Patent Application
20180155478
The present invention relates to a process for preparing water-soluble or water-swellable polymers based on sulfonic acids, phosphonic acids or salts thereof, uncharged monomers, and to the use of these polymers as water loss reducers in cement slurries for cementing deep wells, and as additive in drilling muds for deep wells for reduction of water loss at the well wall.
In the case of deep wells for exploitation of mineral oil and natural gas deposits, it is necessary to use drilling muds and cement slurries. During the drilling operation, what are called drilling muds are used, the tasks of which include conveying the drillings to the surface and cooling the drill head. During the drilling operation, the well can pass through porous rock layers. As a result, there can be release of water from the drilling mud to the porous rock. In order to prevent this, additives such as water loss reducers, called “fluid loss additives”, are used.
Once the well has reached a particular depth, what are called casing tubes are introduced into the well. For this purpose, the casing tubes have to be fixed, meaning that a cement slurry is pumped into the cavity between the rock and the casing tubes, and solidifies to give a solid rock. The release of water from the cement slurry to the porous rock during the pumping operation should be low, in order that there is no thick filtercake formed at the well wall, which would increase the pumping pressure owing to the annular space constriction to such an extent that the porous rock will break up. Moreover, the cement slurry would not set in an optimal manner in the case of excessive water release and would become permeable to gas and oil. On the other hand, the cement mantle that forms in the annular space must attain adequate strength very quickly and no shrinkage, resulting in flow channels for gas, oil and water, must occur in the course of setting. Optimal adjustment of the properties of the cement slurry is only possible by means of additives. The most important additives are retardants, accelerators, dispersants and water loss reducers.
Synthetic polymers based on the monomer acryloyldimethyltaurate have been found to be effective water loss reducers in drilling muds and have become particularly established as water loss reducers in cement and gypsum slurries.
U.S. Pat. No. 5,472,051 describes polymers formed from acryloyldimethyltaurate and acrylic acid with molecular weights of less than 5000 g/mol and the use thereof as water loss reducers.
EP 1045869 describes polymers formed from acryloyldimethyltaurate and acrylamide and the use thereof as water loss reducers. These polymers are prepared with the aid of a precipitation polymerization as the ammonium salt of acryloyldimethyltaurate in tert-butanol. The preparation of a sodium salt is not described or not possible (comparative example 1).
EP 0116671 discloses the introduction of 5%-60% by weight of vinylamides (e.g.
N-vinylmethylacetamide) in acryloyldimethyltaurate-containing polymers. It was thus possible to significantly extend the high temperature-range of use.
U.S. Pat. No. 5,025,040 describes polymers formed from acryloyldimethyltaurate, acrylamide and at least 20% N-vinylimidazole.
EP 0217608, U.S. Pat. No. 4,555,269 and EP 0157055 describe a copolymer formed from acryloyldimethyltaurate and dimethylacrylamide in a molar ratio of 1:4 to 4:1 as fluid loss additive for saline (about 10% by weight) cement slurries and the use of acryloyldimethyltaurate and acrylic acid in a molar ratio of 1:4 to 4:1 for the same purpose.
EP 1059316 describes the use of polymers containing acryloyldimethyltaurate, vinylphosphonic acid and cationic monomers, the preparation thereof and use as water loss reducers.
U.S. Pat. No. 5,336,316 teaches a cement composition for oil and gas sources, comprising a cement, water and an additive. The additive is a polymer containing phosphonate groups bonded to a polymer backbone. The additive imparts improved water loss and setting properties to the cement compositions.
The synthetic poly(acryloyldimethyltaurate) copolymers can be obtained in two different physical forms in industrial production, as powder and in liquid form. The liquid form is understood to mean polymer solutions, for example polymer emulsions or dispersions, in which the polymer is present dissolved in a solvent or dispersed through the use of an emulsifier.
Poly(acryloyldimethyltaurate) copolymers in powder form have recently been described in patent applications U.S. Pat. No. 5,373,044, U.S. Pat. No. 2,798,053, EP 1045869, EP 301532, EP 816403, EP 1116733 and EP 1069142. All these polymers based on acryloyldimethyltaurate are obtained with the aid of a precipitation polymerization. This involves initially charging the monomers used in an organic solvent, such as toluene, ethyl acetate, hexane, cyclohexane, ethanol or 2-methylpropan-2-ol. The disadvantage of these organic solvents is usually that the acryloyldimethyltaurate does not dissolve completely therein, the result being excessively high residual monomer contents of the polymers obtained after the polymerization. Moreover, the molar masses obtained are usually not high, since the polymer becomes insoluble in the solvent too quickly during the polymerization.
Poly(acryloyldimethyltaurate) copolymers which have been prepared with the aid of a precipitation polymerization have the advantage compared to inverse emulsion polymerization that no residues of oil and the emulsifiers are present in the final product. Some of the oils used and the emulsifiers used in the polymerization processes mentioned can cause skin irritation. Moreover, the polymers which have been prepared with the aid of an inverse emulsion polymerization usually have the disadvantage that the oil present in the polymer from the process leads to cloudiness in aqueous polymer solutions.
WO 2010/108634, WO 2012/119747, WO 2012/119746, EP 1045869, EP 0816403, EP 2227498, U.S. Pat. No. 7,151,137 and WO 0244268 describe, inter alia, processes for preparing poly(acryloyldimethyltaurate) copolymers with the aid of a precipitation polymerization in 2-methylpropan-2-ol.
The use of 2-methylpropan-2-ol or 2-methylpropan-2-ol/water mixtures makes it necessary to neutralize the acryloyldimethyltaurate with gaseous ammonia or an ammonium salt, since these are the only salts of acryloyldimethyltaurate that have sufficient solubility in 2-methylpropan-2-ol for polymers of the desired molecular weight to form. The low solubility of these alkali metal or alkaline earth metal salts of poly(acryloyldimethyltaurate) copolymers has an adverse effect on the molecular weight of the polymers obtained and the performance thereof.
EP 1033378 describes a process for preparing poly(acryloyldimethyltaurate) copolymer ammonium salt in 2-methylpropan-2-ol. The polymers prepared were used in barite-weighted seawater drilling muds with 3% KCl and a specific weight of 2.1 kg/L (comparative examples 2 and 3).
The use of ammonium salts of the poly(acryloyldimethyltaurate) copolymers in cement slurries or alkaline drilling muds, because of the high pH values (pH>10) that exist, has the crucial drawback of resulting in the release of ammonia gas. As a result, an unpleasant, irritating odor is perceived at the site of use, which is caused by the release of toxic ammonia into the environment. It necessitates special technical equipment in order, for example, to rule out endangerment of personnel or the release of this gas into the environment. The unwanted release of ammonia gas likewise hinders the use of gas sensors in mineral oil and natural gas drilling plants.
It was therefore an object of the present invention to provide a process for preparing polymers and copolymers of acryloyldimethyltaurate, with the aid of which the metal salts, preferably alkali metal and alkaline earth metal salts, of these polymers and copolymers are preparable directly. These polymers and copolymers are to exhibit improved performance in use as a water loss reducer in cement slurries or as additive in drilling muds. In the use thereof, there is no release of ammonia, as was typical of prior art water loss reducers.
It has now been found that, surprisingly, linear or branched polymers or copolymers of acryloyldimethyltaurate which, as metal salts, preferably alkali metal or alkaline earth metal salts, are free of ammonium salts, can be prepared with the aid of a process, by polymerizing the acryloyldimethyltaurate as a neutralized metal salt, preferably alkali metal salt or alkaline earth metal salt, especially preferably as sodium salt.
The present invention provides a process for preparing water-soluble or water-swellable polymers containing
The monomers that result in the structural units a), in one embodiment, are used in the form of Li+, Na+, K+, Ca++, Mg++, Zn++, Al+++, Zr++++ salts. In another embodiment, they are neutralized prior to the polymerization, or the resulting polymer is neutralized after the polymerization, with an Li+-, Na+-, K+-, Ca++-, Mg++-, Zn++-, Al+++- or Zr++++-containing base, preferably with the corresponding hydroxides, hydrogencarbonates and carbonates.
The polymers prepared by the process of the invention are referred to hereinafter as “polymer D” or as “polymers D”.
The weight-average molecular weights of these polymers D are preferably 300 000 to 5 000 000, preferably 500 000 to 4 000 000 and especially 600 000 to 2 500 000 g/mol. The weight-average molecular weights can be determined with the aid of gel permeation chromatography (GPC). The procedure for determination of the weight-average molecular weight with the aid of GPC is described in detail in chapter 3 in “Makromolekulare Chemie: Eine Einführung” [Macromolecular Chemistry: an Introduction] by Bernd Tieke, Wiley-VCH, second fully revised and extended edition (Sep. 9, 2005) ISBN-10: 3527313796. The polymers are analyzed against a polystyrenesulfonate standard.
Indicators used for the molecular weight are the relative viscosity or the k value. To determine the k value, the polymer D is dissolved in distilled water in a concentration of 0.5% by weight, and the outflow time at 20° C. is determined by means of an Ubbelohde viscometer. This value gives the absolute viscosity of the solution (ηc). The absolute viscosity of the solvent is (η0). The ratio of the two absolute viscosities gives the relative viscosity:
The relative viscosity Z and the concentration C can be used to calculate the k value by means of the following equation:
The k value of the polymers D is preferably from 100 to 300, further preferably from 150 to 270 and especially preferably from 180 to 250.
The polymers D may each contain various structural units of the formula (1) or of component b). A polymer D may contain, for example, two or more structural units that derive from polymerizable sulfonic acids or phosphonic acids of the formula (1). A further polymer D may, for example, also contain two or more uncharged structural units of component b) which differ, for example, by different R1 radicals. References to structural units a) or b) should always be understood hereinafter such that they describe either the case of one such structural unit or the case of two or more such structural units.
The structural units of the formula (1) of the polymers D are preferably derived from monomers from the group consisting of acryloyldimethyltaurate, acryloyl-1,1-dimethyl-2-methyltaurate, acryloyltaurate, acryloyl-N-methyltaurate, 3-allyloxy-2-hydroxy-1-propanesulfonic acid, vinylsulfonic acid, styrenesulfonic acid, vinylphosphonic acid, 2-acrylamido-2-methylpropanephosphonic acid, especially preferably acryloyldimethyltaurate, vinylsulfonic acid, vinylphosphonic acid and styrenesulfonic acid.
Preferably, the neutralization level of the structural units of the formula (1) of the polymers D is from 50.0 to 100 mol %, more preferably from 80.0 to 100 mol %, especially preferably from 90.0 to 100 mol % and exceptionally preferably from 95.0 to 100 mol %.
In the structural units of the formula (1) of the polymers D, the counterion Q+ which is different than H+ is preferably an alkali metal ion, of which Na+ is preferred, an alkaline earth metal ion or mixtures of these ions. More preferably, the counterion Q+ which is different than H+ is Na+.
The mutually independent uncharged repeat structural units preferably derive from functionalized acrylic or methacrylic esters, acrylamides or methacrylamides, polyglycol acrylates or methacrylates, polyglycol acrylamides or methacrylamides, dipropylene glycol acrylates or methacrylates, dipropylene glycol acrylamides or methacrylamides, ethoxylated fatty alcohol acrylates or methacrylates, propoxylated fatty alcohol acrylates or linear or cyclic N-vinylamides or N-methvinyl amides.
The structural units of component b) preferably derive from monomers of the formula (2)
Particularly preferred structural units of the formula (2) are derived from monomers from the group consisting of N-vinylformamide, N-vinylacetamide, N-methyl-N-vinylformamide, N-methyl-N-vinylacetamide.
Further preferably, the structural units of component b) derive from monomers of the formula (3)
Particularly preferred structural units of the formula (3) are derived from monomers from the group consisting of N-vinyl-2-pyrrolidone (NVP) and N-vinylcaprolactam.
In a further preferred embodiment of the polymers D, the structural units of component b) derive from monomers of the formula (4)
In the compounds of the formula (4), R8 is preferably hydrogen or methyl.
In the compounds of the formula (4), R9 is preferably H, a linear or branched alkyl group having 1 to 50 carbon atoms, a linear or branched monohydroxyalkyl group having 2 to 6 carbon atoms or a linear or branched dihydroxyalkyl group having 2 to 6 carbon atoms.
In the compounds of the formula (4), Y2 is preferably OC(O), C(O)NR10 or NR10C(O).
Particularly preferred structural units of the formula (4) are derived from monomers from the group consisting of vinyl acetate, methyl vinyl ether, ethyl vinyl ether, methyl allyl ether, ethyl methallyl ether, methyl methallyl ether, ethyl allyl ether, tert-butylacrylamide, N,N-diethylacrylamide, N,N-dimethylacrylamide, N,N-dimethylmethacrylamide, N,N-dipropylacrylamide, N-isopropylacrylamide, N-propylacrylamide, acrylamide, methacrylamide, methyl acrylate, methymethyl acrylate, tert-butyl acrylate, tert-butyl methacrylate, n-butyl acrylate, n-butyl methacrylate, lauryl acrylate, lauryl methacrylate, behenyl acrylate, behenyl methacrylate, cetyl acrylate, cetyl methacrylate, stearyl acrylate, stearyl methacrylate, tridecyl acrylate, tridecyl methacrylate, polyethoxy-(5) methacrylate, polyethoxy-(5) acrylate, polyethoxy-(10) methacrylate, polyethoxy-(10) acrylate, behenyl polyethoxy-(7) methacrylate, behenyl polyethoxy-(7) acrylate, behenyl polyethoxy-(8) methacrylate, behenyl polyethoxy-(8) acrylate, behenyl polyethoxy-(12) methacrylate, behenyl polyethoxy-(12) acrylate, behenyl polyethoxy-(16) methacrylate, behenyl polyethoxy-(16) acrylate, behenyl polyethoxy-(25) methacrylate, behenyl polyethoxy-(25) acrylate, lauryl polyethoxy-(7) methacrylate, lauryl polyethoxy-(7) acrylate, lauryl polyethoxy-(8) methacrylate, lauryl polyethoxy-(8) acrylate, lauryl polyethoxy-(12) methacrylate, lauryl polyethoxy-(12) acrylate, lauryl polyethoxy-(16) methacrylate, lauryl polyethoxy-(16) acrylate, lauryl polyethoxy-(22) methacrylate, lauryl polyethoxy-(22) acrylate, lauryl polyethoxy-(23) methacrylate, lauryl polyethoxy-(23) acrylate, cetyl polyethoxy-(2) methacrylate, cetyl polyethoxy-(2) acrylate, cetyl polyethoxy-(7) methacrylate, cetyl polyethoxy-(7) acrylate, cetyl polyethoxy-(10) methacrylate, cetyl polyethoxy-(10) acrylate, cetyl polyethoxy-(12) methacrylate, cetyl polyethoxy-(12) acrylat, cetyl polyethoxy-(16) methacrylate, cetyl polyethoxy-(16) acrylate, cetyl polyethoxy-(20) methacrylate, cetyl polyethoxy-(20) acrylate, cetyl polyethoxy-(25) methacrylate, cetyl polyethoxy-(25) acrylate, cetyl polyethoxy-(25) methacrylate, cetyl polyethoxy-(25) acrylate, stearyl polyethoxy-(7) methacrylate, stearyl polyethoxy-(7) acrylate, stearyl polyethoxy-(8) methacrylate, stearyl polyethoxy-(8) acrylate, stearyl polyethoxy-(12) methacrylate, stearyl polyethoxy-(12) acrylate, stearyl polyethoxy-(16) methacrylate, stearyl polyethoxy-(16) acrylate, stearyl polyethoxy-(22) methacrylate, stearyl polyethoxy-(22) acrylate, stearyl polyethoxy-(23) methacrylate, stearyl polyethoxy-(23) acrylate, stearyl polyethoxy-(25) methacrylate, stearyl polyethoxy-(25) acrylate, tridecyl polyethoxy-(7) methacrylate, tridecyl polyethoxy-(7) acrylate, tridecyl polyethoxy-(10) methacrylate, tridecyl polyethoxy-(10) acrylate, tridecyl polyethoxy-(12) methacrylate, tridecyl polyethoxy-(12) acrylate, tridecyl polyethoxy-(16) methacrylate, tridecyl polyethoxy-(16) acrylate, tridecyl polyethoxy-(22) methacrylate, tridecyl polyethoxy-(22) acrylate, tridecyl polyethoxy-(23) methacrylate, tridecyl polyethoxy-(23) acrylate, tridecyl polyethoxy-(25) methacrylate, tridecyl polyethoxy-(25) acrylate, methoxy polyethoxy-(7) methacrylate, methoxy polyethoxy-(7) acrylate, methoxy polyethoxy-(12) methacrylate, methoxy polyethoxy-(12) acrylate, methoxy polyethoxy-(16) methacrylate, methoxy polyethoxy-(16) acrylate, methoxy polyethoxy-(25) methacrylate, methoxy polyethoxy-(25) acrylate.
Each of the polymers D may include various structural units of component b) that derive from one or more of the structural units of the formulae (2) to (4). A polymer D may contain, for example, two or more structural units of the formula (2) which differ from one another by different R5 and R6 radicals. For example, it is possible for both N-vinylformamide and N-methyl-N-vinylacetamide to occur in a polymer D. A further polymer D may also contain, for example, two or more structural units of the formula (2) and formula (4) which differ in their chemical construction. For example, both N-vinylformamide and acrylamide may occur in a polymer D. A further polymer D may, for example, also contain two or more uncharged structural units of the formulae (2) to (4). For example, N-methyl-N-vinylacetamide, acrylamide and also N-vinyl-2-pyrrolidone may occur in a polymer D.
Preferred polymers D contain 37.5 to 75 mol %, especially 40 to 72.5 mol %, of structural units of the formula (1), preferably derived from the sodium salt of acryloyldimethyltaurate, vinylsulfonic acid or vinylphosphonic acid, 25 to 62.5 mol %, especially 27.5 to 60 mol %, of structural units b), preferably acrylamide, N-methyl-N-vinylacetamide, N-vinylformamide, or N-vinyl-2-pyrrolidone.
Particularly preferred polymers D contain 42.5 to 70 mol % of structural units of the formula (1), preferably derived from the sodium salt of acryloyldimethyltaurate, vinylsulfonic acid or vinylphosphonic acid, 30 to 57.5 mol % of the structural units b), preferably acrylamide, N-methyl-N-vinylacetamide, N-vinylformamide or N-vinyl-2-pyrrolidone.
The distribution of the different structural units in the polymers D may be random, in blocks, alternating or in a gradient.
The polymers D are prepared by means of free-radical precipitation polymerization in a polar solvent or solvent mixture. In this case, the corresponding monomers from which the structural units of components a) and b) derive are dissolved or dispersed in a polar solvent or solvent mixture and the polymerization is initiated in a manner known per se, for example by addition of a free-radical-forming compound. It is possible here, for example, to “directly” polymerize the initially charged monomers. Alternatively, they can be neutralized prior to the polymerization, for example by reacting acid groups in monomers used with bases prior to the polymerization, forming the counterions Q+ of the structural units of formula (1). Rather than the neutralization of the monomers prior to the polymerization, however, it is also possible to neutralize the polymers with the bases on completion of polymerization.
In a further preferred embodiment of the process of the invention for preparation of the polymers D, the monomers from which the structural units of components a) and b) derive are free-radically polymerized in a polar solvent or solvent mixture, and, optionally, the monomers prior to the polymerization or the polymer D after the polymerization are neutralized with an Li+-, Na+-, K+-, Ca++-, Mg++- or Zn++-containing base, preferably with the appropriate hydroxides, hydrogencarbonates and carbonates and more preferably with hydrogencarbonates and carbonates.
Preferred bases for neutralization of the structural units of components a) are sodium hydrogencarbonate, sodium carbonate, sodium hydroxide, potassium hydrogencarbonate potassium carbonate, potassium hydroxide, lithium hydrogencarbonate, lithium carbonate, lithium hydroxide, calcium hydrogencarbonate, calcium carbonate, calcium hydroxide, preferably sodium hydrogencarbonate, sodium carbonate, sodium hydroxide, potassium hydrogencarbonate, potassium carbonate, potassium hydroxide, particular preference being given to sodium hydrogencarbonate, sodium carbonate, sodium hydroxide, and especial preference being given to sodium hydrogencarbonate and sodium carbonate.
In a further preferred embodiment of the process of the invention for preparation of the polymers D, the free-radical precipitation polymerization is effected in a polar solvent or solvent mixture which has the characteristic feature of having a boiling point of 60 to 110° C., preferably of 60 to 95° C., more preferably of 65 to 90° C.
In a further preferred embodiment of the process of the invention for preparation of the polymers D, the polar solvent comprises a mixture of:
In a further preferred embodiment of the process of the invention, component d) consists of a solvent mixture comprising one or more polar organic solvents.
In a particularly preferred embodiment of the process of the invention, component d) consists of a solvent mixture comprising one or more alcohols and one or more ketones.
In a further preferred embodiment of the process of the invention, component d) comprises one or more polar solvents selected from the group of methanol, ethanol, 1-propanol, 2-propanol, 2-methyl-2-propanol, 1-butanol, 2-butanol, dimethyl ketone, diethyl ketone, pentan-2-one, butanone, tetrahydropyran, tetrahydrofuran, 2-methyltetrahydrofuran, 1,3-dioxane, 1,4-dioxane, preferably ethanol, 1-propanol, 2-propanol, 2-methylpropan-2-ol, 1-butanol, 2-butanol, dimethyl ketone, tetrahydrofuran, 2-methyltetrahydrofuran, 1,3-dioxane, more preferably 2-propanol, 2-methylpropan-2-ol, dimethyl ketone, tetrahydrofuran, 2-methyltetrahydrofuran, 1,3-dioxane, especially preferably 2-methylpropan-2-ol and dimethyl ketone.
In the process of the invention, various polar solvents may be present within component d). An inventive polar solvent in component d) may comprise dimethyl ketone, for example. A further inventive polar solvent of component d) may comprise, for example, a mixture of 2-methylpropan-2-ol and dimethyl ketone. A further inventive solvent of component d) may comprise, for example, a mixture of dimethyl ketone, 2-methylpropan-2-ol and tetrahydrofuran.
In a particular embodiment of the process of the invention, the polar solvent mixture comprises 0.5% to 10% by weight, preferably 1% to 8% by weight of water and more preferably 2% to 5% by weight of water.
In a further particular embodiment of the process of the invention, the polar solvent mixture comprises 1% to 99.5% by weight, preferably 5% to 95% by weight and more preferably 10% to 90% by weight of 2-methylpropan-2-ol.
In a further particular embodiment of the process of the invention, the polar solvent mixture comprises 0.5% to 10% by weight of water, 1% to 98.5% by weight of 2-methylpropan-2-ol and 1% to 98.5% by weight of dimethyl ketone, preferably 0.5% to 7.5% by weight of water, 5% to 94.5% by weight of 2-methylpropan-2-ol and 5% to 94.5% by weight of dimethyl ketone, more preferably 1% to 5% by weight of water, 7.5% to 91.5% by weight of 2-methylpropan-2-ol and 7.5% to 91.5% by weight of dimethyl ketone.
A particularly preferred embodiment of the process of the invention is preferably effected in a mixture of 2-methylpropan-2-ol, dimethyl ketone and water. The water content of this mixture must not exceed 10% by weight, since formation of lumps can otherwise occur over the course of the polymerization. Specifically, the choice of the amount and type of solvent mixture has to be made such that the salt of the repeat structural unit of the formula (1), especially of the acryloyldimethyltaurate, is substantially soluble or dispersible therein. “Substantially soluble or dispersible” is understood to mean that no solid material settles out of the solution or dispersion even after the stirrer has been switched off. The polymer D that forms in the course of the reaction, by contrast, is to be substantially insoluble in the solvent mixture chosen. “Substantially insoluble” is understood to mean here that a well-stirrable, slurry-like polymer paste forms in the course of the polymerization, in which there must be no formation of lumps or conglutinations. The filtrate obtainable by filtering the paste with suction must not have a solids content of more than 5% by weight. If the copolymers are soluble in the solvent or solvent mixture chosen to any greater degree, lumps may be formed in the course of drying of the polymer paste.
The polymerization reaction itself is triggered in a manner known per se by free-radical-forming compounds such as azo initiators (e.g. azobisisobutyronitrile, 2,2′-azobis(4-methoxy-2,4-dimethylvaleronitrile), 2,2′-azobis(2,4-dimethyl-valeronitrile), dimethyl 2,2′-azobis(2-methylpropionate), 2,2′-azobis(2-methyl-butyronitrile), 1,1′-azobis(cyclohexane-1-carbonitrile) or 2,2′-azobis[N-(2-propenyl)-2-methylpropionamide]), peroxides (e.g. dilauryl peroxide, tert-butyl hydroperoxide, di-tert-butyl peroxide, triphenylmethyl hydroperoxide, benzoyl peroxide), or persulfates within a suitable temperature range from 20 to 120° C., preferably between 30 and 80° C. and especially preferably between 40 and 70° C., and continued over a period of 30 min to several hours.
The polymers D are obtained as a white voluminous precipitate in the polar solvent mixture. Isolation can be accomplished by using all standard evaporation and drying isolation processes. More particularly, the polar solvent mixture can be separated from the product by a pressure filtration or distillation. A minor residue of the polar solvent mixture is not an issue either from a safety point of view or for application-related reasons.
The polymers D prepared by the process of the invention are advantageously suitable for use as water loss reducers in drilling muds and cement slurries. These are used in the deep wells for reduction of water loss at the well wall and as a means of reducing the water loss in cement slurries. Such additives are also called fluid loss additives or fluid loss control additives.
The present invention further provides for the use of the polymers D in water-based drilling fluids. These drilling fluids may comprise further additives as well as the polymers C. Additives of this kind are, for example, bentonites, clay stabilizers, lignin/lignosulfonates, pH stabilizers (e.g. hydroxides), thermal stabilizers (e.g. monoethanolamine or sulfonated synthetic polymers) and weighting agents (e.g. barite, magnetite, calcium carbonate, ilmenite) for establishment of the desired density.
The present invention further provides a method of cementing deep wells, in which a cement slurry is introduced into the well and contains the polymers D in a concentration of 0.01%-5% bwoc (by weight of cement), preferably 0.05% to 2.5% bwoc. Further components of the cement slurries are water in different salinity and cement. It is also possible to use dispersants, retardants, accelerators, extenders, defoamers or silicate derivatives as auxiliaries.
In the examples, the polar solvent used which was used to prepare the polymers D was varied. With the aid of process examples 1 to 20, further polymers D of the invention were prepared by the variation of the monomers and variation of component e). These polymers D and the process examples used for the synthesis are compiled in table 1 a) to 1c).
In a 2 liter Quickfit flask with anchor stirrer, reflux condenser with offgas scrubber, combined thermometer/pH meter and a gas inlet tube, 234 g of anhydrous 2-methylpropan-2-ol and 158 g of dimethyl ketone are admixed with 8 g of distilled water.
The reaction vessel is in a heating bath thermostat. This reaction vessel is blanketed with nitrogen gas and, in a gentle opposing nitrogen stream, 80 g of acryloyldimethyltaurate and 32.4 g of sodium hydrogencarbonate are introduced. The acryloyldimethyltaurate sodium salt does not dissolve completely in the 2-methylpropan-2-ol/dimethyl ketone/water mixture and is partly in the form of a dispersion of solids. The reaction vessel is blanketed with nitrogen, and 15 g of acrylamide and 2.5 g of N-vinylpyrrolidone are introduced. After introduction of the acrylamide and N-vinylpyrrolidone, the pH is checked once again and corrected if necessary by addition of sodium hydrogencarbonate to pH 7 to 8. A constant nitrogen stream is passed through the solution for at least 1 hour. After this inertization period, the residual oxygen is monitored by means of an oxygen electrode. Should the measured residual oxygen value in the liquid phase exceed the value of 1 ppm, inertization must be repeated until this value is attained. Thereafter, the reaction vessel is heated to 60° C., and 1.0 g of azobis(isobutyronitrile) is added in a gentle nitrogen stream. The initiation of the polymerization becomes apparent from a rise in the internal temperature. After the initiation, the introduction of nitrogen gas is ended. About 5-10 minutes after onset of the polymerization reaction, the temperature maximum has been exceeded and the temperature in the reaction vessel is increased by the heating bath up to the boiling point of the 2-methylpropan-2-ol:dimethyl ketone water mixture. Under gentle reflux, the now viscous mass is stirred for a further two hours. The reaction product, in the form of a viscous suspension of polymer in the 2-methylpropan-2-ol:dimethyl ketone water mixture, is isolated by filtration and subsequent drying in a vacuum drying cabinet.
In a 2 liter Quickfit flask with anchor stirrer, reflux condenser with offgas scrubber, combined thermometer/pH meter and a gas inlet tube, 234 g of anhydrous 2-methylpropan-2-ol and 154 g of dimethyl ketone are admixed with 12 g of distilled water. The reaction vessel is in a heating bath thermostat. The further steps of polymerization process 2 are conducted analogously to polymerization process 1. The changes in the monomer compositions are listed accurately in table 1.
In a 2 liter Quickfit flask with anchor stirrer, reflux condenser with offgas scrubber, combined thermometer/pH meter and a gas inlet tube, 234 g of anhydrous 2-methylpropan-2-ol and 154 g of dimethyl ketone are admixed with 16 g of distilled water. The reaction vessel is in a heating bath thermostat. The further steps of polymerization process 3 are conducted analogously to polymerization process 1. The changes in the monomer compositions are listed accurately in table 1.
In a 2 liter Quickfit flask with anchor stirrer, reflux condenser with offgas scrubber, combined thermometer/pH meter and a gas inlet tube, 296 g of anhydrous 2-methylpropan-2-ol and 94 g of dimethyl ketone are admixed with 10 g of distilled water. The reaction vessel is in a heating bath thermostat. The further steps of polymerization process 4 are conducted analogously to polymerization process 1. The changes in the monomer compositions are listed accurately in table 1.
In a 2 liter Quickfit flask with anchor stirrer, reflux condenser with offgas scrubber, combined thermometer/pH meter and a gas inlet tube, 296 g of anhydrous 2-methylpropan-2-ol and 86 g of dimethyl ketone are admixed with 14 g of distilled water. The reaction vessel is in a heating bath thermostat. The further steps of polymerization process 5 are conducted analogously to polymerization process 1. The changes in the monomer compositions are listed accurately in table 1.
In a 2 liter Quickfit flask with anchor stirrer, reflux condenser with offgas scrubber, combined thermometer/pH meter and a gas inlet tube, 296 g of anhydrous 2-methylpropan-2-ol and 90 g of dimethyl ketone are admixed with 18 g of distilled water. The reaction vessel is in a heating bath thermostat. The further steps of polymerization process 6 are conducted analogously to polymerization process 1. The changes in the monomer compositions are listed accurately in table 1.
In a 2 liter Quickfit flask with anchor stirrer, reflux condenser with offgas scrubber, combined thermometer/pH meter and a gas inlet tube, 197 g of anhydrous 2-methylpropan-2-ol and 197 g of dimethyl ketone are admixed with 6 g of distilled water. The reaction vessel is in a heating bath thermostat. The further steps of polymerization process 7 are conducted analogously to polymerization process 1. The changes in the monomer compositions are listed accurately in table 1.
In a 2 liter Quickfit flask with anchor stirrer, reflux condenser with offgas scrubber, combined thermometer/pH meter and a gas inlet tube, 195 g of anhydrous 2-methylpropan-2-ol and 197 g of dimethyl ketone are admixed with 10 g of distilled water. The reaction vessel is in a heating bath thermostat. The further steps of polymerization process 8 are conducted analogously to polymerization process 1. The changes in the monomer compositions are listed accurately in table 1.
In a 2 liter Quickfit flask with anchor stirrer, reflux condenser with offgas scrubber, combined thermometer/pH meter and a gas inlet tube, 193 g of anhydrous 2-methylpropan-2-ol and 193 g of dimethyl ketone are admixed with 14 g of distilled water. The reaction vessel is in a heating bath thermostat. The further steps of polymerization process 9 are conducted analogously to polymerization process 1. The changes in the monomer compositions are listed accurately in table 1.
In a 2 liter Quickfit flask with anchor stirrer, reflux condenser with offgas scrubber, combined thermometer/pH meter and a gas inlet tube, 191 g of anhydrous 2-methylpropan-2-ol and 191 g of dimethyl ketone are admixed with 18 g of distilled water. The reaction vessel is in a heating bath thermostat. The further steps of polymerization process 10 are conducted analogously to polymerization process 1. The changes in the monomer compositions are listed accurately in table 1.
In a 2 liter Quickfit flask with anchor stirrer, reflux condenser with offgas scrubber, combined thermometer/pH meter and a gas inlet tube, 90 g of anhydrous 2-methylpropan-2-ol and 298 g of dimethyl ketone are admixed with 12 g of distilled water. The reaction vessel is in a heating bath thermostat. The further steps of polymerization process 11 are conducted analogously to polymerization process 1. The changes in the monomer compositions are listed accurately in table 1.
In a 2 liter Quickfit flask with anchor stirrer, reflux condenser with offgas scrubber, combined thermometer/pH meter and a gas inlet tube, 90 g of anhydrous 2-methylpropan-2-ol and 294 g of dimethyl ketone are admixed with 16 g of distilled water. The reaction vessel is in a heating bath thermostat. The further steps of polymerization process 12 are conducted analogously to polymerization process 1. The changes in the monomer compositions are listed accurately in table 1.
In a 2 liter Quickfit flask with anchor stirrer, reflux condenser with offgas scrubber, combined thermometer/pH meter and a gas inlet tube, 90 g of anhydrous 2-methylpropan-2-ol and 290 g of dimethyl ketone are admixed with 20 g of distilled water. The reaction vessel is in a heating bath thermostat. The further steps of polymerization process 13 are conducted analogously to polymerization process 1. The changes in the monomer compositions are listed accurately in table 1.
In a 2 liter Quickfit flask with anchor stirrer, reflux condenser with offgas scrubber, combined thermometer/pH meter and a gas inlet tube, 60 g of anhydrous 2-methylpropan-2-ol and 320 g of dimethyl ketone are admixed with 20 g of distilled water. The reaction vessel is in a heating bath thermostat. The further steps of polymerization process 14 are conducted analogously to polymerization process 1. The changes in the monomer compositions are listed accurately in table 1.
In a 2 liter Quickfit flask with anchor stirrer, reflux condenser with offgas scrubber, combined thermometer/pH meter and a gas inlet tube, 60 g of anhydrous 2-methylpropan-2-ol and 316 g of dimethyl ketone are admixed with 24 g of distilled water. The reaction vessel is in a heating bath thermostat. The further steps of polymerization process 15 are conducted analogously to polymerization process 1. The changes in the monomer compositions are listed accurately in table 1.
In a 2 liter Quickfit flask with anchor stirrer, reflux condenser with offgas scrubber, combined thermometer/pH meter and a gas inlet tube, 384 g of tetrahydrofuran and 16 g of distilled water are initially charged. The reaction vessel is in a heating bath thermostat. This reaction vessel is blanketed with nitrogen gas and, in a gentle opposing nitrogen stream, 85 g of acryloyldimethyltaurate, 1.15 g of vinylphosphonic acid and 42.1 g of sodium hydrogencarbonate are introduced. The acryloyldimethyltaurate potassium salt does not dissolve completely in the tetrahydrofuran/water mixture and is partly in the form of a dispersion of solids. The reaction vessel is blanketed with nitrogen, and 5 g of acrylamide, 5 g of N-vinyl-2-pyrrolidone and 5 g of N-vinyl-formamide are introduced. After introduction of the neutral monomers, the pH is checked once again and corrected if necessary by addition of potassium hydrogencarbonate to pH 7 to 8. A constant nitrogen stream is passed through the solution for at least 1 hour. After this inertization period, the residual oxygen is monitored by means of an oxygen electrode. Should the measured residual oxygen value in the liquid phase exceed the value of 1 ppm, inertization must be repeated until this value is attained. Thereafter, the reaction vessel is heated to 60° C., and 1.0 g of azobis(isobutyronitrile) is added in a gentle nitrogen stream. The initiation of the polymerization becomes apparent from a rise in the internal temperature. After the initiation, the introduction of nitrogen gas is ended. About 5-10 minutes after onset of the polymerization reaction, the temperature maximum has been exceeded and the temperature in the reaction vessel is increased by the heating bath up to the boiling point of the tetrahydrofuran/water mixture. Under gentle reflux, the now viscous mass is stirred for a further two hours. The reaction product, in the form of a viscous suspension of polymer in the tetrahydrofuran/water mixture, is isolated by filtration and subsequent drying in a vacuum drying cabinet.
A 2 liter Quickfit flask with anchor stirrer, reflux condenser with offgas scrubber, combined thermometer/pH meter and a gas inlet tube is initially charged with 394 g of tetrahydrofuran and 6 g of distilled water. The reaction vessel is in a heating bath thermostat. The further steps of polymerization process 17 are conducted analogously to polymerization process 16. The changes in the monomer compositions are listed accurately in table 1.
In a 2 liter Quickfit flask with anchor stirrer, reflux condenser with offgas scrubber, combined thermometer/pH meter and a gas inlet tube, 390 g of anhydrous 2-methyltetrahydrofuran are admixed with 10 g of distilled water. The reaction vessel is in a heating bath thermostat. The further steps of polymerization process 18 are conducted analogously to polymerization process 1. The changes in the monomer compositions are listed accurately in table 1.
In a 2 liter Quickfit flask with anchor stirrer, reflux condenser with offgas scrubber, combined thermometer/pH meter and a gas inlet tube, 300 g of anhydrous 2-methylpropan-2-ol and 86 g of 2-methyltetrahydrofuran are admixed with 14 g of distilled water. The reaction vessel is in a heating bath thermostat. The further steps of polymerization process 19 are conducted analogously to polymerization process 1. The changes in the monomer compositions are listed accurately in table 1.
In a 2 liter Quickfit flask with anchor stirrer, reflux condenser with offgas scrubber, combined thermometer/pH meter and a gas inlet tube, 90 g of anhydrous 2-methylpropan-2-ol and 300 g of 2-methyltetrahydrofuran are admixed with 5 g of distilled water. The reaction vessel is in a heating bath thermostat. The further steps of polymerization process 20 are conducted analogously to polymerization process 1. The changes in the monomer compositions are listed accurately in table 1.
The polymers D which have been prepared according to inventive process examples 1 to 20 are listed in table 1 below. Changes made, for example the use of another base and the amount used for neutralization of the acryloyldimethyltaurate or the use of another initiator and the amount used, are set out in table 1.
(noninventive, prepared according to EP 1045869 copolymer prepared in precipitation polymerization 44.5 mol % acryloyldimethyltaurate and 55.5 mol % acrylamide with ammonia gas as neutralizing reagent)
In a 3 liter Quickfit flask with anchor stirrer, reflux condenser with offgas scrubber, combined thermometer/pH meter and a gas inlet tube, 1700 g of anhydrous 2-methylpropan-2-ol are admixed with 50 mL of distilled water. The reaction vessel is in a heating bath thermostat.
This reaction vessel is blanketed with nitrogen gas, and 245 g of acryloyldimethyltaurate are introduced in a gentle opposing nitrogen stream. The acryloyldimethyltaurate does not dissolve completely in the 2-methylpropan-2-ol/water mixture and is partly in the form of a dispersion of solids. The pH of this mixture is below pH 1. Above the liquid phase, gaseous ammonia is introduced through the gas inlet tube until the pH of the dispersion is between 7 and 8. On attainment of the desired pH range, stirring is continued for another 1 hour and the pH is recorded continuously. The reaction vessel is blanketed with nitrogen, and 105 g of acrylamide are introduced. After the acrylamide has been introduced, the pH is checked again and if necessary corrected to the range of pH 7 to 8. A constant nitrogen stream is passed through the solution for at least 1 hour. After this inertization period, the residual oxygen is checked by means of an oxygen electrode. Should the measured residual oxygen value in the liquid phase exceed the value of 1 ppm, inertization has to be repeated until this value is attained. Thereafter, in a gentle nitrogen stream, 2 g of AIBN are added and the reaction vessel is heated to 60° C. Shortly after attainment of an internal temperature of 60° C., the introduction of nitrogen gas is ended and commencement of the polymerization reaction is observed, which can be determined by an increase in temperature of 10-15° C. About 5-15 minutes after onset of the polymerization reaction, the temperature has been exceeded and the temperature in the reaction vessel is increased by means of the heating bath up to the boiling point of the 2-methylpropan-2-ol/water mixture. Under gentle reflux, the now viscous mass is stirred for a further two hours. The reaction product, in the form of a viscous suspension of polymer in the 2-methylpropan-2-ol/water mixture, is separated off by filtration and subsequent drying in a vacuum drying cabinet.
Yield: 365 g
A polymerization flask of capacity 2 L, equipped with stirrer, reflux condenser, dropping funnel, gas inlet tube and electrically heated water bath, is initially charged with 600 mL of 2-methylpropan-2-ol, and 77.5 g of acryloyldimethyltaurate are suspended therein while stirring, then 8.5 L of NH3 gas are introduced and then 7.5 g of acrylamide, 7.5 g of N-vinylformamide and 7.5 g of N-vinylpyrrolidone are added. With introduction of nitrogen, the electrical water bath is used to heat the reaction mixture to 50° C., and 1.0 g of azoisobutyronitrile is added. After an induction time of about 2 hours, polymerization sets in, the reaction temperature rises up to 70° C. and the polymer precipitates out. The mixture is heated at 80° C. for another 2 hours, forming a viscous suspension. The polymer can be isolated by filtration with suction and drying under reduced pressure at 50° C. However, it is also possible to distill the solvent out of the reaction mixture directly under reduced pressure. The polymer is obtained in the form of a white lightweight powder having good solubility in water. K value according to Fikentscher 170.
A 2 L glass reactor with an internal temperature of 20° C. is initially charged with 344 g of dimethyl ketone, 9.6 g of deionized water and the monomers specified in table 2 and the neutralizing reagent. The contents of the reactor are stirred and inertized with introduction of a strong nitrogen stream for 1 h. The reaction medium is heated to 55° C. and then 0.7 g of DLP (dilauryl peroxide) is added to initiate the polymerization. The reaction mixture is heated to reflux and kept there for 2 h. After cooling to room temperature, the reaction medium is filtered and the polymer residue is dried under reduced pressure.
B) Cement Slurry Application Tests
The testing is effected according to API spec. 10. In an atmospheric consistometer, the cement slurry is stirred/conditioned at the study temperature and then at the same temperature the rheology with the FANN model 35SA viscometer (in the case of high temperature, conditioning is effected at 93° C. and the viscosity is measured). At temperatures>93° C., water loss is measured with a stirring fluid loss apparatus (SFLA).
Table 3 shows the water loss-reducing properties of selected abovementioned examples according to API spec. 10 at 121.1° C. (250° F.) in the stirred filtration test in the FANN HTHP filter press (stirring fluid loss apparatus, SFLA). The test was based on two assessment questions: was ammonia gas emitted during the making-up of the formulation and was it possible to improve the water loss reduction properties of the polymers C? It becomes clear here that no ammonia gas emission occurs any more with the polymers D. Direct comparison of the polymers D against the prior art likewise shows an improvement in the fluid loss properties. The polymer of EP 1045869 had an average fluid loss of 52 mL (mean value from three measurements) in the test conducted. Some of the polymers D were much lower in terms of their fluid loss values. Values of 40 to 45 mL were attained here.
Formulation of the cement slurries:
600 g of Dyckerhoff Class G cement
210 g of silica flour
328.8 g of distilled water
Polymer in the concentration specified in table 1
1.8 g of dispersant (polynaphthalenesulfonate, PNS)
1.8 g of retardant (lignosulfonate)
As shown by the comparison of the inventive examples in table 3 with the comparative examples VGP-2, VGP-2-1 to VGP-2-4, the process of the invention that utilizes a solvent mixture gives a product which differs from products that have been obtained with just one solvent according to the prior art. The products obtained by the process of the invention show lower water loss when they are used as additive in cement slurries and drilling mud.
Drilling Mud Application Tests
In the examples which follow, the polymers C are compared with comparative polymer 2 from EP 10033378, known from the prior art, in a barite-weighted seawater drilling mud with 3% KCl and a specific weight of 2.1 kg/L. Prior to use, a drilling mud is adjusted with sodium hydroxide to a pH of 9-11. The amount used in each case was 2.5% by weight.
The quality of the mud and hence the efficacy of the additives is assessed by the following criteria:
The following additives were used for the studies:
The test results show comparable values to comparative example 2, with regard to the uniform rheological properties of the drilling mud after makeup and after ageing over the temperature range from 130 to 200° C. The polymers D have a broad temperature range with regard to their efficacy as a fluid loss additive.
As shown by the comparison of the inventive examples in table 4 with the comparative examples VGP-1, VGP-2-1 to VGP-2-4, the process of the invention that utilizes a solvent mixture gives a product which differs from products which have been obtained with just one solvent according to the prior art. The products obtained by the process of the invention show a lower water loss when used as additive in cement slurries and drilling mud.
The process of WO-99/26991 is conducted in a 2-methyl-2-propanol/water mixture and a corresponding sodium salt is obtained by the addition of sodium carbonate according to the general process description at page 10 line 4 to page 11 line 22.
The object of the process of the invention was the preparation of polymeric AMPS-Na salts which are particularly suitable as a water loss reducer in drilling muds and as additives for the cementing of deep wells and additionally have better properties as water loss reducers than the prior art polymers described. These polymeric AMPS-Na salts from the process of the invention are intended to be free of ammonium ions, which release toxic ammonia gas in an alkaline medium. Even in comparative examples 1 and 2, it was possible to show clearly that polymeric AMPS-Na salts prepared by means of a precipitation polymerization in a 2-methyl-2-propanol/water mixture have poorer water loss-reducing properties in drilling muds than the polymers of the process of the invention. It can be concluded from these results of comparative examples 1 and 2 in the present application that example 2 from WO-99/26991 will lead to a similar deterioration in the water loss-reducing properties.
In order to test this thesis, example 2 from WO-99/26991 hereinafter was repeated twice by the process described and compared with the polymers from the process of the invention:
A 3 Liter Quickfit flask with anchor stirrer, reflux condenser and offgas scrubber, combined thermometer/pH meter and a gas inlet tube is initially charged with 1700 g of tert-butanol, and 50 mL of distilled water are added. The reaction vessel is in a heating bath thermostat.
This reaction vessel is blanketed with nitrogen and, in a gentle opposing nitrogen stream, 245 g of acrylamido-2-methylpropanesulfonic acid are introduced. The acrylamido-2-methylpropanesulfonic acid does not dissolve completely and is partly in the form of a dispersion of solids. The pH of this mixture is below 1. 140.5 g of sodium carbonate are metered in. The reaction vessel is blanketed again with nitrogen, and 105 g of acrylamide are introduced. A constant nitrogen stream is passed through the solution for at least 1 hour. Thereafter, in a gentle nitrogen stream, 1.5 g of AIBN are added and the reaction vessel is heated to 60° C. Shortly after the attainment of an internal temperature of 60° C., the introduction of nitrogen gas is ended and the polymerization reaction typically commences after a few minutes, which can be identified by an increase in temperature of 10-15° C. About 30 minutes after onset of the polymerization reaction, the temperature maximum has been exceeded and the temperature in the reaction vessel is increased by the heating bath up to the boiling point of the tert-butanol/water mixture. Under gentle reflux, the now viscous mass is stirred for a further two hours.
The reaction product, in the form of a viscous suspension of polymer in tert-butanol, is separated from the tert-butanol by filtration and dried in a vacuum drying cabinet.
Yield: about 383 g of polymer D3-1
Dry matter 97% by weight
k value of 0.5% by weight solution: 148
Yield: about 377 g of polymer D3-2
Dry matter 95.8% by weight
k value of 0.5% by weight solution: 164
Note with regard to the described polymerization method according to WO-99/26991 example 2:
WO-99/26991 states, at page 11 lines 17-20, that following the addition of sodium carbonate the pH of the dispersion is in the range between 7 and 8. This was not observed in the reworking. Nor was it possible to observe any evolution of CO2 gas, as occurs in the process of the invention, as a result of the neutralization reaction between the sodium carbonate and the sulfonic acid after the addition. Even after the required hour of inertization time, no change in pH was apparent.
This was not altered by the two-fold molar ratio of sodium carbonate described in WO-99/26991 (ratio of sulfonic acid to Na+ ions corresponds to 1 mol to 2.2 mol). The analysis of the polymers D3-1 and polymer D3-2 showed that a large portion of the unreacted sodium carbonate has remained in the polymer.
The reported yield in WO-99/26991 example 2 with 380 g of polymer (WO-99/26991, page 11 line 19) demonstrates incomplete conversion, since, in the case of a 100% conversion of the monomers, 1.3 mol (270.5 g) of sodium acrylamido-2-methylpropanesulfonic acid and 105 g of acrylamide may be present in the polymer after the reaction. There is an additional 0.65 mol (68.9 g) of unreacted sodium carbonate, which is insoluble in tert-butanol. In the case of a complete conversion of the monomers to the polymers with a dry matter level of 94% by weight, there must accordingly be a theoretical overall yield of 472.77 g=((270.5+105 g+68.9)/0.94)) in the process according to WO-99/26991.
Comparative examples D3-1 and D3-2 also showed by a much lower K value than the polymers by the process of the invention. This, together with the abovementioned reduced yield, suggests incomplete polymerization, since the sodium salt was only of limited to zero solubility in the solvent mixture of the in the describe process of WO-99/26991 and hence was not available for the polymerization.
Acrylamide and polyacrylamide are in contrast is very readily soluble in tert-butanol. This also suggests incomplete copolymerization since both the acrylamide and the polyacrylamide have been removed by the filtration process and thus would explain the losses of mass in the yield.
Cement slurry application tests with polymer D3-1 and D3-2 The testing is effected according to API spec. 10. In an atmospheric consistometer, the cement slurry is stirred/conditioned at the study temperature and then at the same temperature the rheology with the FANN model 35SA viscometer (in the case of high temperature, conditioning is effected at 93° C. and the viscosity is measured). At temperatures >93° C., water loss is measured with a stirring fluid loss apparatus (SFLA).
Table 5 shows the water loss-reducing properties of selected abovementioned examples according to API spec. 10 at 121.1° C. (250° F.) in the stirred filtration test in the Fann HTHP filter press (stirring fluid loss apparatus, SFLA). Formulation of the cement slurries for an application at 250° F., about 121° C.:
100 g of Dyckerhoff Class G cement
35 g of silica flour
54.8 g of distilled water
Polymer in the in table 1 a) to 1c) in the specified concentration
0.3 g of dispersant (polynaphthalenesulfonate, PNS)
0.5 g of retardant (lignosulfonate)
For testing of the polymers obtained, these were used as water loss reducers in cement slurries. The use of sodium hydroxide and sodium carbonate did not result in any release of ammonia, but comparative examples D3-1 and D3-2, by contrast with the polymers of the process of the invention, showed a much poorer “API fluid loss at 250° F.” of >100 mL. This shows clearly that the process of the invention is technologically superior to the process described in WO-99/26991, and that the resulting polymers of the process of the invention are distinctly notable as water loss reducers by way of their improved physical properties in spite of the same composition.
| Number | Date | Country | Kind |
|---|---|---|---|
| 15001794.5 | Jun 2015 | EP | regional |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2016/062287 | 5/31/2016 | WO | 00 |
