WO2014058696A1 - Boron removal system and method - Google Patents
Boron removal system and method Download PDFInfo
- Publication number
- WO2014058696A1 WO2014058696A1 PCT/US2013/063196 US2013063196W WO2014058696A1 WO 2014058696 A1 WO2014058696 A1 WO 2014058696A1 US 2013063196 W US2013063196 W US 2013063196W WO 2014058696 A1 WO2014058696 A1 WO 2014058696A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- boron
- water
- exchange resin
- effluent
- vessel
- Prior art date
Links
- 229910052796 boron Inorganic materials 0.000 title claims abstract description 206
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 title claims abstract description 205
- 238000000034 method Methods 0.000 title claims abstract description 50
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 125
- 239000011347 resin Substances 0.000 claims abstract description 89
- 229920005989 resin Polymers 0.000 claims abstract description 89
- 239000012530 fluid Substances 0.000 claims abstract description 86
- 230000015572 biosynthetic process Effects 0.000 claims abstract description 30
- 239000002562 thickening agent Substances 0.000 claims abstract description 22
- 238000005086 pumping Methods 0.000 claims abstract description 14
- 238000005553 drilling Methods 0.000 claims abstract description 11
- 238000002156 mixing Methods 0.000 claims abstract description 5
- 229930195733 hydrocarbon Natural products 0.000 claims description 14
- 150000002430 hydrocarbons Chemical class 0.000 claims description 14
- 239000003431 cross linking reagent Substances 0.000 claims description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 8
- 239000004094 surface-active agent Substances 0.000 claims description 8
- 239000007787 solid Substances 0.000 claims description 7
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 6
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 5
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 5
- 239000004793 Polystyrene Substances 0.000 claims description 5
- 239000011575 calcium Substances 0.000 claims description 5
- 229910052791 calcium Inorganic materials 0.000 claims description 5
- 239000011777 magnesium Substances 0.000 claims description 5
- 229910052749 magnesium Inorganic materials 0.000 claims description 5
- 229920002223 polystyrene Polymers 0.000 claims description 5
- 239000013505 freshwater Substances 0.000 claims description 4
- 230000001172 regenerating effect Effects 0.000 claims description 4
- MBBZMMPHUWSWHV-BDVNFPICSA-N N-methylglucamine Chemical compound CNC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO MBBZMMPHUWSWHV-BDVNFPICSA-N 0.000 claims description 3
- 239000000701 coagulant Substances 0.000 claims description 2
- 229920000642 polymer Polymers 0.000 claims description 2
- 230000005484 gravity Effects 0.000 claims 1
- 238000005755 formation reaction Methods 0.000 description 27
- 239000000463 material Substances 0.000 description 12
- -1 drill cuttings Substances 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- 230000008569 process Effects 0.000 description 7
- 238000002203 pretreatment Methods 0.000 description 6
- 239000004971 Cross linker Substances 0.000 description 5
- 239000000654 additive Substances 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 230000035699 permeability Effects 0.000 description 5
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 4
- 239000011324 bead Substances 0.000 description 4
- 239000000356 contaminant Substances 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 239000003456 ion exchange resin Substances 0.000 description 4
- 229920003303 ion-exchange polymer Polymers 0.000 description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
- 230000008929 regeneration Effects 0.000 description 4
- 238000011069 regeneration method Methods 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 230000002411 adverse Effects 0.000 description 3
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 3
- 239000004327 boric acid Substances 0.000 description 3
- 150000001642 boronic acid derivatives Chemical class 0.000 description 3
- 239000003638 chemical reducing agent Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000004132 cross linking Methods 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000012492 regenerant Substances 0.000 description 3
- 239000004576 sand Substances 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 240000007049 Juglans regia Species 0.000 description 2
- 235000009496 Juglans regia Nutrition 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- 244000166071 Shorea robusta Species 0.000 description 2
- 235000015076 Shorea robusta Nutrition 0.000 description 2
- 150000001450 anions Chemical class 0.000 description 2
- 229910001570 bauxite Inorganic materials 0.000 description 2
- 239000000919 ceramic Substances 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 229920001429 chelating resin Polymers 0.000 description 2
- 229910052729 chemical element Inorganic materials 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 229920002401 polyacrylamide Polymers 0.000 description 2
- 239000011435 rock Substances 0.000 description 2
- 235000020234 walnut Nutrition 0.000 description 2
- CUNWUEBNSZSNRX-RKGWDQTMSA-N (2r,3r,4r,5s)-hexane-1,2,3,4,5,6-hexol;(z)-octadec-9-enoic acid Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.CCCCCCCC\C=C/CCCCCCCC(O)=O.CCCCCCCC\C=C/CCCCCCCC(O)=O.CCCCCCCC\C=C/CCCCCCCC(O)=O CUNWUEBNSZSNRX-RKGWDQTMSA-N 0.000 description 1
- UCWYGNTYSWIDSW-QXMHVHEDSA-N (z)-n-[3-(dimethylamino)propyl]octadec-9-enamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)NCCCN(C)C UCWYGNTYSWIDSW-QXMHVHEDSA-N 0.000 description 1
- ZORQXIQZAOLNGE-UHFFFAOYSA-N 1,1-difluorocyclohexane Chemical compound FC1(F)CCCCC1 ZORQXIQZAOLNGE-UHFFFAOYSA-N 0.000 description 1
- AOSFMYBATFLTAQ-UHFFFAOYSA-N 1-amino-3-(benzimidazol-1-yl)propan-2-ol Chemical compound C1=CC=C2N(CC(O)CN)C=NC2=C1 AOSFMYBATFLTAQ-UHFFFAOYSA-N 0.000 description 1
- BCFOOQRXUXKJCL-UHFFFAOYSA-N 4-amino-4-oxo-2-sulfobutanoic acid Chemical class NC(=O)CC(C(O)=O)S(O)(=O)=O BCFOOQRXUXKJCL-UHFFFAOYSA-N 0.000 description 1
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 244000303965 Cyamopsis psoralioides Species 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 description 1
- 229920002907 Guar gum Polymers 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229940123973 Oxygen scavenger Drugs 0.000 description 1
- 229920001214 Polysorbate 60 Polymers 0.000 description 1
- 239000004147 Sorbitan trioleate Substances 0.000 description 1
- PRXRUNOAOLTIEF-ADSICKODSA-N Sorbitan trioleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCC\C=C/CCCCCCCC)[C@H]1OC[C@H](O)[C@H]1OC(=O)CCCCCCC\C=C/CCCCCCCC PRXRUNOAOLTIEF-ADSICKODSA-N 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- WERKSKAQRVDLDW-ANOHMWSOSA-N [(2s,3r,4r,5r)-2,3,4,5,6-pentahydroxyhexyl] (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO WERKSKAQRVDLDW-ANOHMWSOSA-N 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000004645 aluminates Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 238000011001 backwashing Methods 0.000 description 1
- 239000003139 biocide Substances 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000002734 clay mineral Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- 238000003795 desorption Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- ZMXDDKWLCZADIW-UHFFFAOYSA-N dimethylformamide Substances CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 1
- 235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 description 1
- YHAIUSTWZPMYGG-UHFFFAOYSA-L disodium;2,2-dioctyl-3-sulfobutanedioate Chemical compound [Na+].[Na+].CCCCCCCCC(C([O-])=O)(C(C([O-])=O)S(O)(=O)=O)CCCCCCCC YHAIUSTWZPMYGG-UHFFFAOYSA-L 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000000665 guar gum Substances 0.000 description 1
- 235000010417 guar gum Nutrition 0.000 description 1
- 229960002154 guar gum Drugs 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 230000003165 hydrotropic effect Effects 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 239000013618 particulate matter Substances 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- 229920003053 polystyrene-divinylbenzene Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000002455 scale inhibitor Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000001593 sorbitan monooleate Substances 0.000 description 1
- 235000011069 sorbitan monooleate Nutrition 0.000 description 1
- 229940035049 sorbitan monooleate Drugs 0.000 description 1
- 229960005078 sorbitan sesquioleate Drugs 0.000 description 1
- 235000019337 sorbitan trioleate Nutrition 0.000 description 1
- 229960000391 sorbitan trioleate Drugs 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J45/00—Ion-exchange in which a complex or a chelate is formed; Use of material as complex or chelate forming ion-exchangers; Treatment of material for improving the complex or chelate forming ion-exchange properties
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J49/00—Regeneration or reactivation of ion-exchangers; Apparatus therefor
- B01J49/50—Regeneration or reactivation of ion-exchangers; Apparatus therefor characterised by the regeneration reagents
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/42—Treatment of water, waste water, or sewage by ion-exchange
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/66—Treatment of water, waste water, or sewage by neutralisation; pH adjustment
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/42—Treatment of water, waste water, or sewage by ion-exchange
- C02F2001/425—Treatment of water, waste water, or sewage by ion-exchange using cation exchangers
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2101/00—Nature of the contaminant
- C02F2101/10—Inorganic compounds
- C02F2101/108—Boron compounds
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2103/00—Nature of the water, waste water, sewage or sludge to be treated
- C02F2103/10—Nature of the water, waste water, sewage or sludge to be treated from quarries or from mining activities
Definitions
- Hydrocarbons are found in subterranean formations. Production of such hydrocarbons is generally accomplished through the use of rotary drilling technology which includes the drilling, completing, and working over of wells penetrating producing formations.
- the types of subterranean formations intersected by a well may include formations having clay minerals as major constituents, such as shales, mudstones, siltstones, and claystones.
- Shale may be a troublesome rock type to drill in order to reach oil and gas deposits.
- One aspect that makes shales troublesome is that they have a very low (nano-Darcy) permeability with relatively small (nanometer) sized pore throats, which makes profitable extraction of entrained hydrocarbons particularly difficult.
- Other low permeability formations include sandstone, carbonates, and coal bed methane.
- Hydrocarbons may be produced from shale formations in various ways.
- gas derived from organic content such as kerogen
- hydrocarbons may be produced from shale through desorption directly from the kerogen. Hydraulic fracturing has conventionally been used to recover hydrocarbons from shale formations.
- Hydraulic fracturing is a common stimulation technique used to enhance production of fluids from subterranean formations, and it is often used in recovering hydrocarbon fluids from low permeability formations that produce mainly dry natural gas.
- Shale formations in particular, have low permeability such that hydrocarbon fluid production in commercial quantities occurs when fractures exhibit permeability.
- vertical wells have been drilled through shale formations and hydraulically fractured. This drilling and completion strategy has evolved so that horizontal wells are now commonly drilled through shale formations and include multistage fracturing.
- fracturing treatment fluid containing a solid proppant material is injected into the formation at a pressure sufficiently high enough to cause the formation or enlargement of fractures in the reservoir.
- proppants including, but not limited to, sand, glass beads, walnut hulls, metal shot, resin-coated sands, ceramics, sintered bauxite, and deformable materials.
- a thickening agent e.g., gel
- the proppant material is deposited in a fracture, where it remains after the treatment is completed.
- the proppant material serves to hold the fracture open, thereby enhancing the ability of fluids to migrate from the formation to the wellbore through the fracture. Because fractured well productivity depends on the ability of a fracture to conduct fluids from a formation to a wellbore, fracture conductivity is a parameter in determining the degree of success of a hydraulic fracturing treatment.
- embodiments disclosed herein relate to a method of forming a fracturing fluid including selectively removing boron from water, the selectively removing boron including flowing water through a boron exchange resin to provide an effluent having a lower boron concentration than the water, and mixing the effluent with a thickening agent.
- embodiments disclosed herein relate to a method including drilling a borehole in an earth formation, producing a produced water from the borehole, and selectively removing boron from the produced water, the selectively removing including pumping the produced water through a vessel comprising a boron exchange resin.
- the method further includes flowing an effluent having a lower boron concentration than the produced water out of the vessel and adding a thickening agent to the effluent.
- embodiments disclosed herein relate to a method of treating boron-containing water for a fracturing fluid including disposing a boron exchange resin in a vessel having an inlet and an outlet, and pumping the boron-containing water into the inlet and through the boron exchange resin.
- the method further includes selectively removing boron from the boron-containing water, flowing an effluent out of the outlet, and adding a thickening agent to the effluent.
- Embodiments disclosed herein relate to systems and methods for removal of boron from water for oilfield applications.
- embodiments disclosed herein relate to removal of boron from freshwater or produced water.
- embodiments disclosed herein relate to removal of boron from water using an ion exchange resin, and specifically a boron exchange resin.
- embodiments disclosed herein relate to methods of forming a fracturing fluid with water that is boron- free or that contains a low concentration of boron.
- Water is often used in various oilfield applications.
- water may be used as a base fluid or additive drilling fluids, often called “mud,” or fracturing fluid (also called a “frac fluid”), for treatment of cuttings (solid pieces of the rock formation generated during drilling of a borehole), for cleaning of equipment, and for providing hydraulic pressure or actuation.
- Water may be obtained from freshwater sources, such as water wells, subsurface aquifers, brackish waters, streams, or lakes, or may be obtained from fluids produced during drilling a formation for production of oil and/or gas (i.e., produced water).
- water obtained from freshwater sources may contain certain concentrations of boron in addition to other chemical elements, compounds and/or contaminants.
- produced water may include boron, other chemical elements, hydrocarbons, chemical additives, drill cuttings, and other contaminants that may come from the drilling fluids used or from the formation being drilled.
- boron may be removed or the concentration of boron reduced.
- boron refers to boron in any form, including borates and boric acid.
- Water is often used in fracturing (or fracking) operations.
- fracturing operations fracturing fluids are injected into a well to stimulate the formation, which enhances production of fluids form subterranean formations.
- Fracturing is often used in low-permeability reservoirs.
- the fracturing fluid may be pumped at a high pressure and rate into the reservoir interval to be treated to cause a vertical fracture to be opened.
- the fracturing fluid may include water, proppant, and other frac fluid chemicals including a thickening agent.
- the proppant may include, for example, grains of sand, glass beads, walnut hulls, metal shot, resin-coated sands, ceramics, sintered bauxite, and deformable materials.
- the proppant is mixed with the water or fracturing fluid to keep the fracture open when the treatment is complete.
- the frac fluid chemicals may be used to reduce friction pressure while pumping the fracturing fluid into the wellbore or to adjust viscosity of the fracturing fluid.
- the frac fluid chemicals may include thickening agents, friction reducers, crosslinkers, breakers, and surfactants. Crosslinkers may be used to change the viscosity of the fracturing fluid as necessary.
- Thickening agents such as guar gum, derivatized guar, cellulose derivatives, xanthan gum, and polyacrylamide, for example, may be used in accordance with embodiments disclosed herein to thicken the fluid to help transport the proppant material.
- Crosslinkers in accordance with the present disclosure may be used to enhance the characteristics and ability of the thickening agent to transport the proppant material.
- Crosslinkers may be used independently or as a mixture of crosslinker compounds.
- Example crosslinking agents may include borates, zirconates, titanates, and aluminates.
- Friction reducing agents in accordance with the present disclosure may include, for example, potassium chloride or polyacrylamide-based compounds to reduce tubular friction and subsequently reduce the pressure to pump the fracturing fluid into the wellbore.
- Surfactants used in accordance with embodiments disclosed herein may include, for example, anionic, cationic, nonionic, and hydrotropic surfactants or one or more hydrophobic organic alcohols, in an aqueous medium.
- Surfactants which may be used in accordance with the present disclosure may be a low benzene or benzene-free surfactant.
- surfactants may include sulfosuccinates, sulfosuccinamates, polyoxyethylene sorbitol fatty acids, sorbitan sesquioleate, polyoxyethylene sorbitan trioleate, sorbitan monooleate, polyoxyethylene (20) sorbitan monooleate, sodium dioctylsulfosuccinate, oleamidopropyldimethyl amine, sodium isostearyl-2-lactate, polyoxyethylene sorbitol monooleate or mixtures thereof and the like.
- additives may be added to the fracturing fluid, including, but not limited to, scale inhibitors, such as ethylene glycol, iron control/stabilizing agents, such as citric acid or hydrochloric acid, biocides or disinfectants, such as bromine -based solutions or glutaraldehyde, corrosion inhibitors, such as ⁇ , ⁇ -dimethyl formamide, oxygen scavengers, such as ammonium bisulfite, etc.
- scale inhibitors such as ethylene glycol
- iron control/stabilizing agents such as citric acid or hydrochloric acid
- biocides or disinfectants such as bromine -based solutions or glutaraldehyde
- corrosion inhibitors such as ⁇ , ⁇ -dimethyl formamide
- oxygen scavengers such as ammonium bisulfite, etc.
- the presence of additional boron (or borate) in the water used to form the fracturing fluid may undesirably crosslink with other components of the fracturing fluid or otherwise negatively affect the fracturing fluid.
- Such crosslinking may destabilize the fracturing fluid.
- the boron may act as a crosslinking agent and change the viscosity of the fracturing fluid from a designed viscosity.
- adding water having boron therein may speed up crosslinking of the thickening agent, which may adversely increase the viscosity of the fracturing fluid before the fracturing fluid is at a downhole location.
- a viscous fracturing fluid may make it difficult to pump the fracturing fluid downhole and may wear or damage the pump or other equipment. If boron is present in the water used to make the fracturing fluid, the boron may prematurely crosslink the thickening agent before it is able to sufficiently hydrate in the water.
- the thickening agent may lose its viscosity and ability to transport sand at elevated temperatures downhole.
- the boron can interfere with the ability of the fract fluid to maintain the proper viscosity at wellbore temperatures to successfully transport proppant downhold.
- embodiments disclosed herein provide a system and method for removing boron or reducing the boron concentration in water.
- One of ordinary skill in the art will appreciate that the system and methods disclosed herein may be used for other oilfield applications where boron-containing water is problematic.
- Embodiments disclosed herein relate to systems and methods for removing boron from water.
- boron may be selectively removed from water so that the water may be used in oilfield applications that may require low concentrations of boron (e.g., less than 30 ppm boron).
- selectively removed refers to the removal of boron, specifically, while allowing other elements or ions to be retained within the water.
- a system for removing boron from water may include a vessel having a specified volume.
- the vessel may include an inlet and an outlet.
- An ion exchange resin is disposed in the vessel.
- a boron exchange resin is disposed in the vessel.
- a boron exchange resin is a resin that is designed to remove borates and/or other forms of boron from a solution.
- the boron exchange resin may include a matrix of macroporous polystyrene with a functional group of N-Methylglucamine.
- the resin may be formed as beads having a harmonic mean particle size of about 0.400 to 0.800 mm.
- the boron ion generates a stable complex with the glucamine group while other anions do not react as well.
- typical ion exchangers remove, for example, magnesium and calcium before removing boron
- the boron exchange resin disclosed herein removes boron while leaving magnesium and calcium in the solution.
- a commercially available boron exchange resin is AMBERLITE IRA743 chelating resin from The Dow Chemical Company (Philadelphia, PA).
- the boron exchange resin may include a macroporous polystyrene crosslinked with divinylbenzene. In this embodiment, the resin may be formed as beads having a mean particle size of about 0.400 to 0.800 mm.
- Another example of a commercially available boron exchange resin is ULTRACLEAN UCW 1080 polystyrene divinylbenzene tertiary amino saccharide from The PUROLITE Company (Bala Cynwyd, PA).
- the boron exchange resin may be disposed in the vessel to provide a resin bed through which water (or a water-based solution) is passed.
- the water is introduced through the inlet of the vessel, passed through the boron exchange resin, which removes the boron from the water, and the effluent is flowed out through the outlet of the vessel.
- a pump may be coupled to the inlet of the vessel to provide a pressure differential across the boron exchange resin to facilitate a flow of the water through the boron exchange resin.
- the pump may provide a steady flow of water at about 2 to 20 psi.
- the pump may provide a flow of water at approximately 10 psi.
- the boron exchange resin may be disposed on a surface of the vessel (i.e., line the surface of the vessel) across which the water is passed.
- the system for removing boron from water may also include one or more components of pre-treatment equipment. Specifically, before introducing water to the vessel, the water may be passed through pre-treatment equipment to remove other contaminants from the water. Specifically, contaminants that may damage the boron exchange resin may be removed from the water before the water is passed through the boron exchange resin. For example, hydrocarbons and particulate matter may be removed from the water before pumping the water to the vessel having the boron exchange resin disposed therein.
- the pre-treatment equipment may include one or more of a filter, a vibratory separator, a centrifuge, a settling tank, and a hydrocyclone.
- the removal or separation of hydrocarbons and/or solids may be facilitated by the addition of a chemical.
- a coagulant, surfactant, polymer, or combinations thereof may be added to the water before the water is passed through the boron exchange resin in the vessel.
- the chemicals may be injected into the water in the pre-treatment equipment discussed above.
- the system may also include components for providing a backwashing of the resin.
- the system may include a second pump configured to pump a backwash fluid back through the boron exchange resin.
- the second pump may be coupled to the outlet of the vessel to introduce a backwash fluid to the vessel and create a pressure differential across the boron exchange resin to facilitate flow of the backwash fluid back through the boron exchange resin.
- the pump coupled to the inlet of the vessel may also be coupled to the outlet of the vessel with a valve operatively coupled to the pump to direct the flow of fluids to the inlet and/or outlet.
- the backwash fluid may be an acid.
- the backwash fluid may be hydrochloric acid or sulfuric acid.
- the pump coupled to the inlet and/or the second pump may also be configured to provide a regenerant material to the vessel to regenerate the boron exchange resin.
- the regenerant material may be a base fluid that is added to the vessel and flowed through the boron exchange resin.
- the base fluid may be sodium hydroxide.
- a method of treating a boron-containing water for oilfield applications includes disposing a boron exchange resin in a vessel.
- the boron exchange resin may be a resin as discussed above for selectively removing boron from water.
- the boron-containing water is pumped into the vessel and through the boron exchange resin.
- the boron-containing water may be pumped into an inlet of the vessel and a pressure applied by a pump may facilitate the flow of the boron-containing water through the boron exchange resin.
- An effluent i.e., water with a boron concentration lower than the boron-containing water introduced to the vessel
- an effluent i.e., water with a boron concentration lower than the boron-containing water introduced to the vessel
- a continuous stream of boron-containing water may be passed through the boron exchange resin for a predetermined amount of time or volume of fluid.
- the size of the vessel, the amount of the boron exchange resin, and the flow rate of the boron-containing water through the vessel may be adjusted and optimized for a particular application to provide a certain boron concentration in the resulting effluent.
- a boron-containing water may have a boron concentration of from about 80 to 100 ppm boron, from about 60 to 80 ppm boron, from about 40 to 60 ppm boron, or from about 20 to 40 ppm boron.
- the boron removal system may be designed such that the size of the vessel, the amount of the boron exchange resin, and the flow rate of boron-containing water through the system may provide an effluent having an optimal boron concentration.
- a water having less than 30 ppm boron, less than 20 ppm boron, less than 10 ppm or less than 5 ppm boron may be desired.
- the flow rate of boron-containing water into the vessel may be between 4 and 30 BV/h.
- BV refers to bed volume.
- BV/h is the volume per hours of liquid to be treated over the volume of resin.
- the flow rate may be 10 BV/h, 17 BV/h, 25 BV/h, or other flow rates to achieve an optimized flow rate for a desired boron concentration in the effluent water flow.
- the size of the vessel, the amount of the boron exchange resin, and the flow rate of boron-containing water may also be selected so as to provide a desired cycle time for the boron removal process.
- the boron exchange resin may be stopped and the regeneration process of the boron exchange resin may be initiated.
- the boron exchange resin may be regenerated or restored to its proper ionic form for continued use in the boron removal process. Regeneration of the boron exchange resin may include a backwash cycle and a base fluid cycle.
- a backwash cycle may be used to pump an acid into the vessel. That is, an acid backflow is applied to the boron exchange resin.
- acids may be used as a backwash for the boron exchange resin without departing from the scope of embodiments disclosed herein. Examples of acids that may be used to backwash the boron exchange resin include hydrochloric acid and sulfuric acid.
- the backwash fluid may be pumped into the outlet, through the boron exchange resin, and out the inlet of the vessel. The backwash fluid may expand the resin bed from its settled and packed condition and may clean the resin by flushing out any suspended solids (that may have bypassed the pre -treatment equipment discussed above) and/or any damaged resin particles.
- regenerating the boron exchange resin may further include pumping a base fluid through the boron exchange resin.
- a regenerant fluid that may be used is sodium hydroxide.
- a predetermined regeneration cycle time may be selected.
- replacement or additional boron exchange resin may be added to the vessel to replace any damaged resin.
- a 1 day cycle time for the boron removal process may be desired.
- the regeneration cycle including the backwash cycle and the base fluid cycle discussed above
- the boron removal cycle i.e., flow of boron-containing fluid through the boron exchange resin
- the desired cycle time for the boron removal process may be determined.
- One of ordinary skill in the art will appreciate that other cycle times may be desired and that the size of the vessel, the amount of the boron exchange resin, and the flow rate of boron-containing water may be adjusted to achieve a desired boron removal process cycle.
- a method of forming a fracturing fluid according to embodiments of the present disclosure may include selectively removing boron from water, and mixing the effluent with a thickening agent.
- the selectively removing boron includes flowing water through a boron exchange resin to provide an effluent having a lower boron concentration than the water introduced to the boron exchange resin.
- an effluent obtained from the outlet of the boron removal system described above may be mixed with a thickening agent to form a fracturing fluid for pumping down hole.
- the effluent has a lower boron concentration, for example, less than 10 ppm boron, the effluent may be used in a fracturing fluid without adversely affecting the fracturing fluid or without causing premature crosslinking of the thickening agent of the fracturing fluid.
- fracturing fluids may be added to the water and thickening agent in forming a fracturing fluid, as discussed above.
- at least one crosslinking agent may be added to the water and thickening agent to increase the viscosity of the fracturing fluid downhole.
- the crosslinking agent may be boric acid. The fracturing fluid may then be pumped downhole and used to fracture the earth formation.
- the boron removed from the boron-containing water may be reused.
- boron removed from the boron-containing water by the boron exchange resin may be collected during the backwash cycle.
- acids used to clean and flush the boron exchange cycle may be collected and treated to separate the removed boron.
- the boron may then be reused in other oilfield applications.
- the removed boron may be used as a crosslinking agent in subsequent fracturing fluids.
- a method according to the present disclosure includes drilling a borehole in an earth formation, producing a produced water from the borehole, and selectively removing boron from the produced water.
- the selectively removing boron from the produced water includes pumping the produced water through a vessel, the vessel having an ion exchange resin, and flowing an effluent having a lower boron concentration than the produced water out of the vessel.
- the ion exchange resin is a boron exchange resin as discussed above.
- the produced water pumped through the boron exchange resin at a predetermined flow rate produces an effluent having no or low concentrations of boron.
- the effluent may be further diluted by adding a volume of water having no boron or a concentration of boron less than the concentration of boron of the effluent.
- the effluent may then be used in various oilfield applications.
- the effluent may be used to form a fracturing fluid.
- a fracturing fluid may be formed by mixing the effluent water with a thickening agent.
- other chemical additives may be added to the fracturing fluid including crosslinking agents, friction reducing agents, etc.
- the fracturing fluid may then be pumped into a borehole and used to fracture the earth formation.
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Abstract
A method of forming a fracturing fluid includes selectively removing boron from water, the selectively removing boron including flowing water through a boron exchange resin to provide an effluent having a lower boron concentration than the water, and mixing the effluent with a thickening agent. A method includes drilling a borehole in an earth formation, producing a produced water from the borehole, and selectively removing boron from the produced water, the selectively removing including pumping the produced water through a vessel, the vessel having a boron exchange resin, and flowing an effluent having a lower boron concentration than the produced water out of the vessel to be used with a thickening agent.
Description
BORON REMOVAL SYSTEM AND METHOD
BACKGROUND
[0001] Hydrocarbons are found in subterranean formations. Production of such hydrocarbons is generally accomplished through the use of rotary drilling technology which includes the drilling, completing, and working over of wells penetrating producing formations.
[0002] The types of subterranean formations intersected by a well may include formations having clay minerals as major constituents, such as shales, mudstones, siltstones, and claystones. Shale may be a troublesome rock type to drill in order to reach oil and gas deposits. One aspect that makes shales troublesome is that they have a very low (nano-Darcy) permeability with relatively small (nanometer) sized pore throats, which makes profitable extraction of entrained hydrocarbons particularly difficult. Other low permeability formations include sandstone, carbonates, and coal bed methane.
[0003] Hydrocarbons may be produced from shale formations in various ways. For example, gas derived from organic content, such as kerogen, may be stored in the natural fractures inherently present in shale formations so that the shale formation may be a large repository for gas that has formed. Also, hydrocarbons may be produced from shale through desorption directly from the kerogen. Hydraulic fracturing has conventionally been used to recover hydrocarbons from shale formations.
[0004] Hydraulic fracturing is a common stimulation technique used to enhance production of fluids from subterranean formations, and it is often used in recovering hydrocarbon fluids from low permeability formations that produce mainly dry natural gas. Shale formations, in particular, have low permeability such that hydrocarbon fluid production in commercial quantities occurs when fractures exhibit permeability. For example, in the past, vertical wells have been drilled through shale formations and hydraulically fractured. This drilling and completion strategy has evolved so that horizontal wells are now commonly drilled through shale formations and include multistage fracturing.
[0005] In a typical hydraulic fracturing treatment, fracturing treatment fluid containing a solid proppant material is injected into the formation at a pressure sufficiently high enough to cause the formation or enlargement of fractures in the reservoir. Various materials may be used as proppants including, but not limited to, sand, glass beads, walnut hulls, metal shot, resin-coated sands, ceramics, sintered bauxite, and deformable materials. A thickening agent (e.g., gel) may be used to help the proppant material stay in suspension as the proppant travels downhole. The proppant material is deposited in a fracture, where it remains after the treatment is completed. After deposition, the proppant material serves to hold the fracture open, thereby enhancing the ability of fluids to migrate from the formation to the wellbore through the fracture. Because fractured well productivity depends on the ability of a fracture to conduct fluids from a formation to a wellbore, fracture conductivity is a parameter in determining the degree of success of a hydraulic fracturing treatment.
SUMMARY
[0006] In one aspect, embodiments disclosed herein relate to a method of forming a fracturing fluid including selectively removing boron from water, the selectively removing boron including flowing water through a boron exchange resin to provide an effluent having a lower boron concentration than the water, and mixing the effluent with a thickening agent.
[0007] In another aspect, embodiments disclosed herein relate to a method including drilling a borehole in an earth formation, producing a produced water from the borehole, and selectively removing boron from the produced water, the selectively removing including pumping the produced water through a vessel comprising a boron exchange resin. The method further includes flowing an effluent having a lower boron concentration than the produced water out of the vessel and adding a thickening agent to the effluent.
[0008] In another aspect, embodiments disclosed herein relate to a method of treating boron-containing water for a fracturing fluid including disposing a boron exchange resin in a vessel having an inlet and an outlet, and pumping the boron-containing water into the
inlet and through the boron exchange resin. The method further includes selectively removing boron from the boron-containing water, flowing an effluent out of the outlet, and adding a thickening agent to the effluent.
[0009] This summary is provided to introduce a selection of concepts that are further described below in the detailed description. This summary is not intended to identify key or essential features of the claimed subject matter, nor is it intended to be used as an aid in limiting the scope of the claimed subject matter.
DETAILED DESCRIPTION
[0010] Embodiments disclosed herein relate to systems and methods for removal of boron from water for oilfield applications. In particular, embodiments disclosed herein relate to removal of boron from freshwater or produced water. More specifically, embodiments disclosed herein relate to removal of boron from water using an ion exchange resin, and specifically a boron exchange resin. Furthermore, embodiments disclosed herein relate to methods of forming a fracturing fluid with water that is boron- free or that contains a low concentration of boron.
[0011] Water is often used in various oilfield applications. For example, water may be used as a base fluid or additive drilling fluids, often called "mud," or fracturing fluid (also called a "frac fluid"), for treatment of cuttings (solid pieces of the rock formation generated during drilling of a borehole), for cleaning of equipment, and for providing hydraulic pressure or actuation. Water may be obtained from freshwater sources, such as water wells, subsurface aquifers, brackish waters, streams, or lakes, or may be obtained from fluids produced during drilling a formation for production of oil and/or gas (i.e., produced water).
[0012] Depending on the location of a drill site, water obtained from freshwater sources may contain certain concentrations of boron in addition to other chemical elements, compounds and/or contaminants. Similarly, produced water may include boron, other chemical elements, hydrocarbons, chemical additives, drill cuttings, and other contaminants that may come from the drilling fluids used or from the formation being
drilled. In order to use the water in certain oilfield applications, boron may be removed or the concentration of boron reduced. As used herein, boron refers to boron in any form, including borates and boric acid.
[0013] Water is often used in fracturing (or fracking) operations. In fracturing operations, fracturing fluids are injected into a well to stimulate the formation, which enhances production of fluids form subterranean formations. Fracturing is often used in low-permeability reservoirs. The fracturing fluid may be pumped at a high pressure and rate into the reservoir interval to be treated to cause a vertical fracture to be opened. The fracturing fluid may include water, proppant, and other frac fluid chemicals including a thickening agent. The proppant may include, for example, grains of sand, glass beads, walnut hulls, metal shot, resin-coated sands, ceramics, sintered bauxite, and deformable materials. The proppant is mixed with the water or fracturing fluid to keep the fracture open when the treatment is complete. The frac fluid chemicals may be used to reduce friction pressure while pumping the fracturing fluid into the wellbore or to adjust viscosity of the fracturing fluid. The frac fluid chemicals may include thickening agents, friction reducers, crosslinkers, breakers, and surfactants. Crosslinkers may be used to change the viscosity of the fracturing fluid as necessary.
[0014] Thickening agents, such as guar gum, derivatized guar, cellulose derivatives, xanthan gum, and polyacrylamide, for example, may be used in accordance with embodiments disclosed herein to thicken the fluid to help transport the proppant material. Crosslinkers (or crosslinking agents) in accordance with the present disclosure may be used to enhance the characteristics and ability of the thickening agent to transport the proppant material. Crosslinkers may be used independently or as a mixture of crosslinker compounds. Example crosslinking agents may include borates, zirconates, titanates, and aluminates. Friction reducing agents in accordance with the present disclosure may include, for example, potassium chloride or polyacrylamide-based compounds to reduce tubular friction and subsequently reduce the pressure to pump the fracturing fluid into the wellbore. Surfactants used in accordance with embodiments disclosed herein may include, for example, anionic, cationic, nonionic, and hydrotropic surfactants or one or more hydrophobic organic alcohols, in an aqueous medium. Surfactants which may be
used in accordance with the present disclosure may be a low benzene or benzene-free surfactant. Other example surfactants may include sulfosuccinates, sulfosuccinamates, polyoxyethylene sorbitol fatty acids, sorbitan sesquioleate, polyoxyethylene sorbitan trioleate, sorbitan monooleate, polyoxyethylene (20) sorbitan monooleate, sodium dioctylsulfosuccinate, oleamidopropyldimethyl amine, sodium isostearyl-2-lactate, polyoxyethylene sorbitol monooleate or mixtures thereof and the like. Other additives may be added to the fracturing fluid, including, but not limited to, scale inhibitors, such as ethylene glycol, iron control/stabilizing agents, such as citric acid or hydrochloric acid, biocides or disinfectants, such as bromine -based solutions or glutaraldehyde, corrosion inhibitors, such as Ν,η-dimethyl formamide, oxygen scavengers, such as ammonium bisulfite, etc.
[0015] The presence of additional boron (or borate) in the water used to form the fracturing fluid may undesirably crosslink with other components of the fracturing fluid or otherwise negatively affect the fracturing fluid. Such crosslinking may destabilize the fracturing fluid. For example, if water used in forming a fracturing fluid includes boron, the boron may act as a crosslinking agent and change the viscosity of the fracturing fluid from a designed viscosity. In certain fracturing fluids where the fracturing fluid includes a crosslinking agent, such as boric acid, adding water having boron therein may speed up crosslinking of the thickening agent, which may adversely increase the viscosity of the fracturing fluid before the fracturing fluid is at a downhole location. A viscous fracturing fluid may make it difficult to pump the fracturing fluid downhole and may wear or damage the pump or other equipment. If boron is present in the water used to make the fracturing fluid, the boron may prematurely crosslink the thickening agent before it is able to sufficiently hydrate in the water. If not sufficiently hydrated, the thickening agent may lose its viscosity and ability to transport sand at elevated temperatures downhole. Above a given concentration of boron in water, the boron can interfere with the ability of the fract fluid to maintain the proper viscosity at wellbore temperatures to successfully transport proppant downhold.
[0016] Because the presence of boron in water may adversely affect a fracturing fluid, embodiments disclosed herein provide a system and method for removing boron or
reducing the boron concentration in water. One of ordinary skill in the art will appreciate that the system and methods disclosed herein may be used for other oilfield applications where boron-containing water is problematic.
[0017] Embodiments disclosed herein relate to systems and methods for removing boron from water. In particular, boron may be selectively removed from water so that the water may be used in oilfield applications that may require low concentrations of boron (e.g., less than 30 ppm boron). As used herein, selectively removed refers to the removal of boron, specifically, while allowing other elements or ions to be retained within the water.
[0018] A system for removing boron from water may include a vessel having a specified volume. The vessel may include an inlet and an outlet. An ion exchange resin is disposed in the vessel. Specifically, a boron exchange resin is disposed in the vessel. As used herein, a boron exchange resin is a resin that is designed to remove borates and/or other forms of boron from a solution. Specifically, the boron exchange resin may include a matrix of macroporous polystyrene with a functional group of N-Methylglucamine. The resin may be formed as beads having a harmonic mean particle size of about 0.400 to 0.800 mm. The boron ion generates a stable complex with the glucamine group while other anions do not react as well. Thus, while typical ion exchangers remove, for example, magnesium and calcium before removing boron, the boron exchange resin disclosed herein removes boron while leaving magnesium and calcium in the solution. One example of a commercially available boron exchange resin is AMBERLITE IRA743 chelating resin from The Dow Chemical Company (Philadelphia, PA). In some embodiments, the boron exchange resin may include a macroporous polystyrene crosslinked with divinylbenzene. In this embodiment, the resin may be formed as beads having a mean particle size of about 0.400 to 0.800 mm. Another example of a commercially available boron exchange resin is ULTRACLEAN UCW 1080 polystyrene divinylbenzene tertiary amino saccharide from The PUROLITE Company (Bala Cynwyd, PA).
[0019] The boron exchange resin may be disposed in the vessel to provide a resin bed through which water (or a water-based solution) is passed. In some embodiments, the
water is introduced through the inlet of the vessel, passed through the boron exchange resin, which removes the boron from the water, and the effluent is flowed out through the outlet of the vessel. In some embodiments, a pump may be coupled to the inlet of the vessel to provide a pressure differential across the boron exchange resin to facilitate a flow of the water through the boron exchange resin. For example, the pump may provide a steady flow of water at about 2 to 20 psi. In certain embodiments, the pump may provide a flow of water at approximately 10 psi. In other embodiments, the boron exchange resin may be disposed on a surface of the vessel (i.e., line the surface of the vessel) across which the water is passed.
[0020] The system for removing boron from water may also include one or more components of pre-treatment equipment. Specifically, before introducing water to the vessel, the water may be passed through pre-treatment equipment to remove other contaminants from the water. Specifically, contaminants that may damage the boron exchange resin may be removed from the water before the water is passed through the boron exchange resin. For example, hydrocarbons and particulate matter may be removed from the water before pumping the water to the vessel having the boron exchange resin disposed therein. The pre-treatment equipment may include one or more of a filter, a vibratory separator, a centrifuge, a settling tank, and a hydrocyclone. One of ordinary skill in the art will appreciate that other pre-treatment equipment may be used without departing from the scope of embodiments disclosed herein. In some embodiments, the removal or separation of hydrocarbons and/or solids may be facilitated by the addition of a chemical. For example, a coagulant, surfactant, polymer, or combinations thereof may be added to the water before the water is passed through the boron exchange resin in the vessel. The chemicals may be injected into the water in the pre-treatment equipment discussed above.
[0021] The system may also include components for providing a backwashing of the resin. Specifically, the system may include a second pump configured to pump a backwash fluid back through the boron exchange resin. The second pump may be coupled to the outlet of the vessel to introduce a backwash fluid to the vessel and create a pressure differential across the boron exchange resin to facilitate flow of the backwash
fluid back through the boron exchange resin. In other embodiments, the pump coupled to the inlet of the vessel may also be coupled to the outlet of the vessel with a valve operatively coupled to the pump to direct the flow of fluids to the inlet and/or outlet. In some embodiments, the backwash fluid may be an acid. For example, the backwash fluid may be hydrochloric acid or sulfuric acid. The pump coupled to the inlet and/or the second pump may also be configured to provide a regenerant material to the vessel to regenerate the boron exchange resin. The regenerant material may be a base fluid that is added to the vessel and flowed through the boron exchange resin. In some embodiments, the base fluid may be sodium hydroxide.
[0022] A method of treating a boron-containing water for oilfield applications, such as for forming a fracturing fluid, includes disposing a boron exchange resin in a vessel. The boron exchange resin may be a resin as discussed above for selectively removing boron from water. The boron-containing water is pumped into the vessel and through the boron exchange resin. The boron-containing water may be pumped into an inlet of the vessel and a pressure applied by a pump may facilitate the flow of the boron-containing water through the boron exchange resin. As the boron-containing water flows through the boron exchange resin, boron is removed from the boron-containing water by the boron exchange resin. An effluent (i.e., water with a boron concentration lower than the boron-containing water introduced to the vessel) is flowed out of the vessel, for example, through an outlet of the vessel.
[0023] While boron is removed from the boron-containing fluid pumped through the boron exchange resin, other anions will not react with the boron exchange resin, and therefore are not removed from the boron-containing water. For example calcium and magnesium in the boron-containing fluid will pass through the boron exchange resin with the water. In other words, the calcium concentration of the boron-containing water and the effluent may be approximately equal. Similarly, the magnesium concentration of the boron-containing water and the effluent may be approximately equal.
[0024] In some embodiments, a continuous stream of boron-containing water may be passed through the boron exchange resin for a predetermined amount of time or volume
of fluid. The size of the vessel, the amount of the boron exchange resin, and the flow rate of the boron-containing water through the vessel may be adjusted and optimized for a particular application to provide a certain boron concentration in the resulting effluent. For example, a boron-containing water may have a boron concentration of from about 80 to 100 ppm boron, from about 60 to 80 ppm boron, from about 40 to 60 ppm boron, or from about 20 to 40 ppm boron. To obtain such a specific boron concentration, the boron removal system may be designed such that the size of the vessel, the amount of the boron exchange resin, and the flow rate of boron-containing water through the system may provide an effluent having an optimal boron concentration. For example, in a fracturing fluid application a water having less than 30 ppm boron, less than 20 ppm boron, less than 10 ppm or less than 5 ppm boron may be desired.
[0025] In certain embodiments, the flow rate of boron-containing water into the vessel may be between 4 and 30 BV/h. As used herein, BV refers to bed volume. BV/h is the volume per hours of liquid to be treated over the volume of resin. For example, in certain embodiments, the flow rate may be 10 BV/h, 17 BV/h, 25 BV/h, or other flow rates to achieve an optimized flow rate for a desired boron concentration in the effluent water flow. Additionally, the size of the vessel, the amount of the boron exchange resin, and the flow rate of boron-containing water may also be selected so as to provide a desired cycle time for the boron removal process.
[0026] Specifically, continually flowing a boron-containing water through the boron exchange resin will exhaust the boron exchange resin, i.e., reduce or eliminate the ability of the boron exchange resin to effectively remove boron from the boron-containing water. Therefore, the boron removal process may be stopped and the regeneration process of the boron exchange resin may be initiated. In other words, the boron exchange resin may be regenerated or restored to its proper ionic form for continued use in the boron removal process. Regeneration of the boron exchange resin may include a backwash cycle and a base fluid cycle.
[0027] To regenerate the boron exchange resin, a backwash cycle may be used to pump an acid into the vessel. That is, an acid backflow is applied to the boron exchange resin.
One of ordinary skill in the art will appreciate that various acids may be used as a backwash for the boron exchange resin without departing from the scope of embodiments disclosed herein. Examples of acids that may be used to backwash the boron exchange resin include hydrochloric acid and sulfuric acid. As discussed above, the backwash fluid may be pumped into the outlet, through the boron exchange resin, and out the inlet of the vessel. The backwash fluid may expand the resin bed from its settled and packed condition and may clean the resin by flushing out any suspended solids (that may have bypassed the pre -treatment equipment discussed above) and/or any damaged resin particles.
[0028] After the backwash cycle, regenerating the boron exchange resin may further include pumping a base fluid through the boron exchange resin. One of ordinary skill in the art will appreciate that various based fluids may be used to regenerate the boron exchange resin without departing from the scope of embodiments disclosed herein. One example of a regenerant fluid that may be used is sodium hydroxide. In order to ensure that the boron exchange resin is adequately regenerated, a predetermined regeneration cycle time may be selected. In some embodiments, replacement or additional boron exchange resin may be added to the vessel to replace any damaged resin.
[0029] In certain embodiments, a 1 day cycle time for the boron removal process may be desired. In this example, the regeneration cycle (including the backwash cycle and the base fluid cycle discussed above) may be 4 hours while the boron removal cycle (i.e., flow of boron-containing fluid through the boron exchange resin) may be 20 hours. By adjusting the size of the vessel, the amount of the boron exchange resin, and the flow rate of boron-containing water the desired cycle time for the boron removal process may be determined. One of ordinary skill in the art will appreciate that other cycle times may be desired and that the size of the vessel, the amount of the boron exchange resin, and the flow rate of boron-containing water may be adjusted to achieve a desired boron removal process cycle.
[0030] A method of forming a fracturing fluid according to embodiments of the present disclosure may include selectively removing boron from water, and mixing the effluent
with a thickening agent. The selectively removing boron includes flowing water through a boron exchange resin to provide an effluent having a lower boron concentration than the water introduced to the boron exchange resin. In other words, an effluent obtained from the outlet of the boron removal system described above may be mixed with a thickening agent to form a fracturing fluid for pumping down hole. Because the effluent has a lower boron concentration, for example, less than 10 ppm boron, the effluent may be used in a fracturing fluid without adversely affecting the fracturing fluid or without causing premature crosslinking of the thickening agent of the fracturing fluid.
[0031] Other fluids or additives may be added to the water and thickening agent in forming a fracturing fluid, as discussed above. For example, at least one crosslinking agent may be added to the water and thickening agent to increase the viscosity of the fracturing fluid downhole. In one embodiment, the crosslinking agent may be boric acid. The fracturing fluid may then be pumped downhole and used to fracture the earth formation.
[0032] In some embodiments, the boron removed from the boron-containing water may be reused. For example, boron removed from the boron-containing water by the boron exchange resin may be collected during the backwash cycle. For example, during the backwash cycle, acids used to clean and flush the boron exchange cycle may be collected and treated to separate the removed boron. The boron may then be reused in other oilfield applications. For example, the removed boron may be used as a crosslinking agent in subsequent fracturing fluids.
[0033] In another embodiment, a method according to the present disclosure includes drilling a borehole in an earth formation, producing a produced water from the borehole, and selectively removing boron from the produced water. The selectively removing boron from the produced water includes pumping the produced water through a vessel, the vessel having an ion exchange resin, and flowing an effluent having a lower boron concentration than the produced water out of the vessel. The ion exchange resin is a boron exchange resin as discussed above.
[0034] The produced water pumped through the boron exchange resin at a predetermined flow rate produces an effluent having no or low concentrations of boron. In some embodiments, the effluent may be further diluted by adding a volume of water having no boron or a concentration of boron less than the concentration of boron of the effluent. The effluent may then be used in various oilfield applications. For example, the effluent may be used to form a fracturing fluid. As discussed above, a fracturing fluid may be formed by mixing the effluent water with a thickening agent. Further, other chemical additives may be added to the fracturing fluid including crosslinking agents, friction reducing agents, etc. The fracturing fluid may then be pumped into a borehole and used to fracture the earth formation.
[0035] Although only a few example means, materials, and embodiments have been described in detail above, those skilled in the art will readily appreciate that many modifications are possible in the example embodiments without materially departing from the systems and methods disclosed herein. Accordingly, all such modifications are intended to be included within the scope of this disclosure as defined in the following claims. In the claims, means-plus-function clauses are intended to cover the structures described herein as performing the recited function and not only structural equivalents, but also equivalent structures. It is the express intention of the applicant not to invoke 35 U.S.C. § 112, paragraph 6 for any limitations of any of the claims herein, except for those in which the claim expressly uses the words 'means for' together with an associated function.
Claims
1. A method of forming a fracturing fluid, the method comprising:
selectively removing boron from water; the selectively removing boron comprising: flowing the water through a boron exchange resin to provide an effluent having a lower boron concentration than the water; and
mixing the effluent with a thickening agent.
2. The method of claim 1, wherein the boron exchange resin comprises a polystyrene.
3. The method of claim 2, wherein the boron exchange resin further comprises methy lglucamine .
4. The method of claim 1, wherein a calcium concentration of the water and the effluent is approximately equal.
5. The method of claim 1, wherein a magnesium concentration of the water and the effluent is approximately equal.
6. The method of claim 1, further comprising adding at least one crosslinking agent to the effluent.
7. The method of claim 1 , wherein the water is produced from a well.
8. The method of claim 1, wherein the water is freshwater.
9. A method comprising:
drilling a borehole in an earth formation;
producing a produced water from the borehole; and
selectively removing boron from the produced water, the selectively removing comprising:
pumping the produced water through a vessel comprising a boron exchange resin;
flowing an effluent having a lower boron concentration than the produced water out of the vessel; and
adding a thickening agent to the effluent.
10. The method of claim 9, wherein the boron exchange resin comprises at least a polystyrene and methylglucamine.
11. The method of claim 10, further comprising pumping the fracturing fluid into the borehole, and fracturing the earth formation.
12. The method of claim 10, further comprising adding a crosslinking agent to the fracturing fluid.
13. A method of treating boron-containing water for a fracturing fluid, the method comprising:
disposing a boron exchange resin in a vessel having an inlet and an outlet;
pumping the boron-containing water into the inlet and through the boron exchange resin;
selectively removing boron from the boron-containing water;
flowing an effluent out of the outlet; and
adding a thickening agent to the effluent.
14. The method of claim 13, wherein the boron exchange resin comprises at least a polystyrene and methyglucamine.
15. The method of claim 13, further comprising regenerating the boron exchange resin.
16. The method of claim 15, wherein the regenerating comprises pumping an acid into the outlet, through the boron exchange resin, and out the inlet.
17. The method of claim 16, wherein the acid is at least one selected from hydrochloric acid and sulfuric acid.
18. The method of claim 16, wherein the regenerating further comprises pumping a base fluid through the boron exchange resin.
19. The method of claim 18, wherein the base fluid is sodium hydroxide.
20. The method of claim 13, further comprising pre-treating the boron-containing water before pumping the boron-containing water into the inlet, the pre-treating comprising removing at least one of hydrocarbons and solids from the water.
21. The method of claim 20, wherein the removing at least one of hydrocarbons and solids from the water comprises flowing the water through at least one of a filter, a gravity separator, a centrifuge and a hydrocyclone.
22. The method of claim 20, wherein the removing at least one of hydrocarbons and solids from the water comprises injecting at least one of a coagulant, a surfactant, a polymer, and combinations thereof.
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US201261712114P | 2012-10-10 | 2012-10-10 | |
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