EP0247754B1 - Appareil et procédé pour la fabrication d'écume comprenant des particules - Google Patents
Appareil et procédé pour la fabrication d'écume comprenant des particules Download PDFInfo
- Publication number
- EP0247754B1 EP0247754B1 EP87304214A EP87304214A EP0247754B1 EP 0247754 B1 EP0247754 B1 EP 0247754B1 EP 87304214 A EP87304214 A EP 87304214A EP 87304214 A EP87304214 A EP 87304214A EP 0247754 B1 EP0247754 B1 EP 0247754B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- foam
- sand
- flow passage
- liquid
- annular
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000006260 foam Substances 0.000 title claims description 149
- 238000000034 method Methods 0.000 title claims description 46
- 239000002245 particle Substances 0.000 title description 3
- 239000004576 sand Substances 0.000 claims description 148
- 239000007788 liquid Substances 0.000 claims description 82
- 239000007789 gas Substances 0.000 claims description 56
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 29
- 239000007791 liquid phase Substances 0.000 claims description 13
- 239000011236 particulate material Substances 0.000 claims description 13
- 238000002156 mixing Methods 0.000 claims description 10
- 229910052757 nitrogen Inorganic materials 0.000 claims description 10
- 239000004094 surface-active agent Substances 0.000 claims description 10
- 239000012530 fluid Substances 0.000 description 41
- 230000008569 process Effects 0.000 description 20
- 238000012360 testing method Methods 0.000 description 18
- 230000015572 biosynthetic process Effects 0.000 description 16
- 238000005755 formation reaction Methods 0.000 description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- 239000002002 slurry Substances 0.000 description 9
- 230000000153 supplemental effect Effects 0.000 description 9
- 229910001873 dinitrogen Inorganic materials 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- 230000008901 benefit Effects 0.000 description 5
- 238000005187 foaming Methods 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- 238000005086 pumping Methods 0.000 description 4
- 239000011800 void material Substances 0.000 description 4
- 241000237858 Gastropoda Species 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000007792 gaseous phase Substances 0.000 description 3
- -1 i.e. Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000011282 treatment Methods 0.000 description 3
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 238000013459 approach Methods 0.000 description 2
- 229910001570 bauxite Inorganic materials 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 230000000295 complement effect Effects 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- 230000002706 hydrostatic effect Effects 0.000 description 2
- 238000009533 lab test Methods 0.000 description 2
- 238000012886 linear function Methods 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 1
- 241000416162 Astragalus gummifer Species 0.000 description 1
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- 235000017399 Caesalpinia tinctoria Nutrition 0.000 description 1
- 244000303965 Cyamopsis psoralioides Species 0.000 description 1
- 229920002907 Guar gum Polymers 0.000 description 1
- 206010019233 Headaches Diseases 0.000 description 1
- 229920002752 Konjac Polymers 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 235000015125 Sterculia urens Nutrition 0.000 description 1
- 240000001058 Sterculia urens Species 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical group [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 235000004298 Tamarindus indica Nutrition 0.000 description 1
- 240000004584 Tamarindus indica Species 0.000 description 1
- 241000388430 Tara Species 0.000 description 1
- LCKIEQZJEYYRIY-UHFFFAOYSA-N Titanium ion Chemical compound [Ti+4] LCKIEQZJEYYRIY-UHFFFAOYSA-N 0.000 description 1
- 229920001615 Tragacanth Polymers 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 150000001408 amides Chemical group 0.000 description 1
- 150000001412 amines Chemical group 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000000679 carrageenan Substances 0.000 description 1
- 235000010418 carrageenan Nutrition 0.000 description 1
- 229920001525 carrageenan Polymers 0.000 description 1
- 229940113118 carrageenan Drugs 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 230000005484 gravity Effects 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
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 235000010485 konjac Nutrition 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
- 229910052756 noble gas Inorganic materials 0.000 description 1
- 150000002835 noble gases Chemical class 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical group [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 239000013526 supercooled liquid Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 239000000196 tragacanth Substances 0.000 description 1
- 235000010487 tragacanth Nutrition 0.000 description 1
- 229940116362 tragacanth Drugs 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Images
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
- E21B21/00—Methods or apparatus for flushing boreholes, e.g. by use of exhaust air from motor
- E21B21/06—Arrangements for treating drilling fluids outside the borehole
- E21B21/062—Arrangements for treating drilling fluids outside the borehole by mixing components
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F23/00—Mixing according to the phases to be mixed, e.g. dispersing or emulsifying
- B01F23/20—Mixing gases with liquids
- B01F23/23—Mixing gases with liquids by introducing gases into liquid media, e.g. for producing aerated liquids
- B01F23/235—Mixing gases with liquids by introducing gases into liquid media, e.g. for producing aerated liquids for making foam
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F25/00—Flow mixers; Mixers for falling materials, e.g. solid particles
- B01F25/30—Injector mixers
- B01F25/31—Injector mixers in conduits or tubes through which the main component flows
- B01F25/311—Injector mixers in conduits or tubes through which the main component flows for mixing more than two components; Devices specially adapted for generating foam
-
- 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
- E21B43/25—Methods for stimulating production
- E21B43/26—Methods for stimulating production by forming crevices or fractures
- E21B43/2607—Surface equipment specially adapted for fracturing operations
Definitions
- the invention relates generally to apparatus and methods for creating particle-containing foams, especially (but not exclusively) foamed fracturing fluids carrying high concentrations of proppant material.
- one technique which is sometimes used to stimulate production is the facturing of the subsurface producing formation. This is accomplished by pumping a fluid at a very high pressure and rate into the formation to hydraulically create a fracture extending from the well bore out into the formation.
- a proppant material such as sand is included in the fracturing fluid, and subsequently deposited in the fracture to prop the fracture so that it remains open after the fracturing pressure has been released from the formation.
- foamed fracturing fluids which are at this point generally recognized.
- one advantage of foamed fracturing fluids is that they have low fluid loss characteristics resulting in more efficient fracture treatments and reduced damage to water sensitive formations.
- foamed fracturing fluids have a relatively low hydrostatic head, thus minimizing fluid entry into the formation and its resulting damage. Also, foamed fracturing fluids have a high effective viscosity permitting the creation of wider vertical fractures and horizontal fractures having greater area. Another advantage is that foamed fracturing fluids typically have a high proppant carrying capacity allowing more proppant to be delivered to the site of the fracture and more proppant to remain suspended until the fracture heals.
- fracturing fluids do have at least one major disadvantage, and this pertains to the proppant concentrations available with currently practiced foam generator techniques.
- current techniques involve blending a mixture of proppant and liquid containing a suitable surfactant. The mixture is pumped to high pressure after which the gaseous phase, typically nitrogen or carbon dioxide, is added to produce the foamed proppant-laden fracturing fluid.
- gaseous phase typically nitrogen or carbon dioxide
- This technique involves an inherent proppant concentration limitation due to the concentration limitation of the proppant/liquid mixture.
- the theoretical maximum concentration of a sand/ liquid mixture is approximately 34 pounds of sand per gallon (4.1 g/cm 3 ) of liquid. This corresponds to a liquid volume just sufficient to fill the void spaces of bulk sand. In common practice, this maximum is further limited by the blending and pumping equipment capabilities and lies in a range of 15 to 25 Ib/gal. (1.8 to 3.0 g/cm 3 ).
- foams are produced which have approximately three unit volumes of gaeous phase per unit volume of liquid phase corresponding to a foam quality, that is a gaseous volume fraction, of 75%.
- a foam quality that is a gaseous volume fraction, of 75%.
- the gas expands the carrier fluid to approximately four times its original volume.
- a sand concentration of 25 pounds of sand per gallon (3.0 g/cm 3 ) of liquid in a sand/liquid slurry is reduced to approximately 6 pounds of sand per gallon (0.7 g/cm 3 of carrier fluid, i.e., foam by the procsss of foaming.
- Even the theoretical maximum sand concentration of 34 Ib/gal (4.1 g/cm 3 ) in the sand/liquid slurry would only produce an 8.5 Ib/gal (1.0 g/cm 3 ) concentration in a 75% quality foam.
- the concentration of proppant in the fracturing fluid is of considerable importance since this determines the final propped thickness of the fracture.
- a fracturing fluid with a sand concentration of 34 pounds of sand per gallon (4.1 g/cm 3 ) of carrier fluid could theoretically prop the fracture at its hydraulically created width.
- Another problem encountered with many fracturing fluids including foam also involves proppant concentration and this pertains to the fracturing fluid's compatibility with the formation core and formation fluids, particularly in gas wells.
- many formations contain clays which swell when contacted by water base fluids resulting in reduced formation permeability.
- Foamed fracturing fluids reduce this problem due to their low fluid loss and low hydrostatic head characteristics, both of which result in less fluid entering the formation.
- the theoretical maximum sand concentration is 34 pounds of sand per gallon (4.1 g/cm 3 ) of liquid phase of the foam and as previously mentioned, the current practical limit is about 25 pounds per gallon (3.0 g/cm 3 ).
- a foamed fracturing fluid with a greater concentration of sand to liquid would be highly desirable for water sensitive formations since a given amount of sand could be delivered to the formation with less liquid in the carrier fluid.
- the Bullen concentrator is stated to be capable of removing about 50% of the liquid from the slurry, thus doubling the proppant concentration in the subsequent foam to a maximum of about 5 pounds per gallon (0.6 g/cm 3 ) of 75% quality foam, that is 20 pounds per gallon (2.4 g/cm 3 ) of liquid in the resulting foam.
- the invention thus provides a method of generating a foam containing particulate material, comprising:
- French patent specification FR-A-2521869 describes a foam-forming head particularly for attachment to an agricultural spray boom, which comprises a body, a main flow passage (for a frother eg. gas) disposed through the body and having an inlet and an outlet, an annular plenum disposed in said body and surrounding said main flow passage; a second flow passage (for the foam base material) disposed in the body and having a first inlet end and a second end communicated with the annular plenum.
- a main flow passage for a frother eg. gas
- the present invention provides apparatus for use in the method of the invention, which apparatus comprises a body; a main flow passage disposed through said body and having an inlet and an outlet; and annular plenum disposed in said body and surrounding said main flow passage; a second flow passage disposed in said body and having a first inlet end and a second end communicated with said annular plenum; characterised by adjustable annular nozzle means, disposed in said body between said annular plenum and said main flow passage, for providing an annular flow path of adjustable width communicating said annular plenum with said main flow passage.
- a system generally designated by the numeral 10 for producing foamed fracturing fluids carrying high concentrations of proppant material in accordance with the principles of the present invention.
- the system 10 is based upon the use of a dry sand foam generating apparatus generally designated by the numeral 12.
- the foam generating apparatus 12 may also be generally referred to as a vessel 12.
- the invention is being disclosed in the context of the production of a proppant carrying foam for hydraulic fracturing of a well, the invention is also useful in other areas such as foamed gravel packing wherein said or the like is packed in an annulus surrounding a well casing.
- foamed gravel packing wherein said or the like is packed in an annulus surrounding a well casing.
- any other particulate may be utilized such as, for example, sintered bauxite, glass beads, calcined bauxite, and resin particles, as well as any other conventionally known particulates for use in the treatment of subterranean formations.
- the foam generating apparatus 12 has a body 14 with a straight vertical main flow passage 16 disposed therethrough.
- Main flow passage 16 has an inlet 18 at its upper end, and an outlet 20 at its lower end.
- Foam generating apparatus 12 includes an upper first nozzle insert 22 threadably engaged at 24 with an upper threaded counterbore 26 of body 14.
- Nozzle insert 22 has an inner end 28 received in the body 14 and adjustably positioned relative to an annular conically tapered first seat 30 surrounding main flow passage 16.
- Inner end 28 of nozzle insert 22 has a conically tapered annular surface 32 defined thereon.
- the conical taper of surface 32 is complementary with that of annular seat 30, that is, the taper on both the surface 32 and seat 30 are substantially the same.
- surface 32 and seat 30 are each tapered 60° from the horizontal.
- An annular conical first flow path 34 is defined between tapered surface 32 and seat 30 and has a width defined vertically in Fig. 1 which is adjustable by adjustment of the threaded engagement 24 between insert 22 and body 14.
- insert 22 has a reduced diameter cylindrical outer portion 36 closely received within an upper cylindrical bore 38 of body 14 with a seal being provided therebetween by 0-ring 40.
- nozzle end portion 42 of insert 22 having a further reduced diameter.
- An upper annular plenum 44 is defined between nozzle portion 42 of insert 22 and upper bore 38 of body 14, and surrounds the main flow passage 16.
- a transverse liquid inlet passage 46 which may generally be referred to as a second flow passage 46, is disposed in the body 14.
- Inlet passage 46 has an outer inlet end 48, and an inner second end 50 which is communicated with the annular plenum 44.
- liquid inlet passage 46 is utilized to introduce a liquid stream, generally a water based liquid including surfactant, into the foam generating apparatus 12.
- the liquid stream also may contain other additives such as viscosifying agent, crosslinking agent, gel breakers, corrosion inhibitors, clay stabilizers, various salts such as potassium chloride and the like which are well-known conventional additives for fluids utilized in the treatment of subterranean formations.
- the viscosifying agent can comprise, for example, hydratable polymers which contain in sufficient concentration and reactive position, one or more functional groups such as hydroxyl or hydroxylalkyl, cis-hydroxyl, carboxyl, sulfate, sulfonate, amino or amide.
- Particularly suitable such polymers are polysaccharides and derivatives thereof, which include but are not limited to, guar gum and derivatives thereof, locust beam gum, tara, konjak, tamarind, starch, karaya, tragacanth, carrageenan, xanthan and cellulose derivatives.
- Hydratable synthetic polymers include, but are not limited to, polyacrylate, polymethacrylate, polyacrylamide, maleic anhydride-methylvinyl ether copolymers, polyvinyl alcohol and the like.
- crosslinking agents for the above viscosifying agents include, but are not limited to, compounds containing titanium (IV) such as various organotitanium chelates, compounds containing zirconium IV such as various organozirconium chelates, various borate-containing compounds, pyroan- timonates and the like.
- a lower second nozzle insert 52 is threadably engaged at 54 with an internally threaded lower counterbore 56 of body 14.
- Second nozzle insert 52 is constructed similar to first nozzle insert 22, except that its upper inner end has a radially inner conical tapered surface 58 which is complementary with a downward facing conically tapered second annular seat 60 defined on body 14 and surrounding main flow passage 16.
- surface 58 and seat 60 are each tapered 15° from the horizontal.
- the apparatus 12 can be inverted with the seats 30 and 60 then being tapered upwardly so that the conical fluid jets ejected therefrom are directed against the downward flow of gas and sand through flow passage 16.
- a lower second annular plenum 62 is defined between second nozzle insert 52 and a lower counterbore 64 of body 14.
- a transverse supplemental gas inlet passage 66 is disposed in body 14 and communicates a supplemental gas inlet 68 thereof with the second plenum 62.
- transverse gas inlet passage 66 and the adjustable lower nozzle insert 52 are utilized to provide supplemental gas, if necessary, to the proppant carrying foam. In some instances, however, such supplemental gas may not be necessary, and the transverse gas inlet passage 66 will not be used. In fact, the methods of the present invention can in many instances be satisfactorily performed with a foam generator in which the lower second nozzle insert 52 and the associated transverse gas inlet passage 66 are eliminated.
- the main flow passage 16 can generally be described as including an upper portion 70 disposed through first nozzle insert 22, a middle portion 72 defined within the body 14 itself, and a lower portion 74 defined in second nozzle insert 52.
- FIG. 1 Also schematically illustrated in Fig. 1 are a plurality of associated apparatus which are utilized with the foam generating apparatus 12 to produce a proppant laden foamed fracturing fluid.
- a high pressure sand tank 76 is located vertically directly above the foam generating apparatus 12.
- Sand tank 76 is substantially filled with a particulate material such as sand 78 through a sand fill inlet valve 80.
- the sand tank 76 is then filled with high pressure nitrogen gas from a nitrogen gas supply 82 through primary nitrogen supply line 84.
- a pressure regulator 86 and other conventional equipment (not shown) for controlling the pressure of the gas supplied to sand tank 76 are included in supply line 84.
- the gas supply 82 is disclosed as nitrogen, many other gases are suitable for use in generating a foam according to the methods and using the apparatus of the present invention. Such other gases include, without limitation, air, carbon dioxide, as well as any inert gas, such as any of the noble gases.
- the sand tank 76 After the sand tank 76 is filled with sand 78, it is pressurized with nitrogen gas to a relatively high pressure, preferably above 500 psi (3.45 MPa) for reasons that are further explained below.
- This dry sand 78 is introduced into the foam generating apparatus 12 by opening a valve 88 in sand supply line 90 which extends from a bottom 92 of sand tank 76 to inlet 18 of main flow passage 16 of foam generating apparatus 12.
- the sand supply line 90 preferably is a straight vertical conduit, and the valve 88 is preferably a full opening type valve such as a full opening ball valve.
- valve 88 When the valve 88 is opened, a stream of gas and sand is introduced into the main flow passage 16 of apparatus 12.
- the dry sand 78 flows by the action of gravity and differential gas pressure downward through sand supply line 90 into the vertical bore 16 of foam generating apparatus 12.
- a water based liquid 94 is contained in a liquid supply tank 96.
- a high pressure pump 98 takes the liquid 94 from supply tank 96 through a suction line 100 and discharges it under high pressure through a high pressure liquid discharge line 102 to the inlet 48 of transverse liquid inlet passage 46.
- the liquid 94 in supply tank 96 will have a sufficient concentration of a suitable surfactant mixed therewith in tank 96, so that upon mixing the liquid 94 with gas and sand in flow passage 16, a stable foam will be formed.
- suitable surfactants are well known in the art and include, by way of example and not limitation, betaines, sulfated or sulfonated alkoxylates, alkyl quaternary amines, alkoxylated linear alcohols, alkyl sulfonates, alkyl aryl sulfonates, C 'o- C 2o alkyldiphenyl ether sulfonates and the like.
- the liquid and surfactant flow through the transverse liquid inlet passage 46 into the annular plenum 44.
- the liquid and surfactant then flow from the annular plenum 44 in the form of a self-impinging conical jet flowing substantially symmetrically through the first annular flow passage 34 and impinging upon the vertically downward flowing stream of gas and sand flowing through main flow passage 16.
- This high pressure, high speed, self-impinging conical jet of water based liquid and surfactant mixes with the downward flowing stream of gas and dry sand in a highly turbulent manner so as to produce a foam comprised of a liquid matrix of bubbles filled with nitrogen gas.
- This foam carries the sand in suspension therein.
- Supplemental gas supply line 110 connects to supplemental gas inlet 68 of transverse gas inlet passage 66 so that gas is introduced into the second annular plenum 62 and then through the conical flow passage defined between conically tapered surface 58 on the inner end of lower nozzle insert 52 and the tapered annular lower seat 60 of body 14.
- the proppant laden foam generated in the foam generating apparatus 12 exits the outl'et 20 and is conducted through a conduit 114 to a well 116.
- the foam fracturing fluid is directed downwardly through tubing (not shown) in the well 116 to a subsurface formation (not shown) which is to be fractured.
- the pressure of the fracturing fluids contained in conduit 114 when introduced into the well head 116 are substantially in excess of atmospheric pressure.
- Well head pressures in a range from 1000 psi to 10,000 psi (6.89 to 68.9 MPa) are common for hydraulic fracturing operations.
- the delivery rate of dry sand 78 into the foam generator 12 is controlled by the differential gas pressure between the sand tank 76 and the bore 16 of the foam generator apparatus 12.
- flow rate of the liquid jet entering transverse liquid inlet passage 46 determines the liquid sand concentration, that is the pounds of sand per gallon of liquid phase in the carrier fluid, of the generated foam.
- the volumetric flow rate of gas through said supply line 90 required to deliver the dry sand together with the volumetric flow rate of supplemental gas, if any, supplied through transverse gas inlet passage 66 determine the quality, that is the gaseous volume fraction of fluid phases, of the generated foam.
- the setting of the threaded engagement of upper nozzle insert 22 with body 14 permits adjustment of the width of the first annular flow path 34.
- This adjustment is generally utilized for the purpose of achieving an appropriate mixing energy and thus a satisfactory foaming of the materials which are mixing with the main flow passage 16.
- This adjustment also conceivably could be used to affect the flow rate of liquid therethrough.
- suitable flowmeters may be placed in lines 84, 102 and 110 to measure the flow of fluids therethrough. Flow of sand out of tank 76 can be measured by measuring a change in weight of the tank 76 and its contents.
- the high pressure nitrogren supply illustrated in Fig. 1, namely the cylinder 82 of compressed nitrogen gas and the pressure regulator 86, are respresentative of the equipment utilized for the laboratory tests described below.
- nitrogen will typically by supplied by a positive displacement cryogenic pump which pumps nitrogen in a supercooled liquid state into the supply lines 84 and/or 110.
- the mass flow rate of nitrogen will be known and controlled by the volumetric rate of the cryogenic pump.
- Fig. 2 a graphical representation is presented of the theoretical maximum sand concentration of a foam as a function of foam quality, both for wet sand foam generation such as has been practiced in the prior art where the sand is introduced in a sand/liquid slurry, and for dry sand foam generation as disclosed in the present application wherein the sand is introduced with a stream of gas.
- Foam sand concentration e.g., the pounds of sand per gallon of foam
- the values displayed on the right-hand vertical axis of Fig. 2 are for liquid sand concentrations, e.g., the pounds of sand per gallon of liquid phase of the foam.
- the theoretical maximum foam sand concentration for a wet sand foam generation process like that utilized in the prior art is shown by the dashed line 118 and is seen to be a decreasing linear function of foam quality.
- the plotted maximum concentrations for the wet sand foam generation process as represented by line 118 are obtained by adding sufficient gas volume to the liquid occupying the void volume of bulk sand to obtain a given foam quality.
- the theoretical maximum foam sand concentration for the dry sand foam generation process of the present invention is represented by the solid line 120 and is seen to be an increasing linear function of foam quality.
- the plotted maximum concentrations for the dry sand foam generation process as represented by straight line 120 are obtained by adding sufficient liquid to the gas volume occupying the void volume of bulk sand to obtain a given foam quality.
- both the wet sand foam generation process represented by line 118 and the dry sand foam generation process represented by line 120 provide an identical foam since they both contain equal volumes of gas and liquid and an identical amount of sand.
- the foam produced by the present invention have a "Mitchell quality", that is, a volume ratio of the gaseous phase to the total gaseous and liquid phases and disregarding the volume of the particulate solids, in the range from about 0.53 to 0.99. This can also be expressed as a quality in the range from about 53% to about 99%.
- a general discussion of the Mitchell quality concept can be found in U.S. Patents Nos. 4,480,696 to Almond et al., 4,448,709 to Bullen, and 3,937,283 to Blauer et al.
- an upper limit of foam quality be about 96%, because the properties of the foam become somewhat unpredictable at higher quality levels where the foam may convert to a mist.
- the generally preferred range of quality for foams generated by the dry sand foam generation process of the present invention is in a range from about 53% to about 96%.
- line 124 shows a constant 34lb/gal (4.1 g/cm 3 ) theoretical maximum liquid sand concentration. As previously explained, this is determined by the volume of liquid required to fill the void spaces in tightly packed sand.
- proppant carrying foamed fracturing fluids can be produced which contain a ratio of sand to the liquid phase of the foam, that is, a liquid sand concentration such as that represented on the right-hand vertical axis of Fig. 2, substantially in excess of both the theoretical maximum ratio of particulate material to liquid which could have been contained in the liquid, i.e., 34 lbs/gal (4.1 g/ cm 3 ), and the somewhat lower practical maximum ratio, i.e., 15 to 25 Ibs/gal (1.8 to 3.0 g/cm 3 ), which could have been contained in the liquid as a result of limitations on pumping equipment and the like.
- the preferred compositions of foams produced by the present invention include those compositions denoted by the trapezoidal region defined by the points, A, B, C and D.
- the sand tank 76 was pressurized to approximately 75 psi (520 kPa) with compressed air.
- the differential pressure between sand tank 76 and main flow passage 16 of the foam generator was about 50 psi (345 kPa).
- the test was run until a five-gallon bucket (1.9x10- Z m 3 ) was filled with foam exiting outlet 20.
- the weight of sand delivered from sand tank 76, and water delivered from supply tank 96 were determined, and converted to a volume basis.
- the five gallons (1.9x 10- 2 m 3 ) of foam collected included 1.32 gallons (5.Ox10- 3 m 3 ) of sand and 0.37 gallons (1.4x10- 3 m 3 ) of water.
- the remaining volume of the five gallons (1.9x10 -2 m 3 ) of foam, 3.31 gallons (1.3x10 -2 m 3 ) was comprised of air. From this data, a foam quality of 89.9% was calculated.
- the liquid sand concentration was calculated to be 74.9 pounds of sand per gallon (9.0 g/cm 3 ) of water in the foam, which corresponds to 7.53 pounds of sand per gallon (0.9 g/ cm 3 ) of foam.
- This test was run using a foam generator with a 5/8 inch (15.9mm) bore.
- the liquid stream was injected into passage 46 so that it entered the mainflow passage 16 at a downward angle of 60° to the horizontal.
- the test apparatus was modified to allow the generated foam to be collected in a receiver vessel (not shown) at approximately the same pressure as that at which it was generated.
- the volume of generated foam was determined by measuring the volume of water displaced from the receiver vessel.
- An average nitrogen pressure in sand tank 76 was 756 psig (5.2 MPa gauge).
- Average pressure in the bore 16 of foam generating apparatus 12 was 750 psig (5.2 MPa gauge).
- Average pressure in the foam receiver vessel was 730 psig (5.0 MPa gauge).
- the test was run for 5.0 mintues.
- Total sand weight delivered was 292 lb. (133 kg) for a sand rate of 58.4 Ib/min (26.5 kg/ min).
- Total liquid supplied was 3.0 gal (1.1 x 1 0- 2 m 3 ) for a liquid rate of 0.60 gallons per minute (2.3x10- 2 m 3 per minute).
- the gas flow rate of the apparatus 12 was calculated to be 55.7 standard cubic feet (1.56 m 3 ) per minute.
- Total foam generated was 57.37 gal (0.22 m 3 ). From this data, a foam quality at the foam generator 12 of 93% was calculated.
- a liquid sand concentration of 97.3 pounds of sand per gallon (11.7 g/cm 3 ) of liquid phase of the foam was calculated.
Landscapes
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Geology (AREA)
- Mining & Mineral Resources (AREA)
- Physics & Mathematics (AREA)
- Environmental & Geological Engineering (AREA)
- Fluid Mechanics (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Mechanical Engineering (AREA)
Claims (15)
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US86462186A | 1986-05-16 | 1986-05-16 | |
US864621 | 1986-05-16 | ||
US06/864,696 US4780243A (en) | 1986-05-19 | 1986-05-19 | Dry sand foam generator |
US864696 | 1986-05-19 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0247754A1 EP0247754A1 (fr) | 1987-12-02 |
EP0247754B1 true EP0247754B1 (fr) | 1990-10-24 |
Family
ID=27127849
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP87304214A Expired EP0247754B1 (fr) | 1986-05-16 | 1987-05-12 | Appareil et procédé pour la fabrication d'écume comprenant des particules |
EP87304213A Withdrawn EP0246800A1 (fr) | 1986-05-16 | 1987-05-12 | Ecume comprenant des particules |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP87304213A Withdrawn EP0246800A1 (fr) | 1986-05-16 | 1987-05-12 | Ecume comprenant des particules |
Country Status (4)
Country | Link |
---|---|
EP (2) | EP0247754B1 (fr) |
DE (1) | DE3765698D1 (fr) |
ES (1) | ES2018546B3 (fr) |
SG (1) | SG5791G (fr) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2519634A (en) * | 2013-08-23 | 2015-04-29 | Chevron Usa Inc | System, apparatus and method for well deliquification |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7213651B2 (en) | 2004-06-10 | 2007-05-08 | Bj Services Company | Methods and compositions for introducing conductive channels into a hydraulic fracturing treatment |
GB201112754D0 (en) * | 2011-07-25 | 2011-09-07 | Clyde Union Ltd | Particulate material delivery method and system |
US10408026B2 (en) | 2013-08-23 | 2019-09-10 | Chevron U.S.A. Inc. | System, apparatus, and method for well deliquification |
CN107130953B (zh) * | 2017-05-17 | 2020-04-14 | 成都百联油田技术服务有限公司 | 一种化学强化采气工艺 |
EP3658264A4 (fr) * | 2017-07-07 | 2021-04-07 | Linde GmbH | Systeme de refroidissement de farine cryogenique et lco2 |
CN108035700B (zh) * | 2017-11-30 | 2023-04-18 | 青岛海洋地质研究所 | 海洋天然气水合物生产井井筒携砂规律仿真系统及方法 |
CN114262607B (zh) * | 2021-12-31 | 2023-05-16 | 昆山京昆油田化学科技有限公司 | 一种铝钛复合交联剂及其制备方法和应用、瓜尔胶酸性压裂液体系 |
CN115945115B (zh) * | 2022-12-16 | 2024-05-17 | 重庆科技学院 | 一种三级搅拌一级增速油套环空起泡装置 |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4126181A (en) * | 1977-06-20 | 1978-11-21 | Palmer Engineering Company Ltd. | Method and apparatus for formation fracturing with foam having greater proppant concentration |
US4354552A (en) * | 1980-09-08 | 1982-10-19 | The Dow Chemical Company | Slurry concentrator |
CA1151527A (fr) * | 1980-11-06 | 1983-08-09 | Ronald S. Bullen | Concentrateur de bouillies de fractionnement |
HU185090B (en) * | 1982-02-25 | 1984-11-28 | Debreceni Mezoegazdasagi | Foam forming head, control apparatus as well as device from these first for agricultural row marking by foam |
AU3450284A (en) * | 1983-12-13 | 1985-06-20 | Halliburton Company | Foam generator |
US4512405A (en) * | 1984-02-29 | 1985-04-23 | Hughes Tool Company | Pneumatic transfer of solids into wells |
-
1987
- 1987-05-12 EP EP87304214A patent/EP0247754B1/fr not_active Expired
- 1987-05-12 EP EP87304213A patent/EP0246800A1/fr not_active Withdrawn
- 1987-05-12 ES ES87304214T patent/ES2018546B3/es not_active Expired - Lifetime
- 1987-05-12 DE DE8787304214T patent/DE3765698D1/de not_active Expired - Fee Related
-
1991
- 1991-02-07 SG SG57/91A patent/SG5791G/en unknown
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2519634A (en) * | 2013-08-23 | 2015-04-29 | Chevron Usa Inc | System, apparatus and method for well deliquification |
GB2519634B (en) * | 2013-08-23 | 2020-06-24 | Chevron Usa Inc | System, apparatus and method for well deliquification |
Also Published As
Publication number | Publication date |
---|---|
SG5791G (en) | 1991-04-05 |
ES2018546B3 (es) | 1991-04-16 |
DE3765698D1 (de) | 1990-11-29 |
EP0247754A1 (fr) | 1987-12-02 |
EP0246800A1 (fr) | 1987-11-25 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4780243A (en) | Dry sand foam generator | |
US4830794A (en) | Dry sand foam generator | |
CA1149732A (fr) | Methode de cimentation des forages | |
AU2002300782B2 (en) | System and method for fracturing a subterranean well formation for improving hydrocarbon production | |
CA1220412A (fr) | Methode et dispositif d'accroissement de la concentration des agents de chasse pour stimuler le rendement des forages petroliferes et gaziferes | |
US7059591B2 (en) | Method and apparatus for enhanced oil recovery by injection of a micro-dispersed gas-liquid mixture into the oil-bearing formation | |
CA2584373C (fr) | Appareil d'hydratation de polymere sec et procedes d'utilisation correspondants | |
CA1215640A (fr) | Injection pneumatique de solides dans un forage | |
EP1398458B1 (fr) | Réduction du refoulement particulaire dans les puits | |
US4730676A (en) | Downhole foam generator | |
US6209641B1 (en) | Method and apparatus for producing fluids while injecting gas through the same wellbore | |
CN105683489B (zh) | 用于无水压裂流体的输送的控制系统和设备 | |
EP0247754B1 (fr) | Appareil et procédé pour la fabrication d'écume comprenant des particules | |
US4470727A (en) | Apparatus and process for foamed cementing | |
US20060272735A1 (en) | Method of supplying a powdered chemical composition to a wellsite | |
CN110898741B (zh) | 一种油田用粉煤灰强化泡沫形成装置及其应用 | |
CN107813229A (zh) | 可循环磨料射流冲蚀测试系统与方法 | |
WO2009048337A1 (fr) | Moyens et procédé pour mélanger une matière particulaire et un liquide | |
CN115853485A (zh) | 一种页岩气压裂试气抽取装置及方法 | |
US3470957A (en) | Well sealing with atomized resin | |
EP2812410B1 (fr) | Procédé de fracturation par utilisation de suspensions d'agent de soutènement ultraléger et de flux gazeux | |
CN210798942U (zh) | 一种新型泡沫压裂液携砂施工装置 | |
US11313212B1 (en) | Pre-hydration of friction reducers for wellbore fluids | |
CN221119884U (zh) | 一种防止堵漏泥浆沉淀的配置装置 | |
RU2306414C2 (ru) | Способ временной изоляции интервала продуктивного пласта |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): DE ES FR GB IT NL |
|
17P | Request for examination filed |
Effective date: 19880331 |
|
17Q | First examination report despatched |
Effective date: 19890508 |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
ITF | It: translation for a ep patent filed | ||
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): DE ES FR GB IT NL |
|
REF | Corresponds to: |
Ref document number: 3765698 Country of ref document: DE Date of ref document: 19901129 |
|
ET | Fr: translation filed | ||
ITTA | It: last paid annual fee | ||
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
26N | No opposition filed | ||
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 19940504 Year of fee payment: 8 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 19940511 Year of fee payment: 8 Ref country code: DE Payment date: 19940511 Year of fee payment: 8 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: NL Payment date: 19940531 Year of fee payment: 8 Ref country code: ES Payment date: 19940531 Year of fee payment: 8 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Effective date: 19950512 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: ES Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 19950513 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: NL Effective date: 19951201 |
|
GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 19950512 |
|
NLV4 | Nl: lapsed or anulled due to non-payment of the annual fee |
Effective date: 19951201 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DE Effective date: 19960201 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FR Effective date: 19960229 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST |
|
REG | Reference to a national code |
Ref country code: ES Ref legal event code: FD2A Effective date: 19990301 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IT Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES;WARNING: LAPSES OF ITALIAN PATENTS WITH EFFECTIVE DATE BEFORE 2007 MAY HAVE OCCURRED AT ANY TIME BEFORE 2007. THE CORRECT EFFECTIVE DATE MAY BE DIFFERENT FROM THE ONE RECORDED. Effective date: 20050512 |