JPH10324555A - Cement admixture and method for placing jointed concrete - Google Patents
Cement admixture and method for placing jointed concreteInfo
- Publication number
- JPH10324555A JPH10324555A JP9134710A JP13471097A JPH10324555A JP H10324555 A JPH10324555 A JP H10324555A JP 9134710 A JP9134710 A JP 9134710A JP 13471097 A JP13471097 A JP 13471097A JP H10324555 A JPH10324555 A JP H10324555A
- Authority
- JP
- Japan
- Prior art keywords
- concrete
- reducing agent
- weight
- cement
- parts
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000004567 concrete Substances 0.000 title claims abstract description 69
- 239000004568 cement Substances 0.000 title claims abstract description 41
- 238000000034 method Methods 0.000 title claims abstract description 22
- 239000003638 chemical reducing agent Substances 0.000 claims abstract description 44
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 40
- 239000000463 material Substances 0.000 claims abstract description 30
- 239000004815 dispersion polymer Substances 0.000 claims abstract description 7
- 238000010998 test method Methods 0.000 claims abstract 2
- 238000001035 drying Methods 0.000 claims description 20
- 238000005266 casting Methods 0.000 claims description 9
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- 239000011248 coating agent Substances 0.000 claims description 5
- 238000000576 coating method Methods 0.000 claims description 5
- 238000005336 cracking Methods 0.000 abstract description 5
- 238000012856 packing Methods 0.000 abstract 3
- 229920000642 polymer Polymers 0.000 description 24
- 239000000843 powder Substances 0.000 description 16
- 239000004575 stone Substances 0.000 description 13
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 11
- 239000000853 adhesive Substances 0.000 description 8
- 230000001070 adhesive effect Effects 0.000 description 8
- 239000007787 solid Substances 0.000 description 8
- 230000000694 effects Effects 0.000 description 6
- 230000005484 gravity Effects 0.000 description 6
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 6
- 238000006703 hydration reaction Methods 0.000 description 5
- 238000000926 separation method Methods 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 4
- 239000011398 Portland cement Substances 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 230000036571 hydration Effects 0.000 description 4
- -1 hydroxypolyacrylate Polymers 0.000 description 4
- 239000004570 mortar (masonry) Substances 0.000 description 4
- 239000011150 reinforced concrete Substances 0.000 description 4
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 230000000740 bleeding effect Effects 0.000 description 3
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 3
- 239000001913 cellulose Substances 0.000 description 3
- 239000005038 ethylene vinyl acetate Substances 0.000 description 3
- 229920000126 latex Polymers 0.000 description 3
- 239000004816 latex Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 3
- 239000004576 sand Substances 0.000 description 3
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 235000011941 Tilia x europaea Nutrition 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- JHLNERQLKQQLRZ-UHFFFAOYSA-N calcium silicate Chemical compound [Ca+2].[Ca+2].[O-][Si]([O-])([O-])[O-] JHLNERQLKQQLRZ-UHFFFAOYSA-N 0.000 description 2
- 229910052918 calcium silicate Inorganic materials 0.000 description 2
- 235000012241 calcium silicate Nutrition 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 235000010980 cellulose Nutrition 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 239000010419 fine particle Substances 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 239000004571 lime Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- LUFUWJZCIDKWJV-UHFFFAOYSA-N methanol;oxirane Chemical compound OC.C1CO1 LUFUWJZCIDKWJV-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 229920000881 Modified starch Polymers 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 235000014676 Phragmites communis Nutrition 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 239000004113 Sepiolite Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229920001222 biopolymer Polymers 0.000 description 1
- KLIYQWXIWMRMGR-UHFFFAOYSA-N buta-1,3-diene;methyl 2-methylprop-2-enoate Chemical compound C=CC=C.COC(=O)C(C)=C KLIYQWXIWMRMGR-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000011083 cement mortar Substances 0.000 description 1
- 239000002734 clay mineral Substances 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000010881 fly ash Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 125000003827 glycol group Chemical group 0.000 description 1
- 230000020169 heat generation Effects 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 235000019426 modified starch Nutrition 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-M naphthalene-1-sulfonate Chemical compound C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-M 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920001467 poly(styrenesulfonates) Polymers 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229960002796 polystyrene sulfonate Drugs 0.000 description 1
- 239000011970 polystyrene sulfonate Substances 0.000 description 1
- 229920005996 polystyrene-poly(ethylene-butylene)-polystyrene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019814 powdered cellulose Nutrition 0.000 description 1
- 229920003124 powdered cellulose Polymers 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 229910052624 sepiolite Inorganic materials 0.000 description 1
- 235000019355 sepiolite Nutrition 0.000 description 1
- 229910021487 silica fume Inorganic materials 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B28/00—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
- C04B28/02—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing hydraulic cements other than calcium sulfates
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
- C04B2111/00474—Uses not provided for elsewhere in C04B2111/00
- C04B2111/00663—Uses not provided for elsewhere in C04B2111/00 as filling material for cavities or the like
- C04B2111/00672—Pointing or jointing materials
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
- C04B2111/34—Non-shrinking or non-cracking materials
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、既設コンクリート
との付着力が良好な打継コンクリートとするセメント混
和材及びその打継コンクリートの打設方法、特に、逆打
ち工法に使用する、また、床版下面補強コンクリート等
の既設コンクリートとの付着力が良好な打継コンクリー
トの打設方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a cement admixture which is a cast-in-place concrete having a good adhesion to existing concrete, and a method of placing the cast-in concrete, particularly for use in a reverse-casting method. The present invention relates to a method of placing cast concrete having good adhesion to existing concrete such as slab lower surface concrete.
【0002】[0002]
【従来の技術とその課題】鉄筋コンクリート構造物で
は、多量のコンクリートを連続して打設することが不可
能であり、既設のコンクリートに、さらに新しいコンク
リートを打ち継ぐ場合や、既設のコンクリートの補強や
補修のために新しくコンクリートを打設する場合など、
既設のコンクリートと新しく打設したコンクリートとの
間に打継目が生じている。そのため、その箇所の既設の
コンクリートと新しく打設したコンクリートとの間の付
着力が問題となっており、付着力が得られないと構造物
の美観、強度、及び耐久性等を損なう恐れがある等の課
題があった。2. Description of the Related Art In a reinforced concrete structure, it is impossible to pour a large amount of concrete continuously, and it is necessary to transfer new concrete to existing concrete or to reinforce existing concrete. For example, when casting new concrete for repair
There is a seam between the existing concrete and the newly cast concrete. Therefore, the adhesive force between the existing concrete and the newly cast concrete at that location is a problem, and if the adhesive force is not obtained, the appearance, strength, durability, etc. of the structure may be impaired. And other issues.
【0003】一方、都市部等では土地を有効に利用する
ため地下階を大きく、例えば、境界ぎりぎりまでに利用
することが多くなっており、地下階の柱・壁などの躯体
工事を進めると同時に地上階の建物の工事も併行して実
施でき、作業の安全性、騒音や振動の低減、及び生産性
の向上等が図れる逆打ちコンクリート工法が採用されて
おり、この逆打ちコンクリート工法にグラウト材が使用
されている。On the other hand, in an urban area or the like, the underground floor is large in order to make effective use of the land, for example, it is often used just before the boundary. The construction of the ground floor can be carried out at the same time, and the upside-down concrete method has been adopted to improve work safety, reduce noise and vibration, and improve productivity. Is used.
【0004】また、既設の床版コンクリート下部の補修
や補強に、交通を遮断せず施工できる床版下面補強コン
クリートを充填することが、交通渋滞を引き起こさない
ことから注目されている。[0004] In addition, it has been noted that the repair and reinforcement of the lower part of the existing slab concrete is filled with a slab lower surface reinforced concrete that can be constructed without interrupting traffic, because it does not cause traffic congestion.
【0005】既設のコンクリートと新しく打設したコン
クリートとの打継目の付着力を向上するためには、既設
コンクリート面を、粗にする、吸水させる、又はペース
トを界面に塗布する等の処理をすることが可能である。
通常の打継は既設のコンクリートの上面又は上面と側面
であり、既設コンクリート面の処理によって、通常、使
用されるモルタル又はコンクリートでも良好な付着力が
得られている。しかしながら、逆打ちコンクリートや床
版下面補強コンクリートでは、既設コンクリートと新し
く打設したコンクリートとの付着力が得られるのは、既
設コンクリートの下面又は下面と側面であり、新しく打
設するコンクリートは充填性が悪くなる傾向があり、ブ
リーデングやコンクリートの沈下などが生じやすくなる
ためにその付着力は得られにくいという課題があった。[0005] In order to improve the adhesion between the existing concrete and the newly cast concrete, the existing concrete surface is roughened, water-absorbed, or a paste is applied to the interface. It is possible.
The usual joint is the upper surface or the upper surface and the side surface of the existing concrete, and by the treatment of the existing concrete surface, a good adhesive force is obtained even with mortar or concrete that is usually used. However, in the case of reverse-casting concrete or floor slab bottom reinforced concrete, the adhesive force between the existing concrete and the newly cast concrete is obtained from the lower surface or the lower surface and the side surface of the existing concrete. However, there is a problem that bleeding and settlement of concrete are apt to occur, so that it is difficult to obtain the adhesive force.
【0006】そのため減水剤、無機微粉、増粘剤、及び
分離防止剤等に金属アルミニウムを併用し水素ガスを発
生させ、体積減少を補い既設コンクリート面との密着性
を確保している。しかしながら、逆打ちコンクリートに
金属アルミニウムを使用して水素ガスによる体積補償す
る方法は、化学反応のため、季節や日内の気温、セメン
トの種類、混和材、及び減水剤中のアルカリ金属類等に
より反応速度が変化し運搬中に反応が終了するため、膨
張量をコントロールすることが難しい場合があった。特
に、金属アルミニウムの使用量は、通常、1m3当たり数
十グラムと少ないため均一な分散が難しく、偏りがあっ
た場合、欠陥部分となりやすいなどの課題があった。こ
のように、金属アルミニウムにより膨張量をコントロー
ルするのは難しく、多めの膨張量にすると、1%の体積
増加で圧縮強度が5%も低下するため安全率を高くみる
必要がある等の課題があった。Therefore, metal gas is used in combination with a water reducing agent, an inorganic fine powder, a thickening agent, a separation preventing agent, and the like to generate hydrogen gas, thereby compensating for a decrease in volume and ensuring adhesion to an existing concrete surface. However, the method of compensating for volume by hydrogen gas using metal aluminum in back-casting concrete is a chemical reaction, so the reaction depends on the season and day temperature, cement type, admixture, and alkali metals in the water reducing agent. In some cases, it was difficult to control the amount of swelling because the speed was changed and the reaction was terminated during transportation. In particular, since the amount of metallic aluminum used is usually as small as several tens of grams per 1 m 3 , it is difficult to uniformly disperse the metal aluminum. As described above, it is difficult to control the amount of expansion by using aluminum metal, and if the amount of expansion is too large, the compressive strength is reduced by as much as 5% with a volume increase of 1%. there were.
【0007】また、逆打ち工法等に使用されるグラウト
材は、多量施工の場合、水和熱によるひび割れや乾燥収
縮によるひび割れの危険性があり、コスト的にも高いも
のとなる場合があった。[0007] Further, the grouting material used in the back-casting method or the like has a risk of cracking due to heat of hydration or cracking due to drying shrinkage in a large amount of construction, which may be high in cost. .
【0008】本発明者は、特定の材料を使用することに
よって、前記課題を解消できる知見を得て本発明を完成
するに至った。The inventor of the present invention has obtained the knowledge that can solve the above-mentioned problems by using a specific material, and has completed the present invention.
【0009】[0009]
【課題を解決するための手段】即ち、本発明は、膨張
材、乾燥収縮低減剤、減水剤、及び水性ポリマーディス
パージョンを含有してなるセメント混和材であり、既設
コンクリートの打継面に水性ポリマーディスパージョン
を被覆し、セメント、膨張材、乾燥収縮低減剤、及び減
水剤を含有してなる打継コンクリートを打ち継ぐことを
特徴とする打継コンクリートの打設方法であり、U型充
填試験方法で30cmを越える充填性を有する打継コンクリ
ートを、また、既設コンクリートの下面及び/又は側面
に該打継コンクリートを打ち継ぐ打継コンクリートの打
設方法である。That is, the present invention is a cement admixture containing an expanding material, a drying shrinkage reducing agent, a water reducing agent, and an aqueous polymer dispersion. A U-type filling test, which is a method of placing cast concrete, characterized by covering a polymer dispersion with a cast concrete containing a cement, an expanding material, a drying shrinkage reducing agent, and a water reducing agent. This is a method of casting cast concrete having a fillability exceeding 30 cm by a method, and casting the cast concrete on the lower surface and / or side surface of existing concrete.
【0010】以下、本発明を詳細に説明する。Hereinafter, the present invention will be described in detail.
【0011】本発明で使用するセメントとしては、普
通、早強、及び超早強等の各種ポルトランドセメント、
これらポルトランドセメントに高炉スラグ又はフライア
ッシュなどを混合した各種混合セメント、並びに、高ビ
ーライトセメント等の低発熱セメント等が挙げられる。
セメントの単位量は、300 〜900kg/m3が好ましい。300k
g/m3未満だと付着強度が得られない場合があり、900kg/
m3を超えると乾燥収縮や水和熱によるひび割れが発生す
る場合がある。As the cement used in the present invention, various portland cements such as ordinary, fast and super fast,
Various mixed cements obtained by mixing blast furnace slag or fly ash with these Portland cements, and low heat-generating cements such as high belite cements and the like can be mentioned.
Unit amount of cement, preferably 300 ~900kg / m 3. 300k
may a less than g / m 3 bonding strength can not be obtained, 900 kg /
sometimes cracking occurs due to the drying shrinkage and heat of hydration greater than m 3.
【0012】本発明で使用する膨張材としては、カルシ
ウムサルホアルミネート系膨張材や石灰系膨張材などが
あり、マスコン用水和熱抑制タイプや通常タイプいずれ
も使用可能である。膨張材の粒度は特に限定されるもの
ではないが、通常、2,000 〜4,000cm2/gが好ましい。2,
000cm2/g未満では未反応物が長期間残存して耐久性が低
下する場合があり、4,000cm2/gを越えると水和反応が早
く、所定の膨張が得られない場合がある。膨張材の使用
量は、セメント 100重量部に対して、3〜15重量部が好
ましく、5〜13重量部がより好ましい。3重量部未満で
は収縮低減効果が少ない場合があり、15重量部を越える
と膨張量が大きすぎて強度が低下する場合がある。As the expanding material used in the present invention, there are calcium-sulfoaluminate-based expanding material and lime-based expanding material, and any of hydration heat suppression type for mascon and normal type can be used. The particle size of the expansive material is not particularly limited, but is usually preferably 2,000 to 4,000 cm 2 / g. 2,
If it is less than 000 cm 2 / g, unreacted substances may remain for a long period of time and the durability may be reduced. If it exceeds 4,000 cm 2 / g, the hydration reaction may be too fast and the desired expansion may not be obtained. The amount of the expanding material to be used is preferably 3 to 15 parts by weight, more preferably 5 to 13 parts by weight, based on 100 parts by weight of cement. If the amount is less than 3 parts by weight, the effect of reducing shrinkage may be small, and if it exceeds 15 parts by weight, the amount of expansion may be too large to lower the strength.
【0013】本発明で使用する乾燥収縮低減剤は、ノニ
オン系界面活性剤の一種で、通常、純分99%以上の液体
であって、水に溶解してその表面張力を低下させる作用
をもつものである。その基本構造は、ポリオキシアルキ
レン重合物を有し、末端に低級アルコール、フェノー
ル、及びアミノ結合物等を付加したものである。具体的
には、ポリプロピレングリコール、エチレンオキシドメ
タノール付加物、エチレンオキシド・プロピレンオキシ
ドブロック重合物、エチレンオキシド・プロピレンオキ
シドランダム重合物、グリコールのシクロアルキル基付
加物、グリコールの両端にメチル基を付加した付加物、
グリコールのフェニル基付加物、グリコールにメチルフ
ェニル基を付加したブロック重合物、グリコールの両端
にエチレンオキサイドメタノールを付加した付加物、及
びグリコールにジメチルアミンを付加した付加物等が使
用可能である。乾燥収縮低減剤は、セメント粒子に吸着
されないでセメントの強アルカリ水溶液中で作用するも
ので、揮発性が低く、異常に多量な空気連行性がなく、
セメントの水和を妨げず減水剤に比べ低分子量のもので
ある。乾燥収縮低減剤は、混練り水の一部又は全部と置
き換えて使用することが好ましい。乾燥収縮低減剤の使
用量は、セメント 100重量部に対して1〜12重量部が好
ましく、2〜8重量部がより好ましい。1重量部未満で
は収縮低減効果が少ない場合があり、12重量部を越える
と凝結遅延を生じ流動性が低下する場合がある。The drying shrinkage reducing agent used in the present invention is a kind of nonionic surfactant and is usually a liquid having a pure content of 99% or more, and has a function of dissolving in water to lower its surface tension. Things. Its basic structure has a polyoxyalkylene polymer, and a terminal is added with a lower alcohol, a phenol, an amino bond and the like. Specifically, polypropylene glycol, ethylene oxide methanol adduct, ethylene oxide / propylene oxide block polymer, ethylene oxide / propylene oxide random polymer, cycloalkyl group adduct of glycol, adduct of methyl group added to both ends of glycol,
A phenyl group adduct of glycol, a block polymer obtained by adding a methylphenyl group to glycol, an adduct obtained by adding ethylene oxide methanol to both ends of glycol, and an adduct obtained by adding dimethylamine to glycol can be used. The drying shrinkage reducing agent acts in a strong alkaline aqueous solution of cement without being adsorbed by cement particles, has low volatility, and does not have an abnormally large amount of air entrainment,
It does not hinder the hydration of cement and has a lower molecular weight than the water reducing agent. The drying shrinkage reducing agent is preferably used in place of part or all of the kneading water. The amount of the drying shrinkage reducing agent to be used is preferably 1 to 12 parts by weight, more preferably 2 to 8 parts by weight, based on 100 parts by weight of cement. If the amount is less than 1 part by weight, the effect of reducing shrinkage may be small, and if it exceeds 12 parts by weight, setting delay may occur and the fluidity may decrease.
【0014】本発明で使用する減水剤は、コンクリート
の流動性の改善や、単位水量の低減のため使用するもの
で、高性能AE減水剤、高性能減水剤、及びAE減水剤
等が使用できる。具体的には、ナフタレンスルホン酸塩
のホルマリン縮合物、メラミンスルホン酸塩のホルマリ
ン縮合物、ポリスチレンスルホン酸塩、ヒドロキシポリ
アクリレート、α、β−不飽和ジカルボン酸とオレフィ
ンの共重合体、ポリエチレングリコールモノアルケニル
エーテルとマレイン酸やメタクリル酸系単量体から導か
れる共重合体、スチレン−アクリル酸エステル−マレイ
ン酸系の共重合体、変性リグニンスルホン酸化合物、及
び芳香族アミノスルホン酸化合物等が使用可能である。
さらに、一部架橋反応で高分子化したものやマレイン酸
の一部をエステル化したものも使用可能であり、これら
のうちの一種又は二種以上の使用が可能である。減水剤
の使用量は、セメントと膨張材の合計 100重量部に対し
て、固形分換算で0.01〜4重量部が好ましく、0.05〜2
重量部がより好ましい。0.01重量部未満では所定の流動
性が得にくい場合があり、4重量部を越えると分離や凝
結遅延を生じる場合がある。The water reducing agent used in the present invention is used to improve the fluidity of concrete and to reduce the unit water volume, and high-performance AE water reducing agents, high-performance water reducing agents, AE water reducing agents, and the like can be used. . Specifically, formalin condensate of naphthalene sulfonate, formalin condensate of melamine sulfonate, polystyrene sulfonate, hydroxypolyacrylate, copolymer of α, β-unsaturated dicarboxylic acid and olefin, polyethylene glycol mono Copolymers derived from alkenyl ethers and maleic or methacrylic monomers, styrene-acrylate-maleic copolymers, modified lignin sulfonic acid compounds, aromatic amino sulfonic acid compounds, etc. can be used It is.
Further, a polymer that is partially polymerized by a cross-linking reaction or a partially esterified maleic acid can be used, and one or more of these can be used. The amount of the water reducing agent used is preferably 0.01 to 4 parts by weight in terms of solid content, and
Parts by weight are more preferred. If the amount is less than 0.01 part by weight, it may be difficult to obtain a predetermined fluidity, and if it exceeds 4 parts by weight, separation or setting delay may occur.
【0015】本願発明で使用する水性ポリマーディスパ
ージョン(以下水性ポリマーという)は、水の中に0.05
〜5μmのポリマーの微粒子が均一に分散しているもの
で、微粒子がゴムの場合はラテックスと呼ばれ、樹脂の
場合はエマルジョンと呼ばれている。ラテックスとして
は、クロロプレンゴム、スチレンブタジエンゴム、アク
リロニトリルブタジエンゴム、及びメタクリル酸メチル
ブタジエンゴム等が挙げられる。また、エマルジョンと
しては、ポリアクリル酸エステル、エチレン酢酸ビニ
ル、及びエポキシ樹脂等が挙げられる。The aqueous polymer dispersion (hereinafter referred to as "aqueous polymer") used in the present invention contains 0.05% of water in water.
Fine particles of a polymer of 5 μm are uniformly dispersed. When the fine particles are rubber, they are called latex, and when they are resin, they are called emulsion. Examples of the latex include chloroprene rubber, styrene butadiene rubber, acrylonitrile butadiene rubber, and methyl methacrylate butadiene rubber. Examples of the emulsion include polyacrylate, ethylene vinyl acetate, and epoxy resin.
【0016】水性ポリマーの被覆方法としては、例え
ば、水性ポリマーを水で希釈し、既設コンクリート表面
に塗布する方法や噴霧する方法などが挙げらるが、均一
な塗布層を形成できる面から、塗布する方法が好まし
い。また、水性ポリマーを、セメント、膨張材、乾燥収
縮低減剤、及び減水剤と混合して使用する方法や、モル
タルやペースト中に水性ポリマーを混練した混合物を既
設コンクリート表面に塗布する方法なども可能である。
膨張材、乾燥収縮低減剤、セメント、減水剤、及び水性
ポリマーの混合方法は、均一に混合できれば特に限定さ
れるものではない。The method of coating the aqueous polymer may be, for example, a method of diluting the aqueous polymer with water and applying it to the existing concrete surface or spraying. Is preferred. In addition, it is also possible to use a method in which an aqueous polymer is mixed with a cement, an expanding material, a drying shrinkage reducing agent, and a water reducing agent, and a method in which a mixture obtained by kneading an aqueous polymer in a mortar or paste is applied to an existing concrete surface. It is.
The method of mixing the expanding material, the drying shrinkage reducing agent, the cement, the water reducing agent, and the aqueous polymer is not particularly limited as long as it can be uniformly mixed.
【0017】水性ポリマーを水で希釈して既設コンクリ
ートに塗布して被膜形成する場合の水性ポリマーの塗布
量は、固形分換算で10〜 500g/m2が好ましい。10g/m2未
満の塗布量では高い付着力が得られない場合があり、50
0 g/m2を越えても塗布効果の向上は期待できない。ま
た、セメントモルタルやペースト中に混練りした混合物
を塗布する場合の水性ポリマーの塗布量は、セメント 1
00重量部に対して、固形分換算で2〜30重量部が好まし
い。2重量部未満の添加量では高い付着力が得られず、
30重量部を越えても添加効果の向上は期待できない。When the aqueous polymer is diluted with water and applied to existing concrete to form a film, the amount of the aqueous polymer applied is preferably from 10 to 500 g / m 2 in terms of solid content. Is the coating amount of less than 10 g / m 2 may high adhesion can not be obtained, 50
Even if it exceeds 0 g / m 2 , improvement of the coating effect cannot be expected. When applying a mixture kneaded in cement mortar or paste, the amount of the aqueous polymer applied is
The amount is preferably 2 to 30 parts by weight in terms of solid content based on 00 parts by weight. If the amount is less than 2 parts by weight, a high adhesive force cannot be obtained,
Even if it exceeds 30 parts by weight, no improvement in the effect of addition can be expected.
【0018】本発明で使用する水の量は特に限定される
ものではないが、セメントと膨張材の合計 100重量部に
対して、20〜 100重量部が好ましく、25〜70重量部がよ
り好ましい。20重量部未満では膨張が著しく遅れる場合
があり、100 重量部を越えるとブリーデングや材料分離
が大きくなる場合がある。The amount of water used in the present invention is not particularly limited, but is preferably from 20 to 100 parts by weight, more preferably from 25 to 70 parts by weight, based on 100 parts by weight of the total of cement and expansive material. . If the amount is less than 20 parts by weight, the expansion may be significantly delayed. If the amount exceeds 100 parts by weight, bleeding and material separation may be increased.
【0019】本発明で使用する骨材は特に限定されるも
のではなく、通常使用される砕石、砕砂、川砂、及び石
灰石等の使用が可能である。骨材の使用量は、セメント
と膨張材の合計 100重量部に対して、100 〜 800重量部
が好ましい。100 重量部未満では発熱や収縮が大きくひ
び割れが発生する場合があり、800 重量部を越えると流
動性が低下する場合がある。The aggregate used in the present invention is not particularly limited, and crushed stone, crushed sand, river sand, limestone and the like which are usually used can be used. The amount of the aggregate is preferably 100 to 800 parts by weight based on 100 parts by weight of the total of the cement and the expanding material. If the amount is less than 100 parts by weight, heat generation and shrinkage are so large that cracks may occur. If the amount is more than 800 parts by weight, fluidity may decrease.
【0020】本発明では、高流動のモルタル又はコンク
リートにした場合、材料分離防止や塑性変形能力向上の
面から、炭酸カルシウム粉末等の石粉を使用することが
好ましい。特に、セメントと膨張材の合計の単位量が50
0kg/m3未満の場合、石粉を使用することが好ましい。石
粉の粒度は特に限定されるものではないが、ブレーン値
で 3,000〜10,000cm 2/g が好ましい。石粉の使用量は、
セメントと膨張材の合計 100重量部に対して、80重量部
以下が好ましい。特に、セメントと膨張材の合計の単位
量が500kg/m3未満の場合に、セメント、膨張材、及び石
粉の合計の単位量が500kg/m3以上になるように石粉を加
えることが好ましい。セメント、膨張材、及び石粉の合
計の単位量が500kg/m3未満では充填性が悪くブリーデン
グを生じる場合がある。In the present invention, the mortar or the high-concentration mortar
In the case of a reed, prevention of material separation and improvement of plastic deformation capacity
From the viewpoint, it is possible to use stone powder such as calcium carbonate powder.
preferable. In particular, the total unit amount of cement and expansive material is 50
0kg / mThreeIf less, it is preferable to use stone powder. stone
The particle size of the powder is not particularly limited, but the Blaine value
In 3,000-10,000cm Two/ g is preferred. The amount of stone powder used is
80 parts by weight for the total of 100 parts by weight of cement and expander
The following is preferred. In particular, the total unit of cement and expansive material
500kg / mThreeLess than cement, intumescent, and stone
Total unit weight of powder is 500kg / mThreeAdd the stone powder so that
Is preferably obtained. Combination of cement, expansive material and stone powder
Total unit weight is 500kg / mThreeIf less than, the filling property is poor and bleeden
May occur.
【0021】さらに、本発明では、セルロース系誘導
体、デンプン系誘導体、ポリビニルアルコール、ポリエ
チレンオキサイド、ポリアクリルアミド、及びバイオポ
リマー等の水溶性ポリマー、セルロース等の粉末繊維
素、シリカヒューム等の無機微粉、並びに、セピオライ
ト等の粘土鉱物等のブリージング防止効果のある分離防
止剤等の使用が可能である。既設コンクリートに被覆す
る水性ポリマー以外に、再乳化形粉末樹脂であるエチレ
ン酢酸ビニル等、液状ポリマーである不飽和ポリエステ
ルやエポキシ樹脂などの低分子量の重合性ポリマー又は
プレポリマーに硬化剤等を併用することが可能である。
また、水性ポリマーにフイルム形成時間の調整剤を併用
し被覆から打設までの時間を調整することも可能であ
る。Furthermore, in the present invention, water-soluble polymers such as cellulose derivatives, starch derivatives, polyvinyl alcohol, polyethylene oxide, polyacrylamide, and biopolymers; powdered cellulose such as cellulose; inorganic fine powders such as silica fume; It is possible to use a separation inhibitor having an effect of preventing bleeding of clay minerals such as sepiolite and the like. In addition to the water-based polymer used to coat the existing concrete, low-molecular-weight polymerizable polymers or prepolymers, such as unsaturated polyester or epoxy resin, which are liquid polymers, such as ethylene vinyl acetate, which is a re-emulsifying powder resin, and a curing agent, etc. It is possible.
It is also possible to adjust the time from coating to casting by using an aqueous polymer together with a film forming time regulator.
【0022】[0022]
【実施例】以下、本発明を実施例に基づいて説明する。DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be described below based on embodiments.
【0023】実施例1 セメントAの単位量を500kg/m3とし、セメントA 100重
量部に対して、膨張材α6重量部、細骨材 152重量部、
及び粗骨材 158重量部をミキサに投入し、低速で30秒空
練りし、水0.36重量部、減水剤を固形分換算で 1.0重
量部、及び乾燥収縮低減剤イ4重量部を投入し、150 秒
練り混ぜコンクリートを作製した。作製したコンクリー
トのスランプフローは65cm、U形充填試験結果は30.5c
m、空気量は 4.5%であった。既設コンクリートの下面
を吐出圧力2,300kgf/cm2のウオタージェットで処理し、
水性ポリマーを表1に示すように塗布し充分皮膜形成し
た3日後に、既設コンクリートの下に型枠をセットし、
作製したコンクリートを流し込んだ。硬化後材齢28日に
コアリングし付着強度を測定した。結果を表1に示す。Example 1 A unit amount of cement A was 500 kg / m 3, and 6 parts by weight of an expanding material α, 152 parts by weight of fine aggregate,
And 158 parts by weight of coarse aggregate were put into a mixer, kneaded at a low speed for 30 seconds, and 0.36 parts by weight of water, 1.0 part by weight of a water reducing agent in terms of solid content, and 4 parts by weight of a drying shrinkage reducing agent were added, Concrete mixed for 150 seconds was prepared. Slump flow of prepared concrete is 65cm, U-shaped filling test result is 30.5c
m, air volume was 4.5%. Treat the lower surface of the existing concrete with a water jet with a discharge pressure of 2,300 kgf / cm 2 ,
Three days after the aqueous polymer was applied as shown in Table 1 and the film was sufficiently formed, a mold was set under the existing concrete,
The prepared concrete was poured. On the 28th day after curing, coring was performed to measure the adhesive strength. Table 1 shows the results.
【0024】<使用材料> セメントA:普通ポルトランドセメント、日本セメント
社製 膨張材 α:カルシウムサルホアルミネート系膨張材、
市販品 乾燥収縮低減剤イ:エチレンオキサイドとプロピレンオ
キサイドとの共重合体 減水剤 :高性能AE減水剤、ポリカルボン酸エーテ
ル系と架橋ポリマーの複合体 細骨材 :川砂、5mm下、比重2.56 粗骨材 :砕石、Gmax=20mm、比重2.65 水性ポリマーa:エチレン酢酸ビニルエマルジョン、比
重1.06 水性ポリマーb:スチレンブタジエンゴムラテックス、
比重1.06 水性ポリマーc:ポリアクリル酸エステルエマルジョ
ン、比重1.05<Materials Used> Cement A: Ordinary Portland cement, expanded material manufactured by Nippon Cement Co. α: Calcium sulfoaluminate-based expanded material,
Commercial product Drying shrinkage reducing agent A: Copolymer of ethylene oxide and propylene oxide Water reducing agent: High-performance AE water reducing agent, composite of polycarboxylic acid ether and crosslinked polymer Fine aggregate: River sand, 5 mm below, specific gravity 2.56 coarse Aggregate: crushed stone, Gmax = 20 mm, specific gravity 2.65 Aqueous polymer a: ethylene vinyl acetate emulsion, specific gravity 1.06 aqueous polymer b: styrene butadiene rubber latex,
Specific gravity 1.06 Aqueous polymer c: polyacrylate emulsion, specific gravity 1.05
【0025】<測定方法> スランプフロー:JSCE-F503 に準じ測定 充填性 :土木学会 高流動コンクリート委員会「U
形充填試験方法(案)」に準じ測定 空気量 :JIS A 1128に準じて測定 付着力 :コンクリートの硬化後、コアリングし、φ
5cmの供試体を作成し、上下面を研磨し、引張試験用治
具に接着し、材齢28日の接着力を測定<Measurement method> Slump flow: Measured according to JSCE-F503 Fillability: High fluidity concrete committee “U”
Air filling: Measured according to JIS A 1128 Adhesion: After hardening of concrete, coring, φ
Prepare a 5cm specimen, grind the upper and lower surfaces, adhere to the jig for tensile test, measure the adhesive force of 28 days old
【0026】[0026]
【表1】 [Table 1]
【0027】実施例2 セメントBの単位量を315kg/m3とし、セメントB 100重
量部に対して、膨張材α11重量部、石粉77重量部、細骨
材 280重量部、及び粗骨材 230重量部をミキサに投入し
低速で30秒空練りし、その後、水47重量部、減水剤を
固形分換算で0.7 重量部、及び乾燥収縮低減剤イ7重量
部を投入し 150秒練り混ぜてコンクリートを作製したこ
と以外実施例1と同様に行った。結果を表2に示す。作
製したコンクリートのスランプフローは67cm、U形充填
試験結果は31cm、空気量は 4.3%であった。Example 2 The unit amount of cement B was 315 kg / m 3, and based on 100 parts by weight of cement B, 11 parts by weight of expander α, 77 parts by weight of stone powder, 280 parts by weight of fine aggregate, and 230 parts of coarse aggregate Parts by weight into a mixer and knead at low speed for 30 seconds, then add 47 parts by weight of water, 0.7 parts by weight of water reducing agent in terms of solid content, and 7 parts by weight of drying shrinkage reducing agent a and knead for 150 seconds. It carried out like Example 1 except having produced concrete. Table 2 shows the results. The produced concrete had a slump flow of 67 cm, a U-shaped filling test result of 31 cm, and an air volume of 4.3%.
【0028】<使用材料> セメントB:早強ポルトランドセメント、住友大阪セメ
ント社製 石粉 :炭酸カルシウム粉末、比重2.70、ブレーン
値 5,000cm2/g<Materials used> Cement B: Early strength Portland cement, manufactured by Sumitomo Osaka Cement Co., Ltd. Stone powder: Calcium carbonate powder, specific gravity 2.70, Blaine value 5,000 cm 2 / g
【0029】[0029]
【表2】 [Table 2]
【0030】実施例3 表3に示すセメント、セメント 100重量部に対して、表
3に示す量の膨張材、乾燥収縮低減剤、及び石粉、水15
0kg/m3、細骨材 865〜875kg/m3、並びに、粗骨材 731〜
741kg/m3を配合し、コンクリートのスランプフロー値が
65±5cmの範囲に入るように、減水剤を、セメント、
膨張材、及び石粉の合計 100重量部に対して、固形分換
算で0.38〜0.42重量部の範囲で配合した。また、空気量
も 4.5±0.5 %になるように調整した。コンクリート表
面を吐出圧 1,800kg/cm2のウオタージェットで処理し、
水性ポリマーbを 150g/m2塗布し皮膜形成したこと以外
は実施例1と同様に行った。結果を表3に併記する。Example 3 Cement shown in Table 3 and 100 parts by weight of cement were used in the amounts shown in Table 3 for the amount of the expanding material, drying shrinkage reducing agent, stone powder and water 15
0 kg / m 3, fine aggregates 865~875kg / m 3, as well as coarse aggregate 731~
Blended 741kg / m 3, slump flow value of concrete
Fill the water reducing agent with cement,
It was blended in a range of 0.38 to 0.42 parts by weight in terms of solid content with respect to a total of 100 parts by weight of the expanding material and the stone powder. The air volume was also adjusted to be 4.5 ± 0.5%. The concrete surface is treated with a water jet with a discharge pressure of 1,800 kg / cm 2 ,
The procedure was performed in the same manner as in Example 1 except that the aqueous polymer b was applied at 150 g / m 2 to form a film. The results are also shown in Table 3.
【0031】<使用材料> セメントC:高ビーライトセメント、秩父小野田社製 膨張材 β:石灰系膨張材、市販品 乾燥収縮低減剤ロ:低級アルコールアルキレンオキシド
付加物<Materials used> Cement C: high belite cement, expander manufactured by Chichibu Onoda Co., Ltd. β: lime-based expander, commercially available drying shrinkage reducing agent b: lower alcohol alkylene oxide adduct
【0032】[0032]
【表3】 [Table 3]
【0033】実施例4 表4に示す単位量のセメントBを用い、セメント 100重
量部に対して、表4に示す膨張材α、固形分換算の減水
剤、細骨材、粗骨材、水、並びに、乾燥収縮低減剤イ
4重量部を配合し、空気量を 4.5%に調整したコンクリ
ートを調製したこと以外は実施例2と同様に行った。結
果を表4に併記する。Example 4 Using a unit amount of cement B shown in Table 4, and using 100 parts by weight of cement, an expanding agent α shown in Table 4, a water reducing agent in terms of solid content, fine aggregate, coarse aggregate, water , And 4 parts by weight of a drying shrinkage reducing agent A, and the same procedure as in Example 2 was carried out, except that a concrete in which the amount of air was adjusted to 4.5% was prepared. The results are also shown in Table 4.
【0034】[0034]
【表4】 [Table 4]
【0035】実施例5 セメントB 100重量部に対して、表5に示す膨張材αと
乾燥収縮低減剤、さらに減水剤を固形分換算で 0.6重
量部配合したこと以外は実施例2と同様に行った。結果
を表5に併記する。Example 5 The procedure of Example 2 was repeated, except that 0.6 parts by weight, in terms of solids, of an expanding agent α, a drying shrinkage reducing agent and a water reducing agent were added to 100 parts by weight of cement B, as shown in Table 5. went. The results are also shown in Table 5.
【0036】<使用材料> 減水剤 :高性能AE減水剤、無水マレイン酸、メト
キシポリエチレングリコール−アクリレートとスチレン
の共重合物<Materials> Water reducing agent: High-performance AE water reducing agent, maleic anhydride, copolymer of methoxypolyethylene glycol-acrylate and styrene
【0037】[0037]
【表5】 [Table 5]
【0038】[0038]
【発明の効果】本発明の打継コンクリートは、充填性に
優れ、乾燥収縮によるひび割れや自己収縮が少なく、か
つ、既設コンクリートとの付着性が良好であり、本発明
法により、逆打ち工法や床版下面補強コンクリート打設
等で、作業性が向上する、交通渋滞のない施工性を改善
するなどの効果を奏する。The cast-in-place concrete of the present invention has an excellent filling property, has little cracking and self-shrinkage due to drying shrinkage, and has good adhesion to existing concrete. The effect of improving workability and improving workability without traffic congestion is achieved by placing concrete under the floor slab reinforced concrete.
Claims (4)
水性ポリマーディスパージョンを含有してなるセメント
混和材。1. A cement admixture comprising an expanding material, a drying shrinkage reducing agent, a water reducing agent, and an aqueous polymer dispersion.
ーディスパージョンを被覆し、セメント、膨張材、乾燥
収縮低減剤、及び減水剤を含有してなる打継コンクリー
トを打ち継ぐことを特徴とする打継コンクリートの打設
方法。2. A casting method comprising coating a joint surface of existing concrete with an aqueous polymer dispersion, and joining a joint concrete containing a cement, an expanding agent, a drying shrinkage reducing agent, and a water reducing agent. How to put joint concrete.
で30cmを越える充填性を有するコンクリートであること
を特徴とする請求項2記載の打継コンクリートの打設方
法。3. The method according to claim 2, wherein the cast concrete is a concrete having a filling property exceeding 30 cm in a U-type filling test method.
に打継コンクリートを打ち継ぐことを特徴とする請求項
2又は3記載の打継コンクリートの打設方法。4. The method according to claim 2, wherein the cast concrete is joined to a lower surface and / or a side surface of the existing concrete.
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001072456A (en) * | 1999-06-28 | 2001-03-21 | Taiheiyo Cement Corp | Paste or mortar for joining water-permeable concrete, and method for joining water-permeable concrete |
JP2002274912A (en) * | 2001-03-14 | 2002-09-25 | Taiheiyo Cement Corp | Paste or mortar for joining water-permeable concrete |
JP2007161507A (en) * | 2005-12-12 | 2007-06-28 | Taiheiyo Material Kk | Highly durable cross-section repairing material |
JP2008260687A (en) * | 2008-07-16 | 2008-10-30 | Denki Kagaku Kogyo Kk | Method for manufacturing cement concrete cured body |
-
1997
- 1997-05-26 JP JP13471097A patent/JP4001404B2/en not_active Expired - Fee Related
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001072456A (en) * | 1999-06-28 | 2001-03-21 | Taiheiyo Cement Corp | Paste or mortar for joining water-permeable concrete, and method for joining water-permeable concrete |
JP4480856B2 (en) * | 1999-06-28 | 2010-06-16 | 太平洋セメント株式会社 | Permeable concrete joining paste or mortar, and permeable concrete joining method |
JP2002274912A (en) * | 2001-03-14 | 2002-09-25 | Taiheiyo Cement Corp | Paste or mortar for joining water-permeable concrete |
JP4536282B2 (en) * | 2001-03-14 | 2010-09-01 | 太平洋セメント株式会社 | Mortar for permeable concrete splicing |
JP2007161507A (en) * | 2005-12-12 | 2007-06-28 | Taiheiyo Material Kk | Highly durable cross-section repairing material |
JP2008260687A (en) * | 2008-07-16 | 2008-10-30 | Denki Kagaku Kogyo Kk | Method for manufacturing cement concrete cured body |
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JP4001404B2 (en) | 2007-10-31 |
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