JP2003226861A - Water-cutting-off agent and water-cutting-off method - Google Patents
Water-cutting-off agent and water-cutting-off methodInfo
- Publication number
- JP2003226861A JP2003226861A JP2002026157A JP2002026157A JP2003226861A JP 2003226861 A JP2003226861 A JP 2003226861A JP 2002026157 A JP2002026157 A JP 2002026157A JP 2002026157 A JP2002026157 A JP 2002026157A JP 2003226861 A JP2003226861 A JP 2003226861A
- Authority
- JP
- Japan
- Prior art keywords
- water
- liquid
- cutting
- stopping
- concrete structure
- 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.)
- Pending
Links
- 238000000034 method Methods 0.000 title claims abstract description 15
- 239000007788 liquid Substances 0.000 claims abstract description 45
- 229920005862 polyol Polymers 0.000 claims abstract description 30
- 150000003077 polyols Chemical class 0.000 claims abstract description 29
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 28
- 238000002347 injection Methods 0.000 claims abstract description 14
- 239000007924 injection Substances 0.000 claims abstract description 14
- 239000012948 isocyanate Substances 0.000 claims abstract description 11
- 150000002513 isocyanates Chemical class 0.000 claims abstract description 11
- 238000006243 chemical reaction Methods 0.000 claims abstract description 7
- 230000000903 blocking effect Effects 0.000 claims abstract description 4
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- 238000002156 mixing Methods 0.000 claims description 12
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- 239000000243 solution Substances 0.000 abstract description 21
- 239000003795 chemical substances by application Substances 0.000 abstract description 4
- 239000000463 material Substances 0.000 abstract description 4
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- 229920002323 Silicone foam Polymers 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
- 239000007983 Tris buffer Substances 0.000 description 2
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- 150000007513 acids Chemical class 0.000 description 2
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- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 2
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- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- 241001649081 Dina Species 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
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- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
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- 229930006000 Sucrose Natural products 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
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- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- HIFVAOIJYDXIJG-UHFFFAOYSA-N benzylbenzene;isocyanic acid Chemical class N=C=O.N=C=O.C=1C=CC=CC=1CC1=CC=CC=C1 HIFVAOIJYDXIJG-UHFFFAOYSA-N 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- ZFMQKOWCDKKBIF-UHFFFAOYSA-N bis(3,5-difluorophenyl)phosphane Chemical compound FC1=CC(F)=CC(PC=2C=C(F)C=C(F)C=2)=C1 ZFMQKOWCDKKBIF-UHFFFAOYSA-N 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
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Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、止水用薬液及び止
水工法に関する。より詳細には、注入チューブを介して
止水用薬液をコンクリート構造物に注入することにより
コンクリート構造物の漏水を止水する工法(チューブ注
入式止水工法)に関し、特に、道路や鉄道などのトンネ
ルアーチ部のようなコンクリートが注入薬液の発泡圧に
より破壊されやすい部位に好適に用いられる止水用薬液
及びそれを用いた止水工法に関する。TECHNICAL FIELD The present invention relates to a water-stopping chemical solution and a water-stopping method. More specifically, it relates to a method for stopping leakage of water from a concrete structure by injecting a chemical liquid for water stoppage into the concrete structure through an injection tube (tube-injection-type water-stopping method), particularly for roads and railways. The present invention relates to a water-stopping chemical solution suitable for use in a site where concrete such as a tunnel arch is easily broken by the foaming pressure of an injected chemical solution, and a water-stopping method using the same.
【0002】[0002]
【従来の技術】コンクリート構造物は、施工が不十分で
あったり、また、温度や湿度の変化、乾燥収縮、アルカ
リ骨材反応、あるいは地震などの外力が作用すると構造
体に空隙が生じたり、クラックを発生する。従来、この
種の補修を行うには、亀裂内に各種グラウト材を充填し
て行う方法が一般的にとられており、グラウト材として
は水ガラスや水和反応型ウレタンなどが使用されてい
る。2. Description of the Related Art Concrete structures are poorly constructed, and voids are created in the structures when external forces such as temperature and humidity changes, drying shrinkage, alkaline aggregate reaction, or earthquakes act. Generate cracks. Conventionally, in order to carry out this kind of repair, a method of filling various cracks with various grout materials is generally taken, and water glass or hydration reaction type urethane is used as the grout material. .
【0003】[0003]
【発明が解決しようとする課題】しかしながら、水ガラ
スや水和反応型ウレタンは、耐久性に欠け、半永久的な
止水効果は得られない。そこで、特開昭61−1960
70号公報には、止水性と耐久性を有し、2〜120倍
発泡する硬質発泡ウレタンが提案されている。しかし、
発泡ウレタンは発泡硬化する際に非常に大きな発泡圧が
かかり、道路や鉄道などのトンネルのアーチ部のような
背面圧に弱いコンクリート構造物や、こわれやすい部位
には用いることはできない。However, water glass and hydration reaction type urethane lack durability and cannot obtain a semi-permanent water blocking effect. Then, JP-A-61-1960
In Japanese Patent Publication No. 70, a hard urethane foam which has waterproofness and durability and foams by a factor of 2 to 120 is proposed. But,
Urethane foam is subjected to a very large foaming pressure when foamed and hardened, and cannot be used for concrete structures that are vulnerable to back pressure, such as arches of tunnels such as roads and railways, and fragile parts.
【0004】また、コンクリート構造物の止水工法に用
いられる止水用薬液は、その粘度が高いと、微細な亀裂
内に確実に浸透させることが困難である。Further, the water-stopping chemical used in the water-stopping method for concrete structures has a high viscosity, so that it is difficult to surely penetrate into fine cracks.
【0005】本発明は、このような問題点を解決するた
めになされたものであり、特にチューブ注入式止水工法
に用いる止水材として、コンクリート構造物に圧力をか
けず、亀裂などを確実に閉塞し、耐久性に優れた止水用
薬液を提供することを目的としている。The present invention has been made in order to solve such problems, and in particular, as a water-stopping material used in a tube-filling type water-stopping construction method, pressure is not applied to a concrete structure and cracks and the like are surely performed. The purpose of the present invention is to provide a water-stopping chemical solution that is blocked and has excellent durability.
【0006】[0006]
【課題を解決するための手段】上記の目的を達成する本
発明の止水用薬液は、ポリオールを主成分とするA液
と、イソシアネートを主成分とするB液とからなる2液
反応型ポリウレタンの止水用薬液であって、A液及びB
液の粘度がそれぞれ200mPa・s/25℃以下であ
り、A液とB液の反応硬化物の硬度(ショアA)が30
〜80の弾性エラストマーであることを特徴とする。[Means for Solving the Problems] A water-stopping chemical solution of the present invention which achieves the above object is a two-component reactive polyurethane comprising a solution A containing a polyol as a main component and a solution B containing an isocyanate as a main component. Water stopping chemicals of A and B
The viscosity of the liquid is 200 mPa · s / 25 ° C. or less, and the hardness (Shore A) of the reaction cured product of liquid A and liquid B is 30.
It is characterized by being an elastic elastomer of ˜80.
【0007】本発明の止水用薬液においては、A液とB
液が混合されてから硬化するまでの時間が10分以上で
あることが好ましい。In the water-stopping chemical liquid of the present invention, liquid A and liquid B
It is preferable that the time from the mixing of the liquids to the curing is 10 minutes or more.
【0008】また、本発明の止水工法は、コンクリート
構造物に注入チューブを予め埋め込み、漏水した場合あ
るいは漏水するおそれのある場合に該注入チューブを介
して前記止水用薬液を前記コンクリート構造物に注入し
て止水するものである。Further, in the water-stopping method of the present invention, an injection tube is embedded in a concrete structure in advance, and when the water leaks or there is a risk of water leakage, the water-stopping chemical solution is passed through the injection tube to the concrete structure. Water is injected into the water to stop it.
【0009】[0009]
【発明の実施の形態】本発明の止水用薬液においてA液
に用いるポリオールとしては、例えば、1,3-ブタンジオ
ール、1,4-ブタンジオール、1,6-ヘキサンジオールなど
の2価アルコール、エチレングリコール、ジエチレング
リコール、トリエチレングリコール、プロピレングリコ
ール、ジプロピレングリコール、ブチレングリコール、
グリセリン、トリメチロールプロパン、モノ、ジまたは
トリエタノールアミン、ジグリセリン、ソルビトール、
蔗糖などの単独もしくは混合物にプロピレンオキシド、
エチレンオキシドなどのアルキレンオキシドを付加重合
したポリオール、ひまし油などが挙げられる。さらにア
ジピン酸、無水フタル酸などの2塩基酸とエチレングリ
コール、ジエチレングリコール、トリメチロールプロパ
ンなどのグリコールやトリオールとの脱水縮合反応によ
り得られる各種ポリエステルポリオール、ε−カプロラ
クタムの開環重合により得られるラクトン系ポリエステ
ルポリオール、その他ポリカーボネートジオール、アク
リルポリオール、ポリブタジエン系ポリオール、フェノ
ール系ポリオール、さらにポリオール中でアクリロニト
リル、スチレンなどのビニル系モノマーをラジカル重合
させたものや、これらのポリマーをポリオール中に分散
溶解させたポリマーポリオール、テトラヒドロフランの
カチオン重合により得られるポリテトラメチレングリコ
ール、あるいはこれらにアルキレンオキシドを付加重合
した変性ポリオールなどが挙げられる。これらのポリオ
ールの分子量は40〜20000であることが好まし
い。BEST MODE FOR CARRYING OUT THE INVENTION Examples of the polyol used in the liquid A in the water-stopping chemical solution of the present invention include dihydric alcohols such as 1,3-butanediol, 1,4-butanediol, and 1,6-hexanediol. , Ethylene glycol, diethylene glycol, triethylene glycol, propylene glycol, dipropylene glycol, butylene glycol,
Glycerin, trimethylolpropane, mono-, di- or triethanolamine, diglycerin, sorbitol,
Propylene oxide, either alone or in a mixture such as sucrose,
Examples include polyols obtained by addition-polymerizing alkylene oxides such as ethylene oxide, and castor oil. Further, various polyester polyols obtained by dehydration condensation reaction of dibasic acids such as adipic acid and phthalic anhydride with glycols and triols such as ethylene glycol, diethylene glycol and trimethylolpropane, and lactone series obtained by ring-opening polymerization of ε-caprolactam. Polyester polyols, other polycarbonate diols, acrylic polyols, polybutadiene-based polyols, phenol-based polyols, radical-polymerized vinyl-based monomers such as acrylonitrile and styrene in polyols, and polymers obtained by dispersing and dissolving these polymers in polyols. Polytetramethylene glycol obtained by cationic polymerization of polyol or tetrahydrofuran, or modification by addition polymerization of alkylene oxide Estriol and the like. The molecular weight of these polyols is preferably 40 to 20,000.
【0010】上記ポリオールのなかでも、コンクリート
構造物中の水との反応を抑えて非発泡の弾性エラストマ
ーとするため、アルキレンオキシドとしてプロピレンオ
キシドのみを用いて付加重合したプロピレンオキシド付
加重合ポリオールや、ポリブタジエンポリオールなどの
疎水性ポリオールが好ましく用いられる。Among the above polyols, in order to suppress the reaction with water in the concrete structure to form a non-foaming elastic elastomer, a propylene oxide addition-polymerized polyol obtained by addition polymerization using only propylene oxide as an alkylene oxide, and a polybutadiene. Hydrophobic polyols such as polyols are preferably used.
【0011】本発明の止水用薬液においてB液に用いる
イソシアネートとしては、例えば、2,2-、2,4-、4,4-な
どの異性体を含むジフェニルメタンジイソシアネート、
ポリメチレンポリフェニルポリイソシアネート、トリレ
ンジイソシネート、キシリレンジイソシアネート、イソ
ホロンジイソシアネート、ヘキサメチレンジイソシアネ
ート、水添ジフェニルメタンジイソシアネートなどの単
独または混合物、これらイソシアネートの2量体、3量
体やカルボジイミド変成したイソシアネート、さらに上
記ポリオールとイソシアネートの一部を予め反応させた
ウレタンプレポリマーなどが用いられる。The isocyanate used in the liquid B in the water-stopping chemical solution of the present invention includes, for example, diphenylmethane diisocyanate containing isomers such as 2,2-, 2,4-, and 4,4-.
Polymethylene polyphenyl polyisocyanate, tolylene diisocyanate, xylylene diisocyanate, isophorone diisocyanate, hexamethylene diisocyanate, hydrogenated diphenylmethane diisocyanate, singly or in a mixture, dimer, trimer or carbodiimide modified isocyanate of these isocyanates, Further, a urethane prepolymer obtained by previously reacting a part of the above-mentioned polyol and isocyanate is used.
【0012】上記A液及びB液には、ポリオールとイソ
シアネートを反応させるための触媒、粘度を下げるため
の粘度調整剤を添加することができる。To the solutions A and B, a catalyst for reacting a polyol with an isocyanate and a viscosity modifier for decreasing the viscosity can be added.
【0013】触媒としては、通常ウレタン樹脂の反応に
使用される触媒が用いられる。例えば、ジメチルオクチ
ルアミン、ジメチルラウリルアミン、モルホリン、ピペ
ラジン、トリエチレンジアミン、ビスジメチルアミノエ
チルエーテル、イミダゾールなどのアミン触媒、ジブチ
ル錫ラウレートなどの金属触媒があげられる。As the catalyst, a catalyst usually used for the reaction of urethane resin is used. Examples thereof include amine catalysts such as dimethyloctylamine, dimethyllaurylamine, morpholine, piperazine, triethylenediamine, bisdimethylaminoethyl ether and imidazole, and metal catalysts such as dibutyltin laurate.
【0014】粘度調整剤としては、通常ウレタン樹脂に
使用される可塑剤や粘度低下剤が用いられる。例えば、
ジオクチルアジぺート、ジイソノニルアジペート、ジオ
クチルフタレートなどの2塩基酸のジアルキルエステ
ル。メチルセロソルブ、エチルセロソルブ、プロピレン
グリコールメチルエーテル、エチルカルビトール、ブチ
ルカルビトールなどのグリコールエーテルのモノアルキ
ルエステル。エチレングリコール、ジエチレングリコー
ル、トリエチレングリコール、プロピレングリコール、
ジプロピレングリコールなどのグリコールのジアルキル
エステル、プロピレンカーボネートなどのアルキレンカ
ーボネート、テトラヒドロフラン、ジオキサンなどの環
状エーテル、γ−ブチルラクトン、ε−カプロラクタム
などの環状エステル、その他パラフィンなどの炭化水素
などが挙げられる。さらに、粘度低下に加え難燃性を付
与するために、トリブチルホスヘートなどのリン酸エス
テル、トリスモノクロロイソプロピルホスヘートなどの
ハロゲン化リン酸エステルなどが用いられる。As the viscosity modifier, a plasticizer or a viscosity reducer usually used for urethane resins is used. For example,
Dialkyl esters of dibasic acids such as dioctyl adipate, diisononyl adipate and dioctyl phthalate. Monoalkyl esters of glycol ethers such as methyl cellosolve, ethyl cellosolve, propylene glycol methyl ether, ethyl carbitol and butyl carbitol. Ethylene glycol, diethylene glycol, triethylene glycol, propylene glycol,
Examples thereof include dialkyl esters of glycols such as dipropylene glycol, alkylene carbonates such as propylene carbonate, cyclic ethers such as tetrahydrofuran and dioxane, cyclic esters such as γ-butyl lactone and ε-caprolactam, and hydrocarbons such as paraffin. Further, in order to impart flame retardancy in addition to viscosity reduction, a phosphoric acid ester such as tributyl phosphate, a halogenated phosphoric acid ester such as tris monochloroisopropyl phosphate, etc. are used.
【0015】上記A液及びB液には、その他必要に応じ
て、着色剤、老化防止剤、界面活性剤などを添加しても
よい。If necessary, a colorant, an antiaging agent, a surfactant, etc. may be added to the solutions A and B.
【0016】A液及びB液それぞれの粘度は、微細な亀
裂に確実に浸透させやすいように200mPa・s/2
5℃以下に調整される。粘度が200mPa・s/25
℃を超えると、注入圧を高めないと薬液を微細な亀裂に
確実に浸透させることができなくなるので、注入圧によ
りコンクリート駆体を傷める恐れが生じるので好ましく
ない。The respective viscosities of the liquids A and B are 200 mPa · s / 2 so as to surely penetrate into fine cracks.
It is adjusted to 5 ° C or lower. Viscosity is 200 mPa · s / 25
If the temperature exceeds ℃, the chemical liquid cannot be surely permeated into the fine cracks unless the injection pressure is increased, so that the concrete pressure may be damaged by the injection pressure, which is not preferable.
【0017】ポリオールを主成分とするA液とイソシア
ネートを主成分とするB液は、両者を混合することによ
り常温で反応が進んでポリウレタンとなる、2液反応型
ポリウレタンである。2液の混合から流動性がなくなる
ゲル化までの硬化時間は、通常10分から2時間程度の
範囲内に調整される。ゲル化が速すぎると微細な亀裂内
に浸透させることが困難になり、ゲル化が遅すぎると空
隙中の水などの影響を受けやすくなるので好ましくな
い。Liquid A containing polyol as a main component and liquid B containing isocyanate as a main component are two-component reactive polyurethanes which react to each other at room temperature to form polyurethane by mixing the two. The curing time from the mixing of the two liquids to the gelation of lack of fluidity is usually adjusted within the range of 10 minutes to 2 hours. If the gelation is too fast, it becomes difficult to permeate into the fine cracks, and if the gelation is too slow, it is likely to be affected by water in the voids, which is not preferable.
【0018】A液、B液の反応硬化物は、硬度(ショア
A)が30〜80の弾性エラストマーである。このよう
に反応硬化物が弾性エラストマーであるために、硬質発
泡ウレタンのように発泡圧でコンクリート駆体に圧力を
かけることがない。そのためコンクリート駆体を傷める
ことはない。ここで、硬度(ショアA)が30未満であ
ると、柔かすぎて水圧などにより変形し、確実な止水効
果が得られない。一方、硬度(ショアA)が80を超え
ると、硬すぎて脆くなるので好ましくない。The reaction cured products of the liquids A and B are elastic elastomers having a hardness (Shore A) of 30 to 80. Since the reaction-cured product is an elastic elastomer in this way, it does not apply pressure to the concrete body with foaming pressure, unlike hard urethane foam. Therefore, it does not damage the concrete structure. Here, if the hardness (Shore A) is less than 30, it is too soft and deforms due to water pressure or the like, so that a reliable waterproofing effect cannot be obtained. On the other hand, if the hardness (Shore A) exceeds 80, it is not preferable because it is too hard and brittle.
【0019】A液とB液の配合比は、通常、重量比で1
/3〜3/1の範囲内に調整することが好ましい。The mixing ratio of the liquid A and the liquid B is usually 1 by weight.
It is preferably adjusted within the range of / 3 to 3/1.
【0020】以上説明した止水用薬液を用いる本発明の
止水工法は、トンネルアーチ部などのコンクリート構造
物を施工する際に注入チューブを埋め込んでおき、打ち
継ぎ部やジャンカ部、ひび割れ部などの水密性の劣る部
位から漏水した場合あるいは漏水するおそれのある場合
に、この注入チューブを通して上記止水用薬液をコンク
リート構造物に注入して止水するものである。In the water-stopping method of the present invention using the above-described water-stopping chemicals, the injection tube is embedded when a concrete structure such as a tunnel arch portion is constructed, and a splice portion, a junker portion, a cracked portion, etc. When water leaks from a part having poor water tightness or there is a risk of water leak, the water blocking chemical is injected into the concrete structure through the injection tube to stop water.
【0021】上記したように本発明の止水用薬液は低粘
度であることから、注入圧を高めなくても薬液をコンク
リート構造物中の微細な亀裂に確実に浸透させることが
できる。注入チューブを介して注入された止水用薬液は
コンクリート構造物中で固結するが、上記のように止水
用薬液の硬化物が非発泡の弾性エラストマーであること
から、固結時に発泡圧がなく、従ってコンクリート構造
物を傷めることなく亀裂などを確実に閉塞して止水性が
発揮される
A液とB液を混合し、注入チューブに注入する方法とし
ては、公知の方法を採用することができる。例えば、A
液とB液を別々のタンクに入れ、注入量、圧力、配合比
などをコントロールしうる比例配合式ポンプを用い、ス
タチックミキサーを通してA液とB液を均一に混合し注
入することができる。あるいはまた、A液とB液を予め
均一に混合したものを、1液ポンプで注入することもで
きる。As described above, since the water-stopping chemical of the present invention has a low viscosity, the chemical can be surely penetrated into fine cracks in the concrete structure without increasing the injection pressure. The water-stopping chemical injected through the injection tube is solidified in the concrete structure, but since the cured product of the water-stopping chemical is a non-foaming elastic elastomer as described above, the foaming pressure during solidification Therefore, it is necessary to adopt a known method as a method of mixing the liquids A and B, which reliably block the cracks without damaging the concrete structure and exert water-stopping property, and inject them into the injection tube. You can For example, A
Liquid A and liquid B can be put in separate tanks, and liquid A and liquid B can be uniformly mixed and injected through a static mixer using a proportional mixing type pump capable of controlling the injection amount, pressure, mixing ratio and the like. Alternatively, it is possible to inject a mixture of the liquid A and the liquid B in advance uniformly with a single liquid pump.
【0022】[0022]
【実施例】以下、実施例により本発明を更に詳細に説明
するが、本発明はこれら実施例により限定されるもので
はない。EXAMPLES The present invention will be described in more detail below with reference to examples, but the present invention is not limited to these examples.
【0023】下記表1に示す配合にて実施例1〜3及び
比較例1,2のA液とB液をそれぞれ調製した。実施例
1〜3が本発明の弾性エラストマー止水用薬液であり、
比較例1及び2が従来の硬質フォーム止水用薬液であ
る。Liquids A and B of Examples 1 to 3 and Comparative Examples 1 and 2 were prepared according to the formulations shown in Table 1 below. Examples 1 to 3 are the elastic elastomer water stop chemicals of the present invention,
Comparative Examples 1 and 2 are conventional rigid foam water-stopping chemicals.
【0024】表中のポリオール、イソシアネート、粘度
調整剤、触媒及びシリコーン整泡剤については以下の通
りである。The polyols, isocyanates, viscosity modifiers, catalysts and silicone foam stabilizers in the table are as follows.
【0025】(ポリオール)
ひまし油D:伊藤製油(株)製品、ひまし油ポリオー
ル。水酸基価=160mgKOH/g
G1000:グリセリンにプロピレンオキシドを付加し
たポリエーテルポリオール。水酸基価=168mgKO
H/g
A480:モノエタノールアミンにプロピレンオキシド
を付加したポリエーテルポリオール。水酸基価=480
mgKOH/g
D400:プロピレングリコールにプロピレンオキシド
を付加したポリエーテルポリオール。水酸基価=280
mgKOH/g
R15HT:出光石油化学(株)製品、ポリブタジエン
ポリオール。水酸基価=106mgKOH/g。(Polyol) Castor oil D: castor oil polyol produced by Ito Oil Co., Ltd. Hydroxyl value = 160 mg KOH / g G1000: Polyether polyol obtained by adding propylene oxide to glycerin. Hydroxyl value = 168mgKO
H / g A480: Polyether polyol obtained by adding propylene oxide to monoethanolamine. Hydroxyl value = 480
mgKOH / g D400: A polyether polyol obtained by adding propylene oxide to propylene glycol. Hydroxyl value = 280
mgKOH / g R15HT: Idemitsu Petrochemical Co., Ltd. product, polybutadiene polyol. Hydroxyl value = 106 mg KOH / g.
【0026】(イソシアネート)コスモネートM50:
三井化学(株)製品、ポリメリックMDI(ポリメチレ
ンポリフェニルポリイソシアネート)
プレポリマー:コスモネートM50を1000gと、ポ
リオールとしてグリセリンにプロピレンオキシドを付加
した水酸基価480mgKOH/gのポリオール27.
5gとプロピレングリコールにプロピレンオキシドを付
加した水酸基価280mgKOH/gのポリオール8
2.5gを混合したポリオールと、を反応させて得られ
る遊離イソシアネート基が25.9%のウレタンプレポ
リマー。(Isocyanate) Cosmonate M50:
Mitsui Chemicals, Inc. product, Polymeric MDI (Polymethylene polyphenyl polyisocyanate) Prepolymer: 1000 g of Cosmonate M50 and polyol of 480 mg KOH / g of hydroxyl value 480 mgKOH / g obtained by adding propylene oxide to glycerin as a polyol.
Polyol 8 having a hydroxyl value of 280 mgKOH / g obtained by adding propylene oxide to 5 g and propylene glycol
A urethane prepolymer having a free isocyanate group of 25.9%, obtained by reacting a polyol mixed with 2.5 g.
【0027】(粘度調整剤) DINA:ジイソノニルアジペート TMCPP:トリスモノクロロイソプロピルホスヘート DBP:ジブチルフタレート。(Viscosity modifier) DINA: diisononyl adipate TMCPP: Tris monochloro isopropyl phosphate DBP: dibutyl phthalate.
【0028】(触媒)TEDA L33:東ソー(株)製
品、トリエチレンジアミン/ジプロピレングリコール=
1/2(重量比)
LDA:ラウリルジメチルアミン。(Catalyst) TEDA L33: product of Tosoh Corporation, triethylenediamine / dipropylene glycol =
1/2 (weight ratio) LDA: lauryl dimethylamine.
【0029】(シリコーン整泡剤)シリコーンSH19
0:トーレシリコーン(株)製品。(Silicone foam stabilizer) Silicone SH19
0: Toray Silicone Co., Ltd. product.
【0030】なお、表1中におけるA液及びB液の粘度
は、JIS K 6833に準じて測定した。The viscosities of solutions A and B in Table 1 were measured according to JIS K6833.
【0031】調製した実施例1〜3及び比較例1,2の
A液とB液を、表1に示す配合割合にて混合して、自由
発泡試験、拘束発泡試験及び止水性試験を行った。各試
験方法は以下の通りである。The prepared solutions A and B of Examples 1 to 3 and Comparative Examples 1 and 2 were mixed at the compounding ratios shown in Table 1, and a free foaming test, a restraining foaming test and a water stopping test were conducted. . Each test method is as follows.
【0032】自由発泡試験:A液及びB液をそれぞれ均
一に混合し、20℃に調整した。次いで、A液とB液を
所定の配合比でスパチュラにより均一に混合した。混合
開始から流動性がなくなるまでの硬化時間をゲルタイム
とした。硬化後の体積を混合開始時の体積で除したもの
を発泡倍率とした。Free foaming test: Solution A and solution B were uniformly mixed and adjusted to 20 ° C. Next, the liquid A and the liquid B were uniformly mixed with a spatula at a predetermined mixing ratio. The gel time was the curing time from the start of mixing until the fluidity disappeared. The volume after curing was divided by the volume at the start of mixing to obtain the expansion ratio.
【0033】拘束発泡試験:A液及びB液をそれぞれ均
一に混合し、20℃に調整した。次いで、A液とB液を
所定の配合比でスパチュラにより均一に混合した。混合
したものを、実施例1〜3の場合は5φ×10cmの金
型に満たし、比較例1及び2の場合は5φ×10cmの
金型の1/2量を注入して、蓋にかかる圧力を測定し、
発泡圧力とした。硬化後、金型から硬化物を取出し、2
0℃で7日間養生した後、ショアA硬度計で硬化物の側
面の硬度を測定した。外観は硬化物を指で押して判断し
た。Constrained foaming test: Solution A and solution B were uniformly mixed and adjusted to 20 ° C. Next, the liquid A and the liquid B were uniformly mixed with a spatula at a predetermined mixing ratio. In the case of Examples 1 to 3, the mixture was filled in a mold of 5φ × 10 cm, and in the case of Comparative Examples 1 and 2, ½ amount of the mold of 5φ × 10 cm was injected, and the pressure applied to the lid. Is measured
The foaming pressure was used. After curing, remove the cured product from the mold, 2
After curing for 7 days at 0 ° C., the hardness of the side surface of the cured product was measured with a Shore A hardness meter. The appearance was judged by pushing the cured product with a finger.
【0034】止水性試験:拘束発泡試験の要領で、15
(縦)×15(横)×1(厚み)cmの金型を用い、そ
れぞれ硬化物を作成した。JIS A 6909の透水試
験B法に従って、透水性を測定し、止水性があるかどう
か判断した。Water stop test: 15 as in the constrained foaming test.
Using a mold of (length) × 15 (width) × 1 (thickness) cm, a cured product was prepared. According to JIS A 6909 water permeability test B method, water permeability was measured and it was judged whether or not there was water stopping property.
【0035】[0035]
【表1】 [Table 1]
【0036】[0036]
【発明の効果】以上のように、本発明の止水用薬液であ
ると、低粘度であり、且つ、反応硬化物が弾性エラスト
マーであることから、薬液を微細な亀裂に確実に浸透さ
せることができ、また、発泡圧がないためコンクリート
駆体を傷めることもない。As described above, the water-stopping chemical solution of the present invention has a low viscosity, and since the reaction-cured product is an elastic elastomer, the chemical solution can surely penetrate into fine cracks. Moreover, since there is no foaming pressure, the concrete body is not damaged.
Claims (3)
アネートを主成分とするB液とからなる2液反応型ポリ
ウレタンの止水用薬液であって、A液及びB液の粘度が
それぞれ200mPa・s/25℃以下であり、A液と
B液の反応硬化物の硬度(ショアA)が30〜80の弾
性エラストマーであることを特徴とする止水用薬液。1. A water-stopping chemical for a two-component reactive polyurethane comprising a liquid A containing a polyol as a main component and a liquid B containing an isocyanate as a main component, wherein the viscosities of the liquids A and B are each 200 mPa. A water-stopping chemical liquid which is s / 25 ° C. or lower and is an elastic elastomer having a hardness (Shore A) of a reaction cured product of liquid A and liquid B of 30 to 80.
の時間が10分以上である請求項1記載の止水用薬液。2. The water-stopping chemical liquid according to claim 1, wherein the time from the mixing of the liquids A and B until hardening is 10 minutes or more.
埋め込み、漏水した場合あるいは漏水するおそれのある
場合に該注入チューブを介して請求項1又は2記載の止
水用薬液を前記コンクリート構造物に注入して止水する
ことを特徴とする止水工法。3. A water blocking chemical according to claim 1 or 2 is injected into the concrete structure through an injection tube when the water is leaked or there is a risk of water leakage when the injection tube is embedded in the concrete structure in advance. The water-stopping method is characterized by stopping the water.
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2009161577A (en) * | 2007-12-28 | 2009-07-23 | Toho Chem Ind Co Ltd | One-component water shutoff material |
JP2009218117A (en) * | 2008-03-11 | 2009-09-24 | Idemitsu Kosan Co Ltd | Organic electroluminescent panel |
JP2010024681A (en) * | 2008-07-17 | 2010-02-04 | Nichiyu Giken Kogyo Co Ltd | Waterproof structure of tunnel and its construction method |
WO2012134878A3 (en) * | 2011-03-25 | 2013-01-10 | Bayer Materialscience Llc | Polyurethane composites produced by a vacuum infusion process |
JP2014020178A (en) * | 2012-07-23 | 2014-02-03 | Ohbayashi Corp | Cut-off structure and cut-off method for cutting off contact surface, and cut-off material used for cut-off structure |
-
2002
- 2002-02-01 JP JP2002026157A patent/JP2003226861A/en active Pending
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2009161577A (en) * | 2007-12-28 | 2009-07-23 | Toho Chem Ind Co Ltd | One-component water shutoff material |
JP2009218117A (en) * | 2008-03-11 | 2009-09-24 | Idemitsu Kosan Co Ltd | Organic electroluminescent panel |
JP2010024681A (en) * | 2008-07-17 | 2010-02-04 | Nichiyu Giken Kogyo Co Ltd | Waterproof structure of tunnel and its construction method |
WO2012134878A3 (en) * | 2011-03-25 | 2013-01-10 | Bayer Materialscience Llc | Polyurethane composites produced by a vacuum infusion process |
RU2598608C2 (en) * | 2011-03-25 | 2016-09-27 | Байер МатириальСайенс ЛЛСИ | Polyurethane composites produced by vacuum infusion process |
US9580598B2 (en) | 2011-03-25 | 2017-02-28 | Covestro Llc | Polyurethane composites produced by a vacuum infusion process |
RU2598608C9 (en) * | 2011-03-25 | 2017-05-10 | Байер МатириальСайенс ЛЛСИ | Polyurethane composites produced by vacuum infusion process |
JP2014020178A (en) * | 2012-07-23 | 2014-02-03 | Ohbayashi Corp | Cut-off structure and cut-off method for cutting off contact surface, and cut-off material used for cut-off structure |
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