JPH0925151A - Primer composition for underwater curing resin concrete and underwater curing resin mortal - Google Patents
Primer composition for underwater curing resin concrete and underwater curing resin mortalInfo
- Publication number
- JPH0925151A JPH0925151A JP17453595A JP17453595A JPH0925151A JP H0925151 A JPH0925151 A JP H0925151A JP 17453595 A JP17453595 A JP 17453595A JP 17453595 A JP17453595 A JP 17453595A JP H0925151 A JPH0925151 A JP H0925151A
- Authority
- JP
- Japan
- Prior art keywords
- concrete
- resin
- cement
- water
- underwater
- 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 48
- 239000011347 resin Substances 0.000 title claims abstract description 48
- 229920005989 resin Polymers 0.000 title claims abstract description 48
- 239000000203 mixture Substances 0.000 title claims abstract description 20
- 230000001459 mortal effect Effects 0.000 title abstract 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 30
- 239000004568 cement Substances 0.000 claims abstract description 27
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 11
- 239000011398 Portland cement Substances 0.000 claims abstract description 7
- 239000004570 mortar (masonry) Substances 0.000 claims description 27
- 238000001723 curing Methods 0.000 claims description 7
- 239000000853 adhesive Substances 0.000 abstract description 13
- 230000001070 adhesive effect Effects 0.000 abstract description 13
- 229920002678 cellulose Polymers 0.000 abstract description 4
- 239000001913 cellulose Substances 0.000 abstract description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 12
- 239000011083 cement mortar Substances 0.000 description 12
- 238000000034 method Methods 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- 239000000463 material Substances 0.000 description 4
- 239000004576 sand Substances 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- 229920000877 Melamine resin Polymers 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 3
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 3
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 3
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- 239000008030 superplasticizer Substances 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
- 229920001479 Hydroxyethyl methyl cellulose Polymers 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 229910003460 diamond Inorganic materials 0.000 description 2
- 239000010432 diamond Substances 0.000 description 2
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 238000005498 polishing Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 229920006305 unsaturated polyester Polymers 0.000 description 2
- RUMACXVDVNRZJZ-UHFFFAOYSA-N 2-methylpropyl 2-methylprop-2-enoate Chemical compound CC(C)COC(=O)C(C)=C RUMACXVDVNRZJZ-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 229920001732 Lignosulfonate Polymers 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- OKKRPWIIYQTPQF-UHFFFAOYSA-N Trimethylolpropane trimethacrylate Chemical compound CC(=C)C(=O)OCC(CC)(COC(=O)C(C)=C)COC(=O)C(C)=C OKKRPWIIYQTPQF-UHFFFAOYSA-N 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- XFWJKVMFIVXPKK-UHFFFAOYSA-N calcium;oxido(oxo)alumane Chemical compound [Ca+2].[O-][Al]=O.[O-][Al]=O XFWJKVMFIVXPKK-UHFFFAOYSA-N 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- NVVZQXQBYZPMLJ-UHFFFAOYSA-N formaldehyde;naphthalene-1-sulfonic acid Chemical compound O=C.C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 NVVZQXQBYZPMLJ-UHFFFAOYSA-N 0.000 description 1
- 230000002262 irrigation Effects 0.000 description 1
- 238000003973 irrigation Methods 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 238000005304 joining Methods 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- GYVGXEWAOAAJEU-UHFFFAOYSA-N n,n,4-trimethylaniline Chemical compound CN(C)C1=CC=C(C)C=C1 GYVGXEWAOAAJEU-UHFFFAOYSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 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
- 229920001567 vinyl ester resin 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
- C04B2111/00482—Coating or impregnation 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
- C04B2111/00474—Uses not provided for elsewhere in C04B2111/00
- C04B2111/00482—Coating or impregnation materials
- C04B2111/00491—Primers
-
- 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
- C04B2111/74—Underwater applications
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Organic Chemistry (AREA)
- Underground Or Underwater Handling Of Building Materials (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、水中硬化性レジンモル
タルおよび水中硬化性レジンコンクリート用プライマー
に関し、さらに詳しくは、海洋、河川や湖等における水
中コンクリート構造物、水利構造物の建設や部分補修材
料として、水中硬化性レジンモルタルおよび水中硬化性
レジンコンクリートを用いる場合のプライマーに関する
ものであり、また本発明は上記プライマーを用いた水中
構造物の補修方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an underwater-curable resin mortar and a primer for underwater-curable resin concrete, and more specifically, construction and partial repair of an underwater concrete structure and a water use structure in the ocean, rivers and lakes. The present invention relates to a primer when using water-curable resin mortar and water-curable resin concrete, and the present invention relates to a method for repairing an underwater structure using the primer.
【0002】[0002]
【従来の技術】海洋、河川や湖等の水中構造物、水利構
造物を部分補修するため、水中で硬化できる各種のモル
タルおよびコンクリートが用いられている。これら水中
で硬化可能なモルタル及びコンクリートとしては、急結
性セメントモルタル又はコンクリートの他に、最近では
エポキシ系、不飽和イソシアネート系、アクリル系、不
飽和ポリエステル系等、合成樹脂を原料とするレジンモ
ルタル組成物およびレジンコンクリート組成物も多く用
いられるようになり、特にアクリル系レジンモルタルま
たはレジンコンクリートは広い温度範囲での優れた作業
性と速硬化性を有し、耐候性、耐薬品性にもすぐれてい
ることから優れた補修材料とされている。2. Description of the Related Art Various mortars and concretes that can be hardened in water are used to partially repair underwater structures such as the ocean, rivers and lakes, and irrigation structures. As these mortars and concretes that can be cured in water, in addition to quick-setting cement mortars and concretes, recently resin mortars made from synthetic resins such as epoxy, unsaturated isocyanate, acrylic, unsaturated polyester, etc. Compositions and resin concrete compositions have also been widely used. Especially, acrylic resin mortar or resin concrete has excellent workability in a wide temperature range and fast curing property, and also has excellent weather resistance and chemical resistance. Therefore, it is regarded as an excellent repair material.
【0003】[0003]
【発明が解決しようとする課題】しかし、これらレジン
モルタルまたはレジンコンクリート組成物は下地コンク
リートの上にそのまま塗布しても接着性が充分ではな
く、大きい強度が得られないという問題があった。However, there is a problem in that the resin mortar or resin concrete composition does not have sufficient adhesiveness even if it is applied as it is on the base concrete, and a large strength cannot be obtained.
【0004】発明者らは上記問題点を解決する方法につ
いて検討した結果、特定の組成を有するプライマーを水
中にてセメントコンクリート下地に塗布した後レジンコ
ンクリート又はレジンモルタルを打継ぐことにより、下
地コンクリートとの接着が良好となり、強度の大きい構
造物又は補修材料が得られることを見出した。As a result of studying a method for solving the above-mentioned problems, the inventors of the present invention applied a primer having a specific composition to a cement concrete base in water and then splicing the resin concrete or resin mortar to form a base concrete. It has been found that the adhesion of the resin is good and a structure or repair material having high strength can be obtained.
【0005】[0005]
【課題を解決するための手段】本発明の第1の発明はポ
ルトランドセメント、セルロース系水中不分離性コンク
リート混和剤、流動化剤及び水からなるセメントペース
トであって、セルロース系水中不分離性コンクリート混
和剤が水及び流動化剤の合計量に対して0.3〜3重量
%配合され、凝結始発時間が30分〜8時間であるレジ
ンコンクリート又はレジンモルタル用プライマー組成物
である。The first invention of the present invention is a cement paste comprising portland cement, a cellulosic underwater non-separable concrete admixture, a superplasticizer and water, which is a cellulosic underwater non-separable concrete. A primer composition for resin concrete or resin mortar, in which an admixture is blended in an amount of 0.3 to 3% by weight based on the total amount of water and a fluidizing agent and the initial setting time is 30 minutes to 8 hours.
【0006】本発明のプライマー組成物は凝結始発時間
が30分〜8時間であり、セメント、セルロース系水中
不分離性コンクリート混和剤、流動化剤及び水を必須成
分とする。The primer composition of the present invention has an initial setting time of 30 minutes to 8 hours, and contains cement, a cellulose-based non-separable concrete admixture in water, a superplasticizer, and water as essential components.
【0007】ここに凝結始発時間とはASTM C 4
03−65Tのプロクター貫入抵抗法により測定した貫
入抵抗が500psiを示す時間であり、本発明で用い
る速硬性のセメントはこの凝結始発時間が30分〜8時
間、好ましくは1時間〜6時間のものである。凝結始発
時間が8時間を超えるような硬化の遅いセメントではレ
ジンコンクリートとの接着強度が不十分であり、強度の
大きい構造物や補修材料が得られない。また凝結始発時
間が30分未満では硬化時間が早すぎて、やはり接着強
度が不十分となる。Here, the setting time of condensation is ASTM C 4
The penetration resistance measured by the Proctor penetration resistance method of 03-65T is 500 psi, and the fast-setting cement used in the present invention has an initial setting time of 30 minutes to 8 hours, preferably 1 hour to 6 hours. Is. Cement having a slow hardening such that the initial setting time exceeds 8 hours has insufficient adhesive strength with resin concrete and a structure or repair material having high strength cannot be obtained. If the initial setting time is less than 30 minutes, the curing time will be too fast and the adhesive strength will be insufficient.
【0008】このような特定の凝結始発時間を有するセ
メントを得るには、超速硬性セメントに凝結遅延剤を配
合して硬化時間を遅らせたり、超早強性ポルトランドセ
メントに凝結促進剤を配合して硬化時間を短縮する等の
方法がある。In order to obtain a cement having such a specific initial setting time, a setting retarder is added to the ultrafast setting cement to delay the setting time, or a setting accelerator is added to the ultrafast setting Portland cement. There are methods such as shortening the curing time.
【0009】ここに超速硬セメントとはポルトランドセ
メントの原料にカルシウムアルミネート等を加えて、超
速硬性が得られるようにしたもので、”ジェットセメン
ト”等の商品名で販売されている。凝結遅延剤としては
オキシカルボン酸塩系、ケイフッ化マグネシウム系等の
化合物が用いられる。超速硬セメント、凝結遅延剤の種
類によっても異なるが、超速硬セメントに対する凝結遅
延剤の配合量は0.5〜2重量%が好ましい。Here, the ultra-rapid hardening cement is obtained by adding calcium aluminate or the like to the raw material of Portland cement so as to obtain the ultra-rapid hardening property, and is sold under the trade name of "jet cement" or the like. As the setting retarder, compounds such as oxycarboxylic acid salt-based compounds and magnesium silicofluoride-based compounds are used. Although depending on the types of the ultra-rapid hardening cement and the setting retarder, the amount of the setting retarder to be added to the ultra-rapid hardening cement is preferably 0.5 to 2% by weight.
【0010】また超早強セメントとはJIS R521
0によって定義されているポルトランドセメントの一種
であり、成分的には強度発現の速い3CaO・SiO2
(C3 S)の含有量が多いことによって特徴づけられて
いる。Ultra fast cement is JIS R521
It is a kind of Portland cement defined by 0, and its composition is 3CaO ・ SiO 2 which has high strength development.
It is characterized by a high content of (C 3 S).
【0011】セルロース系水中不分離性コンクリート混
和剤(以下セルロース系混和剤又は単に混和剤と呼ぶこ
とがある)はセメントモルタルに粘性を与え水中に成分
が拡散するのを防ぐ作用を有するもので、ヒドロキシプ
ロピルメチルセルロース(HPMC)、ヒドロキシエチ
ルメチルセルロース(HEMC)、ヒドロキシエチルセ
ルロース(HEC)等が挙げられる。The cellulosic underwater non-separable concrete admixture (hereinafter sometimes referred to as a cellulosic admixture or simply admixture) has a function of giving viscosity to cement mortar and preventing the components from diffusing into water. Examples thereof include hydroxypropyl methyl cellulose (HPMC), hydroxyethyl methyl cellulose (HEMC) and hydroxyethyl cellulose (HEC).
【0012】流動化剤は混和剤の添加により低下した流
動性を回復するためのもので、ナフタリンスルホン酸ホ
ルマリン縮合物塩(ナフタリン系)、メラミン樹脂スル
ホン酸ホルマリン縮合物塩(メラミン系)、オレフィン
・マレイン酸共重合物塩(カルボン酸系)、リグニンス
ルホン酸塩(リグニン系)等が使用できるが、本発明の
ように混和剤としてセルロース系混和剤を使用する場合
にはメラミン系流動化剤の使用が適している。The fluidizing agent is for recovering the fluidity lowered by the addition of the admixture, and includes a naphthalenesulfonic acid formalin condensate salt (naphthalin type), a melamine resin sulfonic acid formalin condensate salt (melamine type), an olefin. Maleic acid copolymer salt (carboxylic acid type), lignin sulfonate (lignin type), etc. can be used, but when a cellulose type admixture is used as an admixture as in the present invention, a melamine type fluidizing agent Is suitable for use.
【0013】本発明のプライマー組成物には上記の必須
成分のほかに必要に応じてAE(空気連行)剤、減水剤
などの各種添加物を配合することもできる。In addition to the above-mentioned essential components, the primer composition of the present invention may optionally contain various additives such as an AE (air entrainment) agent and a water reducing agent.
【0014】本発明のプライマー組成物におけるセルロ
ース系混和剤の含量は水と流動化剤の合計量に対し0.
3〜3%(重量)である。0.3%未満では水中不分離
性がなくなり、また、3%以上では粘性が上がりすぎて
塗布しにくくなる。水/セメント比は40〜55%、特
に45〜55%が好ましい。The content of the cellulosic admixture in the primer composition of the present invention is 0.
It is 3 to 3% (weight). If it is less than 0.3%, the inseparability in water disappears, and if it is 3% or more, the viscosity becomes too high and it becomes difficult to apply. The water / cement ratio is preferably 40 to 55%, particularly 45 to 55%.
【0015】本発明のプライマー組成物は水中にて硬化
したセメントコンクリート又はモルタル表面にレジンコ
ンクリート又はレジンモルタルを打ち継で水中構造物を
補修するのに用いることができる。即ち本発明の第2の
発明は水中にて硬化したセメントコンクリート又はモル
タル表面に前記第1の発明のプライマー組成物を0.5
mm以上塗布し、次いでレジンコンクリート又はレジン
モルタルを打ち継ぐことを特徴とするコンクリートの水
中硬化方法である。The primer composition of the present invention can be used for repairing an underwater structure by splicing resin concrete or resin mortar on the surface of cement concrete or mortar hardened in water. That is, the second aspect of the present invention is to apply 0.5% of the primer composition of the first aspect to the surface of cement concrete or mortar cured in water.
It is a method for hardening concrete underwater, characterized in that it is applied in an amount of not less than mm, and then resin concrete or resin mortar is spliced.
【0016】プライマー塗布量は厚み0.5mm以上が
必要である。厚みが0.5mm未満では接着強度が不足
する。The coating amount of the primer must be 0.5 mm or more. If the thickness is less than 0.5 mm, the adhesive strength will be insufficient.
【0017】プライマーを塗布した後のレジンコンクリ
ートの打ち込みはなるべく速やかに行ない、遅くともプ
ライマー塗布後40分以内とするのが好ましい。40分
以上経過すると接着強度が不足する。It is preferable to drive the resin concrete after applying the primer as quickly as possible, and at the latest, within 40 minutes after applying the primer. After 40 minutes or more, the adhesive strength becomes insufficient.
【0018】レジンコンクリートとしてはエポキシ、不
飽和ポリエステル、ビニルエステル、フラン、アクリル
系のものが使用できるが、特にアクリル(メタクリル酸
エステル又はアクリル酸エステル)系レジンコンクリー
トが好ましい。As the resin concrete, epoxy, unsaturated polyester, vinyl ester, furan and acrylic type can be used, but acrylic (methacrylic acid ester or acrylic acid ester) type resin concrete is particularly preferable.
【0019】[0019]
【実施例】以下に実施例を挙げて本発明を具体的に説明
する。なお実施例及び比較例に用いたセメントモルタル
下地及びレジンモルタルは下記の方法で製造した。 (1)セメントモルタル下地の作製 JIS R 5201に従って、セメント:標準砂=
1:2(重量比)、水セメント比65%とした調合のセ
メントモルタルを練混ぜ、寸法50×100×200m
mのブロックに成形した。成形後、24時間湿空(20
℃,80%R.H.)、24時間温水(70℃)及び7
日間乾燥(20℃,50%R.H.)養生を行った。養
生後、そのブロックの100×200mmの一面を被着
面とし、JIS R 6252に規定するAA−150
番研磨紙を用いて研磨し、圧縮空気で被着面のごみをと
り除き、セメントモルタル下地とした。EXAMPLES The present invention will be specifically described below with reference to examples. The cement mortar base and resin mortar used in Examples and Comparative Examples were manufactured by the following method. (1) Preparation of cement mortar base Cement: standard sand = according to JIS R5201
Mix 1: 2 (weight ratio), cement mortar with water cement ratio 65%, size 50 × 100 × 200m
Molded into m blocks. After molding, moist air (20
C, 80% R.C. H. ), 24 hours warm water (70 ° C) and 7
Curing was carried out for a day by drying (20 ° C., 50% RH). After curing, one surface of the block of 100 × 200 mm is used as an adherend, and AA-150 specified in JIS R 6252 is used.
Polishing was carried out using a No. polishing paper, and dust on the adhered surface was removed with compressed air to obtain a cement mortar base.
【0020】 (2)レジンモルタルの製造 バインダーの液状レジンとして (1) メタクリル酸メチル ・・67.4%、 (2) トリメチロールプロパントリメタクリレート ・・・1.8%、 (3) オルトフタル酸系不飽和ポリエステル樹脂 [商品名:エポラックG−13PC(日本触媒(株)製]・・・23.1%、 (4) メタクリル酸イソブチル樹脂 [商品名:ダイヤナールBRレジンBR−101 (三菱レイヨン(株)製] ・・・7.7%、 (5) N,N−ジメチルパラトルイジン(重合促進剤) ・・・0.5%、 (6) 過酸化ベンゾイル(重合開始剤) [川口薬品(株)製、50%可塑剤希釈品] ・・・2% (モルタル調整時に直前に加える) を配合したものを使用し、この液状レジンを15重量
部、充填材の重質炭酸カルシウム(商品名:A印(三井
製粉(株)製)を15重量部、4号硅砂(東北硅砂
(株)製)を35重量部、7号硅砂(東北硅砂(株)
製)を35重量部を調合、混練したものを使用した。(2) Manufacture of resin mortar As liquid resin for binder (1) Methyl methacrylate ... 67.4%, (2) Trimethylolpropane trimethacrylate ... 1.8%, (3) Orthophthalic acid-based Unsaturated polyester resin [Brand name: Epolak G-13PC (manufactured by Nippon Shokubai Co., Ltd.) ... 23.1%, (4) Isobutyl methacrylate resin [Brand name: Dianal BR Resin BR-101 (Mitsubishi Rayon ( Co., Ltd.] ... 7.7%, (5) N, N-dimethylparatoluidine (polymerization accelerator) ... 0.5%, (6) Benzoyl peroxide (polymerization initiator) [Kawaguchi Yakuhin ( Co., Ltd., 50% diluted plasticizer] ... 2% (added just before mortar adjustment) is used, and 15 parts by weight of this liquid resin, heavy calcium carbonate filler (trade name) : A mark (Mitsui Powder Co., Ltd.) 15 parts by weight, No. 4 silica sand 35 parts by weight (Tohoku silica sand Ltd.), No. 7 Silica sand (Tohoku silica sand Co.
(Manufactured) was mixed and kneaded.
【0021】[実施例1]プライマー(A)の調製 (1) 超速硬セメント [商品名:ジェットセメント(秩父小野田セメント(株)製)] ・・・・100 重量部 (2) 水 ・・・・・47.68重量部 (3) メチルセルロース系水中不分離性コンクリート用混和剤 [商品名:UWB−D(三井石化産資(株)製)HPMC系混和剤] ・・0.58重量部 (4) 水中不分離性コンクリート用流動化剤 [商品名:ポゾリスUC−150((株)エヌエムビー製、メラミンスルホン酸 塩系流動化剤] (以下流動化剤という) ・・2.32重量部 (5) 凝結遅延剤 (商品名ジェットセッター(秩父小野田セメント(株)製)) ・・1 重量部 を調合して練混ぜ、プライマーを調製した。このセメン
トの凝結始発時間は3時間40分であった。[Example 1] Preparation of primer (A) (1) Super fast cement [Product name: Jet cement (manufactured by Chichibu Onoda Cement Co., Ltd.)] ... 100 parts by weight (2) Water ...・ ・ 47.68 parts by weight (3) Methylcellulose-based admixture for non-separable concrete in water [Brand name: UWB-D (manufactured by Mitsui Petrochemical Co., Ltd.) HPMC-based admixture] ・ ・ 0.58 parts by weight ( 4) Fluidizing agent for water-separable concrete [Brand name: Pozzolith UC-150 (manufactured by NMB Co., Ltd., melaminesulfonic acid salt-based fluidizing agent] (hereinafter referred to as fluidizing agent) ... 2.32 parts by weight ( 5) Set retarder (trade name: Jet Setter (manufactured by Chichibu Onoda Cement Co., Ltd.)) 1 part by weight was mixed and kneaded to prepare a primer, and the initial setting time of this cement was 3 hours and 40 minutes. It was
【0022】上記(1)により作製したセメントモルタ
ル下地の被着面に、寸法10×100×200mmの型
枠を設置し、24時間水中(20℃)に静置した後、水
中にて上記プライマー(A)を塗厚1.5mm塗布し、
引き続きすぐに上記(2)のレジンモルタルを10mm
打継いだ。A mold having a size of 10 × 100 × 200 mm was set on the adherend of the cement mortar base prepared in (1) above, and allowed to stand still in water (20 ° C.) for 24 hours, and then the primer in water. Apply (A) a coating thickness of 1.5 mm,
Immediately afterwards, apply the resin mortar (2) above to 10 mm
I succeeded.
【0023】その後1日水中で養生した後、打継ぎ面に
ダイヤモンドカッターにて40×40mmで下地セメン
トモルタルの2mm深さまで切り込みをいれ、JIS
A6915に従って、打継ぎ部分に鋼製ジグを取付け、
簡易引張試験器(商品名:プルゲージ((株)モトフジ
製))にて引張接着強度を測定した。引張接着強度の値
は、2.1MPaであった。After curing for one day in water, a diamond cutter is used to make a cut with a diamond cutter to the depth of 2 mm of the base cement mortar on the joining surface according to JIS.
According to A6915, attach a steel jig to the joint,
The tensile adhesive strength was measured with a simple tensile tester (trade name: pull gauge (manufactured by Motofuji Co., Ltd.)). The value of tensile adhesive strength was 2.1 MPa.
【0024】[比較例1]実施例1において凝結遅延剤
を配合せしなかった以外は実施例1と同様に調合して練
混ぜ、プライマーを調製した。このセメントの凝結始発
時間は10分であった。実施例1と同様の方法でセメン
トモルタル下地にレジンモルタルを打継ぎ、実施例1と
同様にして引張接着強度を測定した。引張接着強度の値
は0.0MPaであった。Comparative Example 1 A primer was prepared by mixing and kneading in the same manner as in Example 1 except that the setting retarder was not added. The initial setting time of this cement was 10 minutes. In the same manner as in Example 1, resin mortar was spliced on the cement mortar base, and tensile adhesive strength was measured in the same manner as in Example 1. The value of tensile adhesive strength was 0.0 MPa.
【0025】[実施例2〜4、比較例2]実施例1にお
いてプライマーの塗り厚を表1記載の厚さに代えた以外
は、実施例1と同様の方法でセメントモルタル下地にレ
ジンモルタルを打継ぎ、実施例1と同様にして引張接着
強度を測定した。実施例1の結果とともにその結果を表
1に示す。[Examples 2 to 4 and Comparative Example 2] Resin mortar was applied to a cement mortar substrate in the same manner as in Example 1 except that the coating thickness of the primer in Example 1 was changed to the thickness shown in Table 1. The splicing was performed and the tensile adhesive strength was measured in the same manner as in Example 1. The results are shown in Table 1 together with the results of Example 1.
【0026】[0026]
【表1】 [Table 1]
【0027】[実施例5〜7、比較例3]実施例1にお
いてプライマー中の混和剤、流動化剤、水の添加量を代
えた。混和剤の配合量によっても凝結始発時間は若干変
動し、実施例7では凝結始発時間が4時間であった。得
られたプライマーを用いて、実施例1と同様の方法でセ
メントモルタル下地に塗布した後レジンモルタルを打継
ぎ、引張接着強度を測定した。その結果を実施例1の結
果とともに表2に示す。[Examples 5 to 7 and Comparative Example 3] In Example 1, the amounts of the admixture, superplasticizer and water added in the primer were changed. The initial setting time also varied slightly depending on the blending amount of the admixture, and in Example 7, the initial setting time was 4 hours. The obtained primer was applied to a cement mortar underlayer in the same manner as in Example 1 and then the resin mortar was spliced to measure the tensile adhesive strength. The results are shown in Table 2 together with the results of Example 1.
【0028】[0028]
【表2】 [Table 2]
【0029】[実施例9、比較例4]実施例1において
プライマーを塗布し、レジンモルタルを打込むまでの時
間を直後から変化させ、実施例1と同様な方法でセメン
トモルタル下地にレンジモルタルを打継ぎ、引張接着強
度を測定した。その結果を実施例1の結果とともに表2
に示す。[Example 9 and Comparative Example 4] In Example 1, the primer was applied and the time until the resin mortar was driven was changed from immediately after, and range mortar was applied to the cement mortar substrate in the same manner as in Example 1. Splicing and tensile adhesive strength were measured. The results are shown in Table 2 together with the results of Example 1.
Shown in
【0030】[0030]
【表3】 [Table 3]
【0031】[0031]
【発明の効果】水中にてセメントコンクリート下地にレ
ジンコンクリート又はレジンモルタルを打継ぐ際に、本
発明の組成物をプライマーとして使用することにより、
下地コンクリートとの接着強度の大きい水中構造物が得
られるので、水中構造物の構築、補修用の材料として利
用価値が大きい。[Effect of the Invention] When the resin concrete or resin mortar is spliced on the cement concrete substrate in water, by using the composition of the present invention as a primer,
Since an underwater structure having a high adhesive strength with the base concrete can be obtained, it has great utility value as a material for construction and repair of the underwater structure.
Claims (3)
中不分離性コンクリート混和剤、流動化剤及び水からな
るセメントペーストであって、セルロース系水中不分離
性コンクリート混和剤が水及び流動化剤の合計量に対し
て0.3〜3重量%配合され、凝結始発時間が30分〜
8時間であるレジンコンクリート又はレジンモルタル用
プライマー組成物。1. A cement paste comprising Portland cement, a cellulosic water inseparable concrete admixture, a fluidizing agent and water, wherein the cellulosic water inseparable concrete admixture is added to the total amount of water and fluidizing agent. On the other hand, 0.3 to 3% by weight is added, and the initial setting time is 30 minutes.
A primer composition for resin concrete or resin mortar for 8 hours.
トに凝結遅延剤を配合したものであることを特徴とする
請求項1記載のレジンコンクリート又はレジンモルタル
用プライマー組成物。2. The primer composition for resin concrete or resin mortar according to claim 1, wherein the Portland cement is an ultra-rapid setting cement mixed with a setting retarder.
又はモルタル表面に請求項1〜3記載のプライマー組成
物を0.5mm以上塗布し、次いでレジンコンクリート
又はレジンモルタルを打ち継ぐことを特徴とするコンク
リートの水中硬化方法。3. The surface of a cement concrete or mortar hardened in water is coated with the primer composition according to claim 1 in an amount of 0.5 mm or more, and then resin concrete or resin mortar is spliced. Underwater curing method.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17453595A JP3640707B2 (en) | 1995-07-11 | 1995-07-11 | Underwater curable resin concrete and primer composition for underwater curable resin mortar |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17453595A JP3640707B2 (en) | 1995-07-11 | 1995-07-11 | Underwater curable resin concrete and primer composition for underwater curable resin mortar |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0925151A true JPH0925151A (en) | 1997-01-28 |
| JP3640707B2 JP3640707B2 (en) | 2005-04-20 |
Family
ID=15980240
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP17453595A Expired - Lifetime JP3640707B2 (en) | 1995-07-11 | 1995-07-11 | Underwater curable resin concrete and primer composition for underwater curable resin mortar |
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| Country | Link |
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106545016A (en) * | 2016-11-07 | 2017-03-29 | 中建三局集团有限公司 | Super-large diameter pressure bearing pile DLC underwater gliders method |
-
1995
- 1995-07-11 JP JP17453595A patent/JP3640707B2/en not_active Expired - Lifetime
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106545016A (en) * | 2016-11-07 | 2017-03-29 | 中建三局集团有限公司 | Super-large diameter pressure bearing pile DLC underwater gliders method |
| CN106545016B (en) * | 2016-11-07 | 2018-09-11 | 中建三局集团有限公司 | Super-large diameter pressure bearing pile double duct underwater gliders method |
Also Published As
| Publication number | Publication date |
|---|---|
| JP3640707B2 (en) | 2005-04-20 |
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