Cement compositions with improved fluid loss characteristics and methods of cementing using such cement compositions

Information

  • Patent Grant
  • 7216707
  • Patent Number
    7,216,707
  • Date Filed
    Monday, June 21, 2004
    20 years ago
  • Date Issued
    Tuesday, May 15, 2007
    17 years ago
Abstract
The present invention provides a method of cementing in a subterranean formation that includes providing a cement composition that includes water, cement, and a fluid loss control additive that includes a water-soluble hydrophobically modified polymer or a hydrophilically modified water-soluble polymer; placing the cement composition into the subterranean formation; and allowing the cement composition to set therein. In certain embodiments, the water-soluble hydrophobically modified polymer or the hydrophilically modified water-soluble polymer may include a polymer backbone that comprises polar heteroatoms. In another embodiment, the water-soluble hydrophobically modified polymer may be a reaction product of a hydrophobic compound with a polyvinylamine, a poly(vinylamine/vinyl alcohol), or an alkyl acrylate polymer.
Description
BACKGROUND OF THE INVENTION

The present invention relates to cementing operations. More particularly, the present invention relates to cement compositions comprising improved fluid loss control additives, and methods of using such cement compositions.


Hydraulic cement compositions are commonly utilized in subterranean operations, particularly subterranean well completion and remedial operations. For example, hydraulic cement compositions are used in primary cementing operations whereby pipe strings such as casings and liners are cemented in well bores. In performing primary cementing, hydraulic cement compositions are pumped into the annular space between the walls of a well bore and the exterior surface of the pipe string disposed therein. The cement composition is permitted to set in the annular space, thereby forming an annular sheath of hardened substantially impermeable cement therein that substantially supports and positions the pipe string in the well bore and bonds the exterior surface of the pipe string to the walls of the well bore. Hydraulic cement compositions also are used in remedial cementing operations such as plugging highly permeable zones or fractures in well bores, plugging cracks and holes in pipe strings, and the like.


In some cases, subterranean formations may be unable to withstand the hydrostatic head pressure normally associated with fluids (e.g., cement compositions and the like) being injected into the formation. In such cases, the hydrostatic pressure may be sufficient to force such fluids into the permeable zones of the formation, which may result in a significant loss of fluid into the formation. This fluid loss into the formation is problematic for a number of reasons. For example, where the fluid loss occurs during a cementing operation, excessive fluid loss may cause a cement composition to be prematurely dehydrated, which may limit the amount of the cement composition that can be pumped and decrease the compressive strength of the cement composition. Excessive fluid loss into the formation also may prevent or reduce bond strength between the set cement composition and the subterranean zone, the walls of pipe, and/or the walls of the well bore.


In order to counteract these problems, fluid loss control additives may be added to cement compositions to reduce the loss of fluid from the cement compositions when they contact permeable zones of the subterranean formation. Fluid loss control additives also may be suitable for cement compositions used in surface cementing operations. Conventional synthetic fluid loss control additives may be high molecular weight, water-soluble polymers, such as copolymers and copolymer salts of N,N-dimethylacrylamide and 2-acrylamido-2-methylpropane sulfonic acid. While these conventional fluid loss control additives have been used with some success, there is a continuing need for improved fluid loss control additives that achieve fluid loss control in well cement compositions.


SUMMARY OF THE INVENTION

The present invention relates to cementing operations. More particularly, the present invention relates to cement compositions comprising improved fluid loss control additives, and methods of using such cement compositions.


In one embodiment, the present invention provides a method of cementing in a subterranean formation comprising: providing a cement composition that comprises water, cement, and a fluid loss control additive that comprises a water-soluble hydrophobically modified polymer that comprises a polymer backbone comprising polar heteroatoms; placing the cement composition into the subterranean formation; and allowing the cement composition to set therein.


In another embodiment, the present invention provides a method of cementing in a subterranean formation comprising: providing a cement composition that comprises water, cement, and a fluid loss control additive that comprises a water-soluble hydrophobically modified polymer that is a reaction product of a hydrophobic compound with a polyvinylamine, a poly(vinylamine/vinyl alcohol), or an alkyl acrylate polymer; placing the cement composition into the subterranean formation; and allowing the cement composition to set therein.


In another embodiment, the present invention provides a method of cementing in a subterranean formation comprising: providing a cement composition that comprises water, cement, and a fluid loss control additive that comprises a hydrophilically modified water-soluble polymer; placing the cement composition into the subterranean formation; and allowing the cement composition to set therein.


In another embodiment, the present invention provides a cement composition that comprises water, cement, and a fluid loss control additive that comprises a water-soluble hydrophobically modified polymer that comprises a polymer backbone comprising polar heteroatoms.


In another embodiment, the present invention provides a cement composition that comprises water, cement, and a fluid loss control additive comprising a water-soluble hydrophobically modified polymer that is a reaction product of a hydrophobic compound with a polyvinylamine, a poly(vinylamine/vinyl alcohol), or an alkyl acrylate polymer.


In yet another embodiment, the present invention provides a cement composition that comprises water, cement, and a fluid loss control additive that comprises a hydrophilically modified water-soluble polymer.


The features and advantages of the present invention will be readily apparent to those skilled in the art upon a reading of the description of the exemplary embodiments which follows







DESCRIPTION OF EXEMPLARY EMBODIMENTS

The present invention relates to cementing operations. More particularly, the present invention relates to cement compositions comprising improved fluid loss control additives, and methods of using such cement compositions. While the compositions and methods of the present invention are useful in a variety of applications, they are particularly useful for subterranean well completion and remedial operations, such as primary cementing, e.g., cementing casings and liners in well bores, including those in production wells, which include multi-lateral subterranean wells. They are also useful for surface cementing operations, such as construction cementing.


The cement compositions of the present invention generally comprise water, cement, and a fluid loss control additive of the present invention. A wide variety of other additives optionally may be included in the cement compositions of the present invention if desired. Generally, the cement compositions of the present invention may have a density in the range of from about 5 lb/gallon to about 30 lb/gallon. The cement compositions of the present invention may be foamed or unfoamed or may comprise other means to reduce their densities. One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate density of the cement composition for a chosen application.


The water utilized in the cement compositions of the present invention can 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 can be from any source provided that it does not contain an excess of compounds, e.g., dissolved organics, that may adversely affect other components in the cement composition. Further, water may be present in an amount sufficient to make the cement composition a pumpable slurry. In certain exemplary embodiments, water is present in the cement compositions in an amount in the range of from about 30% to about 200% by weight of the cement (“bwoc”) therein. One of ordinary skill in the art with the benefit of this disclosure will recognize the appropriate amount of water to use for a chosen application.


Any cement suitable for use in subterranean applications is suitable for use in the present invention. In one embodiment, the cement compositions of the present invention comprise hydraulic cement. A variety of hydraulic cements are suitable for use, including those comprised of calcium, aluminum, silicon, oxygen, and/or sulfur, which 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.


Generally, the fluid loss control additives of the present invention comprise water-soluble hydrophobically modified polymers or hydrophilically modified water-soluble polymers. As used herein, “hydrophobically modified” refers to the incorporation into the hydrophilic polymer structure of hydrophobic groups, wherein the alkyl chain length is from about 4 to about 22 carbons. As used herein, “hydrophilically modified” refers to the incorporation into the hydrophilic polymer structure of hydrophilic groups. As used herein, “water-soluble” refers to at least 0.01 weight percent soluble in distilled water. Among other things, the fluid loss control additives of the present invention may act to reduce the fluid loss from the cement compositions therein.


The water-soluble hydrophobically modified polymers of the fluid loss control additives of the present invention typically have a molecular weight in the range of from about 100,000 to about 10,000,000. In an exemplary embodiment, the water-soluble hydrophobically modified polymers may comprise a polymer backbone that comprises polar heteroatoms. Generally, the polar heteroatoms present within the polymer backbone of the water-soluble hydrophobically modified polymers include, but are not limited to, oxygen, nitrogen, sulfur, or phosphorous.


In certain embodiments of the present invention, the water-soluble hydrophobically modified polymers may be a reaction product of a hydrophilic polymer and a hydrophobic compound. The hydrophilic polymers suitable for forming the water-soluble hydrophobically modified polymers used in the present invention should be capable of reacting with hydrophobic compounds. Suitable hydrophilic polymers include, homo-, co-, or terpolymers such as, but not limited to, polyvinylamines, poly(vinylamines/vinyl alcohols), and alkyl acrylate polymers in general. Additional examples of alkyl acrylate polymers include, but are not limited to, polydimethylaminoethyl methacrylate, polydimethylaminopropyl methacrylamide, poly(acrylamide/dimethylaminoethyl methacrylate), poly(methacrylic acid/dimethylaminoethyl methacrylate), poly(acrylamide/dimethylaminopropyl methacrylamide), poly(2-acrylamido-2-methyl propane sulfonic acid/dimethylaminoethyl methacrylate), poly (acrylic acid/dimethylaminopropyl methacrylamide), and poly(methacrylic acid/dimethylaminopropyl methacrylamide). In certain embodiments, the hydrophilic polymers contain reactive amino groups in the polymer backbone or as pendant groups, which are capable of reacting with hydrophobic compounds. In an exemplary embodiment, the hydrophilic polymers comprise dialkyl amino pendant groups. In an exemplary embodiment, the hydrophilic polymers comprise a dimethyl amino pendant group and at least one monomer comprising dimethylaminoethyl methacrylate or dimethylaminopropyl methacrylamide. In certain exemplary embodiments of the present invention, the hydrophilic polymers comprise a polymer backbone that comprises polar heteroatoms, wherein the polar heteroatoms present within the polymer backbone of the hydrophilic polymers include, but are not limited to, oxygen, nitrogen, sulfur, or phosphorous. Suitable hydrophilic polymers comprising polar heteroatoms within the polymer backbone include homo-, co-, or terpolymers, such as, but not limited to, celluloses, polyamides, polyetheramines, polyethyleneimines, polyhydroxyetheramines, polylysines, polysulfones, gums, and starches. In an exemplary embodiment, the starch is a cationic starch. A suitable cationic starch may be formed by reacting a starch, such as corn, maize, waxy maize, potato, tapioca, and the like, with the reaction product of epichlorohydrin and trialkylamine.


The hydrophobic compounds that are capable of reacting with the hydrophilic polymers of the present invention include, but are not limited to, alkyl halides, sulfonates, sulfates, and organic acid derivatives. Examples of suitable organic acid derivatives include, but are not limited to, octenyl succinic acid; dodecenyl succinic acid; and anhydrides, esters, and amides of octenyl succinic acid or dodecenyl succinic acid. In certain exemplary embodiments, the hydrophobic compounds may have an alkyl chain length of from about 4 to about 22 carbons. For example, where the hydrophobic compound is an alkyl halide, the reaction between the hydrophobic compound and hydrophilic polymer may result in the quaternization of at least some of the hydrophilic polymer amino groups with an alkyl halide, wherein the alkyl chain length is from about 4 to about 22 carbons.


In another embodiment of the present invention, the fluid loss control additives of the present invention comprise a hydrophilically modified water-soluble polymer. The hydrophilically modified water-soluble polymers used in the present invention typically have a molecular weight in the range of from about 100,000 to about 10,000,000. In an exemplary embodiment, the hydrophilically modified water-soluble polymers comprise a polymer backbone that comprises polar heteroatoms. Generally, the polar heteroatoms present within the polymer backbone of the hydrophilically modified water-soluble polymers include, but are not limited to, oxygen, nitrogen, sulfur, or phosphorous.


In certain embodiments of the present invention, the hydrophilically modified water-soluble polymers may be a reaction product of a water-soluble hydrophilic polymer and a hydrophilic compound. The water-soluble hydrophilic polymers suitable for forming the hydrophilically modified water-soluble polymers used in the present invention should be capable of reacting with hydrophilic compounds. In certain exemplary embodiments, suitable hydrophilic polymers include, homo-, co-, or terpolymers, such as, but not limited to, polyvinylamines, poly(vinylamines/vinyl alcohols), and alkyl acrylate polymers in general. Additional examples of alkyl acrylate polymers include, but are not limited to, polydimethylaminoethyl methacrylate, polydimethylaminopropyl methacrylamide, poly(acrylamide/dimethylaminoethyl methacrylate), poly(methacrylic acid/dimethylaminoethyl methacrylate), poly(2-acrylamido-2-methyl propane sulfonic acid/dimethylaminoethyl methacrylate), poly(acrylamide/dimethylaminopropyl methacrylamide), poly (acrylic acid/dimethylaminopropyl methacrylamide), and poly(methacrylic acid/dimethylaminopropyl methacrylamide). In certain embodiments, the water-soluble hydrophilic polymers contain reactive amino groups in the polymer backbone or as pendant groups, which are capable of reacting with hydrophilic compounds. In an exemplary embodiment, the water-soluble hydrophilic polymers comprise dialkyl amino pendant groups. In an exemplary embodiment, the water-soluble hydrophilic polymers comprise a dimethyl amino pendant group and at least one monomer comprising dimethylaminoethyl methacrylate or dimethylaminopropyl methacrylamide. In another exemplary embodiment of the present invention, the water-soluble hydrophilic polymers comprise a polymer backbone that comprises polar heteroatoms, wherein the polar heteroatoms present within the polymer backbone of the hydrophilic polymers include, but are not limited to, oxygen, nitrogen, sulfur, or phosphorous. Suitable hydrophilic polymers comprising polar heteroatoms within the polymer backbone include homo-, co-, or terpolymers such as, but not limited to, celluloses, polyamides, polyetheramines, polyethyleneimines, polyhydroxyetheramines, polylysines, polysulfones, gums, and starches. In an exemplary embodiment the starch is a cationic starch. A suitable cationic starch may be formed by reacting a starch, such as corn, maize, waxy maize, potato, tapioca, and the like, with the reaction product of epichlorohydrin and trialkylamine.


The hydrophilic compounds suitable for reaction with the water-soluble hydrophilic polymers include, but are not limited to, polyethers comprising halogen, sulfonates, sulfates, and organic acid derivatives. Examples of suitable polyethers include, but are not limited to, polyethylene oxides, polypropylene oxides, polybutylene oxides, and mixtures thereof. In an exemplary embodiment, the polyether comprises an epichlorohydrin terminated polyethylene oxide methyl ether.


The hydrophilically modified water-soluble polymers formed from the reaction of a water-soluble hydrophilic polymer with a hydrophilic compound may have estimated molecular weights in the range of from about 100,000 to about 10,000,000 and may have weight ratios of the water-soluble hydrophilic polymers to the polyethers in the range of from about 1:1 to about 10:1. Suitable hydrophilically modified water-soluble polymers having molecular weights and weight ratios in the ranges set forth above include, but are not limited to, the reaction product of polydimethylaminoethyl methacrylate with epichlorohydrin terminated polyethyleneoxide methyl ether; the reaction product of polydimethylaminopropyl methacrylamide with epichlorohydrin terminated polyethyleneoxide methyl ether; and the reaction product of poly(acrylamide/dimethylaminopropyl methacrylamide) with epichlorohydrin terminated polyethyleneoxide methyl ether. In an exemplary embodiment, the hydrophilically modified water-soluble polymers comprise the reaction product of a polydimethylaminoethyl methacrylate with epichlorohydrin terminated polyethyleneoxide methyl ether having a weight ratio of polydimethylaminoethyl methacrylate to epichlorohydrin terminated polyethyleneoxide methyl ether of 3:1.


The fluid loss control additives of the present invention should be present in the cement compositions of the present invention in an amount sufficient to provide the desired degree of fluid loss control. In an exemplary embodiment, the fluid loss control additive of the present invention is present in the cement compositions of the present invention in an amount in the range of from about 0.1% to about 4% bwoc.


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, but are not limited to, fly ash, silica compounds, surfactants, dispersants, accelerators, retarders, salts, micas, fibers, formation conditioning agents, fumed silica, expanding additives, weighting materials, defoamers, lightweight additives (e.g., bentonite, microspheres, and sodium silicate), and the like.


In one embodiment, the present invention provides a method of cementing in a subterranean formation comprising: providing a cement composition that comprises water, cement, and a fluid loss control additive that comprises a water-soluble hydrophobically modified polymer that comprises a polymer backbone comprising polar heteroatoms; placing the cement composition into the subterranean formation; and allowing the cement composition to set therein.


In another embodiment, the present invention provides a method of cementing in a subterranean formation comprising: providing a cement composition that comprises water, cement, and a fluid loss control additive that comprises a water-soluble hydrophobically modified polymer that is a reaction product of a hydrophobic compound with a polyvinylamine, a poly(vinylamine/vinyl alcohol), or an alkyl acrylate polymer; placing the cement composition into the subterranean formation; and allowing the cement composition to set therein.


In another embodiment, the present invention provides a method of cementing in a subterranean formation comprising: providing a cement composition that comprises water, cement, and a fluid loss control additive that comprises a hydrophilically modified water-soluble polymer; placing the cement composition into the subterranean formation; and allowing the cement composition to set therein.


In another embodiment, the present invention provides a cement composition that comprises water, cement, and a fluid loss control additive that comprises a water-soluble hydrophobically modified polymer that comprises a polymer backbone comprising polar heteroatoms.


In another embodiment, the present invention provides a cement composition that comprises water, cement, and a fluid loss control additive that comprises a water-soluble hydrophobically modified polymer that is a reaction product of a hydrophobic compound with a polyvinylamine, a poly(vinylamine/vinyl alcohol), or an alkyl acrylate polymer.


In yet another embodiment, the present invention provides a cement composition that comprises water, cement, and a fluid loss control additive that comprises a hydrophilically modified water-soluble polymer.


To facilitate a better understanding of the present invention, the following examples of the preferred embodiments are given. In no way should the following examples be read to limit, or define, the scope of the invention.


EXAMPLES

Sample compositions were prepared by mixing a cement slurry with a fluid loss control additive. The sample cement compositions were tested for fluid loss in accordance with the procedure described in Recommended Practice for Testing Well Cements, API Recommended Practice 10B, 22nd Edition, dated December, 1997. The fluid loss tests were performed at 80° F.


Sample Composition No. 1 (comparative) comprises Portland Class H cement, 38% of fresh water bwoc, and 1% of polyethyleneimine (“PEI”) bwoc. The fluid loss was found to be 48 milliliters (“ml”) in 0.3 minutes.


Sample Composition No. 2 comprises Portland Class H cement, 38% of fresh water bwoc, and 1% of a water-soluble hydrophobically modified polymer bwoc. The water-soluble hydrophobically modified polymer used in Sample Composition No. 2 was PEI hydrophobically modified with hexadecyl bromide (“C16Br”), wherein the water-soluble hydrophobically modified polymer comprises 5.7% C16Br by weight. The fluid loss was found to be 49 ml in 5.4 minutes.


Sample Composition No. 3 comprises Portland Class H cement, 38% of fresh water bwoc, and 1% of a water-soluble hydrophobically modified polymer bwoc. The water-soluble hydrophobically modified polymer used in Sample Composition No. 3 was PEI hydrophobically modified with C16Br, wherein the water-soluble hydrophobically modified polymer comprises 15.3% C16Br by weight. The fluid loss was found to be 52 ml in 9.7 minutes.


Sample Composition No. 4 (comparative) comprises Portland Class H cement, 47% of fresh water bwoc, and 1% of poly(dimethylaminoethyl methacrylate) (“PDMAEMA”). The fluid loss was found to be 47 ml in 0.75 minutes.


Sample Composition No. 5 comprises Portland Class H cement, 63% of fresh water bwoc, and 1% of a water-soluble hydrophobically modified polymer bwoc. The water-soluble hydrophobically modified polymer used in Sample Composition No. 5 was PDMAEMA hydrophobically modified with C16Br, wherein the water-soluble hydrophobically modified polymer comprises 9.2% C16Br by weight. The fluid loss was found to be 38 ml in 29.5 minutes.


A summary of the fluid loss demonstrated by each of the samples is depicted in Table 1, below.












TABLE 1






Fluid Loss Control
% C16Br in the
Fluid Loss


Fluid
Additive
modified polymer
(ml/minutes)


















Sample
PEI
0
48/0.3


Composition


No. 1


Sample
PEI modified with
5.7
49/5.4


Composition
C16Br


No.2


Sample
PEI modified with
15.3
52/9.7


Composition
C16Br


No.3


Sample
PDMAEMA
0
47/0.75


Composition


No. 4


Sample
PDMAEMA modified
9.2
38/29.5


Composition
with C16Br


No. 5









Thus, the Example demonstrates, inter alia, that hydrophobic modification improves the fluid loss control characteristics of a polymer.


Therefore, the present invention is well adapted to carry out the objects and attain the ends and advantages mentioned as well as those which 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.

Claims
  • 1. A method of cementing in a subterranean formation comprising the steps of: providing a cement composition that comprises: water,cement, anda fluid loss control additive comprising a water-soluble hydrophobically modified polymer that comprises a polymer backbone comprising polar heteroatoms;placing the cement composition into the subterranean formation; andallowing the cement composition to set therein.
  • 2. The method of claim 1 wherein the water is present in the cement composition in an amount in the range of from about 30% to about 200% by weight of the cement.
  • 3. The method of claim 1 wherein the fluid loss control additive is present in the cement composition in an amount in the range of from about 0.1% to about 4% by weight of the cement.
  • 4. The method of claim 1 wherein the water-soluble hydrophobically modified polymer has a molecular weight in the range of from about 100,000 to about 10,000,000.
  • 5. The method of claim 1 wherein at least one of the polar heteroatoms is selected from the group consisting of: oxygen, nitrogen, sulfur, and phosphorous.
  • 6. The method of claim 1 wherein the water-soluble hydrophobically modified polymer is a reaction product of hydrophobic compound and a hydrophilic polymer that comprises a polymer backbone comprising polar heteroatoms.
  • 7. The method of claim 6 wherein the hydrophilic polymer is selected from the group consisting of: a cellulose, a polyamide, a polyetheramine, a polyethyleneimine, a polyhydroxyetheramine, a polylysine, a polysulfone, a gum, and a starch.
  • 8. The method of claim 6 wherein the hydrophobic compound is selected from the group consisting of: an alkyl halide, a sulfonate, a sulfate, and an organic acid derivative.
  • 9. The method of claim 8 wherein the organic acid derivative is selected from the group consisting of: an octenyl succinic acid; a dodecenyl succinic acid; and an anhydride, ester, or amide of octenyl succinic acid or dodecenyl succinic acid.
  • 10. The method of claim 6 wherein the hydrophobic compound has an alkyl chain length of from about 4 to about 22 carbons.
  • 11. A method of cementing in a subterranean formation comprising: providing a cement composition that comprises: water,cement, anda fluid loss control additive comprising a water-soluble hydrophobically modified polymer that is a reaction product of a hydrophobic compound with a polymer comprising a reactive amino group;placing the cement composition into the subterranean formation; andallowing the cement composition to set therein.
  • 12. The method of claim 11 wherein the water is present in the cement composition in an amount in the range of from about 30% to about 200% by weight of the cement.
  • 13. The method of claim 11 wherein the fluid loss control additive is present in the cement composition in an amount in the range of from about 0.1% to about 4% by weight of the cement.
  • 14. The method of claim 11 wherein the water-soluble hydrophobically modified polymer has a molecular weight in the range of from about 100,000 to about 10,000,000.
  • 15. The method of claim 11 wherein the polymer comprising a reactive amino group is selected from the group consisting of: polydimethylaminoethyl methacrylate, polydimethylaminopropyl methacrylamide, poly(acrylamide/dimethylaminoethyl methacrylate), poly(acrylic acid/dimethylaminoethyl methacrylate), poly(methacrylic acid/dimethylaminoethyl methacrylate), poly(2-acrylamido-2-methyl propane sulfonic acid/dimethylaminoethyl methacrylate), poly(acrylamide/dimethylaminopropyl methacrylamide), poly(acrylic acid/dimethylaminopropyl methacrylamide), and poly(methacrylic acid/dimethylaminopropyl methacrylamide).
  • 16. The method of claim 11 wherein the hydrophobic compound is selected from the group consisting of: an alkyl halide, a sulfonate, a sulfate, and an organic acid derivative.
  • 17. The method of claim 16 wherein the organic acid derivative is selected from the group consisting of: an octenyl succinic acid; a dodecenyl succinic acid; and an anhydride, ester, or amide of octenyl succinic acid or dodecenyl succinic acid.
  • 18. The method of claim 11 wherein the hydrophobic compound has an alkyl chain length of from about 4 to about 22 carbons.
US Referenced Citations (104)
Number Name Date Kind
2863832 Perrine Dec 1958 A
2910436 Fatt et al. Oct 1959 A
3215199 Dilgren Nov 1965 A
3251415 Bombardieri et al. May 1966 A
3297090 Dilgren Jan 1967 A
3307630 Dilgren et al. Mar 1967 A
3382924 Veley et al. May 1968 A
3434971 Atkins Mar 1969 A
3441085 Gidley Apr 1969 A
3451818 Wareham Jun 1969 A
3744566 Szabo et al. Jul 1973 A
3910862 Barabas et al. Oct 1975 A
4129183 Kalfoglou Dec 1978 A
4142595 Anderson et al. Mar 1979 A
4152274 Phillips et al. May 1979 A
4158521 Anderson et al. Jun 1979 A
4158726 Kamada et al. Jun 1979 A
4299710 Dupre et al. Nov 1981 A
4366071 McLaughlin et al. Dec 1982 A
4366072 McLaughlin et al. Dec 1982 A
4366073 McLaughlin et al. Dec 1982 A
4366074 McLaughlin et al. Dec 1982 A
4374739 McLaughlin et al. Feb 1983 A
4393939 Smith et al. Jul 1983 A
4395340 McLaughlin Jul 1983 A
4401789 Gideon Aug 1983 A
4439334 Borchardt Mar 1984 A
4440649 Loftin et al. Apr 1984 A
4447342 Borchardt et al. May 1984 A
4460627 Weaver et al. Jul 1984 A
4462718 McLaughlin et al. Jul 1984 A
4532052 Weaver et al. Jul 1985 A
4536297 Loftin et al. Aug 1985 A
4536303 Borchardt Aug 1985 A
4536305 Borchardt et al. Aug 1985 A
4552670 Lipowski et al. Nov 1985 A
4554081 Borchardt et al. Nov 1985 A
4563292 Borchardt Jan 1986 A
4604216 Irvin et al. Aug 1986 A
4627926 Peiffer et al. Dec 1986 A
4671883 Connell Jun 1987 A
4693639 Hollenbeak et al. Sep 1987 A
4699722 Dymond et al. Oct 1987 A
4730028 Bock et al. Mar 1988 A
4814096 Evani Mar 1989 A
4828726 Himes et al. May 1989 A
4959432 Fan et al. Sep 1990 A
5071934 Peiffer Dec 1991 A
5097904 Himes Mar 1992 A
5146986 Dalrymple Sep 1992 A
5160642 Schield et al. Nov 1992 A
5197544 Himes Mar 1993 A
5208216 Williamson et al. May 1993 A
5244042 Dovan et al. Sep 1993 A
5271466 Harms Dec 1993 A
5342530 Aften et al. Aug 1994 A
5379841 Pusch et al. Jan 1995 A
5382371 Stahl et al. Jan 1995 A
5597783 Audibert et al. Jan 1997 A
5607902 Smith et al. Mar 1997 A
5637556 Argillier et al. Jun 1997 A
5646093 Dino Jul 1997 A
5669456 Audibert et al. Sep 1997 A
5720347 Audibert et al. Feb 1998 A
5728653 Audibert et al. Mar 1998 A
5735349 Dawson et al. Apr 1998 A
5887653 Bishop et al. Mar 1999 A
5944106 Dalrymple et al. Aug 1999 A
5972848 Audibert et al. Oct 1999 A
5979557 Card et al. Nov 1999 A
6020289 Dymond Feb 2000 A
6070664 Dalrymple et al. Jun 2000 A
6124245 Patel Sep 2000 A
6187839 Eoff et al. Feb 2001 B1
6228812 Dawson et al. May 2001 B1
6237687 Barbee, Jr. et al. May 2001 B1
6253851 Schroeder, Jr. et al. Jul 2001 B1
6277900 Oswald et al. Aug 2001 B1
6283210 Soliman et al. Sep 2001 B1
6359047 Thieu et al. Mar 2002 B1
6364016 Dalrymple et al. Apr 2002 B1
6380137 Heier et al. Apr 2002 B1
6441102 Akasaki et al. Aug 2002 B2
6476169 Eoff et al. Nov 2002 B1
6476283 Devore et al. Nov 2002 B1
6497283 Eoff et al. Dec 2002 B1
6516885 Munday Feb 2003 B1
6569983 Treybig et al. May 2003 B1
6609578 Patel et al. Aug 2003 B2
6627719 Whipple et al. Sep 2003 B2
6710107 Audibert et al. Mar 2004 B2
6787506 Blair et al. Sep 2004 B2
6803348 Jones et al. Oct 2004 B2
6855672 Poelker et al. Feb 2005 B2
7091159 Eoff et al. Aug 2006 B2
20030019627 Qu et al. Jan 2003 A1
20030104948 Poelker et al. Jun 2003 A1
20030191030 Blair et al. Oct 2003 A1
20040102331 Chan et al. May 2004 A1
20040171495 Zamora et al. Sep 2004 A1
20040220058 Eoff et al. Nov 2004 A1
20040229756 Eoff et al. Nov 2004 A1
20040229757 Eoff et al. Nov 2004 A1
20050230116 Nguyen et al. Oct 2005 A1
Foreign Referenced Citations (16)
Number Date Country
2 250 552 Apr 1974 DE
0 383 337 Aug 1990 EP
0 896 122 Feb 1999 EP
1 033 378 Sep 2000 EP
1 193 365 Apr 2002 EP
1 312 753 May 2003 EP
2 221 940 Feb 1990 GB
2335428 Sep 1999 GB
WO 9315164 Aug 1993 WO
WO 9949183 Sep 1999 WO
WO 9950530 Oct 1999 WO
WO 0078890 Dec 2000 WO
WO 02097236 Dec 2002 WO
WO 2003056130 Jul 2003 WO
WO 2004094781 Nov 2004 WO
WO 2004101706 Nov 2004 WO
Related Publications (1)
Number Date Country
20050279502 A1 Dec 2005 US