US20080023199A1 - Cement Compositions Comprising Environmentally Compatible Defoaming Agents and Methods of Use - Google Patents
Cement Compositions Comprising Environmentally Compatible Defoaming Agents and Methods of Use Download PDFInfo
- Publication number
- US20080023199A1 US20080023199A1 US11/860,308 US86030807A US2008023199A1 US 20080023199 A1 US20080023199 A1 US 20080023199A1 US 86030807 A US86030807 A US 86030807A US 2008023199 A1 US2008023199 A1 US 2008023199A1
- Authority
- US
- United States
- Prior art keywords
- solvent
- agent
- lecithin
- fluid
- present
- 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.)
- Abandoned
Links
- 238000000034 method Methods 0.000 title claims abstract description 48
- 239000000203 mixture Substances 0.000 title claims description 79
- 239000004568 cement Substances 0.000 title claims description 67
- 239000002518 antifoaming agent Substances 0.000 title abstract description 80
- 239000012530 fluid Substances 0.000 claims abstract description 82
- 239000000787 lecithin Substances 0.000 claims abstract description 51
- 235000010445 lecithin Nutrition 0.000 claims abstract description 51
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 claims abstract description 47
- 229940067606 lecithin Drugs 0.000 claims abstract description 47
- 239000006260 foam Substances 0.000 claims abstract description 42
- 239000002904 solvent Substances 0.000 claims abstract description 37
- 230000002209 hydrophobic effect Effects 0.000 claims abstract description 28
- 239000002245 particle Substances 0.000 claims abstract description 28
- 230000015572 biosynthetic process Effects 0.000 claims description 29
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 21
- 239000003795 chemical substances by application Substances 0.000 claims description 19
- 238000005553 drilling Methods 0.000 claims description 18
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 14
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 6
- 239000004094 surface-active agent Substances 0.000 claims description 6
- 239000002199 base oil Substances 0.000 claims description 5
- 238000002156 mixing Methods 0.000 claims description 5
- 239000003921 oil Substances 0.000 claims description 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 4
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 4
- 239000000194 fatty acid Substances 0.000 claims description 4
- 229930195729 fatty acid Natural products 0.000 claims description 4
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 4
- 239000010703 silicon Substances 0.000 claims description 4
- 229910052710 silicon Inorganic materials 0.000 claims description 4
- 239000010696 ester oil Substances 0.000 claims description 3
- 150000002148 esters Chemical class 0.000 claims description 3
- 150000004665 fatty acids Chemical class 0.000 claims description 3
- 229930195733 hydrocarbon Natural products 0.000 claims description 3
- 150000002430 hydrocarbons Chemical group 0.000 claims description 3
- 230000000149 penetrating effect Effects 0.000 claims description 3
- 230000000638 stimulation Effects 0.000 claims description 3
- 238000004140 cleaning Methods 0.000 claims description 2
- 238000002347 injection Methods 0.000 claims description 2
- 239000007924 injection Substances 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims description 2
- 238000005507 spraying Methods 0.000 claims description 2
- 239000004215 Carbon black (E152) Substances 0.000 claims 2
- 150000001336 alkenes Chemical class 0.000 claims 2
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims 2
- 239000012188 paraffin wax Substances 0.000 claims 2
- 230000004936 stimulating effect Effects 0.000 claims 1
- 238000005755 formation reaction Methods 0.000 description 21
- 239000002002 slurry Substances 0.000 description 17
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 16
- 235000013539 calcium stearate Nutrition 0.000 description 15
- 239000008116 calcium stearate Substances 0.000 description 15
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical class O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 12
- 239000000463 material Substances 0.000 description 11
- 239000011396 hydraulic cement Substances 0.000 description 7
- 239000000654 additive Substances 0.000 description 6
- 230000008901 benefit Effects 0.000 description 6
- VFLDPWHFBUODDF-FCXRPNKRSA-N curcumin Chemical compound C1=C(O)C(OC)=CC(\C=C\C(=O)CC(=O)\C=C\C=2C=C(OC)C(O)=CC=2)=C1 VFLDPWHFBUODDF-FCXRPNKRSA-N 0.000 description 5
- 230000007613 environmental effect Effects 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- 239000002270 dispersing agent Substances 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- -1 glycol ethers Chemical class 0.000 description 4
- 239000004576 sand Substances 0.000 description 4
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000010881 fly ash Substances 0.000 description 3
- 150000002334 glycols Chemical class 0.000 description 3
- 239000004816 latex Substances 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-heptanol Chemical compound CCCCCCCO BBMCTIGTTCKYKF-UHFFFAOYSA-N 0.000 description 2
- 239000010755 BS 2869 Class G Substances 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- CEGOLXSVJUTHNZ-UHFFFAOYSA-K aluminium tristearate Chemical compound [Al+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CEGOLXSVJUTHNZ-UHFFFAOYSA-K 0.000 description 2
- 229940063655 aluminum stearate Drugs 0.000 description 2
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
- 238000005187 foaming Methods 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
- 229920000126 latex Polymers 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- 238000005086 pumping Methods 0.000 description 2
- 230000002195 synergetic effect Effects 0.000 description 2
- 230000008719 thickening Effects 0.000 description 2
- 239000003180 well treatment fluid Substances 0.000 description 2
- GGQQNYXPYWCUHG-RMTFUQJTSA-N (3e,6e)-deca-3,6-diene Chemical compound CCC\C=C\C\C=C\CC GGQQNYXPYWCUHG-RMTFUQJTSA-N 0.000 description 1
- 239000010754 BS 2869 Class F Substances 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000011398 Portland cement Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- KUDVWKKHTYKSDR-UHFFFAOYSA-N butan-1-ol;calcium Chemical compound [Ca].CCCCO KUDVWKKHTYKSDR-UHFFFAOYSA-N 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 229910000389 calcium phosphate Inorganic materials 0.000 description 1
- 235000011010 calcium phosphates Nutrition 0.000 description 1
- 210000000170 cell membrane Anatomy 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical compound C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 description 1
- 229960001231 choline Drugs 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- MRUAUOIMASANKQ-UHFFFAOYSA-N cocamidopropyl betaine Chemical compound CCCCCCCCCCCC(=O)NCCC[N+](C)(C)CC([O-])=O MRUAUOIMASANKQ-UHFFFAOYSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000013530 defoamer Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000013505 freshwater Substances 0.000 description 1
- 229910021485 fumed silica Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 235000012907 honey Nutrition 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000004005 microsphere Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 150000003904 phospholipids Chemical class 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000008347 soybean phospholipid Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 230000005641 tunneling Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/42—Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells
- C09K8/46—Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells containing inorganic binders, e.g. Portland cement
- C09K8/467—Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells containing inorganic binders, e.g. Portland cement containing additives for specific purposes
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B24/00—Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
- C04B24/003—Phosphorus-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B24/00—Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
- C04B24/08—Fats; Fatty oils; Ester type waxes; Higher fatty acids, i.e. having at least seven carbon atoms in an unbroken chain bound to a carboxyl group; Oxidised oils or fats
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2103/00—Function or property of ingredients for mortars, concrete or artificial stone
- C04B2103/50—Defoamers, air detrainers
Definitions
- the present invention relates to subterranean operations, and more particularly, to environmentally compatible defoaming agents and methods of using such defoaming agents in subterranean well fluids.
- well fluids When drilling or completing wells in subterranean formations, various fluids may be used for a variety of reasons. These fluids are often aqueous. For the purposes herein, such a fluid will be referred to as a “well fluid.”
- well fluids include, but are not limited to: lubrication and cooling of drill bit cutting surfaces while drilling generally or drilling-in (e.g., drilling in a targeted petroliferous formation); transportation of cuttings to the surface; controlling formation pressure to prevent blowouts; maintaining well stability; suspending solids in the well; fracturing the formation; cementing the well; displacing the fluid within the well with another fluid; cleaning the well; testing the well; and minimizing fluid loss into and stabilizing the formation through which the well is being drilled. Similar fluids also may be used in other applications such as tunnel drilling. Fluids used for such purposes are encompassed within the term “well fluid” as used herein.
- foam is likely to occur. This foaming may be undesirable.
- surfactants may be added to generate desirable foam to assist in removing the particulate products of drilling, or for other purposes.
- foam and its derivatives as used herein refers to both instances of entrained gas and gas bubbles that exist on the surface of a fluid.
- defoaming agents commonly are utilized, for example, as components in well treatment fluids, to prevent the formation of foam or to break a formed foam (i.e., reduce the amount of foam present in the fluid) (both are referred to collectively herein as “breaking” the foam) during the preparation and placement of the well treatment fluid in the subterranean formation.
- “Defoaming agents” are well fluid additives that may lower interfacial tension in a well fluid so that gas trapped in a foam will readily escape from the well fluid. Defoaming agents also may be used to treat a foam in a return fluid to facilitate disposal of the fluid. Additionally, defoaming agents often are included in cement compositions, inter alia, to ensure proper mixing and to provide adequate control over the density of the cement composition.
- defoaming agents are well known in the art. Dodecyl alcohol, aluminum stearate, various glycols, silicones and sulfonated hydrocarbons are examples of conventional defoamers. Many conventional defoamers have undesirable environmental characteristics and/or may be limited by strict environmental regulations in certain areas of the world. Moreover, many defoaming agents that comply with these strict environmental regulations may be relatively expensive and/or may suffer from other drawbacks, such as poorer defoaming performance.
- the present invention relates to subterranean operations, and more particularly, to environmentally compatible defoaming agents and methods of using such defoaming agents in subterranean well fluids.
- the invention provides a method comprising: providing a well fluid that comprises foam; providing a defoaming agent that comprises a lecithin and a solvent; and contacting the well fluid with the defoaming agent so that the amount of foam present in the well fluid is reduced.
- the present invention provides a method comprising: providing a return fluid that comprises foam; providing a defoaming agent that comprises a lecithin and a solvent; and contacting the return fluid with the defoaming agent so as to reduce the amount of foam present in the return fluid.
- the present invention provides a method of cementing comprising: providing a cement composition that comprises water, a hydraulic cement, and foam; providing a defoaming agent, the defoaming agent comprising a lecithin and a solvent; contacting the cement composition with the defoaming agent so as to reduce the amount of foam present in the cement composition; placing the cement composition in a portion of a subterranean formation; and allowing the cement composition to set therein.
- the present invention provides a method comprising: providing a return foamed cement composition that comprises foam; providing a defoaming agent that comprises a lecithin, a solvent, and hydrophobic particles; and contacting the return foamed cement composition with the defoaming agent so as to reduce the amount of foam present in the return foamed cement composition.
- the present invention provides a method comprising: introducing a well fluid comprising lecithin and a solvent into a well bore penetrating a subterranean formation.
- the present invention provides a method comprising: introducing into a well bore a well fluid comprising a solvent and lecithin; wherein the lecithin and the solvent in combination act to reduce foam present in the well bore or in the subterranean formation.
- the present invention provides a method comprising: introducing into a well bore a well fluid comprising a solvent and lecithin; wherein the treatment fluid reduces foam present in the well bore or in the subterranean formation.
- the present invention relates to subterranean operations, and more particularly, to environmentally compatible defoaming agents and methods of using such defoaming agents in subterranean well fluids.
- the defoaming agents of the present invention may be used in any applicable well fluid.
- the defoaming agents of the present invention may be used in conjunction with a cement composition.
- One of the many advantages of the defoaming agents of the present invention is that in many embodiments all of their components are environmentally acceptable according to the OSPAR Convention for the Protection of the Marine Environment in the North-East Atlantic Region regulations (2004-2005).
- the defoaming agents of the present invention comprise lecithin, a solvent, and, optionally, a plurality of hydrophobic particles.
- the lecithin:solvent ratio is about 1:100 to about a 100:1. This ratio may vary depending on pour point, cost, and other issues familiar to those skilled in the art. In more preferred embodiments, the ratio may be from about 1:2 to about 2:1.
- An example of a defoaming agent of the present invention comprises lecithin and butanol in a ratio of about 1:1 to about 2:1. A more preferred example comprises lecithin, 2-butanol, and calcium stearate.
- Lecithin is an oily base that will break a foam. More particularly, lecithin is a phospholipid. Lecithin is found in all living organisms. Lecithin is one of the major components in cell membranes, along with protein and cholesterol. Lecithin may be synthesized from choline. Lecithin is used as a stabilizer and emulsifier in foods. Lecithin is environmentally acceptable according to the OSPAR Convention for the Protection of the Marine Environment in the North-East Atlantic Region regulations (2004-2005). The lecithin used in the defoaming agents of the present invention may be natural or synthetic. In a preferred embodiment, the lecithin may be a CAS No. 8002-46-5 lecithin or a CAS No.
- lecithin may be chemically or enzymatically modified.
- lecithin includes natural, synthetic, and modified lecithins.
- KIRK-OTHMER ENCYCLOPEDIA OF CHEMICAL TECHNOLOGY 4th ed. Volume 15, pages 192-210, John Wiley & Sons, 1995.
- Lecithins Sources, Manufacture & Uses by Bernard F. Szuhaj, AMERICAN OIL CHEMISTS SOCIETY, 1985 and Lecithins, by Bernard F. Szuhaj and Gary R. List, AMERICAN OIL CHEMISTS SOCIETY, 1985.
- a solvent that is capable of reducing this viscosity is preferably included in the defoaming agents of the present invention.
- a preferred solvent also will act as a surface tension reducer in a well fluid, which should help collapse any foam structure present therein. Examples include, but are not limited to, glycol ethers, methanol, ethanol, propanol, isopropanol, hexanol, heptanol, butanol, glycols, esters of fatty acids, paraffins, ester oils, higher internal olefins, polypropylene glycol, silicon oils, surfactants, and base oils.
- the choice of which solvent to use will be guided by the location of the well, applicable environmental regulations, and any handling concerns.
- the solvent is also acceptable under the OSPAR Convention for the Protection of the Marine Environment in the North-East Atlantic Region regulations (2004-2005). Those that would meet these criteria would be C 1 to C 4 alcohols, glycols, and base oils.
- hydrophobic particles may be included in the defoaming agents of the present invention.
- Hydrophobic particles suitable for use in the defoaming agents of the present invention include, but are not limited to, graphite, fatty acid salts, salts of stearates, calcium stearate, aluminum stearate, hydrophobically-modified silica, and hydrophobically-modified clay.
- Commercially available examples of hydrophobic particles that may be suitable include, but are not limited to, those that are commercially available from Southern Clay under the trade names “CLAYTONE” and “CLOISITE.”
- Preferred hydrophobic particles are acceptable under the OSPAR Convention for the Protection of the Marine Environment in the North-East Atlantic Region regulations (2004-2005).
- hydrophobic particles examples include calcium stearate.
- a particularly advantageous synergistic effect may be achieved when using calcium stearate with lecithin.
- Another preferred example of hydrophobic particles is surface-treated sand.
- surface treated sand is not acceptable under the OSPAR Convention for the Protection of the Marine Environment in the North-East Atlantic Region regulations (2004-2005).
- the hydrophobic particles may be present in an amount in the range of from about 0.01% to about 100% by weight of the defoaming agent. In certain embodiments, the hydrophobic particles may be present in an amount in the range of from about 1% to about 20% by weight of the defoaming agent.
- the hydrophobic particles may have a size in the range of from about 0.1 to about 50 micrometers. In certain embodiments, the hydrophobic particles may have a size that may be smaller than about 0.1 micrometers, or that may be greater than about 50 micrometers.
- the defoaming agents of the present invention may be added to any well fluid wherein it is desirable to reduce the amount of foam that may be present therein.
- Suitable well fluids include, but are not limited to, drilling fluids, stimulation fluids, return fluids (which include, but are not limited to, return foamed cement compositions), completion fluids, and cementing compositions.
- the present invention provides a method of reducing foam generation in a well fluid, comprising adding a defoaming agent that comprises lecithin and a solvent to the well fluid.
- a defoaming agent of the present invention should be included in an amount of from about 0.01% to about 10% v/v. A preferred range is from about 0.1% to about 2% v/v.
- the present invention provides a method comprising: providing a well fluid that comprises foam; providing a defoaming agent that comprises lecithin and a solvent; contacting the well fluid with the defoaming agent so that the amount of foam present in the well fluid is reduced; and introducing the well fluid into a subterranean formation.
- the defoaming agent also comprises hydrophobic particles.
- the hydrophobic particles comprise calcium stearate.
- the well fluid may be introduced into the subterranean formation either before or after the well fluid is contacted with the defoaming agent.
- the well fluids in these embodiments may be any aqueous well fluid that comprises foam that may be introduced into a subterranean formation, e.g., a drilling fluid, a cement composition, a stimulation fluid, a completion fluid, or a return fluid.
- the defoaming agent may be added to the well fluid in any suitable manner including, but not limited to, by injection, mixing, or spraying.
- a defoaming agent of the present invention may be added to a return fluid that comprises foam to reduce the amount of foam present therein.
- the present invention provides a method comprising: providing a return fluid that comprises foam; providing a defoaming agent that comprises lecithin, and a solvent; and contacting the return fluid with the defoaming agent so that the amount of foam present in the return fluid is reduced.
- the return fluid can then be handled appropriately.
- the defoaming agent also comprises hydrophobic particles.
- the hydrophobic particles comprise calcium stearate.
- the defoaming agents of the present invention may be added to a cement composition to reduce the amount of any foam present therein.
- Cement compositions of the present invention generally comprise water, a hydraulic cement, and a defoaming agent of the present invention.
- the defoaming agent also comprises hydrophobic particles.
- the hydrophobic particles comprise calcium stearate.
- the defoaming agents of the present invention may be present in the cement compositions in an amount in the range of from about 0.001% to about 10% v/v.
- the defoaming agents of the present invention may be present in the cement compositions in an amount in the range of from about 0.01% to about 2% v/v.
- the water utilized in the cement compositions of the present invention may be fresh water, salt water (e.g., water containing one or more salts dissolved therein), brine (e.g., saturated salt water), or seawater.
- the water may be from any source provided that it does not contain an excess of compounds that may adversely affect other components in the cement composition. Further, the water may be present in an amount sufficient to form a pumpable slurry. In certain embodiments, the water may be present in the cement compositions of the present invention in an amount in the range of from about 10% to about 200% by weight of the cement (“bwoc”) therein.
- the water may be present in the cement compositions of the present invention in an amount in the range of from about 30% to about 90% bwoc therein. In certain embodiments, the water may be present in the cement compositions of the present invention in an amount in the range of from about 30% to about 50% bwoc therein.
- One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of water for a chosen application.
- the cement compositions of the present invention comprise a hydraulic cement.
- hydraulic cements may be suitable for use, including those comprising calcium, aluminum, silicon, oxygen, and/or sulfur, which may set and harden by reaction with water.
- hydraulic cements include, but are not limited to, Portland cements, pozzolanic cements, gypsum cements, soil cements, calcium phosphate cements, high alumina content cements, silica cements, high alkalinity cements, and mixtures thereof.
- the cement compositions of the present invention may comprise a lost circulation material.
- the lost circulation material may be any suitable material that minimizes the loss of fluid circulation into fractures and/or permeable zones of the formation.
- Lost circulation materials typically comprise a variety of materials, which may include, but are not limited to, asphaltenes, ground coal, cellulosic materials, plastic materials, and the like.
- the lost circulation materials may be provided in particulate form.
- additives may be added to the cement compositions of the present invention as deemed appropriate by one skilled in the art with the benefit of this disclosure.
- additives include, inter alia, fly ash, silica compounds, fluid loss control additives, dispersants, accelerators, retarders, salts, mica, sand, fibers, formation conditioning agents, fumed silica, bentonite, microspheres, weighting materials, and the like.
- suitable fluid loss control additives include those that are commercially available from Halliburton Energy Services, Inc., of Duncan, Okla., under the trade names LATEX 2000TM, HALAD®9, HALAD®200, HALAD®344, HALAD®413, and HALAD®600.
- suitable dispersants include those that are commercially available from Halliburton Energy Services, Inc., of Duncan, Okla., under the trade names CFR®2L and CFR®3L.
- An example of a suitable silica compound is a silica flour commercially available from Halliburton Energy Services, Inc., of Duncan, Okla., under the trade name SSA-1.
- An example of a suitable fly ash is an ASTM class F fly ash that is commercially available from Halliburton Energy Services of Dallas, Tex., under the trade name POZMIX®A.
- suitable retarders include those that are commercially available from Halliburton Energy Services, Inc., of Duncan, Okla., under the trade names SCR-500TM, HR®12, HR®6L, and HR®4L.
- the cement composition may be foamed, meaning that it may comprise foam that may be produced by any suitable method including the addition of an expanding additive or a gas to the cement composition.
- the present invention provides a method of cementing in a subterranean formation comprising: providing a cement composition that comprises water, a hydraulic cement, and foam; providing a defoaming agent, the defoaming agent comprising lecithin and a solvent; contacting the cement composition with the defoaming agent so as to reduce the amount of foam present in the cement composition; placing the cement composition in at least a portion of a subterranean formation; and allowing the cement composition to set therein.
- the defoaming agent also comprises hydrophobic particles.
- the hydrophobic particles comprise calcium stearate.
- the present invention provides a method of treating a return foamed cement composition (which is a foamed cement composition that has been sent downhole and then returned to the surface).
- a defoaming agent of the present invention may be added to the return foamed cement composition to reduce the amount of foam present therein.
- the defoaming agent also comprises hydrophobic particles.
- the hydrophobic particles comprise calcium stearate.
- the present invention provides a method of cementing in a subterranean formation, comprising: providing a cement composition that comprises water, hydraulic cement, and a defoaming agent, the defoaming agent comprising lecithin and a solvent; placing the cement composition in at least a portion of a subterranean formation; and permitting the cement composition to set therein.
- the present invention provides a method of treating a drilling fluid that comprises: providing a drilling fluid; pumping the drilling fluid into a well bore penetrating a subterranean formation; circulating the drilling fluid through the well bore and back to a drilling rig; allowing the drilling fluid to incorporate a foam; pumping the drilling fluid into a pit; providing a defoaming agent that comprises lecithin and a solvent; contacting the drilling fluid with the defoaming agent so as to reduce the amount of foam present in the drilling fluid; and repumping the drilling fluid into the well bore.
- the defoaming agent also comprises hydrophobic particles.
- the hydrophobic particles comprise calcium stearate.
- the defoaming agents of the present invention may be useful in tunneling applications as well as oilfield applications.
- Table 1 illustrates the mixtures of defoaming agentstested: TABLE 1 Mixture 1 Mixture 2 Mixture 3 Mixture 4 Lecithin 5 g (50% w) 10 g (66% w) 30 g (69.77%) 30 g (54.55%) 2- 5 g (50% w) 5 g(33% w) 10 g (23.26%) 10 (18.18%) butanol Calcium 0 0 3 g (6.98%) 15 g (27.27%) stearate
- defoaming agent Mixture 1 and defoaming agent Mixture 2 were tested in a foamed fluid.
- the fluids were made by adding 500 ml of tap water to a 1000 ml blender, mixing it at 4000 rpm, and then adding 1 ml of coco-amido propyl betaine as a foaming agent. Foam was allowed to rise in the blender to fill the blender. Defoaming agents Mixture 1 and Mixture 2 were then added (separately) to a foamed fluid in the blender.
- Conventional defoaming agents D-AIR3000TM and NF-6TM both available under these tradenames under Halliburton Energy Services in Duncan, Okla., were tested as controls.
- Table 2 illustrates the amounts of the defoaming agents added to each foamed fluid in the blender. TABLE 2 Test Defoamer ml 1 D-AIR3000L TM 0.3 2 NF-6 TM 1.0 3 Mixture 2 1.0 4 Mixture 2 2.0 5 Mixture 1 1.0
- the dry materials were weighed and then added to a blender. Mixture 2 defoaming agent was added to the mix water. The cement composition was then mixed to form a slurry. The slurry was then poured into a sample holder and let set in atmospheric water bath overnight. The densities of each of the set samples were taken to observe what effect the defoaming agents had on the density of the set cements. The most desired density is about 18.7 pounds per gallon. Table 5 illustrates the results.
- Table 5 illustrates that the addition of a defoaming agent of the present invention to a cement composition gives the cement composition a more desirable density.
- Slurry number 3 has a density closer to the desired density than Slurry 1 or 2. Also, the thickening time data indicates that there is not adverse effect as a result of the defoaming agent used. A synergistic effect may be seen between the lecithin and calcium stearate in Mixture 4.
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Abstract
Provided herein are defoaming agents that comprise lecithin and a solvent. Optionally, they may comprise hydrophobic particles. One embodiment provides a method comprising: providing a well fluid that comprises foam; providing a defoaming agent that comprises lecithin and a solvent; and contacting the well fluid with the defoaming agent so that the amount of foam present in the well fluid is reduced.
Description
- This application is a continuation of U.S. patent application Ser. No. 11/145,277 filed Jun. 3, 2005, entitled “Cement Compositions Comprising Enviornmentally Compatible Defoaming Agents and Methods of Use,” by Micheal J. Szymanski, et al., which is incorporated by reference herein, from which priority is claimed pursuant to 35 U.S.C. § 120.
- The present invention relates to subterranean operations, and more particularly, to environmentally compatible defoaming agents and methods of using such defoaming agents in subterranean well fluids.
- When drilling or completing wells in subterranean formations, various fluids may be used for a variety of reasons. These fluids are often aqueous. For the purposes herein, such a fluid will be referred to as a “well fluid.” Common uses for well fluids include, but are not limited to: lubrication and cooling of drill bit cutting surfaces while drilling generally or drilling-in (e.g., drilling in a targeted petroliferous formation); transportation of cuttings to the surface; controlling formation pressure to prevent blowouts; maintaining well stability; suspending solids in the well; fracturing the formation; cementing the well; displacing the fluid within the well with another fluid; cleaning the well; testing the well; and minimizing fluid loss into and stabilizing the formation through which the well is being drilled. Similar fluids also may be used in other applications such as tunnel drilling. Fluids used for such purposes are encompassed within the term “well fluid” as used herein.
- Where surfactants are included in a well fluid that does not include a classical surfactant foam, foaming is likely to occur. This foaming may be undesirable. On the other hand, surfactants may be added to generate desirable foam to assist in removing the particulate products of drilling, or for other purposes. The term “foam” and its derivatives as used herein refers to both instances of entrained gas and gas bubbles that exist on the surface of a fluid. Oftentimes, defoaming agents commonly are utilized, for example, as components in well treatment fluids, to prevent the formation of foam or to break a formed foam (i.e., reduce the amount of foam present in the fluid) (both are referred to collectively herein as “breaking” the foam) during the preparation and placement of the well treatment fluid in the subterranean formation. “Defoaming agents” are well fluid additives that may lower interfacial tension in a well fluid so that gas trapped in a foam will readily escape from the well fluid. Defoaming agents also may be used to treat a foam in a return fluid to facilitate disposal of the fluid. Additionally, defoaming agents often are included in cement compositions, inter alia, to ensure proper mixing and to provide adequate control over the density of the cement composition.
- A variety of defoaming agents are well known in the art. Dodecyl alcohol, aluminum stearate, various glycols, silicones and sulfonated hydrocarbons are examples of conventional defoamers. Many conventional defoamers have undesirable environmental characteristics and/or may be limited by strict environmental regulations in certain areas of the world. Moreover, many defoaming agents that comply with these strict environmental regulations may be relatively expensive and/or may suffer from other drawbacks, such as poorer defoaming performance.
- The present invention relates to subterranean operations, and more particularly, to environmentally compatible defoaming agents and methods of using such defoaming agents in subterranean well fluids.
- In one embodiment, the invention provides a method comprising: providing a well fluid that comprises foam; providing a defoaming agent that comprises a lecithin and a solvent; and contacting the well fluid with the defoaming agent so that the amount of foam present in the well fluid is reduced.
- In another embodiment, the present invention provides a method comprising: providing a return fluid that comprises foam; providing a defoaming agent that comprises a lecithin and a solvent; and contacting the return fluid with the defoaming agent so as to reduce the amount of foam present in the return fluid.
- In another embodiment, the present invention provides a method of cementing comprising: providing a cement composition that comprises water, a hydraulic cement, and foam; providing a defoaming agent, the defoaming agent comprising a lecithin and a solvent; contacting the cement composition with the defoaming agent so as to reduce the amount of foam present in the cement composition; placing the cement composition in a portion of a subterranean formation; and allowing the cement composition to set therein.
- In another embodiment, the present invention provides a method comprising: providing a return foamed cement composition that comprises foam; providing a defoaming agent that comprises a lecithin, a solvent, and hydrophobic particles; and contacting the return foamed cement composition with the defoaming agent so as to reduce the amount of foam present in the return foamed cement composition.
- In another embodiment, the present invention provides a method comprising: introducing a well fluid comprising lecithin and a solvent into a well bore penetrating a subterranean formation.
- In another embodiment, the present invention provides a method comprising: introducing into a well bore a well fluid comprising a solvent and lecithin; wherein the lecithin and the solvent in combination act to reduce foam present in the well bore or in the subterranean formation.
- In another embodiment, the present invention provides a method comprising: introducing into a well bore a well fluid comprising a solvent and lecithin; wherein the treatment fluid reduces foam present in the well bore or in the subterranean formation.
- The features and advantages of the present invention will be apparent to those skilled in the art. While numerous changes may be made by those skilled in the art, such changes are within the spirit of the invention.
- The present invention relates to subterranean operations, and more particularly, to environmentally compatible defoaming agents and methods of using such defoaming agents in subterranean well fluids. The defoaming agents of the present invention may be used in any applicable well fluid. In some preferred embodiments, the defoaming agents of the present invention may be used in conjunction with a cement composition. One of the many advantages of the defoaming agents of the present invention is that in many embodiments all of their components are environmentally acceptable according to the OSPAR Convention for the Protection of the Marine Environment in the North-East Atlantic Region regulations (2004-2005).
- The defoaming agents of the present invention comprise lecithin, a solvent, and, optionally, a plurality of hydrophobic particles. In some embodiments, the lecithin:solvent ratio is about 1:100 to about a 100:1. This ratio may vary depending on pour point, cost, and other issues familiar to those skilled in the art. In more preferred embodiments, the ratio may be from about 1:2 to about 2:1. An example of a defoaming agent of the present invention comprises lecithin and butanol in a ratio of about 1:1 to about 2:1. A more preferred example comprises lecithin, 2-butanol, and calcium stearate.
- Lecithin is an oily base that will break a foam. More particularly, lecithin is a phospholipid. Lecithin is found in all living organisms. Lecithin is one of the major components in cell membranes, along with protein and cholesterol. Lecithin may be synthesized from choline. Lecithin is used as a stabilizer and emulsifier in foods. Lecithin is environmentally acceptable according to the OSPAR Convention for the Protection of the Marine Environment in the North-East Atlantic Region regulations (2004-2005). The lecithin used in the defoaming agents of the present invention may be natural or synthetic. In a preferred embodiment, the lecithin may be a CAS No. 8002-46-5 lecithin or a CAS No. 8030-76-0 soya lecithin. In another embodiment, the lecithin may be chemically or enzymatically modified. One should note that some modified lecithins may have different environmental considerations than others. The term “lecithin” as used herein includes natural, synthetic, and modified lecithins. For more information on lecithin and its many variants, please see the KIRK-OTHMER ENCYCLOPEDIA OF CHEMICAL TECHNOLOGY, 4th ed. Volume 15, pages 192-210, John Wiley & Sons, 1995. Lecithins Sources, Manufacture & Uses, by Bernard F. Szuhaj, AMERICAN OIL CHEMISTS SOCIETY, 1985 and Lecithins, by Bernard F. Szuhaj and Gary R. List, AMERICAN OIL CHEMISTS SOCIETY, 1985.
- Because of lecithin's inherent viscosity (e.g., thick like honey), a solvent that is capable of reducing this viscosity is preferably included in the defoaming agents of the present invention. A preferred solvent also will act as a surface tension reducer in a well fluid, which should help collapse any foam structure present therein. Examples include, but are not limited to, glycol ethers, methanol, ethanol, propanol, isopropanol, hexanol, heptanol, butanol, glycols, esters of fatty acids, paraffins, ester oils, higher internal olefins, polypropylene glycol, silicon oils, surfactants, and base oils. The choice of which solvent to use will be guided by the location of the well, applicable environmental regulations, and any handling concerns. In preferred embodiments, the solvent is also acceptable under the OSPAR Convention for the Protection of the Marine Environment in the North-East Atlantic Region regulations (2004-2005). Those that would meet these criteria would be C1 to C4 alcohols, glycols, and base oils.
- Optionally, hydrophobic particles may be included in the defoaming agents of the present invention. Hydrophobic particles suitable for use in the defoaming agents of the present invention include, but are not limited to, graphite, fatty acid salts, salts of stearates, calcium stearate, aluminum stearate, hydrophobically-modified silica, and hydrophobically-modified clay. Commercially available examples of hydrophobic particles that may be suitable include, but are not limited to, those that are commercially available from Southern Clay under the trade names “CLAYTONE” and “CLOISITE.” Preferred hydrophobic particles are acceptable under the OSPAR Convention for the Protection of the Marine Environment in the North-East Atlantic Region regulations (2004-2005). Examples of preferred hydrophobic particles include calcium stearate. One should note that a particularly advantageous synergistic effect may be achieved when using calcium stearate with lecithin. Another preferred example of hydrophobic particles is surface-treated sand. One should note, however, that surface treated sand is not acceptable under the OSPAR Convention for the Protection of the Marine Environment in the North-East Atlantic Region regulations (2004-2005). Where included in the defoaming agents of the present invention, the hydrophobic particles may be present in an amount in the range of from about 0.01% to about 100% by weight of the defoaming agent. In certain embodiments, the hydrophobic particles may be present in an amount in the range of from about 1% to about 20% by weight of the defoaming agent. In certain embodiments, the hydrophobic particles may have a size in the range of from about 0.1 to about 50 micrometers. In certain embodiments, the hydrophobic particles may have a size that may be smaller than about 0.1 micrometers, or that may be greater than about 50 micrometers.
- The defoaming agents of the present invention may be added to any well fluid wherein it is desirable to reduce the amount of foam that may be present therein. Suitable well fluids include, but are not limited to, drilling fluids, stimulation fluids, return fluids (which include, but are not limited to, return foamed cement compositions), completion fluids, and cementing compositions. In one embodiment, the present invention provides a method of reducing foam generation in a well fluid, comprising adding a defoaming agent that comprises lecithin and a solvent to the well fluid. Generally, a defoaming agent of the present invention should be included in an amount of from about 0.01% to about 10% v/v. A preferred range is from about 0.1% to about 2% v/v.
- In one embodiment, the present invention provides a method comprising: providing a well fluid that comprises foam; providing a defoaming agent that comprises lecithin and a solvent; contacting the well fluid with the defoaming agent so that the amount of foam present in the well fluid is reduced; and introducing the well fluid into a subterranean formation. In a preferred embodiment, the defoaming agent also comprises hydrophobic particles. In an even more preferred embodiment, the hydrophobic particles comprise calcium stearate.
- Depending on the particular application, the well fluid may be introduced into the subterranean formation either before or after the well fluid is contacted with the defoaming agent. The well fluids in these embodiments may be any aqueous well fluid that comprises foam that may be introduced into a subterranean formation, e.g., a drilling fluid, a cement composition, a stimulation fluid, a completion fluid, or a return fluid. The defoaming agent may be added to the well fluid in any suitable manner including, but not limited to, by injection, mixing, or spraying.
- In a return fluid embodiment, a defoaming agent of the present invention may be added to a return fluid that comprises foam to reduce the amount of foam present therein. In an example of such a method, the present invention provides a method comprising: providing a return fluid that comprises foam; providing a defoaming agent that comprises lecithin, and a solvent; and contacting the return fluid with the defoaming agent so that the amount of foam present in the return fluid is reduced. The return fluid can then be handled appropriately. In a preferred embodiment, the defoaming agent also comprises hydrophobic particles. In an even more preferred embodiment, the hydrophobic particles comprise calcium stearate.
- In examples of specific cementing-related embodiments, the defoaming agents of the present invention may be added to a cement composition to reduce the amount of any foam present therein. Cement compositions of the present invention generally comprise water, a hydraulic cement, and a defoaming agent of the present invention. In a preferred embodiment, the defoaming agent also comprises hydrophobic particles. In an even more preferred embodiment, the hydrophobic particles comprise calcium stearate. In certain embodiments, the defoaming agents of the present invention may be present in the cement compositions in an amount in the range of from about 0.001% to about 10% v/v. In certain embodiments, the defoaming agents of the present invention may be present in the cement compositions in an amount in the range of from about 0.01% to about 2% v/v.
- The water utilized in the cement compositions of the present invention may be fresh water, salt water (e.g., water containing one or more salts dissolved therein), brine (e.g., saturated salt water), or seawater. Generally, the water may be from any source provided that it does not contain an excess of compounds that may adversely affect other components in the cement composition. Further, the water may be present in an amount sufficient to form a pumpable slurry. In certain embodiments, the water may be present in the cement compositions of the present invention in an amount in the range of from about 10% to about 200% by weight of the cement (“bwoc”) therein. In certain embodiments, the water may be present in the cement compositions of the present invention in an amount in the range of from about 30% to about 90% bwoc therein. In certain embodiments, the water may be present in the cement compositions of the present invention in an amount in the range of from about 30% to about 50% bwoc therein. One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of water for a chosen application.
- Any cement suitable for use in subterranean applications may be suitable for use in the present invention. In certain embodiments, the cement compositions of the present invention comprise a hydraulic cement. A variety of hydraulic cements may be suitable for use, including those comprising calcium, aluminum, silicon, oxygen, and/or sulfur, which may set and harden by reaction with water. Such hydraulic cements include, but are not limited to, Portland cements, pozzolanic cements, gypsum cements, soil cements, calcium phosphate cements, high alumina content cements, silica cements, high alkalinity cements, and mixtures thereof.
- Optionally, the cement compositions of the present invention may comprise a lost circulation material. The lost circulation material may be any suitable material that minimizes the loss of fluid circulation into fractures and/or permeable zones of the formation. Lost circulation materials typically comprise a variety of materials, which may include, but are not limited to, asphaltenes, ground coal, cellulosic materials, plastic materials, and the like. The lost circulation materials may be provided in particulate form. One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of lost circulation material for a chosen application.
- Optionally, other additional additives may be added to the cement compositions of the present invention as deemed appropriate by one skilled in the art with the benefit of this disclosure. Examples of such additives include, inter alia, fly ash, silica compounds, fluid loss control additives, dispersants, accelerators, retarders, salts, mica, sand, fibers, formation conditioning agents, fumed silica, bentonite, microspheres, weighting materials, and the like. Examples of suitable fluid loss control additives include those that are commercially available from Halliburton Energy Services, Inc., of Duncan, Okla., under the trade names LATEX 2000™, HALAD®9, HALAD®200, HALAD®344, HALAD®413, and HALAD®600. Examples of suitable dispersants include those that are commercially available from Halliburton Energy Services, Inc., of Duncan, Okla., under the trade names CFR®2L and CFR®3L. An example of a suitable silica compound is a silica flour commercially available from Halliburton Energy Services, Inc., of Duncan, Okla., under the trade name SSA-1. An example of a suitable fly ash is an ASTM class F fly ash that is commercially available from Halliburton Energy Services of Dallas, Tex., under the trade name POZMIX®A. Examples of suitable retarders include those that are commercially available from Halliburton Energy Services, Inc., of Duncan, Okla., under the trade names SCR-500™, HR®12, HR®6L, and HR®4L.
- In some embodiments, the cement composition may be foamed, meaning that it may comprise foam that may be produced by any suitable method including the addition of an expanding additive or a gas to the cement composition.
- In one embodiment, the present invention provides a method of cementing in a subterranean formation comprising: providing a cement composition that comprises water, a hydraulic cement, and foam; providing a defoaming agent, the defoaming agent comprising lecithin and a solvent; contacting the cement composition with the defoaming agent so as to reduce the amount of foam present in the cement composition; placing the cement composition in at least a portion of a subterranean formation; and allowing the cement composition to set therein. In a preferred embodiment, the defoaming agent also comprises hydrophobic particles. In an even more preferred embodiment, the hydrophobic particles comprise calcium stearate.
- In another embodiment, the present invention provides a method of treating a return foamed cement composition (which is a foamed cement composition that has been sent downhole and then returned to the surface). In an example of such a method, a defoaming agent of the present invention may be added to the return foamed cement composition to reduce the amount of foam present therein. In a preferred embodiment, the defoaming agent also comprises hydrophobic particles. In an even more preferred embodiment, the hydrophobic particles comprise calcium stearate.
- In another embodiment, the present invention provides a method of cementing in a subterranean formation, comprising: providing a cement composition that comprises water, hydraulic cement, and a defoaming agent, the defoaming agent comprising lecithin and a solvent; placing the cement composition in at least a portion of a subterranean formation; and permitting the cement composition to set therein.
- In another embodiment, the present invention provides a method of treating a drilling fluid that comprises: providing a drilling fluid; pumping the drilling fluid into a well bore penetrating a subterranean formation; circulating the drilling fluid through the well bore and back to a drilling rig; allowing the drilling fluid to incorporate a foam; pumping the drilling fluid into a pit; providing a defoaming agent that comprises lecithin and a solvent; contacting the drilling fluid with the defoaming agent so as to reduce the amount of foam present in the drilling fluid; and repumping the drilling fluid into the well bore. In a preferred embodiment, the defoaming agent also comprises hydrophobic particles. In an even more preferred embodiment, the hydrophobic particles comprise calcium stearate.
- The defoaming agents of the present invention may be useful in tunneling applications as well as oilfield applications.
- To facilitate a better understanding of the present invention, the following examples of certain aspects of some embodiments are given. In no way should the following examples be read to limit, or define, the scope of the invention.
- Table 1 illustrates the mixtures of defoaming agentstested:
TABLE 1 Mixture 1 Mixture 2 Mixture 3 Mixture 4 Lecithin 5 g (50% w) 10 g (66% w) 30 g (69.77%) 30 g (54.55%) 2- 5 g (50% w) 5 g(33% w) 10 g (23.26%) 10 (18.18%) butanol Calcium 0 0 3 g (6.98%) 15 g (27.27%) stearate - Both defoaming agent Mixture 1 and defoaming agent Mixture 2 were tested in a foamed fluid. The fluids were made by adding 500 ml of tap water to a 1000 ml blender, mixing it at 4000 rpm, and then adding 1 ml of coco-amido propyl betaine as a foaming agent. Foam was allowed to rise in the blender to fill the blender. Defoaming agents Mixture 1 and Mixture 2 were then added (separately) to a foamed fluid in the blender. Conventional defoaming agents D-AIR3000™ and NF-6™, both available under these tradenames under Halliburton Energy Services in Duncan, Okla., were tested as controls. Table 2 illustrates the amounts of the defoaming agents added to each foamed fluid in the blender.
TABLE 2 Test Defoamer ml 1 D-AIR3000L ™ 0.3 2 NF-6 ™ 1.0 3 Mixture 2 1.0 4 Mixture 2 2.0 5 Mixture 1 1.0 - Table 3 lists the results that were observed.
TABLE 3 Observations Regarding Some Defoaming Residual Foam Agent Speed of Present in the Test No. Used Mixing Blender 1 D-AIR3000 ™ Fast No 2 NF-6 ™ Moderate Yes 3 Mixture 2 Moderate Yes 4 Mixture 2 Moderate Yes 5 Mixture 1 Moderate Yes - To illustrate the effects of a defoaming agent of the present invention in a cement composition, Mixture 2 (from Table 1) was tested in cement compositions. Table 4 illustrates the components of the cement compositions:
TABLE 4 Cement Cement Composition 1 Composition 2 Component (g) (g) Water 244.3 244.3 Class H Cement 500 500 SSA-2 Sand 175 175 HiDense #3 (available 244 244 from Halliburton Energy Services) Halad-9 (available 3 3 from Halliburton Energy Services) NaCl 90.4 90.4 Mixture 2 (Defoaming 11.2 0.0 Agent) - The dry materials were weighed and then added to a blender. Mixture 2 defoaming agent was added to the mix water. The cement composition was then mixed to form a slurry. The slurry was then poured into a sample holder and let set in atmospheric water bath overnight. The densities of each of the set samples were taken to observe what effect the defoaming agents had on the density of the set cements. The most desired density is about 18.7 pounds per gallon. Table 5 illustrates the results.
TABLE 5 Theoretical Slurry 1 Slurry 2 Density Sample Density Density Desired Top 18.3 lb/gal 16.8 lb/gal 18.7 lb/gal Middle 19.0 lb/gal 17.4 lb/gal 18.7 lb/gal Bottom 19.4 lb/gal 17.7 lb/gal 18.7 lb/gal - Table 5 illustrates that the addition of a defoaming agent of the present invention to a cement composition gives the cement composition a more desirable density.
- Defoaming agent Mixtures 3 and 4 were added to a cement slurry. Table 6 lists the components of the cement slurry:
TABLE 6 Slurry 1 Slurry 2 Slurry 3 Component Water (liter/sack) 27.55 27.55 27.55 Class G Cement 100 100 100 (kg/sack) Latex 2000 ™ 20 20 20 (available from Halliburton Energy Services) (liter/sack) Stabilizer 434C ™ 2.5 2.5 2.5 (available from Halliburton Energy Services) (liter/sack) CFR-3L ™ 2 2 2 Dispersant (available from Halliburton Energy Services) (liter/sack) HR-4L ™ Retarder 0.5 0.5 0.5 (available from Halliburton Energy Services) (liter/sack) NF-6 ™ Defoaming 0.2 0 0 Agent (available from Halliburton Energy Services) (liter/sack) Defoaming Agent 0 0.2 0 Mixture 3 (liter/sack) Defoaming Agent 0 0 0.2 Mixture 4 (liter/sack) Data Theoretical Density 11.36 11.87 12.65 of 14.99 (lb/gal) Thickening Time 1.42 1.41 1.42 (hr:min) - Slurry number 3 has a density closer to the desired density than Slurry 1 or 2. Also, the thickening time data indicates that there is not adverse effect as a result of the defoaming agent used. A synergistic effect may be seen between the lecithin and calcium stearate in Mixture 4.
- Another experiment was run to observe the comparative effects of Mixture 2, lecithin only, and calcium stearate only in a cement composition. The stearate was mixed with enough butanol to make it fluid. Table 7 lists the components of the cement compositions and the density results.
TABLE 7 Slurry 1 Slurry 2 Slurry 3 Slurry 4 Slurry 5 Component Water 27.55 27.55 27.55 27.55 27.55 (liter/sack) Class G Cement 100 100 100 100 100 (kg/sack) Latex 2000 ™ 20 20 20 20 20 (available from Halliburton Energy Services) (liter/sack) Stabilizer 2.5 2.5 2.5 2.5 2.5 434C ™ (available from Halliburton Energy Services) (liter/sack) CFR-3L ™ 2 2 2 2 2 Dispersant (available from Halliburton Energy Services) (liter/sack) HR-4L ™ 0.5 0.5 0.5 0.5 0.5 Retarder (available from Halliburton Energy Services) (liter/sack) Lecithin (grams) 2.0 3.0 3.0 0 0 Calcium stearate 0 0 0 2.0 3.0 with butanol (grams) Mixture 2 from 0 0 2.0 0 0 Table 1 (grams) Data Specific Gravity 1.31 1.56 1.58 0.78 1.16 - As can be seen in Table 7, as far as specific gravity of a cement composition, the combination of lecithin and calcium stearate appears to be desirable over either lecithin or calcium stearate alone.
- Therefore, the present invention is well adapted to attain the ends and advantages mentioned as well as those that are inherent therein. While numerous changes may be made by those skilled in the art, such changes are encompassed within the spirit of this invention as defined by the appended claims. The terms in the claims have their plain, ordinary meaning unless otherwise explicitly and clearly defined by the patentee.
Claims (25)
1. A method comprising:
introducing an agent comprising lecithin and a solvent into a well bore penetrating a subterranean formation.
2. The method of claim 1 wherein the solvent is selected from the group consisting of: a C1 to C4 alcohol; a glycol; and a base oil.
3. The method of claim 1 wherein the solvent is an alkanol.
4. The method of claim 1 wherein the solvent comprises a solvent selected from the group consisting of: a glycol ether; an ester of a fatty acid; a paraffin; an ester oil; a higher internal olefin; a silicon oil; and a surfactant.
5. The method of claim 1 wherein the agent has a lecithin to solvent ratio of from about 1:100 to about 100:1.
6. The method of claim 1 wherein the agent comprises hydrophobic particles.
7. The method of claim 1 wherein the solvent comprises butanol.
8. The method of claim 1 wherein the agent comprises water.
9. The method of claim 1 wherein the agent is used in a drilling fluid, a stimulation fluid, a completion fluid, or a cement composition.
10. A method comprising:
introducing an agent into a subterranean formation, wherein the fluid comprises lecithin and a solvent that is selected from the group consisting of: a C1 to C4 alcohol; a glycol; and a base oil.
11. The method of claim 10 wherein the agent comprises hydrophobic particles.
12. The method of claim 10 wherein the subterranean formation is a hydrocarbon-bearing formation.
13. The method of claim 10 further comprising the step of stimulating production of the hydrocarbon bearing formation.
14. The method of claim 10 wherein the agent has a lecithin to solvent ratio of from about 1:100 to about 100:1.
15. The method of claim 10 further comprising the step of performing cementing operations.
16. The method of claim 10 wherein the agent is introduced into the subterranean formation during cleaning operations.
17. The method of claim 10 wherein the agent is introduced into the subterranean formation in a manner selected from the group consisting of: injection, mixing, and spraying.
18. The method of claim 10 wherein the agent is sprayed directly onto a foamed surface.
19. A method comprising:
introducing into a well bore an agent comprising a solvent and lecithin; wherein the agent reduces foam present in the well bore or in the subterranean formation.
20. The method of claim 19 wherein the agent comprises hydrophobic particles.
21. The method of claim 19 wherein the solvent is selected from the group consisting of: a C1 to C4 alcohol; a glycol; a base oil; a glycol ether; an ester of a fatty acid; a paraffin; an ester oil; a higher internal olefin; a silicon oil; and a surfactant.
22. The method of claim 19 wherein the solvent is an alkanol.
23. The method of claim 22 wherein the solvent comprises at least one alkanol selected from the group consisting of: methanol, ethanol, propanol, isopropanol, a butanol, monoethylene glycol, and any combination thereof.
24. The method of claim 19 wherein the agent has a ratio of lecithin to solvent is from about 1:100 to about 100:1.
25. The method of claim 19 wherein the solvent is a butanol.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11/860,308 US20080023199A1 (en) | 2005-06-03 | 2007-09-24 | Cement Compositions Comprising Environmentally Compatible Defoaming Agents and Methods of Use |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11/145,277 US7273103B2 (en) | 2005-06-03 | 2005-06-03 | Cement compositions comprising environmentally compatible defoaming agents and methods of use |
| US11/860,308 US20080023199A1 (en) | 2005-06-03 | 2007-09-24 | Cement Compositions Comprising Environmentally Compatible Defoaming Agents and Methods of Use |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US11/145,277 Continuation US7273103B2 (en) | 2005-06-03 | 2005-06-03 | Cement compositions comprising environmentally compatible defoaming agents and methods of use |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20080023199A1 true US20080023199A1 (en) | 2008-01-31 |
Family
ID=36642795
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US11/145,277 Expired - Lifetime US7273103B2 (en) | 2005-06-03 | 2005-06-03 | Cement compositions comprising environmentally compatible defoaming agents and methods of use |
| US11/860,308 Abandoned US20080023199A1 (en) | 2005-06-03 | 2007-09-24 | Cement Compositions Comprising Environmentally Compatible Defoaming Agents and Methods of Use |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US11/145,277 Expired - Lifetime US7273103B2 (en) | 2005-06-03 | 2005-06-03 | Cement compositions comprising environmentally compatible defoaming agents and methods of use |
Country Status (6)
| Country | Link |
|---|---|
| US (2) | US7273103B2 (en) |
| EP (1) | EP1888477A1 (en) |
| BR (1) | BRPI0611066A2 (en) |
| CA (1) | CA2611136A1 (en) |
| NO (1) | NO20074006L (en) |
| WO (1) | WO2006129122A1 (en) |
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| US20060272550A1 (en) * | 2005-06-03 | 2006-12-07 | Szymanski Michael J | Cement composition comprising environmentally compatible defoaming agents and methods of use |
| CN103074041A (en) * | 2012-09-28 | 2013-05-01 | 四川仁智油田技术服务股份有限公司 | Defoaming agent for water-based drilling fluid and preparation method thereof |
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Also Published As
| Publication number | Publication date |
|---|---|
| EP1888477A1 (en) | 2008-02-20 |
| US7273103B2 (en) | 2007-09-25 |
| US20060272820A1 (en) | 2006-12-07 |
| NO20074006L (en) | 2008-02-29 |
| CA2611136A1 (en) | 2006-12-07 |
| WO2006129122A1 (en) | 2006-12-07 |
| BRPI0611066A2 (en) | 2017-10-03 |
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