Well treatment compositions and methods utilizing nano-particles

Abstract
Disclosed embodiments relate to well treatment fluids and methods that utilize nano-particles. Exemplary nano-particles are selected from the group consisting of particulate nano-silica, nano-alumina, nano-zinc oxide, nano-boron, nano-iron oxide, and combinations thereof. Embodiments also relate to methods of cementing that include the use of nano-particles. An exemplary method of cementing comprises introducing a cement composition into a subterranean formation, wherein the cement composition comprises cement, water and a particulate nano-silica. Embodiments also relate to use of nano-particles in drilling fluids, completion fluids, simulation fluids, and well clean-up fluids.
Description
BACKGROUND

The present invention relates to well treatment compositions and methods utilizing nano-particles and, more particularly, in one or more embodiments, to well cement compositions and/or well completion fluids that comprise nano-particles.


In general, well treatments include a wide variety of methods that may be performed in oil, gas, geothermal and/or water wells, such as drilling, completion and workover methods. The drilling, completion and workover methods may include, but are not limited to, drilling, fracturing, acidizing, logging, cementing, gravel packing, perforating and conformance methods. Many of these well treatments are designed to enhance and/or facilitate the recovery of desirable fluids from a subterranean well.


In cementing methods, such as well construction and remedial cementing, well cement compositions are commonly utilized. 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 functions to prevent 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 and the placement of cement plugs.


In operation, the annular sheath of cement formed between the well bore and the pipe string often suffers structural failure due to pipe movements which cause shear stresses to be exerted on the set cement. Such stress conditions are commonly the result of relatively high fluid pressures and/or temperatures inside the cemented pipe string during testing, perforating, fluid injection or fluid production. For example, such stress may occur in wells subjected to steam recovery or production of hot formation fluids from high-temperature formations. The high-internal pipe pressure and/or temperature can result in the expansion of the pipe string, both radially and longitudinally, which places stresses on the cement sheath causing the cement bond between the exterior surfaces of the pipe or the well bore walls, or both, to fail and thus allow leakage of formation fluids and so forth. Accordingly, it may be desirable for the cement composition utilized for cementing pipe strings in the well bores to develop high strength after setting and to have sufficient resiliency (e.g., elasticity and ductility) to resist loss of the cement bond between the exterior surfaces of the pipe or the well bore walls, or both. Also, it may be desirable for the cement composition to be able to resist cracking and/or shattering that may result from other forces on the cement sheath. For example, it may be desirable for the cement sheath to include structural characteristics that protect its structural integrity from forces associated with formation shifting, overburden pressure, subsidence, tectonic creep, pipe movements, impacts and shocks subsequently generated by drilling and other well operations.


In addition to including components that improve mechanical properties of the cement, in a number of cementing methods, it may also be desirable to include one or more set accelerators in the well cement compositions to counteract certain constituents and/or environmental characteristics that excessively slow set times. For example, among other things, low temperatures and cement additives (e.g., fluid loss control additives and dispersants) can cause or contribute to an excessive set time for a cement composition. Accordingly, in certain situations, it may be desirable to reduce the set time by including a set accelerator in the cement composition. That is, the set accelerator may be included in a cement composition to counteract components of the cement composition or conditions surrounding the cement composition that are causing an excessive set time.


Completion fluids are another type of fluid that may be used in well treatments. A completion fluid is typically a solids-free liquid that is used, in part, to control well pressure while completing the well. The completion fluid is typically placed into the well bore after drilling, but before the start of production, to facilitate completion of the well, which typically involves preparing the bottom of the well bore to the required specifications, running in the production tubing and its associated downhole equipment, and optionally carrying out production enhancement operations, if desired. The completion fluid should generally be chemically compatible with the reservoir formation and fluid and should not damage the permeability of the formation or other equipment placed into the well bore, such as production screens. To avoid such damage, the completion fluid is typically filtered to a high degree to remove any solids that could be introduced into the near-well bore region or downhole equipment.


Brines, such as chlorides, bromides, and formates, have typically been used as completion fluids. However, these metal brines can be expensive, corrosive, and difficult to handle. For example, brines may tend to corrode and damage the downhole equipment in many instances, especially those of a delicate nature such as production screens. Brines may also cause undesired precipitation reactions that can damage the permeability of the producing formation. Furthermore, disposal of the brines may be difficult and costly, especially on land where environmental regulations prohibit the placement of high concentrations of chlorides and other ions into landfills.


SUMMARY

The present invention relates to well treatment compositions and methods utilizing nano-particles and, more particularly, in one or more embodiments, to well cement compositions and/or well completion fluids that comprise nano-particles.


An embodiment of the present invention provides a method of completing a well comprising: including nano-particles in a completion fluid; and using the completion fluid in completing the well.


Another embodiment of the present invention provides a method of completing a well comprising: providing a completion fluid comprising nano-particles; and introducing the completion fluid into a well bore.


Another embodiment of the present invention provides a method of completing a well comprising: including nano-particles having a particle size of from about 1 nanometer to about 100 nanometers in a completion fluid, wherein the nano-particles comprise at least one nano-particle selected from the group consisting of nano-alumina, nano-zinc oxide, nano-boron, nano-iron oxide, nano-silica, and any combination thereof; and using the completion fluid in completing the well.


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.







DESCRIPTION OF SPECIFIC EMBODIMENTS

The present invention relates to well treatment compositions and methods utilizing nano-particles and, more particularly, in one or more embodiments, to well cement compositions and/or well completion fluids that comprise nano-particles.


Cement Composition Embodiments


An exemplary embodiment of the cement compositions of the present invention comprises cement, water and particulate nano-silica. Those of ordinary skill in the art will appreciate that the exemplary cement compositions generally should have a density suitable for a particular application. By way of example, the cement composition may have a density in the range of from about 4 pounds per gallon (“lb/gal”) to about 20 lb/gal. In exemplary embodiments, the cement compositions may have a density in the range of from about 8 lb/gal to about 17 lb/gal. Exemplary embodiments of the cement 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.


Exemplary embodiments of the cement compositions of the present invention comprise a cement. Any of a variety of cements suitable for use in subterranean cementing operations may be used in accordance with exemplary 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, silica cements and combinations thereof. In certain embodiments, the hydraulic cement may comprise a Portland cement. The Portland cements that may be suited for use in exemplary embodiments of the present invention are 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.


The water used in exemplary embodiments of the cement 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 exemplary embodiments, the water may be present in the cement compositions in an amount in the range of from about 33% to about 200% by weight of the cement on a dry basis (“bwoc”). In exemplary embodiments, the water may be present in an amount in the range of from about 35% to about 70% bwoc.


In addition, exemplary embodiments of the cement compositions comprise nano-silica. The nano-silica may 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 cement composition as a dry nano-silica powder. Generally, the particulate nano-silica may be defined as nano-silica having a particle size of less than or equal to about 100 nm. For example, the particulate nano-silica may have a particle size in the range of from about 1 nm to about 100 nm (about 1×10−9 m to about 100×10−9 m). In certain exemplary embodiments, the particulate nano-silica may have a particle size of less than or equal to about 50 nm. For example, the particulate nano-silica may have a particle size in the range of from about 5 nm to about 50 nm. In further exemplary embodiments, the particulate nano-silica may have a particle size of less than or equal to about 30 nm. For example, the particulate nano-silica may have a particle size in the range of from about 5 nm to about 30 nm. However, it should be noted that the particulate nano-silica may be utilized in combination with differently sized silica particles in accordance with present embodiments. For example, a number of silica particles with particle sizes greater than 100 nm may be included in a cement composition in accordance with present embodiments.


It is now recognized that the particulate nano-silica utilized with present embodiments, which may include silicon dioxide, may have an impact on certain physical characteristics of resulting cements. For example, relative to inclusion of colloidal silica or larger silica particles in a cement slurry, inclusion of particulate nano-silica in the cement slurry may provide improved mechanical properties, such as compressive strength, tensile strength, Young's modulus and Poisson's ratio. In addition, the particulate nano-silica also may be included in the cement composition as a set accelerator to accelerate the set time of the resultant cement composition. Accordingly, a cement composition in accordance with present embodiments may comprise a sufficient amount of particulate nano-silica to provide the desired characteristics in a resulting cement. In exemplary embodiments, the particulate nano-silica may be present in the cement composition in an amount in the range of from about 1% to about 25% bwoc. In exemplary embodiments, the particulate nano-silica may be present in the cement composition in an amount in the range of from about 5% to about 15% bwoc.


Other additives suitable for use in subterranean cementing operations also may be added to exemplary embodiments of the cement compositions. Examples of such additives include, strength-retrogression additives, set accelerators, weighting agents, weight-reducing additives, heavyweight additives, lost-circulation materials, filtration-control additives, dispersants, defoaming agents, foaming agents, and combinations thereof. Specific examples of these, and other, additives include crystalline silica, amorphous silica, salts, fibers, hydratable clays, vitrified shale, microspheres, fly ash, lime, latex, thixotropic additives, combinations thereof and the like. 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, exemplary embodiments of the cement compositions of the present invention may be used in a variety of subterranean applications, including primary and remedial cementing. Exemplary embodiments of the cement compositions may be introduced into a subterranean formation and allowed to set therein. Exemplary embodiments of the cement compositions may comprise cement, water and the particulate nano-silica. By way of example, in exemplary primary cementing embodiments, a cement composition may be introduced into a space between a subterranean formation and a pipe string located in the subterranean formation. The cement composition may be allowed to set to form a hardened mass in the space between the subterranean formation and the pipe string. In addition, in exemplary remedial cementing embodiments, a cement composition may be used, for example, in squeeze-cementing operations or in the placement of cement plugs. One or more hydrocarbons (e.g., oil, gas, etc.) may be produced from a well bore penetrating the subterranean formation.


While the preceding discussion is directed to the use of particulate nano-silica, those of ordinary skill in the art will also appreciate that it may be desirable to utilize other types of nano-particles, in accordance with embodiments of the present invention. Examples of such nano-particles include nano-alumina, nano-zinc oxide, nano-boron, nano-iron oxide and combinations thereof. In certain exemplary embodiments, the nano-particles may be particulate in nature and not, for example, a colloidal nano-particle or a suspension of the nano-particle in solution. Furthermore, while the preceding discussion is directed to the use of particulate nano-silica in well cementing methods, those of ordinary skill in the art will appreciate that the present technique also encompasses the use of nano-particles in any of a variety of different subterranean treatments. For example, the nano-particles may be included in any of a number of well treatment fluids that may be used in subterranean treatments, including drilling fluids, completion fluids, stimulation fluids and well clean-up fluids. In accordance with another embodiment, the nano-particles may be included as proppant in a well treatment fluid. For example, a well treatment fluid containing the nano-particles may be introduced into a subterranean formation at or above a pressure sufficient to create or enhance or more fractures in the subterranean formation. Enhancing a fracture includes enlarging a pre-existing fracture in the formation. At least a portion of the nano-particles may be deposited in the one or more fractures such that the fractures are prevented from fully closing upon the release of pressure, forming conductive channels through which fluids may flow to (or from) the well bore.


In addition to the use of the nano-particles without encapsulation, embodiments of the present invention may include encapsulation of the nano-particles to facilitate transportation and incorporation of the nano-particles in well treatment fluids (e.g., cement compositions). Specifically, encapsulation of the nano-particles in accordance with present embodiments may include enclosing the nano-particles within an outer coating or container in particulate form. Exemplary 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 relevant disclosures of which are incorporated herein by reference.


Various types of encapsulation may be employed such that the nano-particles (e.g., the particulate nano-silica) are contained but retains its particulate nature and, thus, retains its corresponding impact on physical properties of cement slurries. For example, the nano-particles may be encapsulated within a bag, capsule, layer, coating or the like. Further, the material utilized to encapsulate the nano-particles may be selected to facilitate transportation and/or incorporation of the nano-particles into a well treatment fluid. For example, to facilitate handling of the nano-particles and/or to facilitate timed release of the nano-particles, the encapsulation material may be degradable. This may facilitate handling of the nano-particles by allowing inclusion of the encapsulated nano-particles in a well treatment fluid without requiring that the nano-particles first be removed from the encapsulating material. Further, the encapsulating 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 well treatment fluid at a desired time. Exemplary 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 relevant disclosures of which are incorporated herein by reference.


In accordance with exemplary embodiments, the cement 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 cement compositions.


The present embodiments may include a combination of at least three features to obtain a maximum packing volume fraction. One is the use of at least three particulate materials wherein the at least three particulate materials are in size ranges “disjointed” from one another. In some embodiments, each of the three particulate materials may include a different particle size selected from the following ranges: about 7 nm to about 50 nm, about 0.05 microns to about 0.5 microns, 0.5 microns to about 10 microns, about 10 microns to about 20 microns, about 20 microns to about 200 microns, about 200 microns to about 800 microns, and greater than about 1 millimeter. For example, a first particulate material may include particles sized from about 7 nm to about 50 nm, a second particulate material may include particles sized from about 0.05 microns to about 0.5 microns, and a third particulate material may include particles sized from about 10 microns to about 20 microns. In accordance with present embodiments, the first particulate material includes at least one of nano-silica, nano-alumina, nano-zinc oxide, nano-boron, nano-iron oxide or combinations thereof. Another feature of present embodiments may include a choice of the proportions of the three particulate materials in relation to the mixing, such that the fluid, when mixed, is in a hindered settling state. Another feature may include the choice of the proportions of the three particulate materials between each other, and according to their respective size ranges, such that the maximum packing volume fraction is at least substantially achieved for the sum total of all particulate materials in the fluid system. Packing volume fraction is described in further detail in U.S. Pat. Nos. 5,518,996 and 7,213,646, the relevant portions of which are incorporated herein by reference.


Completion Fluid Embodiments


As previously mentioned, the nano-particles may be included in completion fluids in accordance with embodiments of the present invention. The nano-particles may be included in the completion fluids to provide a number of different benefits. For example, the nano-particles may be used to enhance or otherwise improve the rheological properties of the completions fluids. By way of further example, the nano-particles may be included in the completion fluids as weighting materials to increase the density of the fluid. Because the nano-particles are nano-sized, it is believed that they should not undesirably plug formation permeability or other downhole equipment, such as production screens, and thus can be included in completion fluids. In addition, the inclusion of the nano-particles in completion fluids may have further beneficial effects, especially in shale formations. For example, it is believed that the nano-particles may prevent the influx of well bore fluids into the nano-porosity often found within shale formations, such as oil shales, by sealing these pores, which isolates and stabilizes the shale formation from the destabilizing hydraulic forces from the well bore.


An exemplary embodiment of the completion fluids may comprise nano-particles. Generally, the “nano-particles” may be defined as having a mean particle size of less than 1 micron. For example, nano-particles may have a mean particles size in a range of from about 1 nm to less than 1 micron. In some embodiments, the nano-particles may have a mean particles size in a range of from about 1 nm to about 800 nm and, alternatively, from about 1 nm to about 100 nm. In one particular embodiment, the nano-particles may have a mean particle size in a range of about 20 nm to about 100 nm. In specific embodiments, the nano-particles may have a particle size of about 1 nm, about 10 nm, about 50 nm, about 100 nm, about 200 nm, about 400 nm, about 600 nm, or about 800 nm. In some embodiments, the nano-particles may be provided in colloidal form, for example, a colloidal nano-particle or a suspension of the nano-particle in a fluid. In some embodiments, the nano-particle may be a particulate nano-particle. The nano-particles may be encapsulated or otherwise contained as discussed above. Examples of suitable nano-particles include nano-alumina, nano-zinc oxide, nano-boron, nano-iron oxide, and nano-silica. Additional examples of suitable nano-particles include other nano-sized materials, including nano-barium sulphate, nano-manganese tetraoxide, nano-magnesium oxide, nano-calcium carbonate, nano-graphite, nano-barium oxide, nano-cerium oxide, nano-lanthium oxide, nano-titanium dioxide, nano-clay, and nano-aluminosilicates. Combinations of different nano-particles may also be used. In some embodiments, the nano-particle is not acid-soluble.


The nano-particles may be included in a completion fluid in an amount sufficient for a desired application. For example, the nano-particles may be included in a completion fluid in an amount sufficient to weight the fluid to a desired density. In some embodiments, the nano-particles may be present in the completion fluid in an amount in a range of from about 0.1% to about 70% by volume of the completion fluid. In specific embodiments, the nano-particles may be present in an amount ranging between any of and/or including any of about 0.1%, about 1%, about 10%, about 20%, about 30%, about 40%, about 50%, about 60%, or about 70% by volume of the completion fluid. One of ordinary skill in the art, with the benefit of this disclosure, should be able to select an appropriate amount of the nano-particles to use for a particular application.


In some embodiments, the completion fluids may comprise a base fluid, such as an oil-based fluid or a water-based fluid. Oil-based fluids may comprise olefins, internal olefins, alkanes, aromatic solvents, cycloalkanes, liquefied petroleum gas, kerosene, diesel oils, crude oils, heavy oils, gas oils, fuel oils, paraffin oils, mineral oils, low toxicity mineral oils, esters, amides, synthetic oils (e.g., polyolefins), polydiorganosiloxanes, siloxanes, organosiloxanes, ethers, acetals, dialkylcarbonates, hydrocarbons, and combinations thereof. Water-based fluids may comprise fresh water or salt water, such as a brine or seawater. The base fluid may be present in an amount in a range of from about 25% to about 99% by volume of the completion fluid.


Other additives suitable for use in completion operations may also be included in the completion fluids in embodiments of the present invention. Examples of such additives includes salts, surfactants, fluid-loss-control additives, gases such as nitrogen or carbon dioxide, surface-modifying agents, foamers, corrosion inhibitors, scale inhibitors, clay-control agents, biocides, friction reducers, antifoam agents, dispersants, flocculants, H2S scavengers, CO2 scavengers, oxygen scavengers, lubricants, viscosifiers, breakers, wetting agents, and combinations thereof. A person having ordinary skill in the art, with the benefit of this disclosure, should readily be able to determine the type and amount of additive useful for a particular application.


The completion fluids may have a density as desired for a particular application. In general, the completion fluid should have a density sufficient to, for example, control formation pressures. As previously described, the nano-particles may be used in some embodiments as weighting agents to increase the density of the completion fluid. For example, the nano-particles may be included in the completion fluid in an amount sufficient to weight the completion fluid. In some embodiments, the completion fluid may have a density in the range of from about 7.5 lb/gal to about 22 lb/gal, and alternatively from about 12 lb/gal to about 18 lb/gal. One of ordinary skill in the art, with the benefit of this disclosure, should be able to determine an appropriate density of the completion fluid for a particular application.


As will be appreciated by those of ordinary skill in the art, with the benefit of this disclosure, embodiments of the completions fluids of the present invention may be used in a variety of completion operations. For example, the completion fluids may be used in operations after drilling, but before the start of production. In some embodiments, the completion operation may include preparing the bottom of the well bore to the required specifications, running in production tubing and its associated downhole equipment, or carrying out production enhancement operations. By way of example, the completion fluid may be present in the well bore while equipment, such as screens, production liners, and/or downhole valves, is run into the well bore. In one embodiment, the completion fluid may be present in the well bore while perforations are formed in the casing disposed in the well bore. Among other functions, the completion fluid should act to control formation pressures.


An embodiment of the present invention may comprise a method of completing a well that comprises providing a completion fluid comprising nano-particles and introducing the completion fluid into a well bore. In some embodiments, downhole equipment may be run into the well while the completion fluid is in the well bore. The downhole equipment may include, for example, screens, production liners, and/or downhole valves. One particular example of a type of downhole equipment that is susceptible to plugging by solids-laden fluids, such as drilling fluids, is wire-wrapped screens. Wire-wrapped screens may be used, for example, where a well bore liner having a porous screen may be required to mechanically hold back the formation sand. Because the nano-particles are nano-sized, the nano-particles should not undesirably plug the downhole equipment. In contrast, if micron-sized or larger particles are included in the completion fluids, the downhole equipment, as well as the formation permeability, would be susceptible to plugging events.


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


EXAMPLE 1

Five different cement slurries (i.e., Slurry A, Slurry B, Slurry C, Slurry D and Slurry E) were prepared. The slurries and resulting set cements were then tested to determine setting or thickening times and other physical properties of each of the five different slurries. As set forth below, the respective test results for the five different slurries demonstrate that inclusion of particulate nano-silica in the slurry reduces the set time and increases the strength of the resulting cement relative to cements resulting from inclusion of the other silica components that were tested.


Slurries A, B, C and D were prepared by dry blending dry components with cement prior to adding water to form the respective slurry. Slurry E was prepared by dry blending dry components with cement prior to adding water and then adding colloidal silica to form the respective slurry. Further, each of the five slurries included a different type of silica. Two of the five slurries included particulate nano-silica in accordance with present embodiments, and the other three included silica in different forms and sizes (e.g., colloidal silica and micro-silica). While the silica included in each of the five slurries was different, the other components utilized in each of the five slurries were similar. Specifically, in addition to a specific type of silica, each of the five slurries included 100% bwoc of Class G cement, 0.5% bwoc of a retarder, and sufficient water to make the density of the slurry approximately 12.00 lbs/gal. The specific retarder utilized in the slurries was HR-5 cement retarder, which is a sulfomethylated lignosulfonate. It should be noted that HR5 cement retarder is available from Halliburton Energy Services, Inc. and is described in U.S. Pat. No. RE31,190.


As set forth above, each of the five slurries included a different type of silica and sufficient water to make the resulting slurry have a density of 12.00 lb/gal. Slurries A and B included particulate nano-silica in accordance with present embodiments and 15.36 gal/sk of water. Specifically, Slurry A included 15% bwoc of particulate nano-silica having a particle size of approximately 30 nm, and Slurry B included particulate nano-silica having a particle size of approximately 10 nm. Slurry C included 15% bwoc of SILICALITE cement additive and 15.68 gal/sk of water. SILICALITE (compacted) cement additive, which is available from Halliburton Energy Services, Inc., Duncan, Okla., is an amorphous silica generally sized in a range from about 2.5 microns to about 50 microns. Slurry D included 15% bwoc of MICROSAND cement additive and 15.77 gal/sk of water. MICROSAND cement additive, which is available from Halliburton Energy Services, Inc., Duncan, Okla., is a crystalline silica ground to a substantially uniform particle size distribution of approximately 5 to 10 microns. Slurry E included 5.12 gal/sk of GasCon 469™ lightweight cement additive and 10.09 gal/sk of water. GASCOND 469 lightweight cement additive is available from Halliburton Energy Services, Inc., Duncan, Okla., and may be defined as a colloidal silicic acid suspension containing suspended silicic acid particles generally having a particle size of less than about 20 nm.


After the five slurries were prepared, tests were performed to determine various physical characteristics associated with inclusion of the different silica components in each of the associated cement compositions. One of these tests was performed to measure a thickening time associated with each of the five slurries. Specifically, the total thickening time (TTT) associated with each cement slurry was determined by performing a thickening-time test in accordance with API Recommended Practice 10, API Specification for Materials and Testing for Well Cements. The measurement of the TTT for each slurry was based on the respective slurry reaching a consistency of 70 Bearden units (Bc) at 80° F. The results of these measurements are set forth for each of the five slurries in Table 1 below.


Additional tests were performed on the cement slurries to determine force-resistance properties (e.g., compressive strength, shear-bond strength, and tensile strength) for each of the slurries. Each of the force-resistance property tests was performed on the respective cement slurries at a temperature of 80° F. and after the slurries had set for 72 hours. The force-resistance property tests included nondestructive and destructive ultrasonic strength tests, a compressive-strength test, a shear-bond test, and a tensile-strength test. The nondestructive and destructive ultrasonic analyzer tests were conducted using a UCA ultrasonic cement analyzer to determine a UCA72 hrs value and a UCAcrush value, respectively. The compressive-strength tests and UCA analyzer tests were performed in accordance with API Recommended Practice 10B. Further, shear-bond and Brazilian-tensile-strength tests were performed to determine shear strength and tensile strength values, respectively, for the different cement compositions. The shear-bond-strength tests were performed as described in SPE 764 entitled “A Study of Cement—Pipe Bonding” by L. G. Carter and G. W. Evans. The Brazilian-tensile-strength tests were performed in accordance with ASTM C496-96. The results of the tests performed on each of the five compositions are shown in Table 1 below.
















TABLE 1











Shear-
Brazilian




TTT


Comp.
Bond
Tensile



Silica
to 70 Bc
UCA72 hrs
UCAcrush
Strength
Strength
Strength


Slurry
Type
(Hr:Min)
(psi)
(psi)
(psi)
(psi)
(psi)






















Slurry A
30 nm
2:43
328
419
428
169
148.28



particulate



nano-silica


Slurry B
10 nm
5:00
500
481
402
51
14.72



particulate



nano-silica


Slurry C
Amorphous
14:32 
266
206
211
98
95.5



silica


Slurry D
Crystalline
20:00+
260
285
252
37.2
102.16



Silica


Slurry E
Colloidal
20:00+
225
219
374
42.4
84.71



Silica









EXAMPLE 2

Samples of Slurries A, C, D and E discussed above were also tested to determine various additional physical properties associated with the resulting set cements and to confirm relative differences demonstrated above. While different instruments and calibration settings were used in the additional testing of the slurries, the test data indicates that relative differences between the different slurries are similar to those differences illustrated in Example 1. Indeed, as indicated above in Example 1, the respective test results in Example 2 for the five different cements demonstrate that inclusion of particulate nano-silica in the cement composition increases the strength of the resulting cement relative to cements resulting from inclusion of the other silica components that were tested.


Three samples for each of the three conventional cement slurries (Slurry C, Slurry D, and Slurry E) and four samples of Slurry A were tested to determine compressive strength, Young's modulus, and Poisson's ratio. The compressive-strength tests were performed in accordance with API Specification 10. It should be noted that the compressive-strength measurements in Example 1 are different than those in Example 2 because different equipment and different calibrations were utilized. However, the relative differences between compressive strengths for each of the five slurries are similar. The Young's modulus and Poisson's ratio were statically determined by means of compression testing using a load frame. The Young's modulus or modulus of elasticity for each sample was obtained by taking a ratio of a simple tension stress applied to each sample to a resulting strain parallel to the tension in that sample. The Poisson's ratio for each sample was determined by calculating a ratio of transverse strain to a corresponding axial strain resulting from uniformly distributed axial stress below a proportional limit of each sample. The values determined for the three samples of each of the five different cement slurries are set forth below in Table 2.














TABLE 2








Compres-







sive




Silica
Strength
Young's
Poisson's


Slurry
Sample
Type
(psi)
Modulus
Ratio




















Slurry A
Sample 1
30 nm
1257
2.26E+05
**




particulate




nano-silica


Slurry A
Sample 2
30 nm
1189
2.12E+05
0.109




particulate




nano-silica


Slurry A
Sample 3
30 nm
1249
2.04E+05
0.092




particulate




nano-silica


Slurry A
Sample 4
30 nm
1275
2.13E+05
0.110




particulate




nano-silica


Slurry C
Sample 1
Amorphous
466
2.53E+05
0.064




silica


Slurry C
Sample 2
Amorphous
483
2.38E+05
0.064




silica


Slurry C
Sample 3
Amorphous
506
2.40E+05
0.053




silica


Slurry D
Sample 1
Crystalline
350
1.42E+05
0.068




Silica


Slurry D
Sample 2
Crystalline
397
1.50E+05
0.063




Silica


Slurry D
Sample 3
Crystalline
378
1.46E+05
0.060




Silica


Slurry E
Sample 1
Colloidal
514
1.03E+05
0.063




Silica


Slurry E
Sample 2
Colloidal
598
1.15E+05
0.072




Silica


Slurry E
Sample 3
Colloidal
627
1.23E+05
0.071




Silica









The particular embodiments disclosed above are illustrative only, as the present invention may be susceptible to various modifications and alternative forms. However, it should be understood that the invention is not intended to be limited to the particular embodiments disclosed. Rather, the present invention is to cover all modifications, equivalents and alternatives falling with the scope and spirit of the present invention as defined by the following appended claims. In addition, 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 in the present Description of Specific Embodiments is to be understood as referring to the power set (the set of all subsets) of the respective range of values, and set for the every range encompassed within the broader range of value.

Claims
  • 1. A method of completing a well comprising: including nano-particles in a completion fluid, wherein the nano-particles are selected from the group consisting of nano-silica, nano-alumina, nano-zinc oxide, nano-boron, nano-iron oxide, nano-barium sulphate, nano-manganese tetraoxide, nano-magnesium oxide, nano-calcium carbonate, nano-graphite, nano-barium oxide, nano-cerium oxide, nano-lanthium oxide, nano-titanium dioxide, nano-clay, nano-aluminosilicate, and any combination thereof;wherein the nano-particles are present in the completion fluid in an amount in a range of from about 10% to about 70% by weight of the completion fluid; and wherein the completion fluid has a density in a range of about 7.5 pounds per gallon to about 22 pounds per gallon;introducing the completion fluid into a well bore; andusing the completion fluid in completing the well, wherein micron-sized or larger particles are not present in the completion fluid when completing the well such that the completion fluid does not plug production screens or other downhole equipment.
  • 2. The method of claim 1 wherein the nano-particles have a particle size in a range of from about 1 nanometer to less than 1 micron.
  • 3. The method of claim 1 wherein the nano-particles have a particle size in a range of from about 1 nanometer to about 100 nanometers.
  • 4. The method of claim 1 wherein the completion fluid comprises at least one base fluid selected from the group consisting of an oil-based fluid, a water-based fluid, and a combination thereof.
  • 5. The method of claim 1 wherein the completion fluid comprises at least one oil-based fluid selected from the group consisting of an olefin, an internal olefin, an alkane, an aromatic solvent, a cycloalkane, liquefied petroleum gas, kerosene, diesel oil, crude oil, heavy oil, gas oil, fuel oil, paraffin oil, mineral oil, low toxicity mineral oil, an ester, an amide, a polyolefin, a polydiorganosiloxane, a siloxane, an organosiloxane, an ether, an acetal, a dialkylcarbonate, a hydrocarbon, and any combination thereof.
  • 6. The method of claim 1 wherein the completion fluid further comprises at least one additive selected from the group consisting of a salt, a surfactant, a fluid-loss-control additive, a gas, nitrogen, carbon dioxide, a surface-modifying agent, a foamer, a corrosion inhibitor, a scale inhibitor, a clay-control agent, a biocide, a friction reducer, an antifoam agent, a dispersant, a flocculant, H2S scavenger, CO2 scavenger, an oxygen scavenger, a lubricant, a viscosifier, a breaker, a wetting agent, and any combination thereof.
  • 7. The method of claim 1 further comprising running downhole equipment into the well while the completion fluid is in the well.
  • 8. The method of claim 1 further comprising running a wire-wrapped screen into the well while the completion fluid is in the well.
  • 9. A method of completing a well comprising: providing a cement-free completion fluid comprising nano-particles, wherein the nano-particles are selected from the group consisting of nano-silica, nano-alumina, nano-zinc oxide, nano-boron, nano-iron oxide, nano-barium sulphate, nano-manganese tetraoxide, nano-magnesium oxide, nano-calcium carbonate, nano-graphite, nano-barium oxide, nano-cerium oxide, nano-lanthium oxide, nano-titanium dioxide, nano-clay, nano-aluminosilicate, and any combination thereof; wherein the nano-particles are present in the completion fluid in an amount in a range of from about 10% to about 70% by weight of the completion fluid; and wherein the completion fluid has a density in a range of about 7.5 pounds per gallon to about 22 pounds per gallon;introducing the cement-free completion fluid into a well bore and;using the cement-free completion fluid in completing the well, wherein micron-sized or larger particles are not present in the cement-free completion fluid when completing the well such that the cement-free completion fluid does not plug production screens or other downhole equipment.
  • 10. The method of claim 9 wherein the nano-particles have a particle size in a range of from about 1 nanometer to less than 1 micron.
  • 11. The method of claim 9 wherein the nano-particles have a particle size of from about 1 nanometer to about 100 nanometers.
  • 12. The method of claim 9 wherein the completion fluid comprises at least one base fluid selected from the group consisting of an oil-based fluid, a water-based fluid, or a combination thereof.
  • 13. The method of claim 9 wherein the completion fluid comprises at least one oil-based fluid selected from the group consisting of an olefin, an internal olefin, an alkane, an aromatic solvent, a cycloalkane, liquefied petroleum gas, kerosene, diesel oil, crude oil, heavy oil, gas oil, fuel oil, paraffin oil, mineral oil, low toxicity mineral oil, an ester, an amide, a polyolefin, a polydiorganosiloxane, a siloxane, an organosiloxane, an ether, an acetal, a dialkylcarbonate, a hydrocarbon, and any combination thereof.
  • 14. The method of claim 9 wherein the completion fluid further comprises at least one additive selected from the group consisting of a salt, a surfactant, a fluid-loss-control additive, a gas, nitrogen, carbon dioxide, a surface-modifying agent, a foamer, a corrosion inhibitor, a scale inhibitor, a clay-control agent, a biocide, a friction reducer, an antifoam agent, a dispersant, a flocculant, H2S scavenger, CO2 scavenger, an oxygen scavenger, a lubricant, a viscosifier, a breaker, a wetting agent, and any combination thereof.
  • 15. The method of claim 9 further comprising running downhole equipment into the well bore while the completion fluid is in the well bore.
  • 16. The method of claim 9 further comprising running a wire-wrapped screen into the well bore while the completion fluid is in the well bore.
  • 17. A method of completing a well comprising: including nano-particles having a particle size of from about 1 nanometer to about 100 nanometers in a cement-free completion fluid, wherein the nano-particles comprise at least one nano-particle selected from the group consisting of nano-alumina, nano-zinc oxide, nano-boron, nano-iron oxide, nano-silica, nano-barium sulphate, nano-manganese tetraoxide, nano-magnesium oxide, nano-calcium carbonate, nano-graphite, nano-barium oxide, nano-cerium oxide, nano-lanthium oxide, nano-titanium dioxide, nano-clay, nano-aluminosilicate, and any combination thereof; wherein the nano-particles are present in the completion fluid in an amount in a range of from about 10% to about 70% by weight of the completion fluid; and wherein the completion fluid has a density in a range of about 7.5 pounds per gallon to about 22 pounds per gallon;introducing the cement-free completion fluid into a well bore;using the cement-free completion fluid in completing the well, wherein micron-sized or larger particles are not present in the cement-free completion fluid such that the cement-free completion fluid does not plug production screens or other downhole equipment; andrunning downhole equipment into the cement-free completion fluid in the well.
CROSS-REFERENCE TO RELATED APPLICATIONS

The present application is a continuation-in-part of U.S. patent application Ser. No. 12/567,782, filed Sep. 27, 2009, entitled “Cement Compositions and Methods Utilizing Nano-Clay,” which 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.

US Referenced Citations (448)
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 Gama 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, Jr. 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 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
4515216 Childs et al. May 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 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
6488089 Bour et al. Dec 2002 B1
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
6846357 Reddy et al. Jan 2005 B2
6848519 Reddy et al. Feb 2005 B2
6861392 Shaarpour Mar 2005 B2
6861468 Yoshida et al. Mar 2005 B2
6874578 Garnier et al. Apr 2005 B1
6881708 Reddy et al. Apr 2005 B2
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
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 et al. 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
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
7445668 Sommain Nov 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
7776797 Allin et al. Aug 2010 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
8226879 Genolet et al. Jul 2012 B2
8394744 Woytowich et al. Mar 2013 B2
8476203 Patil et al. Jul 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
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
20030095906 Bauer 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 Bara 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 et al. 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
20050172864 Dingosoyr et al. Aug 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
20060054319 Fyten et al. Mar 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 Roddy 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 et al. Sep 2009 A1
20090260544 Roddy Oct 2009 A1
20100016183 Roddy et al. Jan 2010 A1
20100025039 Roddy et al. Feb 2010 A1
20100075874 Mercado et al. Mar 2010 A1
20100096135 Roddy et al. Apr 2010 A1
20100193982 Genolet et al. Aug 2010 A1
20100243236 Koons Sep 2010 A1
20110162845 Ravi et al. Jul 2011 A1
20110237467 Cornette et al. Sep 2011 A1
20110312857 Amanullah et al. Dec 2011 A1
20120015852 Quintero et al. Jan 2012 A1
20130312641 Chatterji et al. Nov 2013 A1
Foreign Referenced Citations (38)
Number Date Country
2514492 Sep 2004 CA
2153372 Jan 2006 CA
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 Apr 1983 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 0187796 Nov 2001 WO
WO 03008756 Jan 2003 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
WO 2008034461 Mar 2008 WO
WO 2009030758 Mar 2009 WO
Non-Patent Literature Citations (215)
Entry
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.
Naigian, “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, “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”, 2000.
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 “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 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. 11/223,671, Dec. 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. 11, 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.
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.
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.
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.
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.
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.
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.
PCT International Searching Authority for International Application No. PCT/GB2009/002596, Feb. 8, 2010.
Office Action from U.S. Appl. No. 12/426,645, May 5, 2010.
Office Action from U.S. Appl. No. 12/472,561, May 5, 2010.
PCT International Search Report and Written Opinion for International Application No. PCT/GB2010/000485, May 21, 2010.
“Effect of Nano-SiO2 on heat of hydration of portland cement,” Xu et al., Nanjing Gongye Daxue Xuebao, Ziran Kexeuban, 29(4), 45-48, abstract only, 2007.
“Application of nanometer silica in inorganic nonmetallic materials,” Deng et al., Taoci (Xiangyang China), (9), 8-12, abstract only, 2007.
“Reaction mechanism analyses of cement based composite materials modified by nano-silica,” Xu et al., Kuangye Gongcheng (Changsha, China), 27(3), 99-102, abstract only, 2007.
“Research on Reinforcement of cement composites and relevant mechanism,” Yu et al., Qiangdoa Keji Daxue Xuebao, Ziran Kexueban, 27(2), 148-151, abstract only, 2006.
“Antagonistic Effect of superplasticizer and colloidal nanosilica in the hydration of Alite and Belite pastes,” Bjoernstrom et al., Journal of Materials Science, 42(11), 3901-3907, abstract only, 2007.
“Nano-concrete: possibilities and challenges,” Balaguru et al., RILEM Proceedings (2005), PRO 45 (2nd Int'l Symposium on Nanotechnology in construction (NICOM2), 233-243, abstract only, 2005.
“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, 21(3), 153-157, abstract only, 2006.
“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), 495-505, abstract only, 2004.
“Accelerating effects of colloidal nano-silica for beneficial calcium-silicate-hydrate formation in cement,” Bjornstrom et al., Chemical Physics Letters, 392 (1-3), 242-248, abstract only, 2004.
“Experimental study on cement-based composites with nano-SiO2,” Feng et al., Cailiao Kexue Yu Gongcheng Zuebao Bianjibu, 22(2), 224-227, 2004.
“Strong and bioactive composites containing nano-silica-fused whiskers for bone repair,” Xu et al., Biomaterials, 25(19), 4615-4626, abstract only, 2004.
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, vol. 1), 154-161, abstract only, 2003.
“Comparison on properties of high strength concrete with nano-SiO2 and silica fume added,” Ye et al., Jianzhu Cailiao Xuebao, 6(4), 381-385, abstract only, 2003.
“Study on compound effect of silica fume and nano-SiOx for cementing composite materials,” Tang et al., Guisuanyan Xuebao, 3(5), 523-527, abstract only, 2003.
“Effect of nano-SiOx and silica fume on cement paste water demand,” Li et al., Shenyang Jianzhu gongcheng Xueyuan Xuebao, Ziran Kexueban, 18(4), 278-281, abstract only, 2002.
“Hydration reaction between C3S and fly ash, silica fume, nano-SiO2, and microstructure of hydrated pastes,” Ba et al., Guisuanyan Xuebao, 30(6), 780-784, abstract only, 2002.
“Nano-silica—an additive for high-strength concrete,” Wagner et al., Wissenschaftliche Zeitschrift—Hoschule fuer Architektur und Bauwesen Weimar—Universitaet, 40 (5/6/7), 183-87, abstract only, 1994.
“Investigations on the preparation and mechanical properties of the nano-alumina reinforced cement composite,” Li et al., Materials Letters, 0(3), 356-359, abstract only, 2006.
“Effect of secondary interface microstructure on pore structure and performance of cement-based materials,” Feng et al., Cailiao Yanjiu Xuebao, 17(5), 489-494, abstract only, 2003.
“Preparation of multifunctional dry-power paints,” Yanmin Gao, Faming Zhuanli Shenqing gongkai Shuomingshu, 4 pages, abstract only, 2005.
Office Action from U.S. Appl. No. 12/426,393, Jul. 2, 2010.
Notice of Allowance from U.S. Appl. No. 12/472,561, Jun. 29, 2010.
PCT International Search Report and Written Opinion for International Application No. PCT/GB2010/001045, Jul. 21, 2010.
Office Action from U.S. Appl. No. 11/388,645, Aug. 17, 2010.
Office Action from U.S. Appl. No. 12/833,189, Oct. 1, 2010.
Office Action from U.S. Appl. No. 12/833,189, Nov. 10, 2010.
Notice of Allowance from U.S. Appl. No. 12/426,393, Dec. 16, 2010.
PCT International Search Report and Written Opinion for International Application No. PCT/GB2010/001806, Jan. 20, 2011.
English language abstract of CN 101544488, Sep. 30, 2009.
Office Action from U.S. Appl. No. 12/833,189, Feb. 17, 2011.
Howard, “An Analysis and the Control of Lost Circulation”, Petroleum Transactions, AIME, vol. 192, pp. 171-182, 1951.
Darley, “Composition and Properties of Drilling and Completion Fluids”, Fifth Edition, Gulf Publishing Company, pp. 446-454; 595-598, 1988.
HES Brochure “Latex 2000”, Aug. 2006.
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, Apr. 18, 2011.
“Effect of the particle size on the micro and nanostructural features of calcium phosphate cement: a kinetic analysis”, Biomaterials 25, 3453-3462, 2004.
Office Action from U.S. Appl. No. 12/567,782, Apr. 5, 2011.
Office Action from U.S. Appl. No. 12/651,662, Apr. 5, 2011.
Office Action from U.S. Appl. No. 12/567,783, Apr. 6, 2011.
Office Action from U.S. Appl. No. 12/263,954, Apr. 20, 2011.
Office Action from U.S. Appl. No. 12/651,662, Apr. 22, 2011.
Office Action from U.S. Appl. No. 12/567,782, Apr. 25, 2011.
Office Action from U.S. Appl. No. 12/833,189, May 16, 2011.
Office Action from U.S. Appl. No. 12/833,189, Jul. 18, 2011.
Office Action from U.S. Appl. No. 12/263,954, Aug. 8, 2011.
Office Action from U.S. Appl. No. 12/567,783, Aug. 23, 2011.
Office Action from U.S. Appl. No. 12/833,189, Oct. 11, 2011.
Office Action from U.S. Appl. No. 12/651,662, Nov. 28, 2011.
Office Action from U.S. Appl. No. 12/833,189, Feb. 7, 2012.
Office Action from U.S. Appl. No. 12/567,782, Mar. 2, 2012.
Office Action from U.S. Appl. No. 13/052,471, Mar. 6, 2012.
Office Action from U.S. Appl. No. 12/651,662, 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.
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.
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/GB2010/0010445 dated Jul. 21, 2010.
Office Action from U.S. Appl. No. 13/052,471 dated Feb. 4, 2013.
Communication from EPO from Application No. 12159772.8 dated Feb. 14, 2013.
International Preliminary Report on Patentability from PCT/GB2009/002596, dated May 3, 2011.
Office Action for U.S. Appl. No. 12/833,189 dated May 28, 2013.
Office Action for U.S. Appl. No. 13/435,701 dated Jun. 4, 2013.
Office Action for U.S. Appl. No. 12/567,782 dated Jun. 21, 2013.
Office Action for U.S. Appl. No. 13/443,934 dated Jun. 27, 2012.
Office Action for U.S. Appl. No. 13/052,471 dated May 10, 2013.
Office Action for U.S. Appl. No. 13/431,701, dated Jul. 11, 2013.
Office Action for U.S. Appl. No. 12/263,954 dated Mar. 14, 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 for U.S. Appl. No. 12/263,954 dated Oct. 8, 2013.
Office Action for U.S. Appl. No. 12/567,783 dated Oct. 3, 2013.
Office Action for U.S. Appl. No. 13/435,701 dated Oct. 4, 2013.
EPO Office Action for Application No. 09751959.9 dated Sep. 27, 2013.
USPTO Office Action for U.S. Appl. No. 13/458,112 dated Dec. 26, 2013.
USPTO Notice of Allowance for U.S. Appl. No. 13/052,471 dated Jan. 30, 0214.
HES Brochure, “FlexPlug Services” dated Apr. 2008.
HES Brochure, “Thermatek Services” dated May 2005.
HES Brochure, “Fuse-It Circulation Treatment” dated May 2006.
USPTO Office Action for U.S. Appl. No. 13/458,112 dated Apr. 1, 2014.
USPTO Final Office Action for U.S. Appl. No. 13/435,701 dated Feb. 20, 2014.
USPTO Office Action for U.S. Appl. No. 13/620,013 dated Jan. 30, 2014.
USPTO Final Office Action for U.S. Appl. No. 12/263,954 dated May 9, 2014.
USPTO Final Office Action for U.S. Appl. No. 12/567,783 dated May 9, 2014.
Australian Examination Report GCC/P/2009/14628 dated Nov. 21, 2013.
International Report on Patentability for International Application No. PCT/US2013/038343 dated Oct. 28, 2014.
International Preliminary Report on Patentability for PCT/US13/038343 dated Nov. 6, 2014.
Related Publications (1)
Number Date Country
20120211227 A1 Aug 2012 US
Continuation in Parts (3)
Number Date Country
Parent 12567782 Sep 2009 US
Child 13458112 US
Parent 12263954 Nov 2008 US
Child 12567782 US
Parent 11747002 May 2007 US
Child 12263954 US