The present invention relates to well treatment fluids and methods utilizing nano-particles and, in certain embodiments, to sealant compositions and methods utilizing nano-particles.
A variety of different sealant compositions may be used in subterranean operations. For example, in subterranean well construction, a pipe string (e.g., casing and liners) may be run into a well bore and cemented in place using a cement composition. The process of cementing the pipe string in place is commonly referred to as “primary cementing.” In a typical primary cementing method, a cement composition may be pumped into an annulus between the walls of the well bore and the exterior surface of the pipe string disposed therein. The cement composition sets in the annular space, thereby forming an annular sheath of hardened, substantially impermeable cement that supports and positions the pipe string in the well bore and bonds the exterior surface of the pipe string to the subterranean formation. Among other things, the annular sheath of set cement surrounding the pipe string should seal the annulus, preventing the migration of fluids in the annulus, as well as protecting the pipe string from corrosion. Cement compositions also may be used in remedial cementing methods, such as squeeze cementing, repairing casing strings and the placement of cement plugs. In squeeze cementing, for example, a cement composition may be used to plug off and seal undesirable flow passages in a cement sheath, casing, and/or gravel packs. In some instances, cement compositions may be used to change the direction of the well bore, for example, by drilling a pilot hole in a hardened mass of cement, commonly referred to as a “kickoff plug,” placed in the well bore. While a cement composition is one type of sealant composition that may be used in subterranean operations, other non-cement containing cement sealant compositions also may be employed. By way of example, polymeric sealant compositions also may be used.
The present invention relates to well treatment fluids and methods utilizing nano-particles and, in certain embodiments, to sealant compositions and methods utilizing nano-particles.
An embodiment of the present invention includes a method comprising introducing a sealant composition comprising nano-particles and water into a subterranean formation. The nano-particles may comprise at least about 75% by weight of dry particles in the sealant composition.
Another embodiment of the present invention includes a method comprising preparing a sealant composition comprising nano-particles and water. The nano-particles may comprise at least about 20% by weight of dry particles in the sealant composition. At least a portion of the nano-particles may be introduced into the sealant composition in a liquid suspension.
Another embodiment of the present invention includes a method comprising including agglomerated nano-particles in a sealant composition. The method further may comprise introducing the sealant composition into a subterranean formation.
Another embodiment of the present invention includes a method comprising introducing a sealant composition comprising nano-particles, water, and an elastomeric particle into a subterranean formation.
Another embodiment of the present invention includes a method comprising introducing a sealant composition comprising nano-particles, water, and a swellable particle into a subterranean formation.
Yet another embodiment of the present invention includes a sealant composition comprising nano-particles and water. The nano-particles may comprise at least 75% by weight of dry particles in the sealant composition.
The features and advantages of the present invention will be apparent to those skilled in the art upon reading the following description of specific embodiments.
The present invention relates to well treatment fluids and methods utilizing nano-particles and, in certain embodiments, to sealant compositions and methods utilizing nano-particles. As used herein, the term “sealant composition(s)” refers to a composition(s) that hydraulically sets or otherwise develops compressive strength suitable for use in a subterranean formation application.
An embodiment of the sealant compositions of the present invention may comprise nano-particles and water. Generally, the term “nano-particle” may be defined as a particle having a mean particle size of about 1 nanometers (“nm”) to about 100 nm (e.g., about 5 nm, about 10, about 20 nm, about 30 nm, about 40 nm, about 50 nm, about 60 nm, about 70 nm, about 80 nm, about 90 nm, etc.). In accordance with embodiments of the present invention, the nano-particles may be included in the sealant compositions in a number of different forms, including, for example, as discrete nano-particles, encapsulated nano-particles, agglomerated nano-particles, or in a liquid suspension. In certain embodiments, the nano-particles may comprise at least about 1% by weight of the dry particles in the sealant composition. The term “dry particles” refers to the nano-particles and other solid particles that are present in a dry form at some point either prior to or during introduction into the sealant composition. In certain instances, the dry particles may be suspended in a liquid medium prior to introduction in the sealant composition.
One of the many potential advantages of using nano-particles in embodiments of the sealant compositions is that the inclusion of nano-particles can provide sealant compositions having improved mechanical properties after setting. For example, embodiments of the sealant compositions may have improved compressive strength, tensile strength, Young's modulus and Poisson's ratio. In addition, nano-particles (e.g., nano-silica) also may be included in sealant compositions as a set accelerator to accelerate the set time of the sealant composition. Among other advantages of using nano-particles is that since nano-particles are small, the nano-particles should be capable of invading narrow opening that standard cements may not be able to access. Accordingly, sealant compositions comprising nano-particles may be suitable for use, for example, in squeeze operations. For example, embodiments of the sealant compositions may be seal voids in a pipe string, cement sheath, or gravel pack. As used herein, the term “void” refers to any type of space, including fractures, holes, cracks, spaces, channels, and the like. It is believed that the nano-particles should be able to penetrate voids that are not repairable with larger-sized cements.
Examples of suitable nano-particles may include nano-hydraulic cements, nano-silicas, nano-clays, nano-alumina, nano-zinc oxide, nano-boron, nano-iron oxide and combinations thereof. Nano-hydraulic cements have a variety of applications for well cementing, including both primary and remedial cementing operations. A suitable nano-hydraulic cement and technique that may be used to measure particle size, in accordance with embodiments of the present invention, is described by S C Halim, T J Brunner, R N Grass, M Bohner and W J Stark, Preparation of an Ultra Fast Binding Cement from Calcium Silicate-Based Mixed Oxide Nanoparticles, NANOTECHNOLOGY 18 (2007) 395701 (6 pp). Among other advantages of using nano-hydraulic cement is that it should provide a sealant composition with a lower density and reduced set time. It is believed that the reduced set time of the nano-hydraulic cement may be from early reactivity.
Generally, any hydraulic cement suitable for use in subterranean operations and sized to a range of about 1 nm to about 100 nm may be suitable for use as a nano-hydraulic cement in embodiments in the present invention. Suitable cements that may, for example, be ground to nano-hydraulic cements include those classified as Classes A through H according to American Petroleum Institute, API Specification for Materials and Testing for Well Cements, API Specification 10, Fifth Ed., Jul. 1, 1990. In certain embodiments, API Class A, C, G and H hydraulic cements may be preferred. In addition, in some embodiments, other cements that may be suitable for grinding to nano-hydraulic cements suitable for use in the present invention may be classified as ASTM Type I, II, or III. A variety of nano-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 nano-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, or mixtures thereof.
The nano-hydraulic cement may be present in embodiments of the sealant compositions of the present invention in an amount of from about 0.01% to 100% by weight of cementitious material. As used herein, the term “cementitious material” refers to nano-hydraulic cement, hydraulic cement, cement kiln dust, and the like, which set and harden by reaction with water. In some embodiments, the nano-hydraulic cement may be present in the sealant compositions of the present invention in an amount of about 1% to 75% by weight of cementitious material (e.g., about 5%, about 10%, about 20%, about 30%, about 40%, about 50%, about 60%, about 70%, etc.). In some embodiments, the nano-hydraulic cement may be present in the sealant compositions of the present invention in an amount of about 1% to about 50% by weight of cementitious material. In some embodiments, the nano-hydraulic cement may be present in the sealant compositions of the present invention in an amount of about 1% to about 25% by weight of cementitious material.
Another example of a suitable nano-particle that may be included in embodiments of the sealant compositions of the present invention includes nano-silica. It is now recognized that the nano-silica utilized with present embodiments, which may include silicon dioxide, may have an impact on certain physical characteristics of sealant compositions after setting. For example, relative to inclusion of colloidal silica or larger silica particles in a sealant composition, inclusion of particulate nano-silica in the sealant composition may provide improved mechanical properties, such as compressive strength, tensile strength, Young's modulus and Poisson's ratio. In addition, particulate nano-silica also may be included in the sealant composition as a set accelerator to accelerate the set time of the sealant composition. Accordingly, a sealant composition in accordance with present embodiments may comprise a sufficient amount of nano-silica to provide the desired characteristics. In certain embodiments, the nano-silica may be present in the sealant compositions in an amount in the range of from about 1% to about 25% by weight of cementitious materials (e.g., about 2%, about 5%, about 10%, about 15%, about 20%, etc.). In certain embodiments, the nano-silica may be present in the sealant compositions in an amount in the range of from about 5% to about 15% by weight of cementitious materials.
The nano-silica may, for example, be described as particulate nano-silica. That is, the nano-silica may be particulate in nature and not, for example, a colloidal silica or a suspension of silica in solution. Indeed, in one embodiment, the particulate nano-silica may be added to the sealant composition as a dry nano-silica powder. However, colloidal nano-silica also may be suitable for use in embodiments of the present invention. In certain embodiments, the nano-silica may have a mean particle size of less than about 100 nm, for example, in the range of from about 1 nm to about 100 nm. In further embodiments, the nano-silica may have a mean particle size of less than about 50 nm, for example in the range of from about 5 nm to about 50 nm. In further embodiments, the nano-silica may have a particle size of less than or equal to about 30 nm, for example, in the range of from about 5 nm to about 30 nm. However, it should be noted that the nano-silica may be utilized in combination with larger sized silica particles in accordance with present embodiments.
Another example of a suitable nano-particle that may be included in embodiments of the sealant compositions of the present invention includes nano-clay. An example of a suitable nano-clay includes nano-bentonite. In one particular embodiment, the nano-clay may comprise nano-montmorillonite. Nano-montmorillonite is member of the smectite-clay family, and belongs to the general mineral group of clays with a sheet-like structure where the dimensions in two directions far exceed its thickness. Generally, the nano-montmorillonite has of a three-layered structure of aluminum sandwiched between two layers of silicon, similar to the mica-type layered silicates. Montmorillonite is an active and major ingredient in a volcanic ash called bentonite, which has an ability to swell to many times its original weight and volume when it absorbs water. One example of a suitable nano-montmorillonite is NANOMER® nanoclay, which is available from Nanocor, Arlington Heights, Ill.
It is now recognized that the nano-clay utilized with present embodiments may have an impact on certain physical characteristics of sealant compositions after setting. For example, relative to inclusion of larger clay particles in a sealant composition, inclusion of nano-clay in particular sealant compositions may provide improved mechanical properties. In addition, the nano-clay also may be included in embodiments of the sealant composition to reduce the permeability of the resultant set cement, thus potentially reducing the susceptibility of the set cement to problems associated with gas migration or corrosive environments such as those created by CO2. For example, a sealant composition may be designed to have reduced permeability after setting by including nano-clay in the sealant composition. Accordingly, a sealant composition in accordance with present embodiments may comprise a sufficient amount of nano-clay to provide the desired characteristics. By way of example, the nano-clay may be present in the sealant compositions in an amount in the range of from about 0.1% to about 25% by weight of cementitious components (e.g., about 0.5%, about 1%, about 5%, about 10%, about 15%, about 20%, etc.). In certain embodiments, the nano-clay may be present in the sealant compositions in an amount in the range of from about 2% to about 10% by weight of cementitious components.
The nano-clay may be configured in any of a variety of different shapes in accordance with embodiments of the present invention. Examples of suitable shapes include nano-clay in the general shape of platelets, shavings, flakes, rods, strips, spheroids, toroids, pellets, tablets, or any other suitable shape. In certain embodiments, the nano-clay may generally have a plate-type structure. Suitable plate-type nano-clays include nano-montmorillonite. Plate-type nano-clay may have a thickness, in certain embodiments of less than about 10 nm and, alternatively, of less than about 2 nm. In certain embodiments, the plate-type nano-clay may have a thickness of about 1 nm. Embodiments of the plate-type nano-clay may have surface dimensions (length and/or width) of about 1 nm to about 600 nm. In certain embodiments, the plate-type nano-clay may have surface dimensions about 300 nm to about 600 nm. It should be understood that plate-type nano-clay having dimensions outside the specific ranges listed in this disclosure are encompassed by the present invention.
As previously mentioned, the nano-particles may comprise at least about 1% by weight of the dry particles (e.g., about 10%, about 25%, about 50%, about 75%, about 80%, about 90%, about 99% etc.,) that were included in the sealant composition. By way of example, the nano-particles may be comprise about 10% to about 100% by weight of the dry particles that were included in the sealant composition. By way of further example, the nano-particles may comprise about 50% about 100% by weight of the dry particles that were included in the sealant composition. It should be understood that the reference to dry particles generally refers to a variety of different additives that may typically be included in a sealant composition in a solid form. Examples of such additives include, but are not limited to, hydraulic cement, cement kiln dust, amorphous silica, crystalline silica, vitrified shale, lost circulation materials, and the like. It should be not be implied from the term “dry particle” that the nano-particles or other dry particles (or solid particles) are dry when introduced into the sealant composition. In certain embodiments, the dry particles may be suspended in a liquid medium prior to introduction in the sealant composition.
The water used in certain embodiments of the sealant compositions of the present invention may be freshwater or saltwater (e.g., water containing one or more salts dissolved therein, seawater, brines, saturated saltwater, etc.). In general, the water may be present in an amount sufficient to form a pumpable slurry. In certain embodiments, the water may be present in the sealant compositions in an amount in the range of about 33% to about 200% by weight of cementitious materials. In certain embodiments, the water may be present in an amount in the range of about 35% to about 70% by weight of cementitious materials.
Embodiments of the sealant compositions of the present invention may further comprise a hydraulic cement that has a mean particle size of greater than about 1 micron. Generally, any of a variety of cements suitable for use in subterranean cementing operations may be used in accordance with embodiments of the present invention. Suitable examples include hydraulic cements that comprise 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, pozzolana cements, gypsum cements, high-alumina-content cements, slag cements, and combinations thereof. In certain embodiments, the hydraulic cement may comprise a Portland cement. Portland cements that may be suited for use in embodiments of the present invention may be classified as Class 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, hydraulic cements suitable for use in the present invention may be classified as ASTM Type I, II, or III.
Where present, the larger hydraulic cement generally may be included in embodiments of the sealant compositions in an amount sufficient to provide the desired compressive strength, density, and/or cost. In some embodiments, the larger hydraulic cement may be present in the sealant compositions of the present invention in an amount of about 0.1% to about 99% by weight of cementitious materials. In some embodiments, the hydraulic cement may be present in the sealant compositions of the present invention in an amount of about 0.1% to about 75% by weight of cementitious materials. In some embodiments, the hydraulic cement may be present in the sealant compositions of the present invention in an amount of about 0.1% to about 50% by weight by weight of cementitious materials. In some embodiments, the hydraulic cement may be present in the sealant compositions of the present invention in an amount in the range of from about 0.1% to about 25% by weight of cementitious materials.
In certain embodiments of the present invention, a sealant composition described herein may be foamed using a gas and a foaming and stabilizing surfactant. The gas utilized in the foamed sealant compositions of the present invention may be any gas suitable for foaming a sealant composition, including, but not limited to, air or nitrogen, or combinations thereof. Generally, the gas should be present in the foamed sealant compositions of the present invention in an amount sufficient to form a suitable foam. In certain embodiments, the gas may be present in an amount in the range of from about 10% and about 80% by volume of the composition.
Any suitable foaming and stabilizing surfactant may be used in the foamed sealant composition of the present invention. Among other things, the foaming and stabilizing surfactants may facilitate the foaming of a sealant composition and/or also stabilize the resultant foamed sealant composition formed therewith. Suitable foaming and stabilizing surfactants may include, but are not limited to: mixtures of an ammonium salt of an alkyl ether sulfate, a cocoamidopropyl betaine surfactant, a cocoamidopropyl dimethylamine oxide surfactant, sodium chloride, and water; mixtures of an ammonium salt of an alkyl ether sulfate surfactant, a cocoamidopropyl hydroxysultaine surfactant, a cocoamidopropyl dimethylamine oxide surfactant, sodium chloride, and water; hydrolyzed keratin; mixtures of an ethoxylated alcohol ether sulfate surfactant, an alkyl or alkene amidopropyl betaine surfactant, and an alkyl or alkene dimethylamine oxide surfactant; aqueous solutions of an alpha-olefinic sulfonate surfactant and a betaine surfactant; and combinations thereof. An example of a suitable hydrolyzed keratin is described in U.S. Pat. No. 6,547,871, the disclosure of which is incorporated herein by reference. Example of suitable mixtures of an ethoxylated alcohol ether sulfate surfactant, an alkyl or alkene amidopropyl betaine surfactant, and an alkyl or alkene dimethylamine oxide surfactant is described in U.S. Pat. No. 6,063,738, the disclosure of which is incorporated herein by reference. Examples of suitable aqueous solutions of an alpha-olefinic sulfonate surfactant and a betaine surfactant are described in U.S. Pat. No. 5,897,699, the disclosure of which is incorporated herein by reference. In one embodiment, the foaming and stabilizing surfactant comprises a mixture of an ammonium salt of an alkyl ether sulfate, a cocoamidopropyl betaine surfactant, a cocoamidopropyl dimethylamine oxide surfactant, sodium chloride, and water.
Where used, the foaming and stabilizing surfactants may be present in embodiments of the foamed sealant compositions of the present invention in an amount sufficient to provide a suitable foam. In some embodiments, the foaming and stabilizing surfactant may be present in an amount in the range of from about 0.8% and about 5% by volume of the water present in the foamed sealant composition.
Embodiments of the sealant compositions of the present invention may also comprise swellable particles. As used herein, a particle is characterized as swelling when it swells upon contact with oil and/or an aqueous fluid (e.g., water). Swellable particles suitable for use in embodiments of the present invention may generally swell by up to about 50% of their original size at the surface. Under downhole conditions, this swelling may be more, or less, depending on the conditions presented. For example, the swelling may be at least 10% at downhole conditions. In some embodiments, the swelling may be up to about 50% under downhole conditions. However, as those of ordinary skill in the art, with the benefit of this disclosure, will appreciate, the actual swelling when the swellable particles are included in a sealant composition may depend on, for example, the concentration of the swellable particles included in the sealant composition. In accordance with embodiments of the present invention, the swellable particles may be included in the sealant composition, for example, to counteract the formation of cracks in the cement sheath and/or micro-annulus between the cement sheath and the pipe string or the formation. In general, the swellable particles should be capable of swelling when contacted by aqueous fluids and/or oil to inhibit fluid flow through the crack and/or micro-annulus. Accordingly, the swellable particles may prevent and/or reduce the loss of zonal isolation in spite of the formation of cracks and/or micro-annulus, potentially resulting in an improved annular seal for the sealant compositions.
An example of swellable particles that may be utilized in embodiments of the present invention comprises a swellable elastomer. Some specific examples of suitable swellable elastomers include, but are not limited to, natural rubber, acrylate butadiene rubber, polyacrylate rubber, isoprene rubber, choloroprene rubber, butyl rubber (IIR), brominated butyl rubber (BIIR), chlorinated butyl rubber (CIIR), chlorinated polyethylene (CM/CPE), neoprene rubber (CR), styrene butadiene copolymer rubber (SBR), sulphonated polyethylene (CSM), ethylene acrylate rubber (EAM/AEM), epichlorohydrin ethylene oxide copolymer (CO, ECO), ethylene-propylene rubber (EPM and EDPM), ethylene-propylene-diene terpolymer rubber (EPT), ethylene vinyl acetate copolymer, fluorosilicone rubbers (FVMQ), silicone rubbers (VMQ), poly 2,2,1-bicyclo heptene (polynorborneane), and alkylstyrene. One example of a suitable swellable elastomer comprises a block copolymer of a styrene butadiene rubber. Examples of suitable elastomers that swell when in contact with oil include, but are not limited to, nitrile rubber (NBR), hydrogenated nitrile rubber (HNBR, HNS), fluoro rubbers (FKM), perfluoro rubbers (FFKM), tetrafluorethylene/propylene (TFE/P), isobutylene maleic anhydride. Combinations of suitable swellable elastomers also may be used. Other swellable elastomers that behave in a similar fashion with respect to oil or aqueous fluids also may be suitable. Those of ordinary skill in the art, with the benefit of this disclosure, will be able to select an appropriate swellable elastomer for use in embodiments of the sealant compositions of the present invention based on a variety of factors, including the application in which the composition will be used and the desired swelling characteristics.
An example of swellable particles that may be utilized in embodiments of the present invention comprises a water-swellable polymer. Some specific examples of suitable water-swellable polymers, include, but are not limited to starch-polyacrylate acid graft copolymer and salts thereof, polyethylene oxide polymer, carboxymethyl cellulose type polymers, polyacrylamide, poly(acrylic acid) and salts thereof, poly(acrylic acid-co-acrylamide) and salts thereof, graft-poly(ethylene oxide) of poly(acrylic acid) and salts thereof, poly(2-hydroxyethyl methacrylate), and poly(2-hydroxypropyl methacrylate). Combinations of suitable water-swellable polymers also may be used. In certain embodiments, the water-swellable polymers may be crosslinked and/or lightly crosslinked. Other water-swellable polymers that behave in a similar fashion with respect to aqueous fluids also may be suitable. Those of ordinary skill in the art, with the benefit of this disclosure, will be able to select appropriate water-swellable polymers for use in embodiments of the sealant compositions of the present invention based on a variety of factors, including the application in which the composition will be used and the desired swelling characteristics.
Where used, the swellable particles generally may be included in the sealant compositions in an amount sufficient to provide the desired mechanical properties. In some embodiments, the swellable particles may be present in the sealant compositions in an amount up to about 25% by weight of the cementitious component. In some embodiments, the swellable particles may be present in the sealant compositions in a range of about 5% to about 25% by weight of the cementitious component. In some embodiments, the swellable particles may be present in the sealant compositions in a range of about 15% to about 20% by weight of the cementitious component.
In addition, the swellable particles that are utilized may have a wide variety of shapes and sizes of individual particles suitable for use in accordance with embodiments of the present invention. By way of example, the swellable particles may have a well-defined physical shape as well as an irregular geometry, including the physical shape of platelets, shavings, fibers, flakes, ribbons, rods, strips, spheroids, beads, pellets, tablets, or any other physical shape. In some embodiments, the swellable particles may have a particle size in the range of about 5 microns to about 1,500 microns. In some embodiments, the swellable particles may have a particle size in the range of about 20 microns to about 500 microns. However, particle sizes outside these defined ranges also may be suitable for particular applications.
Other additives suitable for use in subterranean cementing operations also may be added to embodiments of the sealant compositions, in accordance with embodiments of the present invention. Examples of such additives include, but are not limited to, strength-retrogression additives, set accelerators, set retarders, weighting agents, lightweight additives, gas-generating additives, mechanical property enhancing additives, lost-circulation materials, filtration-control additives, dispersants, a fluid loss control additive, defoaming agents, foaming agents, thixotropic additives, and combinations thereof. Specific examples of these, and other, additives include crystalline silica, amorphous silica, fumed silica, salts, fibers, hydratable clays, calcined shale, vitrified shale, microspheres, fly ash, slag, diatomaceous earth, metakaolin, rice husk ash, natural pozzolan (e.g., pumicite), zeolite, cement kiln dust, lime, elastomers, elastomeric particles, resins, latex, combinations thereof, and the like. One example of a suitable elastomeric particle comprises a block copolymer of a styrene butadiene rubber as set forth in U.S. Pat. No. 6,832,651, the disclosure of which is incorporated herein by reference. 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.
Embodiments of the sealant compositions of the present invention may have a density suitable for a particular application. By way of example, the sealant compositions may have a density in the range of from about 4 pounds per gallon (“ppg”) to about 20 ppg. In certain embodiments, the sealant compositions may have a density in the range of from about 8 ppg to about 17 ppg. Embodiments of the sealant compositions may be foamed or unfoamed or may comprise other means to reduce their densities, such as hollow microspheres, low-density elastic beads, or other density-reducing additives known in the art. Those of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate density for a particular application.
As will be appreciated by those of ordinary skill in the art, certain embodiments of the sealant compositions of the present invention may be used for forming a seal in a variety of subterranean applications. In certain embodiments, a sealant composition may be introduced into a subterranean formation and allowed to form a seal therein. In certain embodiments, the sealant composition may comprise a cement composition that sets in the subterranean formation to form the seal. By way of example, in certain primary cementing embodiments, a sealant composition may be introduced into a space between a subterranean formation and a pipe string located in the subterranean formation. The sealant composition may be allowed to set to form a hardened mass in the space between the subterranean formation and the pipe string. Embodiments of the present invention further may comprise running the pipe string into a well bore penetrating the subterranean formation. In addition, in certain remedial cementing embodiments, a sealant composition may be used, for example, in squeeze-cementing operations or in the placement of cement plugs. For example, embodiments of the sealant compositions may used to: penetrate a gravel pack to shut off water or gas production, penetrate a gravel pack to divert steam injections, and penetrate a gravel pack to plug and abandon a well. One or more hydrocarbons (e.g., oil, gas, etc.) may be produced from a well bore penetrating the subterranean formation in accordance with embodiments of the present invention.
In addition to incorporation of the nano-particles in a dry free-flowing state, embodiments of the present invention may include incorporating the nano-particles in an agglomerated form. Among other things, use of agglomerated nano-particles should facilitate the use of nano-particles in subterranean applications, for example, by alleviating potential handling problems. In general, agglomerated nano-particles may include discrete nano-particles that have been collected to form a cohesive mass. Any of a variety of different techniques may be used to agglomerate the nano-particles for use in embodiments of the present invention. In certain embodiments, agglomerated nano-particles may comprise nano-particles bound together by a water-soluble binder. By way of example, agglomerated nano-particles may be prepared by depositing the water-soluble binder onto the nano-particles such that the binder holds the nano-particles together. Agglomerated nano-particles also may include nano-particles that have been pelletized. Generally, the nano-particles may be formed into pellets of any desired shape and/or size by any suitable technique, including, but not limited to, compression, extrusion, and casting. Example methods of agglomeration are set forth in U.S. Pat. Nos. 5,454,867; 6,500,253; 6,861,392; and 7,156,174, the disclosures of which are incorporated herein by reference.
Agglomeration of the nano-particles generally may aid with mixing and bulk transfer of nano-particles. However, when the agglomerated nano-particles are contacted with water, the agglomerated nano-particle should disperse into discrete nano-particles in accordance with embodiments of the present invention. For example, the agglomerated nano-particles may be designed to immediately disperse into discrete nano-particles when mixed with water. By way of further example, the agglomerated nano-particles may be designed to disperse after a chosen delay period. In certain embodiments, a degradable material may be incorporated into the agglomerated nano-particles, for example, to facilitate delayed release of the nano-particles. Examples of suitable degradable materials include, but are not limited to, a dextran, a cellulose, a chitin, a chitosan, a liquid ester (e.g., triethyl citrate), a protein (e.g., gelatin), an aliphatic polyester (e.g., polylactic acid), a poly(glycolide), a poly(ε-caprolactone), a poly (hydroxybutyrate), a poly(anhydride), an aliphatic polycarbonate, an ortho ester, a poly(orthoester), a poly(amino acid), a poly(ethylene oxide), a polyphosphazene, and combinations thereof.
Another technique for alleviated potential handling problems associated with incorporation of the nano-particles in a dry free-flowing state may include incorporating nano-particles a liquid suspension (e.g., colloid suspension). For example, the nano-particles dispersed in a continuous liquid phase may be incorporated into embodiments of the sealant compositions. Suspension of the nano-particles in a liquid medium generally may aid with mixing and bulk transfer of nano-particles, but the nano-particles should release from the suspension when mixed with the sealant composition in accordance with present embodiments.
Contained nano-particles also may be used in certain embodiments of the present invention. Specifically, containment of the nano-particles in accordance with embodiments of the present invention may include enclosing the nano-particles within an outer coating or container in particulate form. Certain methods of encapsulation are set forth in U.S. Pat. Nos. 5,373,901; 6,444,316; 6,527,051; 6,554,071; 7,156,174; and 7,204,312, the disclosures of which are incorporated herein by reference.
Various types of containment may be employed, in certain embodiments, such that the nano-particles (e.g., the nano-hydraulic cement) are contained but retain their particulate nature and, thus, retain their corresponding impact on physical properties of sealant composition. For example, the nano-particles may be contained within a bag, capsule, layer, coating or the like. Further, the material utilized to contain the nano-particles may be selected to facilitate transportation and/or incorporation of the nano-particles into a sealant composition. For example, to facilitate handling of the nano-particles and/or to facilitate timed release of the nano-particles, the containment material may be degradable. This may facilitate handling of the nano-particles by allowing inclusion of the contained nano-particles in a sealant composition without requiring that the nano-particles first be removed from the containment material. Further, the containing material may be designed to degrade at a certain rate when in contact with certain materials (e.g., water) so that the nano-particles are released into the sealant composition at a desired time. Certain water-dissolvable materials that may be utilized to encapsulate the nano-particles are described in U.S. Pat. Nos. 4,961,790 and 5,783,541, the disclosures of which are incorporated herein by reference.
In accordance with certain embodiments, the sealant compositions of the present invention may utilize a packing volume fraction suitable for a particular application as desired. As used herein, the term “packing volume fraction” refers to the volume of the particulate materials in a fluid divided by the total volume of the fluid. The size ranges of the preferred particulate materials are selected, as well as their respective proportions, in order to provide a maximized packing volume fraction so that the fluid is in a hindered settling state. It is known that, in such a state, the particulate materials behave “collectively” like a porous solid material. The hindered settling state is believed to correspond, in practice, to a much higher solid material concentration in the fluid than that present in the some traditional sealant compositions. Packing volume fraction is described in further detail in U.S. Pat. No. 7,213,646, the disclosure of which is incorporated herein by reference.
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,” “having,” 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.
The present application is a continuation-in-part of U.S. patent application Ser. No. 12/263,954, filed Nov. 3, 2008, entitled “Cement Compositions and Methods Utilizing Nano-Hydraulic Cement,” which is a continuation-in-part of U.S. patent application Ser. No. 11/747,002, now U.S. Pat. No. 7,559,369, filed on May 10, 2007, entitled “Well Treatment Compositions and Methods Utilizing Nano-Particles.” The entire disclosures of these applications are incorporated herein by reference.
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 |
2857286 | Striker | Oct 1958 | A |
2871133 | Palonen et al. | Jan 1959 | A |
2880096 | Hurley | Mar 1959 | A |
2890169 | Prokop | Jun 1959 | A |
2933135 | Johnson | Apr 1960 | A |
2945769 | Game et al. | Jul 1960 | A |
2952318 | Ritch | Sep 1960 | A |
2959223 | Harmon et al. | Nov 1960 | A |
2978024 | Davis | Apr 1961 | A |
3026938 | Huitt et al. | Mar 1962 | A |
3079268 | Brooks | Feb 1963 | A |
3168139 | Kennedy et al. | Feb 1965 | A |
3219112 | Sauber et al. | Nov 1965 | A |
3336979 | Ingraham et al. | Aug 1967 | A |
3353601 | Dollarhide et al. | Nov 1967 | A |
3366177 | Powers et al. | Jan 1968 | A |
3381748 | Peters et al. | May 1968 | A |
3454095 | Messenger et al. | Jul 1969 | A |
3467193 | Messenger | Sep 1969 | A |
3499491 | Wyant et al. | Mar 1970 | A |
3557876 | Tragesser | Jan 1971 | A |
3607326 | Serafin | Sep 1971 | A |
RE27271 | Hamsberger et al. | Jan 1972 | E |
3748159 | George | Jul 1973 | A |
3854985 | Suzuki et al. | Dec 1974 | A |
3876005 | Fincher et al. | Apr 1975 | A |
3877522 | Knight et al. | Apr 1975 | A |
3887009 | Miller et al. | Jun 1975 | A |
3887385 | Quist et al. | Jun 1975 | A |
3888311 | Cooke, Jr. | Jun 1975 | A |
3958638 | Johnston | May 1976 | A |
4018617 | Nicholson | Apr 1977 | A |
4031184 | McCord | Jun 1977 | A |
4036301 | Powers et al. | Jul 1977 | A |
4142910 | Kraemer et al. | Mar 1979 | A |
4176720 | Wilson | Dec 1979 | A |
4202413 | Messenger | May 1980 | A |
4202795 | Burnham et al. | May 1980 | A |
4235291 | Messenger | Nov 1980 | A |
4268316 | Wills et al. | May 1981 | A |
4274881 | Langton et al. | Jun 1981 | A |
4284433 | Aignesberger et al. | Aug 1981 | A |
4341562 | Ahlbeck | Jul 1982 | A |
4353746 | Birchall et al. | Oct 1982 | A |
RE31190 | Detroit et al. | Mar 1983 | E |
4400474 | Copperthwaite et al. | Aug 1983 | A |
4407677 | Wills et al. | Oct 1983 | A |
4432800 | Kneller et al. | Feb 1984 | A |
4435216 | Diehl et al. | Mar 1984 | A |
4460292 | Durham et al. | Jul 1984 | A |
4494990 | Harris | Jan 1985 | A |
4506734 | Nolte | Mar 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 |
4643362 | Serafin | Feb 1987 | A |
4650520 | Johnsen et al. | Mar 1987 | A |
4660642 | Young | Apr 1987 | A |
4676317 | Fry et al. | Jun 1987 | A |
4676832 | Childs et al. | Jun 1987 | A |
4700777 | Luers | Oct 1987 | A |
4711401 | Serafin | Dec 1987 | A |
4721160 | Parcevaux et al. | Jan 1988 | A |
4741401 | Walles et al. | May 1988 | A |
4741782 | Styron | May 1988 | A |
4770796 | Jacobs | Sep 1988 | A |
4784223 | Worrall et al. | Nov 1988 | A |
4822421 | Crabb | Apr 1989 | A |
4848973 | Yokota et al. | Jul 1989 | A |
4883125 | Wilson et al. | Nov 1989 | A |
4941536 | Brothers et al. | Jul 1990 | A |
4953620 | Bloys et al. | Sep 1990 | A |
4961790 | Smith et al. | Oct 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 |
5102558 | McDougall et al. | Apr 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 |
5149370 | Olaussen et al. | Sep 1992 | A |
5151203 | Riley et al. | Sep 1992 | A |
5183505 | Spinney | Feb 1993 | A |
5203629 | Valle et al. | Apr 1993 | A |
5207832 | Baffreau et al. | May 1993 | A |
5213160 | Nahm et al. | May 1993 | A |
5236501 | Nomachi et al. | Aug 1993 | A |
5238064 | Dahl et al. | Aug 1993 | A |
5253991 | Yokota et al. | Oct 1993 | A |
5263542 | Brothers | Nov 1993 | A |
5266111 | Barbour | Nov 1993 | A |
5292512 | Schaefer et al. | Mar 1994 | A |
5295543 | Terry et al. | Mar 1994 | A |
5305831 | Nahm | Apr 1994 | A |
5314022 | Cowan et al. | May 1994 | A |
5320851 | Mars et al. | Jun 1994 | A |
5327968 | Onan et al. | Jul 1994 | A |
5337824 | Cowan | Aug 1994 | A |
5339903 | Eoff et al. | Aug 1994 | A |
5340397 | Brothers | Aug 1994 | A |
5346012 | Heathman et al. | Sep 1994 | A |
5352288 | Mallow | Oct 1994 | A |
5358044 | Hale et al. | Oct 1994 | A |
5358047 | Himes 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 |
5373901 | Norman et al. | Dec 1994 | A |
5375661 | Daneshy et al. | Dec 1994 | A |
5382290 | Nahm et al. | Jan 1995 | A |
5383521 | Onan et al. | Jan 1995 | A |
5383967 | Chase | Jan 1995 | A |
5389706 | Heathman et al. | Feb 1995 | A |
5398758 | Onan et al. | Mar 1995 | A |
5398759 | Rodrigues et al. | Mar 1995 | A |
5423379 | Hale et al. | Jun 1995 | A |
5439056 | Cowan | Aug 1995 | A |
5454867 | Brothers et al. | Oct 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 |
5476142 | Kajita | Dec 1995 | A |
5476144 | Nahm et al. | Dec 1995 | A |
5484480 | Styron | Jan 1996 | A |
5494513 | Fu et al. | Feb 1996 | A |
5499677 | Cowan | Mar 1996 | A |
5509962 | Tang | Apr 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 |
5551976 | Allen | Sep 1996 | A |
5569324 | Totten et al. | Oct 1996 | A |
5575841 | Dry | Nov 1996 | A |
5580379 | Cowan | Dec 1996 | A |
5585333 | Dahl et al. | Dec 1996 | A |
5588488 | Vijn et al. | Dec 1996 | A |
5588489 | Chatterji et al. | Dec 1996 | A |
5603961 | Suzuki et al. | Feb 1997 | A |
5660624 | Dry | Aug 1997 | A |
5663230 | Haman | Sep 1997 | A |
5673753 | Hale et al. | Oct 1997 | A |
5688844 | Chatterji et al. | Nov 1997 | A |
5693137 | Styron | Dec 1997 | A |
5711383 | Terry et al. | Jan 1998 | A |
5716910 | Totten et al. | Feb 1998 | A |
5728209 | Bury et al. | Mar 1998 | A |
5728654 | Dobson et al. | Mar 1998 | A |
5741357 | Sheikh | Apr 1998 | A |
5766323 | Butler et al. | Jun 1998 | A |
5779787 | Brothers et al. | Jul 1998 | A |
5783541 | Tack et al. | Jul 1998 | A |
5795060 | Stephens | Aug 1998 | A |
5820670 | Chatterji et al. | Oct 1998 | A |
5851960 | Totten et al. | Dec 1998 | A |
5866516 | Costin | Feb 1999 | A |
5874387 | Carpenter et al. | Feb 1999 | A |
5879699 | Lerner | Mar 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 |
5989334 | Dry | Nov 1999 | A |
6022408 | Stokes et al. | Feb 2000 | A |
6027561 | Gruber 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 |
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 |
6261360 | Dry | Jul 2001 | B1 |
6277189 | Chugh | Aug 2001 | B1 |
6279655 | Pafitis et al. | Aug 2001 | B1 |
6312515 | Barlet-Gouedard et al. | Nov 2001 | B1 |
6315042 | Griffith et al. | Nov 2001 | B1 |
6332921 | Brothers et al. | Dec 2001 | B1 |
6367550 | Chatterji et al. | Apr 2002 | B1 |
6379456 | Heathman et al. | Apr 2002 | B1 |
6390197 | Maroy | May 2002 | B1 |
6402833 | O'Hearn et al. | Jun 2002 | B1 |
6409819 | Ko | Jun 2002 | B1 |
6444316 | Reddy et al. | Sep 2002 | B1 |
6457524 | Roddy | Oct 2002 | B1 |
6471975 | Banovetz et al. | 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 |
6500253 | Norman et al. | Dec 2002 | B2 |
6502636 | Chatterji et al. | Jan 2003 | B2 |
6508305 | Brannon et al. | Jan 2003 | B1 |
6524384 | Griffith et al. | Feb 2003 | B2 |
6527051 | Reddy et al. | Mar 2003 | B1 |
6527849 | Dry | Mar 2003 | B2 |
6547871 | Chatterji et al. | Apr 2003 | B2 |
6547891 | Linden et al. | Apr 2003 | B2 |
6554067 | Davies et al. | Apr 2003 | B1 |
6554071 | Reddy et al. | Apr 2003 | B1 |
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 |
6599863 | Palmer et al. | Jul 2003 | B1 |
6610139 | Reddy et al. | Aug 2003 | B2 |
6626243 | Go Boncan | Sep 2003 | B1 |
6631766 | Brothers et al. | Oct 2003 | B2 |
6632527 | McDaniel et al. | Oct 2003 | B1 |
6645288 | Dargaud et al. | Nov 2003 | B1 |
6645290 | Barbour | Nov 2003 | B1 |
6648962 | Berke et al. | Nov 2003 | B2 |
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 |
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 |
6808561 | Genge | Oct 2004 | B2 |
6811603 | Brothers et al. | Nov 2004 | B2 |
6823940 | Reddy et al. | Nov 2004 | B2 |
6832651 | Ravi et al. | Dec 2004 | B2 |
6835243 | Brothers et al. | Dec 2004 | B2 |
6837316 | Reddy et al. | Jan 2005 | B2 |
6840318 | Lee | Jan 2005 | B2 |
6846357 | Reddy et al. | Jan 2005 | B2 |
6848519 | Reddy et al. | Feb 2005 | B2 |
6861392 | Shaarpour | Mar 2005 | B2 |
6874578 | Garnier et al. | Apr 2005 | B1 |
6883609 | Drochon et al. | Apr 2005 | B2 |
6887833 | Brothers et al. | May 2005 | B2 |
6889767 | Reddy et al. | May 2005 | B2 |
6902001 | Dargaud et al. | Jun 2005 | B2 |
6904971 | Brothers et al. | Jun 2005 | B2 |
6907929 | LeRoy-Delage et al. | Jun 2005 | B2 |
6908508 | Brothers | Jun 2005 | B2 |
6911078 | Barlet-Gouedard et al. | Jun 2005 | B2 |
6926081 | Sweatman et al. | Aug 2005 | B2 |
6962201 | Brothers | Nov 2005 | B2 |
7007755 | Reddy et al. | Mar 2006 | B2 |
7022179 | Dry | Apr 2006 | B1 |
7026272 | Reddy et al. | Apr 2006 | B2 |
7032664 | Lord et al. | Apr 2006 | B2 |
7033975 | Baran et al. | Apr 2006 | B2 |
7048053 | Santra et al. | May 2006 | B2 |
7059415 | Bosma et al. | Jun 2006 | B2 |
7077203 | Roddy et al. | Jul 2006 | B1 |
7084092 | Patel et al. | Aug 2006 | B2 |
7086466 | Roddy | Aug 2006 | B2 |
7138446 | Reddy et al. | Nov 2006 | B2 |
7143828 | Reddy et al. | Dec 2006 | B2 |
7143832 | Freyer | Dec 2006 | B2 |
7156173 | Mueller | Jan 2007 | B2 |
7156174 | Roddy et al. | Jan 2007 | B2 |
7172022 | Reddy et al. | Feb 2007 | B2 |
7174962 | Roddy et al. | Feb 2007 | B1 |
7182137 | Fyten et al. | Feb 2007 | B2 |
7199086 | Roddy et al. | Apr 2007 | B1 |
7204307 | Roddy et al. | Apr 2007 | B2 |
7204310 | Roddy et al. | Apr 2007 | B1 |
7204312 | Roddy et al. | Apr 2007 | B2 |
7213646 | Roddy et al. | May 2007 | B2 |
7264053 | Vargo, Jr. et al. | Sep 2007 | B2 |
7279447 | Lal et al. | Oct 2007 | B2 |
7284609 | Roddy et al. | Oct 2007 | B2 |
7284611 | Reddy et al. | Oct 2007 | B2 |
7294194 | Reddy et al. | Nov 2007 | B2 |
7296597 | Freyer et al. | Nov 2007 | B1 |
7303014 | Reddy et al. | Dec 2007 | B2 |
7335252 | Roddy et al. | Feb 2008 | B2 |
7337841 | Ravi | Mar 2008 | B2 |
7337842 | Roddy et al. | Mar 2008 | B2 |
7338923 | Roddy et al. | Mar 2008 | B2 |
7341104 | Roddy | Mar 2008 | B2 |
7351279 | Brothers | Apr 2008 | B2 |
7353870 | Roddy et al. | Apr 2008 | B2 |
7381263 | Roddy et al. | Jun 2008 | B2 |
7387675 | Roddy et al. | Jun 2008 | B2 |
7393407 | Dingsoyr et al. | Jul 2008 | B2 |
7395860 | Roddy et al. | Jul 2008 | B2 |
7404440 | Reddy et al. | Jul 2008 | B2 |
7409991 | Reddy et al. | Aug 2008 | B2 |
7422060 | Hammami et al. | Sep 2008 | B2 |
7424913 | Roddy | Sep 2008 | B2 |
7445669 | Roddy et al. | Nov 2008 | B2 |
7451817 | Reddy et al. | Nov 2008 | B2 |
7461696 | Nguyen et al. | Dec 2008 | B2 |
7478675 | Roddy et al. | Jan 2009 | B2 |
7482309 | Ravi et al. | Jan 2009 | B2 |
7559369 | Roddy et al. | Jul 2009 | B2 |
7784542 | Roddy et al. | Aug 2010 | B2 |
7806183 | Roddy et al. | Oct 2010 | B2 |
7846876 | Koyanagi | Dec 2010 | B2 |
7892352 | Roddy et al. | Feb 2011 | B2 |
8114820 | Crews | Feb 2012 | B2 |
8202824 | Reddy et al. | Jun 2012 | B2 |
8226879 | Genolet et al. | Jul 2012 | B2 |
8394744 | Woytowich et al. | Mar 2013 | B2 |
8499837 | Koons | Aug 2013 | B2 |
8586512 | Roddy et al. | Nov 2013 | B2 |
8598093 | Roddy et al. | Dec 2013 | B2 |
8603952 | Roddy et al. | Dec 2013 | B2 |
8609595 | Morgan et al. | Dec 2013 | B2 |
8685903 | Ravi et al. | Apr 2014 | B2 |
8822386 | Quintero et al. | Sep 2014 | B2 |
20020004464 | Nelson et al. | Jan 2002 | A1 |
20020033121 | Marko | Mar 2002 | A1 |
20020073894 | Genge et al. | Jun 2002 | A1 |
20020073897 | Trato | Jun 2002 | A1 |
20020117090 | Ku | Aug 2002 | A1 |
20020193257 | Lee et al. | Dec 2002 | A1 |
20030089281 | Berke et al. | May 2003 | A1 |
20030116065 | Griffith et al. | Jun 2003 | A1 |
20030116887 | Scott | Jun 2003 | A1 |
20030134751 | Lee et al. | Jul 2003 | A1 |
20030167970 | Polston | Sep 2003 | A1 |
20030168215 | Drochon et al. | Sep 2003 | A1 |
20030220204 | Baran et al. | Nov 2003 | A1 |
20030234103 | Lee et al. | Dec 2003 | A1 |
20040007162 | Morioka et al. | Jan 2004 | A1 |
20040040475 | De La Roij et al. | Mar 2004 | A1 |
20040055748 | Reddy 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 |
20040121916 | Kono | Jun 2004 | A1 |
20040144537 | Reddy et al. | Jul 2004 | A1 |
20040171499 | Ravi et al. | Sep 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 |
20040261990 | Bosma et al. | Dec 2004 | A1 |
20040261999 | Nguyen | Dec 2004 | A1 |
20050000734 | Getzlaf et al. | Jan 2005 | A1 |
20050022991 | Rao | Feb 2005 | A1 |
20050034867 | Griffith et al. | Feb 2005 | A1 |
20050056191 | Brothers et al. | Mar 2005 | A1 |
20050061206 | Reddy et al. | Mar 2005 | A1 |
20050072599 | Luke et al. | Apr 2005 | A1 |
20050084334 | Shi et al. | Apr 2005 | A1 |
20050096207 | Urbanek | May 2005 | A1 |
20050098317 | Reddy et al. | May 2005 | A1 |
20050113260 | Wood | May 2005 | A1 |
20050113262 | Ravi et al. | May 2005 | A1 |
20050133221 | Chatterji et al. | Jun 2005 | A1 |
20050173117 | Roddy | Aug 2005 | A1 |
20050199401 | Patel et al. | Sep 2005 | A1 |
20060016598 | Urbanek | Jan 2006 | A1 |
20060025312 | Santra et al. | Feb 2006 | A1 |
20060086503 | Reddy et al. | Apr 2006 | A1 |
20060089851 | Silby et al. | Apr 2006 | A1 |
20060122071 | Reddy et al. | Jun 2006 | A1 |
20060162926 | Roddy | Jul 2006 | A1 |
20060166834 | Roddy | Jul 2006 | A1 |
20060177661 | Smith et al. | Aug 2006 | A1 |
20060260512 | Nordmeyer | Nov 2006 | A1 |
20060260513 | Guiterrez et al. | Nov 2006 | A1 |
20060278131 | Hunt | Dec 2006 | A1 |
20070012436 | Freyer | Jan 2007 | A1 |
20070015668 | Harrower et al. | Jan 2007 | A1 |
20070017676 | Reddy et al. | Jan 2007 | A1 |
20070056475 | Roddy et al. | Mar 2007 | A1 |
20070056479 | Gray | Mar 2007 | A1 |
20070056732 | Roddy et al. | Mar 2007 | A1 |
20070056733 | Roddy et al. | Mar 2007 | A1 |
20070062691 | Reddy et al. | Mar 2007 | A1 |
20070102157 | Rodldy et al. | May 2007 | A1 |
20070125534 | Reddy et al. | Jun 2007 | A1 |
20070137528 | LeRoy-Deluge et al. | Jun 2007 | A1 |
20070151484 | Reddy et al. | Jul 2007 | A1 |
20070151724 | Ohmer et al. | Jul 2007 | A1 |
20070151730 | Reddy et al. | Jul 2007 | A1 |
20070186820 | O'Hearn | Aug 2007 | A1 |
20070204765 | LeRoy-Deluge et al. | Sep 2007 | A1 |
20070227734 | Freyer | Oct 2007 | A1 |
20070246225 | Hailey, Jr. et al. | Oct 2007 | A1 |
20070255457 | Whitcomb et al. | Nov 2007 | A1 |
20070266903 | Gartner et al. | Nov 2007 | A1 |
20080017376 | Badalamenti et al. | Jan 2008 | A1 |
20080058229 | Berkland et al. | Mar 2008 | A1 |
20080099203 | Mueller et al. | May 2008 | A1 |
20080108524 | Willberg et al. | May 2008 | A1 |
20080135250 | Bosma et al. | Jun 2008 | A1 |
20080156491 | Roddy et al. | Jul 2008 | A1 |
20080261027 | Li et al. | Oct 2008 | A1 |
20080261834 | Simon | Oct 2008 | A1 |
20080277116 | Roddy et al. | Nov 2008 | A1 |
20090088348 | Roddy | Apr 2009 | A1 |
20090114126 | Roddy | May 2009 | A1 |
20090120644 | Roddy | May 2009 | A1 |
20090124522 | Roddy | May 2009 | A1 |
20090139719 | Luo | Jun 2009 | A1 |
20090200029 | Roddy et al. | Aug 2009 | A1 |
20090236097 | Roddy | Sep 2009 | A1 |
20090260544 | Roddy | Oct 2009 | A1 |
20090312201 | Huang et al. | Dec 2009 | A1 |
20100016183 | Roddy et al. | Jan 2010 | A1 |
20100025039 | Roddy et al. | Feb 2010 | A1 |
20100075874 | Mercado et al. | Mar 2010 | A1 |
20100095871 | Patil et al. | Apr 2010 | A1 |
20100096135 | Roddy et al. | Apr 2010 | A1 |
20110162845 | Ravi et al. | Jul 2011 | A1 |
20110237467 | Cornette | Sep 2011 | A1 |
20110312857 | Amanullah | Dec 2011 | A1 |
20130312641 | Chatterji et al. | Nov 2013 | A1 |
Number | Date | Country |
---|---|---|
2514492 | Sep 2004 | CA |
2153372 | Jan 2006 | CA |
101544488 | Sep 2009 | CN |
102007042078 | Mar 2009 | DE |
0748782 | Dec 1996 | EP |
0814067 | Dec 1997 | EP |
1236701 | Sep 2002 | EP |
1394137 | Jul 2003 | EP |
1348831 | Oct 2003 | EP |
1686234 | Aug 2006 | EP |
1719741 | Nov 2006 | EP |
2465910 | Nov 2009 | EP |
2787105 | Jun 2000 | FR |
1469954 | Apr 1997 | GB |
2429725 | Mar 2007 | GB |
52117316 | Oct 1977 | JP |
10110487 | Apr 1998 | JP |
1373781 | Feb 1988 | SU |
WO 8301443 | Sep 1982 | WO |
9011977 | Apr 1990 | WO |
9011977 | Oct 1990 | WO |
WO 9705079 | Feb 1997 | WO |
WO 9749644 | Dec 1997 | WO |
WO 9854108 | Dec 1998 | WO |
WO 0063134 | Jan 2000 | WO |
WO 0049272 | Aug 2000 | WO |
WO 0050357 | Aug 2000 | WO |
WO 03008756 | Jul 2001 | WO |
WO 0187796 | Nov 2001 | WO |
WO 03031364 | Apr 2003 | WO |
WO 2004001188 | Dec 2003 | WO |
WO 2004057715 | Jul 2004 | WO |
WO 2004101951 | Nov 2004 | WO |
WO 2004101952 | Nov 2004 | WO |
WO 2005047212 | May 2005 | WO |
WO 2005061846 | Jul 2005 | WO |
WO 2005080287 | Aug 2005 | WO |
WO 2006053896 | Nov 2005 | WO |
WO 2006032841 | Mar 2006 | WO |
2008034461 | Mar 2008 | WO |
WO 2009030758 | Mar 2009 | WO |
Entry |
---|
U.S. Appl. No. 12/426,645, filed Apr. 20, 2009, Roddy. |
Bartlet-Gouedard, “A Non-Conventional Way of Developing Cement Slurry for Geothermal Wells”, 2001. |
Poon, “A Study of the Hydration of Natural Zeolite Blended Cement Pastes”, 1999. |
“Beneficial use of Solid Waste in Maine”, Apr. 14, 2005. |
Smith, “Cementing” Society of Petroleum Engineers, p. 38, 1990. |
Smith, “Cementing” Society of Professional Engineers, pp. 14, 38, 1987. |
Chan, Comparative Study of the Initial Surface Absorption and Chloride Diffusion of High Performance Zeolite Silica Fume and PFA concretes, 1999. |
Rogers, “Designing a Remedial Acid Treatment for Gulf of Mexico Deepwater Turbidite Sands Containing Zeolite Cement”, 1996. |
Janotka, “Effect of Bentonite and Zeolite on Durability of Cement Suspension Under Sulfate Attack”, 1998. |
Ding, “Extreme Vertices Design of Concrete With Combined Mineral Admixtures”, 1999. |
“Kiln Dusts”, Apr. 14, 2005. |
Sersale, “Portland-Zeolite-Cement for Minimizing Alkali-Aggregate Expansion”, 1987. |
“Standards for the Management of Cement Kiln Dust Waste”, Apr. 14, 2005. |
Naiqian, “Study on the Suppression Effect of Natural Zeolite on Expansion of Concrete Due to Alkali-Aggregate Reaction”, 1998. |
Janotka, “The Properties of Mortar Using Blends With Portland Cement Clinker, Zeolite Tuff and Gypsum”, 1995. |
Herndon, “Setting Downhole Plugs: A State-of-the-Art”, Petroleum Engineer International, Apr. 1978. |
Sugama, “Carbonation of Hydrothermally Treated Phosphate-Bonded Calcium Aluminate Cements”, pp. 1-9 (undated but admitted as prior art). |
Sugama, “Hot Alkali Carbonation of Sodium Metaphosphate Modified Fly Ash/Calcium Aluminate Blend Hydrothermal Cements”, pp. 1661-1672, Sep. 11, 1996. |
“Use of Cement Kiln Dust for the Stabilization of Soils”, R. L. Parsons, et al., Apr. 14, 2005. |
Feng, “Zeolite Ceramiste Cellular Concrete”. |
Marfil, “Zeolite Crystallization in Portland Cement Concrete Due to Alkali-Aggregate Reaction”, 1993. |
Atkins, “Zeolite P in Cements”, “Its Potential for Immobilizing Toxic and Radioactive Waste Species”, 1995. |
Hes Brochure “AQF-2 Foaming Agent”, 1999. |
Hes Brochure “Halad-23 Fluid Loss Additive”, 2000. |
Hes Brochure “Halad-344 Fluid Loss Additive”, 1998. |
Hes Brochure “Halad-413 Fluid Loss Additive”, 1999. |
Hes Brochure “Howco Suds Surfactant”, 1999. |
Hes Brochure “HR-12 Cement Retarder”, 1999. |
Hes Brochure “HR-15 Cement Retarder”, 1999. |
Hes Brochure “HR-25 Cement Retarder”, dated 1999. |
Hes Brochure “HR-4 Cement Retarder”, 1999. |
Hes Brochure HR-5 Cement Additive, 1998. |
Hes Brochure “HR-7 Cement Retarder”, 1999. |
Hes Brochure “Pozmix a Cement Additive”, 1999. |
Hes Brochure “Pozmix Cement and Pozmix 140” (undated but admitted as prior art). |
Hes Brochure “SCR-100 Cement Retarder a Valuable Time Saver”, 1994. |
Hes Brochure “”SCR-100 Cement Retarder, 1999. |
Hes Brochure “SCR-500L High•Temp Retarder”, 2000. |
Hes Brochure “ThermaLock™ Cement for Corrosive CO2 Environments”, 1999. |
“3M Scotchlite, Glass Bubbles Floated Product Series Product Information”, 1999. |
“API Specification for Materials and Testing for Well Cements”, API Spec. 10, 5th ed., pp. 7, 19-21, Jul. 1, 1980. |
“Appendix A”, API RP 13B-2, 2d ed.; pp. 6-8, Dec. 1, 1991. |
Lafarge brochure “TerraCem™ ”Aug. 2006. |
Lafarge MSDS “Cement Kiln Dust”, Mar. 3, 2005. |
Lafarge MSDS “LaFarge Blended Cement (cement)”, Mar. 3, 2005. |
TXI Material Safety Data Sheet for Pressur-Seal, Oct. 2003. |
“Manufacture of supplementary cementitious materials from cement kiln dust”, Mishulovich et al., World Cement Research and Development, p. 116-120, Mar. 1996 |
“Alkali-activated binders by use of industrial by-products”, Buchwald et al., Cement and concrete Research 35, p. 968-793, 2005. |
Answer 13 of 24 Chemical Abstracts on STN “Manufacture of ceramic particles from floatstone and fly ash”, CN 1182062 (abstract only) (undated but admitted as prior art). |
Answer 3 of 24 Chemical Abstracts on STN “Effect of cement kiln dust substitution on chemical and physical properties and compressive strength of Portland and slag cements”, Adb El-aleem et al. (abstract only), 2005. |
Office Action from U.S. Appl. No. 11/223,671Dec. 15, 2005. |
Office Action from U.S. Appl. No. 11/271,431, Mar. 6, 2006. |
Office Action from U.S. Appl. No. 11/223,671, Mar. 31, 2006. |
Office Action from U.S. Appl. No. 11/271,431, May 17, 2006. |
Office Action from U.S. Appl. No. 11/271,431 (Advisory Action), Jul. 17, 2006. |
Office Action from U.S. Appl. No. 11/416,563, Jul. 21, 2006. |
Office Action from U.S. Appl. No. 11/403,032, Jul. 24, 2006. |
Office Action from U.S. Appl. No. 11/271,431, Aug. 15, 2006. |
Office Action from U.S. Appl. No. 11/440,627, Aug. 21, 2006. |
Office Action from U.S. Appl. No. 11/402,741, Oct. 19, 2006. |
Office Action from U.S. Appl. No. 11/484,951, Oct. 26, 2006. |
Office Action from U.S. Appl. No. 11/484,951, Dec. 21, 2006. |
Office Action from U.S. Appl. No. 11/223,703, Jan. 17, 2007. |
Office Action from U.S. Appl. No. 11/402,741, Feb. 2, 2007. |
Office Action from U.S. Appl. No. 11/223,485, Feb. 28, 2007. |
Office Action from U.S. Appl. No. 11/223,669, Feb. 28, 2007. |
Office Action from U.S. Appl. No. 11/271,690, Mar. 13, 2007. |
Office Action from U.S. Appl. No. 11/402,741, Mar. 22, 2007. |
Office Action from U.S. Appl. No. 11/223,703, Apr. 25, 2007. |
Office Action from U.S. Appl. No. 11/402,741, May 29, 2007. |
Office Action from U.S. Appl. No. 11/223,669, Jun. 18, 2007. |
Office Action from U.S. Appl. No. 11/416,754 (Notice of Allowance), Jul. 2, 2007. |
Office Action from U.S. Appl. No. 11/223,485 (Notice of Allowance), Aug. 3, 2007. |
Office Action from U.S. Appl. No. 11/257,261, Aug. 10, 2007. |
Office Action from U.S. Appl. No. 11/271,690 (Notice of Allowance), Aug. 13, 2007. |
Office Action from U.S. Appl. No. 11/402,741, Sep. 6, 2007. |
Office Action from U.S. Appl. No. 11/223,669, Oct. 9, 2007. |
Office Action from U.S. Appl. No. 11/223,750, Oct. 16, 2007. |
Office Action from U.S. Appl. No. 11/416,754 (Notice of Allowance), Oct. 17, 2007. |
Office Action from U.S. Appl. No. 11/257,261 (Notice of Allowance), Oct. 23, 2007. |
Office Action from U.S. Appl. No. 11/402,741, Oct. 24, 2007. |
Office Action from U.S. Appl. No. 11/223,750 (Notice of Allowance), Dec. 11, 2007. |
Office Action from U.S. Appl. No. 11/402,741 (Notice of Allowance), Dec. 13, 2007. |
Office Action from U.S. Appl. No. 11/223,669, Jan. 29, 2008. |
Office Action from U.S. Appl. No. 11/256,824 (Notice of Allowance), Feb. 27, 2008. |
Office Action from U.S. Appl. No. 11/223,703 (Notice of Allowance), Feb. 27, 2008. |
Office Action from U.S. Appl. No. 11/223,669, Apr. 8, 2008. |
Office Action from U.S. Appl. No. 11/223,669 (Notice of Allowance), Jun. 30, 2008. |
Foreign Search Report from a Related Application, Sep. 9, 2005. |
Foreign Search Report from a Related Application, Jul. 5, 2006. |
Foreign Search Report from a Related Application, Oct. 27, 2006. |
Foreign Search Report from a Related Application, Nov. 2, 2006. |
Foreign Search Report from a Related Application, Dec. 1, 2006. |
Foreign Search Report from a Related Application, Dec. 19, 2006. |
Foreign Search Report from a Related Application, May 8, 2007. |
Office Action from U.S. Appl. No. 12/034,886 (Notice of Allowance), Oct. 21, 2008. |
Harris et al., “Successful Remedial Operations Using Ultrafine Cement”, SPE 24294, 1992. |
Heathman et al., “Case Histories Regarding the Application of Microfine Cements”, Cementing Technical Paper SPE 23926, 1992. |
Halliburton brochure entitled “Micro Matrix Cement”, Nov. 2006. |
Dalrymple et al., “A Selective Water Control Process”, SPE 24330, 1992. |
Halim et al., “Preparation of an ultra fast binding cement from calcium silicate-based mixed oxide nanoparticles”, Nanotechnology 18, 2007. |
Epik Energy brochure entitled “Nanocement”. |
Nanocor brochure entitled “Nanoclay Structure”, Jun. 24, 2008. |
He et al., “Chloride Permeability and Microstructure of Portland Cement Mortars Incorporating Nanomaterials”, Abstract, Transportation Research Board Annual Meeting 2007 Paper #08-1041, 2008. |
Chang et al., “Material Properties of Portland Cement Paste with Nano-Montmorillonite,” J. Material Science, May 18, 2007. |
Foreign communication from a related counterpart application, Jul. 5, 2005. |
Office Action from U.S. Appl. No. 10/775,348, Nov. 23, 2005. |
Office Action from U.S. Appl. No. 10/775,348, May 2, 2006. |
Notice of Allowance from U.S. Appl. No. 10/775,348, Jun. 6, 2006. |
Foreign communication from a related counterpart application, Jun. 29, 2007. |
Notice of Allowance from U.S. Appl. No. 11/388,644, Jan. 3, 2008. |
Office Action from U.S. Appl. No. 12/008,923, May 20, 2008. |
Notice of Allowance from U.S. Appl. No. 12/008,923, Jul. 22, 2008. |
Office Action from U.S. Appl. No. 11/388,645, Apr. 3, 2009. |
Office Action from U.S. Appl. No. 11/388,645, Jul. 30, 2009. |
Nanocor Technical brochure entitled “Nanoclay Structures”, Mar. 18, 2009. |
Nanofil SE 3000, “Active nanofiller for polymr applications”, Product Bulletin/Nanofil, Southern Clay Products. |
Halliburton brochure entitled, “Cementing WellLife III Cementing Service”, Apr. 2008. |
Darbe, “Slurry Design Considerations for Mechanically Enhanced Cement Systems”, AADE-08-DF-HO-06, 2008. |
Halamickova, “Water Permeability and Chloride Ion Diffusion in Portland Cement Mortars: Relationship to Sand Content and Critical Pore Diameter”, Cement and Concrete Research, vol. 25, No. 4, pp. 790-802, 1995. |
Montmorillonite, Wikipedia encyclopedia, 2009. |
Ravi, “Interventionless Zonal Isolation”, Cementing, May 2008. |
Schlumberger brochure, “Futur Active set-cement technology for long-term zonal isolation”, 2007. |
Halliburton brochure, “WellLife III Cementing Service for CO2 Environments”, Jun. 2009. |
Hunter, “Three Key Mechanisms Deliver Zonal Isolation”, IADC. |
Office Action from U.S. Appl. No. 11/747,002, Apr. 2, 2008. |
Office Action from U.S. Appl. No. 11/747,002, May 27, 2008. |
Office Action from U.S. Appl. No. 11/747,002, Jul. 10, 2008. |
Office Action from U.S. Appl. No. 11/747,002, Mar. 3, 2009. |
USPTO Office Action for U.S. Appl. No. 11/388,645 dated Aug. 17, 2010. |
USPTO Office Action for U.S. Appl. No. 12/833,189 dated Oct. 1, 2010. |
PCT International Searching Authority for International Application No. PCT/GB2009/002596 dated Feb. 8, 2010. |
International Search Report for PCT/GB/2010/001045 dated Jul. 21, 2010. |
Written Opinion of the International Searching Authority for PCT/GB/2010/001045 dated Jul. 21, 2010. |
“Effect of Nano-SiO2 on heat of hydration of portland cement,” Xu et al., Nanjing Gongye Daxue Xuebao, Ziran Kexeuban (2007), 29(4), 45-48, abstract only. |
“Application of nanometer silica in inorganic nonmetallic materials,” Deng et al., Taoci (Xiangyang China) 2007, (9), 8-12, abstract only. |
“Reaction mechanism analyses of cement based composite materials modified by nano-silica,” Xu et al., Kuangye Gongcheng (Changsha, China), 2007, 27(3), 99-102, abstract only. |
“Research on Reinforcement of cement composites and relevant mechanism,” Yu et al., Qiangdoa Keji Daxue Xuebao, Ziran Kexueban (2006), 27(2), 148-151, abstract only. |
“Antagonistic Effect of superplasticizer and colloidal nanosilica in the hydration of Alite and Belite pastes,” Bjoernstrom et al., Journal of Materials Science, 2007, 42(11), 3901-3907, abstract only. |
“Nano-concrete: possibilities and challenges,” Balaguru et al., RILEM Proceedings (2005), PRO 45 (2nd Int'l Symposium on Nanotechnology in construction (NICOM2), 2005, 233-243, abstract only. |
“A comparative study on the pozzolanic activity between nano-SiO2 and silica fume,” Ye et al., Journal of Wuhan Univ of Technology, Mat'ls Science Edition (2006), 21(3), 153-157, abstract only. |
“Optimization of silica fume, fly ash and amorphous nano-silica in superplasticized high-performance concrete,” Collepardi et al., American Concrete Institute, SP 2004, SP-221 (Eight CANMET/ACI International Conference on Fly Ash, Silica Fume, Slag, and Natrural Pozzolans in Concrete, 2004), 495-505, abstract only. |
“Accelerating effects of colloidal nano-silica for beneficial calcium-silicate-hydrate formation in cement,” Bjornstrom et al., Chemical Physics Letters (2004), 392 (1-3), 242-248, abstract only. |
“Experimental study on cement-based composites with nano-SiO2,” Feng et al., Cailiao Kexue Yu Gongcheng Zuebao Bianjibu (2004), 22(2), 224-227. |
“Strong and bioactive composites containing nano-silica-fused whiskers for bone repair,” Xu et al., Biomaterials (2004), 25(19), 4615-4626, abstract only. |
Research on properties of Portland cement added with nano-SiO2, Wang et al., Rilem Proceedings (2003), PRO 32 (International Conference on Advances in Concrete and Structures, 2003, vol. 1), 154-161, abstract only. |
“Comparison on properties of high strength concrete with nano-SiO2 and silica fume added,” Ye et al., Jianzhu Cailiao Xuebao (2003), 6(4), 381-385, abstract only. |
“Study on compound effect of silica fume and nano-SiOx for cementing composite materials,” Tang et al., Guisuanyan Xuebao (2003), 3(5), 523-527, abstract only. |
“Effect of nano-SiOx and silica fume on cement paste water demand,” Li et al., Shenyang Jianzhu gongcheng Xueyuan Xuebao, Ziran Kexueban (2002), 18(4), 278-281, abstract only. |
“Hydration reaction between C3S and fly ash, silica fume, nano-SiO2, and microstructure of hydrated pastes,” Ba et al., Guisuanyan Xuebao (2002), 30(6), 780-784, abstract only. |
“Nano-silica—an additive for high-strength concrete,” Wagner et al., Wissenschaftliche Zeitschrift—Hoschule fuer Architektur and Bauwesen Weimar—Universitaet (1994), 40 (5/6/7), 183-87, abstract only. |
“Investigations on the preparation and mechanical properties of the nano-alumina reinforced cement composite,” Li et al., Materials Letters (2006), 0(3), 356-359, abstract only. |
“Effect of secondary interface microstructure on pore structure and performance of cement-based materials,” Feng et al., Cailiao Yanjiu Xuebao (2003), 17(5), 489-494, abstract only. |
“Preparation of multifunctional dry-power paints,” Yanmin Gao, Faming Zhuanli Shenqing gongkai Shuomingshu, 4 pages, 2005, abstract only. |
USPTO office action from U.S. Appl. No. 12/426,393, dated Jul. 2, 2010. |
USPTO notice of allowance from U.S. Appl. No. 12/472,561, dated Jun. 29, 2010. |
Office Action from U.S. Appl. No. 12/426,645, dated May 5, 2010. |
Office Action from U.S. Appl. No. 12/472,561, dated May 5, 2010. |
PCT International Search Report for International Application No. PCT/GB2010/001806, dated Jan. 20, 2011. |
PCT Written Opinion for International Application No. PCT/GB2010/001806, dated Jan. 20, 2011. |
English language abstract of CN 101544488, published Sep. 30, 2009. |
USPTO Notice of Allowability from U.S. Appl. No. 12/426,393, dated Dec. 16, 2010. |
USPTO Office Action for U.S. Appl. No. 12/833,189 dated Nov. 10, 2010. |
PCT International Search Report and Written Opinion for International Application No. PCT/GB2010/000485 dated May 21, 2010. |
USPTO Office Action for U.S.Appl. No. 12/833,189 dated Feb. 17, 2011. |
Campillo et al., “Improvement of initial mechanical strength by nanoalumina in belite cements”, Science Direct, Materials Letters 61, pp. 1889-1892, 2007. |
PCT International Search Report and Written Opinion for International Application No. PCT/GB2011/000003 dated Apr. 18, 2011. |
USPTO Office Action for U.S. Appl. No. 12/567,782 dated Apr. 5, 2011. |
USPTO Office Action for U.S. Appl. No. 12/651,662 dated Apr. 5, 2011. |
USPTO Office Action for U.S. Appl. No. 12/263,954 dated Apr. 20, 2011. |
USPTO Office Action for U.S. Appl. No. 12/567,782 dated Apr. 25, 2011. |
USPTO Office Action for U.S. Appl. No. 12/651,662 dated Apr. 22, 2011. |
USPTO Office Action for U.S. Appl. No. 12/833,189 dated May 16, 2011. |
“Effect of the particle size on the micro and nanostructural features of calcium phosphate cement: a kinetic analysis”, Biomaterials 25, 2004, pp. 3453-3462. |
USPTO Office Action for U.S. Appl. No. 12/263,954 dated Aug. 8, 2011. |
USPTO Office Action for U.S. Appl. No. 12/833,189 dated Oct. 11, 2011. |
USPTO Office Action for U.S. Appl. No. 12/651,662 dated Nov. 28, 2011. |
USPTO Office Action for U.S. Appl. No. 12/833,189 dated Jul. 18, 2011. |
International Search Report for PCT/GB2010/001805 dated Mar. 31, 2011. |
Written Opinion for PCT/GB2010/001805 dated Mar. 27, 2012. |
USPTO Office Action for U.S. Appl. No. 13/431,701 dated Nov. 9, 2012. |
USPTO Office Action from U.S. Appl. No. 12/567,782 dated Feb. 8, 2013. |
Office Action from U.S. Appl. No. 13/435,701 dated Feb. 19, 2013. |
Office Action from U.S. Appl. No. 12/651,662 dated Feb. 13, 2013. |
Office Action from U.S. Appl. No. 12/833,189 dated Feb. 6, 2013. |
Office Action from U.S. Appl. No. 13/443,934 dated Mar. 4, 2013. |
International Search Report and Written Opinion for PCT/GB2010/001045 dated Jul. 21, 2010. |
Office Action from U.S. Appl. No. 13/052,471 dated Feb. 4, 2013. |
USPTO Office Action for U.S. Appl. No. 12/567,782 dated Mar. 2, 2012. |
USPTO Office Action for U.S. Appl. No. 13/052,471 dated Mar. 6, 2012. |
USPTO Office Action for U.S. Appl. No. 12/651,662 dated Mar. 14, 2012. |
USPTO Office Action for U.S. Appl. No. 12/567,782 dated Jul. 25, 2012. |
USPTO Office Action for U.S. Appl. No. 12/651,662 dated Aug. 2, 2012. |
USPTO Office Action for U.S. Appl. No. 13/052,471 dated Jun. 28, 2012. |
Written Opinion of the International Searching Authority for PCT/GB/2010/000485 dated Oct. 25, 2011. |
Written Opinion of the International Searching Authority for PCT/GB/2011/000003 dated Jul. 12, 2012. |
Communication from EPO for EPO App. No. 12159772.8 dated May 3, 2012. |
Li et al., “Investigations on the preparation and mechanical properties of the nano-alumina reinforced cement composite”, Science Direct, Materials Letters 60, pp. 356-359, 2006. |
Office Action from USPTO for Application No. 12/263,954 dated Mar. 14, 2013. |
Office Action from USPTO for Application No. 13/458,112 dated Mar. 15, 2013. |
International Preliminary Examination Report for PCT/GB2009/002596 dated May 3, 2011. |
Final Office Action from USPTO for U.S. Appl. No. 12/833,189 dated May 28, 2013. |
Final Office Action from USPTO for U.S. Appl. No. 13/435,701 dated Jun. 4, 2013. |
Office Action from USPTO for U.S. Appl. No. 12/567,782 dated Jun. 21, 2013. |
Office Action from USPTO for U.S. Appl. No. 13/443,934 dated Jun. 27, 2013. |
Final Office Action from USPTO for U.S. Appl. No. 13/052,471 dated May 10, 2013. |
Office Action from USPTO for U.S. Appl. No. 13/431,701 dated Jul. 11, 2013. |
Search report and Written opinion for PCT/US2013/038343 dated Jul. 31, 2013. |
Andrew R. Barron, Chemical composition of Portland Cement, viewed on Aug. 26, 2013, last edited by author on Jan. 4, 2010. |
International Preliminary Report and Written Opinion of PCT/GB2010/001806 dated Mar. 27, 2012. |
Office Action from USPTO for U.S. Appl. No. 13/458,112 dated Sep. 5, 2013. |
USPTO Office Action for U.S. Appl. No. 12/833,189 dated Feb. 7, 2012. |
Hes Brochure “Latex 2000”, Aug. 2006. |
EPO Office Action for EP Patent Application Serial No. 09751959.9 dated Sep. 27, 2013. |
Office Action for U.S. Appl. No. 12/263,954 dated Oct. 8, 2013. |
Office Action for U.S. Appl. No. 13/435,701 dated Oct. 4, 2013. |
Office Action for U.S. Appl. No. 13/458,112 dated Dec. 26, 2013. |
“Drilling Fluid Using PTFE Powder as a Lubricating Agent and Methods of Drilling in Subterranean Formations,” published electronically on Jan. 15, 2007. Disclosed Anonymously on IP.com. |
Agarwhal et al. “Using Nanoparticles and Nanofluids to Tailor Transport Properties of Drilling Fluids for HTHP Operations,” American Association of Drilling Engineers, 2009 National Technical Conference and Exhibition. Published 2009. |
Tran et al. “Nanofluids for Use as Ultra-Deep Drilling Fluids,” Jan. 2007. |
Notice of Allowance from USPTO for Application No. 13/052,471 dated Jan. 30, 2014. |
Hes FlexPlug Services Brochure dated Apr. 2008. |
Hes Thermatek Services Brochure dated May 2005. |
Hes Fuse-It Circulation Treatment Brochure dated May 2005. |
Office Action from USPTO for U.S. Appl. No. 13/458,112 dated Apr. 29, 2014. |
Final Office Action from USPTO for U.S. Appl. No. 13/435,701 dated Feb. 20, 2014. |
Office Action from USPTO for U.S. Appl. No. 13/620,013 dated Jan. 30, 2014. |
Final Official Action for U.S. Appl. No. 13/458,112 dated Jul. 8, 2015. |
Number | Date | Country | |
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20100016183 A1 | Jan 2010 | US |
Number | Date | Country | |
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Parent | 12263954 | Nov 2008 | US |
Child | 12567783 | US | |
Parent | 11747002 | May 2007 | US |
Child | 12263954 | US |