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, , - .The invention relates to the field of oil and gas industry, in particular to the technology of manufacturing ceramic proppants intended for use in oil or gas production by hydraulic fracturing - hydraulic fracturing.
State of the art
. , .Hydraulic fracturing is a way to increase well productivity in oil or gas production. It involves the injection of fluids into an oil or gas-bearing underground formation at sufficiently high speeds and pressures in order to form cracks in the formation, increasing the flow of fluids from the oil or gas reservoir into the well.
, - (), , , , , , , .To maintain open fractures, mechanically strong proppants that do not interact with the well fluid are introduced into them sphere-like granules (proppants), which, penetrating the fluid into the fracture and at least partially filling it, create a strong proppant permeable to oil and gas released from the reservoir.
, . , . . , ( ), , , , , , , , , , , , , , .In general, a proppant is a solid material designed to keep induced hydraulic fracturing open during or after a fracturing process. For hydraulic fracturing, proppants are added to the well treatment fluids, which are then injected into underground formations. Well treatment fluids may vary in composition depending on the type of formation. Traditional proppants include materials such as sand (the most common type), nutshell, aluminum and aluminum alloys, crushed coke, granular slag, coal dust, crushed stone, metal granules such as steel, sintered bauxite, sintered alumina, refractory materials, such as mullite, and glass granules, as well as artificial ceramic materials and polymers.
, , , , (, , ) .The importance of choosing a material suitable for a particular well is due to the fact that proppants must withstand not only high reservoir pressure, which tends to deform proppant particles, which can lead to closure of the fracture, but also withstand the effects of aggressive well medium (moisture, acid gases, salt solutions) when high temperatures.
, , , .It has been found that ceramic proppants generally have advantageous characteristics relative to many other types of materials, for example, in the context of their strength and uniformity of size and shape.
, , , , , , ( ), , .Nevertheless, despite the fact that ceramic proppants are strong enough and effective and can be produced in cost-effective ways, there is a need to create new proppants with improved mechanical characteristics, such as strength, permeability, specific gravity (bulk density), hydrothermal stability and acid resistance, as well as effective methods for their preparation.
, ( US ), , , , , , . %: - 25-40, - 50-65, - 1,6 - 2,6. psi.Known technical solutions for producing proppants, namely proppant proppant (US patent No. ), which is a ceramic spherical granules of sintered kaolin clay containing oxides of aluminum, silicon, iron and titanium, and the oxides in these granules are present in the following proportions, wt. %: alumina - 25-40, silica - 50-65, iron oxide - 1.6 and titanium oxide - 2.6. However, this proppant has insufficient strength and is intended only for wells of intermediate depth with a pressure of less than psi.
1 , - 55 80% ./. , °.In addition, from the patent of the Russian Federation C1, a method for producing ceramic proppants made of magnesium silicate material with a forsterite content of from 55 to 80% wt./wt. According to this method, the forsterite-based ceramic source material is crushed, granulated and fired at a temperature of to ° C.
, , .The disadvantage of this method is that in hydrothermal conditions, forsterite is partially hydrated, so the mechanical strength of the proppant granules is noticeably reduced.
2 , - 40% ./. MgO 60% ./. SiO2. - (Δ 10 20°) . .RF patent C2 shows a similar process in which the magnesium silicate precursor consists of magnesium metasilicate with approximately 40% w / w. MgO and approximately 60% w / w. SiO 2 . Due to the very narrow sintering range (Δ max from 10 to 20 ° ), the manufacture of such proppants is difficult and expensive. Also, due to the narrow sintering temperature range, firing in a rotary kiln under standard industrial conditions will lead to the production of underburned porous proppant particles and overbaked molten proppant particles.
, , , , . , . , .Thus, the actually achieved strength, acid resistance and hydrothermal stability of proppants obtained under industrial conditions are noticeably lower than for batches obtained under laboratory conditions. In addition, the narrow sintering range requires a greater exposure of the proppant material to the sintering temperature to achieve a uniform temperature distribution. This leads to the growth of crystals of magnesium metasilicate and phase transformation during the cooling process, which also reduces the quality of the resulting proppant.
, , , , .Thus, a disadvantage of the known method and the product obtained by it is that the proppant obtained has reduced mechanical characteristics, in particular strength values, which also leads to a decrease in the proppant layer permeability at elevated pressures.
( ) .The objective of the present invention is to obtain a ceramic proppant (proppant particles) with high performance and low cost.
, , , , , .In particular, it is an object of the present invention to provide a new proppant with improved properties and an economical and energy-efficient method for producing a ceramic proppant, which makes it possible to obtain a proppant with increased strength, reduced bulk density, good permeability, hydrothermal stability and acid resistance.
SUMMARY OF THE INVENTION
, .The tasks are achieved by obtaining a ceramic proppant in accordance with a new method for producing a ceramic proppant, which allows the internal structure of the agent to be modified to give it preferential properties.
, :In one aspect, the present invention relates to a method for producing a ceramic proppant, including:
) , , , ;a) preparation, including grinding of raw materials containing magnesium-containing material, and auxiliary materials to obtain a mixture;
) ; b) granulating the mixture to obtain proppant precursor granules; and
) ;c) firing the proppant precursor granules to produce proppant granules;
.and an important feature of this method is the stage of preliminary firing of magnesium-containing material in a reducing atmosphere.
, .In another aspect, the present invention relates to a ceramic proppant obtained by the above production method.
, 50 80 . % 4 8 . %.In another aspect, the present invention relates to a ceramic proppant, characterized by an enstatite content of from 50 to 80 mass. % and magnesioferrite from 4 to 8 mass. %
, , :In addition, the present invention relates to a method for processing an underground formation, including:
) ;a) providing a ceramic proppant;
) ( );b) mixing said ceramic proppant with hydraulic fracturing fluid (hydraulic fracturing fluid);
) ) .C) the introduction of the mixture from stage b) into the underground reservoir.
.Also in one aspect, the present invention relates to the use of a ceramic proppant for fracturing an underground circuit board.
DETAILED DESCRIPTION OF THE INVENTION
, .The present invention relates to a method for producing proppant and proppant, which has improved performance and can be obtained using inexpensive and affordable ceramic materials.
, . , , ., , ( ). , , , , , , .. , , , .In the present description, the proppant or proppant is a granular material, in particular ceramic granules of a substantially spherical shape. Magnesium-containing material, in particular minerals based on magnesium silicates and, possibly, iron (can also be referred to as magnesium silicate materials or magnesia-containing materials), can be used as a starting material for producing a proppant as a result of grinding, granulation, and calcination. Non-limiting examples of such materials include various representatives of minerals of the peridotite class, including olivines, dunite, serpentinite, used as starting materials for ceramic proppants, as well as forsterite, enstatite and fayalite minerals present in them or formed as a result of firing, etc. d. As auxiliary materials, materials and additives are used, for example silica-containing components such as silica sand, hydromica and montmorillonite clays or refractory clays.
, , 0,4-1,7 . , . : 1,3 1,9 /3, psi, , , - « -».The granule size of the finished proppant is typically 0.4-1.7 mm. This size is not limiting, and granules of any size can be obtained depending on the specific application or requirements for a particular well. In general, proppant granules should satisfy the following characteristics: bulk density in the range from 1.3 to 1.9 g / cm 3 , preservation of integrity and permeability at pressures from to psi, sphericity and roundness, acid resistance, as described in GOST R - "Proppants of magnesia-quartz."
) , , , , , , , . , ) , . 45% 70 . % 55 . %, 30 . % 55 . % , / 0 10 . % 0 10 . % .According to the proposed method for producing a proppant in the first stage a), preparation, for example, grinding or grinding, of starting materials containing magnesium-containing material and auxiliary materials, such as silica-containing components, for example silica sand, is carried out to obtain a mixture of starting materials. Thus, according to the method, step a) of preparing the starting materials may include grinding, for example, grinding the starting materials. According to the proposed method, the amount of starting magnesium-containing material in the charge is from 45% to 70 mass. % and the amount of auxiliary materials is up to 55 mass. %, in particular the mixture may contain silica sand in an amount of from 30 mass. % to 55 mass. % by weight of the mixture, hydromica and / or montmorillonite clay in an amount of from 0 to 10 mass. % by weight of the mixture and refractory clay in an amount of from 0 to 10 mass. % of the mass of the charge.
, . . . , , , 1% 40 , 50% 10 .Grinding can be carried out by any method known to specialists in this field of technology. Preferably, the grinding is carried out in ball tube mills. It is also preferable to co-grind the magnesium-containing material and the auxiliary material. Before grinding, auxiliary materials can be pre-dried, in particular quartz sand, as a rule, dried to a moisture content of less than 1% in a tumble dryer or similar devices. Preferably, grinding is carried out to a maximum particle size of less than 40 microns, while at least 50% of the particles must be less than 10 microns.
) . 33-40% , , 30 . , , () (-) 13-20%. .., .. , 4- , . . .: , . - 528 ., .. « », , . - , .. . . , . . - .Stage a) preparation of the starting materials may also include mixing the crushed starting materials with water to obtain a slip. The specified slip with a moisture content of 33-40% can be further ground, for example, in wet ball mills to a maximum particle size of less than 30 microns. After that, the resulting slip is dried, for example, in tower spray dryers (BRS) to obtain a mixture (press powder) with a moisture content of 13-20%. A detailed description of the techniques for preparing the starting materials and compositions for producing ceramic products can also be found in the books Strelov K.K., Mamykin P.S. Refractory Technology, 4th Edition, Revised. and add. - M.: Metallurgy, .-- 528 p., V.L. Balkevich Technical ceramics, Publishing house of building literature, Moscow. - , K.A. Nohratyan. Drying and firing in the building ceramics industry. State publishing house of literature on construction, architecture and building materials. Moscow. - .
) , 0,5-2 . , . .After the preparation stage, step b) granulating the mixture is carried out to obtain proppant precursor granules with a defined granule size, for example 0.5-2 mm. Granulation can be carried out by any method and in any equipment known to specialists in this field of technology. One example of suitable equipment is plate-type granulators.
() , , ) . , - 0,5-0,8 , 0,7-1,0 , 0,9-1,2 , 1,1-1,7 1,6-2,0 , . .. , .: . - , 224 .The method may further include drying and screening by size (fractionation) of the proppant precursor granules to separate and return granules that do not meet the required characteristics to stage a) of preparation. As a rule, before firing, the mixture is sifted into several fractions - 0.5-0.8 mm, 0.7-1.0 mm, 0.9-1.2 mm, 1.1-1.7 mm or 1.6 -2.0 mm, and each of the fractions is fired separately. A description of the methods and equipment for granulation can also be found in Kochetkov V.N. Granulation of mineral fertilizers, M .: Chemistry. - , 224 p.
) . , , ° ° , , . . . . , . .. , .. , .. . . - , , , . .The final step in producing a proppant is step c) firing the proppant precursor granules. Firing is usually carried out at a temperature of from about ° C to about ° C for a period of time sufficient to ensure the production of spherical ceramic granules. The specific time and temperature will vary depending on the source material used and the specific equipment. The optimal firing time and temperature for a specific composition of the starting material can be determined empirically in accordance with the results of physical tests of the obtained granules after firing. Firing is carried out in an oxidizing atmosphere. For example, firing can be carried out in a traditional rotary kiln. Description of firing equipment can also be found in P.S. Mamykin, P.V. Levchenko, K.K. Arrow Furnaces and dried refractories. State Scientific and Technical Publishing House of Literature on Ferrous and Non-Ferrous Metallurgy, Sverdlovsk Branch, Sverdlovsk, . At the end, screening of proppant agent granules of the required size can be carried out and packaging of a commercial product in a storage container.
, , , , , . () . , , .Moreover, the inventors of the present invention unexpectedly found that ceramic proppants with higher performance, in particular with increased strength, permeability and reduced bulk density, can be obtained through an additional preliminary calcination step, i.e., heat treatment of the magnesium-containing material in a reducing atmosphere . Preliminary firing is generally carried out to remove chemically bound moisture (dehydration) from the starting minerals in order to facilitate granulation and final firing. However, it was found that its conduct in a reducing atmosphere is associated with imparting improved properties to the final products.
, .Thus, the method according to the present invention includes the step of pre-firing the magnesium-containing material in a reducing atmosphere.
) . , ) .According to a preferred embodiment, the pre-calcination step is carried out before step a) of the preparation of the starting materials. The inventors have found that conducting preliminary firing before stage a) may be preferable from the point of view of reducing the energy consumption for grinding the magnesium-containing material due to loosening of the magnesium-containing material during the preliminary firing.
, 900° ° . ( ) () 5 . %, 2-3 . %. , , , , , . , , .Further, in the method according to the present invention, the preliminary calcination step is carried out at a temperature of from about 900 ° C to about ° C in a reducing atmosphere. In the present method, a reducing (weakly reducing) atmosphere means a reaction medium (atmosphere) with an oxygen content of less than 5 mass. %, preferably less than 2-3 mass. % A reducing atmosphere in the pre-calcination zone can be achieved by introducing a carbon-containing additive selected from the group including, for example, natural gas, coal, coke, or mixtures thereof. However, it should be noted that the proposed method is not limited to these additives and the specialist in this field can use any means and techniques to ensure a reducing atmosphere in the firing zone.
, , , .The preliminary firing step can be carried out in any firing furnaces known to those skilled in the art, however, shaft type furnaces are preferred, since it is not possible to create a reducing atmosphere in common rotary kilns.
. , . , , . .The behavior of preliminary firing in shaft furnaces is accompanied by a distributed air supply to maintain combustion in the zones of the furnace. Part of the air is fed through the discharge grill at the bottom of the furnace, part of the air is fed through additional windows above the firing zone. Natural gas or another agent or additive is supplied to the combustion zone to provide a reducing atmosphere in the reaction zone, as defined herein. Preliminary firing in a shaft furnace is also characterized by a low specific energy consumption and a reduction in dust losses compared to firing of magnesium-containing material in rotary kilns.
, , .Not limited to a specific theory, the authors of the present invention believe that the improvement in the characteristics of the proppant is due to the following factors.
, 900° (, , , .), ° , () (Fe2SiO4), FeO, , MgO . , , , . , , . , FeO , , .The inventors found that during preliminary firing at temperatures less than 900 ° C, the magnesium-containing material (dunite, olivine, serpentinite, etc.) does not completely dehydrate, and at temperatures above ° C unwanted interactions can occur, for example, in dunite (olivines ) fayalite (Fe 2 SiO 4 ), including FeO contained in fayalite, can interact with MgO with the formation of magnesioferrite. In this case, the formation of magnesioferrite at the preliminary firing stage is undesirable, since magnesioferrite increases the strength of the material and, therefore, complicates further grinding at the stage of preparing the charge of the starting materials. In addition, magnesioferrite is a passivated element that does not participate in the formation of a given structure during the final firing of proppant precursor granules. Thus, conducting preliminary firing in a reducing atmosphere prevents undesirable oxidation of FeO and, as a result, the formation of magnesioferrite to the stage of final firing.
, (FeO) Fe2O3 Fe3O4 (MgO).A preliminary dehydration calcination in a reducing atmosphere leads to the fact that the iron oxide (FeO) present in the mineral material does not transform into Fe 2 O 3 or Fe 3 O 4 and remains in solid solution with magnesium oxide (MgO).
, , - .An increase in the characteristics, especially strength, of the proppant is achieved due to the formation of proppant precursor precursor granules in an oxidizing atmosphere during the final firing, along with quartz of other crystalline phases - enstatites with magnesioferrites embedded in magnesioferrites.
, During preliminary firing of dunite, thermal decomposition of serpentinite and olivine occurs with the formation of forsterite and enstatite and the removal of chemically bound moisture, namely
(Mgn1,Fem1)2SiO4(Mgn2,Fem2)2SiO4+(Mgn3,Fem3)2SiO3,(Mg n1 , Fe m1 ) 2 SiO 4 (Mg n2 , Fe m2 ) 2 SiO 4 + (Mg n3 , Fe m3 ) 2 SiO 3 ,
n1=n2+m2=n3+m3=1 n1<n2, a m1>m2;where n 1 = n 2 + m 2 = n 3 + m 3 = 1 and n 1 <n 2 , am 1 > m 2 ;
3MgO2SiO22H2O2MgOSiO2+MgOSiO2+2H2O3MgO2SiO 2 2H 2 O 2MgOSiO 2 + MgOSiO 2 + 2H 2 O
3MgO4SiO22H2O3(MgOSiO2)+SiO2+2H2O3MgO4SiO 2 2H 2 O 3 (MgOSiO 2 ) + SiO 2 + 2H 2 O
FeO MgOFeO.In this case, iron oxide FeO remains in the form of a solid solution of magnesium oxides and iron oxides MgOFeO.
700°, . , , .The thermal decomposition of serpentinite begins at temperatures above 700 ° C, and the process intensifies with increasing temperature. At the same time, the material is loosened, which, as indicated earlier, can improve productivity during grinding.
, .Then, crystallization of enstatites and forsterite begins, which leads to an increase in the strength of the material.
, :During the final firing of the product, forsterite, iron oxide and silicon oxide react with the formation of the crystal lattice of enstatite with magnesioferrite embedded in it:
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Mg2SiO4+SiO22MgOSiO2 Mg 2 SiO 4 + SiO 2 2MgOSiO 2
2Mg2SiO4+4FeO+O22MgOSiO2+2MgOFe2O3 2Mg 2 SiO 4 + 4FeO + O 2 2MgOSiO 2 + 2MgOFe 2 O 3
, , , Fe2O3, FeO . , , Mg2SiO4-MgFe2O4 , , .In other words, the inventors believe that the incorporation into the crystal lattice of a more active, compared with Fe 2 O 3 , FeO allows you to get a stronger structure. In addition, the inventors also found that the eutectic Mg 2 SiO 4 -MgFe 2 O 4 has a lower melting point and, therefore, reduces energy costs during the firing of the finished product.
, , 50% 80 . % () 4-8% . %. 0,5-2 . %. , , .Thus, according to the present invention, as a result of the final calcination, the proppant obtained can be characterized by a content of magnesium-containing material, in particular from 50% to 80 mass. % enstatitis (clinoenstatitis) and magnesioferrite 4-8% of the mass. % The composition of the finished proppant may also include magnetite in an amount of from 0.5-2 mass. % The remainder may be diopside, pyroxene, quartz, and other minerals, depending on the presence of impurities in the sand and magnesium-containing material.
, , , , () 50 80% 4-8%, , , , , .As a result of studies conducted by the authors of the present invention, it was found that a proppant, characterized by a content of enstatite (clinoenstatite) from 50 to 80% and magnesioferrite 4-8%, has advantageous properties, namely, significantly higher strength, reduced bulk density, good permeability as well as hydrothermal stability.
, , .Therefore, the present invention also relates to a ceramic proppant obtained by the method described above.
, : ) , ) ( ), ) .The invention also relates to a method for treating a subterranean formation using the obtained ceramic proppant, including: a) providing a ceramic proppant, b) mixing said ceramic proppant with hydraulic fracturing fluid (hydraulic fracturing), c) introducing the mixture into the subterranean formation.
, , , , (), , ., , , , , . , , , , , , , . «» ; , , , , , - (), , , , ..Water-based high-viscosity working fluid used in hydraulic fracturing, as a rule, is additionally thickened using high molecular weight natural resins, such as galactomannan or glucomannan resins (guar), acacia resin karaya, tragacanth, etc., natural polysaccharides, such as, for example, starch cellulose and their derivatives. The working fluid must be chemically stable and viscous enough to hold the proppant in suspension while it is subjected to shear deformation and heating in the surface equipment, in the well pipe system, perforation channels and in the fracture itself, to avoid premature proppant deposition and, as consequence, closing the crack. The composition of the hydraulic fluid can include staplers of a linear gel; destructors providing controlled degradation of the high-viscosity polymer to liquid fluid for simplified hydraulic fluid withdrawal from the well, as well as thermal stabilizers, pH adjusting additives, surfactants, bactericides, emulsifiers and demulsifiers, additives that reduce infiltration, clay stabilizers, etc. .d.
, .Thus, the present invention also relates to the use of a ceramic proppant for fracturing an underground circuit board.
MODES FOR CARRYING OUT THE INVENTION
. , .The invention will now be illustrated with reference to the following non-limiting examples. Experimental proppant samples were obtained and studied using dunite and serpentinite, heat-treated in various ways, as the starting magnesium-containing material.
1Comparison Example 1
° , 48:48:4 40 . 1,1-1,7 . 120° . ISO -2: ( ) psi . 1.Dunite was preliminarily fired in a laboratory furnace at a temperature of ° C in an oxidizing atmosphere, then it was ground together with quartz sand and low-melting clay in a ratio of 48: 48: 4 weight percent to a size of 40 μm or less. After that, the resulting material was granulated on a laboratory granulator to a fraction of 1.1-1.7 mm. The material dried at 120 ° C was calcined at various temperatures and scattered. Quality indicators were tested in accordance with the requirements of ISO -2: for crushing resistance (mass fraction of broken granules) at a specific pressure of 10,000 psi and bulk density was determined. The indicators are shown in table 1.
2Comparison Example 2
, -° . , 1.As a magnesium-containing component used dunite, preliminarily calcined at a temperature of - ° C in an oxidizing atmosphere in a rotary kiln. Samples were prepared as in example 1.
3Comparison Example 3
, -° . , 1.As a magnesium-containing component, serpentinite, previously calcined at a temperature of - ° C in an oxidizing atmosphere in a rotary kiln, was used. Samples were prepared as in example 1.
4Example 4
, 950-° . , 1.As a magnesium-containing component, dunite was used, previously calcined at a temperature of 950- ° C in a reducing atmosphere in a shaft furnace. Samples were prepared as in example 1.
5Example 5
, 950-° . , 1 , 65:30:5 .As a magnesium-containing component, dunite was used, previously calcined at a temperature of 950- ° C in a reducing atmosphere in a shaft furnace. Samples were prepared, as in example 1, with a ratio of dunite, sand and clay of 65: 30: 5 weight percent.
, .As can be seen from the results of the table, a change in the preliminary firing modes affects the quality indicators of the finished product and the conduct of preliminary heat treatment in a shaft furnace allowed us to obtain more durable proppants.
6Example 6
ART Workstation .Additionally, the finished samples were investigated in order to determine the quantitative phase composition on an ART Workstation X-ray fluorescence spectrometer with an integrated diffraction system.
1-3 63,8-67,9% 2,4-3,6%. 3,1-4,5%.In the samples of examples 1-3, the content of enstatite was 63.8-67.9% and magnesioferrite 2.4-3.6%. Moreover, magnetites in the amount of 3.1-4.5% are present in the phase composition.
4 5 66,3% 74,6% , 5,2-5,6%, 0,8-1,5%, .In the samples of examples 4 and 5, the content of enstatite was 66.3% and 74.6%, respectively, magnesioferrites 5.2-5.6%, magnetite 0.8-1.5%, while a high content of magnesioferrites and a low content of magnetite says about a more complete reaction to introduce iron into the crystal lattice of enstatite.
A proppant is a solid material, typically sand, treated sand or man-made ceramic materials, designed to keep an induced hydraulic fracture open, during or following a fracturing treatment, most commonly for unconventional reservoirs. It is added to a fracking fluid which may vary in composition depending on the type of fracturing used, and can be gel, foam or slickwaterbased. In addition, there may be unconventional fracking fluids. Fluids make tradeoffs in such material properties as viscosity, where more viscous fluids can carry more concentrated proppant; the energy or pressure demands to maintain a certain flux pump rate (flow velocity) that will conduct the proppant appropriately; pH, various rheological factors, among others. In addition, fluids may be used in low-volume well stimulation of high-permeability sandstone wells (20 to 80 thousand US gallons (76 to 303 kl) per well) to the high-volume operations such as shale gas and tight gas that use millions of gallons of water per well.
Conventional wisdom has often vacillated about the relative superiority of gel, foam and slickwater fluids with respect to each other, which is in turn related to proppant choice. For example, Zuber, Kuskraa and Sawyer () found that gel-based fluids seemed to achieve the best results for coalbed methane operations,[1] but as of , slickwater treatments are more popular.
Other than proppant, slickwater fracturing fluids are mostly water, generally 99% or more by volume, but gel-based fluids can see polymers and surfactants comprising as much as 7 vol%, ignoring other additives. Other common additives include hydrochloric acid (low pH can etch certain rocks, dissolving limestone for instance), friction reducers, guar gum, biocides, emulsion breakers, emulsifiers, 2-butoxyethanol, and radioactive tracer isotopes.
Proppants have greater permeability than small mesh proppants at low closure stresses, but will mechanically fail (i.e. get crushed) and produce very fine particulates ("fines") at high closure stresses such that smaller-mesh proppants overtake large-mesh proppants in permeability after a certain threshold stress.[2]
Though sand is a common proppant, untreated sand is prone to significant fines generation; fines generation is often measured in wt% of initial feed. One manufacturer has claimed untreated sand fines production to be 23.9% compared with 8.2% for lightweight ceramic and 0.5% for their product.[3] One way to maintain an ideal mesh size (i.e. permeability) while having sufficient strength is to choose proppants of sufficient strength; sand might be coated with resin, to form curable resin coated sand or pre-cured resin coated sands. In certain situations a different proppant material might be chosen altogetherpopular alternatives include ceramics and sintered bauxite.
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Increased strength often comes at a cost of increased density, which in turn demands higher flow rates, viscosities or pressures during fracturing, which translates to increased fracturing costs, both environmentally and economically.[4] Lightweight proppants conversely are designed toals can break the strength-density trend, or even afford greater gas permeability. Proppant geometry is also important; certain shapes or forms amplify stress on proppant particles making them especially vulnerable to crushing (a sharp discontinuity can classically allow infinite stresses in linear elastic materials).[5]
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Proppant mesh size also affects fracture length: proppants can be "bridged out" if the fracture width decreases to less than twice the size of the diameter of the proppant.[2] As proppants are deposited in a fracture, proppants can resist further fluid flow or the flow of other proppants, inhibiting further growth of the fracture. In addition, closure stresses (once external fluid pressure is released) may cause proppants to reorganise or "squeeze out" proppants, even if no fines are generated, resulting in smaller effective width of the fracture and decreased permeability. Some companies try to cause weak bonding at rest between proppant particles in order to prevent such reorganisation. The modelling of fluid dynamics and rheology of fracturing fluid and its carried proppants is a subject of active research by the industry.
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Though good proppant choice positively impacts output rate and overall ultimate recovery of a well, commercial proppants are also constrained by cost. Transport costs from supplier to site form a significant component of the cost of proppants.
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Other than proppant, slickwater fracturing fluids are mostly water, generally 99% or more by volume, but gel-based fluids can see polymers and surfactants comprising as much as 7 vol%, ignoring other additives.[6] Other common additives include hydrochloric acid (low pH can etch certain rocks, dissolving limestone for instance), friction reducers, guar gum,[7] biocides, emulsion breakers, emulsifiers, and 2-Butoxyethanol.
Radioactive tracer isotopes are sometimes included in the hydrofracturing fluid to determine the injection profile and location of fractures created by hydraulic fracturing.[8] Patents describe in detail how several tracers are typically used in the same well. Wells are hydraulically fractured in different stages.[9] Tracers with different half-lives are used for each stage.[9][10] Their half-lives range from 40.2 hours (lanthanum-140) to 5.27 years (cobalt-60).[11] Amounts per injection of radionuclide are listed in The US Nuclear Regulatory Commission (NRC) guidelines.[12] The NRC guidelines also list a wide range of radioactive materials in solid, liquid and gaseous forms that are used as field flood or enhanced oil and gas recovery study applications tracers used in single and multiple wells.[12]
In the US, except for diesel-based additive fracturing fluids, noted by the American Environmental Protection Agency to have a higher proportion of volatile organic compounds and carcinogenic BTEX, use of fracturing fluids in hydraulic fracturing operations was explicitly excluded from regulation under the American Clean Water Act in , a legislative move that has since attracted controversy for being the product of special interests lobbying.[citation needed]
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