Patent Application
20200157004
This non-provisional application claims priority under 35 U.S.C. § 119(a) on Patent Application Nos. 2018-215196 and 2019-147503 filed in Japan on Nov. 16, 2018 and Aug. 9, 2019, respectively, the entire contents of which are hereby incorporated by reference.
The present invention relates to a water-reducing composition, a hydraulic composition, and a method for producing the same.
The hydraulic composition is a composition containing at least a hydraulic substance such as cement, an aggregate such as a fine aggregate and/or a coarse aggregate, and water, and is an aggregate of an inorganic substance having different specific gravity, particle shape, and particle diameter. Therefore, it is a composition in which material separation is likely to occur. Thus, attempts have been made to improve the viscosity of the hydraulic composition by adding a water-soluble polymer as a thickener.
For example, water-soluble cellulose, ether is one of a few nonionic water-soluble polymers that can be thickened even in a hydraulic composition under the severe conditions for a water-soluble polymer in that a pH of cement is 12 or higher which is strongly alkaline, and many calcium ions due to the components of the cement are present.
However, since the water-soluble cellulose ether is generally used in a powder form, there is a problem in that it is inferior in handling to other liquid admixtures, and a lump is formed at the time of addition or in a case of adding a trace amount, it scatters and thus it is difficult to add a desired amount
In order to solve these problems, a water-reducing composition (also referred to a one-pack type water-reducing agent) in which water-soluble cellulose ether, a defoamer, gums, and a water reducing agent are mixed in advance has been proposed (for example, JP-A 2016-056081 (Patent Document 1)).
However, in Patent Document 1, although it attempts to improve the storage stability of the water-reducing composition by using gums, the storage stability may be poor depends on solid content concentration and Na+ ion concentration of the polycarboxylic acid-based water reducing agent, and therefore, there is room for improvement.
The present invention has been made in view of the above circumstances, and an object thereof is to provide a water-reducing composition which contains a polycarboxylic acid-based water reducing agent, water-soluble cellulose ether, gums, and a defoamer, and has storage stability improved, a hydraulic composition using the same, and a method for producing the same.
As a result of intensive research to solve the above problems, the inventor of the present invention has found that by using a naphthalene-based water reducing agent in combination with a water-reducing composition contains at least a polycarboxylic acid-based water reducing agent, water-soluble cellulose ether, gums, and a defoamer, the storage stability of the water-reducing composition is improved even if high Na+ ion concentration is maintained, and the fluidity of the hydraulic composition can be maintained at a high level. With this, the present invention has been completed.
That is, the present invention provides a water-reducing composition, a hydraulic composition, and a method for producing the same.
According to the present invention, by using a polycarboxylic acid-based water reducing agent and a naphthalene-based water reducing agent in combination, the storage stability of the water-reducing composition is improved, and a bleeding suppression effect is expected when used in a hydraulic composition. Furthermore, since addition of the naphthalene-based water reducing agent does not cause aggregation with a water-soluble cellulose ether, a water reducing effect can be expected, and a fluid hydraulic composition can be obtained.
Hereinafter, a configuration of a water-reducing composition according to the present invention is described. Meanwhile, the numerical range “A to B” here includes numerical values at both ends, which means A or more and B or less.
The water-reducing composition according to the present invention includes
Notably, a water-reducing composition means a mixture for a hydraulic composition, containing at least a water-reducing agent, a water-soluble cellulose ether, gums and a defoamer, also referred to a one-pack type water-reducing agent.
A component (A) is a water reducing agent containing a polycarboxylic acid-based water, reducing agent and a naphthalene-based water reducing agent, and preferably consists of a polycarboxylic acid-based water reducing agent and a naphthalene-based water reducing agent. The water reducing agent here means a chemical admixture that reduces the unit water amount necessary to obtain a predetermined slump flow, includes all of so-called, a high-performance water reducing agent, AE water reducing agent and high-performance AE water reducing agent, and is preferably any of these.
Specific examples of the polycarboxylic acid-based water reducing agent include a polycarboxylic acid ether-based compound, a composite of a polycarboxylic acid ether-based compound and a crosslinked polymer, a composite of a polycarboxylic acid ether-based compound and an oriented polymer; a composite of a polycarboxylic acid ether-based compound and a highly modified polymer; a polyether carboxylic acid-based polymer compound, a maleic acid copolymer, a maleate ester copolymer, a maleic acid derivative copolymer, a carboxyl group-containing polyether-based compound, a polycarboxylic acid group-containing multi-element polymer having a terminal sulfone group, a polycarboxylic acid-based graft copolymer, and a polycarboxylic acid ether-based polymer.
A commercially available polycarboxylic acid-based water reducing agent can be used. For example, Tuepole HP-11 (produced by TAKEMOTO OIL & FAT Co., Ltd.), MasterGlenium SP8SV X2 (produced by BASF Japan Ltd.) and the like can be exemplified. The property is preferably liquid. Further, a commercially available polycarboxylic acid-based water reducing agent may be appropriately diluted with water as necessary.
Two or more kinds of the polycarboxylic acid-based water reducing agents may be used in combination.
Specific examples of the naphthalene-based water reducing agent include those containing naphthalene sulfonate or a derivative thereof as a main component. A commercially available product can be used as the naphthalene-based water reducing agent, and examples thereof include MIGHTY 150 (produced by Kao Corporation). The property is preferably liquid. Further, a commercially available naphthalene-based water reducing agent may be appropriately diluted with water as necessary.
Two or more kinds of the naphthalene-based water reducing agents may be used in combination.
The solid content concentration in the mixture (that is, (A) water reducing agent) of the polycarboxylic acid-based water reducing agent and the naphthalene-based water reducing agent is preferably 10% by weight or more, more preferably 10% to 50% by weight, still more preferably 12.5% to 30% by weight, and particularly preferably 13% to 20% by weight from the viewpoint of the storage stability after one-pack composing (uniform dispersion). If the solid content concentration in the component (A) is less than 10% by weight or more than 50% by weight, the storage stability after one-pack composing (uniform dispersion) may be deteriorated.
In addition, the solid content concentration of a water reducing, agent can be measured as follows.
First, a predetermined amount (for example, about 5 g) of a water reducing agent is placed in a weighing bottle (for example, a bottle capacity of 16 ml), and the weight thereof, that is, the weight (g) of the water reducing agent before drying is measured. Then, drying is performed with a dryer at 105° C. until the weight becomes constant weight, and the weight (g) of the water reducing agent after drying is measured. The solid content concentration is calculated by the following calculation formula using the measured weight of the water reducing agent before and after drying (the same applies hereafter).
Solid content concentration (% by weight)={weight (g) of water reducing agent after drying/weight (g) of water reducing agent before drying}×100
The ratio (weight ratio; SCpc:SCnp) of the solid content weight (SCpc) of the polycarboxylic acid-based water reducing agent and the solid content weight (SCnp) of the naphthalene-based water reducing agent in the component (A) is preferably 1:99 to 80:20, more preferably 5:95 to 70:30, and still more preferably 10:90 to 55:45 from the viewpoint of the storage stability after one-pack composing (uniform dispersion). If the ratio is outside the above range, the storage stability after one-pack composing (uniform dispersion) may be deteriorated.
The Na+ ion concentration in the mixture of the polycarboxylic acid-based water reducing agent and the naphthalene-based water reducing agent (that is, (A) water reducing agent) is preferably 8,500 ppm or more, more preferably 9,000 to 30,000 ppm, still more preferably 9,500 to 25,000 ppm, and particularly preferably 10,000 to 20,000 ppm from the viewpoint of the storage stability after one-pack composing (uniform dispersion). In the Na+ ion concentration in the component (A) is less than 8,500 ppm, the storage stability after one-pack composing (uniform dispersion) may be deteriorated.
The Na+ ion concentration of the water reducing agent can be measured by an ion chromatography method (the same applies hereafter). Details are described in Examples.
In producing the water-reducing composition of the present invention, the polycarboxylic acid-based water reducing agent and the naphthalene-based water reducing, agent under the following conditions, may be used.
That is, the solid content concentration of the polycarboxylic acid-based water reducing agent is preferably 10% to 25% by weight, more preferably 12% to 24.5% by weight, and still more preferably 13% to 20% by weight, from the viewpoint of economy or the amount added in the production of the hydraulic composition.
In addition, the Na+ ion concentration of the polycarboxylic acid-based water reducing agent is preferably 8,500 ppm or more, more preferably 9,000 to 18,000 ppm, and still more preferably 9,000 to 16,000 ppm, and particularly preferably 9,000 to 12,000 ppm from the viewpoint of the storage stability after one-pack composing (uniform dispersion).
The water reduction rate of the polycarboxylic acid-based water reducing agent is preferably 18% or more, and more preferably 19% to 30%, from the viewpoint of economy or the amount added in the production of the hydraulic composition.
In addition, the water reduction rate of the water reducing agent can be obtained by calculation from the unit water amounts of the standard concrete and test concrete specified in JIS A6204 (the same applies hereafter).
The solid content concentration of the naphthalene-based water reducing agent is preferably 10% to 50% by weight, more preferably 10% to 40% by weight, and still more preferably 10% to 20% by weight, from the viewpoint of economy or the amount added in the production of the hydraulic composition.
In addition, the Na+ ion concentration of the naphthalene-based water reducing agent is preferably 8,500 ppm or more, more preferably 9,000 to 40,000 ppm, still more preferably 10.000 to 35,000 ppm, and, particularly preferably 10,000 to 20,000 ppm, from the viewpoint of the storage stability after one-pack composing (uniform dispersion).
The water reduction rate of the naphthalene-based water reducing agent is preferably 10% or more, and more preferably 12% to 30%, from the viewpoint of fluidity of the hydraulic composition.
Furthermore, the absolute value of a difference between the Na+ ion concentration of the polycarboxylic acid-based water reducing agent and the Na+ ion concentration of the naphthalene-based water reducing agent is preferably 1,000 ppm or more, more preferably is 1,500 to 30,000 ppm, still more preferably 1,750 to 25,000 ppm, and particularly preferably 2,000 to 10,000 ppm from the viewpoint of the storage stability after one-pack composing (uniform dispersion).
Further, from the viewpoint of the storage stability after one-pack composing (uniform dispersion), the Na+ ion concentration of the naphthalene-based water reducing agent is preferably larger than the Na+ ion concentration of the polycarboxylic acid-based water reducing agent.
In the water-reducing composition of the present invention, (A) the water reducing agent (total weight of polycarboxylic acid-based water reducing agent and naphthalene-based water reducing agent) is a reference amount (for example, 100 parts by weight), and water-soluble cellulose ether, gums, and a defoamer are added to this water reducing agent at a predetermined rate.
The water-soluble cellulose ether is preferably nonionic, and examples thereof include alkyl cellulose such as methyl cellulose; hydroxyalkyl cellulose such as hydroxyethyl cellulose and hydroxypropyl cellulose; and hydroxyalkylalkyl cellulose such as hydroxypropyl methyl cellulose, hydroxyethyl methyl cellulose, and hydroxyethyl ethyl cellulose.
Among the above alkyl celluloses, in methyl cellulose, the substitution degree (DS) of a methoxy group is preferably 1.0 to 2.2, and more preferably 1.2 to 2.0. In addition, the substitution degree (DS) of the alkoxy group in the alkyl cellulose can be obtained by converting a value that can be measured by a methyl cellulose substitution degree analysis method of the 17th revised Japanese pharmacopoeia.
Among the hydroxyalkyl celluloses, in the hydroxyethyl cellulose, the number of molar substitution (MS) of a hydroxyethoxy group is preferably 0.3 to 3.0, and more preferably 0.5 to 2.8, and in the hydroxypropyl cellulose, the number of molar substitution (MS) of a hydroxypropoxy group is preferably 0.1 to 3.3 and more preferably 0.3 to 3.0. In addition, the number of molar substitution (MS) of the hydroxyalkoxy group in the hydroxyalkyl cellulose can be obtained by converting a value that can be measured by a hydroxypropyl cellulose substitution degree analysis method of the 17th revised Japanese pharmacopoeia.
Among the hydroxyalkylalkyl celluloses described above, in the hydroxypropylmethyl cellulose, the substitution, degree (DS) of the methoxy group is preferably 1.0 to 2.2, and more, preferably 1.3 to 1.9, and the number of molar substitution (MS) of the hydroxypropoxy group is preferably 0.1 to 0.6, and more preferably 0.1 to 0.5. In the hydroxyethylmethyl cellulose, the substitution degree (DS) of the methoxy group is preferably 1.0 to 2.2 and more preferably 1.3 to 1.9, and the number of molar substitution (MS) of the hydroxyethoxy group is preferably 0.1 to 0.6 and more preferably 0.15 to 0.4. In the hydroxyethylethyl cellulose, the substitution degree (DS) of the ethoxy group is preferably 1.0 to 2.2 and more preferably 1.2 to 2.0, and the number of molar substitution (MS) of the hydroxyethoxy group is preferably 0.05 to 0.6 and more preferably 0.1 to 0.5. In addition, the substitution degree of the alkoxy group and the number of molar substitution of the hydroxyalkoxy group in the hydroxyalkylalkyl cellulose can be obtained by converting a value that can be measured by a hydroxypropyl cellulose substitution degree analysis method of hypromellose (hydroxypropylmethyl cellulose) described in the 17th revised Japanese pharmacopoeia.
In addition, DS of the alkoxy group in the alkyl cellulose, hydroxyalkyl cellulose, and hydroxyalkylalkyl cellulose represents the degree of substitution and refers to the average number of methoxy groups per anhydroglucose unit.
In addition, MS of the hydroxyalkoxy group in the alkyl cellulose, hydroxyalkyl cellulose, and hydroxyalkylalkyl cellulose represents the number of molar substitution, and means the average number of moles of hydroxyalkoxy groups per mole of anhydrous glucose.
As the water-soluble cellulose ether, the hydroxyalkylalkyl celluloses such as hydroxypropylmethyl cellulose and hydroxyethylmethyl cellulose are preferable among those exemplified above from the viewpoint of imparting material separation resistance in the hydraulic composition.
The viscosity of a 1% by weight aqueous solution of water-soluble cellulose ether at 20° C. is preferably 30 to 30,000 mPa·s, more preferably 300 to 25,000 mPa·s, still more preferably 500 to 20,000 mPa·s, and particularly preferably 500 to 3,000 mPa·s, from the viewpoint of giving a predetermined viscosity to the hydraulic composition.
The viscosity of a 1% by weight aqueous solution of water-soluble cellulose ether at 20° C. of can be measured under a measurement condition of 12 rpm using a B-type viscometer.
The addition amount of the water-soluble cellulose ether is preferably 0.1 to 5 parts by weight and more preferably 0.4 to 3 parts by weight, per total 100 parts by weight (that is, the component (A)) of the polycarboxylic acid-based water reducing agent and the naphthalene-based water reducing agent from the viewpoint of giving a predetermined viscosity to the hydraulic composition.
The water-soluble cellulose ethers may be used alone or two or more kinds thereof may be used in combination. Moreover, as the water-soluble cellulose ether, a commercially available one may be used, or one produced by a known method may be used.
Examples of gums include diutan gum, welan gum, xanthan gum, and gellan gum.
The diutan gum is composed of D-glucose, D-glucuronic acid, D-glucose and L-rhamnose, and two L-rhamnoses.
The welan gum has a structure in which L-rhamnose or L-mannose side chain is bound to a main chain in which D-glucose, D-glucuronic acid, and L-rhamnose are bound at a ratio of 2:2:1.
Similar to cellulose, the xanthan gum has a main chain composed of β-1,4-linked D-glucose, and a side chain composed of two mannose and one glucuronic acid.
The gellan gum is a heteropolysaccharide consisting of four sugars in which D-glucose, D-glucuronic acid, and L-rhamnose are bound at a ratio of 2:1:1 as a repeating unit.
By using gums, it is possible to improve the apparent viscosity of the water reducing agent, improve the dispersion state in the water-reducing composition of the water-soluble cellulose ether, and improve the storage stability after one-pack composing (uniform dispersion).
The addition amount of the gums, from the viewpoint of improving the dispersion state in the water-reducing composition of the water-soluble cellulose ether and improving the storage stability after one-pack composing (dispersion), in the case of the diutan gum, is preferably 0.005 to 2 parts by weight, more preferably 0.01 to 1 part by weight, and still more preferably 0.1 to 0.8 parts by weight per total 100 parts by weight of the polycarboxylic acid-based water reducing agent and the naphthalene-based water reducing agent (that is, the component (A)). In the cases of the welan gum, xanthan gum, and gellan gum, it is preferably 0.01 to 20 parts by weight, more preferably 0.05 to 10 parts by weight, and still more preferably 0.1 to 8 parts by weight per total 100 parts by weight of the polycarboxylic acid-based water reducing agent and the naphthalene-based water reducing agent (that is, the component (A)).
The gums may be used alone or two or more kinds thereof may be used in combination. In addition, commercially available gums can be used.
Examples of the defoamer include an oxyalkylene-based defoamer, a silicone-based defoamer, an alcohol-based defoamer, a mineral oil-based defoamer, a fatty acid-based defoamer, and a fatty acid ester-based defoamer.
Specific examples of the oxyalkylene-based defoamer include polyoxyalkylenes such as a (poly)oxyethylene (poly)oxypropylene adduct; (poly)oxyalkylene alkyl ethers such as diethylene glycol heptyl, ether, polyoxyethylene oleyl ether, polyoxypropylene butyl ether, polyoxyethylene polyoxypropylene 2-ethylhexyl ether, and an oxyethyleneoxypropylene adduct of higher alcohol with 8 or more carbon atoms or secondary alcohol with 12 to 14 carbon atoms; (poly)oxyalkylene (alkyl) aryl ethers such as polyoxypropylene phenyl ether and polyoxyethylene nonyl phenyl, ether; acetylene ethers obtained by addition polymerization of alkylene oxide to acetylene alcohol such as 2,4,7,9-tetramethyl-5-decyne-4,7-diol and 2,5-dimethyl-3-hexyne-2,5-diol, 3-methyl-1-butyn-3-ol; (poly)oxyalkylene fatty acid esters such as diethylene glycol oleate, diethylene glycol laurate, ethylene glycol distearate, and polyoxyalkylene oleate; (poly)oxyalkylene sorbitan fatty acid esters such as polyoxyethylene sorbitan monolaurate and polyoxyethylene sorbitan trioleate; (poly)oxyalkylene alkyl (aryl) ether sulfate ester salts such as sodium polyoxypropylene methyl ether sulfate and sodium polyoxyethylene, dodecylphenol ether sulfate; (poly)oxyalkylene alkyl phosphate esters such as (poly)oxyethylene stearyl phosphate; (poly)oxyalkylene alkylamines such as polyoxyethylene laurylamine; and polyoxyalkylene amide.
Specific examples of the silicone-based defoamer include dimethyl silicone oil, silicone paste, silicone emulsion, organically modified polysiloxane (polyorganosiloxane such as dimethylpolysiloxane), and fluorosilicone oil.
Specific examples of the alcohol-based defoamer include octyl alcohol, 2-ethylhexyl alcohol, hexadecyl alcohol, acetylene alcohol, and glycols.
Specific examples of the mineral oil-based defoamer include kerosene and liquid paraffin.
Specific examples of the fatty acid-based defoamer include oleic acid, stearic acid, and alkylene oxide adducts thereof.
Specific examples of the fatty acid ester-based defoamer include glycerin monoricinoleate, an alkenyl succinic acid derivative, sorbitol monolaurate, sorbitol trioleate, and natural wax.
Among these, the oxyalkylene-based defoamer is preferable from the viewpoint of efficiently defoaming entrained air of water-soluble cellulose ether and gums and improving the storage stability after one-pack composing (uniform dispersion).
The addition amount of the defoamer is preferably 0.001 to 16 parts by weight and more preferably 0.002 to 10 parts by weight per total 100 parts by weight of the polycarboxylic acid-based water reducing agent and the naphthalene-based water reducing agent (that is, the component (A)), from the viewpoint of efficiently defoaming entrained air of water-soluble cellulose ether and gums and improving the storage stability after one-pack composing (uniform dispersion).
The defoamer may be used alone or two or more kinds thereof may be used in combination, A commercially available defoamer can be used.
According to the water-reducing composition of the present invention, the storage stability is improved. For example, sedimentation volume after standing for 72 hours immediately after one-pack composing (uniform dispersion) becomes 65% by volume or more. In addition, according to the present invention, the sedimentation volume after standing for 168 hours immediately after one-pack composing (uniform dispersion) of the water-reducing composition can be 50% by volume or more.
Here, the sedimentation volume means a volume ratio (suspension maintenance ratio) of a suspension layer (water-reducing composition layer) to the whole liquid observed when a predetermined amount (for example, 100 ml) of the water-reducing composition immediately after one-pack composing (uniform dispersion) (immediately after mixing) is poured into a graduated cylinder having a plug with a predetermined outer diameter (for example, 32 mm), and then left standing for a certain time at room temperature (20±3° C.). The amount of the water-reducing composition immediately after one-pack composing (uniform dispersion) (immediately after mixing) and the size (outer diameter and height) of the graduated cylinder to be used are not particularly limited as long as the height (that is, a boundary position between the supernatant and the suspension layer in the entire liquid) of the suspension layer (water-reducing composition layer) in the entire liquid during the above observation can be clearly confirmed visually.
The water-reducing composition of the present invention can be produced by a step of obtaining a water-reducing composition by mixing a polycarboxylic acid-based water reducing agent, a naphthalene-based water reducing agent, water-soluble cellulose ether, gums, and a defoamer.
At this time, the order (that is, the order in which materials are added and mixed) of addition of the polycarboxylic acid-based water reducing agent, the naphthalene-based water reducing agent, the water-soluble cellulose ether, the gums, and the defoamer is not particularly limited.
Further, the polycarboxylic acid-based water reducing agent and the naphthalene-based water reducing agent may be added separately, or may be added after mixing in advance. In addition, the order of addition of the polycarboxylic acid-based water reducing agent and the naphthalene-based water reducing agent may be the same or either one may be added first. For example, in a state where a stirring bar of a stirrer described later is rotating, the polycarboxylic acid-based water reducing agent, the naphthalene-based water reducing agent, the water-soluble cellulose ether, the gums, and the defoamer may be added and mixed in any order, and alternatively, a water reducing agent mixture in which the polycarboxylic acid-based water reducing agent and the naphthalene-based water reducing agent are mixed in advance, the water-soluble cellulose ether, the gums, and the defoamer may be added and mixed in any order. Furthermore, either the polycarboxylic acid-based water reducing agent or the naphthalene-based water reducing agent is added, then a mixture in which the water-soluble cellulose ether, the gums, and the defoamer are mixed in advance is added and mixed for a certain period of time (about 1 minute), and the remaining water reducing agent may be added and mixed at the end.
Furthermore, the gums may be added in either form of powder or aqueous solution.
The mixing method is not particularly limited, and can be performed using, for example, a stirrer.
The stirrer is a device provided with a stirring bar (rotating blade) that rotates at high speed and a container in which the above materials can be mixed by the rotation of the stirring bar, and examples thereof include a homomixer (HM-310, manufactured by AS ONE Corporation), a rotor-stator type mixer such as high speed, homomixer (LZI314-HM-1, manufactured by CHUORIKA, CO., LTD.), a cylindrical wall swirl mixer such as a thin film swivel type high speed mixer (FILMIX, manufactured by PRIMIX PLUS Inc.), a homogenizer (PH91, manufactured by SMT Co., Ltd.), or a high-speed stirrer to which those principles are applied. Among them, the rotor-stator type mixer or the cylindrical wall swirling mixer is preferable.
Examples of the types of stirring bar (rotating blades) in the stirrer include a turbine-stator type, a thin film swirl type (PC wheel), a disper type, and a perforated cage type, and from the viewpoint of the stirring efficiency and the storage stability of the water-reducing composition, the turbine-stator type and the thin-film swivel type (PC wheel) are preferable.
The peripheral speed of the stirring bar in the stirrer is preferably 7 to 30 m/s, and more preferably 7 to 15 m/s, from the viewpoint of efficient productivity of the water-reducing composition.
The peripheral speed of the stirring bar is the speed of the fastest part of the stirring bar (rotating blade) that rotates in the stirrer (that is, the outermost periphery of the stirring bar).
The peripheral speed v (m/s) of the stirring bar is obtained by the following formula from the diameter d (mm) of the stirring bar and the rotation speed n (rpm (number of rotations per minute)) of the stirring bar.
v=π×d×n/60,000
The mixing time (stirring time) is the time after all the materials of the water reducing agent, the water-soluble cellulose ether, the gums, and the defoamer are added and the target peripheral speed of the stirring bar is reached, or the time after all the materials of the water reducing agent, the water-soluble cellulose ether, the gums, and the defoamer have been added after the target peripheral speed of the stirring bar has been reached, and is not particularly limited. For example, it is preferably 30 seconds or longer, and more preferably 1 minute or longer, from the viewpoint of efficient productivity of the water-reducing composition. The upper limit of the mixing time is not particularly limited, and is preferably 60 minutes or shorter, and more preferably 10 minutes or shorter from the viewpoint of efficient productivity of the water-reducing composition.
The hydraulic composition according to the present invention is characterized by containing the water-reducing composition of the present invention described above, a hydraulic substance, and water.
Moreover, the manufacturing method of the hydraulic composition according to the present invention is characterized by including at least a step of mixing the water-reducing composition of the present invention described above, a hydraulic substance, and water.
Specific applications of the hydraulic composition include concrete, mortar, and cement paste.
The hydraulic composition for concrete is preferably one containing the water-reducing composition of the present invention, the hydraulic substance (cement), water, a fine aggregate (sand), and a coarse aggregate (gravel). Examples of the kinds thereof include ordinary concrete, medium fluidized concrete, highly fluidized concrete, underwater inseparable concrete, and sprayed concrete.
The hydraulic composition for mortar preferably contains the water-reducing composition of the present invention, and the hydraulic substance (cement), water, and the fine aggregate (sand). Examples of the kinds thereof include a tiled mortar, a repair mortar, and a self-leveling material.
The hydraulic composition for cement paste preferably contains the water-reducing composition of the present invention, the hydraulic substance (cement), and water. Examples thereof include a tile-based inorganic building material adhesive and a grout material to embed empty walls between parts.
Examples of the hydraulic substance, include hydraulic cement such as ordinary Portland cement, high-early-strength Portland cement, moderate heat Portland cement, blast furnace cement, silica cement, fly ash cement, alumina cement, and ultra-high-early strong Portland cement.
The hydraulic substances may be used alone or two or more kinds thereof may be used in combination. In addition, a commercially available hydraulic substance can be used.
The content of the hydraulic substance (cement) is preferably 270 to 800 kg per 1 m3 of concrete in a case where the hydraulic composition is used for concrete from the viewpoint of securing strength.
In a case where the hydraulic composition is used for a mortar, the content is preferably 300 to 1,000 kg per 1 m3 of mortar.
In a case where the hydraulic composition is used for cement paste, the content is preferably 500 to 1,600 kg per 1 m3 of cement paste.
The addition amount of the water-reducing composition of the present invention is preferably 0.1 to 5% by weight and more preferably 0.3% to 3% by weight per unit cement amount (kg/m3) from the viewpoint of fluidity, material separation resistance, setting delay, and the like in the hydraulic composition.
Examples of water include tap water, and seawater, and tap water is preferable from the viewpoint of preventing salt damage.
The water/cement ratio (W/C) in the hydraulic composition is preferably 30% to 75% by weight, more preferably 45% to 65% by weight, from the viewpoint of material separation in the hydraulic composition.
The hydraulic composition further includes an aggregate depending on the application thereof. Examples of the aggregate include a fine aggregate and a coarse aggregate.
As the fine aggregate, river sand, mountain sand, land sand, crushed sand and the like are preferable.
The sand cement ratio in the hydraulic composition is preferably 0.5 to 3.0 from the viewpoint of fluidity, preventing cracks, and cost of the hydraulic composition.
The particle size (maximum particle size) of the fine aggregate is preferably 5 mm or less.
The particle size distribution of the fine aggregate is preferably from 0.075 to 5 mm, more preferably from 0.075 to 2 mm, and still more preferably from 0.075 to 1 mm, from the viewpoint of the troweling workability of the mortar composition. The particle size distribution of the fine aggregate can be measured using a sieve having openings of 5 mm, 2.5 mm, 1.2 mm, 850 μm, 600 μm, 425 μm, 300 μm, 212 μm, 150 μm, 106 μm, 75 μm, and 53 μm.
In a case where the hydraulic composition is for concrete, the content of the fine aggregates is preferably 400 to 1,100 kg, more preferably 500 to 1,000 kg per 1 m3 of concrete, and in a case where the hydraulic composition is used for a mortar, the content is preferably 500 to 2,000 kg and more preferably 600 to 1,600 kg per 1 m3 of mortar.
As the coarse aggregate, river gravel, mountain gravel, land gravel, crushed stone, and the like are preferable.
The particle size (maximum particle size) of the coarse aggregate is larger than the particle size of the fine aggregate, and is preferably 40 mm or less and more preferably 25 mm or less.
In a case where the hydraulic composition is used for concrete, the content of the coarse aggregate is preferably 600 to 1,200 kg and more preferably 650 to 1,150 kg per 1 m3 of concrete.
In a case where the hydraulic composition is used for concrete, the fine aggregate ratio (volume percentage) in the aggregate is preferably 30% to 55% by volume, more preferably 35% to 55% by volume, and more preferably 35% to 50% by volume, from the viewpoint of maintaining the fluidity or sufficient strength. The following expression is established:
Fine aggregate ratio (volume %)=fine aggregate volume/(fine aggregate volume+coarse aggregate volume)×100
The aggregates may be used alone or two or more kinds thereof may be used in combination. In addition, a commercially available aggregate, can be used.
An admixture can be added to the hydraulic composition as necessary in order to suppress heat generation during curing and to increase durability after curing. Examples of the admixture include blast furnace slag and fly ash.
In a case of adding the admixture, the content thereof is preferably more than 0% by weight and 70% by weight or less from the viewpoint of the initial strength development and durability of the hydraulic composition. The admixtures may be used alone or two or more kinds thereof, may be used in combination. In addition, a commercially available admixture can be used.
In the hydraulic composition, an AE, agent (air entraining agent) may be used in combination as necessary in order to secure a predetermined amount of air and obtain the durability of the hydraulic composition.
Examples of the AE agent include AE agents of an anionic surfactant, a cationic surfactant, a nonionic surfactant, an amphoteric surfactant, and a rosin surfactant.
Examples of the anionic surfactant include a carboxylic acid type, a sulfuric acid ester type, a sulfonic acid type, and a phosphoric acid ester type.
Examples of the cationic surfactant include an amine salt type, a primary amine salt type, a secondary amine salt type, a tertiary amine salt type, and a quaternary amine salt type.
Examples of the nonionic surfactant include an ester type, an ester and ether type, an ether type, and an alkanolamide type.
Examples of the amphoteric surfactant include an amino acid type and a sulfobetaine type.
Examples of the rosin surfactant include abietic acid, neoabietic acid, parastrinic acid, pimaric acid, isopimaric acid, and dehydroabietic acid.
The addition amount of the AE agent, is preferably 0.0001 to 0.01% by weight per unit cement amount (kg/m3) from the viewpoint of the air amount of the hydraulic composition.
The AE agents may be used alone or two or more kinds thereof may be used in combination, A commercially available AE agent can be used.
In order to obtain the strength of the hydraulic composition, a defoamer may be added to the hydraulic composition as necessary. Examples of the defoamer include those used in the water-reducing composition.
The addition amount of the defoamer is preferably 1 to 50 parts by weight per 100 parts by weight of the water-soluble cellulose ether from the viewpoint of dispersibility.
In addition, in the hydraulic composition of the present invention, in order to manage the physical properties of the hydraulic composition (fresh concrete, fresh mortar, or fresh cement paste) immediately after kneading, a set acceleration agent such as calcium chloride, lithium chloride, and calcium formate or a setting retarder such as sodium citrate or sodium gluconate can be used as necessary. Furthermore, in order to prevent shrinkage cracking due to hardening and drying and cracking by a temperature stress due to heat of hydration reaction of cement, a drying shrinkage reducing agent and an Auin or lime expansion material can be added in the hydraulic composition of the present invention as necessary.
The hydraulic composition described, above can be produced by a usual method. For example, first, the water-reducing composition of the present invention, the hydraulic substance, and the aggregates (fine aggregate and/or coarse aggregate) and the defoamer as necessary are put into a mixer and air-kneaded. Thereafter, water is added and kneaded to obtain the hydraulic composition.
Moreover, the water-reducing composition and water may be mixed in advance to be added.
As described above, according to the method for producing the hydraulic composition of the present invention, bleeding is suppressed and thus a fluid hydraulic composition is obtained.
Hereinafter, the present invention is specifically described below with reference to Examples and Comparative Examples, but the present invention is not limited to the following Examples.
Water reducing agents, water-soluble cellulose ether, gums, and a defoamer described below were weighed to be the addition amounts indicated in Table 1, and these materials were stirred and mixed as follows using a stirrer to produce a water-reducing composition.
The stirring time in all of Examples 1 to 8 and Comparative Examples 1 and 2 was 2 minutes after all of the water reducing agent, the water-soluble cellulose ether, the gums, and the defoamer were added after having the stirring bar reached the target peripheral speed.
In addition, as for the water reducing agent, a polycarboxylic acid-based water reducing agent and a naphthalene-based water reducing agent were mixed in advance and added as a mixture, of the water reducing agents. The gums were added in the form of powder.
In Example 9, after having the stirring bar reached the target peripheral speed, a mixture of the water-soluble cellulose ether, the gums, and the defoamer was added to the polycarboxylic acid-based water reducing agent, and after stirring for 1 minute, the naphthalene-based water reducing agent was added and stirred for another 1 minute.
The water-soluble cellulose ether, the gums, and the defoamer were added in a powder state.
In Example 10, after having the stirring bar reached the target, peripheral speed, a mixture of the water-soluble cellulose ether, the gums, and the defoamer was added to the naphthalene-based water reducing agent, and after stirring for 1 minute, the polycarboxylic acid-based water reducing agent was added and stirred for another 1 minute.
The water-soluble cellulose ether, the gums, and the defoamer were added in a powder state.
The Na+ ion concentration of the water reducing agent (the above carboxylic acid-based water reducing agent, the naphthalene-based water reducing agent, and a mixture thereof) was measured by the following method.
A water reducing agent sample used in the production of the water-reducing composition was diluted with pure water to 1/10,000 concentration, and filtrated using a 0.2 μm filter (trade name, liquid chromatography disc (made by PTFE), manufactured by Thermo Fisher Scientific), and measured with an ion chromatograph DIONEX ICS-1600 (manufactured by Thermo Fisher Scientific) under the following measurement conditions.
The eluent was prepared by diluting 2 mol of metasulfonic acid with pure water to 10 mmol of concentration.
The sedimentation volume of the obtained water-reducing composition was measured with the following method.
Immediately after the above production, 100 ml of the water-reducing composition Immediately after one-pack composing (uniform dispersion) was collected in a graduated cylinder (outer diameter 32 mm, capacity 100 ml, manufactured by IWAKI) having a plug and left (standing) at room temperature (20±3° C.), and a boundary with a supernatant was visually observed immediately (after 0 hour), 24 hours, 72 hours, and 168 hours after collection. Based on the scale corresponding to the boundary, the volume ratio (suspension maintenance ratio) of the suspension layer (water-reducing composition layer) to the whole liquid was determined as the sedimentation volume. For example, in a case where the boundary with the supernatant is 0 mL, the sedimentation volume is 100% by volume, in a case where the boundary with the supernatant is 90 mL, the sedimentation volume is 90% by volume, and in a case where the boundary with the supernatant is 50 mL, the sedimentation volume is 50% by volume.
Next, using the water-reducing composition produced as described above, a mortar was produced as a hydraulic composition as follows.
That is, a dry mortar was prepared by putting a predetermined amount of cement and fine aggregates into a 5 liter mortar mixer (C138A-48, manufactured by MARUTO Testing Machine Company) defined in JIS R 5201 and performing dry blending for 1 minute. Subsequently, a mortar was produced by adding a mixture of the above water-reducing composition and a predetermined amount of water mixed in advance, and mixing the mixture for 3 minutes at a low speed (rotation speed: 140 rpm, revolution speed: 62 rp defined in JIS R 5201. The conditions at this time are as follows.
Note that, W represents a unit water amount (kg/m3), and C represents a unit cement amount (kg/m).
The material temperature was adjusted so that mortar temperature at the end of kneading was 20±3° C.
The obtained hydraulic composition (mortar) was subjected to the following table flow test, and the table flow value was measured.
Table Flow Test
The test was conducted according to HS R 5201. Here, after placing the mortar, on the table, an operation of giving 15 impacts (falling motion) to the defined table was not performed, and the table flow value (0 stroke, flow) in the state without impact was measured. That is, the spread when the flow stopped after placing the mortar on the table was set as a table flow value (mortar flow value).
The results are indicated in Table 1.
As a result of the above, regarding the storage stability of the water-reducing composition, as compared with the water-reducing composition containing only the polycarboxylic acid-based water reducing agent of Comparative Example 1, in the water-reducing composition containing the polycarboxylic acid-based water reducing agent and the naphthalene-based water reducing agent of Examples 1 to 10, the storage stability up to 168 hours later was improved. In any of Examples 1 to 10, the storage stability of the water-reducing composition was improved while maintaining Na+ ion concentration of 10,000 ppm or more. Furthermore, in Examples 5 to 8, a combination of water-soluble cellulose ethers and gums, one of which is different from that in Example 4, is used; however, it has been found that in either case, the water-reducing composition storage stability is improved.
Next, regarding the fluidity of the hydraulic composition (mortar) using the water-reducing composition, in the mortar using the water-reducing composition containing the polycarboxylic acid-based water reducing agent and the naphthalene-based water reducing agent of Examples 1 to 10, excellent fluidity is exhibited in all cases. On the other hand, in Comparative Example 2, due to the mortar using the water-reducing composition containing only the naphthalene-based water reducing agent, the result is inferior in the fluidity. In particular, in Examples 2 to 4, although the proportion of the naphthalene-based water reducing agent is increased, the fluidity is excellent.
It is known that when the naphthalene-based water reducing agent and the water-soluble cellulose are used in combination as in Comparative Example 2, both form a certain complex, resulting in a decrease in the fluidity of the hydraulic composition.
In contrast, in the present invention, by using the polycarboxylic acid-based water reducing agent and the naphthalene-based water reducing agent in combination as the water reducing agent, the formation of this complex is avoided, and the fluidity of the hydraulic composition is, prevented from being reduced so that the storage stability of the water-reducing composition and the fluidity of the hydraulic composition are realized at a high level.
Although the present invention has been described with the embodiment described above, the present invention is not limited to this embodiment, and can be changed within the range that can be conceived by those skilled in the art such as other embodiments, additions, changes, and deletions, and any embodiment is included in the scope of the present invention as long as the effects of the present invention pare exhibited.
Japanese Patent Application Nos. 2018-215196 and 2019-147503 are incorporated herein, by reference.
Although some preferred embodiments have been described, many modifications and variations may be made thereto in light of the above teachings. It is therefore to be understood that the invention may be practiced otherwise than as specifically described without departing from the scope of the appended claims.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2018-215196 | Nov 2018 | JP | national |
| 2019-147503 | Aug 2019 | JP | national |
