JPH11256159A - Grouting material and grouting using the same - Google Patents

Grouting material and grouting using the same

Info

Publication number
JPH11256159A
JPH11256159A JP6529398A JP6529398A JPH11256159A JP H11256159 A JPH11256159 A JP H11256159A JP 6529398 A JP6529398 A JP 6529398A JP 6529398 A JP6529398 A JP 6529398A JP H11256159 A JPH11256159 A JP H11256159A
Authority
JP
Japan
Prior art keywords
calcium silicate
agent
silicate
aqueous solution
ground
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
Application number
JP6529398A
Other languages
Japanese (ja)
Inventor
Yasukiyo Nakazato
保清 中里
Takahiko Okada
能彦 岡田
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Taiheiyo Cement Corp
Onoda Co Ltd
Original Assignee
Taiheiyo Cement Corp
Onoda Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Taiheiyo Cement Corp, Onoda Co Ltd filed Critical Taiheiyo Cement Corp
Priority to JP6529398A priority Critical patent/JPH11256159A/en
Publication of JPH11256159A publication Critical patent/JPH11256159A/en
Pending legal-status Critical Current

Links

Classifications

    • 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
    • C04B28/24Compositions 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 alkyl, ammonium or metal silicates; containing silica sols
    • C04B28/26Silicates of the alkali metals
    • 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
    • C04B2111/00474Uses not provided for elsewhere in C04B2111/00
    • C04B2111/00732Uses not provided for elsewhere in C04B2111/00 for soil stabilisation
    • 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
    • C04B2111/70Grouts, e.g. injection mixtures for cables for prestressed concrete

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)
  • Consolidation Of Soil By Introduction Of Solidifying Substances Into Soil (AREA)
  • Curing Cements, Concrete, And Artificial Stone (AREA)
  • Soil Conditioners And Soil-Stabilizing Materials (AREA)

Abstract

PROBLEM TO BE SOLVED: To obtain a grouting material excellent in permeability, capable of being grouted into fine gaps and readily controlling the gelation time and useful for reinforcing the ground or stopping water by using an alkali silicate (an aqueous solution) and a specific calcium silicate (a slurry) in combination. SOLUTION: This grouting material is obtained by using (A) an alkali silicate (an aqueous solution) [e.g. sodium silicate in the form of an aqueous solution, a colloid or an aqueous dispersion at respective concentrations of 10-70 wt.% SiO2 and 0.2-35 wt.% Na2 O] and (B) a calcium silicate having <=2 μm average particle diameter without any hydrating activity at normal temperatures under atmospheric pressure or a slurry containing the calcium silicate (e.g. wollastonite or a baked material of calcium silicate hydrate having <=1.0 molar ratio of Ca/Si) in combination. The grouting material is used by, as necessary, adding water to the components A and B, mixing the components A with B and grouting the resultant material into the ground.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明が属する技術分野】本発明は、浸透性に優れ、か
つゲル化時間の制御が容易な注入材料、及びこれを用い
た注入工法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an injection material having excellent permeability and easily controlling the gelation time, and an injection method using the same.

【0002】[0002]

【従来の技術】橋脚、トンネル、ダム、ビル等の構造物
の建設においてその地盤が軟弱であったり、地下水の湧
出がある場合、また地震時に噴泥がある場合など、地盤
の強化や止水が必要になるが、このような目的には地盤
注入材が使用されている。
2. Description of the Related Art In the construction of piers, tunnels, dams, buildings, and other structures, when the ground is soft, when there is groundwater seepage, or when there is mud during an earthquake, the ground is strengthened or water is stopped. However, a ground injection material is used for such a purpose.

【0003】注入材料としては、従来、水ガラス−セメ
ントスラリー系が主として用いられてきているが、この
系の材料は、注入後の地盤の強度は十分である反面、粒
子が大きいため、微細な間隙を持った地盤には注入でき
ないという欠点があった。また、この系では、ゲル化時
間を任意にコントロールすることは困難であった。
Conventionally, a water glass-cement slurry system has been mainly used as an injecting material. The material of this system has sufficient strength of the ground after the injection, but has a fine particle due to large particles. There is a drawback that it cannot be injected into the ground with a gap. In this system, it was difficult to arbitrarily control the gel time.

【0004】[0004]

【発明が解決しようとする課題】そこで、本発明は、浸
透性に優れ微細な間隙への注入にも好適に使用でき、か
つゲル化時間の制御が容易な注入材料を提供することを
目的とする。
SUMMARY OF THE INVENTION Accordingly, an object of the present invention is to provide an injection material which has excellent permeability and can be suitably used for injection into fine gaps, and which can easily control the gel time. I do.

【0005】[0005]

【課題を解決するための手段】かかる実情において、本
発明者らは、上記要求を満たす凝固系を開発すべく、微
細な間隙を持った地盤への注入が可能となる平均粒径2
μm以下のものが容易に得られ、かつ常温常圧での水和
が可能な材料を種々探索した。しかし、適度な水和活性
を有するもの、例えば合成ケイ酸カルシウム水和物等で
は、その粒子の平均粒径が数μm〜数十μmと非常に大
きく、浸透性に優れたものとはなり得ないものであっ
た。
Under such circumstances, the present inventors have developed an average particle size of 2 which can be injected into the ground having fine gaps in order to develop a solidification system satisfying the above requirements.
We have searched for various materials that can be easily obtained with a thickness of less than μm and that can be hydrated at normal temperature and pressure. However, those having an appropriate hydration activity, such as synthetic calcium silicate hydrate, have an extremely large average particle size of several μm to several tens of μm, and may have excellent permeability. There was nothing.

【0006】ここにおいて、ウォラストナイトに代表さ
れるケイ酸カルシウム無水和物は、常温常圧では水和活
性がなく、従って注入材料としては使用できないとされ
ていた材料であるが、本発明者らは、このものはアルカ
リ金属イオンの存在により刺激され、その水和活性が向
上することを見出した。そして更に本発明者らは、この
ケイ酸カルシウム無水和物は、合成ケイ酸カルシウム水
和物等と比較して微細な粒径のものを得やすく、しかも
微細であるほどアルカリ金属イオンにより水和活性が向
上し、常温常圧においても合成ケイ酸カルシウム水和物
と同等の硬化特性を示すに至ることを見出し、本発明を
完成するに至った。
[0006] Here, calcium silicate anhydrate represented by wollastonite has no hydration activity at normal temperature and normal pressure, and is therefore a material which cannot be used as an injection material. Have found that this is stimulated by the presence of an alkali metal ion, and its hydration activity is improved. Further, the present inventors have found that this calcium silicate anhydrate can be easily obtained in a fine particle size as compared with synthetic calcium silicate hydrate and the like. It has been found that the activity is improved, and even at normal temperature and normal pressure, the same hardening characteristics as those of the synthetic calcium silicate hydrate are exhibited, and the present invention has been completed.

【0007】すなわち、本発明は、ケイ酸アルカリ又は
その水溶液(A剤)、及び平均粒径が2μm以下で常温
常圧において水和活性のないケイ酸カルシウム又はこれ
を含有するスラリー(B剤)からなる注入材料、並びに
当該注入材料のA剤とB剤を、必要により水を加え、混
合して地盤中に注入することを特徴とする注入工法を提
供するものである。
That is, the present invention provides an alkali silicate or an aqueous solution thereof (agent A), a calcium silicate having an average particle diameter of 2 μm or less and having no hydration activity at normal temperature and pressure, or a slurry containing the same (agent B) And a method of injecting into the ground by adding water if necessary, mixing and injecting the injecting material consisting of

【0008】[0008]

【発明の実施の形態】本発明に用いられるA剤における
ケイ酸アルカリとしては、ケイ酸ナトリウム及びケイ酸
カリウムが挙げられ、特にケイ酸ナトリウムが好まし
い。また、ケイ酸アルカリの水溶液としては、そのSiO2
濃度が10〜70重量%、Na2O濃度が0.2〜35重量%である
ものが好ましい。なお、ここでいうケイ酸アルカリ水溶
液には、水ガラスのように完全な溶液状態のもののほ
か、シリカゾル、コロイダルシリカ等、更にはシリカの
微粉末を水酸化ナトリウム水溶液に分散させて得られた
ものなど、コロイド状ないし分散液状のものも含まれる
ものとし、この場合、上記濃度は固形分を含めた数値で
ある。
BEST MODE FOR CARRYING OUT THE INVENTION Examples of the alkali silicate in Agent A used in the present invention include sodium silicate and potassium silicate, with sodium silicate being particularly preferred. In addition, as an aqueous solution of alkali silicate, SiO 2
Concentration of 10 to 70 wt%, Na 2 O concentration of those is preferably 0.2 to 35 wt%. The aqueous solution of alkali silicate referred to here may be obtained by dispersing a fine powder of silica, such as silica sol, colloidal silica, or the like, in addition to a completely solution state such as water glass, in an aqueous solution of sodium hydroxide. In this case, the concentration is a numerical value including the solid content in this case.

【0009】なお、シリカの微粉末を水酸化ナトリウム
水溶液に分散させて得られたものは、上記のNa2O濃度の
範囲であれば、シリカ微粉末の表面がアルカリで溶出す
ることにより活性が高められるため、水ガラスと同等の
特性を有している。しかし、反応性をより高めるために
は、溶液状又はコロイド状のものが好ましく、その濃度
は、注入材料に求められる粘性、ゲル化に要する時間、
ゲル化後の強度等に応じて適宜調節することができる。
[0009] The silica powder obtained by dispersing the silica fine powder in an aqueous sodium hydroxide solution has an activity within a range of the above-mentioned Na 2 O concentration due to elution of the surface of the silica fine powder with alkali. Because it is enhanced, it has the same properties as water glass. However, in order to further enhance the reactivity, a solution or a colloid is preferable, and the concentration is determined by the viscosity required for the injection material, the time required for gelation,
It can be appropriately adjusted according to the strength after gelation and the like.

【0010】また、本発明で用いられるB剤におけるケ
イ酸カルシウムとしては、常温常圧において水和活性の
ないものであればいずれのものであってもよく、例えば
合成又は天然のウォラストナイト、Ca/Siのモル比が1.
0以下のケイ酸カルシウム水和物の焼成物等が挙げられ
る。C3S、C2S、セメント等のCa/Siが1.0より高く、水
和活性が高いケイ酸カルシウムは、カルシウムの溶出に
よってA剤のケイ酸アルカリとの反応が急激に進行する
ため、硬化時間が極端に短く、地盤への浸透性、作業性
に欠け、好ましくない。
The calcium silicate in the agent B used in the present invention may be any one having no hydration activity at normal temperature and normal pressure, such as synthetic or natural wollastonite, Ca / Si molar ratio is 1.
Examples include calcined products of calcium silicate hydrate of 0 or less. Calcium silicate with high Ca / Si such as C3S, C2S, cement, etc. having a high hydration activity of 1.0 is used because the reaction with the alkali silicate of the A agent progresses rapidly due to the dissolution of calcium. It is short and lacks ground permeability and workability, which is not preferable.

【0011】また、ケイ酸カルシウムの平均粒径は2μ
m以下である必要があり、0.2〜2μmであるのが好ま
しい。ケイ酸カルシウムの平均粒径が2μmを超える
と、微細な間隙への浸透性に劣り、好ましくない。ケイ
酸カルシウム含有スラリーの濃度は、ケイ酸カルシウム
が5〜50重量%(残部は水)、特に5〜35重量%が好ま
しい。ケイ酸カルシウム濃度が50重量%を超えると、ス
ラリーの粘性が高くなり、浸透性が低下する。また、ケ
イ酸カルシウム濃度が5重量%未満では、分散性が低下
するとともに、良好な強度発現が得られない。
The average particle size of calcium silicate is 2 μm.
m, and preferably 0.2 to 2 μm. If the average particle size of calcium silicate exceeds 2 μm, the permeability to fine gaps is poor, which is not preferable. The concentration of the calcium silicate-containing slurry is preferably 5 to 50% by weight of calcium silicate (the remainder being water), and particularly preferably 5 to 35% by weight. If the calcium silicate concentration exceeds 50% by weight, the viscosity of the slurry increases, and the permeability decreases. On the other hand, if the calcium silicate concentration is less than 5% by weight, the dispersibility is reduced and good strength cannot be obtained.

【0012】本発明の注入材料の製造時の固体・液体の
混練時間は、ケイ酸カルシウム原料の種類や粒度に応じ
て適宜調整することが望ましい。また、混練時に、前記
各原料のほか、必要に応じ、例えば分散剤、ゲルタイム
調整剤等の地盤注入材作製用に一般に使用されている公
知の混和剤の類を添加することもできる。
[0012] The kneading time of the solid / liquid at the time of manufacturing the injection material of the present invention is desirably adjusted as appropriate according to the type and particle size of the calcium silicate raw material. In addition, at the time of kneading, in addition to the above-mentioned raw materials, if necessary, known admixtures generally used for preparing a ground injection material such as a dispersant and a gel time adjuster can be added.

【0013】本発明の注入材料は、A剤とB剤を、必要
により水を加え、混合して地盤中に注入することにより
使用される。すなわち、A剤及びB剤が粉体又は高濃度
の場合には、水を加えて所期の濃度の溶液、分散液、ス
ラリーとした上で両者を混合し、地盤中に注入する。こ
こで、A剤及びB剤中にあらかじめ含まれている水分量
を含めて必要となる水の全量は、良好な浸透性と強度発
現性を確保するためには、A剤及びB剤中の固形分相当
量100重量部に対し、200〜1000重量部が好ましい。この
水分は、A剤の水溶液やB剤のスラリーの水分として用
い、あらかじめ液剤として調製しておいてもよいが、A
剤及びB剤を粉体とし、又は高濃度のものとしておき、
上記のように使用に際して水を追加してもよい。また、
A剤のケイ酸アルカリ水溶液と、B剤のケイ酸カルシウ
ム含有スラリーとの混合比は、ケイ酸アルカリ溶液中の
ケイ酸分の濃度、ケイ酸アルカリ溶液のpH、注入材料に
求められる粘性、ゲル化に要する時間及びゲル化後の強
度に応じて適宜調節することができる。
The injection material of the present invention is used by mixing the agent A and the agent B with water, if necessary, mixing and injecting the mixture into the ground. That is, when the agent A and the agent B are in a powder or high concentration, water is added to obtain a solution, dispersion, or slurry having a desired concentration, and both are mixed and injected into the ground. Here, the total amount of water required, including the amount of water previously contained in the A agent and the B agent, is required to ensure good permeability and strength development. The amount is preferably 200 to 1000 parts by weight based on 100 parts by weight of the solid equivalent. This water may be used as an aqueous solution of the agent A or water of a slurry of the agent B, and may be prepared in advance as a liquid agent.
Agent and B agent as powder or high concentration,
Water may be added during use as described above. Also,
The mixing ratio of the alkali silicate aqueous solution of the agent A and the calcium silicate-containing slurry of the agent B is determined by the concentration of the silicic acid component in the alkali silicate solution, the pH of the alkali silicate solution, the viscosity required for the injection material, and the gel. It can be appropriately adjusted according to the time required for the gelation and the strength after gelation.

【0014】本発明の注入材料を地盤中に注入する具体
的工法としては、注入材料のゲル化時間に応じて適宜2
ショット、1.5ショット及び1ショットのいずれかの工
法を選択して用いることができる。すなわち、注入材料
のゲル化時間が短い場合には、A液とB液を注入管の先
端部で混合して注入(2ショット)し、ゲル化時間がや
や長い場合には、A液とB液を注入管の中で混合して注
入(1.5ショット)し、ゲル化時間が十分に長い場合に
は、A液とB液をミキサー内又は注入ポンプ内で混合し
て注入(1ショット)することができる。
As a concrete method of injecting the injection material of the present invention into the ground, two methods are appropriately selected according to the gelation time of the injection material.
Any one of the shot, 1.5 shot, and 1 shot method can be selected and used. That is, when the gelation time of the injection material is short, the liquid A and the liquid B are mixed at the tip of the injection tube and injected (two shots). When the gelation time is slightly long, the liquid A and the liquid B are mixed. The liquids are mixed and injected (1.5 shots) in an injection tube. If the gelation time is sufficiently long, the liquids A and B are mixed and injected in a mixer or an injection pump (one shot). be able to.

【0015】[0015]

【作用】従来の懸濁型注入材では、その粒子の平均粒径
は数μm〜数十μmと非常に大きく、浸透性に限界があっ
たが、これは、粒子の水和活性が高いために粒子が凝集
していることによるものと考えられる。すなわち、本発
明では、B剤として常温常圧において水和活性のないケ
イ酸カルシウムを用いることにより、サブミクロンまで
微粒子化が可能となり、微細な間隙を持った地盤にも注
入できる優れた浸透性が得られる。また、A剤のケイ酸
アルカリの水溶液と混合することにより、ケイ酸カルシ
ウム微粒子の表面がアルカリで刺激されケイ酸イオンが
溶出するため、ケイ酸カルシウムの水和活性が高くな
り、常温常圧においてもゲル化が可能となる。従って、
B剤におけるケイ酸カルシウムの粒度、濃度、あるいは
混合するA剤におけるケイ酸アルカリの混合比、濃度に
よってケイ酸カルシウムの溶出量が異なるため、これら
を調整することによりゲル化時間の制御が可能である。
With the conventional suspension-type injection material, the average particle size of the particles is as large as several μm to several tens μm, and there is a limit to the permeability. However, this is because the hydration activity of the particles is high. It is considered that the particles are agglomerated. That is, in the present invention, by using calcium silicate having no hydration activity at normal temperature and normal pressure as the agent B, fine particles down to submicron can be obtained, and excellent permeability that can be injected into the ground having fine gaps Is obtained. In addition, by mixing with the aqueous solution of the alkali silicate of the agent A, the surface of the calcium silicate fine particles is stimulated by the alkali and silicate ions are eluted, so that the hydration activity of the calcium silicate increases, and at normal temperature and normal pressure, Can also be gelled. Therefore,
The amount of calcium silicate eluted varies depending on the particle size and concentration of calcium silicate in agent B, or the mixing ratio and concentration of alkali silicate in agent A to be mixed. Therefore, the gelation time can be controlled by adjusting these. is there.

【0016】[0016]

【実施例】以下、実施例を挙げて本発明を更に詳細に説
明するが、本発明はこれらに限定されるものではない。
EXAMPLES The present invention will be described in more detail with reference to the following Examples, but it should not be construed that the invention is limited thereto.

【0017】なお、以下の実施例において、注入材料の
ゲル化時間、圧縮強度、及び浸透量の測定は、以下のよ
うにして行った。
In the following examples, the gelation time, compressive strength, and permeation amount of the injection material were measured as follows.

【0018】〈ゲル化時間の測定〉所定量のA液及びB
液をそれぞれカップに計量し、その内容物を交互に移す
「カップ倒立法」により、混合物の自己流動性が無くな
った時間をゲル化時間とした。
<Measurement of gelation time> A predetermined amount of solution A and B
The liquid was weighed into cups, and the contents were alternately transferred. The time when the self-fluidity of the mixture was lost by the "cup inversion method" was defined as the gelation time.

【0019】〈一軸圧縮強度の測定〉所定量のA液及び
B液を混合し、ゲル化時間以内に直径50mm×高さ100mm
の型枠に流し込み成形して得られた硬化体を20℃、水中
で所定日数養生したものを土質試験法(JSF T 511-199
0:土の一軸圧縮強度試験方法)に基づいて圧縮強度試
験を行った。
<Measurement of Uniaxial Compressive Strength> A predetermined amount of Solution A and Solution B are mixed, and within 50 minutes of gelation time, diameter 50 mm × height 100 mm
The cured product obtained by casting in a mold of No. 1 was cured in water at 20 ° C. for a predetermined number of days, and then subjected to a soil test method (JSF T 511-199).
0: soil uniaxial compressive strength test method).

【0020】〈浸透性の評価〉豊浦標準砂を直径50mm×
高さ500mmのモールドに間隙率が40%となるように充填
し、透水係数を2.0±0.1×10-2cm/秒としたものを用
い、豊浦標準砂をあらかじめ水で飽和させた。ここに注
入材料を1kgf/cm2の圧力で注入し、豊浦標準砂の間隙
が閉塞現象(毎分50ml以下の注入量)を生じるまでに、
注入口と異なる他端から排出した体積を浸透量とした。
<Evaluation of permeability> Toyoura standard sand was 50 mm in diameter.
A mold having a height of 500 mm was filled so as to have a porosity of 40%, and a Toura standard sand was previously saturated with water using a mold having a water permeability of 2.0 ± 0.1 × 10 -2 cm / sec. The injection material is injected here at a pressure of 1 kgf / cm 2 , and until the gap in the Toyoura standard sand causes a clogging phenomenon (injection rate of 50 ml or less per minute)
The volume discharged from the other end different from the inlet was defined as the permeation amount.

【0021】実施例1〜5及び比較例1〜2 A液として、シリカゾル(カタロイドSi-30,触媒化成
工業社製,SiO2=28重量%,Na2O=0.4重量%)又は3
号水ガラス(SiO2=35重量%,Na2O=10重量%)を用
い、B液として、天然のウォラストナイトを水/ウォラ
ストナイト重量比=10で湿式粉砕し、所定の平均粒径と
したウォラストナイトスラリー又はCa/Si=1.0に水熱
合成したCSHスラリー(水/合成CSH重量比=10)を用
い、A液/B液体積比=1となるよう混合した。この場
合のゲル化時間、地盤への浸透性及び硬化体のホモゲル
一軸圧縮強度を前記方法に従い測定した結果を表1に示
す。
Examples 1 to 5 and Comparative Examples 1 and 2 As solution A, silica sol (cataloid Si-30, manufactured by Catalyst Chemicals, Inc., SiO 2 = 28% by weight, Na 2 O = 0.4% by weight) or 3
No. 2 water glass (SiO 2 = 35% by weight, Na 2 O = 10% by weight), and as a liquid B, natural wollastonite is wet-pulverized at a water / wollastonite weight ratio of 10 to obtain a predetermined average particle size. Using a wollastonite slurry having a diameter or a CSH slurry hydrothermally synthesized to Ca / Si = 1.0 (water / synthetic CSH weight ratio = 10), mixing was performed so that the A liquid / B liquid volume ratio = 1. Table 1 shows the results obtained by measuring the gel time, the permeability into the ground, and the homogel uniaxial compressive strength of the cured product in this case according to the above method.

【0022】[0022]

【表1】 [Table 1]

【0023】表1より、ケイ酸カルシウム微粒子の平均
粒径を2μm以下とすることが、良好な浸透性を保つ上
で重要であることが明らかとなった。また、ゲル化時間
は、瞬結から十数分の範囲で制御可能である。
Table 1 shows that it is important to keep the average particle size of the calcium silicate fine particles at 2 μm or less in order to maintain good permeability. Further, the gel time can be controlled within a range of ten minutes or more from the instantaneous setting.

【0024】実施例6〜10及び比較例3〜4 A液として、シリカゾル(カタロイドSi-30,触媒化成
工業社製,SiO2=28重量%,Na2O=0.4重量%)又は3
号水ガラス(SiO2=35重量%,Na2O=10重量%)を用
い、B液として、Ca/Si=0.8に合成したCSHを1000℃で
焼成したもの(焼成CSH)を水/焼成CSH重量比=10で湿
式粉砕し、所定の平均粒径とした焼成CSH含有スラリー
及びCa/Si=0.8に水熱合成したCSHスラリー(水/合成
CSH重量比=10)を用い、A液/B液体積比=1となる
よう混合した。この場合のゲル化時間及び硬化体のホモ
ゲル一軸圧縮強度を前記方法に従い測定した結果を表2
に示す。
Examples 6 to 10 and Comparative Examples 3 to 4 As solution A, silica sol (cataloid Si-30, manufactured by Catalyst Chemicals, Inc., SiO 2 = 28% by weight, Na 2 O = 0.4% by weight) or 3
No. 2 water glass (SiO 2 = 35% by weight, Na 2 O = 10% by weight) was used, and as a B solution, CSH synthesized to Ca / Si = 0.8 was baked at 1000 ° C (fired CSH) with water / firing. A slurry containing calcined CSH having a predetermined average particle size by wet grinding with a CSH weight ratio of 10 and a CSH slurry (water / synthesis) hydrothermally synthesized to Ca / Si = 0.8
Using a CSH weight ratio = 10), mixing was performed so that the A liquid / B liquid volume ratio = 1. Table 2 shows the results obtained by measuring the gel time and the homogel uniaxial compressive strength of the cured product according to the above method.
Shown in

【0025】[0025]

【表2】 [Table 2]

【0026】[0026]

【発明の効果】本発明によれば、微細な間隙を持った地
盤にも注入できる優れた浸透性を有し、しかもゲル化時
間を容易にコントロール可能な注入材料、及びこれを用
いた注入工法が提供される。
According to the present invention, an injection material having an excellent permeability that can be injected into the ground having fine gaps and capable of easily controlling the gelation time, and an injection method using the same. Is provided.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 FI C09K 103:00 ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 6 Identification code FI C09K 103: 00

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】 ケイ酸アルカリ又はその水溶液(A
剤)、及び平均粒径が2μm以下で常温常圧において水
和活性のないケイ酸カルシウム又はこれを含有するスラ
リー(B剤)からなる注入材料。
An alkali silicate or an aqueous solution thereof (A)
An injection material comprising calcium silicate having an average particle size of 2 μm or less and having no hydration activity at normal temperature and normal pressure, or a slurry containing the same (agent B).
【請求項2】 A剤が、SiO2濃度が10〜70重量%、Na2O
濃度が0.2〜35重量%であるケイ酸アルカリの水溶液で
ある請求項1記載の注入材料。
2. The agent A has an SiO 2 concentration of 10 to 70% by weight, Na 2 O
The injection material according to claim 1, which is an aqueous solution of an alkali silicate having a concentration of 0.2 to 35% by weight.
【請求項3】 B剤が、ウォラストナイト及びCa/Siの
モル比が1.0以下のケイ酸カルシウム水和物の焼成物か
ら選ばれる1種もしくは2種以上、又はこれを含有する
スラリーである請求項1又は2記載の注入材料。
3. The agent B is one or more selected from calcined products of wollastonite and calcium silicate hydrate having a Ca / Si molar ratio of 1.0 or less, or a slurry containing the same. The injection material according to claim 1 or 2.
【請求項4】 請求項1〜3のいずれかに記載の注入材
料のA剤とB剤を、必要により水を加え、混合して地盤
中に注入することを特徴とする注入工法。
4. An injection method, wherein the A agent and the B agent of the injection material according to any one of claims 1 to 3 are added to water if necessary, mixed, and injected into the ground.
JP6529398A 1998-03-16 1998-03-16 Grouting material and grouting using the same Pending JPH11256159A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6529398A JPH11256159A (en) 1998-03-16 1998-03-16 Grouting material and grouting using the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6529398A JPH11256159A (en) 1998-03-16 1998-03-16 Grouting material and grouting using the same

Publications (1)

Publication Number Publication Date
JPH11256159A true JPH11256159A (en) 1999-09-21

Family

ID=13282748

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6529398A Pending JPH11256159A (en) 1998-03-16 1998-03-16 Grouting material and grouting using the same

Country Status (1)

Country Link
JP (1) JPH11256159A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006138171A (en) * 2004-11-15 2006-06-01 Soma Takafumi Service life extension method and repair method with reforming material

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006138171A (en) * 2004-11-15 2006-06-01 Soma Takafumi Service life extension method and repair method with reforming material

Similar Documents

Publication Publication Date Title
JPH07166163A (en) Chemical agent solution for injection into ground
JP2505295B2 (en) Injection products for watertightening and / or compacting soil and construction materials and their use
JPH10168452A (en) Water glass based suspension grout and method for grouting and solidifying ground by using it
JPH11256159A (en) Grouting material and grouting using the same
JPS6118593B2 (en)
JPH1161125A (en) Grouting material
JP2549949B2 (en) Ground improvement agent
JP3435122B2 (en) Plastic injection material
JP3186829B2 (en) Materials for civil engineering
JP3396789B2 (en) Ground injection material
JP2001098271A (en) Ground solidification material
JP2884395B2 (en) Ground consolidated material
JP3483903B2 (en) Injection material
JP3166960B2 (en) Ground injection method
JPH11157895A (en) Irritant for retarding soil stabilizer and retarding stabilizer containing the same
JP2808252B2 (en) Ground consolidated material
JPH0554520B2 (en)
JP2568221B2 (en) Method for forming cement suspension composition
KR102619095B1 (en) Eco-friendly Grout revealing early high-strength
JP2003013062A (en) Slope surface anchor-setting material and method for producing the same
JPH09165576A (en) Slag-based high-strength grouting agent
JP2004204102A (en) Packing material for cavity and packing construction method using the same
JPS62172088A (en) Ground grouting process
JPH1161123A (en) Material for civil engineering and its application
JP2000109834A (en) Chemical liquid to be injected in soil