JP5460956B2 - Coating composition, concrete anticorrosion construction method, and concrete anticorrosion structure thereby - Google Patents

Coating composition, concrete anticorrosion construction method, and concrete anticorrosion structure thereby Download PDF

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JP5460956B2
JP5460956B2 JP2007324362A JP2007324362A JP5460956B2 JP 5460956 B2 JP5460956 B2 JP 5460956B2 JP 2007324362 A JP2007324362 A JP 2007324362A JP 2007324362 A JP2007324362 A JP 2007324362A JP 5460956 B2 JP5460956 B2 JP 5460956B2
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concrete
water
epoxy resin
weight
coating material
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JP2009143776A (en
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昌宏 内田
文男 浅川
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Aica Kogyo Co Ltd
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    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C04B28/02Compositions 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
    • C04B28/04Portland cements
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/009After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone characterised by the material treated
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/45Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
    • C04B41/52Multiple coating or impregnating multiple coating or impregnating with the same composition or with compositions only differing in the concentration of the constituents, is classified as single coating or impregnation
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2111/00Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
    • C04B2111/20Resistance against chemical, physical or biological attack
    • C04B2111/26Corrosion of reinforcement resistance

Description

本発明は、水処理施設、農業用集落排水施設、下水道処理施設等のコンクリート構造物の保護のために塗布する耐薬品性を有する防食ライニング材の下地調整に使用される塗材組成物及び当該塗材組成物によるコンクリート防食施工方法並びにこれによって形成されるコンクリート防食構造に関するものである。   The present invention relates to a coating composition for use in the preparation of a base for a corrosion-resistant lining material having chemical resistance applied for the protection of concrete structures such as water treatment facilities, agricultural settlement drainage facilities, sewerage treatment facilities, and the like. The present invention relates to a concrete anticorrosion construction method using a coating material composition and a concrete anticorrosion structure formed thereby.

従来、水処理施設、農業用集落排水施設、下水道処理施設等のコンクリート構造物の貯水槽等の槽内防食には、高い耐薬品性が要求される場合はビニルエステル樹脂塗材によるライニング材が施工され、上水道用の貯水槽等ではエポキシ樹脂塗材によるライニング材の施工が行われている。しかしこれらの塗材が施工される下地コンクリートは、短工期化により十分な養生乾燥期間を確保することが難しいためコンクリート型枠が脱型された直後であったり、乾燥が不十分な高含水率状態にあることが多く、当該状態で上記ライニング材を施工すると施工後に剥離やふくれが発生することがあった。特にビニルエステル樹脂塗材によるライニング材が施工される場合は、塗材の硬化収縮によって下地からの剥離は顕著であった。   Conventionally, lining materials made of vinyl ester resin coating have been used for anti-corrosion in tanks such as water tanks for concrete structures such as water treatment facilities, agricultural settlement drainage facilities, and sewerage treatment facilities when high chemical resistance is required. It is constructed, and lining materials are being constructed with epoxy resin coatings in water tanks for waterworks. However, the foundation concrete on which these coating materials are applied is difficult to ensure a sufficient curing and drying period due to the shortened construction period. In many cases, when the lining material is applied in this state, peeling or blistering may occur after the application. In particular, when a lining material made of a vinyl ester resin coating material was applied, the peeling from the base was remarkable due to the curing shrinkage of the coating material.

これに対して、コンクリートやモルタル等からなる建築構造物における表面滲出水圧のある下地表面に、反応硬化型のエポキシ樹脂エマルジヨンと水硬性セメントとの混合物からなる下地調整層を形成した後、この下地調整層の上に急速反応型弾性エポキシ樹脂塗膜を塗着することを特徴とする防湿・防水層の施工方法では、下地調整層用の混合物は、上記エポキシ樹脂エマルジヨンの固形分を25%以上で、この樹脂エマルジヨンの水分に対して400〜200重量%の範囲で水硬性セメントを混入したものが、エポキシ樹脂エマルジョンの分散媒体である水分と反応し、エマルジョンの造膜を促進させるとともに、下地から滲出してくる水分をその水和反応の過程で吸着・保水せしめ、表面滲出水圧の影響を低減させ、下地との同質性を高め、下地調整層の接着力を増強させることが開示されている(特許文献1)。   On the other hand, after forming an undercoat adjustment layer made of a mixture of a reaction-curing epoxy resin emulsion and hydraulic cement on the undersurface with surface seepage water pressure in a building structure made of concrete, mortar, etc. In the construction method of the moisture-proof / waterproof layer, characterized in that a rapid reaction type elastic epoxy resin coating is applied on the adjustment layer, the mixture for the base adjustment layer has a solid content of 25% or more of the epoxy resin emulsion. The mixture of hydraulic cement in the range of 400 to 200% by weight with respect to the moisture of the resin emulsion reacts with the moisture that is the dispersion medium of the epoxy resin emulsion, and promotes film formation of the emulsion. Moisture that exudes from the surface is adsorbed and retained during the hydration process, reducing the effect of surface exudation water pressure and ensuring homogeneity with the substrate. Because, it is disclosed that enhancing the adhesion of the base adjustment layer (Patent Document 1).

また、コンクリート表面に乳化可能な二液反応形エポキシ樹脂又はアルカリ水存在下で反応可能なエポキシ樹脂の中から選ばれた常温硬化形エポキシ樹脂混合物、若しくはこれと細骨材、或いはセメント、水との混合物を任意の厚みで塗付することによりコンクリート打設直後から任意の材令のコンクリートまで塗布することができ、当該組成物が下地コンクリートと強固に結合したコンクリート表層の強化方法が開示されている(特許文献2)。   Also, a two-component reactive epoxy resin that can be emulsified on the concrete surface or an epoxy resin mixture that can be reacted in the presence of alkaline water, a room temperature-curable epoxy resin mixture, or a fine aggregate, cement, water, and the like A concrete surface layer strengthening method in which the composition is firmly bonded to the ground concrete is disclosed by applying a mixture of the above to a concrete of an arbitrary age immediately after casting the concrete. (Patent Document 2).

また、(A)素地調整剤がエポキシ樹脂と自己乳化性を有するアミン系硬化剤及び骨材を含有し、(B)プライマー剤がエポキシ樹脂と自己乳化性を有するアミン系硬化剤及び充填材を含有し、(C)上塗り材がエポキシ樹脂とアミン系硬化剤、充填材、希釈剤、及び層状揺変剤を含有する、これら3層からなるエポキシライニング材組成物により塗布作業性と防食性に優れた素地調整材、プライマー材及び上塗り材が開示されている(特許文献3)。
特公平3−79494号公報 特開平7−187860号公報 特開2004−136525号公報
In addition, (A) the base conditioner contains an epoxy resin and an amine-based curing agent and aggregate having self-emulsifying properties, and (B) the primer agent includes an epoxy resin and an amine-based curing agent and filler having self-emulsifying properties. (C) The top coat material contains an epoxy resin, an amine-based curing agent, a filler, a diluent, and a layered thixotropic agent. An excellent substrate preparation material, primer material, and topcoat material are disclosed (Patent Document 3).
Japanese Patent Publication No. 3-79494 JP-A-7-187860 JP 2004-136525 A

特許文献1ではエポキシ樹脂エマルションと混合する水硬性セメントが下地から滲出してくる水分をその水和反応の過程で吸着・保水せしめて表面滲出水圧の影響を低減させるとし、特許文献2ではコンクリート表面が打設直後の高含水率であっても、表面強化層は十分な付着力を有するとし、特許文献3では開示されている素地調整材、プライマー材、上塗り材を順次、塗膜が乾燥した時点で塗り重ねることで、接着性と防食性に優れた塗膜が得られるとしている。   In Patent Document 1, the hydraulic cement mixed with the epoxy resin emulsion adsorbs and retains the water that exudes from the base during the hydration reaction, thereby reducing the effect of surface exudation water pressure. Even if it has a high water content immediately after placement, the surface reinforcing layer has sufficient adhesion, and the coating material is dried in order by applying the substrate preparation material, primer material, and topcoat material disclosed in Patent Document 3. It is said that a coating film excellent in adhesiveness and anticorrosiveness can be obtained by recoating at this point.

しかしながら、これらの文献に示されたコンクリート表面に塗付する下地調整層、表面強化層、又は素地調整剤(以下下地調整層という)はコンクリートとの初期の接着性に優れてはいても、下地コンクリート内に多量の自由水が含まれている場合や、何らかの原因で水分がコンクリートに供給され続けるような場合には、仕上塗材である上塗りにふくれが発生したり、長期的には下地調整層にコンクリート中の水分が浸透して上塗りとの接着性が低下し、当該上塗りの剥離を生じることがあった。   However, even if the foundation adjustment layer, surface reinforcing layer, or substrate conditioner (hereinafter referred to as the foundation adjustment layer) applied to the concrete surface shown in these documents is excellent in the initial adhesiveness to concrete, If the concrete contains a large amount of free water or if moisture continues to be supplied to the concrete for some reason, blistering may occur in the top coat, which is the finish coating material, and in the long-term, the base is adjusted. In some cases, moisture in the concrete permeated into the layer, resulting in a decrease in adhesiveness with the top coat, and peeling of the top coat.

特に上塗りが硬化収縮を生じて下地との付着界面に大きな剥離応力が発生しやすいビニルエステル樹脂塗材の場合は、下地調整層の強度が元来十分でないことに加えて、その後下地調整層内に水分が滲出したことでさらに下地調整層の強度が低下し、このため下地調整層の表層が破壊して上塗りが下地調整層の表層と共に剥離することがあった。   In particular, in the case of vinyl ester resin coating materials, where the top coat causes curing shrinkage and a large peeling stress is likely to occur at the adhesion interface with the base, the strength of the base adjustment layer is not originally sufficient, and then within the base adjustment layer When the moisture exudes to the surface, the strength of the base adjustment layer is further reduced. For this reason, the surface layer of the base adjustment layer may be broken and the top coat may be peeled off together with the surface layer of the base adjustment layer.

本発明が解決しようとする課題は、コンクリート型枠の脱型直後や若材齢コンクリートのような高含水率のコンクリート下地であっても付着性に優れ、強靭で、下地コンクリートからの水分の透過を防止する塗材組成物及びコンクリート防食施工方法並びにそれによるコンクリート防食構造を提供することにある。   The problem to be solved by the present invention is that it is excellent in adhesiveness, toughness, and moisture permeation from the foundation concrete even immediately after demolding of the concrete formwork or even in a high moisture content concrete foundation such as young age concrete. It is providing the coating material composition and concrete anticorrosion construction method which prevent a corrosion, and the concrete anticorrosion structure by it.

請求項1記載の発明は、水硬性セメントと骨材と水系エポキシ樹脂と減水剤と粘弾性調整剤を含む水系エポキシ樹脂モルタル組成物であって、水と水硬性セメントの重量比が0.3:1以上0.4:1以下であり、樹脂固形分重量が全固形分重量に対して4%以上10%以下であり、減水剤は水硬性セメント100重量部に対し0.1〜1重量部であり、粘弾性調整剤は水硬性セメント100重量部に対して0.05〜0.15重量部であり、硬化物の総細孔量が0.05cc/g以上0.2cc/g以下であり、混合直後における粘度が5Pa・s以上40Pa・s以下/23℃であり且つT.I値が4.0〜7.0であり、JISA6909の透水試験B法の透水量が0.2ml以下であり、水硬性セメントと骨材と減水剤と粘弾性調整剤から成る1粉体と、液状エポキシ樹脂の1液と、水系硬化剤と水とから成る1液、とから成ることを特徴とする塗材組成物であり、付着性に優れ、強靭で、下地コンクリートから上昇してくる水分のライニング材裏面への透過を防ぎ、ライニング材に剥がれ、膨れ等の不具合を生じさせず、鏝さばきが良く、垂直面へ塗付してもタレが生じない。
The invention according to claim 1 is a water-based epoxy resin mortar composition containing hydraulic cement, aggregate, water-based epoxy resin, water reducing agent, and viscoelasticity modifier, wherein the weight ratio of water to hydraulic cement is 0.3. 1 to 0.4: 1, the resin solid weight is 4% to 10% with respect to the total solid weight, and the water reducing agent is 0.1 to 1 weight with respect to 100 parts by weight of hydraulic cement. The viscoelasticity adjusting agent is 0.05 to 0.15 parts by weight with respect to 100 parts by weight of the hydraulic cement, and the total pore amount of the cured product is 0.05 cc / g or more and 0.2 cc / g or less. The viscosity immediately after mixing is 5 Pa · s to 40 Pa · s / 23 ° C. and T.I. An I value of 4.0 to 7.0, a water permeability of the water permeability test B method of JISA 6909 is 0.2 ml or less, and one powder composed of hydraulic cement, aggregate, water reducing agent, and viscoelasticity modifier; A coating composition characterized by comprising one liquid epoxy resin liquid and one liquid water-based curing agent and water, having excellent adhesion, toughness, and rising from the underlying concrete Prevents moisture from penetrating to the back of the lining material, does not cause problems such as peeling or swelling on the lining material, has a good grip, and does not cause sagging even when applied to a vertical surface.

請求項2記載の発明は,請求項1記載の塗材組成物において,水系エポキシ樹脂が非乳化型のエポキシ樹脂と自己乳化型の硬化剤とを配合したもので,特に下地コンクリート中に打設時の水分だけでなく断続的に多量の水分が供給される海岸の埋立地や切土上に打設された下地コンクリートであっても,下地コンクリートから上昇してくる水分のライニング材裏面への透過を長期に亘って防ぎ,ライニング材に剥がれ,膨れ等の不具合を生じさせない。
The invention according to claim 2 is the coating material composition according to claim 1, wherein the water-based epoxy resin is a mixture of a non-emulsifying type epoxy resin and a self-emulsifying type curing agent, and is particularly placed in the ground concrete. Even if the ground concrete is placed on landfills or cuts where coastal water is intermittently supplied in addition to the moisture at the time, moisture rising from the ground concrete is applied to the back of the lining material. Permeation is prevented over a long period of time, and it does not cause problems such as peeling off and swelling on the lining material.

請求項3記載の発明は,水硬性セメントが白セメントであることを特徴とする請求項1または請求項2記載の塗材組成物であり,鏝さばきが良く,垂直面へ塗付してもタレが生じない。
The invention according to claim 3 is the coating material composition according to claim 1 or 2 , characterized in that the hydraulic cement is white cement. Sauce does not occur.

請求項4記載の発明は,コンクリート表面に請求項1乃至請求項3のいずれか記載の塗材組成物を塗付して硬化させ,一液湿気硬化型ウレタンプライマーを塗付した後、ビニルエステル樹脂塗材をライニングすることを特徴とするコンクリート防食施工方法であり,ライニング材及び下地との付着性がよく,ライニング材に膨れ等の不具合が生じることがない。
According to a fourth aspect of the invention, the coating composition according to any one of the first to third aspects is applied to a concrete surface and cured, and after applying a one-component moisture-curing urethane primer, a vinyl ester It is a concrete anticorrosion method characterized by lining a resin coating material, has good adhesion to the lining material and the base, and does not cause problems such as swelling in the lining material.

請求項5記載の発明は,コンクリート表面に請求項1乃至請求項3のいずれか記載の塗材組成物を塗付して硬化させ,エポキシ樹脂塗材をライニングすることを特徴とするコンクリート防食施工方法であり,ライニング材及び下地との付着性がよく,ライニング材に膨れ等の不具合が生じることがない。
The invention according to claim 5 is a concrete anticorrosion construction characterized in that the coating material composition according to any one of claims 1 to 3 is applied to a concrete surface and cured, and an epoxy resin coating is lined. This method has good adhesion to the lining material and the base, and does not cause problems such as swelling in the lining material.

請求項6記載の発明は,前記コンクリートが打設後1日以上10以下の若材齢コンクリートであることを特徴とする請求項4または請求項5記載のコンクリート防食施工方法であり,コンクリート打設からライニング材施工終了までの施工期間が短く,ライニング材及び下地との付着性がよく,ライニング材に剥離当の不具合が生じることがない。
The invention according to claim 6 is the concrete anticorrosion construction method according to claim 4 or 5 , characterized in that the concrete is a young age concrete of 1 day to 10 days after placing. The construction period from the lining material to the end of the lining material construction is short, it has good adhesion to the lining material and the groundwork, and the lining material does not suffer from peeling problems.

請求項7記載の発明は,コンクリート表面に請求項1乃至請求項3のいずれか記載の塗材組成物を塗付して硬化させ,一液湿気硬化型ウレタンプライマーを塗付した後,ビニルエステル樹脂塗材をライニングすることを特徴とするコンクリート防食構造であり,ライニング材にフクレ等の不具合が生じることがない,強靭なコンクリート防食構造と成る。
The invention according to claim 7 is the vinyl ester after the coating material composition according to any one of claims 1 to 3 is applied to the concrete surface and cured, and a one-part moisture-curing urethane primer is applied. It is a concrete anticorrosion structure characterized by lining a resin coating material, and it has a tough concrete anticorrosion structure that does not cause defects such as blistering in the lining material.

請求項8記載の発明は,コンクリート表面に請求項1乃至請求項3のいずれか記載の塗材組成物を塗付して硬化させ,エポキシ樹脂塗材をライニングすることを特徴とするコンクリート防食構造であり,ライニング材にフクレ等の不具合が生じることがない,強靭なコンクリート防食構造と成る。
The invention according to claim 8 is a concrete anticorrosion structure characterized in that the coating material composition according to any one of claims 1 to 3 is applied to a concrete surface and cured, and an epoxy resin coating is lined. Therefore, it becomes a strong concrete anticorrosion structure that does not cause defects such as blistering in the lining material.

請求項9記載の発明は,前記コンクリートが打設後1日以上10日以下の若材齢コンクリートであることを特徴とする請求項7または請求項8記載のコンクリート防食構造であり,表面水分率が高い若材齢コンクリート上であっても,ライニング材に膨れ等の不具合が生じることがない,強靭なコンクリート防食構造となる。
The invention according to claim 9 is the concrete anticorrosive structure according to claim 7 or 8 , characterized in that the concrete is a young age concrete of 1 day or more and 10 days or less after pouring. Even if it is on high-age young concrete, it becomes a tough concrete anticorrosion structure that does not cause problems such as swelling in the lining material.

本発明の塗材組成物は,水硬性セメントと骨材と水系エポキシ樹脂と減水剤と粘弾性調整剤を含む水系エポキシ樹脂モルタル組成物であって,水と水硬性セメントの重量比が0.3:1以上0.4:1以下で,かつ樹脂固形分重量が全固形分重量に対して4%以上10%以下であることで,硬化したあとの硬化物の総細孔量が0.05cc/g以上0.2cc/g以下となり,これにより下地コンクリート及び重層されるライニング材との付着性が高く,また下地コンクリートから上昇してくる水分のライニング材裏面への透過を防止して,強靭なコンクリート防食構造になり,ライニング材に剥離や膨れ等の不具合が生じることがない。ここで総細孔量とは塗材組成物の数nmから数十μm程度の非常に小さな穴の総量をいい,水銀圧入法により水銀の注入圧と注入量から細孔分布を求め,各細孔半径ごとの体積(細孔量)を合算したものである。
The coating material composition of the present invention is a water-based epoxy resin mortar composition containing a hydraulic cement, an aggregate, a water-based epoxy resin, a water reducing agent, and a viscoelasticity modifier, and the weight ratio of water to the hydraulic cement is 0. When the resin solid content weight is 3% or more and 0.4: 1 or less, and the resin solid content weight is 4% or more and 10% or less with respect to the total solid content weight, the total pore amount of the cured product after curing is 0.00. 05cc / g or more and 0.2cc / g or less, which has high adhesion to the base concrete and the lining material to be layered, and prevents the water rising from the base concrete from permeating to the back of the lining material, It has a tough concrete anticorrosion structure, and there are no problems such as peeling or swelling in the lining material. Here, the total amount of pores means the total amount of very small holes of several nanometers to several tens of micrometers in the coating composition, and the pore distribution is determined from the injection pressure and injection amount of mercury by the mercury intrusion method. The total volume (the amount of pores) is summed up.

全固形分重量についてであるが,本発明が水硬性セメントを配合するものであり,水と水硬性セメントの重量比は少なくとも0.3:1以上0.5:1以下の低水セメント比の組成物であるため,水系エポキシ樹脂に含まれる水分は当該水硬性セメントの水和にその殆んどが消費されて結晶水となるため,水を含んだ全配合物の重量を全固形分重量とした。
As for the total solid weight, the present invention is a mixture of hydraulic cement, and the weight ratio of water to hydraulic cement is at least 0.3: 1 to 0.5: 1 . Because it is a composition, most of the water contained in the water-based epoxy resin is consumed in the hydration of the hydraulic cement and becomes crystal water, so the weight of the total formulation including water is the total solid weight. It was.

本発明の塗材組成物はその混合直後の粘度が5Pa・s以上40Pa・s以下/23℃、かつT.I値が4.0〜7.0であり、さらに樹脂固形分重量が4%以上10%以下であれば、鏝さばきが良く、垂直面へ塗布してもタレが生じない。さらに水硬性セメントが白セメントであると、本発明の塗材組成物は全体が白色となり、この上層に淡色系ライニング材を塗付した際にも、ライニング材の色ムラが目立ちにくく、また鏝さばきが良好となる。   The coating composition of the present invention has a viscosity immediately after mixing of 5 Pa · s to 40 Pa · s / 23 ° C. When the I value is 4.0 to 7.0 and the resin solid content weight is 4% or more and 10% or less, it is easy to handle, and no sagging occurs even when applied to a vertical surface. Further, when the hydraulic cement is white cement, the coating composition of the present invention is entirely white, and even when a light-colored lining material is applied to the upper layer, the color unevenness of the lining material is not noticeable. Good judgment.

さらに本発明の塗材組成物をコンクリートに塗付した後にプライマーを塗布し、さらにビニルエステル樹脂塗材をライニングすることにより、ライニング材及び下地との付着性が良好で、ライニング材に膨れや剥離等の不具合が生じることがない強靱なコンクリート防食構造となる。   Furthermore, by applying a primer after applying the coating composition of the present invention to concrete, and further lining the vinyl ester resin coating material, the adhesion to the lining material and the base is good, and the lining material is swollen or peeled off It becomes a tough concrete anticorrosion structure that does not cause such defects.

加えて本発明の塗材組成物は、下地コンクリートが打設10日以下の若材齢であっても十分な付着性を有し、下地コンクリートから上昇してくる水分のライニング材裏面への透過が無いためライニング材等に膨れや剥離を生じることがなく、長期にわたって強靱なコンクリート防食構造を保持する。なおここでいう若材齢のコンクリートとはコンクリートを打設して10日以下であることはもちろん、これに加えて表面水分率が高い状態にあるコンクリートをいい、例えばケット水分計HI−520(測定レンジ:コンクリートレンジ)で8%以上のコンクリートをいう。   In addition, the coating composition of the present invention has sufficient adhesion even when the foundation concrete is younger than 10 days after placement, and allows the moisture rising from the foundation concrete to permeate the back of the lining material. Therefore, the lining material is not swollen or peeled off, and a strong concrete anticorrosive structure is maintained over a long period of time. In addition, the concrete of the young age here means the concrete in which the concrete has a high surface moisture content in addition to the concrete being put in the concrete for 10 days or less, for example, a ket moisture meter HI-520 ( (Measurement range: concrete range) means 8% or more concrete.

本発明の水系エポキシ樹脂モルタル組成物は下地コンクリートの表面に塗付することにより、下地コンクリートの表面を改質する塗材組成物であり、液状エポキシ樹脂と水系硬化剤とを撹拌混合することにより強制的に乳化させた分散組成物と、水硬性セメント、骨材、減水材及び粘弾性調整剤を混合したものである。   The water-based epoxy resin mortar composition of the present invention is a coating composition that modifies the surface of the base concrete by applying it to the surface of the base concrete, and by stirring and mixing the liquid epoxy resin and the water-based curing agent. The dispersion composition forcibly emulsified is mixed with hydraulic cement, aggregate, water reducing material and viscoelasticity modifier.

また、本発明の塗材組成物は、硬化物の総細孔量が0.05cc/g以上0.2cc/g以下では、その空隙は極めて小さく、連続した導管が無い。従ってライニング材であるビニルエステル樹脂塗材やエポキシ樹脂塗材の裏面に水分が供給されることが無く、ふくれの駆動力となる浸透圧が発生することがない。   In the coating composition of the present invention, when the total pore amount of the cured product is 0.05 cc / g or more and 0.2 cc / g or less, the void is extremely small and there is no continuous conduit. Therefore, moisture is not supplied to the back surface of the vinyl ester resin coating material or epoxy resin coating material, which is a lining material, and osmotic pressure as a driving force for blistering does not occur.

また、全固形分重量に対する樹脂固形分重量の割合が4%以上10%以下の本発明の塗材組成物は、付着性が良好で、プライマーやビニルエステル樹脂塗材或いはエポキシ樹脂塗材であるラインング材と十分な付着性を有する。   Further, the coating material composition of the present invention having a resin solid content weight ratio with respect to the total solid weight weight of 4% or more and 10% or less has good adhesion and is a primer, a vinyl ester resin coating material or an epoxy resin coating material. Adhesive enough with the line material.

さらには、エポキシ樹脂ライニング材を塗付する際、一般的に必要とされるプライマーが不要で、本発明である塗材組成物の表面にエポキシ樹脂ライニング材を直接塗付することが出来る。なお塗布に際しては本発明である塗材組成物の表面を目粗しすることが好ましい。   Furthermore, when applying an epoxy resin lining material, a generally required primer is unnecessary, and the epoxy resin lining material can be directly applied to the surface of the coating material composition of the present invention. In addition, it is preferable to roughen the surface of the coating material composition which is this invention in the case of application | coating.

本発明のエポキシ樹脂は、液状であり、常温硬化するものであればよく、ビスフェノールA型エポキシ樹脂、ビスフェノールF型エポキシ樹脂、フェノールノボラック型エポキシ樹脂、ビスフェノールAD型エポキシ樹脂、ビフェニル型エポキシ樹脂、ナフタレン型エポキシ樹脂、脂環式エポキシ樹脂、グリシジルエステル型エポキシ樹脂、グリシジルアミン型エポキシ樹脂、複素環式エポキシ樹脂、ジアリールスルホン型エポキシ樹脂、ヒドロキノン型エポキシ樹脂およびそれらの変性物などを単独あるいは併せて用いてもよく、また、希釈剤を用いて液状化してもよい。また好ましくはエポキシ樹脂が水に乳化せず不溶なものが良く、本願ではこれを非乳化型と称している。最も多く配合するエポキシ樹脂の軟化点は、35℃以下が好ましく、このような液状エポキシ樹脂としては、液状ビスフェノールA型エポキシ樹脂が、汎用性、コスト等で適当である。なおこれらのエポキシ樹脂組成物の市販品例としてジョリエースJEX210A(アイカ工業(株)製エポキシ樹脂、商品名、エポキシ当量180、固形分100%、粘度0.7Pa・s/25℃)がある。   The epoxy resin of the present invention may be liquid and can be cured at room temperature. Bisphenol A type epoxy resin, bisphenol F type epoxy resin, phenol novolac type epoxy resin, bisphenol AD type epoxy resin, biphenyl type epoxy resin, naphthalene Type epoxy resin, cycloaliphatic epoxy resin, glycidyl ester type epoxy resin, glycidyl amine type epoxy resin, heterocyclic epoxy resin, diaryl sulfone type epoxy resin, hydroquinone type epoxy resin and their modified products, either alone or in combination Alternatively, it may be liquefied using a diluent. Preferably, the epoxy resin is not emulsified in water and insoluble, and this is referred to as a non-emulsifying type in the present application. The softening point of the epoxy resin to be blended most is preferably 35 ° C. or less, and as such a liquid epoxy resin, a liquid bisphenol A type epoxy resin is suitable in view of versatility and cost. Examples of commercially available products of these epoxy resin compositions include Joliace JEX210A (epoxy resin manufactured by Aika Kogyo Co., Ltd., trade name, epoxy equivalent 180, solid content 100%, viscosity 0.7 Pa · s / 25 ° C.).

本発明の水系硬化剤は、前記エポキシ樹脂と混合し、また水分を良好に分散させることができるものであればよく、下記脂肪族ポリアミン、脂環式ポリアミン等を選択し、単独或いは組み合わせて使用する。   The aqueous curing agent of the present invention may be any one that can be mixed with the epoxy resin and can disperse water well. The following aliphatic polyamines and alicyclic polyamines are selected and used alone or in combination. To do.

脂肪族ポリアミンは、アミノ基及びイミノ基を分子中に少なくとも2個以上有する脂肪族化合物であり、ジエチレントリアミン、トリエチレンテトラミン、テトラエチレンペンタミン、ペンタエチレンヘキサミン、ジエチルアミノプロピルアミン、ヘキサメチレンジアミン、トリメチルヘキサメチレンジアミン、ポリオキシプロピレンジアミン、イミノビスヘキシルアミン等がある。   An aliphatic polyamine is an aliphatic compound having at least two amino groups and imino groups in the molecule, and is diethylenetriamine, triethylenetetramine, tetraethylenepentamine, pentaethylenehexamine, diethylaminopropylamine, hexamethylenediamine, trimethylhexa There are methylenediamine, polyoxypropylenediamine, iminobishexylamine, and the like.

脂環式ポリアミンは、アミノ基及びイミノ基を分子中に少なくとも2個以上有する脂環式化合物であり、キシリレンジアミン、3,9ビス(3−アミノプロピル)−2,4,8,10テトラオキサスピロ[5,5]ウンデカン、N−アミノエチルピペラジン、ビス(4−アミノシクロヘキシル)メタン等がある。   The alicyclic polyamine is an alicyclic compound having at least two amino groups and imino groups in the molecule, and xylylenediamine, 3,9bis (3-aminopropyl) -2,4,8,10 tetra. There are oxaspiro [5,5] undecane, N-aminoethylpiperazine, bis (4-aminocyclohexyl) methane and the like.

この他、ポリエーテル等の親水性主鎖をエポキシ樹脂に導入し、過剰のアミンを反応させた自己乳化型硬化剤、脂肪族ポリアミンのエチレンオキサイド付加物、エポキシ樹脂付加物、ポリエチレンポリアミン変性物等の変性脂肪族ポリアミンや脂環式ポリアミンのモノグリシジルエーテル付加物、エポキシ樹脂付加物、アクリルニトリル付加物、フェノールホルマリン変性物(マンニッヒ変成物)、脂肪酸グリシジルエーテル付加物の変性脂環式ポリアミンやポリエチレンポリアミンへの脂肪酸、ポリエチレンポリアミンへのダイマー酸、キシリレンジアミン−ダイマー酸等の縮合反応生成物であるポリアミドアミン並びにこれらの変性物等が挙げられる。前記自己乳化型硬化剤の市販品例としてジョリエースJEX210B(アイカ工業(株)製エポキシ樹脂硬化剤、商品名、活性水素当量750、固形分18%水溶液、粘度7mPa・s/25℃)がある。   In addition, a self-emulsifying curing agent in which a hydrophilic main chain such as polyether is introduced into an epoxy resin and an excess amine is reacted, an ethylene oxide adduct of an aliphatic polyamine, an epoxy resin adduct, a polyethylene polyamine modified product, etc. Modified Aliphatic Polyamines and Alicyclic Polyamine Monoglycidyl Ether Adducts, Epoxy Resin Additives, Acrylonitrile Adducts, Phenol Formalin Modified Products (Mannich Modified Products), Fatty Acid Glycidyl Ether Adducts Modified Alicyclic Polyamines and Polyethylene Examples include polyamidoamines which are condensation reaction products such as fatty acids to polyamines, dimer acids to polyethylene polyamines, xylylenediamine-dimer acids, and modified products thereof. As an example of a commercial product of the self-emulsifying curing agent, there is Jolie's JEX210B (epoxy resin curing agent manufactured by Aika Industry Co., Ltd., trade name, active hydrogen equivalent 750, solid content 18% aqueous solution, viscosity 7 mPa · s / 25 ° C.). .

本発明においてビニルエステル樹脂をライニングする際に硬化した塗材組成物に塗布するプライマーには、一般公知のプライマーが使用でき、たとえば一液湿気硬化型ウレタンプライマー、常温硬化型エポキシプライマー、不飽和ポリエステル系プライマーを挙げることが出来る。   In the present invention, as a primer to be applied to the coating composition cured when the vinyl ester resin is lined, a generally known primer can be used. For example, a one-part moisture curable urethane primer, a room temperature curable epoxy primer, an unsaturated polyester. System primers.

本発明の塗材組成物は樹脂固形分重量が4%以上10%以下であって、その混合直後の粘度が5Pa・s以上40Pa・s以下/23℃でT.I値が4.0〜7.0で鏝さばきが良く垂直面へ塗布してもタレが生じることがないが、ここで言うT.I値はJIS A6024のチクソトロピックインデックスの試験方法に準じ、BH型回転粘度計の2rpmの粘度を20rpmの粘度で除したときの値である。T.I値が4.0〜7.0の際は垂直面に塗付した場合タレが生ぜず作業性が良好である。粘度はBH型回転粘度計で6号ローター20rpm時の粘度(ただし粘度が50Pa・s以上の場合は7号ローター20rpm時の粘度)、5Pa・s未満40Pa・s超では鏝さばきが不良となる。   The coating material composition of the present invention has a resin solid content weight of 4% to 10% and a viscosity immediately after mixing of 5 Pa · s to 40 Pa · s / 23 ° C. at 23 ° C. Although the I value is 4.0 to 7.0 and the wiping is good, there is no sagging even when applied to a vertical surface. The I value is a value obtained by dividing the viscosity of 2 rpm of the BH type rotational viscometer by the viscosity of 20 rpm in accordance with the thixotropic index test method of JIS A6024. T.A. When the I value is 4.0 to 7.0, sagging does not occur when applied to a vertical surface, and workability is good. Viscosity of BH-type rotational viscometer with No. 6 rotor at 20 rpm (however, when the viscosity is 50 Pa · s or more, No. 7 rotor at 20 rpm) If the viscosity is less than 5 Pa · s and more than 40 Pa · s, the crispness is poor. .

水硬性成分はセメント、水硬性ポゾランであり、セメントとしては、水硬性セメントであれば特に限定されることはない。普通ポルトランドセメント、早強ポルトランドセメント、中庸熱ポルトランドセメント、耐硫酸塩ポルトランドセメント、白色ポルトランドセメント等の各種ポルトランドセメントや高炉セメント、シリカセメント、フライアッシュセメント等の混合セメントや、アルミン酸石灰質セメント、ケイ酸アルミン酸石灰質セメント、リン酸セメント等がある。白セメントすなわち白色ポルトランドセメントが、流動性が良い点で好ましい。水硬性ポゾランとしてメタカオリンが挙げられる。市販メタカオリンとしてはメタマックスHRM((株)デグサコンストラクション、商品名)がある。   The hydraulic component is cement or hydraulic pozzolan, and the cement is not particularly limited as long as it is a hydraulic cement. Various Portland cements such as ordinary Portland cement, early-strength Portland cement, moderately hot Portland cement, sulfate-resistant Portland cement, white Portland cement, mixed cements such as blast furnace cement, silica cement, fly ash cement, calcined aluminate, silica Examples include acid aluminate calcareous cement and phosphate cement. White cement, that is, white Portland cement, is preferable in terms of good fluidity. Examples of hydraulic pozzolans include metakaolin. Commercially available metakaolin is Metamax HRM (Degussa Construction Co., Ltd., trade name).

減水剤は陰イオン系、非イオン系、陽イオン系又は両性イオン系のAE剤とリグニンスルホン酸塩系、高級多価アルコールのスルホン酸塩系、オキシ有機酸、アルキルアリールスルホン酸塩、ポリオキシエチレンアルキルエーテル系、ポリカルボン酸系又はポリオール複合体の減水剤、これらの複合または混合したものが使うことができるが、最も効果を有するものに変性ポリカルボン酸系又はポリエーテル・ポリカルボン酸系の高性能AE減水剤がある。変性ポリカルボン酸系AE減水剤の市販品例としてはMelfluxAP101F((株)デグサコンストラクション、商品名)が、ポリエーテル・ポリカルボン酸系の高性能AE減水剤の市販品例としてはMelflux2641F((株)デグサコンストラクション、商品名)が挙げられる。これらのAE減水剤は水硬性セメント100重量部に対し0.1重量部から1重量部を配合することで水硬性セメントを十分に分散させた上で塗材組成物の粘度を低下させ、次に示す粘弾性調整剤をさらに配合することによって本発明の所定の粘度とT.I値に調整することが出来る。
Water reducing agents include anionic, nonionic, cationic or amphoteric AE agents and lignin sulfonates, sulfonates of higher polyhydric alcohols, oxyorganic acids, alkylaryl sulfonates, polyoxys A water reducing agent of ethylene alkyl ether, polycarboxylic acid or polyol complex, or a complex or mixture thereof can be used, but the modified polycarboxylic acid or polyether / polycarboxylic acid is most effective. There is a high-performance AE water reducing agent. Melflux AP101F (Degussa Construction Co., Ltd., trade name) is an example of a commercial product of a modified polycarboxylic acid-based AE water reducing agent, and Mellux2641F ((Co., Ltd.) is an example of a commercial product of a polyether / polycarboxylic acid-based high-performance AE water reducing agent ) Degussa Construction, trade name). These AE water reducing agent reduces the viscosity of the coating material composition on to sufficiently disperse the hydraulic cement by blending 1 part by weight from 0.1 parts by weight per 100 parts by weight of hydraulic cement, following Further blending the viscoelasticity adjusting agent shown in FIG. It can be adjusted to I value.

粘弾性調整剤は、塗材組成物のダレを防止する目的で配合するものであり、一般に無機系、金属石鹸系、天然物系、セルロース誘導体系、ポリカルボン酸系、ポリエーテル誘導体系、ポリビニル系があり、本発明に於いては高分子の強固な網目構造を有する高分子型が最も好ましい。市販粘弾性調整剤としては高分子型のVPWR40F((株)デグサコンストラクション、商品名)がある。配合量は水硬性セメント100重量部に対して0.05〜0.15重量部の割合で混合され、この範囲であれば垂直面への塗付時にタレが生ぜず塗付作業性が良好となる。
The viscoelasticity modifier is blended for the purpose of preventing sagging of the coating composition, and is generally inorganic, metal soap, natural product, cellulose derivative, polycarboxylic acid, polyether derivative, polyvinyl. In the present invention, the polymer type having a strong polymer network structure is most preferred. As a commercially available viscoelasticity adjusting agent, there is a polymer type VPWR40F (Degussa Construction Co., Ltd., trade name). The blending amount is mixed at a ratio of 0.05 to 0.15 parts by weight with respect to 100 parts by weight of hydraulic cement, and if it is within this range, no sagging occurs when applying to a vertical surface and the coating workability is good. Become.

骨材は通常水硬性材料と混合して使用できるものであれば良いが、鏝さばきを良好とするにはJISG5901の48号〜150号のけい砂であることが好ましく、前記、水硬性セメントと水の重量比、及び全固形分重量に対する樹脂固形分重量にて配合成分と配合量が確定するので、実際には残る成分となる。骨材は粒径等が同じであれば、等しい効果が得られるものの、コスト、入手性から、けい砂が最適となる。JISG5901の150号より細かいと粘度が高くなり、鏝作業性が低下し、48号より大きいと強度、収縮による割れ、骨材の凹凸により表面仕上り性が劣る結果となる。市販品としては東北珪砂6、7号(北日本産業(株)、商品名)等がある。   The aggregate may be any material as long as it can be used in combination with a hydraulic material. However, in order to improve the cocoon handling, it is preferably JIS G5901 No. 48-150 silica sand, Since the blending component and blending amount are determined by the weight ratio of water and the resin solid content weight relative to the total solid weight, it is actually the remaining component. If the aggregate has the same particle size and the like, the same effect can be obtained, but silica sand is optimal from the viewpoint of cost and availability. If it is finer than JIS G5901, No. 150, the viscosity becomes high, and the workability of dredging is lowered. Commercially available products include Tohoku Silica Sand 6 and 7 (Kitanippon Sangyo Co., Ltd., trade name).

配合物の混合形態として、エポキシ樹脂、水系硬化剤、水、水硬性成分、骨材、減水剤、粘弾性調整剤が主たる配合物であるが、2液、1粉体とするのが使用に際して好ましい。すなわち、水系硬化剤と水、エポキシ樹脂、骨材と減水剤と粘弾性調整剤と水硬性成分とするのが、混合・分散不十分、特性の失活、計量ミス・誤差を防ぐには好ましいが、別個に配合しても構わない。   As the mixing form of the compound, epoxy resin, water-based curing agent, water, hydraulic component, aggregate, water reducing agent, viscoelasticity adjusting agent are the main compounds. preferable. That is, it is preferable to use an aqueous curing agent and water, an epoxy resin, an aggregate, a water reducing agent, a viscoelasticity modifier, and a hydraulic component in order to prevent insufficient mixing / dispersion, property deactivation, measurement errors, and errors. However, you may mix | blend separately.

本発明の塗材組成物はコンクリートに1.0〜6.0kg/m塗付できるが、2.0kg/m程度が塗付作業性の点で適当である。1.0kg/m未満では下地上に均一な厚みに塗付することが難しく、6.0kg/m超では垂直面に塗布することが難しくなる。コンクリートが打設後10日以上のコンクリート下地に対しては、コンクリート表面の水分が揮散してコンクリート表面の細孔が空洞状態になっていることから、塗付した塗材組成物の水分だけがコンクリート表面に吸い込まれて水成分が減少し塗付した塗材組成物の組成が硬化前に変化して硬化不良となる恐れがあり、これを防止するため予めプライマーとして、本発明の樹脂部(エポキシ樹脂と水系硬化剤及び水を混合したもの)を0.1kg/m程度塗付するか、当該樹脂部に普通ポルトランドセメンとを1:1で配合し、金鏝で下地コンクリート表面に擦り込むように塗布しておくことが望ましい。 Coating material composition of the present invention can 2 with coating 1.0~6.0kg / m concrete, about 2.0 kg / m 2 is appropriate from the viewpoint of coating workability. If it is less than 1.0 kg / m 2 , it is difficult to apply a uniform thickness on the substrate, and if it exceeds 6.0 kg / m 2 , it is difficult to apply to a vertical surface. For concrete foundations of 10 days or more after the concrete is placed, the moisture on the concrete surface is volatilized and the pores on the concrete surface are in a hollow state, so only the moisture of the applied coating composition is There is a risk that the composition of the coating composition applied by reducing the water component by being sucked into the concrete surface will change before curing, resulting in poor curing, and as a primer to prevent this, the resin part ( Apply a mixture of epoxy resin, water-based curing agent and water (approx. 0.1 kg / m 2 ), or mix 1: 1 with normal Portland cement in the resin part, and rub against the surface of the underlying concrete with a hammer. It is desirable to apply it so that

本発明の塗材組成物を塗付後、重層できるライニング材としてはビニルエステル樹脂塗材及びエポキシ樹脂塗材に限定されない。例えば衝突混合型のポリウレア樹脂塗材やローラー刷毛で塗付可能なポリウレア樹脂塗材であってもよく、これらのポリウレア樹脂塗材は、本発明の塗材組成物が硬化後、エポキシプライマーを塗付した上で吹付け又はローラー刷毛により塗付する。ライニング材の市販品としてはビニルエステル樹脂塗材としてジョリエースJE−2503(アイカ工業(株)、商品名)、エポキシ樹脂塗材としてダイナミックレジンC333(アイカ工業(株)、商品名)等がある。   The lining material that can be overlaid after applying the coating composition of the present invention is not limited to vinyl ester resin coating materials and epoxy resin coating materials. For example, a collision-mixing type polyurea resin coating material or a polyurea resin coating material that can be applied with a roller brush may be used. These polyurea resin coating materials are coated with an epoxy primer after the coating composition of the present invention is cured. Apply with spray or roller brush. Commercially available lining materials include Joliace JE-2503 (Aika Industry Co., Ltd., trade name) as a vinyl ester resin coating material, and Dynamic Resin C333 (Aika Industry Co., Ltd., trade name) as an epoxy resin coating material. .

以下、実施例及び比較例にて詳細に説明する。 Hereinafter, it demonstrates in detail in an Example and a comparative example.

攪拌機にジョリエースJEX210A(アイカ工業(株)製エポキシ樹脂、商品名、エポキシ当量180、固形分100%、粘度0.7Pa・s/25℃)100重量部とジョリエースJEX210B(アイカ工業(株)製エポキシ樹脂硬化剤、商品名、活性水素当量750、固形分18%水溶液、粘度7mPa・s/25℃)400重量部を入れ、けい砂(JISけい砂100号)400重量部、ホワイトセメント(太平洋セメント(株)、白色ポルトランドセメント)820重量部、減水剤Melflux AP101F((株)デグサコンストラクション、商品名、変成ポリカルボン酸系減水剤)5重量部、粘弾性調整剤としてVPWR40F((株)デグサコンストラクション、商品名)を1重量部配合し、水と水硬性セメントの重量比0.4:1、樹脂固形分重量が全固形分重量に対して10%の塗材組成物を調製し、実施例1とした。
Jolies JEX210A (epoxy resin manufactured by Aika Kogyo Co., Ltd., trade name, epoxy equivalent 180, solid content 100%, viscosity 0.7 Pa · s / 25 ° C.) and Jolias JEX210B (Aika Kogyo Co., Ltd.) Epoxy resin curing agent, trade name, active hydrogen equivalent 750, solid content 18% aqueous solution, viscosity 7 mPa · s / 25 ° C) 400 parts by weight, silica sand (JIS silica sand No. 100) 400 parts by weight, white cement ( Taiheiyo Cement Co., Ltd., White Portland Cement) 820 parts by weight, water reducing agent Melflux AP101F (Degussa Construction Co., Ltd., trade name, modified polycarboxylic acid water reducing agent) 5 parts by weight, VPWR40F (Co) Degussa construction, trade name) were blended 1 part by weight, the weight ratio of water to hydraulic cement .4: 1, the resin solids weight of 10 percent of the coating material composition was prepared based on the total solid content weight was as in Example 1.

実施例1の白色ポルトランドセメントを普通ポルトランドセメント(太平洋セメント(株)製)に換えた以外同じに行い、実施例2とした。   Example 2 was carried out in the same manner except that the white Portland cement of Example 1 was replaced with ordinary Portland cement (manufactured by Taiheiyo Cement Co., Ltd.).

実施例1のけい砂を830重量部とし、水と水硬性セメントの重量比0.4:1、樹脂固形分重量8%とした以外同じに行い、実施例3とした。
Example 3 was carried out in the same manner except that the silica sand of Example 1 was changed to 830 parts by weight, the weight ratio of water to hydraulic cement was 0.4: 1 , and the resin solid content was 8%.

実施例3のホワイトセメント1090重量部、けい砂を560重量部とし、水と水硬性セメントの重量比0.3:1、樹脂固形分重量8%とした以外同じに行い、実施例4とした。
Example 4 was carried out in the same manner as in Example 3, except that 1090 parts by weight of white cement and 560 parts by weight of silica sand were used, and the weight ratio of water to hydraulic cement was 0.3: 1 and the resin solid content was 8%. .

実施例3のホワイトセメントを1385重量部、けい砂を825重量部とし、水160重量部を追加し、水と水硬性セメントの重量比0.35:1、樹脂固形分重量6%とした以外同じに行い、実施例5とした。
The white cement of Example 3 was 1385 parts by weight, the silica sand was 825 parts by weight, 160 parts by weight of water was added, and the weight ratio of water to hydraulic cement was 0.35: 1 and the resin solid content was 6%. This was done in the same way as Example 5.

実施例3のホワイトセメントを2120重量部、けい砂を1265重量部とし、水を415重量部を追加し、水と水硬性セメントの重量比0.35:1、樹脂固形分重量4%とした以外同じに行い、実施例6とした。
The white cement of Example 3 was 2120 parts by weight, the silica sand was 1265 parts by weight, 415 parts by weight of water was added, and the weight ratio of water to hydraulic cement was 0.35: 1 , and the resin solid content was 4% by weight. Example 6 was performed in the same manner.

比較例1
実施例3のホワイトセメントを1090重量部,けい砂を1280重量部とし,水と水硬性セメントの重量比0.3:1,樹脂固形分重量6%とした以外同じに行い,比較例1とした。
Comparative Example 1
Comparative Example 1 was carried out in the same manner as in Example 3 except that the white cement was 1090 parts by weight, the silica sand was 1280 parts by weight, and the weight ratio of water to hydraulic cement was 0.3: 1 and the resin solid content was 6%. did.

比較例2
実施例3のけい砂を1550重量部とし,水と水硬性セメントの重量比0.4:1,樹脂固形分重量6%とした以外同じに行い,比較例2とした。
Comparative Example 2
Comparative Example 2 was carried out in the same manner except that the silica sand of Example 3 was changed to 1550 parts by weight and the weight ratio of water to hydraulic cement was 0.4: 1 and the resin solid content was 6%.

比較例3
実施例1のホワイトセメントを4330重量部,けい砂を2580重量部とし,水1190重量部を追加し,水と水硬性セメントの重量比0.35:1,樹脂固形分重量2%とした以外同じに行い,比較例3とした。
Comparative Example 3
The white cement of Example 1 was 4330 parts by weight, the silica sand was 2580 parts by weight, 1190 parts by weight of water was added, and the weight ratio of water to hydraulic cement was 0.35: 1, and the resin solid content was 2% by weight. This was done in the same manner as Comparative Example 3 .

比較例4
実施例1のホワイトセメントを660重量部,けい砂を990重量部とし,水と水硬性セメントの重量比0.5:1,樹脂固形分重量8%とした以外同じに行い,比較例4とした。
Comparative Example 4
Comparative Example 4 was carried out in the same manner as in Example 1 except that 660 parts by weight of white cement and 990 parts by weight of silica sand were used, and the weight ratio of water to hydraulic cement was 0.5: 1 and the resin solid content was 8%. did.

比較例5
塗材組成物なし,下塗りを行なわないものとして比較例5とした。
Comparative Example 5
Comparative Example 5 was designated as having no coating composition and no undercoating.

表1に実施例及び比較例の結果を示す。   Table 1 shows the results of Examples and Comparative Examples.

Figure 0005460956
Figure 0005460956

評価方法 Evaluation method

総細孔量:本発明の塗材組成物をガラスシャーレ内に厚さ3mmで流し込み、24時間後にシャーレ内より取り出した後、ハンマーで細かく砕く。次にふるいにより2.5〜5.0mmの破砕片を取り出し真空脱水とドライアイスによるトラップ処理(D−dry処理)をして、塗材組成物中の水分を除去した上で水銀圧入法により測定した。測定には島津製作所製自動ポロシメータオートポアIV9500を使用した。   Total pore amount: The coating composition of the present invention is poured into a glass petri dish at a thickness of 3 mm, taken out from the petri dish after 24 hours, and then finely crushed with a hammer. Next, 2.5 to 5.0 mm fragments are removed by sieving, vacuum dehydration and trapping with dry ice (D-dry treatment) are performed, water in the coating composition is removed, and mercury intrusion is used. It was measured. For the measurement, an automatic porosimeter Autopore IV9500 manufactured by Shimadzu Corporation was used.

耐ふくれ性:水硬性セメントと水の重量比0.8のコンクリートをφ200×150mmの円柱型とし、材齢1日、4日、10日のものを調製する。この上面に実施例の塗材組成物を2.0kg/m塗付1日後、プライマーである一液湿気硬化型ウレタンプライマーのジョリエースJU‐1270(アイカ工業(株)、商品名)を0.1kg/m塗付し、指触乾燥後、ビニルエステル樹脂塗材としてジョリエースJE2503を0.4kg/m塗布し直ちにJR−94KM(ガラスマット#380、アイカ工業(株)、商品名)を貼り付け含浸させ、更にビニルエステル樹脂塗材ジョリエースJE2503を0.6kg/m塗布することによりビニルエステル樹脂塗材でライニングした。またこれとは別に当該ビニルエステル樹脂塗材の代わりにエポキシ樹脂塗材としてダイナミックレジンC−333を0.7kg/m塗布し、硬化後更に同塗材を0.7kg/m塗布し、エポキシ樹脂塗材によりライニングした。これらを7日間23℃にて静置後、試験体とし、試験体の上面より、10mmを残して、28日30℃温水に浸漬する。発生したふくれの状態を目視にて観察するとともにふくれを透明なシートに写し取る。中央部100φ部分をふくれ観察部位とし、100φ部分に発生したふくれ面積を100φ部分の面積で除してふくれ面積%とする。各材齢全てのふくれ面積%が1%未満のものを○、前記以外を×とする。 Swelling resistance: Concrete having a weight ratio of 0.8 and a hydraulic cement and water is made into a cylindrical shape of φ200 × 150 mm, and those having a material age of 1 day, 4 days, and 10 days are prepared. One day after the coating composition of the example was applied to the upper surface at a rate of 2.0 kg / m 2 , the one-part moisture-curing urethane primer Jolieth JU-1270 (Aika Industry Co., Ltd., trade name) was set to 0. Apply 1 kg / m 2 , dry to the touch, and then apply 0.4 kg / m 2 of Jolieth JE2503 as a vinyl ester resin coating material and immediately apply JR-94KM (Glass Mat # 380, Aika Industry Co., Ltd., trade name) ) Was applied and impregnated, and further coated with a vinyl ester resin coating material by applying 0.6 kg / m 2 of a vinyl ester resin coating material Joliase JE2503. It also Separately dynamic Resin C-333 0.7kg / m 2 was applied in place of the vinyl ester resin coating material as epoxy resin coating material, further the same coating material 0.7 kg / m 2 was applied after curing, Lined with epoxy resin coating. These were allowed to stand at 23 ° C. for 7 days, then used as test specimens, and immersed in 30 ° C. warm water for 28 days, leaving 10 mm from the top surface of the test specimens. Observe the state of the blisters generated visually and copy the blisters onto a transparent sheet. The center 100φ portion is defined as a blister observation site, and the blister area generated in the 100φ portion is divided by the area of the 100φ portion to obtain a blister area%. The bulging area% of all ages is less than 1%, and the others are marked with x.

鏝作業性:90×90cmの8mm厚フレキシブル板を水平に置き、これに塗材組成物を塗付し評価する。全ての目隠しサンプルを官能評価し、金鏝が重くないものを○とし、それ以外のものを×とした。金鏝が重くないというのは、金鏝にかかる力がおおよそ1N以下となるものである。   鏝 Workability: An 8 mm thick flexible plate of 90 × 90 cm is placed horizontally, and a coating material composition is applied thereto for evaluation. All the blindfold samples were subjected to sensory evaluation, and those that were not heavy were marked with ◯, and those other than that were marked with ×. The fact that the hammer is not heavy means that the force applied to the hammer is about 1 N or less.

タレ性:JISA5371付属書2普通平板呼び300の規定に適合する300×300×60mmのコンクリート平板表面を高圧水洗して表面の脆弱部を除去する。平板の表面が垂直になるように保持したまま塗材組成物を金鏝で塗り付け、タレが生じないものを○、それ以外を×とした。   Sagging property: The surface of a 300 × 300 × 60 mm concrete flat plate that complies with the provisions of JIS A5371 Annex 2 normal flat plate nominal 300 is washed with high-pressure water to remove weak portions on the surface. The coating material composition was applied with a hammer while keeping the surface of the flat plate vertical.

遮水性:厚さ1mmの塩ビ板の上に塗材組成物を2kg/m(1mm厚み)で塗布し、48時間後に塩ビ板を脱型する。その後塗材組成物を7日間養生して試験体とし下地の無い塗材組成物層のみで JISA6909の透水試験B法の透水量を測定した。0.2ml以下で防水性能を有すると判断し、これを○とした。 Water impermeability: A coating composition is applied at a rate of 2 kg / m 2 (1 mm thickness) onto a 1 mm thick PVC plate, and the PVC plate is demolded after 48 hours. Thereafter, the coating material composition was cured for 7 days to obtain a test body, and the water permeability of the water permeability test B method of JISA 6909 was measured only with the coating material composition layer having no base. It was judged that it had waterproof performance at 0.2 ml or less, and this was set as (circle).

上塗り付着性1:上記耐ふくれ性試験終了後の試験体のうちビニルエステル樹脂塗材をライニングした試験体を使用し、試験終了後ヒーターの電源を遮断し水温を23℃とする。この状態で24時間放置し、水中から試験体を取り出し、カッターナイフにて前記ビニルエステル樹脂塗材が3cm×5cm残るようにその周囲を除去する。その上で残ったビニルエステル樹脂塗材の短辺側(3cm)部分の塗材(図1及び図2においては塗材10)と塗材組成物層(図1及び図2においては被塗物11)との界面に図1及び図2に示す付着力測定器の刃先1を挿入させ、刃先1に荷重することによりビニルエステル樹脂塗材と塗材組成物層との界面に刃先1をさらに挿入進展させ、ビニルエステル樹脂塗材を塗材組成物表層から剥離させ、剥離時の荷重を付着力とし付着性を評価した。付着力測定器の正面図を図1に、同平面図を図2に示す。刃先角度は11°とし、本付着力測定器での測定値が10N/cm以上を○とし、それ以外を×とする。   Top coat adhesion 1: Use the test body lined with the vinyl ester resin coating material among the test bodies after completion of the blistering resistance test, and turn off the heater power and set the water temperature to 23 ° C. after the test. The sample is left in this state for 24 hours, and the specimen is taken out of the water, and its periphery is removed with a cutter knife so that the vinyl ester resin coating material remains 3 cm × 5 cm. The coating material (the coating material 10 in FIGS. 1 and 2) and the coating material composition layer (the objects to be coated in FIGS. 1 and 2) on the short side (3 cm) portion of the remaining vinyl ester resin coating material. 11) is inserted into the interface with the adhesive force measuring device shown in FIGS. 1 and 2, and the blade edge 1 is further applied to the interface between the vinyl ester resin coating material and the coating composition layer by loading the blade edge 1. Insertion progressed, the vinyl ester resin coating material was peeled from the coating composition surface layer, and the adhesiveness was evaluated using the load at the time of peeling as the adhesive force. A front view of the adhesion measuring device is shown in FIG. 1, and a plan view thereof is shown in FIG. The cutting edge angle is 11 °, and the measured value with this adhesive force measuring instrument is 10 N / cm or more as ◯, and the others are as x.

上塗り付着性2:上記耐ふくれ性試験終了後の試験体のうちエポキシ樹脂塗材をライニングした試験体を使用し、試験終了後ヒーターの電源を遮断し水温を23℃とする。この状態で24時間放置し、水中から試験体を取り出し、カッターナイフにて前記エポキシ樹脂塗材が3cm×5cm残るようにその周囲を除去する。その上で残ったエポキシ樹脂塗材の短辺側(3cm)部分の塗材(図1及び図2においては塗材10)と塗材組成物層(図1及び図2においては被塗物11)との界面に図1及び図2に示す付着力測定器の刃先1を挿入させ、刃先1に荷重することによりエポキシ樹脂塗材と塗材組成物層との界面に刃先1をさらに挿入進展させ、エポキシ樹脂塗材を塗材組成物表層から剥離させ、剥離時の荷重を付着力とし付着性を評価した。付着力測定機の正面図を図1に、同平面図を図2に示す。刃先角度は11°とし、本付着力測定機での測定値が10N/cm以上を○とし、それ以外を×とする。   Top coat adhesion 2: A test body lined with an epoxy resin coating material is used among the test bodies after completion of the above-mentioned blistering resistance test, and after the test is completed, the heater is turned off and the water temperature is set to 23 ° C. The sample is left in this state for 24 hours, and the specimen is taken out from the water, and the periphery thereof is removed with a cutter knife so that the epoxy resin coating material remains 3 cm × 5 cm. The coating material (the coating material 10 in FIGS. 1 and 2) and the coating material composition layer (the coating object 11 in FIGS. 1 and 2) on the short side (3 cm) portion of the epoxy resin coating material remaining thereon. 1 and FIG. 2 is inserted into the interface with the cutting edge 1 and the cutting edge 1 is further inserted into the interface between the epoxy resin coating material and the coating composition layer by loading the cutting edge 1. Then, the epoxy resin coating material was peeled from the surface layer of the coating material composition, and the adhesiveness was evaluated using the load at the time of peeling as the adhesive force. A front view of the adhesion measuring machine is shown in FIG. 1, and a plan view thereof is shown in FIG. The cutting edge angle is 11 °, and the measured value with this adhesive force measuring machine is 10 N / cm or more as ◯, and the others are as x.

評価結果のまとめ:実施例1乃至実施例6ではすべての評価結果が良好であった。従って総細孔量が0.05cc/g以上0.2cc/g以下であって、水硬性セメントと水の重量比が0.3以上0.4以下、かつ樹脂固形分重量が全固形分重量に対して4%以上10%以下であって、粘度が5Pa・s以上40Pa・s以下/23℃、かつT.I値が4.0〜7.0であり,JISA6909の透水試験B法の透水量が0.2ml以下あれば、防食ライニング材下地に好適に使用でき、高含水率のコンクリート下地であっても付着性に優れ、強靭で、下地コンクリートからの水分の透過を防止する塗材組成物及びコンクリート防食施工方法並びにそれによるコンクリート防食構造となる。
Summary of evaluation results: In Examples 1 to 6, all the evaluation results were good. Accordingly, the total pore amount is 0.05 cc / g or more and 0.2 cc / g or less, the weight ratio of hydraulic cement to water is 0.3 or more and 0.4 or less, and the resin solid content weight is the total solid content weight. And a viscosity of 5 Pa · s to 40 Pa · s / 23 ° C. If the I value is 4.0 to 7.0 and the water permeability of the water permeability test B method of JISA 6909 is 0.2 ml or less, it can be suitably used as an anticorrosion lining material base, and even a high water content concrete base The coating composition and the concrete anticorrosion construction method are excellent in adhesion, tough, and prevent the permeation of moisture from the base concrete, and the concrete anticorrosion structure thereby.

以下、上記上塗り付着性1で使用した付着力測定器の概念の詳細を示す。   Hereinafter, the details of the concept of the adhesive force measuring device used in the above-mentioned top coat adhesion 1 will be described.

図1及び図2に示した付着力測定器であるが、当該付着力測定器は刃先(刃物)1と、刃先1に角度(図1においては11°)を保持させる支持輪2と、刃先1を先端方向に被測定物である塗材10側に連結棒6及び秤外筒8を介して押し付けるための取っ手3と、この押力の最大を測定する器具4(筒状のばね秤)からなる。当該付着力測定器は、被塗物11に塗材10が塗付されて硬化した後、所定の幅に切り出された被測定物である塗材10の端部において、塗材10と被塗物11の付着界面に刃先1の先端を、取って3を手で握りながら押し付け、塗材10が被塗物11より剥離する際の最大応力を、押力の最大を測定する器具4によって測定するものである。   1 and FIG. 2, the adhesive force measuring device includes a blade edge (blade) 1, a support wheel 2 that holds the blade edge 1 at an angle (11 ° in FIG. 1), and a blade edge. A handle 3 for pressing 1 to the coating material 10 side to be measured in the tip direction via a connecting rod 6 and a scale outer cylinder 8, and an instrument 4 for measuring the maximum pressing force (cylindrical spring balance) Consists of. The adhesive force measuring device applies the coating material 10 to the coating material 10 at the end of the coating material 10 which is the measurement object cut out to a predetermined width after the coating material 10 is applied to the coating material 11 and cured. The tip of the blade edge 1 is taken against the adhesion interface of the object 11 and pressed while grasping the hand 3 by hand, and the maximum stress when the coating material 10 is peeled off from the object 11 is measured by the instrument 4 that measures the maximum pressing force. To do.

押力の最大を測定する器具4は秤外筒8に秤内筒9が擦動自在に内接され、該秤内筒9の下側前後には連結棒6が略垂直に固着され、該連結棒6には刃先1と一体となったカワスキが固着されている。秤内筒9は秤外筒8の内部において秤外秤8の取って3側の端部にコイルバネ(図示せず)によって張着されている。従って秤内筒9の後端部(図1において右側)は秤外筒8の開放右端(図1において右側)より突出し、刃先1が塗材10に押し付けられると、その押力が大きくなるにつれ、秤内筒9の後端部が序々に秤外筒8の開放右端から遠ざかるように摺動する。つまり、前記コイルバネ(図示せず)が伸展することによって刃先1が塗材10に押し付けられる力も大きくなることになる。測定時において秤内筒9が最大に摺動した時点が刃先1が塗材10に最も大きな力で押されたこととなり、その際塗材10は被塗物11より剥離することになる。この秤内筒9の最大の摺動位置が置き針5によって秤外筒8の所定位置に添着されて、塗材10が被塗物11より剥離して秤内筒9が秤外筒8内にすべて収納され図1の状態になった後でも、置き針5が置かれた位置によって刃先1が塗材10に押し付けられた力を読み取ることが出来るものである。なお12は秤外筒8の下部前後に渡って細長に設けられた秤外筒の切り欠き部であり、この秤外筒の切り欠き部12を連通して連結部6が秤内筒9と固着されている。また7は両側に配置された2個の支持輪2を回転自在に固着する支持輪台であり、前記刃先1と一体となったカワスキの下側に固着されている。刃先1の角度は当該支持輪2の位置を前後することや支持輪2の直径を変化させることにより変えることが出来る。つまり支持輪2の位置を図1において左側に移動させ、又は支持輪2の直径を小さくすることにより刃先1の角度を小さくすることが出来る。   In the instrument 4 for measuring the maximum pressing force, a scale inner cylinder 9 is slidably inscribed on a scale outer cylinder 8, and connecting rods 6 are fixed substantially vertically on the lower and front sides of the scale inner cylinder 9. A kawaski integrated with the cutting edge 1 is fixed to the connecting rod 6. The inner cylinder 9 is attached to the end of the outer scale 8 inside the outer cylinder 8 by a coil spring (not shown). Accordingly, the rear end portion (right side in FIG. 1) of the inner cylinder 9 protrudes from the open right end (right side in FIG. 1) of the balance outer cylinder 8, and when the cutting edge 1 is pressed against the coating material 10, the pressing force increases. The rear end portion of the inner cylinder 9 slides gradually away from the open right end of the outer cylinder 8. That is, the force with which the blade edge 1 is pressed against the coating material 10 is increased by the extension of the coil spring (not shown). At the time of measurement, the point at which the inner cylinder 9 slides to the maximum is that the cutting edge 1 is pressed against the coating material 10 with the greatest force, and the coating material 10 is peeled off from the article 11 at that time. The maximum sliding position of the inner cylinder 9 is attached to a predetermined position of the outer cylinder 8 by the placing needle 5, the coating material 10 is peeled off from the object 11 to be coated, and the inner cylinder 9 is in the outer cylinder 8. Even after all the components are stored in the state shown in FIG. 1, the force with which the blade edge 1 is pressed against the coating material 10 can be read according to the position where the setting needle 5 is placed. Reference numeral 12 denotes a notch portion of the outer scale cylinder that is provided in a slender shape across the lower part of the outer scale cylinder 8. The notch 12 of the outer scale cylinder communicates with the connecting portion 6 to connect with the inner scale cylinder 9. It is fixed. Reference numeral 7 denotes a support wheel base for rotatably fixing the two support wheels 2 arranged on both sides, and is fixed to the lower side of the Kawasuki integrated with the blade edge 1. The angle of the blade edge 1 can be changed by moving the position of the support wheel 2 back and forth or changing the diameter of the support wheel 2. That is, the angle of the blade edge 1 can be reduced by moving the position of the support wheel 2 to the left in FIG. 1 or reducing the diameter of the support wheel 2.

なお押力の最大を測定する器具4は図1及び図2では円筒状のバネ秤を用いたが、デジタルセンサー式でも構わない。   The instrument 4 for measuring the maximum pressing force uses a cylindrical spring balance in FIGS. 1 and 2, but may be a digital sensor type.

付着力測定器の正面図である。It is a front view of an adhesive force measuring device. 付着力測定器の平面図である。It is a top view of an adhesive force measuring device.

符号の説明Explanation of symbols

1 刃先(刃物)
2 支持輪
3 取っ手(秤外筒に固定する。)
4 押力の最大を測定する器具
5 置き針(最大値を示す針)
6 連結棒(刃物と秤内筒を固定する。)
7 支持輪台(刃先方向に前後させることに角度を変える。)
8 秤外筒
9 秤内筒
10 塗材
11 被塗物
12 秤外筒の切り欠き部

1 Cutting edge (blade)
2 Support wheel 3 Handle (fixed to the balance outer cylinder)
4 Instrument for measuring maximum pressing force 5 Placement needle (needle showing maximum value)
6 Connecting rod (fix the blade and inner cylinder)
7 Support wheel base (change the angle to move back and forth in the direction of the blade edge)
8 Weighing outer cylinder 9 Weighing inner cylinder 10 Coating material 11 Object to be coated 12 Notch of scale outer cylinder

Claims (9)

水硬性セメントと骨材と水系エポキシ樹脂と減水剤と粘弾性調整剤を含む水系エポキシ樹脂モルタル組成物であって、水と水硬性セメントの重量比が0.3:1以上0.4:1以下であり、樹脂固形分重量が全固形分重量に対して4%以上10%以下であり、減水剤は水硬性セメント100重量部に対し0.1〜1重量部であり、粘弾性調整剤は水硬性セメント100重量部に対して0.05〜0.15重量部であり、硬化物の総細孔量が0.05cc/g以上0.2cc/g以下であり、混合直後における粘度が5Pa・s以上40Pa・s以下/23℃であり且つT.I値が4.0〜7.0であり、JISA6909の透水試験B法の透水量が0.2ml以下であり、水硬性セメントと骨材と減水剤と粘弾性調整剤から成る1粉体と、液状エポキシ樹脂の1液と、水系硬化剤と水とから成る1液、とから成ることを特徴とする塗材組成物。 A water-based epoxy resin mortar composition comprising a hydraulic cement, an aggregate, a water-based epoxy resin, a water reducing agent, and a viscoelasticity modifier, wherein the weight ratio of water to the hydraulic cement is 0.3: 1 or more and 0.4: 1. The resin solid content weight is 4% or more and 10% or less with respect to the total solid content weight, and the water reducing agent is 0.1 to 1 part by weight with respect to 100 parts by weight of the hydraulic cement. Is 0.05 to 0.15 parts by weight with respect to 100 parts by weight of hydraulic cement , the total pore amount of the cured product is 0.05 cc / g or more and 0.2 cc / g or less, and the viscosity immediately after mixing is 5 Pa · s to 40 Pa · s / 23 ° C. An I value of 4.0 to 7.0, a water permeability of the water permeability test B method of JISA 6909 is 0.2 ml or less, and one powder composed of hydraulic cement, aggregate, water reducing agent, and viscoelasticity modifier; A coating composition comprising a liquid epoxy resin, and a liquid composed of an aqueous curing agent and water . 前記水系エポキシ樹脂は、非乳化型のエポキシ樹脂と自己乳化型の硬化剤とを配合したものであることを特徴とする請求項1記載の塗材組成物。   The coating composition according to claim 1, wherein the water-based epoxy resin is a mixture of a non-emulsifying type epoxy resin and a self-emulsifying type curing agent. 前記水硬性セメントが白セメントであることを特徴とする請求項1または請求項2記載の塗材組成物。   The coating material composition according to claim 1, wherein the hydraulic cement is white cement. コンクリート表面に請求項1乃至請求項3のいずれか記載の塗材組成物を塗付して硬化させ、一液湿気硬化型ウレタンプライマーを塗付した後、ビニルエステル樹脂塗材をライニングすることを特徴とするコンクリート防食施工方法。   Applying the coating composition according to any one of claims 1 to 3 to a concrete surface and curing it, applying a one-component moisture-curing urethane primer, and then lining the vinyl ester resin coating material. Concrete anticorrosion construction method. コンクリート表面に請求項1乃至請求項3のいずれか記載の塗材組成物を塗付して硬化させ、エポキシ樹脂塗材をライニングすることを特徴とするコンクリート防食施工方法。   A concrete anticorrosion construction method comprising applying a coating composition according to any one of claims 1 to 3 to a concrete surface and curing the composition, and lining an epoxy resin coating. 前記コンクリートが打設後1日以上10日以下の若材齢コンクリートであることを特徴とする請求項4または請求項5記載のコンクリート防食施工方法。   The concrete anticorrosion construction method according to claim 4 or 5, wherein the concrete is young age concrete of 1 day to 10 days after placement. コンクリート表面に請求項1乃至請求項3のいずれか記載の塗材組成物を塗付して硬化させ、一液湿気硬化型ウレタンプライマーを塗付した後、ビニルエステル樹脂塗材をライニングすることを特徴とするコンクリート防食構造。   Applying the coating composition according to any one of claims 1 to 3 to a concrete surface and curing it, applying a one-component moisture-curing urethane primer, and then lining the vinyl ester resin coating material. Characteristic concrete anticorrosion structure. コンクリート表面に請求項1乃至請求項3のいずれか記載の塗材組成物を塗付して硬化させ、エポキシ樹脂塗材をライニングすることを特徴とするコンクリート防食構造。   A concrete anticorrosive structure, characterized in that the coating composition according to any one of claims 1 to 3 is applied to a concrete surface and cured, and an epoxy resin coating is lined. 前記コンクリートが打設後1日以上10日以下の若材齢コンクリートであることを特徴とする請求項7または請求項8記載のコンクリート防食構造。
The concrete anticorrosive structure according to claim 7 or 8, wherein the concrete is young age concrete of 1 day to 10 days after placement.
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