Admixture composition for hydraulic composition

Abstract

Provided are an admixture composition for a hydraulic composition, which can favorably control the behavior of bubbles in the hydraulic composition adhering to a mold form or a release agent applied to the surface of the mold form, which causes bubble marks on the surface of a hardened body of the hydraulic composition, to improve the surface appearance of the hardened body, and which is excellent in storage stability during high-temperature storage (for example, 30 to 40 °C), a method for producing a hardened body of a hydraulic composition using the same, and a method for improving the surface appearance of a hydraulic composition.SOLUTION: An admixture composition for a hydraulic composition, comprising the following components (A), (B) and (C): (A): a modified silicone functional group having one or more functional groups selected from the following in a side chain: an amino group, a carboxyl group, a hydroxyl group, an epoxy group, a mercapto group, a fluorine group, a polyoxyalkylene group, a polyoxazoline group, and a polyglycerin group (B): an anionic surface active agent represented by a specific general formula (b1) SELECTED DRAWING: None

Description

[Technical Field]

[0001] The present invention relates to an admixture composition for a hydraulic composition, a method for producing a set product of a hydraulic composition using the same, and a method for improving the surface appearance of a hydraulic composition. [Background technology]

[0002] Hydraulic compositions, such as concrete, can be produced by filling a formwork with an unhardened hardenable composition, followed by hardening through drying or chemical reaction in a subsequent process to obtain a hardened product. One of the factors that influences the value of a hardened product is the aesthetic appearance of its surface. This literally refers to the beauty of the surface of the hardened product, and the more aesthetically pleasing the surface is, the more the product tends to be evaluated as having higher value.

[0003] One of the causes of the deterioration of the surface appearance of the cured product is the traces of air bubbles that are exposed on the surface of the cured product. To address this problem, measures have been taken to add a repair process to hide the traces of air bubbles after curing, but this is not desirable from the standpoints of cost and labor.

[0004] Patent Document 1 discloses a drying inhibitor for mortar or concrete that has a high initial drying inhibitory effect after spraying, which comprises (A) a nonionic surfactant represented by general formula (I), (B) a surfactant whose 0.1 wt % aqueous solution at 20°C has a surface tension of 10 to 45 mN / m, and (C) water. Patent Document 2 discloses a method for preventing efflorescence in a hardened self-leveling aqueous composition, which comprises pouring a self-leveling aqueous composition containing a base material made of cement and gypsum or a base material made of cement and an expanding material, water, aggregate, a thickener, and an antifoaming agent, and hardening the composition, the method comprising blending 0.00005 to 0.005 parts by weight of polyoxyalkylene-modified silicone with 100 parts by weight of the self-leveling aqueous composition, and using a cement dispersant made of a water-soluble vinyl copolymer obtained by copolymerizing a vinyl monomer containing 50 to 90 mol % of a structural unit represented by formula (1) as a structural unit. Patent Document 3 discloses a dry composition useful for producing, for example, cement-based materials such as mortar, concrete, and plaster, which comprises at least one binder and at least one silicone oil and enables reduction in dust generation. Patent Document 4 discloses a water-repellent composition for treating porous substrates, which comprises an emulsion containing water, at least one surfactant, and a specific siloxane copolymer. [Prior art documents] [Patent documents]

[0005] [Patent Document 1] Japanese Patent Application Laid-Open No. 2008-273765 [Patent Document 2] Japanese Patent Application Publication No. 7-267712 [Patent Document 3] Japanese Patent Application Laid-Open No. 2015-57369 [Patent Document 4] Special Publication No. 2014-531491 Summary of the Invention [Problem to be solved by the invention]

[0006] In construction sites, particularly in summer construction work environments, additives for hydraulic compositions that have storage stability during high-temperature storage are desired. For example, if a container in which an additive for a hydraulic composition is stored is exposed to direct sunlight during the daytime during a hot summer, the temperature inside the container may reach, for example, 60°C. In such cases, it is desirable to store the container indoors out of direct sunlight, but there are many cases where sufficient storage space cannot be secured at manufacturing sites, and outdoor storage is the only option.

[0007] The present invention provides an admixture composition for hydraulic compositions, which can improve the aesthetic appearance of the surface of a set hydraulic composition by effectively controlling the behavior of air bubbles in the hydraulic composition, which cause air bubble marks on the surface of the set hydraulic composition, adhering to a formwork or a release agent applied to the formwork surface, and which has excellent storage stability when stored at high temperatures (e.g., 30 to 40°C), as well as a method for producing a set hydraulic composition using the same and a method for improving the aesthetic appearance of the surface of a hydraulic composition.

[0008] In the present invention, improving the aesthetic appearance of the surface means reducing the number of bubble traces on the surface of a hardened product of a hydraulic composition to improve the aesthetic appearance of the surface of the hardened product. [Means for solving the problem]

[0009] The present invention relates to an admixture composition for a hydraulic composition, which contains the following component (A), component (B), and component (C): Component (A): Modified silicone having one or more functional groups selected from the following on its side chain: Functional groups: amino group, carboxy group, hydroxy group, epoxy group, mercapto group, fluoro group, polyoxyalkylene group, polyoxazoline group, polyglycerin group Component (B): a compound represented by the following general formula (b1): R 1b -O-[(EO) n (PO) m ]-SO3M b (b1) [In the formula, R 1b is a hydrocarbon group having 4 to 20 carbon atoms, EO is an ethyleneoxy group, PO is a propyleneoxy group, n is the average number of moles of EO added and is a number of 1 to 50, m is the average number of moles of PO added and is a number of 0 to 30, and EO and PO may be bonded in blocks or randomly. b indicates a counter cation. (C) Component: Cement dispersant

[0010] The present invention also provides a method for preparing a hydraulic composition by mixing the admixture composition for hydraulic compositions of the present invention, hydraulic powder, and water; a step of filling the prepared hydraulic composition into a form and hardening it; and A step of demolding the hardened hydraulic composition; The present invention relates to a method for producing a hardened product of a hydraulic composition having the formula (I).

[0011] The present invention also relates to a method for improving the surface appearance of a hydraulic composition, which comprises mixing the admixture composition for hydraulic compositions of the present invention, hydraulic powder, and water. [Effects of the Invention]

[0012] According to the present invention, there are provided an admixture composition for hydraulic compositions which can improve the aesthetic appearance of the surface of a set hydraulic composition by effectively controlling the behavior of air bubbles in the hydraulic composition, which cause air bubble marks on the surface of the set hydraulic composition, adhering to a formwork or a release agent applied to the formwork surface, and which has excellent storage stability when stored at high temperatures (for example, 30 to 40°C), as well as a method for producing a set hydraulic composition using the same and a method for improving the aesthetic appearance of the surface of a hydraulic composition. DETAILED DESCRIPTION OF THE INVENTION

[0013] The reason why the admixture composition for hydraulic compositions of the present invention can better control the behavior of bubbles in the hydraulic composition, which cause bubble marks on the surface of the set body of the hydraulic composition, thereby improving the aesthetic appearance of the surface of the set body, and has excellent storage stability when stored at high temperatures is not necessarily clear, but is presumed to be as follows. A hydraulic composition such as concrete is filled into a metal formwork by applying a release agent to the formwork, pouring the composition into the formwork, and vibrating the mixture, and then hardening the composition. The component (A) contained in the admixture composition for hydraulic compositions of the present invention is a specific modified silicone having a silicone backbone with a high affinity for air and specific functional groups in the side chains with a high affinity for water. It is presumed that the component (A) acts on the interface of air bubbles in the hydraulic composition, interposing water between the air bubbles and the formwork (or the release agent applied to the formwork), preventing the air bubbles in the hydraulic composition from adhering to the formwork (or the release agent applied to the formwork), reducing the number of air bubbles on the surface of the set hydraulic composition, and improving the aesthetic appearance of the set hydraulic composition surface. Furthermore, when the admixture composition for hydraulic compositions contains the component (A) and a cement dispersant (component (C)) containing many salts or hydrophilic groups for the purpose of improving the fluidity of the hydraulic composition, and is formulated as a one-component composition, the hydration of the component (C) inhibits the hydration of the component (A), causing insolubility, clouding, or separation, especially under high temperature conditions. It is presumed that the admixture composition for hydraulic compositions of the present invention further contains component (B) having a specific structure, which allows the hydrocarbon groups of component (B) to interact with the silicone skeleton of component (A), and the hydrophilicity of the sulfonic acid groups of component (B) to strengthen hydration, thereby increasing the water solubility of component (A), allowing it to exist stably in a one-part state at high temperatures (for example, 30 to 40°C). However, the present invention is not limited to the above-mentioned mechanism of action.

[0014] [Admixture composition for hydraulic composition] <Component (A)> The admixture composition for hydraulic compositions of the present invention contains the following component (A): Component (A): Modified silicone having one or more functional groups selected from the following on its side chain: Functional groups: amino group, carboxy group, hydroxy group, epoxy group, mercapto group, fluoro group, polyoxyalkylene group, polyoxazoline group, polyglycerin group

[0015] Examples of modified silicone compounds having an amino group in the side chain include the following. KF-868, KF865, KF864, KF859, KF393, KF860, KF880, KF8004, KF8002, KF8005, KF867, KF8021, KF869, KF861, and KF877 manufactured by Shin-Etsu Chemical Co., Ltd. XF42-B1989, XF42-B8922, XF42-C0330, SF1708fluid, and silfoftAX fluid manufactured by MOMENTIVE. DOWSIL BY16-205, DOWSIL BY16-213, DOWSIL BY16-849Fluid, DOWSIL BY16-853U, DOWSIL BY16-871, DOWSIL BY16-872, DOWSIL BY16-789B, DOWSIL BY16-892, DOWSIL FZ-3705, DOWSIL FZ-3710Fluid, DOWSIL FZ-3760, DOWSIL FZ3785, DOWSIL SF8417Fluid. BELSIL ADM 1370, BELSIL ADM1650, BELSIL ADM6057E, BELSIL ADM6102E, BELSIL ADM6300E, BELSIL ADM8103E, BELSIL ADM8104E, BELSIL ADM8301E, BELSIL ADM9000E, BELSIL ADM9700E, WACKER L652, WACKER L653, WACKER L655, and WACKER L656 manufactured by Wacker Asahi Kasei Silicones.

[0016] Examples of modified silicone compounds having a carboxy group in the side chain include the following. X-22-3701E, X-22-62C, and X-22-3710 manufactured by Shin-Etsu Chemical Co., Ltd. SilsoftINX fluid manufactured by MOMENTIVE. DOWSILBY16-880 Fluid manufactured by DOW. Examples of modified silicone compounds having a hydroxy group in the side chain include the following. X-22-4039, X-22-4015, KF-6000, KF-6001, KF-6002, KF-6003, X-22-170BX, X-22-170DX, X-22-176DX, X-22-176F, and X-22-176GX-A manufactured by Shin-Etsu Chemical Co., Ltd. DOWSIL BY16-201, DOWSIL SF8427 Fluid, DOWSIL SF8428 Fluid manufactured by DOW. Examples of modified silicone compounds having an epoxy group in the side chain include the following. X-22-343, KF-101, KF-1001, X-22-2000, X-22-2046, KF-102, X-22-4741, KF-1002, KF1005, X-22163, KF-105, X-22163A, X-22163B, X-22-163C, X-22-169AS, X-22-169B, X-22-173BX, X-22-1730DX, and X-22-9002 manufactured by Shin-Etsu Chemical Co., Ltd. DOWSILBY16-839 Fluid, DOWSIL BY16-876, DOWSIL FZ-3736Fluid, DOWSIL L-9300, DOWSILSF8411Fluid, DOWSIL SF8421Fluid manufactured by DOW. GENIOSIL GF80, GENIOSIL GF82, and GENIOSIL GF91 manufactured by Wacker Asahi Kasei Silicone.

[0017] Examples of modified silicone compounds having a mercapto group in the side chain include the following. Shin-Etsu Chemical Co., Ltd. KF-2001, KF-2004, X-22-167B, X-22-167C Examples of modified silicone compounds having a fluoro group in the side chain include the following. FL-5, X-22-821, X-22-822, FL-100-100cs, FL-100-450cs, FL-100-1000cs, and FL-100-10000cs manufactured by Shin-Etsu Chemical Co., Ltd. FR-5, XS66-B8226, XS66-B8636 manufactured by MOMENTIVE. DOWSIL FS1265 fluid (300cSt), DOWSIL FS1265 fluid (1000cSt), DOWSIL FS1265 fluid (10000cSt) manufactured by DOW. WACKER AF 98 / 1000 and WACKER AF 98 / 10000 manufactured by Asahi Kasei Wacker Silicone.

[0018] Examples of modified silicone compounds having polyoxyalkylene groups in the side chains include the following. X-22-4952, X-22-4272, KF6123, KF-351A, KF-352A, KF-353, KF-354L, KF-355A, KF-615A, KF-945, KF-640, KF-642, KF-643, KF-644, KF-6020, KF6204, X-22-4515, KF-6011, KF-6012, KF-6015, KF6017, X-22-2516, KF6004, KF-6043, KF-6048, KF-6028, and KF-6038 manufactured by Shin-Etsu Chemical Co., Ltd. SF1188SAfluid, Silsoft840 fluid, Silsoft860 fluid, Silsoft870 fluid, Silsoft875fluid, Silsoft876 fluid, Silsoft895 fluid, Silsoft900 fluid, Silsoft1528 fluid, Silsoft1540 fluid manufactured by MOMENTIVE. DOWSIL 501WAdditive, DOWSIL FZ-2104 Fluid, DOWSIL FZ-2110, DOWSIL FZ-2123, DOWSILFZ-2164, DOWSIL FZ-2191, DOWSIL FZ5609 fluid, DOWSIL L-7001, DOWSIL L-7002, DOWSILL-7604, SYLGARD manufactured by DOW OFX-0309 Fluid. FZ-2203, DOWSILFZ-2215, DOWSIL FZ-2222, DOWSIL FZ-2233. BELSIL DMC6031, BELSIL DMC6038, BELSIL OW1500, WACKER L053, WACKER L060, WACKER L066 manufactured by Asahi Kasei Wacker Silicone Co., Ltd. ABIL8843, ABIL EM90, ABIL EM180, ABIL 8851, ABIL 8852, ABIL EM97S, ABIL 8832 manufactured by EVONIK.

[0019] Examples of modified silicone compounds having a polyoxazoline group in the side chain include the following. Elastomer OS manufactured by Kao Corporation. Examples of modified silicone compounds having a polyglycerin group in the side chain include the following. KF-6100, KF-6104, KF-6106, and KF6105 manufactured by Shin-Etsu Chemical Co., Ltd. Examples of modified silicone compounds having an amino group and a polyether group include the following. Shin-Etsu Chemical Co., Ltd. X-22-3939A and SilfoftA+fluid manufactured by MOMENTIVE, DOWSIL BY-16-891, DOWSIL FZ-3789 manufactured by DOW. Examples of modified silicone compounds having an epoxy group and a polyether group include the following. Shin-Etsu Chemical Co., Ltd.'s X-22-4741, KF-1002, etc. DOWSIL BY16-876, DOWSIL FZ-3736 Fluid, DOWSIL SF8421 Fluid manufactured by DOW.

[0020] From the viewpoint of the effect of reducing the amount of bubble traces on the surface of the cured product, component (A) is preferably a modified silicone having one or more repeating units selected from repeating units (a1) represented by the following general formula (a1) and repeating units (a2) represented by the following general formula (a2):

[0021] [ka]

[0022] [In general formula (a1), R 1a is a hydrocarbon group having 1 to 6 carbon atoms, and R 2a is an alkylene group having 1 to 10 carbon atoms, a is 1 or 0, and * is a bonding site. X is a group containing an amino group, a group containing a carboxy group, a group containing an epoxy group, a group containing a hydroxy group, a group containing a fluoro group, -O-(AO) e R 3a and a group selected from the following general formula (a3):

[0023] [ka]

[0024] AO is an alkyleneoxy group having 2 to 4 carbon atoms, e is the average number of moles of AO added, and is a number of 0 to 50, and R 3a is a hydrogen atom or an alkyl group having 1 to 30 carbon atoms. 4a are each independently a hydrogen atom, an alkyl group having 1 to 30 carbon atoms, or -(CO)-R5a and R 5a is a hydrocarbon group having 1 to 30 carbon atoms; s is an integer of 0 to 3, t is an integer of 0 to 3, and u is an integer of 0 to 20. *-SiR 7a 3-b (R 8a -X) b (a2) [In general formula (a2), R 7a are each independently a hydrocarbon group having 1 to 6 carbon atoms, and R 8a are each independently an alkylene group having 1 to 10 carbon atoms, b is an integer of 1 to 3, and * is a bonding site. X is a group containing an amino group, a group containing a carboxy group, a group containing an epoxy group, a group containing a hydroxy group, a group containing a fluoro group, -O-(AO) e R 3a AO is an alkyleneoxy group having 2 to 4 carbon atoms, e is the average number of moles of AO added, and is a number of 0 to 50, and R 3a is a hydrogen atom or an alkyl group having 1 to 30 carbon atoms. 4a are each independently a hydrogen atom, an alkyl group having 1 to 30 carbon atoms, or -(CO)-R 5a and R 5a is a hydrocarbon group having 1 to 30 carbon atoms; s is an integer of 0 to 3, t is an integer of 0 to 3, and u is an integer of 0 to 20.

[0025] In general formula (a1), R 1a is a hydrocarbon group having 6 or less carbon atoms, preferably 4 or less, more preferably 3 or less, even more preferably 2 or less, and even more preferably 1 carbon atom, preferably an alkyl or alkenyl group, more preferably an alkyl group. R 1a is, for example, a methyl group, an ethyl group, an n-propyl group, an isopropyl group, Examples of the alkyl group include a group selected from the group consisting of butyl, n-butyl, tert-butyl, pentyl, and phenyl. Among these, a methyl group is preferred. In general formula (a1), R 2aThe alkylene group has 10 or less carbon atoms, preferably 8 or less, more preferably 5 or less, even more preferably 4 or less, still more preferably 3 or less, and 1 or more carbon atoms. R 2a is, for example, a group selected from a methanediyl group, an ethane-1,2-diyl group, an ethane-1,1-diyl group, an n-propane-1,3-diyl group, and an n-propane-1,2-diyl group. Among these, a group selected from a methanediyl group, an ethane-1,2-diyl group, an n-propane-1,3-diyl group, and an n-propane-1,2-diyl group is preferred.

[0026] The kinematic viscosity of the modified silicone of component (A) is preferably 1 mm at 25°C from the viewpoint of improving the surface appearance of the cured product of the hydraulic composition and improving workability. 2 / s or more, preferably 5 mm 2 / s or more, more preferably 10 mm 2 / s or more, and preferably 1,000,000 mm 2 / s or less, preferably 5000 mm 2 / s or less, more preferably 1000 mm 2 / s or less, and even more preferably 400 mm 2 / s or less, and even more preferably 300 mm 2 / s or less, and even more preferably 200 mm 2 / s or less. The kinematic viscosity of the modified silicone may be a catalog value, or may be measured using, for example, a fully automatic micro kinematic viscometer (manufactured by Viscotec Co., Ltd.).

[0027] The HLB value of the modified silicone of component (A) is preferably 5 or more, more preferably 7 or more, even more preferably 10 or more, and even more preferably 12 or more, and is preferably 17 or less, more preferably 15 or less, from the viewpoint of improving the surface appearance of the cured product of the hydraulic composition and improving workability. Here, HLB stands for Hydrophile Lipophile Balance, and is an index for determining whether a compound is hydrophilic or lipophilic. The HLB value may be a value found in academic literature or a catalog value, or it may be calculated. In this case, the HLB value is calculated using the Griffin method, which is represented by the following formula: HLB = (sum of molecular weights of hydrophilic parts / molecular weight) × 20 Examples of the hydrophilic group include a hydroxy group, an ethyleneoxy group, and an oxypropylene group.

[0028] <(B) component> The admixture composition for hydraulic compositions of the present invention contains the following component (B): Component (B): a compound represented by the following general formula (b1): R 1b -O-[(EO) n (PO) m ]-SO3M b (b1) [In the formula, R 1b is a hydrocarbon group having 4 to 20 carbon atoms, EO is an ethyleneoxy group, PO is a propyleneoxy group, n is the average number of moles of EO added and is a number of 1 to 50, m is the average number of moles of PO added and is a number of 0 to 30, and EO and PO may be bonded in blocks or randomly. b indicates a counter cation.

[0029] In general formula (b1), R 1b R has, for example, 4 or more carbon atoms, preferably 10 or more carbon atoms, and more preferably 12 or more carbon atoms, from the viewpoints of compatibility between component (A) and component (C) described later, solubility in water, and storage stability during high-temperature storage, and R has, for example, 20 or less carbon atoms, preferably 18 or less carbon atoms, from the viewpoints of compatibility between component (A) and component (C) described later, solubility in water, and storage stability during high-temperature storage. 1b is preferably a linear or branched alkyl group or a linear or branched alkenyl group, more preferably a linear or branched alkyl group, and even more preferably a linear alkyl group. In general formula (b1), n ​​represents the average number of moles of EO added, and from the viewpoints of compatibility between component (A) and component (C) described later, solubility in water, and storage stability during high-temperature storage, n is, for example, 1 or more, preferably 5 or more, more preferably 10 or more, and even more preferably 15 or more; and from the viewpoints of compatibility between component (A) and component (C) described later, solubility in water, and storage stability during high-temperature storage, n is, for example, 50 or less, preferably 40 or less, and more preferably 30 or less. In general formula (b1), m is the average number of moles of PO added, and from the viewpoints of compatibility between component (A) and component (C) described below, solubility in water, and storage stability during high-temperature storage, it is, for example, 0 or more and preferably 5 or less, and more preferably 3 or less. m may be 0. In general formula (b1), M b Examples of the cation include inorganic ions selected from sodium ions, ammonium ions, potassium ions, calcium ions, magnesium ions, etc., and organic ammonium ions selected from monoethanolammonium ions, diethanolammonium ions, triethanolammonium ions, morpholinium ions, etc., and from the viewpoint of availability, sodium ions are preferred. EO and PO may be bonded in block or random combination, and from the viewpoint of manufacturability, for example, block addition is preferred.

[0030] <(C) component> The admixture composition for hydraulic compositions of the present invention contains (C) a cement dispersant (hereinafter referred to as component (C)).

[0031] The cement dispersant of component (C) can be one or more compounds selected from naphthalene-based polymers, polycarboxylic acid-based polymers, lignin sulfonic acid-based polymers, melamine-based polymers, polymers containing phosphate groups in their structures, and polymers containing aromatic compounds having polyalkyleneoxy groups. From the viewpoints of compatibility between components (A) and (C), solubility in water, and storage stability during high-temperature storage, the dispersant is preferably a polymer containing polyalkyleneoxy groups, more preferably one or more compounds selected from polycarboxylic acid-based polymers and polymers containing aromatic compounds having polyalkyleneoxy groups, and even more preferably a polycarboxylic acid-based polymer.

[0032] Examples of polycarboxylic acid polymers that can be used include copolymers of a monoester of polyalkylene glycol and (meth)acrylic acid with a carboxylic acid such as (meth)acrylic acid (e.g., compounds described in JP-A-8-12397), copolymers of an unsaturated alcohol having polyalkylene glycol with a carboxylic acid such as (meth)acrylic acid, and copolymers of an unsaturated alcohol having polyalkylene glycol with a dicarboxylic acid such as maleic acid. Here, (meth)acrylic acid means a carboxylic acid selected from acrylic acid and methacrylic acid.

[0033] Examples of the polycarboxylic acid polymer (hereinafter also referred to as (c1)) include a copolymer containing, as constituent monomers, a monomer (11c) represented by the following general formula (11c) and a monomer (12c) represented by the following general formula (12c):

[0034] [ka]

[0035] [During the ceremony, R 11c , R 12c , R 13c may be the same or different, and may be a hydrogen atom, a methyl group, or (CH2) r COOM 12 and (CH2) r COOM 12 COOM11 or other (CH2) r COOM 12 and an anhydride may be formed, in which case the M 11 , M 12 does not exist. M 11 , M 12 may be the same or different, and may be a hydrogen atom, an alkali metal, an alkaline earth metal (1 / 2 atom), an ammonium group, an alkylammonium group, a substituted alkylammonium group, an alkyl group, a hydroalkyl group, or an alkenyl group r: a number between 0 and 2 indicates.]

[0036] [ka]

[0037] [During the ceremony, R 14c , R 15c , R 16c : may be the same or different, and may be a hydrogen atom, a methyl group, (CH2) s COOM 13 , or (CH2) q1 (CO) p1 O(AO) n1 -R 17c R 17c : a hydrogen atom or an alkyl group having 1 to 4 carbon atoms AO: an alkyleneoxy group having 2 to 4 carbon atoms n1: the average number of moles of AO added, a number of 4 or more and 200 or less q1: A number between 0 and 2 p1: 0 or 1 M 13 : hydrogen atom, alkali metal, alkaline earth metal (1 / 2 atom), ammonium group, alkylammonium group, substituted alkylammonium group, alkyl group, hydroxyalkyl group or alkenyl group s: a number between 0 and 2 indicates.]

[0038] In the general formula (11c), from the viewpoint of availability, R11c is preferably a hydrogen atom. In the general formula (11c), from the viewpoint of availability, R 12c is preferably a hydrogen atom or a methyl group. In the general formula (11c), from the viewpoint of availability, R 13c is preferably a hydrogen atom. (CH2) r COOM 12 About COOM 11 or other (CH2) r COOM 12 and an acid anhydride may be formed, in which case, M 11 , M 12 does not exist. M 11 and M 12 may be the same or different and are a hydrogen atom, an alkali metal, an alkaline earth metal (1 / 2 atom), an ammonium group, an alkylammonium group, a substituted alkylammonium group, an alkyl group, a hydroalkyl group, or an alkenyl group. M 11 and M 12 The alkyl group, the hydroalkyl group, and the alkenyl group each preferably have 1 to 4 carbon atoms. M 11 and M 12 may be the same or different and are preferably a hydrogen atom, an alkali metal, an alkaline earth metal (1 / 2 atom), an ammonium group, or an alkylammonium group, more preferably a hydrogen atom, an alkali metal, an alkaline earth metal (1 / 2 atom), or an ammonium group, even more preferably a hydrogen atom, an alkali metal, or an alkaline earth metal (1 / 2 atom), and still more preferably a hydrogen atom or an alkali metal. (CH2) in general formula (11c) r COOM 12 r is preferably 0.

[0039] In general formula (12c), R 14c is preferably a hydrogen atom from the viewpoint of availability. In general formula (12c), R 15cFrom the viewpoints of availability and dispersibility in the hydraulic composition, is preferably a hydrogen atom or a methyl group, more preferably a methyl group. In general formula (12c), R 16c is preferably a hydrogen atom from the viewpoint of availability. In general formula (12c), R 17c From the viewpoint of availability, is preferably a hydrogen atom or a methyl group, and more preferably a methyl group. In the general formula (12c), AO is preferably a group selected from an ethyleneoxy group, a propyleneoxy group, and a butyleneoxy group, more preferably an ethyleneoxy group, from the viewpoint of dispersibility of the hydraulic composition. AO preferably contains an ethyleneoxy group. In general formula (12c), n1 is the average number of moles of AO added, and from the viewpoint of dispersibility of the hydraulic composition, it is preferably 4 or more, more preferably 20 or more, and preferably 150 or less, more preferably 120 or less, and even more preferably 80 or less. Furthermore, the AOs in the average n1 repeating units may be different, and may be randomly added, block added, or a mixture of these. It is preferable that 70 mol % or more, more preferably 80 mol % or more, even more preferably 90 mol % or more of EO groups are ethyleneoxy groups (EO groups), and furthermore, all AO groups are EO groups. For example, AO may contain propyleneoxy, butyleneoxy, etc. in addition to EO. In the general formula (12c), q1 is preferably 0, 1 or 2, more preferably 0 or 1, and even more preferably 0, from the viewpoint of dispersibility of the hydraulic composition. In the general formula (12c), p1 is preferably 1 from the viewpoint of dispersibility of the hydraulic composition. In general formula (12c), M 13 is a hydrogen atom, an alkali metal, an alkaline earth metal (1 / 2 atom), an ammonium group, an alkylammonium group, a substituted alkylammonium group, an alkyl group, a hydroxyalkyl group, or an alkenyl group. M 13 The alkyl group, the hydroalkyl group, and the alkenyl group each preferably have 1 to 4 carbon atoms. M 13is preferably a hydrogen atom, an alkali metal, an alkaline earth metal (1 / 2 atom), an ammonium group, or an alkylammonium group, more preferably a hydrogen atom, an alkali metal, an alkaline earth metal (1 / 2 atom), or an ammonium group, even more preferably a hydrogen atom, an alkali metal, or an alkaline earth metal (1 / 2 atom), and still more preferably a hydrogen atom or an alkali metal. In the general formula (12c), (CH2) s COOM 13 The s is preferably 0.

[0040] The proportion of the monomer (11c) in the total amount of the monomer (11c) and the monomer (12c) in all the constituent monomers of the copolymer (c1) is, from the viewpoint of dispersibility in the hydraulic composition, preferably 1% by mass or more, more preferably 5% by mass or more, even more preferably 10% by mass or more, still more preferably 15% by mass or more, and preferably 40% by mass or less, more preferably 30% by mass or less, even more preferably 25% by mass or less, and still more preferably 20% by mass or less.

[0041] From the viewpoint of dispersibility in the hydraulic composition, the proportion of the monomer (11c) in all the constituent monomers of the copolymer (c1) is preferably 1% by mass or more, more preferably 5% by mass or more, even more preferably 10% by mass or more, still more preferably 15% by mass or more, and preferably 40% by mass or less, more preferably 30% by mass or less, even more preferably 25% by mass or less, and still more preferably 20% by mass or less.

[0042] The total amount of the monomers (11c) and (12c) in the copolymer (c1) is preferably 70% by mass or more, more preferably 80% by mass or more, even more preferably 90% by mass or more, and preferably 100% by mass or less, from the viewpoint of dispersibility in the hydraulic composition. This total amount may be 100% by mass.

[0043] From the viewpoint of dispersibility in the hydraulic composition, the weight average molecular weight of the copolymer (c1) is preferably 5,000 or more, more preferably 10,000 or more, even more preferably 20,000 or more, still more preferably 30,000 or more, still more preferably 40,000 or more, still more preferably 50,000 or more, and preferably 100,000 or less, more preferably 80,000 or less, even more preferably 70,000 or less.

[0044] The weight average molecular weight of the copolymer was measured by gel permeation chromatography (GPC) under the following conditions. *GPC conditions Apparatus: GPC (HLC-8320GPC) manufactured by Tosoh Corporation Column: G4000PWXL + G2500PWXL (Tosoh Corporation) Eluent: 0.2M phosphate buffer / CH3CN=9 / 1 Flow rate: 1.0mL / min Column temperature: 40℃ Detection: RI Sample size: 0.2 mg / mL Standard substance: Polyethylene glycol equivalent (monodisperse polyethylene glycol with known molecular weight, molecular weight 250,000, 145,000, 87,500, 46,000, 24,000)

[0045] The copolymer (c1) may contain, in addition to the monomer (11c) and the monomer (12c), one or more monomers (13c) copolymerizable with the monomer (11c) and / or the monomer (12c). Examples of the monomer (13c) include acrylic acid esters. In the copolymer (c1), the total of the monomers (11c) and (12c), or the total of the monomers (11c), (12c), and (13c), may account for 100% by mass of all structural units.

[0046] The aromatic-containing polymer having a polyalkyleneoxy group (hereinafter also referred to as (c2)) is preferably a formaldehyde condensation polymer containing a monomer (c21) having a polyalkyleneoxy group in which the average number of moles of alkyleneoxy groups added to the aromatic ring is 5 to 300, and a monomer (c22) having a carboxylic acid group and / or a salt thereof on the aromatic ring or a monomer (c23) having a phosphate group and / or a salt thereof on the aromatic ring.

[0047] Examples of the monomer (c21) include monomers obtained from one or more compounds selected from benzene compounds having polyalkyleneoxy groups with an average number of added moles of alkyleneoxy groups of 5 to 300 and which may have substituents other than polyalkyleneoxy groups, and naphthalene compounds having polyalkyleneoxy groups with an average number of added moles of alkyleneoxy groups of 5 to 300 and which may have substituents other than polyalkyleneoxy groups, and preferred are monomers obtained from benzene compounds having polyalkyleneoxy groups with an average number of added moles of alkyleneoxy groups of 5 to 300 and which may have substituents other than polyalkyleneoxy groups. Examples of the substituent other than the polyalkyleneoxy group include one or more selected from an alkyl group having 1 to 4 carbon atoms, an alkenyl group having 2 to 4 carbon atoms, a hydroxyl group, and a halogeno group.

[0048] In the monomer (c21), the alkyleneoxy group is preferably an alkyleneoxy group having 2 or more and 3 or less carbon atoms, and more preferably an ethyleneoxy group. In the monomer (c21), the average number of moles of alkyleneoxy groups added is 5 or more, preferably 10 or more, more preferably 20 or more, and 300 or less, preferably 150 or less, more preferably 90 or less, even more preferably 50 or less, and still more preferably 30 or less, from the viewpoint of the effect of reducing the number of bubble traces on the surface of the cured body.

[0049] From the viewpoint of the effect of reducing the number of bubble traces on the surface of the cured product, the monomer (c21) is preferably a monomer obtained from a compound represented by the following general formula (c21).

[0050] [ka]

[0051] [wherein AO is an alkyleneoxy group, and m is the average number of moles of alkyleneoxy groups added, which is a number of 5 to 300.] 1 is an optional substituent of the benzene ring, and is at least one selected from an alkyl group having 1 to 4 carbon atoms, an alkenyl group having 2 to 4 carbon atoms, a hydroxyl group, and a halogeno group.

[0052] In general formula (c21), AO is preferably an alkyleneoxy group having 2 or more and 3 or less carbon atoms, and more preferably an ethyleneoxy group. In general formula (c21), m is 5 or more, preferably 10 or more, more preferably 20 or more, and 300 or less, preferably 150 or less, more preferably 90 or less, even more preferably 50 or less, and even more preferably 30 or less, from the viewpoint of the effect of reducing the number of bubble traces on the surface of the cured body. In general formula (c21), Y 1 If Y has 1 is preferably one or more selected from alkyl groups having 1 to 4 carbon atoms, more preferably an alkyl group having 1 to 2 carbon atoms. 1 It is not necessary to have

[0053] The monomer (c21) may be a monomer obtained from one or more compounds selected from polyoxyalkylene phenyl ether and polyoxyalkylene naphthyl ether. Specific examples of the raw material compound for the monomer (c21) include compounds in which an average of 5 to 300 moles of alkyleneoxy groups are added to phenol, cresol, nonylphenol, naphthalene, methylnaphthalene, butylnaphthalene, bisphenol, or the like.

[0054] Examples of the aromatic compound having a carboxylic acid group and / or a salt thereof as the monomer (c22) include a monomer obtained from one or more compounds selected from a benzene compound having a carboxylic acid group and / or a salt thereof and optionally having a substituent other than the carboxylic acid group and / or the salt thereof, and a naphthalene compound having a carboxylic acid group and / or a salt thereof and optionally having a substituent other than the carboxylic acid group and / or the salt thereof, and a monomer obtained from a benzene compound having a carboxylic acid group and / or a salt thereof and optionally having a substituent other than the carboxylic acid group and / or the salt thereof is preferred. The carboxylic acid group and / or its salt is a group selected from a carboxy group and a carboxy group in the form of a salt, and also includes a carboxy group that forms an anhydride with another carboxy group. Examples of the substituent other than the carboxylic acid group and / or its salt include one or more selected from an alkyl group having 1 to 20 carbon atoms, an alkenyl group having 2 to 4 carbon atoms, a hydroxyl group, and a halogeno group.

[0055] From the viewpoint of the effect of reducing the number of bubble traces on the surface of the cured product, the monomer (c22) is preferably a monomer obtained from a compound represented by the following general formula (c22).

[0056] [ka]

[0057] [In the formula, Z 1 is a hydrogen atom, an alkali metal, an alkaline earth metal (1 / 2 atom), an ammonium group, an alkylammonium group, or a substituted alkylammonium group. 2 is an optional substituent of the benzene ring, and is at least one selected from an alkyl group having 1 to 20 carbon atoms, an alkenyl group having 2 to 4 carbon atoms, a hydroxyl group, and a halogeno group.

[0058] In general formula (c22), Z 1 is preferably a hydrogen atom or an alkali metal, more preferably a hydrogen atom. In general formula (c22), Y 2 If Y has 2is preferably at least one selected from a hydroxyl group and an alkyl group having 1 to 20 carbon atoms, and more preferably a hydroxyl group. 2 It is not necessary to have

[0059] The monomer (c22) may be a monomer obtained from a benzene or naphthalene derivative, specifically, one or more compounds selected from hydroxybenzoic acid, benzoic acid, isophthalic acid, hydroxynaphthoic acid, and isomers thereof. From the viewpoint of improving the one-component stability, a monomer obtained from hydroxybenzoic acid and one or more compounds selected from benzoic acid is preferred, and a monomer obtained from hydroxybenzoic acid is more preferred.

[0060] Examples of the aromatic compound having a phosphoric acid group and / or a salt thereof as the monomer (c23) include monomers obtained from one or more compounds selected from a benzene compound having a phosphoric acid group and / or a salt thereof and optionally having a substituent other than a carboxylic acid group and / or a salt thereof, and a naphthalene compound having a phosphoric acid group and / or a salt thereof and optionally having a substituent other than a phosphoric acid group and / or a salt thereof, and a monomer obtained from a benzene compound having a phosphoric acid group and / or a salt thereof and optionally having a substituent other than a phosphoric acid group and / or a salt thereof is preferred. The phosphate group and / or salts thereof also include those in which a phosphate group is dehydrated and condensed with another phosphate group. Examples of substituents other than the phosphate group and / or its salt include one or more selected from an alkyl group having 1 to 20 carbon atoms, an alkenyl group having 2 to 4 carbon atoms, a hydroxyl group, and a halogeno group. The phosphoric acid group and / or its salt may be coordinated as a substituent on an aromatic compound, or may be a phosphoric acid ester or phosphoric acid diester of an aromatic alcohol.

[0061] Monomer (c23) may be a monomer obtained from one or more compounds selected from benzene or naphthalene derivatives, specifically phenylphosphonic acid, phenylphosphinic acid, naphthylphosphonic acid, naphthylphosphinic acid, phenyl phosphate (mono-, di-, or triester, or a mixture thereof), phenoxyethanol phosphate (mono-, di-, or triester, or a mixture thereof), phenoxydiglycol phosphate (mono-, di-, or triester, or a mixture thereof), phenoxy(poly)alkylene glycol phosphate (mono-, di-, or triester, or a mixture thereof), naphthol phosphate (mono-, di-, or triester, or a mixture thereof), polyoxyalkylene naphthalate phosphate (mono-, di-, or triester, or a mixture thereof), isomers thereof, and salts thereof. From the viewpoint of improving the one-component stability, a monomer obtained from phenoxyethanol phosphate (mono-, di-, or triester, or a mixture thereof) is preferred.

[0062] The polymer (c2) may contain other polymerizable monomers in addition to the monomers (c21), (c22), and (c23), as long as the effects of the present invention are not impaired. Examples of the monomers other than the monomers (c21), (c22), and (c23) include monomers obtained from phenol, alkylphenols such as cresol, and benzene or naphthalene derivatives, specifically, monomers obtained from benzenesulfonic acid, phenolsulfonic acid, naphthalenesulfonic acid, alkylnaphthalenesulfonic acid, and naphtholsulfonic acid compounds.

[0063] When the polymer (c2) contains a monomer (c21) and a monomer (c22), the molar ratio (c21) / (c22) of the monomer (c21) to the monomer (c22) in the polymer (c2) is, from the viewpoint of the effect of reducing the amount of bubble traces on the surface of the cured body, preferably 10 / 90 or more, more preferably 50 / 50 or more, even more preferably 60 / 40 or more, and preferably 90 / 10 or less, more preferably 80 / 20 or less, even more preferably 70 / 30 or less. When the polymer (c2) contains the monomer (c21) and the monomer (c22), the molar ratio (c21) / (c22) of the monomer (c21) to the monomer (c22) in the polymer (c2) may be calculated from the charge ratio of the raw material compound that becomes the monomer (c21) and the raw material compound that becomes the monomer (c22) when producing the polymer (c2).

[0064] When the polymer (c2) contains the monomer (c21) and the monomer (c23), the molar ratio (c21) / (c23) of the monomer (c21) to the monomer (c23) in the polymer (c2) is, from the viewpoint of the effect of reducing the amount of bubble traces on the surface of the cured body, preferably 10 / 90 or more, more preferably 50 / 50 or more, even more preferably 60 / 40 or more, and preferably 90 / 10 or less, more preferably 80 / 20 or less, even more preferably 70 / 30 or less. When the polymer (c2) contains the monomer (c21) and the monomer (c23), the molar ratio (c21) / (c23) of the monomer (c21) to the monomer (c23) in the polymer (c2) may be calculated from the charge ratio of the raw material compound that becomes the monomer (c21) and the raw material compound that becomes the monomer (c23) when producing the polymer (c2).

[0065] When the polymer (c2) contains the monomer (c21) and the monomer (c22), the total amount of the monomer (c21) and the monomer (c22) in the total constituent monomers of the polymer (c2) is 70 mol% or more, preferably 80 mol% or more, more preferably 90 mol% or more, and 100 mol% or less. This total amount may be 100 mol%. The total amount of the monomer (c21) and the monomer (c22) in the total constituent monomers of the polymer (c2) is calculated assuming that the constituent monomers of the polymer (c2) do not include formaldehyde used in the condensation polymerization reaction.

[0066] When the polymer (c2) contains the monomer (c21) and the monomer (c23), the total amount of the monomer (c21) and the monomer (c23) in the total constituent monomers of the polymer (c2) is 70 mol% or more, preferably 80 mol% or more, more preferably 90 mol% or more, and 100 mol% or less. This total amount may be 100 mol%. The total amount of the monomer (c21) and the monomer (c23) in the total constituent monomers of the polymer (c2) is calculated assuming that the constituent monomers of the polymer (c2) do not include formaldehyde used in the condensation polymerization reaction.

[0067] From the viewpoint of the effect of reducing the number of bubble traces on the surface of the cured product, the weight-average molecular weight of the polymer (c2) is preferably 5,000 or more, more preferably 8,000 or more, even more preferably 10,000 or more, and preferably 150,000 or less, more preferably 100,000 or less, even more preferably 50,000 or less, and still more preferably 30,000 or less. This weight-average molecular weight is measured by gel permeation chromatography (GPC) under the following conditions. *GPC conditions Apparatus: GPC (HLC-8320GPC) manufactured by Tosoh Corporation Column: G4000SWXL + G2000SWXL + guard column SWXL (manufactured by Tosoh Corporation) Eluent: 30mM CH3COONa / CH3CN=6 / 4 Flow rate: 0.7mL / min Column temperature: room temperature Detection: RI Sample size: 0.2 mg / mL Standard substance: Polyethylene glycol equivalent (monodisperse polyethylene glycol with known molecular weight, molecular weight 250,000, 145,000, 87,500, 46,000, 24,000)

[0068] <Composition, etc.> In the admixture composition for hydraulic compositions of the present invention, the content of component (A) is preferably 0.01% by mass or more, more preferably 0.1% by mass or more, even more preferably 0.5% by mass or more, from the viewpoint of the effect of reducing the amount of bubble traces on the surface of the hardened body, and is preferably 100% by mass or less, more preferably 50% by mass or less, even more preferably 25% by mass or less, still more preferably 10% by mass or less, still more preferably 5% by mass or less, and still more preferably 3% by mass or less.

[0069] In the admixture composition for hydraulic compositions of the present invention, the content of component (B) is preferably 0.1% by mass or more, more preferably 0.5% by mass or more, and even more preferably 1% by mass or more, from the viewpoints of compatibility between components (A) and (C), solubility in water, and storage stability during high-temperature storage, and from the viewpoint of economy, it is preferably 20% by mass or less, more preferably 15% by mass or less, even more preferably 10% by mass or less, still more preferably 5% by mass or less, and even more preferably 3% by mass or less. b The value converted to sodium ion shall be used.

[0070] In the admixture composition for hydraulic compositions of the present invention, the total content of the components (A) and (B) is, for example, preferably 1.0% by mass or more, more preferably 1.5% by mass or more, and even more preferably 2.0% by mass or more from the viewpoint of the surface appearance of the hardened product of the hydraulic composition (reduced bubble traces) and storage stability during high-temperature storage, and from the viewpoint of viscosity, it is preferably 25% by mass or less, more preferably 20% by mass or less, even more preferably 15% by mass or less, still more preferably 10% by mass or less, and even more preferably 5% by mass or less.

[0071] In the admixture composition for hydraulic compositions of the present invention, the mass ratio (A) / (B) of the content of the component (A) to the content of the component (B) is preferably 0.01 or more, more preferably 0.05 or more, even more preferably 0.1 or more, and is preferably 8 or less, more preferably 5 or less, even more preferably 3 or less, and still more preferably 1 or less, from the viewpoints of the surface appearance of the cured product of the hydraulic composition (reduced bubble traces) and storage stability during high-temperature storage.

[0072] The content of component (C) in the admixture composition for hydraulic compositions of the present invention is, in terms of active ingredient, preferably 5% by mass or more, more preferably 10% by mass or more, and even more preferably 15% by mass or more from the viewpoint of dispersibility of the hydraulic composition, and preferably 50% by mass or less, more preferably 40% by mass or less, even more preferably 30% by mass or less, and even more preferably 25% by mass or less from the viewpoint of surface appearance of the cured product of the hydraulic composition (reduced amount of bubble traces). The content of component (C) in the present invention is the value converted into an unneutralized acid type compound.

[0073] In the admixture composition for hydraulic compositions of the present invention, the mass ratio (A) / (C) of the content of the component (A) to the content of the component (C) is preferably 0.001 or more, more preferably 0.01 or more, even more preferably 0.03 or more, and preferably 0.2 or less, more preferably 0.1 or less, even more preferably 0.05 or less, from the viewpoints of the surface appearance of the cured product of the hydraulic composition (reduced bubble traces) and storage stability during high-temperature storage.

[0074] The admixture composition for a hydraulic composition of the present invention may contain water. That is, the admixture composition for a hydraulic composition of the present invention may be in a liquid state, or may be an aqueous solution. When the admixture composition for a hydraulic composition of the present invention contains water, the content of water is, from the viewpoint of viscosity, for example, preferably 40% by mass or more, more preferably 50% by mass or more, even more preferably 60% by mass or more, still more preferably 70% by mass or more, and preferably less than 90% by mass, more preferably 80% by mass or less.

[0075] The admixture composition for hydraulic compositions of the present invention exhibits excellent improvement in the surface appearance of the cured product of the hydraulic composition even in the embodiment containing the component (A), but as a specific embodiment, it can further contain an antifoaming agent. The antifoaming agent is not particularly limited as long as it does not affect the effects of the present invention, and examples thereof include antifoaming agents with an HLB of less than 3 (excluding component (A)). Specific examples of the defoaming agent include polyalkylene glycol alkyl ether-based defoaming agents, polyalkylene glycol alkyl ester-based defoaming agents, polyol polyether-based defoaming agents, polyalkylene glycol block polymer-based defoaming agents, and silicone-based defoaming agents (excluding component (A)). Among these, defoaming agents having an HLB of less than 3 are further included. From the viewpoint of adjusting the amount of air in the hydraulic composition and the storage stability of the admixture composition for hydraulic compositions, for example, the defoaming agent is preferably one or more selected from polyalkylene glycol alkyl ether-based defoaming agents, polyalkylene glycol alkyl ester-based defoaming agents, and silicone-based defoaming agents (excluding component (A)), and more preferably a silicone-based defoaming agent (excluding component (A)).

[0076] The admixture composition for hydraulic compositions of the present invention may contain, as optional components, components such as water-soluble polymer compounds, air-entraining agents, cement wetting agents, expanding agents, retarders, quick-setting agents, thickeners, flocculants, strength enhancers, hardening accelerators, compatibilizers, and preservatives (however, excluding those corresponding to the above-mentioned components (A) to (C)).

[0077] The admixture composition for hydraulic compositions of the present invention can effectively control the behavior of air bubbles in the hydraulic composition, which cause air bubble marks on the surface of the hardened hydraulic composition, adhering to a formwork or a release agent applied to the surface of the formwork, thereby suppressing the occurrence of air bubble marks on the surface of the hardened hydraulic composition and improving the aesthetic appearance of the surface. That is, the admixture composition for a hydraulic composition of the present invention may be a surface appearance improver composition for a hydraulic composition. The admixture composition for a hydraulic composition of the present invention may also be a surface bubble mark inhibitor composition for a hydraulic composition. The surface appearance improver composition for a hydraulic composition of the present invention and the surface bubble mark inhibitor composition for a hydraulic composition of the present invention are the same as the admixture composition for a hydraulic composition of the present invention, and the aspects described for the admixture composition for a hydraulic composition of the present invention can be applied as appropriate.

[0078] [Method for producing admixture composition for hydraulic composition] The present invention provides a method for producing an admixture composition for hydraulic compositions, which comprises mixing component (A), component (B), and component (C). By this production method, the admixture composition for hydraulic compositions of the present invention containing component (A), component (B), and component (C) is produced. In the method for producing an admixture composition for a hydraulic composition of the present invention, water can be further mixed. Specific examples and preferred aspects of the components (A), (B), and (C) used in the method for producing an admixture composition for hydraulic compositions of the present invention are the same as those described for the admixture composition for hydraulic compositions of the present invention. The matters described in relation to the admixture composition for hydraulic compositions of the present invention can be appropriately applied to the method for producing the admixture composition for hydraulic compositions of the present invention. In the method for producing the admixture composition for hydraulic compositions of the present invention, the contents of the components and their mass ratios described in the admixture composition for hydraulic compositions of the present invention can be appropriately applied by replacing the contents of the components with the mixing amounts.

[0079] [Hydraulic composition] The present invention provides a hydraulic composition containing the admixture composition for hydraulic compositions of the present invention, hydraulic powder, and water. That is, the present invention provides a hydraulic composition containing component (A), component (B), component (C), hydraulic powder, and water. Specific examples and preferred embodiments of the components (A), (B), and (C) used in the hydraulic composition of the present invention are the same as those described in the admixture composition for hydraulic compositions of the present invention. The matters described in relation to the admixture composition for hydraulic compositions of the present invention and the method for producing the same can be appropriately applied to the hydraulic composition of the present invention.

[0080] <Hydraulic powder> The hydraulic powder used in the hydraulic composition of the present invention is a powder that hardens when mixed with water. Examples include ordinary Portland cement, high-early-strength Portland cement, ultra-high-early-strength Portland cement, sulfate-resistant Portland cement, low-heat Portland cement, white Portland cement, and ecocement (e.g., JIS R5214). Among these, from the viewpoint of strength development, one or more cements selected from early-strength Portland cement, ordinary Portland cement, sulfate-resistant Portland cement, and white Portland cement are preferred, and one or more cements selected from early-strength Portland cement and ordinary Portland cement are more preferred. The hydraulic powder may also contain blast furnace slag, fly ash, silica fume, anhydrous gypsum, etc., or non-hydraulic limestone fine powder. The hydraulic powder may also contain blast furnace cement, fly ash cement, or silica fume cement, which is a mixture of cement with blast furnace slag, fly ash, silica fume, etc. Clay such as bentonite may also be included. The hydraulic compositions finally obtained by adding sand, sand and gravel as aggregates to these powders are generally called mortar, concrete, etc.

[0081] <Aggregate> The hydraulic composition of the present invention may contain aggregate. Examples of aggregates include one or more types of aggregate selected from fine aggregates and coarse aggregates. Examples of fine aggregates include those specified under No. 2311 in JIS A0203-2014. Examples of fine aggregates include river sand, land sand, mountain sand, sea sand, lime sand, silica sand, and crushed sands thereof, blast furnace slag fine aggregate, ferronickel slag fine aggregate, lightweight fine aggregate (artificial and natural), and recycled fine aggregate. Examples of coarse aggregates include those specified under No. 2312 in JIS A0203-2014. Examples of coarse aggregates include river gravel, land gravel, mountain gravel, sea gravel, lime gravel, crushed stones thereof, blast furnace slag coarse aggregate, ferronickel slag coarse aggregate, lightweight coarse aggregate (artificial and natural), and recycled coarse aggregate. Different types of fine aggregates and coarse aggregates may be used in combination, or a single type may be used.

[0082] <Composition, etc.> In the hydraulic composition of the present invention, the content of the admixture composition for hydraulic compositions, as parts by mass of the solid content, relative to 100 parts by mass of the hydraulic powder, is preferably 0.001 parts by mass or more, more preferably 0.005 parts by mass or more, even more preferably 0.010 parts by mass or more, even more preferably 0.030 parts by mass or more, and still more preferably 0.080 parts by mass or more, from the viewpoint of the surface aesthetics of the hydraulic composition cured body (reduction of the number of bubble traces) and economic efficiency, and is preferably 10 parts by mass or less, more preferably 3 parts by mass or less, even more preferably 2.5 parts by mass or less, even more preferably 2.0 parts by mass or less, even more preferably 1.0 part by mass or less, and still more preferably 0.5 parts by mass or less.

[0083] In the hydraulic composition of the present invention, the content of component (A) is preferably 0.0001 part by mass or more, more preferably 0.001 part by mass or more, even more preferably 0.005 part by mass or more, and preferably 5 parts by mass or less, more preferably 1 part by mass or less, even more preferably 0.5 parts by mass or less, still more preferably 0.1 part by mass or less, and still more preferably 0.05 part by mass or less, relative to 100 parts by mass of hydraulic powder, from the viewpoint of reducing the amount of bubble traces on the surface of the hardened hydraulic composition.

[0084] In the hydraulic composition of the present invention, the content of component (B) is, for example, preferably 0.001 part by mass or more, more preferably 0.005 part by mass or more, and even more preferably 0.010 part by mass or more, relative to 100 parts by mass of hydraulic powder, from the viewpoint of reducing the amount of bubble traces on the surface of the hardened hydraulic composition; and from the viewpoint of economy, it is preferably 10 parts by mass or less, more preferably 3 parts by mass or less, even more preferably 2.5 parts by mass or less, even more preferably 2.0 parts by mass or less, even more preferably 1.0 part by mass or less, still more preferably 0.5 parts by mass or less, still more preferably 0.1 part by mass or less, and even more preferably 0.05 part by mass or less.

[0085] In the hydraulic composition of the present invention, the total content of component (A) and component (B) is preferably 0.001 part by mass or more, more preferably 0.003 part by mass or more, even more preferably 0.006 part by mass or more, and preferably 0.25 part by mass or less, more preferably 0.2 part by mass or less, even more preferably 0.1 part by mass or less, and still more preferably 0.05 part by mass or less, relative to 100 parts by mass of hydraulic powder, from the viewpoint of reducing the amount of bubble traces on the surface of the hardened hydraulic composition.

[0086] In the hydraulic composition of the present invention, the mass ratio (A) / (B) of the content of the component (A) to the content of the component (B) is preferably 0.01 or more, more preferably 0.05 or more, even more preferably 0.1 or more, and is preferably 8 or less, more preferably 5 or less, even more preferably 3 or less, and still more preferably 1 or less, from the viewpoint of the surface appearance of the cured product of the hydraulic composition (reducing the amount of bubble traces).

[0087] In the hydraulic composition of the present invention, the content of component (C) relative to 100 parts by mass of hydraulic powder is preferably 0.001 part by mass or more, more preferably 0.005 part by mass or more, even more preferably 0.010 part by mass or more, even more preferably 0.030 parts by mass or more, and still more preferably 0.080 parts by mass or more, from the viewpoint of improving workability in producing the hydraulic composition, and is preferably 10 parts by mass or less, more preferably 3 parts by mass or less, even more preferably 2.5 parts by mass or less, even more preferably 2.0 parts by mass or less, even more preferably 1.0 part by mass or less, and still more preferably 0.5 parts by mass or less, from the viewpoint of economy.

[0088] In the hydraulic composition of the present invention, the mass ratio (A) / (C) of the content of the component (A) to the content of the component (C) is preferably 0.001 or more, more preferably 0.01 or more, even more preferably 0.03 or more, and preferably 0.2 or less, more preferably 0.1 or less, even more preferably 0.05 or less, from the viewpoint of the surface appearance of the cured product of the hydraulic composition (reducing the amount of bubble traces).

[0089] In the hydraulic composition of the present invention, the mass percentage of the water content to the hydraulic powder content (water / hydraulic powder ratio (W / P)) is preferably 60 mass% or less, more preferably 50 mass% or less, even more preferably 45 mass% or less, and preferably 10 mass% or more, more preferably 20 mass% or more, even more preferably 30 mass% or more, from the viewpoint of the effect of reducing the amount of bubble traces on the surface of the hardened hydraulic composition. Here, the water / hydraulic powder ratio (W / P) is the mass percentage (mass%) of water to hydraulic powder in the hydraulic composition, and is calculated as water / hydraulic powder x 100. The water / hydraulic powder ratio is calculated based on the amount of powder that has the physical property of hardening through a hydration reaction. Furthermore, when the hydraulic powder is cement, W / P may be expressed as W / C. In addition, when the hydraulic powder includes powders selected from powders with pozzolanic action, powders with latent hydraulic properties, and stone powder (calcium carbonate powder) in addition to powders such as cement that harden through hydration, the amounts of these powders are also included in the amount of hydraulic powder in this invention. Furthermore, when the powder that hardens through hydration contains a high-strength admixture, the amount of the high-strength admixture is also included in the amount of hydraulic powder. This also applies to other parts by mass that involve the mass of the hydraulic powder.

[0090] In the hydraulic composition of the present invention, the mass percentage of the hydraulic powder content to the aggregate content (hydraulic powder content / aggregate content x 100) is preferably 60 mass% or less, more preferably 45 mass% or less, even more preferably 30 mass% or less, still more preferably 25 mass% or less, and preferably 5 mass% or more, more preferably 10 mass% or more, even more preferably 15 mass% or more, from the viewpoint of the effect of reducing the amount of bubble traces on the surface of the hardened body.

[0091] The hydraulic composition of the present invention is not particularly limited with respect to the amount of air contained in the hydraulic composition, but from the viewpoint of durability of the set body of the hydraulic composition, it is, for example, preferably 0% or more, more preferably 8.0% or less.

[0092] The aggregate may be used in the usual range used in preparing concrete, mortar, etc. When the hydraulic composition is concrete, the amount of coarse aggregate used is preferably 50% or more by bulk volume, more preferably 55% or more, even more preferably 60% or more, and preferably 100% or less, more preferably 90% or less, even more preferably 80% or less, from the viewpoint of the properties of the concrete. The bulk volume is the amount of coarse aggregate used per 1 m of concrete. 3 The coarse aggregate ratio is the ratio of the volume (including voids) of the coarse aggregate in the concrete. From the viewpoint of the properties of concrete, the coarse aggregate ratio is preferably 9.0% by mass or less, more preferably 8.0% by mass or less, even more preferably 7.0% by mass or less, and preferably 5.0% by mass or more, more preferably 5.5% by mass or more, and even more preferably 6.0% by mass or more. The coarse aggregate ratio can be measured in accordance with JIS A 1102. When the hydraulic composition is concrete, the amount of fine aggregate used is preferably 500 kg / m from the viewpoint of improving the filling property into a formwork or the like. 3 More preferably, 600 kg / m 3 More preferably, 700 kg / m 3 or more, and preferably 1000 kg / m 3 Less than or equal to 900 kg / m 3 When the hydraulic composition is mortar, the amount of fine aggregate used is preferably 800 kg / m 3 More preferably, 900 kg / m 3 More preferably, 1000 kg / m 3 or more, and preferably 2000 kg / m 3 or less, more preferably 1800 kg / m 3 or less, more preferably 1700 kg / m 3 The coarse particle ratio of the fine aggregate is preferably 5.0% by mass or less, more preferably 4.0% by mass or less, even more preferably 3.5% by mass or less, from the viewpoint of improving the packing property into forms, etc., and is preferably 1.0% by mass or more, more preferably 1.5% by mass or more, even more preferably 2.0% by mass or more. The coarse particle ratio can be measured in accordance with JIS A 1102.

[0093] The hydraulic composition of the present invention may further contain other components in addition to the above components, such as retarders, thickeners, air-entraining agents, waterproofing agents, fluidizing agents, early strengthening agents, antifoaming agents, compatibilizers, preservatives, etc. (excluding those corresponding to the above components (A) to (C)). Examples of early-strengthening agents include compounds selected from alkali metal and alkaline earth metal hydrochlorides, sulfates, nitrates, nitrites, cyanates, thiocyanates, thiosulfates, and formates, or organic compounds selected from alkanolamines, glycerin derivatives, formaldehyde derivatives, and catechol derivatives, and nanoparticles of Portland cement hydration products (CSH, calcium carbonate and calcium hydroxide).

[0094] The hydraulic composition of the present invention may be used for concrete or mortar. The hydraulic composition of the present invention is useful in any field such as self-leveling, refractories, plaster, lightweight or heavy-duty concrete, air entrainment, repair, prepacked, trame, ground improvement, grout, and cold weather use.

[0095] [Method for producing hydraulic composition] The present invention provides a method for producing a hydraulic composition, which comprises mixing the admixture composition for hydraulic compositions of the present invention, hydraulic powder, and water. That is, the present invention provides a method for producing a hydraulic composition by mixing component (A), component (B), component (C), hydraulic powder, and water. In the method for producing the hydraulic composition of the present invention, aggregate can be further mixed. Specific examples and preferred embodiments of the components (A), (B), and (C) used in the method for producing the hydraulic composition of the present invention are the same as those described for the admixture composition for hydraulic compositions of the present invention, and specific examples and preferred embodiments of the hydraulic powder and aggregate are the same as those described for the hydraulic composition of the present invention. In the method for producing the hydraulic composition of the present invention, the hydraulic powder is mixed so that the W / P ratio falls within the range described for the hydraulic composition of the present invention. The amount of aggregate used (mixed amount) and the mass percentages of the hydraulic powder content and aggregate content are also within the same ranges as described for the hydraulic composition of the present invention. In the method for producing the hydraulic composition of the present invention, the contents of the components and their mass ratios described for the hydraulic composition of the present invention can be appropriately applied by replacing the contents of the components with the mixing amounts. The matters described in relation to the admixture composition for hydraulic compositions and the method for producing the same, and the hydraulic composition of the present invention can be appropriately applied to the method for producing the hydraulic composition of the present invention.

[0096] As a method for producing the hydraulic composition of the present invention, for example, the admixture composition for hydraulic compositions of the present invention may be mixed with hydraulic powder to prepare the hydraulic composition, or the hydraulic composition may be prepared by separately mixing the components (A), (B), and (C) with hydraulic powder.

[0097] Specifically, in the method for producing the hydraulic composition of the present invention, the mixing amount of the admixture composition for hydraulic compositions of the present invention, as parts by mass of solids, relative to 100 parts by mass of hydraulic powder is, from the viewpoint of the aesthetic appearance of the surface of the hardened product of the hydraulic composition (reduction of the number of bubble traces), preferably 0.001 parts by mass or more, more preferably 0.005 parts by mass or more, even more preferably 0.010 parts by mass or more, even more preferably 0.030 parts by mass or more, and still more preferably 0.080 parts by mass or more, and from the viewpoint of the aesthetic appearance of the surface of the hardened product of the hydraulic composition (reduction of the number of bubble traces) and economic efficiency, preferably 10 parts by mass or less, more preferably 3 parts by mass or less, even more preferably 2.5 parts by mass or less, even more preferably 2.0 parts by mass or less, even more preferably 1.0 part by mass or less, and still more preferably 0.5 parts by mass or less.

[0098] In the method for producing the hydraulic composition of the present invention, mixing may be carried out using a mixer such as a mortar mixer, a forced twin-screw mixer, etc. The mixing time is, for example, preferably 1 minute or more, more preferably 2 minutes or more, and preferably 5 minutes or less, more preferably 3 minutes or less.

[0099] <Method for producing a hardened product of hydraulic composition> The present invention provides a method for producing a hardened hydraulic composition, the method comprising the steps of: preparing a hydraulic composition by mixing the admixture composition for hydraulic compositions of the present invention, hydraulic powder, and water; filling a form with the prepared hydraulic composition and curing it; and demolding the hardened hydraulic composition. That is, the present invention provides a method for producing a hardened hydraulic composition, comprising the steps of: mixing component (A), component (B), component (C), hydraulic powder, and water to prepare a hydraulic composition; filling a form with the prepared hydraulic composition and hardening it; and demolding the hardened hydraulic composition. The matters described in the admixture composition for hydraulic compositions and the method for producing the same, and the hydraulic composition and the method for producing the same of the present invention can be appropriately applied to the method for producing a hardened product of the hydraulic composition of the present invention.

[0100] In the step of preparing the hydraulic composition, which is included in the method for producing a hardened product of the hydraulic composition of the present invention, aggregate can be further mixed in. Specific examples and preferred aspects of components (A), (B), and (C) are the same as those described for the admixture composition for hydraulic compositions of the present invention, and specific examples and preferred aspects of the hydraulic powder and aggregate are the same as those described for the hydraulic composition of the present invention. In the process of preparing the hydraulic composition, the hydraulic powder is mixed so that the W / P ratio falls within the range described for the hydraulic composition of the present invention. The amount of aggregate used (mixed amount) and the mass percentage of the hydraulic powder content and the aggregate content also fall within the ranges described for the hydraulic composition of the present invention. In the process of preparing the hydraulic composition, the contents of the components and their mass ratios described for the hydraulic composition of the present invention can be appropriately applied by replacing the contents of the components with the mixing amounts. The step of preparing the hydraulic composition included in the method for producing a hardened product of the hydraulic composition of the present invention may be the same as that described in the method for producing the hydraulic composition of the present invention.

[0101] The method for producing a hardened product of the hydraulic composition of the present invention includes, for example, a step of filling a formwork with the hydraulic composition prepared in the previous step and hardening the composition. Examples of forms used in the method for producing a hardened product of the hydraulic composition of the present invention include formwork for buildings and formwork for concrete products. Methods for filling the formwork include a method of directly pouring the composition from a mixer and a method of introducing the hydraulic composition into the formwork by pressure-feeding it with a pump.

[0102] The form used in the method for producing a cured product of the hydraulic composition of the present invention may preferably be coated with a release agent, for example, from the viewpoint of the releasability of the cured product of the hydraulic composition when demolded. The release agent may be (1) mineral oil such as kerosene, light oil, spin oil, transformer oil, machine oil, turbine oil, gear oil, bearing oil, or electrical insulating oil, (2) synthetic oil such as polyalkylene glycol, (3) vegetable oil such as rapeseed, coconut, palm, or soybean oil, (4) fats and oils, or (5) fatty acid esters, and may be either an "oil-based release agent" that is applied as is or an "aqueous-based release agent" that is emulsified in water.

[0103] In the method for producing a hardened product of the hydraulic composition of the present invention, for example, when the hydraulic composition of the present invention is filled into a form and cured, heat curing can be carried out to accelerate hardening. Here, heat curing can be carried out by maintaining the hydraulic composition at a temperature of 40°C or higher and 80°C or lower to accelerate hardening, for example.

[0104] The hardened hydraulic composition can be demolded to obtain a hardened product of the hydraulic composition of the present invention. At the time of demolding, it is preferable that the hardened product of the hydraulic composition has sufficient compressive strength. The compressive strength at the time of demolding is preferably equal to or greater than the strength specified in, for example, "2023 Japan Society of Civil Engineers Standard Specifications [Construction Section] Commentary Table 8.8.1."

[0105] Examples of hardened products of hydraulic compositions using formwork for concrete products include civil engineering products such as concrete piles, concrete poles, various block products for revetments, box culvert products, segment products used in tunnel construction and the like, and girder products for bridge piers, and examples of architectural products include curtain wall products and architectural component products used for columns, beams, and floorboards.

[0106] In the present invention, in the preparation of the hydraulic composition, the time from bringing the hydraulic powder into contact with water to demolding is, for example, preferably 16 hours or more and 72 hours or less, from the viewpoint of obtaining the strength required for demolding and improving the production cycle.

[0107] <Method for improving the surface appearance of hydraulic composition> The present invention provides a method for improving the surface appearance of a hydraulic composition, which comprises mixing the admixture composition for hydraulic compositions of the present invention, hydraulic powder, and water. That is, the present invention provides a method for improving the surface appearance of a hydraulic composition, which comprises mixing component (A), component (B), component (C), hydraulic powder, and water. The present invention provides a method for improving the surface appearance of a hydraulic composition, which comprises mixing component (A), component (B), component (C), hydraulic powder, and water. In the method for improving the surface appearance of a hydraulic composition of the present invention, aggregate can be further mixed. Specific examples and preferred embodiments of the components (A), (B), and (C) used in the method for improving the surface appearance of a hydraulic composition of the present invention are the same as those described for the admixture composition for hydraulic compositions of the present invention, and specific examples and preferred embodiments of the hydraulic powder and aggregate are the same as those described for the hydraulic composition of the present invention. In the method for improving the surface appearance of a hydraulic composition of the present invention, the hydraulic powder is mixed so that the W / P ratio falls within the range described for the hydraulic composition of the present invention. The amount of aggregate used (mixed amount) and the mass percentages of the hydraulic powder content and aggregate content are also within the same ranges as described for the hydraulic composition of the present invention. In the method for improving the surface appearance of a hydraulic composition of the present invention, the contents of the components and their mass ratios described for the hydraulic composition of the present invention can be appropriately applied by replacing the contents of the components with the mixing amounts. The matters described in the admixture composition for hydraulic compositions and the method for producing the same, the hydraulic composition and the method for producing the same, and the method for producing a hardened product of the hydraulic composition of the present invention can be appropriately applied to the method for improving the surface appearance of the hydraulic composition of the present invention.

[0108] In the method for improving the surface appearance of a hydraulic composition of the present invention, the preparation of the hydraulic composition may be the same as that described in the method for producing the hydraulic composition of the present invention. Furthermore, the method for producing a hardened product of the hydraulic composition prepared after the hydraulic composition is prepared may be the same as that described in the method for producing a hardened product of the hydraulic composition of the present invention.

[0109] The method for improving the surface appearance of a hydraulic composition of the present invention can effectively control the behavior of air bubbles in the hydraulic composition, which cause air bubble marks on the surface of a hardened hydraulic composition, adhering to a formwork or a release agent applied to the surface of the formwork, thereby reducing air bubble marks on the surface of the hardened hydraulic composition and improving the surface appearance. That is, the method for improving the surface appearance of a hydraulic composition of the present invention may be a method for suppressing bubble marks on the surface of a hydraulic composition. The method for suppressing bubble marks on the surface of a hydraulic composition of the present invention is the same as the method for improving the surface appearance of a hydraulic composition of the present invention, and the matters described in the method for improving the surface appearance of a hydraulic composition of the present invention, the admixture composition for a hydraulic composition and its manufacturing method of the present invention, the hydraulic composition and its manufacturing method, and the method for manufacturing a hardened product of the hydraulic composition can be appropriately applied to the method for suppressing bubble marks on the surface of a hydraulic composition of the present invention. [Example]

[0110] The components (A), (B) and (C) used in the examples and comparative examples were as follows.

[0111] <Component (A)> KF640: Side-chain polyether-modified silicone, manufactured by Shin-Etsu Chemical Co., Ltd., kinematic viscosity 20 mm 2 / s, HLB value: 14 KF6011: PEG-11 methyl ether dimethicone (side-chain polyether-modified silicone), manufactured by Shin-Etsu Chemical Co., Ltd., kinematic viscosity 130 mm 2 / s, HLB value: 14.5 KF6100: Polyglyceryl-3 disiloxane dimethicone, manufactured by Shin-Etsu Chemical Co., Ltd., kinematic viscosity 40,000 mm 2 / s Elastomer OS: Polyoxazoline-modified silicone, 75% by mass of silicone, 25% by mass of polyoxazoline, synthesized in reference to JP-A-5-25025, kinematic viscosity measurement impossible (solid at room temperature)

[0112] <(B) component> (B-1): Polyoxyethylene (18) lauryl ether sulfate sodium salt: In the general formula (b1), R 1b is an alkyl group with 12 carbon atoms, n is 18, m is 0, M b is a sodium compound (B-2): Polyoxyethylene (23) oleyl sulfate sodium salt: In the general formula (b1), R 1b is an alkenyl group having 18 carbon atoms, n is 23, m is 0, M b is a sodium compound

[0113] <(C) component> Each of the polycarboxylic acid polymers (C-1) to (C-8) shown in Table 1 was used. Furthermore, (C-9) was the polymer (B-9) described in paragraph 0120 of JP-A No. 2020-75840.

[0114] [Table 1]

[0115] The proportions of monomer (11c) and monomer (12c) in each copolymer are shown in Table 1. The number of moles of EO in monomer (12c) indicates the average number of moles of ethyleneoxy groups added in each monomer.

[0116] The weight average molecular weight of each polymer of component (C) was measured by gel permeation chromatography (GPC) under the following conditions. *GPC conditions Apparatus: GPC (HLC-8320GPC) manufactured by Tosoh Corporation Column: G4000PWXL + G2500PWXL (Tosoh Corporation) Eluent: 0.2M phosphate buffer / CH3CN=9 / 1 Flow rate: 1.0mL / min Column temperature: 40℃ Detection: RI Sample size: 0.2 mg / mL Standard substance: Polyethylene glycol equivalent (monodisperse polyethylene glycol with known molecular weight, molecular weight 250,000, 145,000, 87,500, 46,000, 24,000)

[0117] (1) Preparation of admixture composition for hydraulic composition The admixture composition for hydraulic compositions of the present invention was prepared by putting each component (A), component (B), and component (C) shown in Table 3 into a glass beaker and mixing with water for 5 minutes using a magnetic stirrer so that the contents of each component (A), component (B), and component (C) were 100% by mass (calculated as active ingredients; the remainder was tap water (clean water)).

[0118] (2) Method for evaluating the high-temperature stability of admixture compositions for hydraulic compositions 40 g of the admixture composition for hydraulic compositions shown in Table 3 was placed in a 50 mL screw tube and stored at 30°C or 40°C for one month. After storage, the admixture in the screw tube was evaluated by visual observation and by measuring the absorbance of the admixture at a wavelength of 660 nm using an ultraviolet spectrophotometer (UV-160A, manufactured by Shimadzu Corporation). These evaluations were performed on admixture compositions for hydraulic compositions at 20°C. Each admixture composition for hydraulic compositions was evaluated according to the following evaluation criteria. The results are shown in Table 3. Evaluation criteria ◯: Visually evaluated as no separation, absorbance (AU) less than 0.5. △: No separation was visually observed, and the absorbance (AU) was 0.5 or more. ×: Separation is visually observed.

[0119] (3) Preparation of hydraulic composition Coarse aggregate (G), half of the fine aggregate (S), cement (C), and the remaining half of the fine aggregate (S) were charged into a forced twin-shaft mixer (manufactured by IHI Corporation) under the mixing conditions shown in Table 2, and dry-mixed for 10 seconds. Then, mixing water (W) of the following composition was charged, and the mixture was mixed for 90 seconds to prepare a hydraulic composition. The mixing water contained the admixture composition for hydraulic compositions, an air-entraining agent (Mighty AE-02, manufactured by Kao Corporation), and an antifoaming agent (Antifoam E20, manufactured by Kao Corporation) shown in Table 3. The concentrations of the components in the mixing water were such that, for the admixture composition for hydraulic compositions, the blend amount per 100 parts by mass of cement in the hydraulic composition was 0.6 parts by mass, and for the air-entraining agent and antifoaming agent, the blend amounts per 100 parts by mass of cement in the hydraulic composition were 0.1 parts by mass and 0.0003 parts by mass. The air content (volume %) in the hydraulic composition obtained above was measured in accordance with JISA1128:2019 and confirmed to be 4.0 to 5.0%.

[0120] [Table 2]

[0121] The ingredients used in Table 2 are as follows: W: Mixing water (tap water (Wakayama City tap water)) C: Ordinary Portland cement (manufactured by Taiheiyo Cement Corporation, density 3.16 g / cm 3 ) ·S: Fine aggregate (yamasand from Joyo, Kyoto Prefecture, density 2.50g / cm 3 , coarse grain ratio 2.9) G: Coarse aggregate (andesite crushed stone from Nishijima, Hyogo Prefecture (crushed stone with a diameter of 10-20 mm and crushed stone with a diameter of 5-10 mm mixed at a mass ratio of 1:1, density 2.63 g / cm 3 , coarse grain ratio 6.7) In Table 2, W / C is the mass ratio of the amount of water to the amount of cement, and is calculated by [amount of water / amount of cement] x 100 (mass%). Note that the amounts of each component contained in water are minute compared to the amount of hydraulic composition, so these amounts were taken into account when calculating W / C. Furthermore, C / (S+G) is the mass ratio of the amount of cement to the total amount of fine aggregate and coarse aggregate, and is calculated by [amount of cement / total amount of fine aggregate and coarse aggregate] x 100 (mass%).

[0122] (4) Measurement of air bubble traces in hardened hydraulic compositions (4-1) Preparation of hardened hydraulic composition A 0.1 m x 0.2 m x 0.5 m steel form was placed on a table vibrator vibrating at 50 Hz, and the hydraulic composition obtained above was filled in and cured at 20°C. 24 hours after the preparation of the hydraulic composition, the hardened hydraulic composition was demolded from the form. The inside of the form was coated with an oil-based straight-type release agent "Resiner NSX-553" (manufactured by Shin-Etsu Chemical Co., Ltd.).

[0123] (4-2) Measurement of air bubble traces in hardened hydraulic compositions One surface (0.2 m × 0.5 m) of the removed hardened body was rubbed with a plastic brush to remove the thin skin, and the surface was photographed with a smartphone. Image data was converted to two colors using ImageJ (areas with air bubble traces were black, and other areas were white). The area percentage of the hardened body surface that was occupied by air bubble traces was calculated from the ratio of each color using the following formula, and this was defined as the air bubble trace amount (area %). The results are shown in Table 3. The smaller the value of the air bubble trace amount (area %), the better the surface appearance of the hardened hydraulic composition body. Bubble trace amount (area%) = Bubble trace area (m 2 ) / 0.2m x 0.5m surface area (m 2 ) x 100 ○: Bubble traces are less than 1% by area ×: Bubble traces are 1% or more by area

[0124] [Table 3]

Claims

1. An admixture composition for a hydraulic composition, comprising the following component (A), component (B), and component (C): Component (A): Modified silicone having one or more functional groups selected from the following on its side chain: Functional groups: amino group, carboxy group, hydroxy group, epoxy group, mercapto group, fluoro group, polyoxyalkylene group, polyoxazoline group, polyglycerin group Component (B): a compound represented by the following general formula (b1): R １ｂ -O-[(EO) ｎ ・(PO) ｍ ]-SO ３ M ｂ (ｬ1) [In the formula, R １ｂ is a hydrocarbon group having 4 to 20 carbon atoms, EO is an ethyleneoxy group, PO is a propyleneoxy group, n is the average number of moles of EO added and is a number of 1 to 50, m is the average number of moles of PO added and is a number of 0 to 30, and EO and PO may be bonded in blocks or randomly. ｂ indicates a counter cation. Component (C): Cement dispersant

2. 2. The admixture composition for hydraulic compositions according to claim 1, wherein component (C) is a polymer having a polyalkyleneoxy group.

3. A step of mixing the admixture composition for hydraulic compositions according to claim 1 or 2, hydraulic powder, and water to prepare a hydraulic composition; a step of filling the prepared hydraulic composition into a form and hardening it; and A step of demolding the hardened hydraulic composition; A method for producing a hardened product of a hydraulic composition comprising the above-mentioned formula (1).

4. A method for improving the surface appearance of a hydraulic composition, comprising mixing the admixture composition for hydraulic compositions according to claim 1 or 2, hydraulic powder, and water.

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