presence of a fluid that may be water or brine to give a mixture. The method further includes at least partially drying the mixture. Additionally the method involves packing the at least partially dried mixture into the flow path of the container of the wellbore device to form a consolidated water sensitive porous medium (WSPM). [0007] There is also provided, in another non-limiting form, a method for controlling a flow of a fluid through a flow path in a wellbore device in a well bore. The method involves flowing the fluid through the flowpath in the wellbore device and controlling a resistance to flow of the fluid through the flow path whereby: resistance to flow increases as water content of the fluid increases, and resistance to flow decreases as water content of the fluid decreases. The WO 2012/009184 PCT/US2011/042993 3 wellbore device used includes a container (which may be coextensive there with) comprising the flow path and a consolidated water sensitive porous medium (WSPM) packed within the flow path of the wellbore device container. In turn the WSPM includes solid particles and at least one water hydrolyzable polymer at least partially coated on the solid particles. BRIEF DESCRIPTION OF THE DRAWINGS [0008] FIG. 1 is a schematic illustration of water sensitive porous media (WSPM) installed inside a wellbore to control the production of water; [0009] FIGS. 2A and 2B are schematic illustrations of different water cuts generating different flow resistance when flowing through a WSPM as a result of different degrees of polymer chain activation (expansion); [0010] FIG. 3 is a graph of the pressure differential of WSPM (cross linked VF-1 copolymer coated on 20-60 mesh (850-250 micron) HSP* proppant) at 200OF (930C) with diesel and simulated formation brine (SFB); [0011] FIG. 4 is a graph of a pressure drop response for different water cut fluids flowing through WSPM at 200OF (93 C); [0012] FIG. 5 is a microphotograph of 20/40 mesh (850/425 micron) HSP ceramic proppant before polymer coating; and [0013] FIG. 6 is a microphotograph of 20/40 mesh (850/425 micron) HSP ceramic proppant after polymer coating. DETAILED DESCRIPTION [0014] A method has been discovered for building a water sensitive porous medium (WSPM) to control downhole water production through a flowpath in a wellbore device installed inside of a wellbore. The WSPM may be constructed of water-soluble or water-hydrolyzable, high molecular weight polymers which are coated on solid particles, such as sand, glass beads, and ceramic proppants. The coated particles are packed under high pressure to form a consolidated homogenous and high porosity porous medium within a container of a wellbore device. The container and the wellbore device may be WO 2012/009184 PCT/US2011/042993 4 separate structures, where the container is part of the wellbore device, or the container and the wellbore device may be the same and coextensive. After the polymers are fully hydrolyzed in water or brine, the polymers may be optionally crosslinked with crosslinking agents. The solid particles may be mixed with the polymer solution, e.g. in a blender or mixer, at a particular ratio. [0015] As a blender or mixer is continuous stirring the mixture of solid particles and polymer solution, blowing ambient air, hot air, nitrogen, or vacuuming is applied to the mixture to at least partially or completely dry the polymer. The polymer coated particles are loaded into a container to pack into consolidated porous medium at high pressure. The packed container, as part of a downhole tool, is installed in a wellbore. When formation water is flowed through the WSPM interstitial flow channels, the coated polymers extend their polymer chains into the pore flow channels, resulting in increased fluid flow resistance. Conversely, when oil flows through the WSPM, the polymer chains shrink back to open the flow channels wider for the desired oil flow. This process has been demonstrated to be repeatable and reversible as water/oil fluid composition varies. [0016] When water mixed with oil flows through the WSPM, the magni tude in pressure drop across the flow channels depends on the percentage of water in the mixture (water/oil ratio, or WOR). Higher water cuts result in higher resulting pressure drops. As will be discussed, lab testing data has confirmed that pressure drops across WSPM change with water percentage of flowing through fluids. [0017] More specifically, the production of unwanted subterranean formation water may be prevented, controlled or inhibited by a method involving treating particles with high molecular weight, water-hydrolyzable polymers, and incorporating the particles into a water sensitive porous medium (WSPM) in a wellbore device placed within the wellbore. The polymer-coated particles are introduced into a container of a wellbore device under high pressure to form a consolidated WSPM in the device before its introduction downhole.
WO 2012/009184 PCT/US2011/042993 5 [0018] Generally, the relatively high molecular weight polymers that have components or functional groups that anchor, affiliate or attach onto the surface of the solid particles. The polymers are hydrophilic and/or hydrolyzable mean ing they swell or expand in physical size upon contact with water. The average particle size of the particles may range from about 10 mesh to about 100 mesh (from about 2000 microns to about 150 microns). Alternatively, the average particle size of the particles may range from about 20 mesh independently to about 60 mesh (from about 840 microns to about 250 microns); where the term "independently" means that any lower threshold may be combined with any upper threshold. Thus, it should be understood that the solid particles which serve as a substrate to the water hydrolyzable polymer are relatively small, particulate matter, but should not be confused with atomic particles or sub atomic particles. [0019] The particles may be any of a wide variety of solid particulate material; suitable materials include, but are not necessarily limited to, sand, glass beads, ceramic beads, metal beads, bauxite grains, walnut shell frag ments, aluminum pellets, nylon pellets and combinations thereof, including conventional proppants and gravel, and, including proppants and gravel of to be-developed materials. Proppants are known in the oilfield as sized particles typically mixed with fracturing fluids to hold open fractures after a hydraulic fracturing treatment. Proppants are sorted for size and sphericity to provide an effective conduit for the production of oil and/or gas from the reservoir to the wellbore. "Gravel" has a particular meaning in the oilfield relating to particles of a specific size or specific size range which are placed between a screen that is positioned in the wellbore and the surrounding annulus. The size of the gravel is selected to prevent the passage of sand from the formation through the gravel pack. [0020] Further, the solid particles, e.g. proppants or gravel, may suitably be a variety of materials including, but not necessarily limited to, sand (the most common component of which is silica, i.e. silicon dioxide, SiO 2 ), glass beads, WO 2012/009184 PCT/US2011/042993 6 ceramic beads, metal beads, bauxite grains, walnut shell fragments, aluminum pellets, nylon pellets and combinations thereof. [0021] The particles may be coated by a method that involves at least partially hydrolyzing the polymer in a liquid including, but not necessarily limited to, water, brine, glycol, ethanol and mixtures thereof. The particles are then inti mately mixed or contacted with the liquid containing the polymer to contact the surfaces of the particles with the polymer. The liquid is then at least partially vaporized or evaporated through vacuum, or the use of heat and/or contact with a dry gas such as air, nitrogen, or the like. The coating method may be conducted at a temperature between ambient up to about 200OF (about 930C), to facilitate quick drying of the coating. It may not be necessary in some embodiments to completely dry the coating. [0022] The loading of the polymers may be a ratio of weight of solid particles to weight of dry water hydrolyzable polymer ranging from about 10,000:1 to about 10:1; alternatively ranging from about 500:1 independently to about 25:1. The solid particles should be at least partially coated by the polymer; that is, while it is desirable to completely coat the solid particles with the polymer, the method and apparatus may still be considered successful if the particles are at least partially coated to the extent the WSPM functions effectively for the purposes noted herein. [0023] The high pressure used to pack the water hydrolyzable polymer coated particles into the container of the wellbore device through which the flow path exists may range from about 50 to about 2000 psi (about 0.3 to about 13.8 MPa), alternatively from about 100 independently to about 1000 psi (about 0.7 to about 6.9 MPa). [0024] The WSPM placed in the wellbore will control unwanted formation water flowing through the wellbore while not adversely affecting the flow of oil and gas. When water flows into the WSPM, the polymers anchored on the solid particles expand to reduce the water flow channel and increase the resistance to water flow. The polymers may be understood to interact chemically, sonically or mechanically with a component of the produced or in-flowing formation WO 2012/009184 PCT/US2011/042993 7 fluids, e.g. water molecules. This desired response may be variously described as resistance, permeability, impedance, etc., where the flow of hydrocarbons (e.g. oil and gas) is desirable, but the flow of water is not. This interaction varies the resistance to flow across the flow path of the wellbore device. When oil and/or gas flow through this special porous media, the polymers shrink to open the flow channel for oil and/or gas flow. The pre-treated particles, (e.g. proppants) are expected to form homogeneous porous media with the polymer uniformly distributed in the media to increase the efficiency of the polymer controlling unwanted water production. [0025] In more detail, suitable water hydrolyzable polymers include those having a weight average molecular weight greater than 100,000. Suitable, more specific examples of water hydrolyzable polymers include, but are not neces sarily limited to, homopolymers and copolymers of acrylamide, sulfonated or quaternized homopolymers and copolymers of acrylamide, polyvinylalcohols, polysiloxanes, hydrophilic natural gum polymers and chemically modified deriv atives thereof. Crosslinked versions of these polymers may also be suitable, including but not necessarily limited to, crosslinked homopolymers and copoly mers of acrylamide, crosslinked sulfonated or quaternized homopolymers and copolymers of acrylamide, crosslinked polyvinylalcohols, crosslinked polysilox anes, crosslinked hydrophilic natural gum polymers and chemically modified derivatives thereof. Further specific examples of suitable water hydrolyzable polymers include, but are not necessarily limited to, copolymers having a hydrophilic monomeric unit, where the hydrophilic monomeric unit is selected from the group consisting of ammonium and alkali metal salt of acrylamido methylpropanesulfonic acid (AMPS), a first anchoring monomeric unit based on N-vinylformamide and a filler monomeric unit, where the filler monomeric unit is selected from the group consisting of acrylamide and methylacrylamide. Addi tional suitable water hydrolyzable polymers include, but are not necessarily limited to, copolymers of vinylamide monomers and monomers containing ammonium or quaternary ammonium moieties, copolymers of vinylamide monomers and monomers comprising vinylcarboxylic acid monomers and/or WO 2012/009184 PCT/US2011/042993 8 vinylsulfonic acid monomers, and salts thereof, and these aforementioned copolymers further comprising a crosslinking monomer selected from the group consisting of bis-acrylamide, diallylamine, N,N-diallylacrylamide, divinyloxy ethane, divinyldimethylsilane. [0026] In an optional embodiment, when the polymers are fully or essentially completely hydrolyzed, they may be cross-linked to increase their molecular weight. Suitable crosslinking agents include, but are not necessarily limited to, aluminum, boron, chromium, zirconium, titanium, and other inorganic based and organic based crosslinking agents and other conventional crosslink ing agents. [0027] These polymers are sometimes referred to as relative permeabil ity modifiers (RPMs) and more information about RPMs suitable to be of use in the method and compositions described herein may be found in U.S. Pat. Nos., 5,735,349; 6,228,812; 7,008,908; 7,207,386 and 7,398,825. [0028] Shown in FIG. 1 is a schematic illustration of an oil well 10 having a wellbore 12, which happens to be vertical in part and horizontal in part, in a subterranean formation 14 that contains both oil and water. Water sensitive porous media (WSPM) within wellbore devices 16 have been installed at four locations between packers 18 along the horizontal section of the wellbore 12 to control the production of water. The flow of oil from the formation 14 into the wellbore 12 is schematically indicated by black arrows 20, whereas the flow of water is schematically indicated by gray arrows 22. The flow of oil 20 is uninhi bited by the WSPM due to the lack of resistance of the unhydrolyzed polymer, whereas the flow of water is inhibited by the increased resistance of the hydrolyzed polymer, as indicated by the lower water flow at small gray arrows 24. [0029] Shown in FIG. 2 is a schematic illustration of different water cuts generating different flow resistance when flowing through a WSPM 16 as a result of different degrees of polymer chain activation (expansion). As pre viously discussed, the WSPM 16 includes solid particles 30 having water hydrolyzable polymers 32 at least partially coated thereon or adhered thereto.
WO 2012/009184 PCT/US2011/042993 9 The water droplets are schematically represented by gray circles 34 and the oil droplets are schematically represented by black circles 36. FIG. 2A schemati cally illustrates the WSPM 16 where a 25% water cut flows in the direction shown (left to right) where the relatively low amount of water droplets 34 cause a relatively small amount of the polymer 32 to swell, enlarge or hydrolyze increasing resistance to flow. FIG. 2B schematically illustrates the WSPM 16 where a larger 50% water cut flows in the direction shown (left to right) where the relatively equal amount of water droplets 34 compared to the oil droplets 36 cause a relatively larger amount of the polymer 32 to swell, enlarge or hydro lyze further increasing resistance to flow, as compared with FIG. 2A. [0030] The invention will now be illustrated with respect to certain exam ples which are not intended to limit the invention in any way but simply to further illustrated it in certain specific embodiments. EXAMPLES [0031] FIG. 5 is a microphotograph of 20/40 mesh (850/425 micron) HSP* ceramic proppant before polymer coating. HSP proppant is available from Carbo Ceramics. FIG. 6 is a microphotograph of the same 20/40 mesh (850/425 micron) HSP ceramic proppant after polymer coating. It may be seen that each proppant particle in FIG. 6 is fully coated and bonded by the polymer using the coating method described. [0032] One non-limiting packing procedure for building a WSPM as a water sensitive flow channel (WSFC) is set out in Table 1. The procedure involves packing polymer coated proppants into 1 inch (2.5 cm) ID and 12 inch (30 cm) long stainless steel tube with both end caps forming a uniform porous medium.
WO 2012/009184 PCT/US2011/042993 10 TABLE I Packing Procedure 1) The stainless steel tube (container, simulating a wellbore device) is affixed on one end with an end cap; a 100 mesh (150 micron) stainless screen is laid inside the end cap to hold the polymer coated proppants; 2) The stainless steel tube is placed into a compressor with open end up; 3) One spoon of polymer coated proppants (about 5 grams) is loaded inside of the tube, and a 0.97 inch (2.5) ID and 18 inch-long (45.7 cm) alumina rod is put against the proppants inside of the tube; 4) 1200 pound force from a compressor is loaded onto the alumina rod to compress the polymer coated proppants into a consolidated porous medium; 5) Steps 3) and 4) are repeated until the length of the porous medium reaches desired porous medium length; 6) Another 100 mesh (150 micron) stainless screen is affixed on the top of the stainless steel tube; 7) Stainless steel spacers are added into the tube if there is any open space inside of the tube; and 8) The top end cap was tightened and the tube is ready for testing. [0033] FIG. 3 is a graph of the pressure differential of crosslinked VF-1 copolymer coated on 20-60 mesh (850-250 micron) HSP proppant at 200OF (930C) with diesel and simulated formation brine (SFB). VF-1 is a cross-linked vinylamide-vinylsulfonate copolymer. The HSP proppants were coated with the VF-1 polymer as described above. The polymer loading was 0.4 % bw (by weight) of the proppant weight. FIG. 3 is a response test graph showing that the pressure differential of the polymer-coated proppant WSPM placed inside of a 12-inch long, 1-inch ID stainless steel tube (about 30 cm long by about 2.5 cm ID) changes when pumping with oil (diesel in this Example) relative to pumping with formation water (Simulated Formation Brine or SFB) flowing through the pack. This graph demonstrates that the pack exhibits high flow resistance for water and low flow resistance for oil.
WO 2012/009184 PCT/US2011/042993 11 [0034] FIG. 4 is a graph of a pressure drop response for different water cut fluids flowing through a WSPM at 200OF (930C). The fluids were blends of brine and diesel. With increasing amounts of water (greater water cut percen tage), the higher the pressure drop. The WSPM was made from VF-1 coated 50-60 mesh (297 to 250 micron) ceramic proppants with polymer loading 0.4%. Different water cuts are marked on FIG 4. [0035] In the foregoing specification, the invention has been described with reference to specific embodiments thereof, and has been demonstrated as effective in providing methods for inhibiting and controlling water flow through wellbores, particularly wellbore devices having flow paths containing solid particles coated with a water hydrolyzable polymer. However, it will be evident that various modifications and changes can be made thereto without departing from the broader scope of the invention as set forth in the appended claims. Accordingly, the specification is to be regarded in an illustrative rather than a restrictive sense. For example, specific combinations of solid particles, water hydrolyzable polymers, wellbore devices and other components falling within the claimed parameters, but not specifically identified or tried in a particular composition or method, are expected to be within the scope of this invention. Further, it is expected that the components and proportions of the solid particles and polymers and steps of constructing the wellbore devices may change somewhat from wellbore device to another and still accomplish the stated purposes and goals of the methods described herein. For example, the assembly methods may use different pressures and additional or different steps than those exemplified herein. [0036] The words "comprising" and "comprises" as used throughout the claims is interpreted "including but not limited to". [0037] The present invention may suitably comprise, consist or consist essentially of the elements disclosed and may be practiced in the absence of an element not disclosed. For instance, a wellbore device for controlling a flow of a fluid through a flow path may consist of or consist essentially of a container WO 2012/009184 PCT/US2011/042993 12 comprising a flow path and a consolidated water sensitive porous medium (WSPM) packed within the flow path of the wellbore device container, where the WSPM consists of or consists essentially of solid particles and at least one water hydrolyzable polymer at least partially coated on the solid particles.
Claims (17)
1. A wellbore device for controlling a flow of a fluid through a flow path therein, the wellbore device comprising: a container comprising the flow path; and a consolidated water sensitive porous medium (WSPM) packed within the flow path of the container, the WSPM comprising: solid particles; and at least one water hydrolyzable polymer at least partially coated on the solid particles.
2. The wellbore device of claim 1 where the average particle size of the solid particles ranges from 10 to 100 mesh (2000 to 150 microns).
3. The wellbore device of claim 1 or 2 where the WSPM is packed within the container at a pressure ranging from 50 to 2000 psi (0.3 to 13.8 MPa).
4. The wellbore device of claim 3 where the ratio of weight of solid particles to weight of dry water hydrolyzable polymer ranges from 10,000:1 to 10:1.
5. The wellbore device of claim 3 where the water hydrolyzable polymer is crosslinked.
6. The wellbore device of claim 1 or 2 where the water hydrolyzable polymer has a weight average molecular weight greater than 100,000 and is selected from the group consisting of: homopolymers and copolymers of acrylamide, sulfonated or quaternized homopolymers and copolymers of acrylamide, polyvinylalcohols, polysiloxanes, hydrophilic natural gum polymers and chemically modified derivatives thereof; WO 2012/009184 PCT/US2011/042993 14 crosslinked homopolymers and copolymers of acrylamide, crosslinked sulfonated or quaternized homopolymers and copolymers of acrylamide, crosslinked polyvinylalcohols, crosslinked polysiloxanes, crosslinked hydrophilic natural gum polymers and chemically modified derivatives thereof; copolymers having a hydrophilic monomeric unit, where the hydrophilic monomeric unit is selected from the group consisting of ammonium and alkali metal salt of acrylamidomethylpropanesulfonic acid, a first anchoring monomeric unit based on N-vinylformamide and a filler monomeric unit, where the filler monomeric unit is selected from the group consisting of acrylamide and methylacrylamide; and copolymers of vinylamide monomers and monomers containing ammonium or quaternary ammonium moieties, copolymers of vinylamide monomers and monomers comprising vinylcarboxylic acid monomers and/or vinylsulfonic acid monomers, and salts thereof, and these copolymers comprising a crosslinking monomer selected from the group consisting of bis-acrylamide, dialylamine, N,N-diallylacrylamide, divinyloxyethane, divinyldimethylsilane; and where the solid particles comprise sand, glass beads, ceramic beads, metal beads, bauxite grains, walnut shell fragments, aluminum pellets, nylon pellets and combinations thereof.
7. A method of constructing a wellbore device for controlling a flow of a fluid through a flow path in the wellbore device, the method comprising: mixing solid particles with at least one water hydrolyzable polymer in the presence of a fluid selected from the group consisting of water and brine to give a mixture; at least partially drying the mixture; WO 2012/009184 PCT/US2011/042993 15 packing the at least partially dried mixture into the flow path of a container of the wellbore device to form a consolidated water sensitive porous medium (WSPM).
8. The method of claim 7 further comprising: where in mixing the solid particles with the water hydrolyzable polymer, the mixing is in the presence of an amount of water effective to fully hydrolyze the water hydrolyzable polymer; and crosslinking the water hydrolyzable polymer with at least one crosslinking agent.
9. The method of claim 7 or 8 where the average particle size of the solid particles ranges from 10 to 100 mesh (2000 to 150 microns).
10. The method of claim 7 or 8 where the WSPM is packed within the wellbore device container at a pressure ranging from 50 to 2000 psi (0.3 to 13.8 MPa).
11. The method of claim 10 where the ratio of weight of solid particles to weight of dry water hydrolyzable polymer ranges from 10,000:1 to 10:1.
12. The method of claim 9 where the water hydrolyzable polymer has a weight average molecular weight greater than 100,000 and is selected from the group consisting of: homopolymers and copolymers of acrylamide, sulfonated or quaternized homopolymers and copolymers of acrylamide, polyvinylalcohols, polysiloxanes, hydrophilic natural gum polymers and chemically modified derivatives thereof; crosslinked homopolymers and copolymers of acrylamide, crosslinked sulfonated or quaternized homopolymers and copolymers of acrylamide, crosslinked polyvinylalcohols, crosslinked WO 2012/009184 PCT/US2011/042993 16 polysiloxanes, crosslinked hydrophilic natural gum polymers and chemically modified derivatives thereof; copolymers having a hydrophilic monomeric unit, where the hydrophilic monomeric unit is selected from the group consisting of ammonium and alkali metal salt of acrylamidomethylpropanesulfonic acid, a first anchoring monomeric unit based on N-vinylformamide and a filler monomeric unit, where the filler monomeric unit is selected from the group consisting of acrylamide and methylacrylamide; and copolymers of vinylamide monomers and monomers containing ammonium or quaternary ammonium moieties, copolymers of vinylamide monomers and monomers comprising vinylcarboxylic acid monomers and/or vinylsulfonic acid monomers, and salts thereof, and these copolymers comprising a crosslinking monomer selected from the group consisting of bis-acrylamide, diallylamine, N,N-diallylacrylamide, divinyloxyethane, divinyldimethylsilane; and where the solid particles comprise sand, glass beads, ceramic beads, metal beads, bauxite grains, walnut shell fragments, aluminum pellets, nylon pellets and combinations thereof.
13. A method for controlling a flow of a fluid through a flow path in a wellbore device within a wellbore, the method comprising: flowing the fluid through the flowpath in the wellbore device; and controlling a resistance to flow of the fluid through the flow path whereby: resistance to flow increases as water content of the fluid increases, and resistance to flow decreases as water content of the fluid decreases; the wellbore device comprising: WO 2012/009184 PCT/US2011/042993 17 a container comprising the flow path; and a consolidated water sensitive porous medium (WSPM) packed within the flow path of the container, the WSPM comprising: solid particles; and at least one water hydrolyzable polymer at least partially coated on the solid particles.
14. The method of claim 13 where the average particle size of the solid particles ranges from 10 to 100 mesh (2000 to 150 microns).
15. The method of claim 13 or 14 where the WSPM is packed within the wellbore device container at a pressure ranging from 50 to 2000 psi (0.3 to 13.8 MPa).
16. The method of claim 15 where the ratio of weight of solid particles to weight of dry water hydrolyzable polymer ranges from 10,000:1 to 10:1.
17. The method of claim 15 where the water hydrolyzable polymer has a weight average molecular weight greater than 100,000 and is selected from the group consisting of: homopolymers and copolymers of acrylamide, sulfonated or quaternized homopolymers and copolymers of acrylamide, polyvinylalcohols, polysiloxanes, hydrophilic natural gum polymers and chemically modified derivatives thereof; crosslinked homopolymers and copolymers of acrylamide, crosslinked sulfonated or quaternized homopolymers and copolymers of acrylamide, crosslinked polyvinylalcohols, crosslinked polysiloxanes, crosslinked hydrophilic natural gum polymers and chemically modified derivatives thereof; copolymers having a hydrophilic monomeric unit, where the hydrophilic monomeric unit is selected from the group consisting of WO 2012/009184 PCT/US2011/042993 18 ammonium and alkali metal salt of acrylamidomethylpropanesulfonic acid, a first anchoring monomeric unit based on N-vinylformamide and a filler monomeric unit, where the filler monomeric unit is selected from the group consisting of acrylamide and methylacrylamide; and copolymers of vinylamide monomers and monomers containing ammonium or quaternary ammonium moieties, copolymers of vinylamide monomers and monomers comprising vinylcarboxylic acid monomers and/or vinylsulfonic acid monomers, and salts thereof, and these copolymers comprising a crosslinking monomer selected from the group consisting of bis-acrylamide, diallylamine, N,N-diallylacrylamide, divinyloxyethane, divinyldimethylsilane; and where the solid particles comprise sand, glass beads, ceramic beads, metal beads, bauxite grains, walnut shell fragments, aluminum pellets, nylon pellets and combinations thereof.
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| US12/835,023 | 2010-07-13 | ||
| US12/835,023 US20110005752A1 (en) | 2008-08-14 | 2010-07-13 | Water Sensitive Porous Medium to Control Downhole Water Production and Method Therefor |
| PCT/US2011/042993 WO2012009184A2 (en) | 2010-07-13 | 2011-07-06 | Water sensitive porous medium to control downhole water production and method therefor |
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| US (1) | US20110005752A1 (en) |
| CN (1) | CN103080472A (en) |
| AU (1) | AU2011279476A1 (en) |
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| CN110486004A (en) * | 2018-05-14 | 2019-11-22 | 中国石油天然气股份有限公司 | Method and device for identifying water flow dominant channels in sandstone reservoirs |
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| US9051819B2 (en) | 2011-08-22 | 2015-06-09 | Baker Hughes Incorporated | Method and apparatus for selectively controlling fluid flow |
| CN102364041B (en) * | 2011-10-26 | 2014-03-26 | 王胜存 | Oil extraction method for establishing oil permeable water stop sieve by filling fusheng sand in horizontal well fracture |
| US9334708B2 (en) | 2012-04-23 | 2016-05-10 | Baker Hughes Incorporated | Flow control device, method and production adjustment arrangement |
| CN109932489B (en) * | 2019-03-20 | 2024-02-13 | 西安航空学院 | Gas pretreatment device with mixing instrument and gas detection device |
| US20230075579A1 (en) * | 2021-09-09 | 2023-03-09 | Baker Hughes Oilfield Operations Llc | Pseudoplastic flow control device, method and system |
| US20250092765A1 (en) * | 2023-09-18 | 2025-03-20 | Halliburton Energy Services, Inc. | Flow control devices for brine production from wellbore |
| WO2025063940A1 (en) * | 2023-09-18 | 2025-03-27 | Halliburton Energy Services, Inc. | Flow control devices for hydrogen production from wellbore |
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| US3336979A (en) * | 1965-07-26 | 1967-08-22 | Dow Chemical Co | Composition and use thereof for water shut-off |
| US3878893A (en) * | 1972-10-06 | 1975-04-22 | Dow Chemical Co | Method for forming a consolidated gravel pack in a well borehole |
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| US5529124A (en) * | 1994-12-19 | 1996-06-25 | Texaco Inc. | Method for retarding water coning |
| US5701956A (en) * | 1996-04-17 | 1997-12-30 | Halliburton Energy Services, Inc. | Methods and compositions for reducing water production from subterranean formations |
| US5735349A (en) * | 1996-08-16 | 1998-04-07 | Bj Services Company | Compositions and methods for modifying the permeability of subterranean formations |
| US5981447A (en) * | 1997-05-28 | 1999-11-09 | Schlumberger Technology Corporation | Method and composition for controlling fluid loss in high permeability hydrocarbon bearing formations |
| US6228812B1 (en) * | 1998-12-10 | 2001-05-08 | Bj Services Company | Compositions and methods for selective modification of subterranean formation permeability |
| US7008908B2 (en) * | 2002-11-22 | 2006-03-07 | Schlumberger Technology Corporation | Selective stimulation with selective water reduction |
| US7117942B2 (en) * | 2004-06-29 | 2006-10-10 | Halliburton Energy Services, Inc. | Methods useful for controlling fluid loss during sand control operations |
| US7207386B2 (en) * | 2003-06-20 | 2007-04-24 | Bj Services Company | Method of hydraulic fracturing to reduce unwanted water production |
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| US20060065396A1 (en) * | 2004-08-13 | 2006-03-30 | Dawson Jeffrey C | Compositions containing water control treatments and formation damage control additives, and methods for their use |
| US7398825B2 (en) * | 2004-12-03 | 2008-07-15 | Halliburton Energy Services, Inc. | Methods of controlling sand and water production in subterranean zones |
| US7493957B2 (en) * | 2005-07-15 | 2009-02-24 | Halliburton Energy Services, Inc. | Methods for controlling water and sand production in subterranean wells |
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| CN110486004A (en) * | 2018-05-14 | 2019-11-22 | 中国石油天然气股份有限公司 | Method and device for identifying water flow dominant channels in sandstone reservoirs |
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| CA2804663C (en) | 2015-06-02 |
| CA2804663A1 (en) | 2012-01-19 |
| US20110005752A1 (en) | 2011-01-13 |
| BR112013000803A2 (en) | 2017-11-14 |
| CN103080472A (en) | 2013-05-01 |
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| NO20130019A1 (en) | 2013-02-13 |
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| GB2494826A (en) | 2013-03-20 |
| WO2012009184A2 (en) | 2012-01-19 |
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