Latex compositions comprising pozzolan and/or cement kiln dust and methods of use

Abstract
The present invention includes methods and compositions that include a latex, and at least one of a natural pozzolan or cement kiln dust. An embodiment includes a method comprising: placing a latex composition in a subterranean formation, wherein the latex composition comprises: latex, a component selected from the group consisting of a natural pozzolan, cement kiln dust, and a combination thereof, and water; and allowing the latex composition to set. Another embodiment of the present invention includes a latex composition comprising: latex, a component selected from the group consisting of a natural pozzolan, cement kiln dust, and a combination thereof.
Description
BACKGROUND

The present invention relates to cementing operations and, more particularly, in certain embodiments, to compositions and methods that include a latex and at least one of a natural pozzolan (e.g., pumicite) or cement kiln dust (“CKD”).


In cementing methods, such as well construction and remedial cementing, cement compositions are commonly utilized. Cement compositions may be used in primary cementing operations whereby pipe strings, such as casing and liners, are cemented in well bores. In performing primary cementing, a cement composition may be pumped into an annulus between a subterranean formation and the pipe string disposed in the subterranean formation. The cement composition should set in the annulus, thereby forming an annular sheath of hardened cement (e.g., a cement sheath) that 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. Cement compositions also may be used in remedial cementing methods, such as the placement of cement plug and squeeze cementing for sealing voids in a pipe string, cement sheath, gravel pack, formation, and the like.


Cement compositions for use in subterranean formations may include a latex to improve various properties of the compositions. For example, the latex may be included in a cement composition for fluid loss control, to provide resiliency to the set cement, and/or to reduce the issues associated with gas channeling. In general, the latex used in cement compositions is often provided as a water-in-oil emulsion containing high quantities of natural or synthetic rubber (such as styrene-butadiene rubber). However, latex-containing cement compositions typically may have reduced strength with respect to comparable cement compositions.


Cement compositions for use in subterranean formations may further include Portland cement. Portland cement generally is a major component of the cost for the cement compositions. To reduce the cost of such cement compositions, other components may be included in the cement composition in addition to, or in place of, the Portland cement. Such components may include fly ash, slag cement, shale, metakaolin, micro-fine cement, and the like. “Fly ash,” as that term is used herein, refers to the residue from the combustion of powdered or ground coal, wherein the fly ash carried by the flue gases may be recovered, for example, by electrostatic precipitation. “Slag,” as that term is used herein, refers to a granulated, blast furnace by-product formed in the production of cast iron and generally comprises the oxidized impurities found in iron ore. Slag cement generally comprises slag and a base, for example, such as sodium hydroxide, sodium bicarbonate, sodium carbonate, or lime, to produce a hydraulic composition that, when combined with water, may set to form a hardened mass.


Cement compositions may further include natural pozzolans. Natural pozzolans are generally present on the Earth's surface and set and harden in the presence of hydrated lime and water. Examples of natural pozzolans include pumicite, diatomaceous earth, volcanic ash, opaline shale, tuff, and combinations thereof.


During the manufacture of cement, a waste material commonly referred to as cement kiln dust (“CKD”) is generated. CKD, as that teem is used herein, refers to a partially calcined kiln feed which is removed from the gas stream and collected, for example, in a dust collector during the manufacture of cement. Usually, large quantities of CKD are collected in the production of cement that are commonly disposed of as waste. Disposal of the waste CKD can add undesirable costs to the manufacture of the cement, as well as the environmental concerns associated with its disposal. The chemical analysis of CKD from various cement manufactures varies depending on a number of factors, including the particular kiln feed, the efficiencies of the cement production operation, and the associated dust collection systems. CKD generally may comprise a variety of oxides, such as SiO2, Al2O3, Fe2O3, CaO, MgO, SO3, Na2O, and K2O.


SUMMARY

The present invention relates to cementing operations and, more particularly, in certain embodiments, to compositions and methods that include a latex and at least one of a natural pozzolan (e.g., pumicite) or CKD.


An embodiment of the present invention includes a method comprising: placing a latex composition in a subterranean formation, wherein the latex composition comprises: latex, a component selected from the group consisting of a natural pozzolan, CKD, and a combination thereof, and water; and allowing the latex composition to set.


Another embodiment of the present invention includes a method comprising: placing a latex composition in a subterranean formation, wherein the latex composition comprises: latex, hydraulic cement, a component selected from the group consisting of a natural pozzolan, CKD, and a combination thereof, and water; and allowing the latex composition to set.


Yet another embodiment of the present invention includes a latex composition comprising: latex, a component selected from the group consisting of a natural pozzolan, CKD, and a combination thereof, and water.


The features and advantages of the present invention will be readily 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.







DESCRIPTION OF PREFERRED EMBODIMENTS

The present invention relates to cementing operations and, more particularly, in certain embodiments, to compositions and methods that include a latex and at least one of a natural pozzolan (e.g., pumicite) or CKD. There may be several potential advantages to the methods and compositions of the present invention, only some of which may be alluded to herein. One of the many potential advantages of the methods and compositions of the present invention is that inclusion of the natural pozzolan may provide for more rapid strength development in a latex cement. Another potential advantage of the methods and compositions of the present invention is that inclusion of the natural pozzolan and/or CKD in the latex composition may reduce the amount of, or potentially eliminate, a higher cost additive, such as Portland cement, resulting in a more economical latex composition.


Embodiments of the latex compositions of the present invention may comprise a latex, at least one of a natural pozzolan or CKD, and water. In certain embodiments, the latex compositions may further comprise a hydraulic cement. An example of a suitable latex composition may comprise a latex, pumicite, a hydraulic cement, and water. Another example of a suitable latex composition may comprise a latex, pumicite, a hydraulic cement, CKD, and water. Other optional additives may also be included in embodiments of the latex compositions of the present invention as desired, including, but not limited to, shale, metakaolin, zeolite, combinations thereof, and the like. In addition, latex stabilizers may be used as needed for a particular application. As described in more detail herein, embodiments of the latex compositions of the present invention may be foamed and/or extended as desired by those of ordinary skill in the art.


The latex compositions of the present invention should have a density suitable for a particular application as desired by those of ordinary skill in the art, with the benefit of this disclosure. In some embodiments, the latex compositions of the present invention may have a density in the range of about 8 pounds per gallon (“ppg”) to about 16 ppg. In the foamed embodiments, the foamed latex compositions of the present invention may have a density in the range of about 8 ppg to about 13 ppg.


Latex may be included in embodiments of the latex compositions of the present invention. As will be understood by those skilled in the art, the latex may comprise any of a variety of rubber materials that are commercially available in latex form. Suitable rubber materials include natural rubber (e.g., cis-1,4-polyisoprene), modified natural rubber, synthetic rubber, and combinations thereof. Synthetic rubber of various types may be utilized, including ethylene-propylene rubbers, styrene-butadiene rubbers, nitrile rubbers, nitrile butadiene rubbers, butyl rubber, neoprene rubber, polybutadiene rubbers, acrylonitrile-styrene-butadiene rubber, polyisoprene rubber, and AMPS-styrene-butadiene rubber, combinations thereof. As used herein, the term “AMPS” refers to 2-acrylamido-2-methylpropanesulfonic acid and salts thereof. Those of ordinary skill in the art will appreciate that other types of synthetic rubbers are also encompassed within the present invention.


One example of a suitable latex may include a water-in-oil emulsion that comprises an AMPS-styrene-butadiene rubber. In general, the aqueous phase of the emulsion may comprise an aqueous colloidal dispersion of the AMPS-styrene-butadiene rubber. In certain embodiments, the AMPS-styrene-butadiene rubber in the latex may comprise AMPS in an amount ranging from about 7.5% to about 10% by weight of the rubber, styrene in an amount ranging from about 30% to about 70% by weight of the rubber, and butadiene in an amount ranging from about 30% to about 70% by weight of the rubber. Examples of suitable AMPS-styrene-butadiene rubbers are described in more detail in U.S. Pat. Nos. 6,488,764 and 6,184,287, the entire disclosures of which are incorporated herein by reference.


Another example of a suitable latex may include a water-in-oil emulsion that comprises a styrene-butadiene rubber. In general, the aqueous phase of the emulsion comprises an aqueous colloidal dispersion of the styrene-butadiene rubber. Moreover, in addition to the dispersed styrene-butadiene rubber, the emulsion may comprise water in the range of about 40% to about 70% by weight of the emulsion and small quantities of an emulsifier, polymerization catalysts, chain modifying agents, and the like. As will be appreciated, styrene-butadiene latex is often produced as a terpolymer emulsion that may include a third monomer to assist in stabilizing the emulsion. Non-ionic groups which exhibit stearic effects and which contain long ethoxylate or hydrocarbon tails also may be present.


In accordance with embodiments of the present invention, the weight ratio of the styrene to the butadiene in the latex may be in the range of about 10:90 to about 90:10. In some embodiments, the weight ratio of the styrene to the butadiene in the latex may be in the range of about 20:80 to about 80:20. An example of a suitable styrene-butadiene latex has a styrene-to-butadiene weight ratio of about 25:75 and comprises water in an amount of about 50% by weight of the emulsion. Another example of a suitable styrene-butadiene latex has a styrene-to-butadiene weight ratio of about 30:70.


Where used, the latex may be provided in the latex compositions of the present invention in an amount sufficient for the desired application. In some embodiments, the latex may be included in the latex compositions in an amount in the range of about 2% to about 45% by weight of cementitious components. The term “cementitious components” refers to the components, or a combination thereof, of the latex compositions that hydraulically set, or otherwise harden, to develop compressive strength, including, for example, latex, CKD, fly ash, natural pozzolans (e.g., pumicite), slag, lime, shale, and the like. In some embodiments, the latex may be included in the latex compositions in an amount in the range of about 5% to about 27% by weight of cementitious components. One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of the latex to include for a chosen application.


A natural pozzolan may be included in embodiments of the latex compositions of the present invention. Natural pozzolans are generally present on the Earth's surface and set and harden in the presence of hydrated lime and water. Examples of natural pozzolans include pumicite, diatomaceous earth, volcanic ash, opaline shale, tuff, and combinations thereof. Generally, pumicite is a volcanic rock that exhibits cementitious properties, in that it may set and harden in the presence of hydrated lime and water. Hydrated lime may be used in combination with the pumicite, for example, to provide sufficient calcium ions for pumicite to set. The natural pozzolan may be used, among other things, to replace higher cost cementitious components, such as Portland cement, in embodiments of the latex compositions, resulting in more economical latex compositions. Where present, the natural pozzolan may be included in an amount in the range of from about 0.1% to about 50% by weight of cementitious components, for example (e.g., about 5%, about 10%, about 20%, about 30%, about 40%, etc.). In some embodiments, the natural pozzolan may be present in an amount in the range of from about 25% to about 50% by weight of cementitious components. One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of the natural pozzolan to include for a chosen application.


CKD may be included in embodiments of the latex compositions of the present invention. The CKD generally may exhibit cementitious properties, in that it may set and harden in the presence of water. The CKD may be used, among other things, to replace higher cost cementitious components, such as Portland cement, in embodiments of the latex compositions, resulting in more economical latex compositions. The CKD may be included in the latex compositions in an amount sufficient to provide the desired compressive strength, density, and/or cost reduction. In some embodiments, the CKD may be present in the latex compositions of the present invention in an amount in the range of about 1% to about 99% by weight of cementitious components (e.g., about 10%, about 20%, about 30%, about 40%, about 50%, about 60%, about 70%, about 80%, about 90%, etc.). In some embodiments, the CKD may be present in the latex compositions of the present invention in an amount in the range of about 5% to about 99% by weight of cementitious components. In some embodiments, the CKD may be present in an amount in the range of about 5% to about 80% by weight of cementitious components. In some embodiments, the CKD may be present in an amount in the range of about 10% to about 50% by weight of cementitious components. One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of CKD to include for a chosen application.


Embodiments of the latex compositions may further comprise water. The water used in embodiments of the latex compositions may include, for example, freshwater, saltwater (e.g., water containing one or more salts dissolved therein), brine (e.g., saturated saltwater produced from subterranean formations), seawater, or combinations thereof. Generally, the water may be from any source, provided that the water does not contain an excess of compounds that may undesirably affect other components in the latex composition. In some embodiments, the water may be included in an amount sufficient to form a pumpable slurry. In some embodiments, the water may be included in the latex compositions of the present invention in an amount in the range of about 40% to about 200% by weight of cementitious components. In some embodiments, the water may be included in an amount in the range of about 40% to about 150% by weight of cementitious components. One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of water to include for a chosen application.


A hydraulic cement may be included in embodiments of the latex compositions of the present invention. A variety of hydraulic cements may be utilized in accordance with the present invention, including, but not limited to, those comprising calcium, aluminum, silicon, oxygen, iron, and/or sulfur, which set and harden by reaction with water. Suitable hydraulic cements include, but are not limited to, Portland cements, pozzolana cements, gypsum cements, high alumina content cements, slag cements, silica cements, and combinations thereof. In certain embodiments, the hydraulic cement may comprise a Portland cement. In some embodiments, the Portland cements that are suited for use in the present invention are classified as Classes A, C, H, and G cements according to American Petroleum Institute, API Specification for Materials and Testing for Well Cements, API Specification 10, Fifth Ed., Jul. 1, 1990. In addition, in some embodiments, cements suitable for use in the present invention may include cements classified as ASTM Type I, II, or III.


Where present, the hydraulic cement generally may be included in the latex compositions in an amount sufficient to provide the desired compressive strength, density, and/or cost. In some embodiments, the hydraulic cement may be present in the latex compositions of the present invention in an amount in the range of 0.1% to about 99% by weight of cementitious components. In some embodiments, the hydraulic cement may be present in the latex compositions in an amount in the range of 0.1% to about 95% by weight of cementitious components. In some embodiments, the hydraulic cement may be present in the latex compositions in an amount in the range of about 20% to about 95% by weight of cementitious components. In some embodiments, the hydraulic cement may be present in the latex compositions in an amount in the range of about 50% to about 90% by weight of cementitious components. One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of the hydraulic cement to include for a chosen application.


In some embodiments, a pozzolana cement that may be suitable for use comprises fly ash. A variety of fly ashes may be suitable, including fly ash classified as Class C and Class F fly ash according to American Petroleum Institute, API Specification for Materials and Testing for Well Cements, API Specification 10, Fifth Ed., Jul. 1, 1990. Class C fly ash comprises both silica and lime so that, when mixed with water, it sets to form a hardened mass. Class F fly ash generally does not contain sufficient lime, so an additional source of calcium ions is required for the Class F fly ash to form a settable composition with water. In some embodiments, lime may be mixed with Class F fly ash in an amount in the range of about 0.1% to about 25% by weight of the fly ash. In some instances, the lime may be hydrated lime. Suitable examples of fly ash include, but are not limited to, POZMIX® A cement additive, commercially available from Halliburton Energy Services, Inc., Duncan, Okla.


Where present, the fly ash generally may be included in the latex compositions in an amount sufficient to provide the desired compressive strength, density, and/or cost. In some embodiments, the fly ash may be present in the latex compositions of the present invention in an amount in the range of about 5% to about 75% by weight of cementitious components. In some embodiments, the fly ash may be present in the latex compositions in an amount in the range of about 10% to about 60% by weight of cementitious components. One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of the fly ash to include for a chosen application.


In some embodiments, a slag cement that may be suitable for use may comprise slag. Slag generally does not contain sufficient basic material, so slag cement may further comprise a base to produce a settable composition that may react with water to set to form a hardened mass. Examples of suitable sources of bases include, but are not limited to, sodium hydroxide, sodium bicarbonate, sodium carbonate, lime, and combinations thereof. Where present, the slag cement generally may be included in the latex compositions in an amount sufficient to provide the desired compressive strength, density, and/or cost. In some embodiments, the slag cement may be present in the latex compositions of the present invention in an amount in the range of 0.1% to about 99% by weight of cementitious components. In some embodiments, the slag cement may be present in the latex compositions in an amount in the range of about 5% to about 75% by weight of cementitious components. One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of the slag cement to include for a chosen application.


A latex stabilizer may be included in embodiments of the latex compositions of the present invention. Among other things, the latex stabilizer may be included in embodiments of the latex compositions for preventing the latex compositions from prematurely coagulating. Suitable latex stabilizers may include a surfactant or combination of surfactants for preventing the premature inversion of the latex emulsion. Examples of suitable latex stabilizers include, but are not limited to, sulfonates and sulfates. Additional examples of suitable latex stabilizing surfactants which are suitable for this purpose may have the formula R—Ph—O(OCH2CH2)mOH where R contains an alkyl group of from about 5 to about 30 carbon atoms, Ph contains a phenyl group, and m is an integer having value between 5 to 50. An example of a surfactant of this formula is ethoxylated nonylphenyl containing in the range of about 20 to about 30 moles of ethylene oxide. Another example of a suitable surfactant is a salt having the formula R1(R2O)nSO3X where R1 contains an alkyl group having 5 to 20 carbon atoms, R2 contains the group —CH2—CH2—, n is an integer having value in between 10 to 40, and X is any suitable cation. An example of surfactant of this formula is the sodium salt of a sulfonated compound derived by reacting a C12-15 alcohol with about 15 moles of ethylene oxide having the formula H(CH2)12-15(CH2CH2O)15SO3Na. Specific examples of suitable latex stabilizers include Stabilizer 434B™ latex stabilizer, Stabilizer 434C™ latex stabilizer, and Stabilizer 434D™ latex stabilizer, which are available from Halliburton Energy Services, Inc. While embodiments of the present invention encompass a wide variety of different latex stabilizers and amounts thereof that may be included in the latex compositions of the present invention depending on the particular latex used and other factors, the latex stabilizer may be included in embodiments of the latex compositions in an amount in the range of about 0.1% to about 30% by weight of the latex in the latex composition and, alternatively, about 10% to about 20% by weight of the latex. One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of the latex stabilizer to include for a chosen application.


Metakaolin may be included in embodiments of the latex compositions of the present invention. Generally, metakaolin is a white pozzolan that may be prepared by heating kaolin clay, for example, to temperatures in the range of about 600° C. to about 800° C. In some embodiments, the metakaolin may be present in the latex compositions of the present invention in an amount in the range of about 5% to about 95% by weight of cementitious components. In some embodiments, the metakaolin may be present in an amount in the range of about 10% to about 50% by weight of cementitious components. One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of the metakaolin to include for a chosen application.


Shale may be included in embodiments of the latex compositions of the present invention. Among other things, shale included in the latex compositions may react with excess lime to form a suitable cementing material, for example, calcium silicate hydrate. A variety of shales may be suitable, including those comprising silicon, aluminum, calcium, and/or magnesium. An example of a suitable shale comprises vitrified shale. Suitable examples of vitrified shale include, but are not limited to, PRESSUR-SEAL FINE LCM material and PRESSUR-SEAL COARSE LCM material, which are commercially available from TXI Energy Services, Inc., Houston, Tex. Generally, the shale may have any particle size distribution as desired for a particular application. In certain embodiments, the shale may have a particle size distribution in the range of about 37 micrometers to about 4,750 micrometers.


Where present, the shale may be included in the latex compositions of the present invention in an amount sufficient to provide the desired compressive strength, density, and/or cost. In some embodiments, the shale may be present in the latex compositions of the present invention in an amount in the range of about 5% to about 75% by weight of cementitious components. In some embodiments, the shale may be present in an amount in the range of about 10% to about 35% by weight of cementitious components. One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of the shale to include for a chosen application.


Zeolite may be included in embodiments of the latex compositions of the present invention. Zeolites generally are porous alumino-silicate minerals that may be either a natural or synthetic material. Synthetic zeolites are based on the same type of structural cell as natural zeolites, and may comprise aluminosilicate hydrates. As used herein, the term “zeolite” refers to all natural and synthetic forms of zeolite. Examples of suitable zeolites are described in more detail in U.S. Patent Publication No. 2007/0056475 A1. An example of a suitable source of zeolite is available from the C2C Zeolite Corporation of Calgary, Canada. In some embodiments, the zeolite may be present in the latex compositions of the present invention in an amount in the range of about 5% to about 65% by weight of cementitious components. In certain embodiments, the zeolite may be present in an amount in the range of about 10% to about 40% by weight of cementitious components. One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of the zeolite to include for a chosen application.


Lime may be included in embodiments of the latex compositions of the present invention. In certain embodiments, the lime may be hydrated lime. The lime may be included in embodiments of the latex compositions, for example to, faun a hydraulic composition with other components of the latex compositions, such as the pumicite, fly ash, slag, and/or shale. Where present, the lime may be included in the latex compositions in an amount in the range of from about 1% to about 40% by weight of cementitious components, for example. In some embodiments, the lime may be present in an amount in the range of from about 5% to about 20% by weight of cementitious components. One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of the lime to include for a chosen application.


A set retarding additive may be included in embodiments of the latex compositions of the present invention. As used herein, the term “set retarding additive” refers to an additive that retards the setting of the latex compositions of the present invention. Examples of suitable set retarding additives include, but are not limited to, ammonium, alkali metals, alkaline earth metals, metal salts of sulfoalkylated lignins, organic acids (e.g., hydroxycarboxy acids), copolymers that comprise acrylic acid or maleic acid, and combinations thereof. One example of a suitable sulfoalkylate lignin comprises a sulfomethylated lignin. Suitable set retarding additives are disclosed in more detail in U.S. Pat. No. Re. 31,190, the entire disclosure of which is incorporated herein by reference. Suitable set retarding additives are commercially available from Halliburton Energy Services, Inc. under the trademarks HR® 4, HR® 5, HR® 7, HR® 12, HR®15, HR®25, HR®601, SCR™ 100, and SCR™ 500 retarders. Generally, where used, the set retarding additive may be included in the latex compositions of the present invention in an amount sufficient to provide the desired set retardation. In some embodiments, the set retarding additive may be present in the latex compositions of the present invention an amount in the range of about 0.1% to about 5% by weight of cementitious components. One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of the set retarding additive to include for a chosen application.


Optionally, other additional additives may be added to the latex 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, strength-retrogression additives, set accelerators, weighting agents, lightweight additives, gas-generating additives, mechanical property enhancing additives, lost-circulation materials, filtration-control additives, dispersants, fluid loss control additives, defoaming agents, foaming agents, oil-swellable particles, water-swellable particles, thixotropic additives, and combinations thereof. Specific examples of these, and other, additives include crystalline silica, amorphous silica, fumed silica, salts, fibers, hydratable clays, microspheres, rice husk ash, combinations thereof, and the like. By way of example, latex compositions may be foamed and further comprise a gas and a foaming agent. A person having ordinary skill in the art, with the benefit of this disclosure, will readily be able to determine the type and amount of additive useful for a particular application and desired result.


As will be appreciated by those of ordinary skill in the art, embodiments of the latex compositions of the present invention may be used for a variety of subterranean cementing applications. By way of example, embodiments of the latex compositions may be used in cementing methods, including primary and remedial cementing. Embodiments of the latex compositions may be introduced into a subterranean formation and allowed to set therein. As desired by one of ordinary skill in the art, with the benefit of this disclosure, the latex compositions of the present invention useful in this method may comprise any of the above-listed additives, as well any of a variety of other additives suitable for use in subterranean applications.


In primary cementing embodiments, for example, a latex composition may be introduced into a space between a subterranean formation and a conduit (e.g., pipe string, casing, expandable casing, liners, etc.) located in the subterranean formation. The latex composition may be allowed to set to form a hardened mass in the space between the subterranean formation and the conduit. Among other things, the set latex composition may faun a barrier, preventing the migration of fluids in the well bore. The set latex composition also may, for example, support the conduit in the well bore.


In remedial cementing embodiments, a latex composition may be used, for example, in squeeze-cementing operations or in the placement of cement plugs. By way of example, the latex composition may be placed in a well bore to plug a void or crack in the conduit, the cement sheath, the formation, a gravel pack or a microannulus between the cement sheath and the conduit.


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.


EXAMPLE 1

Five slurries (i.e., Slurries 1-5) were prepared to determine the effect of including pumicite in latex compositions. Each of the slurries contained Portland Class H cement in an amount of 75% bwoc, 200-mesh pumicite in an amount of 25% bwoc, a cement dispersant (CFR-2L™ cement dispersant from Halliburton Energy Services, Inc.) in an amount of 0.48 gallons per 94-lb sack of dry blend (“gal/sk”), a defoamer (D-AIR 3000L™ defoamer from Halliburton Energy Services, Inc.) in an amount of 0.05 gal/sk, a latex containing an AMPS-styrene-butadiene rubber in an amount of 2.0 gal/sk, and water in an amount of 16.4 gal/sk. In this example, by weight of cement (or “% bwoc”) is based on the amount of the Portland cement and pumicite included in each sample. A cement set retarder and salt were also included in certain samples as indicated in the table below.


After the slurries were prepared, the slurries and resulting set compositions were tested to determine their respective thickening times, fluid loss, and mechanical properties in accordance with API Recommended Practice 10B at the temperature indicated in the table below. For the compressive strength testing, the slurries were allowed to cure in an ultrasonic cement analyzer at the temperature indicated in the table below for twenty-four hours. Immediately after removal from the UCA, compressive strengths were determined using a Tinius Olsen tester. The results of these tests are provided in the table below.









TABLE 1







Latex Test Results: 75% Portland Cement and 25% Pumicite
















NaCl
Thick.
Fluid Loss
24-Hour




Retarder
(% by wt
Time 70 bc
200° F.
Compressive


Slurry
Temp
(% bwoc)
of water)
(hr:min)
(cc/30 min)
Strength (psi)





1
130


2:24
24
2650


2
200
0.2 HR ®-5

5:46
28
3570


3
250
0.6 SCR

3:14
18
4040




100 ™/




0.3 HR ®-25


4
250
0.6 SCR
18
5:49
20
2100




100 ™/




0.3 HR ®-25


5
300
0.4 SCR
37
4:34
46
2530




100 ™/




0.2 HR ®-25









Example 1 thus indicates that the inclusion of pumicite in latex compositions may provide suitable properties for certain applications at a variety of different downhole temperatures.


EXAMPLE 2

Eight additional slurries (i.e., Slurries 6-13) were prepared to determine the effect of including pumicite in latex compositions that comprise Portland cement, CKD, and latex. Each of the slurries had a density of 15.5 ppg and contained Portland Class H cement in an amount of 50% bwoc, 200-mesh pumicite in an amount of 25% bwoc, Joppa CKD in an amount of 25% bwoc, a latex containing an AMPS-styrene-butadiene rubber in an amount of 2.0 gal/sk, a defoamer (D-AIR 3000L™ defoamer from Halliburton Energy Services, Inc.) in an amount of 0.05 gal/sk, and water in the amount indicated in the table below. In this example, by weight of cement (or “% bwoc”) is based on the amount of the Portland cement, pumicite, and CKD included in each sample. Additional additives were also included in each sample in the amount indicated in the table below.


After the slurries were prepared, the slurries and resulting set compositions were tested to determine their respective thickening times, fluid loss, and mechanical properties in accordance with API Recommended Practice 10B at the temperature indicated in the table below. For the compressive strength testing, the slurries were allowed to cure in an ultrasonic cement analyzer at the temperature listed in the table below for twenty-four hours. Immediately after removal from the UCA, compressive strengths were determined using a Tinius Olsen tester. Additionally, the rheological properties of Slurry 7 were also determined using a Fann Model 35 viscometer at the temperature indicated in the table below using a bob and sleeve and spring #1. The results of these tests are provided in the table below.









TABLE 2







Latex Test Results: 50% Portland Cement, 25% Pumicite, and 25% Cement Kiln Dust















Slurry
6
7
8
9
10
11
12
13


















Temperature (° F.)
180
250
300
250
300
180
180
300


Water (% bwoc)
20.58
  32.3
32.3
33.3
33.3
21.74
21.74
36.62


HR ®-5 retarder (% bwoc)
0.2




0.2
0.5


SCR 100 ™ retarder (% bwoc)

   0.4
0.6
0.4
0.6


0.4


HR ®-25 retarder (% bwoc)

   0.2
0.3
0.2
0.3


0.2


Silica Flour1 (% bwoc)

 35
35
35
35


35


Dispersant2 (gal/sk)
0.143
    0.175
0.175
0.175
0.175
0.143
0.143
0.175


Latex Stabilizer3 (gal/sk)



0.2
0.2
0.2
0.2
0.2


NaCl (% by wt of water)



18
18
37
37
37


Rheology (at 80° F.)


 3

 8








 6

 13








100

108








200

170








300

265








600

  330+








Rheology (at 180° F.)


 3

 3








 6

 5








100

 63








200

118








300

223








600

  330+








Thick. Time 70 bc (hr:min)
4:45
4:35
3:57
7:20
9:10
1:25
10:15
10:15


Fluid Loss (cc/30 min)
50
 2
74
16
14
42

80


24-Hour Comp. Strength (psi)
4130
3020 
3210
1088
2360
2190

1327






1The silica flour included was SSA-1 ™ strength stabilizing additive, available from Halliburton Energy Services, Inc.




2The dispersant included was CFR-6L ™ cement dispersant, available from Halliburton Energy Services, Inc.




3The latex stabilizer included was Stabilizer 434-D ™ stabilizer, available from Halliburton Energy Services, Inc.







Example 2 thus indicates that the inclusion of pumicite in latex compositions may provide suitable properties for certain applications at a variety of different downhole temperatures.


EXAMPLE 3

Four additional slurries (i.e., Slurries 14-17) were prepared to further analyze the inclusion of pumicite in latex compositions by comparison with latex compositions that do not contain pumicite. Each of the slurries contained Portland Class H cement in an amount of from 50% to 100% bwoc, 200-mesh pumicite in an amount from 0% to 25% bwoc, Joppa CKD in an amount from 0% to 25% bwoc, a latex containing an AMPS-styrene-butadiene rubber in an amount of 2.0 gal/sk, a defoamer (D-AIR 3000L™ defoamer from Halliburton Energy Services, Inc.) in an amount of 0.05 gal/sk, a cement dispersant (CFR-6L™ cement dispersant from Halliburton Energy Services, Inc.) in an amount of 0.143 gal/sk. In this example, by weight of cement (or “% bwoc”) is based on the amount of the Portland cement, pumicite, and/or CKD included in each sample. Certain samples also included a cement set retarder (HR®-5 retarder) in the amount indicated below to provide comparable thickening times between the slurries.


After the slurries were prepared, the slurries and resulting set compositions were tested to determine their respective thickening times and mechanical properties in accordance with API Recommended Practice 10B at the temperature indicated in the table below. For the compressive strength testing, the slurries were allowed to cure in an ultrasonic cement analyzer at 180° F. for twenty-four hours. Immediately after removal from the UCA, compressive strengths were determined using a Tinius Olsen tester. The results of these tests are provided in the table below.









TABLE 3







Latex Test Results:


Portland Cement, Pumicite, and/or Cement Kiln Dust









Slurry












14
15
16
17















Temperature (° F.)
180
180
180
180


Water (% bwoc)
20.58
29.05
26.19
23.45


Portland Cement (% bwoc)
50
100
75
75


Pumicite (% bwoc)
25


25


CKD (% bwoc)
25

25



Cement Set Retarder
0.5

0.4



(% bwoc)


Thick. Time 70 bc
7:00
6:18
6:10
6:17


(hr:min)


24-Hour Comp. Strength
2620
1676
2100
2740


(psi)









Example 3 thus indicates that the inclusion of pumicite in latex compositions may provide suitable properties for certain applications at a variety of different downhole temperatures. By way of example, this example indicates that the inclusion of pumicite in latex compositions may provide more rapid strength development in slurries containing Portland cement and/or CKD as compared to slurries without pumicite.


EXAMPLE 4

Two additional slurries (i.e., Slurries 18-19) were prepared to determine the effect of including pumicite and cement kiln dust in latex compositions that do not comprise Portland cement. Each of the slurries contained 200-mesh pumicite in an amount from 70% to 80% bwoc, Joppa CKD in an amount from 20% to 30% bwoc, hydrated lime in an amount of 10% bwoc, a cement set retarder (HR®-5 retarder from Halliburton Energy Services, Inc.) in an amount of 0.75% bwoc, a defoamer (D-AIR 3000L™ defoamer from Halliburton Energy Services, Inc.) in an amount of about 0.05 gal/sk, a latex containing an AMPS-styrene-butadiene rubber in an amount of 2.0 gal/sk, and water in an amount of 32.32 gal/sk. In this example, by weight of cement (or “% bwoc”) is based on the amount of the pumicite and CKD included in each sample. Slurry 18 further contained a cement dispersant (CFR-2L™ cement dispersant from Halliburton Energy Services, Inc.) in an amount of 0.29 gal/sk, and Slurry 19 contained the cement dispersant in an amount of 1.0 gal/sk.


After the slurries were prepared, the slurries and resulting set compositions were tested to determine their respective thickening times, fluid loss, and mechanical properties in accordance with API Recommended Practice 10B at the temperature indicated in the table below. For the compressive strength testing, the slurries were allowed to cure in an ultrasonic cement analyzer at 180° F. for forty-eight hours. Immediately after removal from the UCA, compressive strengths were determined using a Tinius Olsen tester. Additionally, the rheological properties were also determined using a Fann Model 35 viscometer at the temperature indicated in the table below using a bob and sleeve and spring #1. The results of these tests are provided in the table below.









TABLE 4







Latex Test Results:


Pumicite and Cement Kiln Dust










Slurry











18
19















Temperature (° F.)
180 
180 



Density (ppg)
14
  13.5



Pumicite (% bwoc)
70
80



Cement Kiln Dust (% bwoc)
30
20



Hydrated Lime (% bwoc)
10
10



Rheology (at 80° F.)



 3
26
 8



 6
34
10



 30
92
26



 60
153 
42



100
227 
62



200
300+
101 



300
300+
153 



600
300+
300+



Rheology (at 180° F.)



 3
15
 4



 6
21
 7



 30
65
17



 60
114 
29



100
177 
41



200
300+
72



300
300+
97



600
300+
172 



Thick. Time 70 bc (hr:min)
8:42
7:58



Fluid Loss (cc/30 min)
36
36



48-Hour Comp. Strength (psi)
1285 
1197 










Example 4 thus indicates that the inclusion of pumicite and CKD in latex compositions that do not contain Portland cement may provide suitable properties for certain applications at a variety of different downhole temperatures.


Therefore, the present invention is well adapted to attain the ends and advantages mentioned as well as those that are inherent therein. The particular embodiments disclosed above are illustrative only, as the present invention may be modified and practiced in different but equivalent manners apparent to those skilled in the art having the benefit of the teachings herein. Furthermore, no limitations are intended to the details of construction or design herein shown, other than as described in the claims below. It is therefore evident that the particular illustrative embodiments disclosed above may be altered or modified and all such variations are considered within the scope and spirit of the present invention. While compositions and methods are described in terms of “comprising,” “containing,” or “including” various components or steps, the compositions and methods can also “consist essentially of” or “consist of” the various components and steps. Whenever a numerical range with a lower limit and an upper limit is disclosed, any number and any included range falling within the range is specifically disclosed. In particular, every range of values (of the form, “from about a to about b,” or, equivalently, “from approximately a to b,” or, equivalently, “from approximately a-b”) disclosed herein is to be understood to set forth every number and range encompassed within the broader range of values. Also, the terms in the claims have their plain, ordinary meaning unless otherwise explicitly and clearly defined by the patentee.

Claims
  • 1. A subterranean latex composition comprising: a synthetic latex;a cementitious component comprising cement kiln dust in an amount of about 70% to about 99% by weight of the cementitious component and hydraulic cement in an amount of about 0.1% to about 10% by weight of the cementitious component; andwater in an amount sufficient to form a pumpable slurry,wherein the synthetic latex is present in the subterranean latex composition in an amount of about 6% to about 45% by weight of the cementitious component.
  • 2. The subterranean latex composition of claim 1 wherein the synthetic latex comprises a rubber selected from the group consisting of an ethylene-propylene rubber, a styrene-butadiene rubber, a nitrile rubber, a nitrile butadiene rubber, a butyl rubber, a neoprene rubber, a polybutadiene rubber, an acrylonitrile-styrene-butadiene rubber, a polyisoprene rubber, an AMPS-styrene-butadiene rubber, and any combination thereof.
  • 3. The subterranean latex composition of claim 1 wherein the synthetic latex comprises an AMPS-styrene-butadiene rubber.
  • 4. The subterranean latex composition of claim 1 wherein the latex composition further comprises a natural pozzolan, and wherein the natural pozzolan comprises at least one pozzolan selected from the group consisting of pumicite, diatomaceous earth, volcanic ash, opaline shale, tuff, and any combination thereof.
  • 5. The subterranean latex composition of claim 1 wherein the latex composition further comprises a natural pozzolan, and wherein the natural pozzolan comprises pumicite.
  • 6. The subterranean latex composition of claim 1 wherein the cement kiln dust is present in an amount of about 80% to about 99% by weight of the cementitious component.
  • 7. The subterranean latex composition of claim 1 wherein the cement kiln dust is present in an amount of about 90% to about 99% by weight of the cementitious component.
  • 8. The subterranean latex composition of claim 1 wherein the cementitious component further comprises pumicite.
  • 9. The subterranean latex composition of claim 1 wherein the latex composition further comprises at least one additive selected from the group consisting of fly ash, slag cement, metakaolin, shale, zeolite, as gas, crystalline silica, amorphous silica, finned silica, a salt, a fiber, a hydratable clay, a microsphere, rice husk ash, lime, and any combination thereof.
  • 10. The subterranean latex composition of claim 1, wherein the latex composition further comprises at least one additive selected from the group consisting of a latex stabilizer, a strength-retrogression additive, a set retarder, a set accelerator, a weighting agent, a lightweight additive, a gas-generating additive, as mechanical property enhancing additive, a lost-circulation material, a filtration-control additive, a dispersant, a fluid loss control additive, a defoaming agent, a foaming agent, an oil-swellable particle, a water-swellable particle, a thixotropic additive, and any combination thereof.
  • 11. The subterranean latex composition of claim 1 wherein the latex composition is foamed.
  • 12. The subterranean latex composition of claim 1 wherein the hydraulic cement comprises at least one cement selected from the group consisting of Portland cement, pozzolana cement, gypsum cement, high alumina content cement, slag cement, silica cement, and any combination thereof.
  • 13. The subterranean latex composition of claim 1 wherein the hydraulic cement comprises Portland cement.
  • 14. A latex composition comprising: a synthetic latex:a cementitious component consisting of: cement kiln dust; andpumicite; andwater in an amount sufficient to form a pumpable slurry,wherein the synthetic latex is present in an amount of about 6% to about 45% by weight of the cementitious component,wherein the latex composition is essentially free of any additional cementitious components other than the cementitious component.
  • 15. The latex composition of claim 14 wherein the pumicite is present in an amount of about 25% to about 75% by weight of the cementitious component.
  • 16. The latex composition of claim 14 wherein the cement kiln dust is present in an amount of about 10% to about 30% by weight of the cementitious component.
  • 17. The latex composition of claim 14 wherein the cement kiln dust is present in an amount of about 10% to about 50% by weight of the cementitious component.
  • 18. A subterranean latex composition comprising: a cementitious component consisting of cement kiln dust;a latex;water in an amount sufficient to form a pumpable slurry; anda set retarder,wherein the latex composition is essentially free of any additional cementitious components other than the cementitious component,wherein the latex comprises a rubber selected from the group consisting of an ethylene-propylene rubber, a styrene-butadiene rubber, a nitrite rubber, a nitrite butadiene rubber, a butyl rubber, a neoprene rubber, a polybutadiene rubber, an acrylonitrile-styrene-butadiene rubber, a polyisoprene rubber, an AMPS-styrene-butadiene rubber, and any combination thereof.
  • 19. The subterranean latex compositions of claim 18 wherein the latex comprises the AMPS-styrene-butadiene rubber.
  • 20. The subterranean latex composition of claim 18 wherein the latex is present in an amount of about 2% to about 45% by weight of the cementitious component.
  • 21. The subterranean latex composition of claim 18 wherein the latex composition further comprises at least one additive selected from the group consisting of gas, crystalline silica, amorphous silica, fumed silica, a salt, a fiber, a microsphere, rice husk ash, and any combination thereof.
  • 22. The subterranean latex composition of claim 18 wherein the latex composition further comprises at least one additive selected from the group consisting of a latex stabilizer, a strength-retrogression additive, a set accelerator, a weighting agent, a lightweight additive, a gas-generating additive, a mechanical property enhancing additive, a lost-circulation material, a filtration-control additive, a dispersant, a fluid loss control additive, a defoaming agent, a foaming agent, an oil-swellable particle, to water-swellable particle, a thixotropic additive, and any combination thereof.
  • 23. The subterranean latex composition of claim 18 wherein the latex composition is foamed.
  • 24. A latex composition comprising: a cementitious component consisting of cement kiln dust;a synthetic latex in an amount of about 6% to about 45% by weight of the cementitious component; andwater in an amount in a range of from about 40% to about 200% by weight of cementitious components,wherein the latex composition is essentially free of any additional cementitious components other than the cementitious component,wherein the latex composition has a density in a range of from about 8 pounds per gallon to about 16 pounds per gallon,wherein the synthetic latex comprises a rubber selected from the group consisting of an ethylene-propylene rubber, a styrene-butadiene rubber, a nitrile rubber, a nitrile butadiene rubber, a butyl rubber, a neoprene rubber, a polybutadiene rubber, an acrylonitrile-styrene-butadiene rubber, a polyisoprene rubber, an AMPS-styrene-butadiene rubber, and any combination thereof.
  • 25. The latex composition of claim 24 wherein the synthetic latex comprises the AMPS-styrene-butadiene rubber.
  • 26. The latex composition of claim 24 wherein the latex composition further comprises at least one additive selected from the group consisting of gas, crystalline silica, amorphous silica, filmed silica, a salt, a fiber, a microsphere, rice husk ash, and any combination thereof.
  • 27. The latex composition of claim 24 wherein the latex composition further comprises at least one additive selected from the group consisting of a latex stabilizer, a strength-retrogression additive, a set retarder, a set accelerator, a weighting agent, a lightweight additive, a gas-generating additive, a mechanical property enhancing additive, a lost-circulation material, a filtration-control additive, a dispersant, as fluid loss control additive, a defoaming agent, a foaming agent, an oil-swellable particle, as water-swellable particle, a thixotropic additive, and any combination thereof.
  • 28. The latex composition of claim 24 wherein the latex composition is foamed.
CROSS-REFERENCE TO RELATED APPLICATIONS

This application is divisional of U.S. application Ser. No. 12/609,993, entitled “Latex Compositions Comprising Pozzolan and/or Cement Kiln Dust and Methods of Use,” filed on Oct. 30, 2009, which is a continuation-in-part of U.S. application Ser. No. 12/420,630, now U.S. Pat. No. 7,631,692, entitled “Cement Compositions Having Cement Kiln Dust and/or Pumicite and Methods of Use,” filed on Apr. 8, 2009, which is a continuation-in-part of U.S. application Ser. No. 12/349,676, now U.S. Pat. No. 7,674,332, entitled “Extended Settable Compositions Comprising Cement Kiln Dust and Associated Methods,” filed on Jan. 7, 2009, which is a divisional of U.S. application Ser. No. 12/034,886, U.S. Pat. No. 7,478,675, entitled “Extended Settable Compositions Comprising Cement Kiln Dust and Associated Methods, filed on Feb. 21, 2008, which is a continuation-in-part of U.S. application Ser. No. 11/223,669, now U.S. Pat. No. 7,445,669, entitled “Settable Compositions Comprising Cement Kiln Dust and Additive(s),” filed Sep. 9, 2005, the entire disclosures of which are incorporated herein by reference.

US Referenced Citations (278)
Number Name Date Kind
2094316 Cross et al. Sep 1937 A
2329940 Ponzer Sep 1943 A
2842205 Allen et al. Jul 1958 A
2848051 Willaims Aug 1958 A
2871133 Palonen et al. Jan 1959 A
2880096 Hurley Mar 1959 A
2945769 Gama et al. Jul 1960 A
3168139 Kennedy et al. Feb 1965 A
3407193 McColl et al. Oct 1968 A
3454095 Messenger et al. Jul 1969 A
3499491 Wyant et al. Mar 1970 A
3557876 Tragesser Jan 1971 A
3748159 George Jul 1973 A
3876005 Fincher et al. Apr 1975 A
3887009 Miller et al. Jun 1975 A
3887385 Quist et al. Jun 1975 A
4018617 Nicholson Apr 1977 A
4031184 McCord Jun 1977 A
4036301 Powers et al. Jul 1977 A
4101332 Nicholson Jul 1978 A
4176720 Wilson Dec 1979 A
4240952 Hulbert et al. Dec 1980 A
4268316 Wills et al. May 1981 A
4341562 Ahlbeck Jul 1982 A
RE31190 Detroit et al. Mar 1983 E
4407677 Wills et al. Oct 1983 A
4432800 Kneller et al. Feb 1984 A
4435216 Diehl et al. Mar 1984 A
4436850 Burdick et al. Mar 1984 A
4460292 Durham et al. Jul 1984 A
4494990 Harris Jan 1985 A
4515635 Rao et al. May 1985 A
4519452 Tsao et al. May 1985 A
4555269 Rao et al. Nov 1985 A
4614599 Walker Sep 1986 A
4624711 Styron Nov 1986 A
4633950 Delhommer et al. Jan 1987 A
4676317 Fry et al. Jun 1987 A
4676832 Childs et al. Jun 1987 A
4741782 Styron May 1988 A
4784223 Worrall et al. Nov 1988 A
4883125 Wilson et al. Nov 1989 A
4941536 Brothers et al. Jul 1990 A
4992102 Barbour Feb 1991 A
5030366 Wilson et al. Jul 1991 A
5049288 Brothers et al. Sep 1991 A
5058679 Hale et al. Oct 1991 A
RE33747 Hartley et al. Nov 1991 E
5086850 Harris et al. Feb 1992 A
5121795 Ewert et al. Jun 1992 A
5123487 Harris et al. Jun 1992 A
5125455 Harris et al. Jun 1992 A
5127473 Harris et al. Jul 1992 A
5183505 Spinney Feb 1993 A
5213160 Nahm et al. May 1993 A
5215585 Luthra et al. Jun 1993 A
5238064 Dahl et al. Aug 1993 A
5252128 Gopalkrishnan Oct 1993 A
5266111 Barbour Nov 1993 A
5295543 Terry et al. Mar 1994 A
5305831 Nahm Apr 1994 A
5314022 Cowan et al. May 1994 A
5327968 Onan et al. Jul 1994 A
5337824 Cowan Aug 1994 A
5352288 Mallow Oct 1994 A
5358044 Hale et al. Oct 1994 A
5358049 Hale et al. Oct 1994 A
5361841 Hale et al. Nov 1994 A
5361842 Hale et al. Nov 1994 A
5368103 Heathman et al. Nov 1994 A
5370185 Cowan et al. Dec 1994 A
5372641 Carpenter Dec 1994 A
5382290 Nahm et al. Jan 1995 A
5383521 Onan et al. Jan 1995 A
5383967 Chase Jan 1995 A
5398758 Onan et al. Mar 1995 A
5417759 Huddleston May 1995 A
5423379 Hale et al. Jun 1995 A
5430235 Hooykaas et al. Jul 1995 A
5439056 Cowan Aug 1995 A
5456751 Zandi et al. Oct 1995 A
5458195 Totten et al. Oct 1995 A
5464060 Hale et al. Nov 1995 A
5472051 Brothers Dec 1995 A
5476144 Nahm et al. Dec 1995 A
5494513 Fu et al. Feb 1996 A
5499677 Cowan Mar 1996 A
5515921 Cowan et al. May 1996 A
5518996 Maroy et al. May 1996 A
5520730 Barbour May 1996 A
5529624 Riegler Jun 1996 A
5536311 Rodrigues Jul 1996 A
5542782 Carter et al. Aug 1996 A
5554352 Jaques et al. Sep 1996 A
5569324 Totten et al. Oct 1996 A
5580379 Cowan Dec 1996 A
5585333 Dahl et al. Dec 1996 A
5588489 Chatterji et al. Dec 1996 A
5641584 Andersen et al. Jun 1997 A
5673753 Hale et al. Oct 1997 A
5685903 Stav et al. Nov 1997 A
5688844 Chatterji et al. Nov 1997 A
5711383 Terry et al. Jan 1998 A
5716910 Totten et al. Feb 1998 A
5728654 Dobson et al. Mar 1998 A
5795924 Chatterji et al. Aug 1998 A
5820670 Chatterji et al. Oct 1998 A
5851960 Totten et al. Dec 1998 A
5866516 Costin Feb 1999 A
5866517 Carpenter et al. Feb 1999 A
5874387 Carpenter et al. Feb 1999 A
5897699 Chatterji et al. Apr 1999 A
5900053 Brothers et al. May 1999 A
5913364 Sweatman Jun 1999 A
5988279 Udarbe et al. Nov 1999 A
6022408 Stokes et al. Feb 2000 A
6060434 Sweatman et al. May 2000 A
6060535 Villar et al. May 2000 A
6063738 Chatterji et al. May 2000 A
6098711 Chatterji et al. Aug 2000 A
6138759 Chatterji et al. Oct 2000 A
6143069 Brothers et al. Nov 2000 A
6145591 Boncan et al. Nov 2000 A
6153562 Villar et al. Nov 2000 A
6167967 Sweatman Jan 2001 B1
6170575 Reddy et al. Jan 2001 B1
6230804 Mueller et al. May 2001 B1
6244343 Brothers et al. Jun 2001 B1
6245142 Reddy et al. Jun 2001 B1
6258757 Sweatman et al. Jul 2001 B1
6277189 Chugh Aug 2001 B1
6312515 Barlet-Gouedard et al. Nov 2001 B1
6315042 Griffith et al. Nov 2001 B1
6328106 Griffith et al. Dec 2001 B1
6332921 Brothers et al. Dec 2001 B1
6367550 Chatterji et al. Apr 2002 B1
6379456 Heathman et al. Apr 2002 B1
6402833 O'Hearn et al. Jun 2002 B1
6409819 Ko Jun 2002 B1
6457524 Roddy Oct 2002 B1
6478869 Reddy et al. Nov 2002 B2
6488763 Brothers et al. Dec 2002 B2
6488764 Westerman Dec 2002 B2
6494951 Reddy et al. Dec 2002 B1
6500252 Chatterji et al. Dec 2002 B1
6508305 Brannon et al. Jan 2003 B1
6516884 Chatterji et al. Feb 2003 B1
6524384 Griffith et al. Feb 2003 B2
6547871 Chatterji et al. Apr 2003 B2
6547891 Linden et al. Apr 2003 B2
6561273 Brothers et al. May 2003 B2
6562122 Dao et al. May 2003 B2
6565647 Day et al. May 2003 B1
6572697 Gleeson et al. Jun 2003 B2
6610139 Reddy et al. Aug 2003 B2
6626243 Go Boncan Sep 2003 B1
6645290 Barbour Nov 2003 B1
6656265 Garnier et al. Dec 2003 B1
6660080 Reddy et al. Dec 2003 B2
6666268 Griffith et al. Dec 2003 B2
6668929 Griffith et al. Dec 2003 B2
6689208 Brothers Feb 2004 B1
6702044 Reddy et al. Mar 2004 B2
6706108 Polston Mar 2004 B2
6708760 Chatterji et al. Mar 2004 B1
6716282 Griffith et al. Apr 2004 B2
6729405 DiLullo et al. May 2004 B2
6767398 Trato Jul 2004 B2
6776237 Dao et al. Aug 2004 B2
6796378 Reddy et al. Sep 2004 B2
6797054 Chatterji et al. Sep 2004 B2
6823940 Reddy et al. Nov 2004 B2
6832652 Dillenbeck et al. Dec 2004 B1
6835243 Brothers et al. Dec 2004 B2
6837316 Reddy et al. Jan 2005 B2
6846357 Reddy et al. Jan 2005 B2
6848519 Reddy et al. Feb 2005 B2
6887833 Brothers et al. May 2005 B2
6889767 Reddy et al. May 2005 B2
6904971 Brothers et al. Jun 2005 B2
6908508 Brothers Jun 2005 B2
6911078 Barlet-Gouedard et al. Jun 2005 B2
7022755 Chatterji et al. Apr 2006 B1
7048053 Santra et al. May 2006 B2
7077203 Roddy et al. Jul 2006 B1
7174962 Roddy et al. Feb 2007 B1
7199086 Roddy et al. Apr 2007 B1
7204307 Roddy et al. Apr 2007 B2
7204310 Roddy et al. Apr 2007 B1
7213646 Roddy et al. May 2007 B2
7284609 Roddy et al. Oct 2007 B2
7335252 Roddy et al. Feb 2008 B2
7337842 Roddy et al. Mar 2008 B2
7338923 Roddy et al. Mar 2008 B2
7341104 Roddy et al. Mar 2008 B2
7353870 Roddy et al. Apr 2008 B2
7381263 Roddy et al. Jun 2008 B2
7387675 Roddy et al. Jun 2008 B2
7395860 Roddy et al. Jul 2008 B2
7404855 Chatterji et al. Jul 2008 B2
7409990 Burts et al. Aug 2008 B1
7445669 Roddy et al. Nov 2008 B2
7478675 Roddy et al. Jan 2009 B2
7607482 Roddy et al. Oct 2009 B2
7607484 Roddy et al. Oct 2009 B2
7631692 Roddy et al. Dec 2009 B2
7674332 Roddy et al. Mar 2010 B2
7743828 Roddy et al. Jun 2010 B2
7789150 Roddy et al. Sep 2010 B2
7815880 Constantz et al. Oct 2010 B2
7922809 Constantz et al. Apr 2011 B1
8006446 Constantz et al. Aug 2011 B2
20020033121 Marko Mar 2002 A1
20020073897 Trato Jun 2002 A1
20020117090 Ku Aug 2002 A1
20030116065 Griffith et al. Jun 2003 A1
20030116887 Scott Jun 2003 A1
20030167970 Polston Sep 2003 A1
20040007162 Morioka et al. Jan 2004 A1
20040040475 De La Roij et al. Mar 2004 A1
20040079260 Datta et al. Apr 2004 A1
20040107877 Getzlaf et al. Jun 2004 A1
20040108113 Luke et al. Jun 2004 A1
20040112600 Luke et al. Jun 2004 A1
20040129181 Lalande et al. Jul 2004 A1
20040187740 Timmons Sep 2004 A1
20040188091 Luke et al. Sep 2004 A1
20040191439 Bour et al. Sep 2004 A1
20040211562 Brothers et al. Oct 2004 A1
20040211564 Brothers et al. Oct 2004 A1
20040244650 Brothers Dec 2004 A1
20040244977 Luke et al. Dec 2004 A1
20040256102 Trato Dec 2004 A1
20040262000 Morgan et al. Dec 2004 A1
20050000734 Getzlaf et al. Jan 2005 A1
20050034867 Griffith et al. Feb 2005 A1
20050056191 Brothers et al. Mar 2005 A1
20050061505 Caveny et al. Mar 2005 A1
20050072599 Luke et al. Apr 2005 A1
20050077045 Chatterj et al. Apr 2005 A1
20050084334 Shi et al. Apr 2005 A1
20050098317 Reddy et al. May 2005 A1
20050133221 Chatterji et al. Jun 2005 A1
20060025312 Santra et al. Feb 2006 A1
20060054319 Fyten Mar 2006 A1
20060081372 Dealy et al. Apr 2006 A1
20060166834 Roddy Jul 2006 A1
20060260512 Nordmeyer Nov 2006 A1
20070056475 Roddy et al. Mar 2007 A1
20070056479 Gray Mar 2007 A1
20070102157 Roddy et al. May 2007 A1
20070137528 Le Roy-Delage et al. Jun 2007 A1
20070186820 O'Hearn Aug 2007 A1
20070289744 Bingamon Dec 2007 A1
20080092780 Bingamon et al. Apr 2008 A1
20080156491 Roddy et al. Jul 2008 A1
20080229979 Lewis Sep 2008 A1
20090044726 Brouillette et al. Feb 2009 A1
20090105099 Warrender et al. Apr 2009 A1
20090120644 Roddy et al. May 2009 A1
20090124522 Roddy et al. May 2009 A1
20090266543 Reddy et al. Oct 2009 A1
20090312445 Roddy et al. Dec 2009 A1
20090320720 Roddy et al. Dec 2009 A1
20100041792 Roddy et al. Feb 2010 A1
20100044043 Roddy et al. Feb 2010 A1
20100077922 Constantz et al. Apr 2010 A1
20100196104 Constantz et al. Aug 2010 A1
20100258035 Constantz et al. Oct 2010 A1
20100258312 Brenneis et al. Oct 2010 A1
20100273912 Roddy et al. Oct 2010 A1
20100282466 Brenneis et al. Nov 2010 A1
20100292365 Roddy et al. Nov 2010 A1
20100294496 Woytowich et al. Nov 2010 A1
20100313793 Constantz et al. Dec 2010 A1
20110000400 Roddy Jan 2011 A1
20110017452 Benkley Jan 2011 A1
20110100626 Brenneis May 2011 A1
Foreign Referenced Citations (29)
Number Date Country
2064682 Apr 1992 CA
2336077 Jan 2000 CA
2153372 Jan 2006 CA
1054620 Nov 1997 CN
0814067 Dec 1997 EP
1092693 Apr 2001 EP
1236701 Sep 2002 EP
1394137 Jul 2003 EP
1348831 Oct 2003 EP
2075303 Jul 2009 EP
1469954 Apr 1997 GB
52117316 Oct 1977 JP
10110487 Apr 1998 JP
2026959 Jan 1995 RU
2003136028 May 2005 RU
1373781 Feb 1988 SU
WO 8301443 Sep 1982 WO
WO 9854108 Dec 1998 WO
WO 0063134 Jan 2000 WO
WO 03031364 Apr 2003 WO
WO 2004101951 Nov 2004 WO
WO 2004101952 Nov 2004 WO
WO 2005047212 May 2005 WO
WO 2005061846 Jul 2005 WO
WO 2006032841 Mar 2006 WO
WO 2007028952 Mar 2007 WO
WO 2007048999 May 2007 WO
WO 2007128945 Nov 2007 WO
WO 2009138747 Nov 2009 WO
Related Publications (1)
Number Date Country
20100292365 A1 Nov 2010 US
Divisions (2)
Number Date Country
Parent 12609993 Oct 2009 US
Child 12844612 US
Parent 12034886 Feb 2008 US
Child 12349676 US
Continuation in Parts (3)
Number Date Country
Parent 12420630 Apr 2009 US
Child 12609993 US
Parent 12349676 Jan 2009 US
Child 12420630 US
Parent 11223669 Sep 2005 US
Child 12034886 US